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
3951 to 3960 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

3951
EF-hand calcium binding domain 3
-
Alzheimer disease

3952
EF-hand calcium binding domain 5
-
Obstructive pulmonary disease

3953
EF-hand calcium binding domain 6
DJBP, HSCBCIP1, dJ185D5.1
Schizophrenia, Teratozoospermia

3954
EF-hand calcium binding domain 7
-
Polydactyly

3955
EF-hand calcium binding domain 8
-
Attention deficit hyperactivity disorder, Diabetic neuropathy, Non-melanoma skin carcinoma

3956
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)

3957
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)

3958
EF-hand domain family member B
CFAP21
Alzheimer disease, Cerebral amyloid angiopathy, Dementia, Migraine

3959
EF-hand domain containing 1
EJM1, POC9, RIB72, dJ304B14.2
Eczema, Asthma, Epilepsy, Absence epilepsy, Juvenile absence epilepsy, Myoclonic epilepsy, Peripheral arterial disease

3960
EF-hand domain containing 2
MRX74, dJ1158H2.1
Open angle glaucoma