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
4021 to 4030 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4021
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, Hepatitis b, Huntington disease, Parkinson disease, Prostatic neoplasms, Scoliosis, Status epilepticus

4022
Eukaryotic translation initiation factor 2 alpha kinase 3
PEK, PERK, WRS
Breast cancer, Connective tissue disease, Desbuquois syndrome, Diabetes mellitus type 1, Epiphyseal dysplasia, Myocardial ischemia, Progressive supranuclear palsy, Sialolithiasis, Status epilepticus, Uterine fibroid, Wolcott-rallison syndrome

4023
Eukaryotic translation initiation factor 2 alpha kinase 4
GCN2, PVOD2
Amino acid metabolism disorder, Dementia, Disorders involving the immune mechanism, Endometrial cancer, Endometrial neoplasms, Pulmonary hypertension, Pulmonary arterial hypertension, Hypertension, Immune system disease, Myopathy

4024
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

4025
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

4026
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

4027
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

4028
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

4029
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

4030
Eukaryotic translation initiation factor 2 subunit beta
EIF2, EIF2B, EIF2beta, PPP1R67, eIF-2-beta
Breast neoplasms