The Human Collagen Mutation Database 1998
- PMID: 9399846
- PMCID: PMC147171
- DOI: 10.1093/nar/26.1.253
The Human Collagen Mutation Database 1998
Abstract
The collagens are a large and diverse family of proteins which are found in the extracellular matrix. In common with one another, the 19 known collagen types have triple-helical domains of variable length but they differ with respect to their overall size and the nature and location of their globular domains. Collagen mutations lead to heritable defects of connective tissues and mutation data for collagen types I and III are presented here. The mutation data are accessible on the world wide web at http://www.le.ac.uk/genetics/collagen/
Similar articles
-
The human type I collagen mutation database.Nucleic Acids Res. 1997 Jan 1;25(1):181-7. doi: 10.1093/nar/25.1.181. Nucleic Acids Res. 1997. PMID: 9016532 Free PMC article.
-
Database of mutations within the adenovirus 5 E1A oncogene.Nucleic Acids Res. 1998 Jan 1;26(1):292-4. doi: 10.1093/nar/26.1.292. Nucleic Acids Res. 1998. PMID: 9399857 Free PMC article.
-
Folding defects in fibrillar collagens.Philos Trans R Soc Lond B Biol Sci. 2001 Feb 28;356(1406):151-7; discussion 157-8. doi: 10.1098/rstb.2000.0760. Philos Trans R Soc Lond B Biol Sci. 2001. PMID: 11260795 Free PMC article. Review.
-
The collagen superfamily.Int Arch Allergy Immunol. 1995 Aug;107(4):484-90. doi: 10.1159/000237090. Int Arch Allergy Immunol. 1995. PMID: 7620364 Review.
-
Pfam: multiple sequence alignments and HMM-profiles of protein domains.Nucleic Acids Res. 1998 Jan 1;26(1):320-2. doi: 10.1093/nar/26.1.320. Nucleic Acids Res. 1998. PMID: 9399864 Free PMC article.
Cited by
-
The type of variants at the COL3A1 gene associates with the phenotype and severity of vascular Ehlers-Danlos syndrome.Eur J Hum Genet. 2015 Dec;23(12):1657-64. doi: 10.1038/ejhg.2015.32. Epub 2015 Mar 11. Eur J Hum Genet. 2015. PMID: 25758994 Free PMC article.
-
A brilliant breakthrough in OI type V.Osteoporos Int. 2014 Feb;25(2):399-405. doi: 10.1007/s00198-013-2465-8. Epub 2013 Sep 13. Osteoporos Int. 2014. PMID: 24030286 Review.
-
Osteogenesis imperfecta type III/Ehlers-Danlos overlap syndrome in a Chinese man.Intractable Rare Dis Res. 2018 Feb;7(1):37-41. doi: 10.5582/irdr.2018.01010. Intractable Rare Dis Res. 2018. PMID: 29552444 Free PMC article.
-
Collagen type III alpha I is a gastro-oesophageal reflux disease susceptibility gene and a male risk factor for hiatus hernia.Gut. 2009 Aug;58(8):1063-9. doi: 10.1136/gut.2008.167353. Epub 2009 Apr 26. Gut. 2009. PMID: 19398442 Free PMC article.
-
Homozygosity for a null allele of COL3A1 results in recessive Ehlers-Danlos syndrome.Eur J Hum Genet. 2009 Nov;17(11):1411-6. doi: 10.1038/ejhg.2009.76. Epub 2009 May 20. Eur J Hum Genet. 2009. PMID: 19455184 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources