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 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3911
Epstein-Barr virus induced 3
IL-27B, IL27B, IL35B
Autism, Stomach neoplasms

3912
Endogenous Bornavirus like nucleoprotein 1
EBLN-1
Atrial fibrillation, B-cell acute lymphoblastic leukemia, Breast cancer, Crohn disease, Inflammatory bowel disease, Multiple sclerosis, Biliary cholangitis

3913
EBNA1 binding protein 2
EBP2, NOBP, P40
Bipolar disorder, Schizophrenia, Diabetes mellitus type 1, Diabetes mellitus type 2

3914
EBP cholestenol delta-isomerase
CDPX2, CHO2, CPX, CPXD, MEND
Chondrodysplasia, Connective tissue disease, Desbuquois syndrome, X-linked chondrodysplasia punctata, X-linked dominant chondrodysplasia punctata

3915
EBP like
EBRP
Atrial fibrillation, Hypertension

3916
Endothelin converting enzyme 1
ECE
Alzheimer disease, Androgenetic alopecia, Autonomic nervous system disease, Breast cancer, Ischemic heart disease, Congenital heart defects, Coronary artery disease, Craniofacial abnormalities, Diabetes mellitus type 2, Hypertension, Congenital heart defect, Hirschsprung disease, Major depressive disorder, Myocardial ischemia, Neurotic disorder
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3917
Endothelin converting enzyme 2
EEF1AKMT4
Alzheimer disease, Atrial fibrillation, Edema, Heart failure, Metabolic syndrome, Obesity, Diabetes mellitus type 2

3918
Endothelin converting enzyme like 1
DA5D, DINE, ECEX, XCE
Arthrogryposis, Arthrogryposis multiplex congenita, Distal arthrogryposis, Desbuquois syndrome, Eye disease

3919
Ethylmalonyl-CoA decarboxylase 1
HEL-S-76, MMCD, dJ351K20.2
Color vision deficiency, Butyryl-coa dehydrogenase deficiency, Melanoma

3920
Enoyl-CoA hydratase domain containing 2
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Alzheimer disease