Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1997 Jan 1;25(1):181-7.
doi: 10.1093/nar/25.1.181.

The human type I collagen mutation database

Affiliations

The human type I collagen mutation database

R Dalgleish. Nucleic Acids Res. .

Abstract

Type I collagen is the most abundant and ubiquitously distributed of the collagen family of proteins. It is a heterotrimer comprising two alpha1(I) chains and one alpha2(I) chain which are encoded by the unlinked loci COL1A1 and COL1A2 respectively. Mutations at these loci result primarily in the connective tissue disorders osteogenesis imperfecta and Ehlers-Danlos syndrome types VIIA and VIIB. Two instances of osteoporosis and a single instance of Marfan syndrome are also the result of mutations at these loci. The mutation data are accessible on the world wide web at http://www.le.ac.uk/depts/ge/collagen/collagen.html

PubMed Disclaimer

References

    1. Nucleic Acids Res. 1991 Aug 11;19(15):4302 - PubMed
    1. Annu Rev Biophys Biophys Chem. 1991;20:137-52 - PubMed
    1. Matrix. 1991 Dec;11(6):375-9 - PubMed
    1. Matrix. 1992 Apr;12(2):87-91 - PubMed
    1. J Med Genet. 1993 Jun;30(6):492-6 - PubMed

Associated data