CRYGS
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn CRYGS yw CRYGS a elwir hefyd yn Crystallin gamma S (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 3, band 3q27.3.[2]
CRYGS | |||||||||||||||
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Dynodwyr | |||||||||||||||
Cyfenwau | CRYGS, CRYG8, CTRCT20, crystallin gamma S | ||||||||||||||
Dynodwyr allanol | OMIM: 123730 HomoloGene: 40695 GeneCards: CRYGS | ||||||||||||||
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Species | Bod dynol | Llygoden | |||||||||||||
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Ensembl |
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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 CRYGS.
- CRYG8
- CTRCT20
Llyfryddiaeth
golygu- "Deamidation of Human γS-Crystallin Increases Attractive Protein Interactions: Implications for Cataract. ". Biochemistry. 2015. PMID 26158710.
- "A G57W Mutation of CRYGS Associated with Autosomal Dominant Pulverulent Cataracts in a Chinese Family. ". Ophthalmic Genet. 2015. PMID 24328668.
- "The cataract-associated V41M mutant of human γS-crystallin shows specific structural changes that directly enhance local surface hydrophobicity. ". Biochem Biophys Res Commun. 2014. PMID 24287181.
- "Structural analysis of the mutant protein D26G of human γS-crystallin, associated with Coppock cataract. ". Mol Vis. 2013. PMID 23761725.
- "The mutation V42M distorts the compact packing of the human gamma-S-crystallin molecule, resulting in congenital cataract.". PLoS One. 2012. PMID 23284690.