GLOD4

GLOD4
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 3ZI1
Identifiers
Aliases	GLOD4 , C17orf25, HC71, CGI-150, glyoxalase domain containing 4
External IDs	MGI: 1914451; HomoloGene: 9376; GeneCards: GLOD4; OMA:GLOD4 - orthologs
Gene location (Human) Chr. Chromosome 17 (human) [1] Band 17p13.3 Start 757,097 bp [1] End 783,390 bp [1]
Gene location (Mouse) Chr. Chromosome 11 (mouse) [2] Band 11|11 B5 Start 76,011,813 bp [2] End 76,134,551 bp [2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in buccal mucosa cell ventricular zone duodenum islet of Langerhans rectum ganglionic eminence epithelium of nasopharynx mucosa of transverse colon palpebral conjunctiva prefrontal cortex Top expressed in endocardial cushion Paneth cell medial ganglionic eminence sciatic nerve medullary collecting duct atrioventricular junction renal corpuscle atrioventricular valve ventricular zone urothelium More reference expression data BioGPS More reference expression data
Gene ontology Molecular function cadherin binding Cellular component extracellular exosome mitochondrion Biological process cell-cell adhesion Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 51031 67201 Ensembl ENSG00000167699 ENSMUSG00000017286 UniProt Q9HC38 Q9CPV4 RefSeq (mRNA) NM_016080 NM_001366247 NM_001366248 NM_001366249 NM_001366250 NM_026029 NM_001362901 RefSeq (protein) NP_057164 NP_001353176 NP_001353177 NP_001353178 NP_001353179 NP_080305 NP_001349830 Location (UCSC) Chr 17: 0.76 – 0.78 Mb Chr 11: 76.01 – 76.13 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Glyoxalase domain-containing protein 4 is an enzyme that in humans is encoded by the GLOD4 gene. ^{[5] [6] [7]}

References

1. GRCh38: Ensembl release 89: ENSG00000167699 – Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000017286 – Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Qin WX, Wan F, Sun FY, Zhang PP, Han LW, Huang Y, Jiang HQ, Zhao XT, He M, Ye Y, Cong WM, Wu MC, Zhang LS, Yang NW, Gu JR (Oct 2001). "Cloning and characterization of a novel gene (C17orf25) from the deletion region on chromosome 17p13.3 in hepatocelular carcinoma". Cell Res. 11 (3): 209–16. doi: 10.1038/sj.cr.7290088 . PMID   11642406.
6. Guo JY, Xu J, Mao Q, Fu LL, Gu JR, De Zhu J (Jan 2003). "The promoter analysis of the human C17orf25 gene, a novel chromosome 17p13.3 gene". Cell Res. 12 (5–6): 339–52. doi: 10.1038/sj.cr.7290136 . PMID   12528892.
7. "Entrez Gene: C17orf25 chromosome 17 open reading frame 25".

Further reading

• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC   528928 . PMID   15489334.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi: 10.1038/ng1285 . PMID   14702039.
• Zhang HT, Yan ZQ, Hu XB, et al. (2004). "Interaction of C17orf25 with ADP-ribose pyrophosphatase NUDT9 detected via yeast two-hybrid method". Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao. 35 (8): 747–51. PMID   12897971.
• Cardoso C, Leventer RJ, Ward HL, et al. (2003). "Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3". Am. J. Hum. Genet. 72 (4): 918–30. doi:10.1086/374320. PMC   1180354 . PMID   12621583.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi: 10.1073/pnas.242603899 . PMC   139241 . PMID   12477932.
• Lai CH, Chou CY, Ch'ang LY, et al. (2000). "Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics". Genome Res. 10 (5): 703–13. doi:10.1101/gr.10.5.703. PMC   310876 . PMID   10810093.