Collagen alpha-4(IV) chain is a protein that in humans is encoded by the COL4A4 gene.[5][6]

Quick Facts COL4A4, Identifiers ...
COL4A4
Identifiers
AliasesCOL4A4, CA44, collagen type IV alpha 4, collagen type IV alpha 4 chain, BFH, ATS2
External IDsOMIM: 120131; MGI: 104687; HomoloGene: 20071; GeneCards: COL4A4; OMA:COL4A4 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000092

NM_007735

RefSeq (protein)

NP_000083

NP_031761

Location (UCSC)Chr 2: 227 – 227.16 MbChr 1: 82.43 – 82.56 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. This particular collagen IV subunit, however, is only found in a subset 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 so that each gene pair shares a common promoter. Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease). Two transcripts, differing only in their transcription start sites, have been identified for this gene and, as is common for collagen genes, multiple polyadenylation sites are found in the 3' UTR.[6]

Disease Database

LOVD Alport gene variant databases (COL4A4, COL4A3, COL4A5)

References

Further reading

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