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
3931 to 3940 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3931
Embryonic ectoderm development
COGIS, HEED, WAIT1
Attention deficit hyperactivity disorder, Autism, Cannabis abuse, Cohen-gibson syndrome, Substance abuse, Weaver syndrome

3932
Eukaryotic translation elongation factor 1 alpha 1
CCS-3, CCS3, EE1A1, EEF-1, EEF1A, EF-Tu, EF1A, EF1A1, EF1alpha1, GRAF-1EF, LENG7, PTI1, eEF1A-1
Carcinoma, Stomach neoplasms

3933
Eukaryotic translation elongation factor 1 alpha 2
DEE33, EEF1AL, EF-1-alpha-2, EF1A, EIEE33, HS1, MRD38, STN, STNL
Autism, Nonsyndromic intellectual disability, Bipolar disorder, Liver cirrhosis, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Developmental disability, Epilepsy, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Schizophrenia, Spastic paraplegia, Stomach neoplasms

3934
EEF1A lysine methyltransferase 1
ESP13, N6AMT2, eEF1A-KMT
Melanoma, Insomnia, Neuroblastoma

3935
EEF1A lysine methyltransferase 2
C10orf138, Efm4, METTL10
B-cell acute lymphoblastic leukemia, Crohn disease, Gout, Inflammatory bowel disease, Obesity, Open angle glaucoma, Ulcerative colitis

3936
EEF1A lysine methyltransferase 4
-
Congenital disorder of glycosylation

3937
EEF1AKMT4-ECE2 readthrough
ECE-2, ECE2
Atrial fibrillation, Congenital disorder of glycosylation, Edema, Heart failure, Metabolic syndrome, Obesity, Diabetes mellitus type 2

3938
Eukaryotic translation elongation factor 1 beta 2
EEF1B, EEF1B1, EF1B
Nonsyndromic intellectual disability, Breast neoplasms, Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorder

3939
Eukaryotic translation elongation factor 1 delta
EF-1D, EF1D, FP1047, NEDTCHAL
Nonsyndromic intellectual disability, Color vision deficiency, Moyamoya angiopathy, Neurodevelopmental disorder

3940
Eukaryotic translation elongation factor 1 epsilon 1
AIMP3, P18
Kidney disease, Diabetic neuropathy, Hearing loss, Orofacial cleft, Hypertension