Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3911 to 3920 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3911
Epithelial cell transforming 2 like
ARHGEF32, C6orf91, FBXO49, LFDH, dJ509I19.2, dJ509I19.3, dJ509I19.5
Colorectal cancer, Endometrial neoplasms, Scoliosis, Diabetes mellitus type 2

3912
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

3913
Ectodysplasin A2 receptor
EDA-A2R, EDAA2R, TNFRSF27, XEDAR
Christ-siemens-touraine syndrome, Hypogonadism, X-linked hypohidrotic ectodermal dysplasia

3914
Ectodysplasin A receptor
DL, ECTD10A, ECTD10B, ED1R, ED3, ED5, EDA-A1R, EDA1R, EDA3, HRM1
Alzheimer disease, Androgenetic alopecia, Hypohidrotic ectodermal dysplasia, Christ-siemens-touraine syndrome, Ectodermal dysplasia, Mitochondrial dna depletion syndrome

3915
EDAR associated via death domain
CR, ECTD11A, ECTD11B, ED3, EDA3
Autoimmune thyroid disease, Hypohidrotic ectodermal dysplasia, Christ-siemens-touraine syndrome, Ectodermal dysplasia, Hypothyroidism, Insomnia, Tooth agenesis, Upper aerodigestive tract neoplasm

3916
Enhancer of mRNA decapping 3
LSM16, MRT50, YJDC, YJEFN2, hYjeF_N2-15q23
Nonsyndromic intellectual disability, Hyperopia, Intellectual developmental disorder, Squamous cell carcinoma

3917
Enhancer of mRNA decapping 4
GE1, Ge-1, HEDL5, HEDLS, RCD-8, RCD8
Metabolic syndrome, Diabetes mellitus type 2

3918
Epididymal protein 13
-
Pancreatic cancer

3919
Epididymal protein 3A
EP3A, FAM12A, HE3-ALPHA, HE3A, HE3ALPHA, RAM1
Hypertension

3920
Epididymal protein 3B
EP3B, FAM12B, HE3-BETA, HE3B, RAM2
Hypertension