Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4011 to 4020 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4011
Euchromatic histone lysine methyltransferase 2
BAT8, C6orf30, G9A, GAT8, KMT1C, NG36
Asthma, Autism, Autoimmune disease, Epithelial ovarian carcinoma, Obstructive pulmonary disease, Idiopathic pulmonary fibrosis, Infertility, Myeloid leukemia, Lung neoplasms, Membranous glomerulonephritis, Migraine, Moyamoya disease, Multiple sclerosis, Neurodevelopmental disorder, Open angle glaucoma
View all (7 more)

4012
EI24 autophagy associated transmembrane protein
EPG4, PIG8, TP53I8
Intellectual developmental disorder, Prostatic neoplasms

4013
EP300 interacting inhibitor of differentiation 1
C15orf3, CRI1, EID-1, IRO45620, PNAS-22, PTD014, RBP21
Mesothelioma

4014
EP300 interacting inhibitor of differentiation 2B
EID-2B, EID-3
Uveitis

4015
Eukaryotic translation initiation factor 1
A121, EIF-1, EIF1A, ISO1, SUI1
Duodenal ulcer, Peptic ulcer disease

4016
Eukaryotic translation initiation factor 1A domain containing
OBELIX, haponin
Melanoma

4017
Eukaryotic translation initiation factor 1A X-linked
EIF1A, EIF1AP1, EIF4C, eIF-1A, eIF-4C
Differentiated thyroid carcinoma, Uveal melanoma

4018
Eukaryotic translation initiation factor 1A Y-linked
eIF-4C
Autism

4019
Eukaryotic translation initiation factor 2A
CDA02, EIF-2A, MST089, MSTP004, MSTP089
Dystonia, Marinesco-sjogren syndrome, Myocardial ischemia

4020
Eukaryotic translation initiation factor 2 alpha kinase 1
HCR, HRI, LEMSPAD, hHRI
Hemolytic anemia, Hypomyelinating leukodystrophy, Nonalcoholic fatty liver disease, Oligodendroglioma, Splenomegaly