Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "G"

481 to 490 of 533 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
481	83550	GPR101	G protein-coupled receptor 101	GPCR6, PAGH2, PITA2	Acanthosis nigricans, Acne, Acromegaly, Anxiety disorder, Arthritis, Cerebral palsy, Congenital macrodactylia, Diabetes mellitus, Erectile dysfunction, Frontal bossing, Hypersomnia, Hypertension, Hypertrophic cardiomyopathy, Hypogonadotropic hypogonadism, Hypopituitarism View all (12 more)
482	83606	GUCD1	Guanylyl cyclase domain containing 1	C22orf13, LLN4	Prostatic neoplasms, Prostate cancer
483	83743	GRWD1	Glutamate rich WD repeat containing 1	CDW4, DIAR14, GRWD, RRB1, WDR28	Lung adenocarcinoma
484	84340	GFM2	GTP dependent ribosome recycling factor mitochondrial 2	EF-G2mt, EFG2, MRRF2, MST027, MSTP027, RRF, RRF2, RRF2mt, hEFG2, mEF-G 2	Arthrogryposis multiplex congenita, Combined oxidative phosphorylation deficiency, Developmental delay, Developmental regression, Dysarthria, Leigh syndrome, Mitochondrial diseases, Necrotizing encephalomyelopathy
485	8443	GNPAT	Glyceronephosphate O-acyltransferase	DAP-AT, DAPAT, DHAPAT, RCDP2	Cataract, Chondrodysplasia punctata, High palate, Mental retardation, Microcephaly, Micrognathism, Osteopenia, Rhizomelia, Rhizomelic chondrodysplasia punctata, Schizophrenia, Scoliosis
486	84572	GNPTG	N-acetylglucosamine-1-phosphate transferase subunit gamma	C16orf27, GNPTAG, LP2537, RJD9	Aortic valve insufficiency, Aortic valve sclerosis, Congenital pectus carinatum, Dwarfism, Mental retardation, Mucolipidosis, Myopia, Pfaundler-hurler syndrome, Scoliosis
487	84656	GLYR1	Glyoxylate reductase 1 homolog	BM045, HIBDL, N-PAC, NP60, NPAC, hNDF	Malignant neoplasm
488	84662	GLIS2	GLIS family zinc finger 2	NKL, NPHP7	Ciliopathies, Gastrointestinal stromal tumor, Kidney disease, Megakaryoblastic leukemia without down syndrome, Nephronophthisis
489	84694	GJA10	Gap junction protein alpha 10	CX62	Kidney failure
490	84705	GTPBP3	GTP binding protein 3, mitochondrial	COXPD23, GTPBG3, MSS1, MTGP1, THDF1	Cardiomyopathy, Combined oxidative phosphorylation deficiency, Congestive heart failure, Developmental delay

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