CTSF
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn CTSF yw CTSF a elwir hefyd yn Cathepsin F (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn ôl o gromosom dynol 11, band 11q13.2.[2]
CTSF | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | CTSF, CATSF, CLN13, cathepsin F | ||||||||||||||||
Dynodwyr allanol | OMIM: 603539 HomoloGene: 31194 GeneCards: CTSF | ||||||||||||||||
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Species | Bod dynol | Llygoden | |||||||||||||||
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RefSeq (mRNA) |
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RefSeq (protein) |
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Lleoliad (UCSC) | n/a | n/a | |||||||||||||||
PubMed search | [1] | n/a | |||||||||||||||
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Cyfystyron
golyguYn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn CTSF.
- CATSF
- CLN13
Llyfryddiaeth
golygu- "The human cathepsin F gene--a fusion product between an ancestral cathepsin and cystatin gene. ". Biol Chem. 1999. PMID 10661872.
- "Full-length cDNA of human cathepsin F predicts the presence of a cystatin domain at the N-terminus of the cysteine protease zymogen. ". Biochem Biophys Res Commun. 1999. PMID 10198209.
- "Exome sequencing in a consanguineous family clinically diagnosed with early-onset Alzheimer's disease identifies a homozygous CTSF mutation. ". Neurobiol Aging. 2016. PMID 27524508.
- "Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis. ". Hum Mol Genet. 2013. PMID 23297359.
- "Cysteine protease cathepsin F is expressed in human atherosclerotic lesions, is secreted by cultured macrophages, and modifies low density lipoprotein particles in vitro.". J Biol Chem. 2004. PMID 15184381.