Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "G"
371 to 380 of 674 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

371
N-acetylglucosamine-1-phosphate transferase subunits alpha and beta
GNPTA, ICD
Avascular necrosis of femoral head, Desbuquois syndrome, Mucolipidosis, Mucopolysaccharidosis

372
N-acetylglucosamine-1-phosphate transferase subunit gamma
C16orf27, GNPTAG, LP2537, RJD9
Desbuquois syndrome, Mucolipidosis, Retinitis pigmentosa, Rod-cone dystrophy, Diabetes mellitus type 2

373
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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374
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

375
Glucosamine (N-acetyl)-6-sulfatase
G6S
Desbuquois syndrome, Mucopolysaccharidosis, Sanfilippo syndrome

376
Golgin A2
DEDHMB, GM130
Developmental delay with hypotonia, myopathy, and brain abnormalities, Neuromuscular disease

377
Golgin A3
GCP170, MEA-2
Attention deficit hyperactivity disorder, Central nervous system cancer, Glioma, Metabolic syndrome, Substance abuse, Diabetes mellitus type 2

378
Golgin A4
CRPF46, GCP2, GOLG, MU-RMS-40.18, p230
Eczema, Color vision deficiency, Colorectal cancer, Dermatologic disorder, Prostatic neoplasms, Skin disease

379
Golgin A5
GOLIM5, RFG5, ret-II
Differentiated thyroid carcinoma

380
Golgin A6 family like 7
GOLGA6L7P
Skin disease