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
4081 to 4090 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

4081
Engulfment and cell motility 2
CED-12, CED12, Ced-12A, ELMO-2, VMPI
Vascular malformation

4082
ELMO domain containing 1
-
Central nervous system cancer, Cerebral amyloid angiopathy, Glioblastoma, Glioma

4083
ELMO domain containing 3
DFNA81, DFNB88, LST3, RBED1, RBM29
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Deafness, Hearing loss, Nonsyndromic hearing loss

4084
Elastin
ADCL1, SVAS, WBS, WS
Androgenetic alopecia, Aortic aneurysm, Aortic stenosis, Atrioventricular septal defect, Cutis laxa, Obstructive airway disease, Obstructive pulmonary disease, Congenital venous anomaly, Accessory skin tag, Congenital stenosis of aortic valve, Dermatitis herpetiformis, Diabetic retinopathy, Digestive system disease, Diverticular disease, Age-related macular degeneration
View all (23 more)

4085
Elongin A
ELOA1, SIII, SIII p110, TCEB3, TCEB3A
Eczema, Inflammatory skin disease, Psoriasis

4086
Elongin C
SIII, TCEB1
Renal cell carcinoma

4087
ELOVL fatty acid elongase 1
CGI-88, IKSHD, Ssc1
Optic atrophy, Retinitis pigmentosa

4088
ELOVL fatty acid elongase 2
SSC2
Male infertility

4089
ELOVL fatty acid elongase 3
CIG-30, CIG30
Alzheimer disease, Atrial fibrillation, Attention deficit hyperactivity disorder, Substance abuse, Systemic lupus erythematosus

4090
ELOVL fatty acid elongase 4
ADMD, CT118, ISQMR, SCA34, STGD2, STGD3
Obstructive pulmonary disease, Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome, Corneal dystrophy, Elsahy-waters syndrome, Erythrokeratodermia with ataxia, Hereditary corneal dystrophy, Retinitis pigmentosa, Rosacea, Spastic ataxia, Spinocerebellar ataxia, Stargardt disease