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
4001 to 4010 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4001
Eukaryotic translation initiation factor 1A Y-linked
eIF-4C
Autism

4002
Eukaryotic translation initiation factor 2A
CDA02, EIF-2A, MST089, MSTP004, MSTP089
Dystonia, Marinesco-sjogren syndrome, Myocardial ischemia

4003
Eukaryotic translation initiation factor 2 alpha kinase 1
HCR, HRI, LEMSPAD, hHRI
Hemolytic anemia, Hypomyelinating leukodystrophy, Nonalcoholic fatty liver disease, Oligodendroglioma, Splenomegaly

4004
Eukaryotic translation initiation factor 2 alpha kinase 2
DYT33, EIF2AK1, LEUDEN, PKR, PPP1R83, PRKR
Alzheimer disease, Developmental regression, Dystonia, Torsion dystonia, Early-onset generalized limb-onset dystonia, Global developmental delay, Gout, Huntington disease, Parkinson disease, Prostatic neoplasms, Scoliosis, Status epilepticus

4005
Eukaryotic translation initiation factor 2 alpha kinase 3
PEK, PERK, WRS
Breast cancer, Connective tissue disease, Desbuquois syndrome, Diabetes mellitus type 1, Multiple epiphyseal dysplasia with early-onset diabetes mellitus, Myocardial ischemia, Progressive supranuclear palsy, Sialolithiasis, Status epilepticus, Uterine fibroid, Wolcott-rallison syndrome

4006
Eukaryotic translation initiation factor 2 alpha kinase 4
GCN2, PVOD2
Amino acid metabolism disorder, Dementia, Immune system disorder, Endometrial cancer, Endometrial neoplasms, Pulmonary hypertension, Pulmonary arterial hypertension, Hypertension, Immune system disease, Myopathy

4007
Eukaryotic translation initiation factor 2B subunit alpha
EIF2B, EIF2BA, EIF2Balpha, VWM1
Childhood ataxia with cns hypomyelination, Congenital or early infantile cach syndrome, Cree leukoencephalopathy, Vanishing white matter disease

4008
Eukaryotic translation initiation factor 2B subunit beta
EIF-2Bbeta, EIF2B, EIF2Bbeta, VWM2
Childhood ataxia with cns hypomyelination, Congenital neurologic anomalies, Congenital or early infantile cach syndrome, Coronary artery disease, Cree leukoencephalopathy, Osteogenesis imperfecta, Vanishing white matter disease

4009
Eukaryotic translation initiation factor 2B subunit gamma
EIF-2B, EIF2Bgamma, VWM3
Alzheimer disease, Brain infarction, Childhood ataxia with cns hypomyelination, Congenital or early infantile cach syndrome, Cree leukoencephalopathy, Vanishing white matter disease

4010
Eukaryotic translation initiation factor 2B subunit delta
EIF-2B, EIF2B, EIF2Bdelta, VWM4
Childhood ataxia with cns hypomyelination, Congenital or early infantile cach syndrome, Cree leukoencephalopathy, Gout, Vanishing white matter disease