HNRNPH2
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn HNRNPH2 yw HNRNPH2 a elwir hefyd yn Heterogeneous nuclear ribonucleoprotein H2 (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn blaen o gromosom X dynol, band Xq22.1.[2]
HNRNPH2 | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | HNRNPH2, FTP3, HNRPH', HNRPH2, hnRNPH', heterogeneous nuclear ribonucleoprotein H2 (H'), heterogeneous nuclear ribonucleoprotein H2, MRXSB, NRPH2 | ||||||||||||||||
Dynodwyr allanol | OMIM: 300610 HomoloGene: 23165 GeneCards: HNRNPH2 | ||||||||||||||||
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Orthologau | |||||||||||||||||
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 golygu
Yn 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 HNRNPH2.
- FTP3
- MRXSB
- NRPH2
- HNRPH'
- HNRPH2
- hnRNPH'
Llyfryddiaeth golygu
- "Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in Females. ". Am J Hum Genet. 2016. PMID 27545675.
- "The hnRNPs F and H2 bind to similar sequences to influence gene expression. ". Biochem J. 2006. PMID 16171461.
- "Determination of the RNA binding specificity of the heterogeneous nuclear ribonucleoprotein (hnRNP) H/H'/F/2H9 family. ". J Biol Chem. 2001. PMID 11571276.
- "Heterogeneous nuclear ribonucleoprotein H1/H2-dependent unsplicing of thymidine phosphorylase results in anticancer drug resistance. ". J Biol Chem. 2011. PMID 21068389.
- "Heterogeneous nuclear ribonucleoproteins F and H/H' show differential expression in normal and selected cancer tissues.". Exp Cell Res. 2004. PMID 14980514.