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Our Hereditary Panels analyze the most frequent syndromes that present predisposition to cancer, which may lead to the development of tumors such as: breast and ovarian, colorectal, prostate, as well as genes that are associated with an increased susceptibility to the development of neoplasia. .

Get to know IntelligeneCG's Hereditary Cancer Panels below:

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Our 30 genes panel analyze genes associated with the following syndromes:

Breast and Ovarian Cancer (19 genes) - ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM**, MLH1, MSH2, MSH6, NBN, PALB2, PMS2***, PTEN, RAD51C, RAD51D, STK11 and TP53.

Colorectal Cancer (17 genes) - APC, BMPR1A, CDH1, CHEK2, EPCAM**, GREM1**, MLH1, MSH2, MSH6, MUTYH, PMS2***, POLD1**, POLE**, PTEN, SMAD4, STK11 and TP53.

Melanoma Cancer (7 genes) - BAP1, BRCA2, CDKN2A, CDK4**, MITF**, PTEN and TP53.

Pancreatic Cancer (10  genes) - APC, ATM, BRCA1, BRCA2, CDK4**, CDKN2A, MLH1, MSH2, PALB2 and TP53.

Prostate Cancer (2 genes) - BRCA2 and CHEK2.

Stomach Cancer (11 genes) - APC, BMPR1A, CDH1, EPCAM**, MLH1, MSH2, MSH6, MUTYH, PMS2***, SMAD4, and  TP53.

Uterine/Endometrial Cancer (6 genes) - (EPCAM**, MLH1, MSH2, MSH6, PMS2*** and PTEN).

The following 30 genes are analyzed: APC, ATM, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDKN2A, CDK4**, CHEK2, EPCAM**, GREM1**, MITF**, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, POLD1**, POLE**, PMS2***, PTEN, RAD51C, RAD51D, SMAD4, STK11 and TP53.

** Only positions known to impact cancer risk analyzed. CDK4: only chr12:g.58145429-58145431 (codon 24) analyzed, EPCAM: only large deletions and duplications including 3’ end of the gene analyzed, GREM1: only duplications in the upstream regulatory region analyzed, MITF: only chr3:g.70014091 (including c.952G>A) analyzed, POLD1: only chr19:g.50909713 (including c.1433G>A) analyzed, POLE: only chr12:g.133250250 (including c.1270C>G) analyzed.

*** PMS2: Exons 12-15 not analyzed.

Approximately 5% of renal (kidney) cancers are hereditary. Several syndromes are associated with an increased risk of renal cancers including: von Hippel-Lindau disease (mutations in VHL gene), Hereditary papillary renal cell carcinoma (mutations in MET gene), Hereditary leiomyoma-renal cell carcinoma (mutations in FH gene), Birt-Hogg-Dube (BHD) syndrome (mutations in FLCN gene) and Familial renal cancer (mutations in SDHB and/or SDHD).


Bladder cancer accounts for about 5% of all new cancers in the US. It is the fourth most common cancer in men, but it is less common in women. People who have family members with bladder cancer have a higher risk of getting it themselves. Some of these cases may be due to inheriting a gene syndrome that increases their risk for bladder cancer. For example:
• RB1 gene mutations can cause cancer of the eye in infants, but also increases the risk of bladder cancer.
• Lynch syndrome, also known as hereditary non-polyposis colorectal cancer (HNPCC), is mainly linked to colon and endometrial cancers, but people with this syndrome may also have an increased risk of bladder and ureter cancers.
• Cowden disease is caused by mutations in the PTEN gene. It is primarily linked to breast and thyroid cancer, but people with this disease also have a higher risk of bladder cancer.

In the Hereditary Cancer Panel - Bladder and Renal Cancer, these are the genes analyzed: CDC73, EPCAM, FH, FLCN, MET, MLH1, MSH2, MSH6, PMS2, PTEN, SDHB, SDHC, SDHD, TSC1, TSC2, including deletions and insertions.

Breast cancer is the most common cancer type among American women with 1 in 8 women in the United States developing breast cancer in their lifetime. It is also the second leading cause of cancer death in women. Men can also develop breast cancer. One out of a thousand men in the United States will develop breast cancer in their lifetime. Most breast cancer is not inherited, however, up to 10% of breast cancers are due to a genetic change (mutation) that can be passed on in the family.

Red Flags for Breast, Ovarian and Uterine Hereditary Cancer

• Personal or close relative with breast cancer diagnosed at or under age 50;
• Personal or close relative with uterine cancer diagnosed under age 50;
• Personal or family history of ovarian cancer at any age;
• Personal or family history of male breast cancer at any age;
• Triple-negative breast cancer diagnosed at or under age 60;
• Two or more separate breast cancers in the same person;
• Ashkenazi Jewish descent;
• Three or more cases of breast, ovarian, pancreatic and/or aggressive prostate cancer in close relatives, including the patient.

The Hereditary Cancer Panel – Breast Cancer and Ovarian Cancer covers 27 genes: ATM, BAP1, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PTEN, RAD51C, RAD51D, SDHB, SDHC, SDHD, SLX4, SMAD4, STK11 and TP53, including deletions and insertions.

Colorectal cancer is the third most common cancer type in the United States. One in 21 men and one in 23 women will develop colorectal cancer in their lifetime. Most colorectal cancer is not inherited, however, up to 10 percent of colorectal cancers are due to a genetic change (mutation) that can be passed on in the family.

Lynch Syndrome
Individuals with Lynch syndrome (also called Hereditary Nonpolyposis Colorectal Cancer or HNPCC) are at a signifi cant risk of developing colorectal and/or uterine cancers. Depending on the specifi c Lynch syndrome gene involved, the colorectal cancer risk can be as high as 82% and uterine cancer risk is up to 60 percent. Also, risks are elevated for stomach, ovarian, liver, urinary tract, small bowel, pancreatic and brain cancers. Between 2 and 4 percent of all colorectal cancer cases are due to Lynch syndrome.

Red Flags for Colorectal Cancer/Lynch Syndrome
 • Colorectal cancer diagnosed under age 50
• 10 or more colon polyps in the same person
• Colorectal cancer diagnosed at or over age 50 if there is a fi rst degree relative with colorectal or uterine cancer at any age
 • Two or more cases of colorectal and/or uterine cancer in the same person

Through the Hereditary Cancer Panel - Colorectal Cancer, 16 genes associated with the CRC are analyzed: APC, BMPR1A, BUB1B, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, PMS2, PTEN, SDHD, SMAD4, STK11 and TP53, including deletions and insertions.

The Lynch Syndrome Panel analyzes the following 5 genes: EPCAM, MLH1, MSH2, MSH6 and PMS2 including deletions and insertions.

The Multiple Endocrine Neoplasia syndromes (MEN) are classified in two major types: type 1 and type 2, although the types occasionally overlap.

Multiple Endocrine Neoplasia Type 1 (MEN1, also known as Wermer's syndrome) is a genetic syndrome characterized by the development of tumors, or excessive growth and activity, of two or more of the following glands: parathyroid glands, pituitary gland, pancreas, thyroid gland (less often affected) or adrenal glands (less often affected). Alterations in the gene MEN1 are found in 70 to 95% of patients with MEN1. Multiple endocrine neoplasia type 1 affects about 1 in 30,000 people.

Multiple Endocrine Neoplasia Type 2 (MEN2, also known as Sipple syndrome) is a group of disorders associated with tumors of the endocrine system. There are three subtypes of this syndrome, MEN 2A, MEN 2B, and Familial Medullary Thyroid Carcinoma (FMTC) with the common feature between the three being the high tendency to develop medullary thyroid carcinoma. It is estimated that about one in 30,000 people has MEN2. Alterations in the gene RET are found in more than 95% of families with MEN2A or MEN2B, and in more than 85% of families with FMTC. Multiple endocrine neoplasia type 2 affects an estimated 1 in 35,000 people. Among the subtypes of type 2, type 2A is the most common form, followed by FMTC. Type 2B is relatively uncommon and accounts for approximately 5 percent of all cases of MEN type 2.

In the Hereditary Cancer Panel - Endocrine System Neoplasia, 7 genes are analyzed: CDC73, HRAS, MEN1, PRKAR1A, PTEN, RET and VHL including deletions and insertions.

Uterine (Endometrial) Cancer is the most common cancer of the female reproductive tract. About 3% of women in the United States will develop uterine cancer in their lifetime. About 10 percent of all uterine cancers are hereditary.
 
Red Flags for Breast, Ovarian and Uterine Hereditary Cancer
 
  • Personal or close relative with breast cancer diagnosed at or under age 50
  • Personal or close relative with uterine cancer diagnosed under age 50
  • Personal or family history of ovarian cancer at any age
  • Personal or family history of male breast cancer at any age
  • Triple-negative breast cancer diagnosed at or under age 60
  • Two or more separate breast cancers in the same person
  • Ashkenazi Jewish descent
  • Three or more cases of breast, ovarian, pancreatic and/or aggressive prostate cancer in close relatives, including the patient
 Also, individuals who do not know their family medical history (for example, if they were adopted) may be appropriate candidates for genetic testing.

Gastric cancer is also known as stomach cancer and is the 4th most common cancer in the world. About 6 of every 10 people diagnosed with stomach cancer each year are 65 or older, with the average age of diagnosis being 69 years old. The average risk that a person will develop stomach cancer in their lifetime is about 1 in 111. This risk is higher in men than in women, and can also be affected by several other factors. The American Cancer Society’s estimates that 28,000 new cases of stomach cancer will be diagnosed (17,750 in men and 10,250 in women) in the United States for 2017. Stomach cancer is much more common in other parts of the world, particularly in less developed countries.

Hereditary diffuse gastric cancer (HDGC) is an inherited disorder that greatly increases the chance of developing a form of stomach (gastric) cancer. In this form, known as diffuse gastric cancer, there is no solid tumor. Instead cancerous (malignant) cells multiply underneath the stomach lining, making the lining thick and rigid. It is estimated that HDGC accounts for less than 1% of all the newly diagnosed gastric cancer cases.

The earlier diagnosis is made, the better the prognosis for the patient. With the help of molecular genetic analysis, patients and their medical care providers may consider their preventative health management strategies and/or familial genetic counseling.

The Hereditary Cancer Panel - Familial Gastric Cancer analyzes the genes: APC, BMPR1A, CDH1, EPCAM, KIT, MLH1, MSH2, MSH6, MUTYH, PMS2, SDHB, SDHC, SDHD, SMAD4 and TP53 including deletions and insertions.

The Hereditary Cancer Panel - Familial Gastric Cancer analyzes the genes: APC, BMPR1A, CDH1, EPCAM, KIT, MLH1, MSH2, MSH6, MUTYH, PMS2, SDHB, SDHC, SDHD, SMAD4 and TP53 including deletions and insertions.

Li-Fraumeni is a rare cancer syndrome in which children and adults are at a high risk of developing cancer. Most common cancers in Li-Fraumeni syndrome include early onset breast cancer, bone cancer (osteosarcoma), cancer of soft tissues (soft tissue sarcoma), brain tumors, leukemia and adrenocortical carcinoma. 

The exact prevalence of Li- Fraumeni syndrome is unknown, but is estimated to be 1 in 5,000 to 1 in 20,000. Approximately half of individuals with Li-Fraumeni syndrome develop cancer by age 30; 90 percent develop cancer by age 60. Also, 15 percent of people with Li-Fraumeni syndrome develop second cancer, 4 percent develop third cancer and 2 percent develop fourth cancer in their lifetime.

Red Flags for Li-Fraumeni Hereditary Cancer
• Personal history of or a first degree relative with breast  cancer diagnosed before age 30
• Personal history of or a first degree relative with an  adrenocortical tumor
• Personal history of or a first degree relative with a cho roid plexus tumor
• Sarcoma diagnosed under age 18
• Two or more close relatives with a tumor in the Li-  Fraumeni Syndrome (LFS) spectrum, one diagnosed at or before age 45
• Personal history of two or more LFS associated tumors,  one diagnosed at or under age 45

In the Hereditary Cancer Panel - Li-Fraumeni Syndrome, we analyze the genes CHEK2 and TP53, including deletions and insertions.

Melanoma is a type of skin cancer that begins in melanocytes (skin cells that produce brown pigment). Melanoma is more dangerous than other types of skin cancer because it is more likely to spread to other parts of the body, if untreated. Individuals who have relatives with melanoma are
at a higher risk of developing melanoma themselves compared to someone with no family history of melanoma.

Hereditary Melanoma, also called familial atypical mole and malignant melanoma, predisposes people to melanoma and pancreatic cancers. Individuals with Hereditary Melanoma have a 17 percent chance of developing pancreatic cancer by age 75. Melanoma risk varies from 28 to 91 percent depending on the population studied. Individuals who have pale skin, blond or red hair and light-colored eyes are at a higher risk of developing melanoma compared to people with darker complexions.

Red Flags for Melanoma cancer:

If you have any of the following you may benefit from genetic counseling and hereditary cancer genetic testing:
• Two or more relatives on the same side of the family  affected with malignant melanoma (especially at an early age), or
• You and/or a close relative have a history of multiple  primary melanomas, or
• You have a family history of both malignant melanoma
 and pancreatic cancer.

The Hereditary Cancer Panel - Familial Melanoma analyzes the following 9 genes: BAP1, BRCA2, CDK4, CDKN2A, PTEN, RB1, TP53, XPA and XPC, including deletions and insertions.

Pancreatic Cancer is a serious, aggressive, and a disease with a high-mortality-rate. The most common type of pancreatic cancer is the ductal adenocarcinoma, which accounts for approximately 85% of cases.

Pancreatic cancer accounts for about 3% of all cancers in the US and about 7% of cancer deaths. Approximately 10% of pancreatic cancers have hereditary basis.


According to the ACMG Practice Guidelines published in January 2015, the indications for referring a patient for genetic counseling and/or genetic testing include:
  • Pancreatic cancer diagnosed at any age, if any of the following criteria are met:
    • 2 or more cases of pancreatic cancer in close relatives
    • 2 or more cases of breast, ovarian, and/or aggressive prostate cancer in close relatives
    • Ashkenazi Jewish ancestry
  • Pancreatic cancer and 1 or more PJ polyp in the same person
  • Pancreatic cancer and two additional cases of any Lynch Syndrome-associated cancer in the same person or in close relatives
  • 3 or more cases of pancreatic cancer and/or melanoma in close relatives
  • Pancreatic cancer and melanoma in the same person
In the Hereditary Cancer Panel - Pancreatic Cancer, the following genes are analyzed: APC, ATM, BRCA1, BRCA2, CDK4, CDKN2A, MLH1, MSH2, PALB2 and TP53, including deletions and insertions.

Prostate cancer is the most common cancer in American men. About 1 man in 7 will be diagnosed with prostate cancer during his lifetime. About 5 to 10 percent of all prostate cancers diagnosed are hereditary, meaning that an increased risk for the disease runs in the family. Family history is the strongest risk factor for prostate cancer.

Patients have an increased risk of developing this disease if they have:
• 2 or more close relatives who had prostate cancer diagnosed under the age of 55;
• 3 or more first degree relatives with prostate cancer at any age; or
• had a close relative diagnosed with aggressive prostate cancer and 2 or more cases of breast, ovarian and/or pancreatic cancer in close relatives

In the Hereditary Cancer Panel - Prostate Cancer, the following genes are analyzed: BRCA2 and TP53, including deletions and insertions.

The CompleteRisk (Hereditary – 94 genes) is indicated when criteria are met for multiple hereditary panels. This panel tests all of the genes included in our other hereditary cancer panels.

Current NCCN guidelines, adopted by IntelligeneDx Cancer Genomics Laboratory, support the use of DNA sequencing technologies (Sanger, MLPA, and Next Generation Sequencing (NGS) to detect mutations that allow providers to create personalized health management plans for their patients. The detection of a pathogenic genetic variant or mutation in germline DNA analysis is crucial in the identification of individuals or even clusters of families who may be susceptible to a hereditary cancer syndrome.

These are the genes analyzed: AIP, ALK, APC, ATM, BAP1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, BUB1B, CDC73, CDH1, CDK4, CDKN1C, CDKN2A, CEBPA, CEP57, CHEK2, CYLD, DDB2, DICER1, DIS3L2, EGFR, EPCAM, ERCC2, ERCC3, ERCC4, ERCC5, EXT1, EXT2, EZH2, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FH, FLCN, GATA2, GPC3, HNF1A, HRAS, KIT, MAX, MEN1, MET, MLH1, MSH2, MSH6, MUTYH, NBN, NF1, NF2, NSD1, PALB2, PHOX2B, PMS1, PMS2, PRF1, PRKAR1A, PTCH1, PTEN, RAD51C, RAD51D, RB1, RECQL4, RET, RHBDF2, RUNX1, SBDS, SDHAF2, SDHB, SDHC, SDHD, SLX4, SMAD4, SMARCB1, STK11, SUFU, TMEM127, TP53, TSC1, TSC2, VHL, WRN, WT1, XPA and XPC, including deletions and insertions.

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The Prosigna® Breast Cancer Prognostic Gene Signature Assay is a Medicare covered diagnostic exam, performed in vitro, using FFPE breast tumor tissue from patients previously diagnosed with invasive breast carcinoma. This qualitative assay utilizes gene expression data, weighted together with clinical variables to generate a risk category and a numerical score, to assess a patient’s risk of distant recurrence of disease. 

The Prosigna® Breast Cancer Prognostic Gene Signature Assay is indicated in female breast cancer patients who have undergone surgery in conjunction with locoregional treatment consistent with standard of care, either as: 

1. A prognostic indicator for distant recurrence-free survival at 10 years in post-menopausal women with Hormone Receptor-Positive (HR+), lymph node-negative, Stage I or II breast cancer to be treated with adjuvant endocrine therapy alone, when used in conjunction other clinicopathological factors. 

2. A prognostic indicator for distant recurrence-free survival at 10 years in post-menopausal women with Hormone Receptor-Positive (HR+), lymph node-positive (1-3 lymph nodes), Stage II breast cancer to be treated with adjuvant endocrine therapy alone, when used in conjunction other clinicopathological factors. 

Test Description: Prosigna® Breast Cancer Prognostic Gene Signature Assay 

The Prosigna Score is a numerical value on a 0-to-100 scale that correlates with the probability of distant recurrence within 10 years. The gene expression profile of a patient’s tumor is compared with each of the four PAM50 prototypical molecular profiles to determine the degree of similarity. The results in combination with a proliferation score and tumor size produce an individualized Prosigna Score. 

The clinical performance of Prosigna® has been validated in two large independent studies using retrospective tissue samples from over 2,400 patients within the intended use population (postmenopausal women with hormone receptor-positive early stage breast cancer). Both the ATAC and ABCSG-8 trials assessed the benefit of adjuvant treatment (tamoxifen and anastrozole alone or in combinations for 5 years) in post-menopausal women with hormone receptor-positive early stage breast cancer. A subset of tumor samples from the TransATAC (translational arm of the ATAC trial) and ABCSG-8 trials were analyzed by Prosigna to assess the assay’s ability to predict risk of distant recurrence. Both studies demonstrated that the Prosigna Score provided substantial prognostic information over and above the standard clinical variables (nodal status, tumor size and grade, age, and treatment) in predicting risk of distant recurrence.

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This panel consists of a set of 4,813 genes that were chosen from the Human Gene Mutation Database (HGMD) emphasizing regions where mutations are pathogenic and proven to be important in inherited conditions. 

This panel allows physicians to make a possible diagnosis of cases whose common analysis of genes and other different approaches were inconclusive. It also helps to obtain faster test results of rare genes that would normally take a long time for a standardization. It was developed by Illumina, based on the Human Gene Mutation Database (HGMD).

The genes analyzed in this panel are: 2M, A4GALT, A4GNT, AAAS, AADAC, AADACL2, AANAT, AARS, AARS2, AASS, ABAT, ABCA1, ABCA10, ABCA12, ABCA13, ABCA2, ABCA3, ABCA4, ABCA7, ABCB1, ABCB11, ABCB4, ABCB6, ABCB7, ABCC1, ABCC11, ABCC2, ABCC3, ABCC4, ABCC6, ABCC8, ABCC9, ABCD1, ABCD3, ABCD4, ABCG1, ABCG2, ABCG5, ABCG8, ABHD12, ABHD5, ABI3BP, ABO, ACACA, ACACB, ACAD8, ACAD9, ACADL, ACADM, ACADS, ACADSB, ACADVL, ACAN, ACAT1, ACAT2, ACBD5, ACBD6, ACCS, ACE, ACHE, ACLY, ACO2, ACOX1, ACP5, ACSF3, ACSL4, ACSL5, ACSM2B, ACSM3, ACTA1, ACTA2, ACTB, ACTC1, ACTG1, ACTN2, ACTN3, ACTN4, ACVR1, ACVR1B, ACVR1C, ACVR2B, ACVRL1, ACY1, ADA, ADAM10, ADAM12, ADAM17, ADAM19, ADAM33, ADAM7, ADAM9, ADAMTS10, ADAMTS13, ADAMTS16, ADAMTS17, ADAMTS18, ADAMTS2, ADAMTSL2, ADAMTSL3, ADAMTSL4, ADAR, ADARB1, ADC, ADCK3, ADCY10, ADCY3, ADCY5, ADCY6, ADCY9, ADCYAP1, ADD1, ADH1B, ADH1C, ADH4, ADH5, ADH7, ADIPOQ, ADIPOR1, ADK, ADM, ADNP, ADORA1, ADORA2A, ADORA3, ADRA1A, ADRA2A, ADRA2B, ADRA2C, ADRB1, ADRB2, ADRB3, ADRBK2, ADSL, ADTRP, AFF2, AFF3, AFG3L2, AFP, AGA, AGBL4, AGER, AGGF1, AGK, AGL, AGMO, ago/01, ago/02, AGPAT2, AGPS, AGRN, AGRP, AGT, AGTR1, AGTR2, AGXT, AGXT2, AHCY, AHI1, AHR, AHRR, AHSG, AHSP, AICDA, AIF1, AIFM1, AIMP1, AIP, AIPL1, AIRE, AK1, AK2, AKAP10, AKAP13, AKAP2, AKAP9, AKR1B1, AKR1C2, AKR1C3, AKR1C4, AKR1D1, AKR7A2, AKR7A3, AKT1, AKT2, AKT3, ALAD, ALAS2, ALB, ALCAM, ALDH16A1, ALDH18A1, ALDH1A1, ALDH1A2, ALDH2, ALDH3A2, ALDH4A1, ALDH5A1, ALDH6A1, ALDH7A1, ALDOA, ALDOB, ALG1, ALG10B, ALG11, ALG12, ALG13, ALG2, ALG3, ALG6, ALG8, ALG9, ALK, ALMS1, ALOX12, ALOX12B, ALOX15, ALOX5, ALOX5AP, ALOXE3, ALPL, ALS2, ALS2CL, ALX1, ALX3, ALX4, AMACR, AMELX, AMELY, AMER1, AMH, AMHR2, AMN, AMPD1, AMPD3, AMT, ANAPC1, ANG, ANGPT1, ANGPTL3, ANGPTL4, ANGPTL5, ANK1, ANK2, ANK3, ANKH, ANKK1, ANKRD1, ANKRD11, ANKRD26, ANKS1A, ANKS1B, ANO10, ANO5, ANO6, ANO7, ANTXR1, ANTXR2, ANXA11, ANXA5, AOAH, AOC1, AP1S1, AP1S2, AP3B1, AP3B2, AP4B1, AP4E1, AP4M1, AP4S1, AP5Z1, APAF1, APBA2, APBB1, APBB3, APC, APCDD1, APEX1, APH1A, APH1B, APLNR, APOA1, APOA2, APOA4, APOA5, APOB, APOBEC3B, APOBEC3G, APOBEC3H, APOC1, APOC2, APOC3, APOC4, APOD, APOE, APOH, APOL1, APOL3, APOM, APP, APRT, APTX, AQP1, AQP2, AQP3, AQP4, AQP5, AQP7, AR, AREL1, ARF4, ARFGEF2, ARG1, ARHGAP24, ARHGAP31, ARHGAP6, ARHGAP9, ARHGEF10, ARHGEF11, ARHGEF12, ARHGEF6, ARHGEF7, ARHGEF9, ARID1A, ARID1B, ARL11, ARL13B, ARL14EP, ARL6, ARL6IP5, ARMS2, ARPC3, ARSA, ARSB, ARSE, ARSF, ART4, ARVCF, ARX, AS3MT, ASAH1, ASAH2, ASB10, ASCC1, ASCC3, ASCL1, ASIC3, ASIP, ASL, ASMT, ASMTL, ASNS, ASPA, ASPM, ASPN, ASPRV1, ASS1, ASTN2, ASXL1, ATCAY, ATF1, ATF3, ATF5, ATF6, ATG16L1, ATG7, ATIC, ATL1, ATM, ATN1, ATOH7, ATP10A, ATP10D, ATP13A2, ATP13A4, ATP1A2, ATP1A3, ATP1B1, ATP2A1, ATP2A2, ATP2A3, ATP2B2, ATP2B4, ATP2C1, ATP5E, ATP5SL, ATP6AP2, ATP6V0A1, ATP6V0A2, ATP6V0A4, ATP6V1B1, ATP7A, ATP7B, ATP8A2, ATP8B1, ATPAF2, ATR, ATRNL1, ATRX, ATXN1, ATXN10, ATXN2, ATXN3, ATXN3L, ATXN7, ATXN8OS, AUH, AURKA, AURKC, AUTS2, AVP, AVPR1A, AVPR1B, AVPR2, AXIN1, AXIN2, AXL, B2M, B3GALNT1, B3GALT6, B3GALTL, B3GAT3, B3GNT2, B3GNT3, B4GALT1, B4GALT7, B9D1, B9D2, BAALC, BAAT, BACE1, BAG3, BAG6, BANF1, BANK1, BAP1, BARD1, BAX, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCAM, BCAP31, BCAT1, BCAT2, BCHE, BCKDHA, BCKDHB, BCL10, BCL11A, BCL2, BCL2A1, BCL2L11, BCL2L2, BCL9, BCMO1, BCOR, BCORL1, BCR, BCS1L, BDKRB2, BDNF, BEAN1, BEST1, BEX4, BFSP1, BFSP2, BHLHA9, BHLHE41, BHMT, BICC1, BICD1, BIN1, BIRC5, BLK, BLM, BLMH, BLNK, BLOC1S3, BLOC1S6, BLVRA, BMI1, BMP1, BMP10, BMP15, BMP2, BMP2K, BMP4, BMP5, BMP7, BMPER, BMPR1A, BMPR1B, BMPR2, BNC2, BOLA3, BPGM, BPI, BPIFA1, BPY2, BRAF, BRAP, BRAT1, BRCA1, BRCA2, BRCC3, BRD1, BRIP1, BRSK2, BRWD1, BRWD3, BSCL2, BSG, BSND, BST1, BTAF1, BTBD9, BTC, BTD, BTK, BTLA, BTN1A1, BTN2A1, BTNL2, BTRC, BUB1B, C10orf11, C10orf137, C10orf2, C12orf10, C12orf57, C12orf65, C19orf12, C1GALT1, C1QA, C1QB, C1QC, C1QTNF5, C1R, C1S, C2, C2orf71, C3, C3AR1, C4A, C4B, C4BPA, C5, C5AR2, C5orf42, C6, C6orf15, C7, C7orf10, C8A, C8B, C8orf37, C9, C9orf72, CA1, CA12, CA2, CA4, CA6, CA8, CABIN1, CABP4, CACNA1A, CACNA1C, CACNA1D, CACNA1E, CACNA1F, CACNA1G, CACNA1H, CACNA1S, CACNA2D1, CACNA2D3, CACNA2D4, CACNB2, CACNB4, CACNG2, CADM1, CALCA, CALCR, CALHM1, CALM1, CALM3, CALR, CALR3, CAMK4, CAMKK1, CAMKK2, CAMP, CAMTA1, CANT1, CAPN10, CAPN13, CAPN3, CARD14, CARD8, CARD9, CARTPT, CASC16, CASC5, CASK, CASP1, CASP10, CASP12, CASP2, CASP3, CASP5, CASP8, CASP9, CASQ2, CASR, CAST, CAT, CATSPER1, CATSPER2, CATSPER3, CATSPER4, CAV1, CAV3, CBFB, CBL, CBLB, CBR1, CBR3, CBS, CBX2, CBX4, CC2D1A, CC2D2A, CCBE1, CCDC103, CCDC14, CCDC170, CCDC22, CCDC28B, CCDC39, CCDC40, CCDC50, CCDC8, CCDC88C, CCHCR1, CCK, CCKAR, CCKBR, CCL11, CCL13, CCL17, CCL2, CCL22, CCL26, CCL3L1, CCL4L1, CCL5, CCL7, CCM2, CCNA2, CCND1, CCR1, CCR2, CCR3, CCR5, CCR6, CCR7, CCRL2, CCT5, CD109, CD14, CD151, CD177, CD19, CD1A, CD1E, CD207, CD209, CD22, CD226, CD24, CD244, CD247, CD27, CD2AP, CD320, CD36, CD38, CD3D, CD3E, CD3EAP, CD3G, CD4, CD40, CD40LG, CD44, CD46, CD5, CD55, CD58, CD59, CD72, CD79A, CD79B, CD81, CD86, CD8A, CD96, CDA, CDAN1, CDC42BPB, CDC6, CDC73, CDH1, CDH12, CDH13, CDH15, CDH23, CDH3, CDH5, CDH8, CDHR1, CDK11A, CDK4, CDK5R1, CDK5RAP2, CDK5RAP3, CDK7, CDKL3, CDKL5, CDKN1A, CDKN1B, CDKN1C, CDKN2A, CDKN2B, CDKN2B-AS1, CDKN2C, CDON, CDSN, CDT1, CDY1, CDY2A, CEACAM16, CEBPA, CEBPE, CEL, CELSR1, CENPJ, CEP135, CEP152, CEP290, CEP41, CEP57, CEP63, CEP68, CEP85L, CER1, CERKL, CERS6, CES1, CES2, CETP, CFB, CFC1, CFC1B, CFD, CFH, CFHR1, CFHR2, CFHR3, CFHR4, CFHR5, CFI, CFL2, CFLAR, CFP, CFTR, CGA, CGB, CHAT, CHD1L, CHD2, CHD3, CHD6, CHD7, CHD8, CHDH, CHEK2, CHFR, CHGA, CHGB, CHI3L1, CHI3L2, CHIA, CHIT1, CHKB, CHL1, CHM, CHMP2B, CHMP4B, CHN1, CHRDL1, CHRFAM7A, CHRM1, CHRM2, CHRM3, CHRNA1, CHRNA2, CHRNA3, CHRNA4, CHRNA5, CHRNA7, CHRNA9, CHRNB1, CHRNB2, CHRNB4, CHRND, CHRNE, CHRNG, CHST14, CHST3, CHST6, CHST8, CHSY1, CHUK, CIB2, CIC, CIDEA, CIDEC, CIITA, CILP, CIRH1A, CISD2, CISH, CITED2, CKM, CLCA1, CLCA2, CLCF1, CLCN1, CLCN2, CLCN5, CLCN7, CLCNKA, CLCNKB, CLDN1, CLDN14, CLDN16, CLDN19, CLEC11A, CLEC2D, CLEC4M, CLEC7A, CLIC2, CLK2, CLMP, CLN3, CLN5, CLN6, CLN8, CLNK, CLOCK, CLPS, CLPTM1, CLRN1, CLSTN2, CLTCL1, CLU, CLUL1, CLYBL, CMA1, CMPK1, CNBP, CNDP1, CNGA1, CNGA3, CNGB1, CNGB3, CNKSR1, CNKSR2, CNNM2, CNNM4, CNOT3, CNOT4, CNPY3, CNR1, CNR2, CNTF, CNTN1, CNTN4, CNTNAP2, CNTNAP4, CNTNAP5, COA5, COCH, COG1, COG4, COG5, COG6, COG7, COG8, COL10A1, COL11A1, COL11A2, COL12A1, COL17A1, COL18A1, COL1A1, COL1A2, COL25A1, COL2A1, COL3A1, COL4A1, COL4A2, COL4A3, COL4A4, COL4A5, COL4A6, COL5A1, COL5A2, COL6A1, COL6A2, COL6A3, COL6A4P2, COL6A5, COL7A1, COL8A2, COL9A1, COL9A2, COL9A3, COLEC11, COLQ, COMMD1, COMP, COMT, COQ2, COQ4, COQ5, COQ6, COQ9, CORIN, CORO1A, COX10, COX14, COX15, COX4I1, COX4I2, COX6B1, COX7A1, COX7A2, CP, CPA4, CPA6, CPB2, CPE, CPLX2, CPN1, CPOX, CPS1, CPT1A, CPT1B, CPT2, CPZ, CR1, CR2, CRADD, CRB1, CRBN, CREB1, CREB3L3, CREBBP, CRELD1, CRH, CRHR1, CRISP2, CRK, CRKL, CRLF1, CRP, CRTAP, CRX, CRYAA, CRYAB, CRYBA1, CRYBA4, CRYBB1, CRYBB2, CRYBB3, CRYGB, CRYGC, CRYGD, CRYGEP, CRYGS, CRYM, CSAG1, CSDE1, CSF1, CSF1R, CSF2, CSF2RA, CSF2RB, CSF3R, CSGALNACT1, CSH1, CSMD1, CSMD3, CSNK1A1L, CSNK1D, CSNK1E, CSNK2A2, CSNK2A3, CSRP3, CST3, CSTA, CSTB, CSTF2T, CTC1, CTDP1, CTF1, CTGF, CTH, CTHRC1, CTLA4, CTNNA3, CTNNB1, CTNND1, CTNS, CTRC, CTSA, CTSB, CTSC, CTSD, CTSG, CTSK, CTSZ, CTTNBP2, CUBN, CUL3, CUL4B, CUL5, CUL7, CX3CR1, CXCL10, CXCL11, CXCL12, CXCL16, CXCL5, CXCR1, CXCR3, CXCR4, CYB5A, CYB5R3, CYBA, CYBB, CYBRD1, CYCS, CYLD, CYP11A1, CYP11B1, CYP11B2, CYP17A1, CYP19A1, CYP1A1, CYP1A2, CYP1B1, CYP21A2, CYP24A1, CYP26A1, CYP26B1, CYP27A1, CYP27B1, CYP2A13, CYP2A6, CYP2B6, CYP2C18, CYP2C19, CYP2C8, CYP2C9, CYP2D6, CYP2D7P1, CYP2E1, CYP2F1, CYP2G1P, CYP2J2, CYP2R1, CYP2W1, CYP3A4, CYP3A43, CYP3A5, CYP3A5P1, CYP3A7, CYP46A1, CYP4A11, CYP4A22, CYP4B1, CYP4F12, CYP4F2, CYP4F22, CYP4F3, CYP4V2, CYP7A1, CYP7B1, CYSLTR1, CYSLTR2, D2HGDH, DAG1, DAO, DAOA, DAPK1, DARC, DARS2, DAZ1, DAZ2, DAZ3, DAZL, DBH, DBI, DBT, DCAF13, DCAF17, DCC, DCDC2, DCK, DCLK1, DCLRE1C, DCN, DCP1B, DCTD, DCTN1, DCX, DCXR, DDAH1, DDAH2, DDB2, DDC, DDOST, DDR1, DDR2, DDX11, DDX20, DDX25, DDX39B, DDX3Y, DDX5, DDX53, DDX58, DEAF1, DEC1 , DECR1, DEFB1, DEFB126, DEFB4A, DES, DFNA5, DFNB31, DFNB59, DGAT1, DGCR14, DGCR2, DGCR5, DGCR6, DGCR8, DGKD, DGUOK, DHCR24, DHCR7, DHDDS, DHFR, DHH, DHODH, DHRS4L1, DHX16, DHX36, DHX37, DIABLO, DIAPH1, DIAPH2, DIAPH3, DICER1, DIO1, DIO2, DIP2A, DIP2B, DIP2C, DIRC2, DIS3L2, DISC1, DISP1, DKC1, DKK2, DKK3, DLAT, DLD, DLG3, DLG5, DLGAP2, DLGAP3, DLL1, DLL3, DLX3, DLX5, DLX6, DMBT1, DMC1, DMD, DMGDH, DMP1, DMPK, DMRT1, DMXL1, DNAAF1, DNAAF2, DNAAF3, DNAH11, DNAH5, DNAH9, DNAI1, DNAI2, DNAJA4, DNAJB2, DNAJB6, DNAJC19, DNAJC5, DNAJC6, DNAL1, DNASE1, DNASE1L3, DNASE2, DND1, DNM1, DNM1L, DNM2, DNMT1, DNMT3A, DNMT3B, DNMT3L, DOC2A, DOCK3, DOCK4, DOCK6, DOCK8, DOCK9, DOK7, DOLK, DPAGT1, DPM1, DPM3, DPP10, DPP6, DPY19L2, DPYD, DPYS, DPYSL2, DRD1, DRD2, DRD3, DRD4, DRD5, DROSHA, DRP2, DSC2, DSC3, DSCAM, DSCR8, DSG1, DSG2, DSG4, DSP, DSPP, DST, DTNA, DTNBP1, DUOX2, DUOXA2, DUSP23, DUX4, DXO, DYM, DYNC1H1, DYNC2H1, DYRK1A, DYSF, DYX1C1, DYX1C1-CCPG1, EARS2, EBAG9, EBP, ECE1, ECI1, ECM1, ECM2, ECSIT, EDA, EDA2R, EDAR, EDARADD, EDN1, EDN2, EDN3, EDNRA, EDNRB, EEF1B2, EEF2K, EFCAB5, EFEMP1, EFEMP2, EFHC1, EFHC2, EFNB1, EFR3A, EFTUD2, EGF, EGFR, EGLN1, EGR2, EGR3, EHD2, EHMT1, EHMT2, EIF2AK3, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EIF3H, EIF4E, EIF4G1, ELAC2, ELANE, ELAVL2, ELF4, ELK1, ELN, ELOVL4, ELP2, ELP4, EMC4, EMD, EME1, EMG1, EMX2, EN2, ENAM, ENG, ENO1, ENO3, ENPP1, ENSA, ENTPD1, EOMES, EP300, EPAS1, EPB41, EPB41L1, EPB42, EPC2, EPCAM, EPHA2, EPHA3, EPHA5, EPHA7, EPHB2, EPHB6, EPHX1, EPHX2, EPM2A, EPO, EPOR, EPX, ERAP1, ERAP2, ERBB2, ERBB3, ERBB4, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERCC8, ERLIN2, ERMAP, ESAM, ESCO2, ESPN, ESR1, ESR2, ESRRB, ESRRG, ETFA, ETFB, ETFDH, ETHE1, ETNPPL, ETS1, EVC, EVC2, EVI5, EXO1, EXO5, EXOC4, EXOSC3, EXT1, EXT2, EXTL3, EYA1, EYA4, EYS, EZH2, F10, F11, F12, F13A1, F13B, F2, F2R, F2RL1, F3, F5, F7, F8, F9, FA2H, FAAH, FAAH2, FABP1, FABP2, FABP3, FABP4, FABP6, FABP7, FADD, FADS2, FAH, FAM120A, FAM126A, FAM134B, FAM161A, FAM205A, FAM20A, FAM20C, FAM58A, FAM83H, FAM8A1, FAM91A1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FARS2, FAS, FASLG, FASN, FASTKD2, FBLIM1, FBLN1, FBLN5, FBN1, FBN2, FBN3, FBP1, FBXL6, FBXO10, FBXO18, FBXO7, FBXW11, FBXW4, FBXW7, FCAR, FCER1A, FCER2, FCGR1A, FCGR2A, FCGR2B, FCGR3A, FCGR3B, FCGRT, FCN2, FCN3, FCRL3, FDFT1, FECH, FEM1A, FEN1, FERMT1, FERMT3, FEV, FEZF2, FFAR1, FFAR4, FGA, FGB, FGD1, FGD3, FGD4, FGF1, FGF10, FGF14, FGF2, FGF20, FGF23, FGF3, FGF8, FGF9, FGFBP1, FGFR1, FGFR2, FGFR3, FGFR4, FGFRL1, FGG, FH, FHL1, FHL2, FIG4, FIGLA, FIP1L1, FKBP10, FKBP14, FKBP5, FKBP6, FKBPL, FKRP, FKTN, FLCN, FLG, FLNA, FLNB, FLNC, FLT1, FLT3, FLT4, FLVCR1, FLVCR2, FMN1, FMN2, FMO1, FMO2, FMO3, FMO4, FMO5, FMO6P, FMR1, FN1, FN3K, FOLH1, FOLR1, FOXA1, FOXA2, FOXA3, FOXC1, FOXC2, FOXD3, FOXE1, FOXE3, FOXF1, FOXF2, FOXG1, FOXH1, FOXI1, FOXL2, FOXN1, FOXP1, FOXP2, FOXP3, FOXRED1, FPGS, FPR1, FPR2, FRA10AC1, FRAS1, FREM1, FREM2, FREM3, FRG1, FRK, FRMD6, FRMD7, FRMPD4, FRY, FRZB, FSCB, FSCN2, FSHB, FSHR, FTCD, FTH1, FTHL17, FTL, FTO, FTSJ1, FUCA1, FURIN, FUS, FUT1, FUT2, FUT3, FUT6, FUT7, FUT8, FUZ, FXN, FXYD2, FXYD6, FYCO1, FZD1, FZD3, FZD4, FZD6, FZD9, G6PC, G6PC2, G6PC3, G6PD, GAA, GAB2, GABBR1, GABRA1, GABRA5, GABRA6, GABRB3, GABRD, GABRG1, GABRG2, GABRG3, GABRR2, GAD1, GAD2, GADD45B, GAK, GAL3ST3, GALC, GALE, GALK1, GALNS, GALNT12, GALNT18, GALNT2, GALNT3, GALNT9, GALNTL5, GALP, GALT, GAMT, GAN, GAP43, GARS, GAS1, GAS2L2, GAS6, GATA1, GATA2, GATA3, GATA4, GATA6, GATAD1, GATM, GBA, GBA3, GBE1, GBGT1, GC, GCDH, GCGR, GCH1, GCK, GCKR, GCLC, GCLM, GCM2, GCNT2, GCSH, GDAP1, GDF1, GDF15, GDF3, GDF5, GDF6, GDF9, GDI1, GDNF, GEMIN2, GEMIN4, GFAP, GFER, GFI1, GFI1B, GFM1, GFPT1, GFPT2, GFRA1, GGCX, GGH, GGT5, GH1, GH2, GHR, GHRH, GHRHR, GHRL, GHSR, GIF, GIGYF2, GIMAP8, GIP, GIPC3, GIPR, GIT1, GJA1, GJA3, GJA4, GJA5, GJA8, GJB1, GJB2, GJB3, GJB4, GJB6, GJC2, GJC3, GJD2, GK, GLA, GLB1, GLCCI1, GLDC, GLE1, GLI1, GLI2, GLI3, GLIS2, GLIS3, GLMN, GLO1, GLP1R, GLRA1, GLRB, GLRX5, GLS, GLTSCR1, GLUD1, GLUD2, GLUL, GLYCTK, GM2A, GMIP, GNA14, GNAI2, GNAQ, GNAS, GNAS-AS1, GNAT1, GNAT2, GNB1L, GNB3, GNB5, GNE, GNMT, GNPAT, GNPTAB, GNPTG, GNRH1, GNRHR, GNS, GOLGA3, GOLGA5, GON4L, GORAB, GOSR2, GOT1, GP1BA, GP1BB, GP2, GP6, GP9, GPAM, GPANK1, GPATCH8, GPBAR1, GPC3, GPC4, GPC6, GPD1, GPD1L, GPD2, GPHN, GPI, GPIHBP1, GPR1, GPR12, GPR139, GPR143, GPR179, GPR33, GPR55, GPR56, GPR68, GPR98, GPS1, GPSM2, GPT, GPX1, GPX4, GRB10, GREM1, GRHL2, GRHPR, GRIA3, GRID1, GRIK1, GRIK3, GRIK4, GRIK5, GRIN1, GRIN2A, GRIN2B, GRIN3A, GRIP1, GRK1, GRK4, GRK5, GRM1, GRM3, GRM5, GRM6, GRM7, GRM8, GRN, GRPR, GRXCR1, GSC, GSDMA, GSDMB, GSE1, GSK3B, GSN, GSPT1, GSPT2, GSR, GSS, GSTA1, GSTA2, GSTA3, GSTK1, GSTM1, GSTM3, GSTM4, GSTO1, GSTO2, GSTP1, GSTT1, GSTT2, GSTT2B, GSTZ1, GTF2E1, GTF2H1, GTF2H5, GTF2IRD1, GTF2IRD2, GUCA1A, GUCA1B, GUCY2C, GUCY2D, GUSB, GYG1, GYLTL1B, GYPA, GYPB, GYPC, GYPE, GYS1, GYS2, GZMB, H19, H2BFWT, H6PD, HABP2, HACE1, HADH, HADHA, HADHB, HAL, HAMP, HAND1, HAND2, HARS, HARS2, HAS1, HAVCR1, HAX1, HBA1, HBA2, HBB, HBD, HBE1, HBEGF, HBG1, HBG2, HBM, HBS1L, HBZ, HCCS, HCK, HCLS1, HCN1, HCN2, HCN4, HCP5, HCRT, HCRTR1, HCRTR2, HDAC4, HDAC8, HDAC9, HDC, HDLBP, HDX, HEATR2, HELQ, HEPACAM, HERC2, HES6, HES7, HESX1, HEXA, HEXB, HEY1, HFE, HFE2, HGD, HGF, HGSNAT, HHEX, HHIP, HIBCH, HIF1A, HIF1AN, HIGD2A, HIP1, HIST1H2AE, HIST3H3, HK1, HK2, HLA-A, HLA-B, HLA-C, HLA-DMB, HLA-DOA, HLA-DPB1, HLA-DPB2, HLA-DQA1, HLA-DQB1, HLA-DRA, HLA-DRB1, HLA-DRB5, HLA-E, HLA-G, HLCS, HLX, HMBS, HMCN1, HMGA1, HMGA2, HMGCL, HMGCR, HMGCS2, HMHA1, HMOX1, HMOX2, HMSD, HMX1, HMX2, HNF1A, HNF1B, HNF4A, HNMT, HNRNPH3, HNRNPU, HOGA1, HOMER2, HOXA1, HOXA10, HOXA11, HOXA13, HOXA2, HOXA4, HOXB13, HOXB6, HOXD10, HOXD13, HOXD4, HP, HPD, HPGD, HPRT1, HPS1, HPS3, HPS4, HPS5, HPS6, HPSE2, HR, HRAS, HRC, HRG, HRH2, HRH3, HS1BP3, HS6ST1, HSD11B1, HSD11B2, HSD17B1, HSD17B10, HSD17B2, HSD17B3, HSD17B4, HSD3B1, HSD3B2, HSD3B7, HSF4, HSFY1, HSN2, HSP90AA1, HSP90B1, HSPA1A, HSPA1B, HSPA1L, HSPA5, HSPA8, HSPA9, HSPB1, HSPB3, HSPB6, HSPB7, HSPB8, HSPD1, HSPG2, HTN3, HTR1A, HTR1B, HTR2A, HTR2B, HTR2C, HTR3A, HTR3B, HTR3C, HTR3E, HTR5A, HTR6, HTR7, HTRA1, HTRA2, HTT, HUS1B, HUWE1, HVCN1, HYAL1, HYDIN, HYLS1, HYMAI, IAPP, IBSP, ICAM1, ICAM4, ICAM5, ICK, ICOS, ID3, IDE, IDH1, IDH2, IDH3B, IDO1, IDS, IDUA, IER3IP1, IFI30, IFI44L, IFIH1, IFITM3, IFITM5, IFNA10, IFNA17, IFNA2, IFNAR1, IFNAR2, IFNG, IFNGR1, IFNGR2, IFNL3, IFRD1, IFT122, IFT140, IFT43, IFT80, IGBP1, IGF1, IGF1R, IGF2, IGF2R, IGFALS, IGFBP1, IGFBP3, IGFBP5, IGFBP7, IGHA1, IGHG2, IGHM, IGHMBP2, IGKV, IGLL1, IHH, IKBIP, IKBKAP, IKBKG, IL10, IL10RA, IL10RB, IL11RA, IL12A, IL12B, IL12RB1, IL12RB2, IL13, IL16, IL17A, IL17F, IL17RA, IL17RB, IL17REL, IL18, IL18R1, IL18RAP, IL19, IL1A, IL1B, IL1R1, IL1RAPL1, IL1RL1, IL1RN, IL2, IL20RA, IL20RB, IL21, IL21R, IL23R, IL2RA, IL2RG, IL3, IL31RA, IL36RN, IL4, IL4R, IL5, IL6, IL6R, IL7, IL7R, IL8, IL9, IL9R, ILDR1, ILK, IMMP2L, IMMT, IMPA2, IMPAD1, IMPDH1, IMPDH2, IMPG2, INF2, INHA, INMT, INPP4A, INS, INSIG1, INSIG2, INSL3, INSL6, INSR, INVS, IQCB1, IQGAP1, IQGAP2, IQGAP3, IQSEC2, IRAK1, IRAK3, IRAK4, IRF1, IRF2, IRF4, IRF5, IRF6, IRF7, IRF8, IRGM, IRS1, IRS2, IRS4, IRX4, IRX5, ISCU, ISL1, ISPD, ISYNA1, ITCH, ITGA11, ITGA2, ITGA2B, ITGA3, ITGA4, ITGA6, ITGA7, ITGA9, ITGAE, ITGAM, ITGB2, ITGB3, ITGB4, ITIH1, ITIH3, ITIH4, ITIH6, ITK, ITM2B, ITPA, ITPKC, ITPR1, ITPR3, ITSN2, IVD, IYD, JAG1, JAG2, JAK2, JAK3, JAM3, JMJD1C, JPH2, JPH3, JRK, JUN, JUP, KAL1, KALRN, KANK1, KANSL1, KARS, KAT6B, KATNAL2, KBTBD13, KCNA1, KCNA3, KCNA5, KCNAB2, KCNC3, KCND2, KCND3, KCNE1, KCNE1L, KCNE2, KCNE3, KCNE4, KCNH2, KCNIP4, KCNJ1, KCNJ10, KCNJ11, KCNJ13, KCNJ15, KCNJ2, KCNJ3, KCNJ5, KCNJ6, KCNJ8, KCNJ9, KCNK18, KCNK6, KCNK9, KCNMA1, KCNMB1, KCNMB3, KCNN3, KCNQ1, KCNQ2, KCNQ3, KCNQ4, KCNS1, KCNS3, KCNV2, KCTD13, KCTD7, KDM4C, KDM5A, KDM5C, KDM5D, KDM6A, KDM6B, KDR, KEL, KERA, KHDC3L, KHK, KIAA0100, KIAA0196, KIAA0226, KIAA0232, KIAA0319, KIAA0513, KIAA1033, KIAA1199, KIAA1279, KIAA1377, KIAA1432, KIAA1462, KIAA2022, KIF11, KIF17, KIF18A, KIF1A, KIF1B, KIF21A, KIF22, KIF5A, KIF5B, KIF6, KIF7, KIFAP3, KIR2DL1, KIR2DL3, KIR2DL4, KIR3DL1, KIR3DL2, KIRREL3, KISS1, KISS1R, KIT, KITLG, KL, KLB, KLF1, KLF10, KLF11, KLF5, KLF6, KLF7, KLHDC8B, KLHL10, KLHL3, KLHL7, KLHL9, KLK1, KLK12, KLK15, KLK3, KLK4, KLK7, KLKB1, KLRK1, KMT2C, KMT2D, KMT2E, KNG1, KPNA1, KRAS, KRIT1, KRT1, KRT10, KRT12, KRT13, KRT14, KRT16, KRT17, KRT18, KRT2, KRT3, KRT31, KRT37, KRT38, KRT4, KRT5, KRT6A, KRT6B, KRT6C, KRT74, KRT75, KRT8, KRT81, KRT83, KRT85, KRT86, KRT9, KRTAP1-1, KYNU, L1CAM, L2HGDH, L3MBTL1, LAMA1, LAMA2, LAMA3, LAMA4, LAMA5, LAMB1, LAMB2, LAMB3, LAMC1, LAMC2, LAMC3, LAMP2, LAMTOR2, LARGE, LARS2, LBP, LBR, LCA5, LCAT, LCE3B, LCE3C, LCE5A, LCN10, LCT, LDB3, LDHA, LDHB, LDLR, LDLRAD4, LDLRAP1, LEFTY2, LEMD3, LEP, LEPR, LEPRE1, LEPREL1, LETM1, LFNG, LGALS13, LGALS2, LGALS3, LGI1, LHB, LHCGR, LHFPL5, LHX1, LHX3, LHX4, LHX8, LIAS, LIF, LIFR, LIG1, LIG3, LIG4, LILRA3, LIM2, LIMK1, LIN28A, LIN28B, LINS, LIPA, LIPC, LIPE, LIPG, LIPH, LIPI, LIPN, LITAF, LLGL1, LMAN1, LMBR1, LMBRD1, LMF1, LMNA, LMNB1, LMNB2, LMTK3, LMX1B, LNX2, loc344967, LOR, LOX, LOXHD1, LOXL1, LOXL2, LPA, LPAR1, LPAR6, LPIN1, LPIN2, LPIN3, LPL, LPP, LRAT, LRCH1, LRFN5, LRP1, LRP2, LRP4, LRP5, LRP6, LRP8, LRPAP1, LRPPRC, LRRC4, LRRC6, LRRC8A, LRRK2, LRSAM1, LRTOMT, LTA, LTBP1, LTBP2, LTBP3, LTBP4, LTC4S, LTF, LTK, LTN1, LUM, LY96, LYN, LYST, LYZ, LZTFL1, LZTS1, MACROD2, MAD1L1, MAD2L1, MADD, MAF, MAFB, MAGEE2, MAGEL2, MAGI2, MAGT1, MAK, MAMLD1, MAN1A2, MAN1B1, MAN2B1, MANBA, MAOA, MAOB, MAP2, MAP2K1, MAP2K2, MAP2K3, MAP2K4, MAP3K1, MAP3K15, MAP4K5, MAP6, MAP7D3, MAPK10, MAPK8IP1, MAPT, MARS2, MARVELD2, MASP1, MASP2, MAST4, MASTL, MAT1A, MATN3, MATR3, MAVS, MAX, MBD1, MBD3, MBD4, MBD5, MBL2, MBTPS2, MC1R, MC2R, MC3R, MC4R, MCCC1, MCCC2, MCEE, MCF2L2, MCFD2, MCHR1, MCL1, MCM3AP, MCM4, MCM5, MCM6, MCOLN1, MCPH1, MDH1, MDM2, MDM4, MDN1, MECP2, MED12, MED13, MED13L, MED17, MED23, MED25, MEF2A, MEF2C, MEFV, MEGF10, MEGF11, MEIS1, MEIS2, MEN1, MEP1B, MERTK, MESDC2, MESP2, MEST, MET, MFF, MFGE8, MFI2, MFN2, MFRP, MFSD2A, MFSD8, MGAT1, MGAT2, MGAT4C, MGEA5, MGLL, MGMT, MGP, MGST2, MGST3, MIA3, MIAT, MICA, MICB, MID1, MIF, MIIP, MINPP1, MIP, MIPOL1, MIR106B, MIR124-1, MIR125A, MIR126, MIR140, MIR146A, MIR16-1, MIR17, MIR17HG, MIR182, MIR184, MIR191, MIR196A2, MIR206, MIR24-1, MIR27A, MIR2861, MIR30C1, MIR34B, MIR499A, MIR502, MIR510, MIR890, MIR892B, MIR934, MIR96, MIRLET7E, MITF, MKKS, MKL1, MKRN3, MKS1, MLC1, MLH1, MLH3, MLLT3, MLPH, MLXIPL, MLYCD, MMAA, MMAB, MMACHC, MMADHC, MME, MMEL1, MMP1, MMP10, MMP12, MMP13, MMP14, MMP2, MMP20, MMP3, MMP7, MMP8, MMP9, MNX1, MOCOS, MOCS1, MOCS2, MOG, MOGS, MOK, MPDU1, MPDZ, MPG, MPHOSPH8, MPI, MPL, MPLKIP, MPO, MPP3, MPP4, MPP6, MPP7, MPST, MPV17, MPZ, MR1, MRAP, MRC1, MRE11A, MRPL3, MRPL48, MRPS16, MRPS22, MRRF, MS4A1, MS4A12, MS4A2, MS4A3, MS4A6A, MS4A6E, MSH2, MSH3, MSH4, MSH5, MSH6, MSMB, MSMO1, MSR1, MSRB3, MST1, MST1R, MSTN, MSX1, MSX2, MT1A, MT2A, MTAP, MTCH2, MTFMT, MTHFD1, MTHFD1L, MTHFR, MTHFS, MTM1, MTMR14, MTMR2, MTMR9, MTNR1A, MTNR1B, MTO1, MTPAP, MTR, MTRR, MTTP, MTUS1, MUC1, MUC13, MUC2, MUC3A, MUC4, MUC5B, MUC6, MUC7, MURC, MUSK, MUT, MUTYH, MVK, MX1, MYB, MYBL2, MYBPC1, MYBPC3, MYC, MYCL, MYCN, MYD88, MYF6, MYH11, MYH13, MYH14, MYH15, MYH2, MYH3, MYH6, MYH7, MYH8, MYH9, MYL2, MYL3, MYLIP, MYLK, MYLK2, MYO15A, MYO18B, MYO1A, MYO1C, MYO1E, MYO1F, MYO3A, MYO5A, MYO5B, MYO6, MYO7A, MYO7B, MYO9B, MYOC, MYOCD, MYOM1, MYOT, MYOZ2, MYPN, MYT1, MYT1L, NAA10, NAGA, NAGLU, NAGPA, NAGS, NAIP, NAMPT, NAPRT1, NARS2, NAT1, NAT2, NAT8L, NAV2, NBAS, NBEA, NBEAL2, NBN, NBPF1, NCALD, NCAM1, NCAN, NCAPD2, NCF1, NCF2, NCF4, NCKAP1, NCOA1, NCOA3, NCR3, NCS1, NCSTN, NDE1, NDN, NDOR1, NDP, NDRG1, NDST1, NDUFA1, NDUFA10, NDUFA11, NDUFA12, NDUFA13, NDUFA2, NDUFA4, NDUFA6, NDUFA7, NDUFA8, NDUFA9, NDUFAF1, NDUFAF2, NDUFAF3, NDUFAF4, NDUFAF5, NDUFAF6, NDUFAF7, NDUFB1, NDUFB3, NDUFB6, NDUFB9, NDUFC2, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS5, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV2, NDUFV3, NEB, NEBL, NEDD4L, NEDD9, NEFH, NEFL, NEFM, NEGR1, NEIL1, NEIL2, NEK1, NEK8, NELFA, NELL1, NEU1, NEU2, NEUROD1, NEUROG3, NEXN, NF1, NF2, NFATC4, NFE2L2, NFIA, NFIX, NFKB1, NFKBIA, NFKBIL1, NFU1, NGF, NGFR, NHEJ1, NHLRC1, NHP2, NHS, NID1, NINJ1, NIPA1, NIPAL4, NIPBL, NIPSNAP1, NIPSNAP3A, NKAIN2, NKX2-1, NKX2-3, NKX2-5, NKX2-6, NKX3-1, NKX3-2, NLGN1, NLGN2, NLGN3, NLGN4X, NLGN4Y, NLRP1, NLRP12, NLRP14, NLRP2, NLRP3, NLRP7, NLRX1, NMB, NME1, NME8, NMNAT1, NMT2, NMU, NOBOX, NOD1, NOD2, NODAL, NOG, NOP10, NOP56, NOS1, NOS1AP, NOS2, NOS3, NOTCH1, NOTCH2, NOTCH3, NOTCH4, NPAP1, NPAS2, NPAS3, NPAT, NPC1, NPC1L1, NPC2, NPFFR2, NPHP1, NPHP3, NPHP4, NPHS1, NPHS2, NPL, NPM1, NPPA, NPPB, NPPC, NPR1, NPR2, NPR3, NPSR1, NPTN, NPY, NPY1R, NPY2R, NQO1, NQO2, NR0B1, NR0B2, NR1H2, NR1H3, NR1H4, NR1I2, NR1I3, NR2E1, NR2E3, NR2F1, NR3C1, NR3C2, NR4A2, NR5A1, NRAS, NRG1, NRG3, NRIP1, NRL, NRP2, NRTN, NRXN1, NRXN2, NRXN3, NSD1, NSDHL, NSMF, NSUN2, NSUN7, NT5C1B, NT5C3A, NT5E, NTF3, NTF4, NTHL1, NTNG1, NTRK1, NTRK2, NTRK3, NUAK1, NUBPL, NUDC, NUDT1, NUDT6, NUMBL, NUP155, NUP62, NXF3, NXF5, NXNL1, NYX, OAS1, OAS2, OAT, OAZ1, OBSCN, OBSL1, OCA2, OCLN, OCRL, ODC1, OFD1, OGG1, OLFM2, OLR1, OMG, OPA1, OPA3, OPCML, OPHN1, OPN1LW, OPN1MW, OPN1SW, OPN4, OPRD1, OPRK1, OPRL1, OPRM1, OPTC, OPTN, OR13G1, OR7D4, ORAI1, ORC1, ORC4, ORC6, ORMDL3, OSMR, OSR1, OSTM1, OTC, OTOA, OTOF, OTOR, OTX2, OVGP1, OXCT1, OXTR, P2RX1, P2RX4, P2RX5, P2RX7, P2RY11, P2RY12, P2RY4, PABPC4L, PABPN1, PACRG, PAFAH1B1, PAFAH1B3, PAH, PAK3, PAK7, PALB2, PALLD, PANK2, PAPD7, PAPSS2, PARD3B, PARD6A, PARK2, PARK7, PARL, PARP1, PARP2, PASK, PAWR, PAX1, PAX2, PAX3, PAX4, PAX5, PAX6, PAX7, PAX8, PAX9, PC, PCBD1, PCCA, PCCB, PCDH11X, PCDH15, PCDH18, PCDH19, PCDH9, PCDHA10, PCDHA13, PCDHB4, PCK1, PCK2, PCM1, PCMT1, PCNT, PCOLCE, PCSK1, PCSK2, PCSK9, PDCD1, PDCD10, PDCD5, PDE10A, PDE11A, PDE4B, PDE4D, PDE6A, PDE6B, PDE6C, PDE6G, PDE6H, PDE7B, PDE8B, PDGFB, PDGFC, PDGFRA, PDHA1, PDHB, PDHX, PDLIM3, PDLIM5, PDP1, PDPK1, PDSS1, PDSS2, PDX1, PDXK, PDYN, PDZD7, PEAR1, PECAM1, PECR, PEMT, PENK, PEPD, PER1, PER2, PER3, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PFAS, PFKM, PFN1, PGAM1, PGAM2, PGAM5, PGBD1, PGC, PGD, PGK1, PGM1, PGR, PGRMC1, PHB, PHEX, PHF11, PHF2, PHF3, PHF6, PHF8, PHGDH, PHIP, PHKA1, PHKA2, PHKB, PHKG2, PHLDA2, PHLPP2, PHOX2A, PHOX2B, PHYH, PI3, PICALM, PICK1, PIEZO2, PIF1, PIGA, PIGL, PIGM, PIGN, PIGO, PIGR, PIGV, PIK3C2G, PIK3C3, PIK3CA, PIK3CB, PIK3CD, PIK3CG, PIK3R1, PIK3R2, PIK3R4, PIK3R5, PIKFYVE, PIN1, PINK1, PIP4K2A, PIP5K1B, PIP5K1C, PITPNM3, PITX1, PITX2, PITX3, PIWIL3, PKD1, PKD1L1, PKD2, PKHD1, PKLR, PKM, PKN3, PKP1, PKP2, PLA2G10, PLA2G2A, PLA2G2D, PLA2G4A, PLA2G4C, PLA2G5, PLA2G6, PLA2G7, PLAGL1, PLAT, PLAU, PLAUR, PLCB1, PLCB4, PLCD1, PLCE1, PLCG2, PLCZ1, PLD2, PLEC, PLEKHG4, PLEKHG5, PLEKHM1, PLG, PLIN1, PLIN4, PLN, PLOD1, PLOD2, PLOD3, PLP1, PLP2, PLTP, PLXND1, PMAIP1, PML, PMM2, PMP22, PMPCA, PMS1, PMS2, PMS2P3, PNKD, PNKP, PNMT, PNP, PNPLA1, PNPLA2, PNPLA3, PNPLA6, PNPO, POF1B, POGZ, POLB, POLD1, POLE2, POLG, POLG2, POLH, POLL, POLR1C, POLR1D, POLR2E, POLR2M, POLR3A, POLR3B, POLRMT, POMC, POMGNT1, POMGNT2, POMP, POMT1, POMT2, PON1, PON2, PON3, POP1, POR, PORCN, POU1F1, POU3F4, POU4F3, POU5F1, POU5F1B, POU6F2, PPARA, PPARD, PPARG, PPARGC1A, PPARGC1B, PPAT, PPIA, PPIB, PPIG, PPM1D, PPOX, PPP1R1A, PPP1R3A, PPP1R3C, PPP2R1A, PPP2R1B, PPP2R2B, PPP2R2C, PPT1, PQBP1, PRB1, PRB3, PRB4, PRCD, PRCP, PRDM2, PRDM5, PRDM9, PREPL, PRF1, PRG4, PRICKLE1, PRICKLE2, PRKAA2, PRKACA, PRKAG2, PRKAG3, PRKAR1A, PRKCB, PRKCG, PRKCH, PRKCSH, PRKD3, PRKDC, PRKRA, PRL, PRLHR, PRLR, PRM1, PRM2, PRMT10, PRMT3, PRMT7, PRND, PRNP, PROC, PROCR, PRODH, PROK1, PROK2, PROKR1, PROKR2, PROM1, PROP1, PROS1, PROZ, PRPF3, PRPF31, PRPF6, PRPF8, PRPH, PRPH2, PRPS1, PRRC2A, PRRT2, PRRX1, PRSS1, PRSS12, PRSS2, PRSS3P2, PRSS56, PRSS8, PRX, PRY, PRY2, PSAP, PSAT1, PSCA, PSEN1, PSEN2, PSENEN, PSMA6, PSMB8, PSMB9, PSMC3IP, PSMD7, PSPH, PSPN, PSTPIP1, PTAFR, PTCD1, PTCH1, PTCH2, PTCHD1, PTCHD3, PTCSC3, PTEN, PTF1A, PTGDR, PTGDR2, PTGDS, PTGER2, PTGER4, PTGES2, PTGIR, PTGIS, PTGS1, PTGS2, PTH, PTH1R, PTHLH, PTK7, PTPN1, PTPN11, PTPN13, PTPN14, PTPN2, PTPN21, PTPN22, PTPN6, PTPRB, PTPRC, PTPRCAP, PTPRD, PTPRF, PTPRJ, PTPRK, PTPRO, PTPRQ, PTPRT, PTRF, PTS, PUS1, PVR, PVRL1, PVRL3, PVRL4, PVT1, PWRN1, PXDN, PYCR1, PYCRL, PYGL, PYGM, PYY, PZP, QDPR, QKI, RAB11FIP5, RAB18, RAB23, RAB27A, RAB28, RAB2A, RAB39B, RAB3GAP1, RAB3GAP2, RAB40AL, RAB7A, RAB7L1, RABGGTA, RABL6, RAC1, RAC2, RAD21, RAD21L1, RAD23B, RAD50, RAD51, RAD51C, RAD51D, RAD52, RAD54B, RAD54L, RAD9A, RAET1L, RAF1, RAG1, RAG2, RAI1, RALGAPA1, RALGDS, RANBP2, RANGRF, RAPSN, RARS2, RASA1, RASGRP2, RASSF1, RAX, RAX2, RB1, RB1CC1, RBBP8, RBFOX1, RBM10, RBM15, RBM20, RBM28, RBM8A, RBMXL2, RBMY1A1, RBP3, RBP4, RCAN1, RD3, RDH12, RDH5, RDX, RECQL4, REEP1, RELN, REN, REPS2, RET, RETN, REV3L, RFC2, RFT1, RFWD2, RFX2, RFX5, RFX6, RFX8, RFXANK, RFXAP, RGMA, RGR, RGS2, RGS6, RGS7, RGS9, RGS9BP, RHAG, RHBDF2, RHCE, RHD, RHO, RHOB, RHOG, RHPN2, RIMS1, RIMS3, RIN2, RIPK3, RIPK4, RLBP1, RMI1, RMRP, RNASE3, RNASEH2A, RNASEH2B, RNASEH2C, RNASEL, RNASET2, RNF113A, RNF114, RNF135, RNF139, RNF168, RNF170, RNF213, RNLS, RNU4ATAC, ROBO1, ROBO2, ROBO3, ROCK1, ROCK2, ROGDI, ROM1, ROPN1L, ROR2, RORA, ROS1, RP1, RP1L1, RP2, RP9, RPA1, RPA4, RPE65, RPGR, RPGRIP1, RPGRIP1L, RPH3AL, RPIA, RPL10, RPL11, RPL21, RPL35A, RPL36, RPL5, RPN2, RPS10, RPS15, RPS17, RPS19, RPS24, RPS26, RPS27A, RPS3, RPS4Y2, RPS6KA3, RPS6KB1, RPS6KL1, RPS7, RPTOR, RRH, RRM1, RRM2B, RRP1B, RS1, RSPH4A, RSPH9, RSPO1, RSPO4, RSRC1, RTN2, RTN4R, RUNX1, RUNX2, RUNX3, RUVBL1, RXFP2, RXRG, RYK, RYR1, RYR2, RYR3, S100A11P1, S100B, S1PR1, SAA1, SAA2, SACS, SAG, SAGE1, SALL1, SALL4, SAMD9, SAMHD1, SAR1B, SARDH, SARS2, SART1, SART3, SAT1, SATB2, SATL1, SBDS, SBF2, SBNO1, SCAP, SCARB1, SCARB2, SCARF2, SCG2, SCG3, SCGB1A1, SCGB1D2, SCGB3A2, SCN10A, SCN1A, SCN1B, SCN2A, SCN2B, SCN3A, SCN3B, SCN4A, SCN4B, SCN5A, SCN8A, SCN9A, SCNN1A, SCNN1B, SCNN1G, SCO1, SCO2, SCP2, SCRIB, SCT, SCUBE2, SDC3, SDCCAG8, SDHA, SDHAF1, SDHAF2, SDHB, SDHC, SDHD, SEC23A, SEC23B, SEC63, SECISBP2, SEL1L, SELE, SELL, SELP, SELPLG, SEMA3A, SEMA3E, SEMA4A, SEMA4C, SEMA4G, SEMA6D, SEMG1, SEP15, SEPN1, SEPP1, SEPSECS, SEPT12, SEPT9, SERPINA1, SERPINA10, SERPINA3, SERPINA6, SERPINA7, SERPINB11, SERPINB3, SERPINB5, SERPINB6, SERPINC1, SERPIND1, SERPINE1, SERPINF1, SERPINF2, SERPING1, SERPINH1, SERPINI1, SERPINI2, SERTAD1, SESN2, SETBP1, SETD2, SETD8, SETDB2, SETX, SEZ6, SEZ6L2, SF3B4, SFTPA1, SFTPA2, SFTPB, SFTPC, SFTPD, SGCA, SGCB, SGCD, SGCE, SGCG, SGK1, SGK110, SGK223, SGSH, SH2B1, SH2B3, SH2D1A, SH3BP2, SH3GL1, SH3PXD2B, SH3TC2, SHANK2, SHANK3, SHBG, SHFM1, SHH, SHMT1, SHOC2, SHOX, SHROOM3, SHROOM4, SI, SIAE, SIGLEC12, SIGLEC14, SIGLEC16, SIGMAR1, SIL1, SIM1, SIPA1, SIRT1, SIRT3, SIRT5, SIX1, SIX2, SIX3, SIX5, SIX6, SKI, SKIV2L, SLBP, SLC10A1, SLC10A2, SLC11A1, SLC11A2, SLC12A1, SLC12A3, SLC12A6, SLC13A2, SLC14A1, SLC14A2, SLC15A1, SLC16A1, SLC16A12, SLC16A2, SLC16A3, SLC17A1, SLC17A3, SLC17A5, SLC17A8, SLC18A1, SLC19A1, SLC19A2, SLC19A3, SLC1A1, SLC1A2, SLC1A3, SLC20A2, SLC22A1, SLC22A11, SLC22A12, SLC22A14, SLC22A2, SLC22A3, SLC22A4, SLC22A5, SLC22A6, SLC22A9, SLC23A2, SLC24A1, SLC24A2, SLC24A5, SLC25A12, SLC25A13, SLC25A15, SLC25A19, SLC25A20, SLC25A22, SLC25A3, SLC25A38, SLC25A39, SLC25A4, SLC26A1, SLC26A10, SLC26A2, SLC26A3, SLC26A4, SLC26A5, SLC26A6, SLC26A9, SLC27A4, SLC27A5, SLC28A1, SLC28A2, SLC28A3, SLC29A1, SLC29A2, SLC29A3, SLC29A4, SLC2A1, SLC2A10, SLC2A2, SLC2A4, SLC2A9, SLC30A10, SLC30A2, SLC30A5, SLC30A8, SLC31A1, SLC33A1, SLC34A1, SLC34A2, SLC34A3, SLC35A1, SLC35C1, SLC35D1, SLC35G2, SLC36A2, SLC37A4, SLC39A13, SLC39A4, SLC3A1, SLC40A1, SLC41A1, SLC44A2, SLC45A2, SLC46A1, SLC47A1, SLC47A2, SLC4A1, SLC4A10, SLC4A11, SLC4A3, SLC4A4, SLC52A1, SLC52A3, SLC5A1, SLC5A11, SLC5A2, SLC5A5, SLC5A7, SLC6A1, SLC6A11, SLC6A12, SLC6A13, SLC6A14, SLC6A18, SLC6A19, SLC6A2, SLC6A20, SLC6A3, SLC6A4, SLC6A5, SLC6A8, SLC7A1, SLC7A10, SLC7A2, SLC7A5, SLC7A7, SLC7A9, SLC8A1, SLC9A3R1, SLC9A6, SLC9A9, SLCO1A2, SLCO1B1, SLCO1B3, SLCO1C1, SLCO2A1, SLCO2B1, SLFN5, SLIT3, SLITRK1, SLURP1, SLX4, SMAD1, SMAD2, SMAD3, SMAD4, SMAD6, SMAD7, SMAD9, SMARCA2, SMARCA4, SMARCAD1, SMARCAL1, SMARCB1, SMARCE1, SMC1A, SMC1B, SMC3, SMG1, SMG6, SMN1, SMN2, SMNDC1, SMOC1, SMOC2, SMPD1, SMPX, SMS, SMUG1, SMYD3, SNAI2, SNAP29, SNAPC4, SNAPC5, SNCA, SNCAIP, SNCB, SNIP1, SNORD115-1, SNORD116, SNORD116-1, SNORD50A, SNRK, SNRNP200, SNRPN, SNTA1, SNTG2, SNURF, SNURF-SNRPN, SNX10, SNX19, SNX3, SOBP, SOCS1, SOCS3, SOD1, SOD2, SOD3, SOGA3, SOHLH1, SORBS1, SORCS1, SORL1, SORT1, SOS1, SOST, SOX10, SOX17, SOX18, SOX2, SOX3, SOX5, SOX6, SOX8, SOX9, SP100, SP110, SP7, SP8, SPAG16, SPAG17, SPANXN5, SPAST, SPATA13, SPATA16, SPATA21, SPATA31C1, SPATA7, SPECC1L, SPG11, SPG20, SPG21, SPG7, SPI1, SPINK1, SPINK5, SPINT2, SPP1, SPR, SPRED1, SPRN, SPRR3, SPRY2, SPRY3, SPTA1, SPTAN1, SPTB, SPTBN2, SPTBN5, SPTLC1, SPTLC2, SQSTM1, SRC, SRCAP, SRD5A2, SRD5A3, SREBF1, SREBF2, SREK1, SRGAP2, SRGAP3, SRI, SRP72, SRPX, SRPX2, SRR, SRY, SSH1, SST, SSTR2, SSTR5, SSX7, ST14, ST3GAL3, ST3GAL5, ST5, ST7, ST8SIA2, STAR, STAT1, STAT3, STAT5B, STAT6, STEAP3, STEAP4, STH, STIL, STIM1, STK10, STK11, STK19, STK3, STK32A, STK33, STK39, STK4, STMN1, STOX1, STRA6, STRADA, STRC, STS, STX11, STX16, STX1A, STXBP1, STXBP2, STXBP5, SUCLA2, SUCLG1, SUFU, SULF1, SULT1A1, SULT1A3, SULT1C4, SULT1E1, SULT2A1, SULT2B1, SULT4A1, SUMF1, SUMO1, SUMO4, SUN2, SUOX, SUPT16H, SURF1, SUV420H1, SV2B, SYCP3, SYN1, SYN3, SYNE1, SYNE2, SYNGAP1, SYNGR1, SYNM, SYNPO, SYP, SYT11, SYT14, SYT2, SYTL3, SYTL5, T, TAAR6, TAAR9, TAB2, TAC3, TACO1, TACR3, TACSTD2, TAF1, TAF15, TAF1C, TAF1L, TAF2, TAF7L, TAL1, TALDO1, TAP1, TAP2, TAPBP, TARDBP, TAS1R1, TAS1R2, TAS1R3, TAS2R16, TAS2R19, TAS2R3, TAS2R38, TAS2R43, TAS2R46, TAS2R50, TAS2R9, TAT, TAZ, TBC1D1, TBC1D23, TBC1D24, TBC1D4, TBCE, TBK1, TBL1X, TBL1XR1, TBL1Y, TBP, TBX1, TBX10, TBX15, TBX19, TBX2, TBX20, TBX21, TBX22, TBX3, TBX4, TBX5, TBX6, TBXA2R, TBXAS1, TCAP, TCF21, TCF4, TCF7, TCF7L1, TCF7L2, TCIRG1, TCN1, TCN2, TCOF1, TCP1, TCTE1, TCTE3, TCTN1, TCTN2, TDGF1, TDO2, TDP1, TDRD7, TEAD1, TECR, TECTA, TEK, TEKT2, TENM4, TEP1, TERC, TERT, TET1, TEX14, TF, TFAM, TFAP2A, TFAP2B, TFB1M, TFCP2, TFF1, TFPI, TFR2, TFRC, TG, TGFB1, TGFB2, TGFB3, TGFBI, TGFBR1, TGFBR2, TGFBR3, TGFBRAP1, TGIF1, TGM1, TGM2, TGM5, TGM6, TH, THADA, THAP1, THBD, THBS1, THBS2, THBS4, THPO, THRA, THRB, THSD7A, TICAM1, TIMM44, TIMM8A, TIMP1, TIMP2, TIMP3, TINAG, TINF2, TIRAP, TJP2, TK2, TLK1, TLL1, TLR1, TLR10, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TM4SF19, TMC1, TMC6, TMC8, TMCO1, TMEM114, TMEM126A, TMEM127, TMEM135, TMEM138, TMEM165, TMEM173, TMEM185A, TMEM187, TMEM2, TMEM216, TMEM237, TMEM39A, TMEM43, TMEM67, TMEM70, TMEM8A, TMEM9, TMIE, TMLHE, TMPO, TMPRSS11A, TMPRSS15, TMPRSS3, TMPRSS4, TMPRSS5, TMPRSS6, TNC, TNF, TNFAIP2, TNFAIP3, TNFRSF10A, TNFRSF10B, TNFRSF11A, TNFRSF11B, TNFRSF13B, TNFRSF13C, TNFRSF1A, TNFRSF1B, TNFRSF25, TNFRSF4, TNFSF10, TNFSF11, TNFSF13B, TNFSF14, TNFSF15, TNFSF4, TNFSF8, TNKS, TNNC1, TNNI2, TNNI3, TNNI3K, TNNT1, TNNT2, TNNT3, TNP1, TNR, TNS3, TNXB, TOMM40, TOP1MT, TOPBP1, TOPORS, TOR1A, TOX3, TP53, TP53AIP1, TP53BP1, TP53I3, TP53RK, TP63, TP73, TPCN2, TPH1, TPH2, TPI1, TPK1, TPM1, TPM2, TPM3, TPMT, TPO, TPP1, TPP2, TPRN, TPSB2, TPTE, TRAC, TRADD, TRAF3, TRAF3IP1, TRAF3IP2, TRAF6, TRAK2, TRAPPC10, TRAPPC2, TRAPPC9, TRB, TRBV9, TRDN, TREM2, TRERF1, TREX1, TRHR, TRIB1, TRIB3, TRIL, TRIM17, TRIM21, TRIM22, TRIM32, TRIM37, TRIM5, TRIO, TRIOBP, TRIP11, TRIP12, TRMT1, TRMU, TRNAD1, TROAP, TROVE2, TRPA1, TRPC3, TRPC4, TRPC5, TRPC6, TRPM1, TRPM2, TRPM3, TRPM4, TRPM6, TRPM7, TRPS1, TRPV1, TRPV3, TRPV4, TRPV5, TRRAP, TSC1, TSC2, TSEN2, TSEN34, TSEN54, TSFM, TSHB, TSHR, TSHZ1, TSLP, TSPAN12, TSPAN17, TSPAN7, TSPO, TSPYL1, TSSC4, TSSK2, TSSK3, TSSK4, TST, TTBK2, TTC19, TTC21B, TTC37, TTC8, TTI2, TTLL11, TTN, TTPA, TTR, TTTY13, TUBA1A, TUBA8, TUBB1, TUBB2B, TUBB3, TUBGCP4, TUBGCP5, TUBGCP6, TUFM, TULP1, TULP3, TUSC3, TWIST1, TWIST2, TXN2, TXNRD2, TYK2, TYMP, TYMS, TYR, TYROBP, TYRP1, UBA1, UBA3, UBAC2, UBD, UBE2A, UBE2B, UBE2I, UBE2NL, UBE3A, UBE3C, UBIAD1, UBN2, UBQLN2, UBR1, UBR3, UBR7, UCHL1, UCP1, UCP2, UCP3, UFD1L, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT2A1, UGT2A3, UGT2B10, UGT2B15, UGT2B17, UGT2B28, UGT2B7, UHRF1BP1, UIMC1, UMOD, UMPS, UNC119, UNC13D, UNC5C, UNC5CL, UNC80, UNC93A, UNC93B1, UNG, UNKL, UPB1, UPF3B, UPK3A, UQCRB, UQCRQ, UROC1, UROD, UROS, USB1, USF1, USH1C, USH1G, USH2A, USP15, USP24, USP26, USP46, USP7, USP9X, USP9Y, UTF1, UTRN, UTS2, UVSSA, VAMP7, VANGL1, VANGL2, VAPB, VAX1, VCAM1, VCAN, VCL, VCP, VCX3A, VCY, VDR, VEGFA, VHL, VIM, VIMP, VIP, VIPAS39, VIPR2, VKORC1, VLDLR, VMA21, VNN1, VPREB1, VPS13A, VPS13B, VPS33B, VPS35, VRK1, VSIG4, VSX1, VSX2, VTN, VWF, WAS, WASF3, WDFY3, WDFY4, WDPCP, WDR11, WDR13, WDR19, WDR35, WDR36, WDR4, WDR45, WDR45B, WDR62, WDR65, WDR72, WDR81, WFS1, WHSC1, WIPF1, WISP3, WNK1, WNK4, WNT10A, WNT10B, WNT3, WNT4, WNT5A, WNT5B, WNT7A, WRAP53, WRN, WT1, WT1-AS, WWC1, WWOX, XBP1, XDH, XIAP, XIST, XK, XKR4, XKRY, XPA, XPC, XPNPEP2, XPNPEP3, XRCC1, XRCC2, XRCC3, XRCC4, XRCC5, XRCC6, XYLT1, XYLT2, YAP1, YARS, YARS2, YBX2, YTHDF2, YWHAE, YY1, ZAN, ZAP70, ZBTB16, ZBTB18, ZBTB24, ZBTB40, ZBTB41, ZC3H14, ZC3H3, ZC3HAV1, ZCCHC12, ZCCHC13, ZCCHC8, ZDHHC15, ZDHHC8, ZDHHC9, ZEB1, ZEB2, ZFAT, ZFHX3, ZFHX4, ZFP36, ZFP36L1, ZFP57, ZFP90, ZFPM2, ZFY, ZFYVE26, ZFYVE27, ZHX3, ZIC1, ZIC2, ZIC3, ZMPSTE24, ZMYND11, ZNF202, ZNF213, ZNF224, ZNF24, ZNF335, ZNF350, ZNF365, ZNF385B, ZNF41, ZNF469, ZNF480, ZNF507, ZNF513, ZNF526, ZNF592, ZNF627, ZNF644, ZNF674, ZNF711, ZNF750, ZNF75D, ZNF80, ZNF804A, ZNF81, ZNHIT6, ZNRF1, ZPBP, ZPBP.