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
Showing genes starting with "E"
51 to 60 of 465 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

51
Endothelin 3
ET-3, ET3, HSCR4, PPET3, WS4B
Biliary atresia, Bradycardia, Haddad syndrome, Congenital central hypoventilation syndrome, Hirschsprung disease, Hypertension, Hypotension, Kleins syndrome, Hearing loss, Tricuspid valve disease, Waardenburg syndrome, Waardenburg-shah syndrome

52
Endothelin receptor type A
ET-A, ETA, ETA-R, ETAR, ETRA, MFDA, hET-AR
Atherosclerosis, Brain aneurysm, Carotid atherosclerosis, Cerebrovascular disorder, Congenital heart defects, Congestive heart failure, Coronary artery disease, Craniofacial abnormalities, Cystic fibrosis, Desbuquois syndrome, Diabetes mellitus type 2, Erectile dysfunction, Congenital heart defect, Heart disease, Heart failure
View all (16 more)

53
Endothelin receptor type B
ABCDS, ET-B, ET-BR, ETB, ETB1, ETBR, ETRB, HSCR, HSCR2, WS4A
Abcd syndrome, Androgenetic alopecia, Asthma, Breast neoplasms, Congestive heart failure, Deafness, Diabetes mellitus type 2, Hearing impairment, Heart failure, Hirschsprung disease, Pulmonary hypertension, Kleins syndrome, Nephrotic syndrome, Intestinal aganglionosis, Waardenburg syndrome
View all (1 more)

54
Early endosome antigen 1
MST105, MSTP105, ZFYVE2
Alzheimer disease, Neurotic disorder

55
Embryonic ectoderm development
COGIS, HEED, WAIT1
Attention deficit hyperactivity disorder, Autism, Cannabis abuse, Cohen-gibson syndrome, Substance abuse, Weaver syndrome

56
Eukaryotic translation elongation factor 1 alpha 1
CCS-3, CCS3, EE1A1, EEF-1, EEF1A, EF-Tu, EF1A, EF1A1, EF1alpha1, GRAF-1EF, LENG7, PTI1, eEF1A-1
Carcinoma, Stomach neoplasms

57
Eukaryotic translation elongation factor 1 alpha 2
DEE33, EEF1AL, EF-1-alpha-2, EF1A, EIEE33, HS1, MRD38, STN, STNL
Autism, Nonsyndromic intellectual disability, Bipolar disorder, Liver cirrhosis, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Developmental disability, Epilepsy, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Schizophrenia, Spastic paraplegia, Stomach neoplasms

58
EEF1A lysine methyltransferase 1
ESP13, N6AMT2, eEF1A-KMT
Melanoma, Insomnia, Neuroblastoma

59
EEF1A lysine methyltransferase 2
C10orf138, Efm4, METTL10
B-cell acute lymphoblastic leukemia, Crohn disease, Gout, Inflammatory bowel disease, Obesity, Open angle glaucoma, Ulcerative colitis

60
EEF1A lysine methyltransferase 4
-
Congenital disorder of glycosylation