SGCZ
| SGCZ | ||||||
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| Identifiers | ||||||
| Aliases | SGCZ, ZSG1, sarcoglycan zeta | |||||
| External IDs | MGI: 2388820 HomoloGene: 26726 GeneCards: SGCZ | |||||
| Genetically Related Diseases | ||||||
| obesity[1] | ||||||
| Orthologs | ||||||
| Species | Human | Mouse | ||||
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| Location (UCSC) | Chr 8: 14.09 – 15.24 Mb | Chr 8: 37.52 – 38.66 Mb | ||||
| PubMed search | [2] | [3] | ||||
| Wikidata | ||||||
| View/Edit Human | View/Edit Mouse | |||||
Sarcoglycan zeta also known as SGCZ is a protein which in humans is encoded by the SGCZ gene.[4]
Function[edit]
The zeta-sarcoglycan gene measures over 465 kb and localizes to 8p22. This protein is part of the sarcoglycan complex, a group of 6 proteins. The sarcoglycans are all N-glycosylated transmembrane proteins with a short intra-cellular domain, a single transmembrane region and a large extra-cellular domain containing a carboxyl-terminal cluster with several conserved cysteine residues. The sarcoglycan complex is part of the dystrophin-associated glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix.[5]
Clinical significance[edit]
Zeta-sarcoglycan is reduced in mouse models of muscular dystrophy and SGCZ is found as a component of the vascular smooth muscle sarcoglycan complex. Hence SGCZ may be important in the pathogenesis of muscular dystrophy.[4]
References[edit]
- ^ "Diseases that are genetically associated with SGCZ view/edit references on wikidata".
- ^ "Human PubMed Reference:".
- ^ "Mouse PubMed Reference:".
- ^ a b Wheeler MT, Zarnegar S, McNally EM (September 2002). "Zeta-sarcoglycan, a novel component of the sarcoglycan complex, is reduced in muscular dystrophy". Hum. Mol. Genet. 11 (18): 2147–54. doi:10.1093/hmg/11.18.2147. PMID 12189167.
- ^ "Entrez Gene: SGCZ Sarcoglycan zeta".
External links[edit]
Further reading[edit]
- Strausberg RL, Feingold EA, Grouse LH, et al. (2002). "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. doi:10.1073/pnas.242603899. PMC 139241
. PMID 12477932. - Anastasi G, Cutroneo G, Sidoti A, et al. (2007). "Sarcoglycan subcomplex expression in normal human smooth muscle.". J. Histochem. Cytochem. 55 (8): 831–43. doi:10.1369/jhc.6A7145.2007. PMID 17438352.
- Aurino S, Piluso G, Saccone V, et al. (2008). "Candidate-gene testing for orphan limb-girdle muscular dystrophies.". Acta Myol. 27: 90–7. PMC 2858943. PMID 19472918.
- 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.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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