Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3971 to 3980 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3971
EF-hand calcium binding domain 7
-
Polydactyly

3972
EF-hand calcium binding domain 8
-
Attention deficit hyperactivity disorder, Diabetic neuropathy, Non-melanoma skin carcinoma

3973
EGF containing fibulin extracellular matrix protein 1
ARCL1D, DHRD, DRAD, FBLN3, FBNL, FIBL-3, GLC1H, MLVT, MTLV, S1-5
Amyotrophic lateral sclerosis, Androgenetic alopecia, Arachnodactyly, Atrial fibrillation, Biliary atresia, Blindness, Breast neoplasms, Carcinoma, Carpal tunnel syndrome, Obstructive pulmonary disease, Venous insufficiency, Colorectal neoplasms, Congenital contractural arachnodactyly, Congenital hernia of foramen of bochdalek, Connective tissue disease
View all (25 more)

3974
EGF containing fibulin extracellular matrix protein 2
ARCL1B, FBLN4, MBP1, UPH1
Aortic aneurysm, Arterial tortuosity syndrome, Cutis laxa, Basal cell carcinoma, Accessory skin tag, Congenital contractural arachnodactyly, Crohn disease, Benign pemphigus, Thoracic aortic aneurysm and aortic dissection, Inflammatory bowel disease, Darier disease, Prostatic neoplasms, Retinal detachment, Rothmund-thomson syndrome, Ruptured abdominal aortic aneurysm
View all (4 more)

3975
EF-hand domain family member B
CFAP21
Alzheimer disease, Cerebral amyloid angiopathy, Dementia, Migraine

3976
EF-hand domain containing 1
EJM1, POC9, RIB72, dJ304B14.2
Eczema, Asthma, Epilepsy, Absence epilepsy, Juvenile absence epilepsy, Myoclonic epilepsy, Myocarditis, Peripheral arterial disease

3977
EF-hand domain containing 2
MRX74, dJ1158H2.1
Open angle glaucoma

3978
EF-hand domain family member D1
MST133, MSTP133, PP3051, SWS2
Asthma, Breast cancer, Cancer, Adenoid cystic carcinoma, Colorectal cancer, Coronary artery disease, Estrogen-receptor negative breast cancer, Lung cancer, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Salivary gland neoplasms, Schizophrenia, Squamous cell carcinoma

3979
EF-hand domain family member D2
SWS1
Binge drinking

3980
Elongation factor like GTPase 1
EFTUD1, FAM42A, HsT19294, RIA1, SDS2
Alzheimer disease, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Desbuquois syndrome, Glioma, Shwachman-diamond syndrome, Tourette syndrome