Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3921 to 3930 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3921
Enoyl-CoA hydratase domain containing 3
-
Alzheimer disease, Androgenetic alopecia, Breast cancer, Color vision deficiency, Dementia, Estrogen-receptor negative breast cancer, Lewy body disease, Obesity

3922
Enoyl-CoA hydratase, short chain 1
ECHS1D, SCEH, mECH, mECH1
Leigh syndrome, Obesity, Stomach neoplasms

3923
Extracellular matrix protein 1
URBWD
Autism, Hepatocellular carcinoma, Ulcerative colitis, Stomach neoplasms

3924
Extracellular matrix protein 2
-
Kidney disease, Obstructive sleep apnea syndrome

3925
Ecm29 proteasome adaptor and scaffold
ECM29, KIAA0368
Anxiety disorder, Dry eye syndrome, Squamous cell carcinoma

3926
ECRG4 augurin precursor
C2orf40
Alzheimer disease, Cerebral amyloid angiopathy, Dementia, Esophageal cancer, Gastric cancer, Osteoarthritis

3927
Epithelial cell transforming 2
ARHGEF31
Hepatocellular carcinoma, Liver cirrhosis, Obesity

3928
Epithelial cell transforming 2 like
ARHGEF32, C6orf91, FBXO49, LFDH, dJ509I19.2, dJ509I19.3, dJ509I19.5
Colorectal cancer, Endometrial neoplasms, Scoliosis, Diabetes mellitus type 2

3929
Ectodysplasin A
ECTD1, ED1, ED1-A1, ED1-A2, EDA-A1, EDA-A2, EDA1, EDA2, HED, HED1, ODT1, STHAGX1, TNLG7C, XHED, XLHED
Androgenetic alopecia, Anhidrotic ectodermal dysplasia, Christ-siemens-touraine syndrome, Craniofrontonasal dysplasia, Tooth agenesis, Ectodermal dysplasia, Melanoma, Neurotic disorder, X-linked hypohidrotic ectodermal dysplasia

3930
Ectodysplasin A2 receptor
EDA-A2R, EDAA2R, TNFRSF27, XEDAR
Christ-siemens-touraine syndrome, Hypogonadism, X-linked hypohidrotic ectodermal dysplasia