Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "G"
481 to 490 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

481
G protein-coupled receptor 101
GPCR6, PAGH2, PITA2
Acromegaly, Chromosome xq26.3 duplication syndrome, Growth hormone-secreting pituitary adenoma, X-linked acrogigantism due to xq26 microduplication

482
Guanylyl cyclase domain containing 1
C22orf13, LLN4
Prostatic neoplasm

483
Glutamate rich WD repeat containing 1
CDW4, DIAR14, GRWD, RRB1, WDR28

484
GTP dependent ribosome recycling factor mitochondrial 2
EF-G2mt, EFG2, MRRF2, MST027, MSTP027, RRF, RRF2, RRF2mt, hEFG2, mEF-G 2
Combined oxidative phosphorylation deficiency, Leigh syndrome, Mitochondrial disease, Sandhoff disease

485
Glyceronephosphate O-acyltransferase
DAP-AT, DAPAT, DHAPAT, RCDP2
Chondrodysplasia, Desbuquois syndrome, Rhizomelic chondrodysplasia punctata, Schizophrenia

486
N-acetylglucosamine-1-phosphate transferase subunit gamma
C16orf27, GNPTAG, LP2537, RJD9
Desbuquois syndrome, Mucolipidosis, Retinitis pigmentosa, Diabetes mellitus, type 2

487
Glyoxylate reductase 1 homolog
BM045, HIBDL, N-PAC, NP60, NPAC, hNDF

488
GLIS family zinc finger 2
NKL, NPHP7
Gastrointestinal stromal tumor, Nephronophthisis, Kidney disease, Nephronophthisis, familial juvenile, Diabetes mellitus, type 2

489
Gap junction protein alpha 10
CX62

490
GTP binding protein 3, mitochondrial
COXPD23, GTPBG3, MSS1, MTGP1, THDF1
Combined oxidative phosphorylation deficiency, Hypertrophic cardiomyopathy, Leigh syndrome, Breast cancer, Mitochondrial disease, Triple-negative breast cancer