Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4961 to 4970 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4961
Glutamate decarboxylase like 1
ADC, CSADC, HuADC, HuCSADC
Angioedema, Bipolar disorder, Color vision deficiency, Eating disorder, Liver neoplasms, Diabetes mellitus type 2

4962
G antigen 1
CT4.1, CT4.4, GAGE-1, GAGE-4, GAGE4
Asthma, Pancreatic neoplasms, Vitiligo

4963
Cyclin G associated kinase
DNAJ26, DNAJC26
Alzheimer disease, Behcet disease, Parkinson disease, Vasculitis

4964
Galanin and GMAP prepropeptide
ETL8, GAL-GMAP, GALN, GLNN, GMAP
Lateral temporal lobe epilepsy, Bipolar disorder, Major depressive disorder, Familial temporal lobe epilepsy, Temporal lobe epilepsy, Hyperalgesia, Hypertension, Mood disorder

4965
Galactose-3-O-sulfotransferase 1
CST
Autism, Schizophrenia, Creutzfeldt-jakob disease

4966
Galactose-3-O-sulfotransferase 2
GAL3ST-2, GP3ST
Ankylosing spondylitis, Asthma, Crohn disease, Inflammatory bowel disease, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

4967
Galactose-3-O-sulfotransferase 3
GAL3ST-3, GAL3ST2
Autism

4968
Galactosylceramidase
-
Amblyopia, Breast cancer, Congenital neurologic anomalies, Crohn disease, Developmental regression, Fabry disease, Global developmental delay, Hypertension, Inflammatory bowel disease, Intellectual developmental disorder, Leukodystrophy, Metabolic syndrome, Multiple sclerosis, Nystagmus, Obsessive-compulsive disorder
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4969
UDP-galactose-4-epimerase
SDR1E1, THC13
Erythrocyte galactose epimerase deficiency, Erythrocyte udp-galactose-4-epimerase deficiency, Galactosemia, Thrombocytopenia, Udp-glucose 4-epimerase deficiency

4970
Galactokinase 1
GALK, GK1, HEL-S-19
Asthma, Cataract, Galactokinase deficiency, Junctional epidermolysis bullosa, Galactosemia, Hypothyroidism, Diabetes mellitus type 2, Weber-cockayne syndrome