NSUN5

NSUN5
Strwythurau PDB Human UniProt search: PDBe RCSB Rhestr o ddynodwyr PDB 2B9E
Dynodwyr
Cyfenwau	NSUN5, NOL1, NOL1R, NSUN5A, WBSCR20, WBSCR20A, p120, p120(NOL1), NOP2/Sun RNA methyltransferase family member 5, NOP2/Sun RNA methyltransferase 5
Dynodwyr allanol	OMIM: 615732 HomoloGene: 6828 GeneCards: NSUN5
Patrwm RNA pattern Rhagor o gyfeiriadau
Ontoleg y genyn Gweithrediad moleciwlaidd • GO:0102674, GO:0102675 methyltransferase activity • transferase activity • S-adenosylmethionine-dependent methyltransferase activity • RNA methyltransferase activity • RNA binding Cydrannau o'r gell • cnewyllyn cell • nucleolus Prosesau biolegol • rRNA processing • methylation • rRNA base methylation Sources:Amigo / QuickGO
Orthologau
Species	Bod dynol	Llygoden
Entrez	55695	n/a
Ensembl	ENSG00000130305	n/a
UniProt	Q96P11	n/a
RefSeq (mRNA)	NM_001168347 NM_001168348 NM_018044 NM_148956	n/a
RefSeq (protein)	NP_001161819 NP_001161820 NP_060514 NP_683759	n/a
Lleoliad (UCSC)	n/a	n/a
PubMed search		n/a
Wicidata
Gweld/Golygu Bod dynol

Protein sy'n cael ei godio yn y corff dynol gan y genyn NSUN5 yw NSUN5 a elwir hefyd yn NOP2/Sun RNA methyltransferase family member 5 (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 7q11.23.

Cyfystyron

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 NSUN5.

• NOL1
• p120
• NOL1R
• NSUN5A
• WBSCR20
• WBSCR20A
• p120(NOL1)

Llyfryddiaeth

• "hnRNPA1 couples nuclear export and translation of specific mRNAs downstream of FGF-2/S6K2 signalling. ". Nucleic Acids Res. 2014. PMID 25324306.
• "The variant Polycomb Repressor Complex 1 component PCGF1 interacts with a pluripotency sub-network that includes DPPA4, a regulator of embryogenesis. ". Sci Rep. 2015. PMID 26687479.
• "Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome. ". Cytogenet Cell Genet. 2001. PMID 11978965.
• "Identification of additional transcripts in the Williams-Beuren syndrome critical region. ". Hum Genet. 2002. PMID 12073013.
• "Proteomic analysis of the epidermal growth factor receptor (EGFR) interactome and post-translational modifications associated with receptor endocytosis in response to EGF and stress.". Mol Cell Proteomics. 2014. PMID 24797263.