Cystatin C: Difference between revisions
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'''Cystatin 3''', usually called '''Cystatin C''' (also '''CST3''' and '''Gamma trace''') is a [[serum]] protein used mainly as a measure of [[glomerular filtration rate]]. It is a single 120-residue polypeptide belonging to the type 2 [[cystatin]] gene family. Studies have shown that Cystatin C allows a more precise testing of kidney function than [[creatinine]]. |
'''Cystatin 3''', usually called '''Cystatin C''' (also '''CST3''' and '''Gamma trace''') is a [[serum]] protein used mainly as a measure of [[glomerular filtration rate]]. It is a single 120-residue polypeptide belonging to the type 2 [[cystatin]] gene family. Studies have shown that Cystatin C allows a more precise testing of kidney function than [[creatinine]]. |
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[[Mutation]]s in the cystatin 3 [[gene]] are responsible for the Icelandic type of hereditary [[cerebral amyloid angiopathy]], a condition predisposing to [[intracerebral haemorrhage]]. |
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== External links == |
== External links == |
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* [http://www.medterms.com/script/main/art.asp?articlekey=39781 Definition of Cystatin C] |
* [http://www.medterms.com/script/main/art.asp?articlekey=39781 Definition of Cystatin C] |
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[[Category:Proteins]] |
[[Category:Proteins]] |
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[[Category:Nephrology]] |
[[Category:Nephrology]] |
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[[ru:Цистатин C]] |
[[ru:Цистатин C]] |
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[[sv:Cystatin C]] |
[[sv:Cystatin C]] |
Revision as of 22:42, 6 October 2007
cystatin C (amyloid angiopathy and cerebral hemorrhage) | |||||||
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Identifiers | |||||||
Symbol | CST3 | ||||||
NCBI gene | 1471 | ||||||
HGNC | 2475 | ||||||
OMIM | 604312 | ||||||
RefSeq | NM_000099 | ||||||
UniProt | P01034 | ||||||
Other data | |||||||
Locus | Chr. 20 p11.2 | ||||||
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Cystatin 3, usually called Cystatin C (also CST3 and Gamma trace) is a serum protein used mainly as a measure of glomerular filtration rate. It is a single 120-residue polypeptide belonging to the type 2 cystatin gene family. Studies have shown that Cystatin C allows a more precise testing of kidney function than creatinine.
Mutations in the cystatin 3 gene are responsible for the Icelandic type of hereditary cerebral amyloid angiopathy, a condition predisposing to intracerebral haemorrhage.