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
Gene location (Human)
Chr.	Chromosome 17 (human)
End	783,390 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	76,134,551 bp
RNA expression pattern
	Top expressed in
	duodenum; ; islet of Langerhans; ; rectum; ; ganglionic eminence; ; palpebral conjunctiva; ; prefrontal cortex; ; body of stomach; ; skin of abdomen; ; Achilles tendon; ; gallbladder;
	Top expressed in
	endocardial cushion; ; Paneth cell; ; medial ganglionic eminence; ; sciatic nerve; ; medullary collecting duct; ; renal corpuscle; ; atrioventricular valve; ; urothelium; ; otic placode; ; mirror;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	cadherin binding ;
Cellular component	extracellular exosome ; mitochondrion ;
Biological process	cell-cell adhesion ;
	Sources:Amigo / QuickGO
Orthologs
	51031
	67201
	ENSG00000167699
	ENSMUSG00000017286
	Q9HC38
	Q9CPV4
	NM_016080 ; NM_001366247 ; NM_001366248 ; NM_001366249 ; NM_001366250
	NM_026029 ; NM_001362901
	NP_057164 ; NP_001353176 ; NP_001353177 ; NP_001353178 ; NP_001353179
	NP_080305 ; NP_001349830
	Wikidata
View/Edit Human	View/Edit Mouse

Last updated October 12, 2022

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

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References

1 2 3 GRCh38: Ensembl release 89: ENSG00000167699 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000017286 - Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ 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.
↑ 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.
↑ "Entrez Gene: C17orf25 chromosome 17 open reading frame 25".

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.

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[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000167699 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 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.

[pmid11642406-5] 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.

[pmid12528892-6] 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.

[entrez-7] "Entrez Gene: C17orf25 chromosome 17 open reading frame 25".

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GLOD4

Related Research Articles

References

Further reading