Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "E"
371 to 380 of 465 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

371
Endogenous retrovirus group 48 member 1, envelope
C21orf105, HERV-Fb1, NDUFV3-AS1, SUPYN
Schizophrenia

372
Endogenous retrovirus group W member 1, envelope
ENV, ENVW, ERVWE1, HERV-7q, HERV-W-ENV, HERV7Q, HERVW, HERVWENV
Bipolar disorder, Color vision deficiency, Respiratory system disease, Schizophrenia

373
Endothelial cell adhesion molecule
NEDIHSS, W117m
Neurodevelopmental disorder, Schizophrenia

374
Establishment of sister chromatid cohesion N-acetyltransferase 2
2410004I17Rik, EFO2, EFO2p, JHS, RBS, hEFO2
Cleft lip/palate with abnormal thumbs and microcephaly, Desbuquois syndrome, Kidney neoplasms, Roberts syndrome, Roberts-sc phocomelia syndrome

375
Esterase D
FGH
Hypoxia, Osteoarthritis

376
ESF1 nucleolar pre-rRNA processing protein
ABTAP, C20orf6, HDCMC28P, bA526K24.1
Lung cancer

377
Endothelial cell specific molecule 1
endocan
Hepatocellular carcinoma, Liver neoplasms, Squamous cell carcinoma

378
Extra spindle pole bodies like 1, separase
ESP1, SEPA
Adenoid cystic carcinoma, Transitional cell carcinoma, Salivary gland neoplasms, Urinary bladder neoplasms

379
Espin
DFNB36, LP2654, USH1M
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing loss, Hereditary hearing loss, Multiple sclerosis, Optic atrophy, Retinitis pigmentosa, Usher syndrome, Vestibular disease

380
Espin like
-
Alzheimer disease, Eosinophilia