Integrin alpha 10

Integrin alpha-10 also known as ITGA10 is a protein that in humans is encoded by the ITGA10 gene.[4][5][6]

ITGA10
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesITGA10, PRO827, integrin subunit alpha 10
External IDsOMIM: 604042 MGI: 2153482 HomoloGene: 2697 GeneCards: ITGA10
Gene location (Human)
Chr.Chromosome 1 (human)[1]
Band1q21.1Start145,891,208 bp[1]
End145,910,111 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

8515

213119

Ensembl

ENSG00000143127

n/a

UniProt

O75578

n/a

RefSeq (mRNA)

NM_001303040
NM_001303041
NM_003637

NM_001081053
NM_001302471

RefSeq (protein)

NP_001289969
NP_001289970
NP_003628

n/a

Location (UCSC)Chr 1: 145.89 – 145.91 Mbn/a
PubMed search[2][3]
Wikidata
View/Edit HumanView/Edit Mouse

Function

Integrins are integral membrane proteins composed of an alpha chain and a beta chain, and are known to participate in cell adhesion as well as cell-surface mediated signalling. The I-domain containing alpha 10 combines with the integrin beta 1 chain (ITGB1) to form a novel collagen type II-binding integrin expressed in cartilage tissue.[4]

References

  1. GRCh38: Ensembl release 89: ENSG00000143127 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Entrez Gene: ITGA10 integrin, alpha 10".
  5. Camper L, Hellman U, Lundgren-Akerlund E (August 1998). "Isolation, cloning, and sequence analysis of the integrin subunit alpha10, a beta1-associated collagen binding integrin expressed on chondrocytes". J. Biol. Chem. 273 (32): 20383–9. doi:10.1074/jbc.273.32.20383. PMID 9685391.
  6. Lehnert K, Ni J, Leung E, Gough S, Morris CM, Liu D, Wang SX, Langley R, Krissansen GW (1999). "The integrin alpha10 subunit: expression pattern, partial gene structure, and chromosomal localization". Cytogenet. Cell Genet. 87 (3–4): 238–44. doi:10.1159/000015434. PMID 10702680.
  7. Klopocki E, Schulze H, Strauss G, et al. (February 2007). "Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome". Am. J. Hum. Genet. 80 (2): 232–40. doi:10.1086/510919. PMC 1785342. PMID 17236129.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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