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"
201 to 210 of 465 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

201
Elongator acetyltransferase complex subunit 1
DYS, FD, IKAP, IKBKAP, IKI3, TOT1
Asthma, Attention deficit hyperactivity disorder, Breast neoplasms, Charcot-marie-tooth disease, Dysautonomia, Gaucher disease, Medulloblastoma, Hereditary sensory and autonomic neuropathy, Riley-day syndrome, Scoliosis, Substance abuse

202
Elongator acetyltransferase complex subunit 2
MRT58, SHINC-2, STATIP1, StIP
Intellectual developmental disorder, Major depressive disorder, Oligodendroglioma

203
Elongator acetyltransferase complex subunit 3
KAT9
Amyotrophic lateral sclerosis, Breast neoplasms, Metabolic syndrome, Scoliosis, Systemic lupus erythematosus, Hypertension, Diabetes mellitus type 2

204
Elongator acetyltransferase complex subunit 4
AN, AN2, C11orf19, PAX6NEB, PAXNEB, dJ68P15A.1, hELP4
Aniridia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Anophthalmia, Autism, Coloboma, Congenital ocular coloboma, Gastrointestinal stromal tumor, Glaucoma, Global developmental delay, Insomnia, Anterior segment dysgenesis, Keratitis, Macular telangiectasia, Neurotic disorder, Nystagmus
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205
Elongator acetyltransferase complex subunit 5
C17orf81, DERP6, HSPC002, MST071, MSTP071
Hypertension

206
Elongator acetyltransferase complex subunit 6
C3orf75, TMEM103
Crohn disease

207
Epididymal sperm binding protein 1
E12, EDDM12, EL149, HE12
Gastric cancer

208
Embigin
GP70
Alzheimer disease, Breast cancer, Coronary artery disease, Allergic contact dermatitis, Diabetes mellitus, Estrogen-receptor negative breast cancer, Liver cirrhosis, Major depressive disorder, Mood disorder, Movement disorder, Neurotic disorder, Periodic limb movement disorder, Schizophrenia, Squamous cell carcinoma, Diabetes mellitus type 2
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209
ER membrane protein complex subunit 1
CAVIPMR, KIAA0090
Retinitis pigmentosa, Congenital anomalies of the kidney and urinary tract, Cerebellar atrophy, Cerebellar atrophy with seizures and variable developmental delay, Neurodevelopmental disorder, Global developmental delay, Obesity

210
ER membrane protein complex subunit 10
C19orf63, HSM1, HSS1, NEDDFAS
Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorder, Non-specific syndromic intellectual disability