Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5311 to 5320 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5311
Glyceronephosphate O-acyltransferase
DAP-AT, DAPAT, DHAPAT, RCDP2
Chondrodysplasia, Desbuquois syndrome, Rhizomelic chondrodysplasia punctata, Schizophrenia

5312
Glucosamine-6-phosphate deaminase 1
GNP1, GNPDA, GNPI, GPI, HLN
Asthma, Corneal astigmatism, Crohn disease, Dementia, Inflammatory bowel disease, Liver cirrhosis, Respiratory system disease, Squamous cell carcinoma

5313
Glucosamine-6-phosphate deaminase 2
GNP2, SB52
Body weight, Insomnia, Obesity, Scoliosis

5314
Glucosamine-phosphate N-acetyltransferase 1
GNA1, GNPNAT, Gpnat1, RHZDAN
Alzheimer disease, Atrial fibrillation, Desbuquois syndrome, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Osteochondrodysplasias, Rhizomelic dysplasia, ain-naz type

5315
N-acetylglucosamine-1-phosphate transferase subunits alpha and beta
GNPTA, ICD
Avascular necrosis of femoral head, Desbuquois syndrome, Mucolipidosis, Mucopolysaccharidosis

5316
N-acetylglucosamine-1-phosphate transferase subunit gamma
C16orf27, GNPTAG, LP2537, RJD9
Desbuquois syndrome, Mucolipidosis, Retinitis pigmentosa, Rod-cone dystrophy, Diabetes mellitus type 2

5317
Gonadotropin releasing hormone 1
GNRH, GRH, LHRH, LNRH
Bradycardia, Chiari-frommel syndrome, Headache, Hyperproinsulinemia, Hypertension, Hypogonadism, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Male infertility, Intestinal polyps, Kallmann syndrome, Panhypopituitarism, Periodontitis, Pituitary dwarfism
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5318
Gonadotropin releasing hormone receptor
GNRHR1, GRHR, HH7, LHRHR, LRHR
Hypogonadism, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Sheehan syndrome

5319
Glucosamine (N-acetyl)-6-sulfatase
G6S
Desbuquois syndrome, Mucopolysaccharidosis, Sanfilippo syndrome

5320
Golgin A2
DEDHMB, GM130
Developmental delay with hypotonia, myopathy, and brain abnormalities, Neuromuscular disease