ASCC2

Protein sy'n cael ei godio yn y corff dynol gan y genyn ASCC2 yw ASCC2 a elwir hefyd yn Activating signal cointegrator 1 complex subunit 2 (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 22, band 22q12.2.

ASCC2
Strwythurau PDB Human UniProt search: PDBe RCSB Rhestr o ddynodwyr PDB 2DI0
Dynodwyr
Cyfenwau	ASCC2, ASC1p100, p100, activating signal cointegrator 1 complex subunit 2
Dynodwyr allanol	OMIM: 614216 HomoloGene: 41774 GeneCards: ASCC2
Patrwm RNA pattern Rhagor o gyfeiriadau
Orthologau
Species	Bod dynol	Llygoden
Entrez	84164	n/a
Ensembl	ENSG00000100325	n/a
UniProt	Q9H1I8	n/a
RefSeq (mRNA)	NM_001242906 NM_032204	n/a
RefSeq (protein)	NP_001229835 NP_115580 NP_001356849 NP_001356850 NP_001356851 NP_001356852 NP_001356853 NP_001356854 NP_001356855 NP_001356856 NP_001356857 NP_001356858 NP_001356859 NP_001356860 NP_001356861 NP_001356862 NP_001356863 NP_001356864 NP_001356865 NP_001356866 NP_001356867 NP_001356868 NP_001356869 NP_001356870 NP_001356871 NP_001356872 NP_001356873 NP_001356874 NP_001356875 NP_001356876 NP_001356877 NP_001356878 NP_001356879	n/a
Lleoliad (UCSC)	n/a	n/a
PubMed search		n/a
Wicidata
Gweld/Golygu Bod dynol

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 ASCC2.

• p100
• ASC1p100

Llyfryddiaeth

• "Chromosome-wide mapping of estrogen receptor binding reveals long-range regulation requiring the forkhead protein FoxA1. ". Cell. 2005. PMID 16009131.
• "The MEKK1 PHD ubiquitinates TAB1 to activate MAPKs in response to cytokines. ". EMBO J. 2014. PMID 25260751.
• "Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study. ". Front Genet. 2013. PMID 24478790.
• "Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures. ". Am J Hum Genet. 2016. PMID 26924529.
• "Novel transcription coactivator complex containing activating signal cointegrator 1.". Mol Cell Biol. 2002. PMID 12077347.