GLOD4

3ZI1

GLOD4

Identifiers

GLOD4, C17orf25, HC71, CGI-150, glyoxalase domain containing 4

External IDs

MGI: 1914451; GeneCards: GLOD4

Available structures

Ortholog search: PDBe RCSB

List of PDB id codes
3ZI1

Gene location (Human)

Chr.	Chromosome 17 (human)^[1]

Band	17p13.3	Start	757,097 bp^[1]
Band	17p13.3	End	783,390 bp^[1]

Gene location (Mouse)

Chr.	Chromosome 11 (mouse)^[2]

Band	11\|11 B5	Start	76,011,813 bp^[2]
Band	11\|11 B5	End	76,134,551 bp^[2]

RNA expression pattern

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


More reference expression data

Gene ontology
Molecular function	cadherin binding
Cellular component	extracellular exosome mitochondrion
Biological process	cell-cell adhesion
Sources:Amigo / QuickGO

Databases

NCBI: entry; OMA: entry

Species

Human

Mouse


51031


67201


ENSG00000167699


ENSMUSG00000017286


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]

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

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000167699 – Ensembl, May 2017
^ ^a ^b ^c 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".

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.

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