RBM28
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn RBM28 yw RBM28 a elwir hefyd yn RNA-binding protein 28 a RNA binding motif protein 28 (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 7, band 7q32.1.[2]
RBM28 | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | RBM28, ANES, RNA binding motif protein 28 | ||||||||||||||||
Dynodwyr allanol | OMIM: 612074 HomoloGene: 135952 GeneCards: RBM28 | ||||||||||||||||
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Orthologau | |||||||||||||||||
Species | Bod dynol | Llygoden | |||||||||||||||
Entrez |
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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 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 RBM28.
- ANES
Llyfryddiaeth golygu
- "RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR-203 and p63. ". Exp Dermatol. 2015. PMID 25939713.
- "The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome. ". Elife. 2016. PMID 27077951.
- "ANE syndrome caused by mutated RBM28 gene: a novel etiology of combined pituitary hormone deficiency. ". Eur J Endocrinol. 2010. PMID 20231366.
- "Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesis. ". Am J Hum Genet. 2008. PMID 18439547.
- "Human RBM28 protein is a specific nucleolar component of the spliceosomal snRNPs.". Biol Chem. 2006. PMID 17081119.