HIST1H2BL
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn HIST1H2BL yw HIST1H2BL a elwir hefyd yn Histone cluster 1 H2B family member l (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 6, band 6p22.1.[2]
H2BC13 | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | H2BC13, H2B/c, H2BFC, dJ97D16.4, histone cluster 1, H2bl, histone cluster 1 H2B family member l, H2B clustered histone 13, HIST1H2BL | ||||||||||||||||
Dynodwyr allanol | OMIM: 602800 HomoloGene: 136771 GeneCards: H2BC13 | ||||||||||||||||
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Species | Bod dynol | Llygoden | |||||||||||||||
Entrez |
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Ensembl |
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UniProt |
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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 HIST1H2BL.
- H2B/c
- H2BFC
- dJ97D16.4
Llyfryddiaeth
golygu- "Alpha thalassemia/mental retardation syndrome X-linked gene product ATRX is required for proper replication restart and cellular resistance to replication stress. ". J Biol Chem. 2013. PMID 23329831.
- "Inhibition of core histones acetylation by carcinogenic nickel(II). ". Mol Cell Biochem. 2005. PMID 16283522.
- "The human H2A and H2B histone gene complement. ". Biol Chem. 1999. PMID 10064132.
- "Disease mutant analysis identifies a new function of DAXX in telomerase regulation and telomere maintenance. ". J Cell Sci. 2015. PMID 25416818.
- "Quantitative proteomic analysis of post-translational modifications of human histones.". Mol Cell Proteomics. 2006. PMID 16627869.