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 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4011
Eukaryotic translation initiation factor 2B subunit epsilon
CACH, CLE, EIF-2B, EIF2Bepsilon, LVWM, VWM5
Childhood ataxia with cns hypomyelination, Congenital or early infantile cach syndrome, Cree leukoencephalopathy, Vanishing white matter disease

4012
Eukaryotic translation initiation factor 2 subunit alpha
EIF-2, EIF-2A, EIF-2alpha, EIF2, EIF2A
Alzheimer disease, Cognition disorder, Delirium, dementia, and cognitive disorders, Osteosarcoma, Schizophrenia, Status epilepticus

4013
Eukaryotic translation initiation factor 2 subunit beta
EIF2, EIF2B, EIF2beta, PPP1R67, eIF-2-beta
Breast neoplasms

4014
Eukaryotic translation initiation factor 2 subunit gamma
EIF2, EIF2G, EIF2gamma, MEHMO, MRXSBRK, eIF-2gA, eIF2gX
Diabetes mellitus

4015
Eukaryotic translation initiation factor 3 subunit A
EIF3, EIF3S10, P167, TIF32, eIF3-p170, eIF3-theta, p180, p185
Keratoconus, Prostatic neoplasms

4016
Eukaryotic translation initiation factor 3 subunit B
EIF3-ETA, EIF3-P110, EIF3-P116, EIF3S9, PRT1
Color vision deficiency

4017
Eukaryotic translation initiation factor 3 subunit D
EIF3S7, eIF3-p66, eIF3-zeta
Preeclampsia

4018
Eukaryotic translation initiation factor 3 subunit E
EIF3-P48, EIF3S6, INT6, eIF3-p46
Androgenetic alopecia, Obstructive pulmonary disease, Dupuytren contracture, Gastroesophageal reflux disease, Inflammatory bowel disease, Oligodendroglioma, Prostate cancer

4019
Eukaryotic translation initiation factor 3 subunit F
EIF3S5, MRT67, eIF3-p47
Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorder

4020
Eukaryotic translation initiation factor 3 subunit G
EIF3-P42, EIF3S4, eIF3-delta, eIF3-p44
Cataplexy and narcolepsy