Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "E"
61 to 70 of 465 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

61
EEF1AKMT4-ECE2 readthrough
ECE-2, ECE2
Atrial fibrillation, Congenital disorder of glycosylation, Edema, Heart failure, Metabolic syndrome, Obesity, Diabetes mellitus type 2

62
Eukaryotic translation elongation factor 1 beta 2
EEF1B, EEF1B1, EF1B
Nonsyndromic intellectual disability, Breast neoplasms, Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorder

63
Eukaryotic translation elongation factor 1 delta
EF-1D, EF1D, FP1047, NEDTCHAL
Nonsyndromic intellectual disability, Color vision deficiency, Moyamoya angiopathy, Neurodevelopmental disorder

64
Eukaryotic translation elongation factor 1 epsilon 1
AIMP3, P18
Kidney disease, Diabetic neuropathy, Hearing loss, Orofacial cleft, Hypertension

65
Eukaryotic translation elongation factor 2
EEF-2, EF-2, EF2, SCA26
Breast neoplasms, Renal cell carcinoma, Glaucoma, Lung neoplasms, Neurodevelopmental disorder, Osteoarthritis, Spinocerebellar ataxia

66
Eukaryotic elongation factor 2 lysine methyltransferase
EFM3, FAM86A, SB153, eEF2-KMT
Congenital disorder of glycosylation

67
Eukaryotic elongation factor, selenocysteine-tRNA specific
EFSEC, NEDPSB, SELB
Asthma, Atrial fibrillation, Nonsyndromic intellectual disability, Obstructive airway disease, Obstructive pulmonary disease, Endometrial cancer, Endometrial neoplasms, Endometriosis, Gastroesophageal reflux disease, Hypertension, Hypospadias, Microcephaly, Neurodevelopmental disorder, Prostate cancer, Chronic obstructive pulmonary disease
View all (5 more)

68
Estrogen-induced osteoclastogenesis regulator 1
C9orf132, FAM102A, SYM-3A, bA203J24.7
Glaucoma, Gout, Primary angle closure glaucoma

69
EEIG family member 2
FAM102B, SYM-3B
Color vision deficiency, Liver cirrhosis

70
Endonuclease/exonuclease/phosphatase family domain containing 1
HSPC107
Color vision deficiency, Obesity, Schizophrenia, Hypertension