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
4001 to 4010 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4001
Early growth response 3
EGR-3, PILOT
Ataxia, Bipolar disorder, Cataract, Color vision deficiency, Major depressive disorder, Otosclerosis, Post-traumatic stress disorder, Schizophrenia

4002
Early growth response 4
AT133, NGFI-C, NGFIC, PAT133
Schizophrenia

4003
EH domain binding protein 1
HPC12, NACSIN
Androgenetic alopecia, Obstructive pulmonary disease, Colorectal cancer, Coronary artery disease, Essential tremor, Hemorrhoid, Major depressive disorder, Metabolic syndrome, Myocardial infarction, Neurotic disorder, Prostate cancer, Prostatic neoplasms, Schizophrenia, Diabetes mellitus type 2, Vesicoureteral reflux

4004
EH domain binding protein 1 like 1
-
Breast cancer, Liver cirrhosis, Coronary artery disease, Non-immune hydrops fetalis, Migraine, Myocardial infarction, Nonalcoholic fatty liver disease, Osteoarthritis, Diabetes mellitus type 2

4005
EH domain containing 1
H-PAST, HPAST1, PAST, PAST1
Glioma, Hyperuricemia

4006
EH domain containing 3
PAST3
Androgenetic alopecia, Hepatocellular carcinoma, Myeloid leukemia, Major depressive disorder, Depression

4007
EH domain containing 4
PAST4
Progressive supranuclear palsy, Diabetes mellitus type 2

4008
ETS homologous factor
ESE3, ESE3B, ESEJ
Cholecystitis, Cholecystolithiasis, Obstructive pulmonary disease, Cystic fibrosis, Lung disease, Obesity, Prostate cancer, Prostatic neoplasms, Psychiatric disorders, Systemic lupus erythematosus, Systemic sclerosis, Diabetes mellitus type 2

4009
Enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase
ECHD, FRTS3, L-PBE, LBFP, LBP, MFE1, PBFE
Alzheimer disease, Bifunctional enzyme deficiency, Bipolar disorder, Kidney disease, De toni-debre-fanconi syndrome, Fanconi renotubular syndrome, Fanconi syndrome, Insomnia, Prostatic neoplasms

4010
Euchromatic histone lysine methyltransferase 1
EHMT1-IT1, EUHMTASE1, Eu-HMTase1, FP13812, GLP, GLP1, KLEFS1, KMT1D
Asthma, Eczema, Atrial fibrillation, Autism, Global developmental delay, Intellectual developmental disorder, Kleefstra syndrome, Medulloblastoma, Metabolic syndrome, Migraine, Neurodevelopmental disorder, Polymicrogyria, Schizophrenia, Tetralogy of fallot, Diabetes mellitus type 2