Integrin, beta 6

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ITGB6
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases ITGB6, AI1H, Integrin, beta 6, integrin subunit beta 6
External IDs MGI: 96615 HomoloGene: 685 GeneCards: ITGB6
Gene location (Human)
Chromosome 2 (human)
Chr. Chromosome 2 (human)[1]
Chromosome 2 (human)
Genomic location for ITGB6
Genomic location for ITGB6
Band 2q24.2 Start 160,099,666 bp[1]
End 160,271,888 bp[1]
RNA expression pattern
PBB GE ITGB6 208084 at fs.png

PBB GE ITGB6 208083 s at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001159564
NM_021359

RefSeq (protein)

NP_001153036
NP_067334

Location (UCSC) Chr 2: 160.1 – 160.27 Mb Chr 2: 60.6 – 60.72 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Integrin beta-6 is a protein that in humans is encoded by the ITGB6 gene.[5][6][7]


Clinical effects[edit]

Mutations in ITGB6 cause amelogenesis imperfecta .[8]

Interactions[edit]

Integrin, beta 6 has been shown to interact with FHL2.[9]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000115221 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000026971 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". 
  4. ^ "Mouse PubMed Reference:". 
  5. ^ Krissansen GW, Yuan Q, Jenkins D, Jiang WM, Rooke L, Spurr NK, Eccles M, Leung E, Watson JD (February 1992). "Chromosomal locations of the genes coding for the integrin beta 6 and beta 7 subunits". Immunogenetics. 35 (1): 58–61. doi:10.1007/bf00216629. PMID 1729173. 
  6. ^ Weinacker A, Chen A, Agrez M, Cone RI, Nishimura S, Wayner E, Pytela R, Sheppard D (April 1994). "Role of the integrin alpha v beta 6 in cell attachment to fibronectin. Heterologous expression of intact and secreted forms of the receptor". J Biol Chem. 269 (9): 6940–8. PMID 8120056. 
  7. ^ "Entrez Gene: ITGB6 integrin, beta 6". 
  8. ^ Wang, S. K.; Choi, M; Richardson, A. S.; Reid, B. M.; Lin, B. P.; Wang, S. J.; Kim, J. W.; Simmer, J. P.; Hu, J. C. (2014). "ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta". Human Molecular Genetics. 23 (8): 2157–63. doi:10.1093/hmg/ddt611. PMC 3959820Freely accessible. PMID 24305999. 
  9. ^ Wixler, V; Geerts D; Laplantine E; Westhoff D; Smyth N; Aumailley M; Sonnenberg A; Paulsson M (October 2000). "The LIM-only protein DRAL/FHL2 binds to the cytoplasmic domain of several alpha and beta integrin chains and is recruited to adhesion complexes". J. Biol. Chem. UNITED STATES. 275 (43): 33669–78. doi:10.1074/jbc.M002519200. ISSN 0021-9258. PMID 10906324. 

Further reading[edit]

External links[edit]