Integrin beta 5

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Integrin beta-5 is a protein that in humans is encoded by the ITGB5 gene.[5][6]

AliasesITGB5, Integrin, beta 5, integrin subunit beta 5
End124,901,418 bp[1]
Quick facts ITGB5, Identifiers ...
ITGB5
Identifiers
AliasesITGB5, Integrin, beta 5, integrin subunit beta 5
External IDsOMIM: 147561; MGI: 96614; HomoloGene: 20511; GeneCards: ITGB5; OMA:ITGB5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002213
NM_001354764
NM_001354765
NM_001354766

NM_001145884
NM_010580

RefSeq (protein)

NP_002204
NP_001341693
NP_001341694
NP_001341695

NP_001139356
NP_034710
NP_001391992

Location (UCSC)Chr 3: 124.76 – 124.9 MbChr 16: 33.65 – 33.77 Mb
PubMed search[3][4]
Wikidata
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Interactions

Integrin, beta 5 has been shown to interact with PTK2,[7] Annexin A5[8] and PAK4.[9]

Functions

ITGB5 encodes a subunit of integrin that can interact with several alpha chains to form a variety of integrin heterodimers. It also plays a potential role in intercellular communication during tumor progression and metastasis.[10]

Clinical significance

Research

Elevated levels of ITGB5 have been found in patients with autosomal dominant osteopetrosis type II, a rare disease of bones.[11]

References

Further reading

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