Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4301 to 4310 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4301
ETS variant transcription factor 3 like
-
Multiple sclerosis

4302
ETS variant transcription factor 4
E1A-F, E1AF, PEA3, PEAS3
Alzheimer disease, Breast neoplasms, Congenital anomalies of the kidney and urinary tract, Prostatic neoplasms, Skeletal ewing sarcoma

4303
ETS variant transcription factor 5
ERM
Bipolar disorder, Hyperuricemia, Major depressive disorder, Obesity, Obstructive sleep apnea syndrome, Osteoarthritis, Prostatic neoplasms, Sleep apnea, Diabetes mellitus type 2

4304
ETS variant transcription factor 6
TEL, TEL/ABL, THC5
Myeloid leukemia, Juvenile arthritis, Asthma, Thrombocytopenia with normal platelets, B-lymphoblastic leukemia/lymphoma, Myelomonocytic leukemia, Colorectal cancer, Congenital mesoblastic nephroma, Connective tissue disease, Differentiated thyroid carcinoma, Endometriosis, Hematologic neoplasms, Juvenile idiopathic arthritis, Major depressive disorder, Migraine
View all (9 more)

4305
ETS variant transcription factor 7
TEL-2, TEL2, TELB
Multiple sclerosis, Systemic lupus erythematosus

4306
Eva-1 homolog A, regulator of programmed cell death
FAM176A, TMEM166
Alzheimer disease, Gout, Large artery stroke, Obesity

4307
Eva-1 homolog B
C1orf78, FAM176B
Diabetes mellitus type 2

4308
Eva-1 homolog C
B18, B19, C21orf63, C21orf64, FAM176C, PRED34, SUE21
Cerebral amyloid angiopathy, Hepatocellular carcinoma, Neuroblastoma

4309
EvC ciliary complex subunit 1
DWF-1, EVC1, EVCL
Acrofacial dysostosis, Curry-hall syndrome, Desbuquois syndrome, Ellis-van creveld syndrome, Majewski syndrome, Nephronophthisis, Osteonecrosis, Prostate cancer, Ventricular septal defect, Weyers acrofacial dysostosis

4310
EvC ciliary complex subunit 2
LBN, WAD
Acrofacial dysostosis, Curry-hall syndrome, Desbuquois syndrome, Ellis-van creveld syndrome, Jeune thoracic dystrophy, Majewski syndrome, Meckel-gruber syndrome, Myopathy, Short rib dysplasia-polydactyly syndrome, Tooth agenesis, Weyers acrofacial dysostosis