Collagen, type IV, alpha 6

Mammalian protein found in humans From Wikipedia, the free encyclopedia

Collagen alpha-6(IV) chain is a protein that in humans is encoded by the COL4A6 gene.[5][6]

AliasesCOL4A6, CXDELq22.3, DELXq22.3, DFNX6, collagen type IV alpha 6, collagen type IV alpha 6 chain
End108,439,497 bp[1]
Quick facts COL4A6, Identifiers ...
COL4A6
Identifiers
AliasesCOL4A6, CXDELq22.3, DELXq22.3, DFNX6, collagen type IV alpha 6, collagen type IV alpha 6 chain
External IDsOMIM: 303631; MGI: 2152695; HomoloGene: 48050; GeneCards: COL4A6; OMA:COL4A6 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001287758
NM_001287759
NM_001287760
NM_001847
NM_033641

NM_053185

RefSeq (protein)

n/a

Location (UCSC)Chr X: 108.16 – 108.44 MbChr X: 139.95 – 140.26 Mb
PubMed search[3][4]
Wikidata
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This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene, alpha 5 type IV collagen, so that the gene pair shares a common promoter. Deletions in the alpha 5 gene that extend into the alpha 6 gene result in diffuse leiomyomatosis accompanying the X-linked Alport syndrome caused by the deletion in the alpha 5 gene. Two splice variants have been identified for this gene.[6]

References

Further reading

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