TRAPPC2

TRAPPC2
Dynodwyr
Cyfenwau	TRAPPC2, MIP2A, SEDL, SEDT, TRAPPC2P1, TRS20, ZNF547L, hYP38334, trafficking protein particle complex 2, trafficking protein particle complex subunit 2
Dynodwyr allanol	OMIM: 300202 HomoloGene: 5436 GeneCards: TRAPPC2
Patrwm RNA pattern Rhagor o gyfeiriadau
Ontoleg y genyn Gweithrediad moleciwlaidd • transmembrane transporter binding • transcription factor binding • GO:0001948, GO:0016582 protein binding Cydrannau o'r gell • cytoplasm • cytosol • intracellular anatomical structure • perinuclear region of cytoplasm • Golgi membrane • cnewyllyn cell • nucleoplasm • Reticwlwm endoplasmig • endoplasmic reticulum-Golgi intermediate compartment • intracellular membrane-bounded organelle • TRAPP complex Prosesau biolegol • skeletal system development • GO:0009373 regulation of transcription, DNA-templated • transcription, DNA-templated • COPII vesicle coating • vesicle-mediated transport • endoplasmic reticulum to Golgi vesicle-mediated transport Sources:Amigo / QuickGO
Orthologau
Species	Bod dynol	Llygoden
Entrez	6399	n/a
Ensembl	ENSG00000196459	n/a
UniProt	P0DI81 P0DI82	n/a
RefSeq (mRNA)	NM_001011658 NM_001128835 NM_014563	n/a
RefSeq (protein)	NP_001011658 NP_001122307 NP_055378 NP_001011658.1 NP_055378.1	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 TRAPPC2 yw TRAPPC2 a elwir hefyd yn Trafficking protein particle complex subunit 2B a Trafficking protein particle complex 2 (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn ôl Q61333, band Xp22.2.

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 TRAPPC2.

• SEDL
• SEDT
• MIP2A
• TRS20
• ZNF547L
• hYP38334
• TRAPPC2P1

Llyfryddiaeth

• "A novel splicing mutation in the SEDL gene causes spondyloepiphyseal dysplasia tarda in a large Chinese pedigree. ". Clin Chim Acta. 2013. PMID 23876379.
• "Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes SEDT. ". Clin Genet. 2014. PMID 23656395.
• "[Mutation analysis of the TRAPPC2 gene in a Chinese family with X-linked spondyloepiphyseal dysplasia tarda]. ". Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID 26252088.
• "[Analysis of SEDL gene mutation in a Chinese pedigree with X-linked spondyloepiphyseal dysplasia tarda]. ". Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID 25297591.
• "A novel nonsense mutation in the sedlin gene (SEDL) causes severe spondyloepiphyseal dysplasia tarda in a five-generation Chinese pedigree.". Genet Mol Res. 2014. PMID 24841781.