CRYGB
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn CRYGB yw CRYGB a elwir hefyd yn Crystallin gamma B (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 2, band 2q33.3.[2]
CRYGB | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | CRYGB, CRYG2, CTRCT39, crystallin gamma B | ||||||||||||||||
Dynodwyr allanol | OMIM: 123670 HomoloGene: 3816 GeneCards: CRYGB | ||||||||||||||||
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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 CRYGB.
- CRYG2
- CTRCT39
Llyfryddiaeth
golygu- "Glycation of human γB-crystallin: A biophysical investigation. ". Int J Biol Macromol. 2017. PMID 28013006.
- "[ALLELIC VARIANT FREQUENCY OF PROMOTER (G(-47)-->A) γ-CRYSTALLIN GENE AFFECTS THE LEVEL OF ITS EXPRESSION IN PLATELETS]. ". Fiziol Zh. 2015. PMID 26552302.
- "Novel crystallin gamma B mutations in a Kuwaiti family with autosomal dominant congenital cataracts reveal genetic and clinical heterogeneity. ". Mol Vis. 2012. PMID 23288985.
- "Polymorphisms of the gamma crystallin A and B genes among Indian patients with pediatric cataract. ". J Postgrad Med. 2011. PMID 21941057.
- "Prediction of possible sites for posttranslational modifications in human gamma crystallins: effect of glycation on the structure of human gamma-B-crystallin as analyzed by molecular modeling.". Proteins. 2003. PMID 14517968.