Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "G"
491 to 500 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

491
Glutamic--pyruvic transaminase 2
ALT2, GPT 2, MRT49, NEDSPM
Developmental delay, Dysarthria, Dysmorphic features, Epileptic encephalopathy, Febrile seizures, Hypoplasia of corpus callosum, Mental retardation, Microcephaly, Movement disorders, Seizure, Spastic paraplegia, Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome

492
G protein-coupled receptor 65
TDAG8, hTDAG8
Asthma, Crohn disease, Inflammatory bowel disease, Parkinson disease, Ulcerative colitis

493
Glycerol-3-phosphate acyltransferase 3
AGPAT 10, AGPAT10, AGPAT8, AGPAT9, HMFN0839, LPAAT-theta, MAG1
Leukemia

494
Galanin receptor 3
-
Involutional depression, Involutional paraphrenia, Mental depression, Psychosis

495
Growth arrest specific 7
-
Obesity

496
G elongation factor mitochondrial 1
COXPD1, EFG, EFG1, EFGM, EGF1, GFM, hEFG1, mtEF-G1
Basal ganglia cysts, Cholestasis, Combined oxidative phosphorylation deficiency, Hepatoencephalopathy, Hypoplasia of corpus callosum, Leigh syndrome, Liver failure, Microcephaly, Motor delay, Necrotizing encephalomyelopathy, Nystagmus

497
Polypeptide N-acetylgalactosaminyltransferase 4
GALNAC-T4, GALNACT4
Schizophrenia

498
Golgi brefeldin A resistant guanine nucleotide exchange factor 1
ARF1GEF, CMT2GG, CMTDI2, CMTDIA
Parkinson disease

499
Glycosylphosphatidylinositol anchor attachment 1
GAA1, GPIBD15, hGAA1
Apraxia, Cerebellar atrophy, Cerebellar hypoplasia, Developmental delay, Dysarthria, Glycosylphosphatidylinositol deficiency, Mental retardation, Myopia, Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Optic atrophy, Osteopenia, Osteoporosis
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500
Gamma-glutamylamine cyclotransferase
A2LD1
Alzheimer disease