AP1S1
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn AP1S1 yw AP1S1 a elwir hefyd yn Adaptor related protein complex 1 sigma 1 subunit (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn blaen o gromosom dynol 7, band 7q22.1.[2]
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| Cyfenwau | AP1S1, AP19, CLAPS1, EKV3, MEDNIK, SIGMA1A, WUGSC:H_DJ0747G18.2, adaptor related protein complex 1 sigma 1 subunit, adaptor related protein complex 1 subunit sigma 1 | ||||||||||||||
| Dynodwyr allanol | OMIM: 603531 HomoloGene: 20342 GeneCards: AP1S1 | ||||||||||||||
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| Species | Bod dynol | Llygoden | |||||||||||||
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| Lleoliad (UCSC) | n/a | n/a | |||||||||||||
| PubMed search | [1] | n/a | |||||||||||||
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Cyfystyron
golyguYn 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 AP1S1.
- AP19
- EKV3
- CLAPS1
- MEDNIK
- SIGMA1A
Llyfryddiaeth
golygu- "MEDNIK syndrome: a novel defect of copper metabolism treatable by zinc acetate therapy. ". Brain. 2013. PMID 23423674.
- "An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22. ". Hum Genet. 2005. PMID 15668823.
- "Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord. ". PLoS Genet. 2008. PMID 19057675.
- "Cooperation of GGAs and AP-1 in packaging MPRs at the trans-Golgi network. ". Science. 2002. PMID 12215646.
- "An ear-core interaction regulates the recruitment of the AP-3 complex to membranes.". Dev Cell. 2004. PMID 15469849.