Collagen, type IV, alpha 5: Difference between revisions

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*{{cite journal  | vauthors=Lemmink HH, Schröder CH, Monnens LA, Smeets HJ |title=The clinical spectrum of type IV collagen mutations. |journal=Hum. Mutat. |volume=9 |issue= 6 |pages= 477–99 |year= 1997 |pmid= 9195222 |doi= 10.1002/(SICI)1098-1004(1997)9:6<477::AID-HUMU1>3.0.CO;2-# }}
*{{cite journal  | vauthors=Lemmink HH, Schröder CH, Monnens LA, Smeets HJ |title=The clinical spectrum of type IV collagen mutations |journal=Hum. Mutat. |volume=9 |issue= 6 |pages= 477–99 |year= 1997 |pmid= 9195222 |doi= 10.1002/(SICI)1098-1004(1997)9:6<477::AID-HUMU1>3.0.CO;2-# |doi-broken-date=2018-09-06 }}
*{{cite journal  | vauthors=Ständer M, Naumann U, Wick W, Weller M |title=Transforming growth factor-beta and p-21: multiple molecular targets of decorin-mediated suppression of neoplastic growth. |journal=Cell Tissue Res. |volume=296 |issue= 2 |pages= 221–7 |year= 1999 |pmid= 10382266 |doi=10.1007/s004410051283  }}
*{{cite journal  | vauthors=Ständer M, Naumann U, Wick W, Weller M |title=Transforming growth factor-beta and p-21: multiple molecular targets of decorin-mediated suppression of neoplastic growth |journal=Cell Tissue Res. |volume=296 |issue= 2 |pages= 221–7 |year= 1999 |pmid= 10382266 |doi=10.1007/s004410051283  }}
*{{cite journal  | vauthors=Kurpakus Wheater M, Kernacki KA, Hazlett LD |title=Corneal cell proteins and ocular surface pathology. |journal=Biotechnic & Histochemistry |volume=74 |issue= 3 |pages= 146–59 |year= 1999 |pmid= 10416788 |doi=  10.3109/10520299909047967}}
*{{cite journal  | vauthors=Kurpakus Wheater M, Kernacki KA, Hazlett LD |title=Corneal cell proteins and ocular surface pathology |journal=Biotechnic & Histochemistry |volume=74 |issue= 3 |pages= 146–59 |year= 1999 |pmid= 10416788 |doi=  10.3109/10520299909047967}}
*{{cite journal  | vauthors=Zhou J, Hertz JM, Leinonen A, Tryggvason K |title=Complete amino acid sequence of the human alpha 5 (IV) collagen chain and identification of a single-base mutation in exon 23 converting glycine 521 in the collagenous domain to cysteine in an Alport syndrome patient. |journal=J. Biol. Chem. |volume=267 |issue= 18 |pages= 12475–81 |year= 1992 |pmid= 1352287 |doi=  }}
*{{cite journal  | vauthors=Zhou J, Hertz JM, Leinonen A, Tryggvason K |title=Complete amino acid sequence of the human alpha 5 (IV) collagen chain and identification of a single-base mutation in exon 23 converting glycine 521 in the collagenous domain to cysteine in an Alport syndrome patient |journal=J. Biol. Chem. |volume=267 |issue= 18 |pages= 12475–81 |year= 1992 |pmid= 1352287 |doi=  }}
*{{cite journal  | author=Renieri A |title=De novo mutation in the COL4A5 gene converting glycine 325 to glutamic acid in Alport syndrome |journal=Hum. Mol. Genet. |volume=1 |issue= 2 |pages= 127–9 |year= 1993 |pmid= 1363780 |doi=10.1093/hmg/1.2.127  |name-list-format=vanc| author2=Seri M  | author3=Myers JC  | display-authors=3  | last4=Pihlajaniemi  | first4=Taina  | last5=Massella  | first5=Laura  | last6=Rizzoni  | first6=Gianfranco  | last7=Marchi  | first7=Mario De  }}
*{{cite journal  | author=Renieri A |title=De novo mutation in the COL4A5 gene converting glycine 325 to glutamic acid in Alport syndrome |journal=Hum. Mol. Genet. |volume=1 |issue= 2 |pages= 127–9 |year= 1993 |pmid= 1363780 |doi=10.1093/hmg/1.2.127  |name-list-format=vanc| author2=Seri M  | author3=Myers JC  | display-authors=3  | last4=Pihlajaniemi  | first4=Taina  | last5=Massella  | first5=Laura  | last6=Rizzoni  | first6=Gianfranco  | last7=Marchi  | first7=Mario De  }}
*{{cite journal  | author=Knebelmann B |title=Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-amplified lymphoblast cDNA fragments |journal=Am. J. Hum. Genet. |volume=51 |issue= 1 |pages= 135–42 |year= 1992 |pmid= 1376965 |doi=  | pmc=1682875  |name-list-format=vanc| author2=Deschenes G  | author3=Gros F  | display-authors=3  | last4=Hors  | first4=MC  | last5=Grünfeld  | first5=JP  | last6=Zhou  | first6=J  | last7=Tryggvason  | first7=K  | last8=Gubler  | first8=MC  | last9=Antignac  | first9=C  }}
*{{cite journal  | author=Knebelmann B |title=Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-amplified lymphoblast cDNA fragments |journal=Am. J. Hum. Genet. |volume=51 |issue= 1 |pages= 135–42 |year= 1992 |pmid= 1376965 |doi=  | pmc=1682875  |name-list-format=vanc| author2=Deschenes G  | author3=Gros F  | display-authors=3  | last4=Hors  | first4=MC  | last5=Grünfeld  | first5=JP  | last6=Zhou  | first6=J  | last7=Tryggvason  | first7=K  | last8=Gubler  | first8=MC  | last9=Antignac  | first9=C  }}

Latest revision as of 00:07, 6 September 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

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RefSeq (protein)

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Collagen alpha-5(IV) chain is a protein that in humans is encoded by the COL4A5 gene.

This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. 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. Three transcript variants have been identified for this gene.[1]

Disease Databases

ARUP COL4A5 gene variant database

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

See also

References

  1. "Entrez Gene: COL4A5 collagen, type IV, alpha 5 (Alport syndrome)".

Further reading