ASMTL

Protein sy'n cael ei godio yn y corff dynol gan y genyn ASMTL yw ASMTL a elwir hefyd yn Acetylserotonin O-methyltransferase like (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 X dynol, band Xp22.33 and Yp11.2.

ASMTL
Strwythurau PDB Human UniProt search: PDBe RCSB Rhestr o ddynodwyr PDB 2P5X
Dynodwyr
Cyfenwau	ASMTL, ASMTLX, ASMTLY, ASTML, acetylserotonin O-methyltransferase-like, acetylserotonin O-methyltransferase like
Dynodwyr allanol	OMIM: 300162, 400011 HomoloGene: 36273 GeneCards: ASMTL
Patrwm RNA pattern Rhagor o gyfeiriadau
Ontoleg y genyn Gweithrediad moleciwlaidd • GO:0102674, GO:0102675 methyltransferase activity • transferase activity • GO:0001948, GO:0016582 protein binding • O-methyltransferase activity • nucleoside-triphosphate diphosphatase activity • molecular function • nucleotide diphosphatase activity • NADH pyrophosphatase activity • hydrolase activity Cydrannau o'r gell • cytosol Prosesau biolegol • methylation • GO:0022610 proses fiolegol • nucleotide metabolic process Sources:Amigo / QuickGO
Orthologau
Species	Bod dynol	Llygoden
Entrez	8623	n/a
Ensembl	ENSG00000169093	n/a
UniProt	O95671	n/a
RefSeq (mRNA)	NM_001173473 NM_001173474 NM_004192	n/a
RefSeq (protein)	NP_001166944 NP_001166945 NP_004183	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 ASMTL.

• ASTML
• ASMTLX
• ASMTLY

Llyfryddiaeth

• "A high-throughput approach for measuring temporal changes in the interactome. ". Nat Methods. 2012. PMID 22863883.
• "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. ". Cell. 2006. PMID 17081983.
• "Gene duplications as a recurrent theme in the evolution of the human pseudoautosomal region 1: isolation of the gene ASMTL. ". Hum Mol Genet. 1998. PMID 9736779.
• "Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism. ". Nat Commun. 2014. PMID 24722188.
• "Proteomic analyses reveal distinct chromatin-associated and soluble transcription factor complexes.". Mol Syst Biol. 2015. PMID 25609649.