PAPSS2
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn PAPSS2 yw PAPSS2 a elwir hefyd yn 3'-phosphoadenosine 5'-phosphosulfate synthase 2, isoform CRA_b (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 10, band 10q23.2-q23.31.[2]
PAPSS2 | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | PAPSS2, ATPSK2, BCYM4, SK2, 3'-phosphoadenosine 5'-phosphosulfate synthase 2 | ||||||||||||||||
Dynodwyr allanol | OMIM: 603005 HomoloGene: 55840 GeneCards: PAPSS2 | ||||||||||||||||
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Orthologau | |||||||||||||||||
Species | Bod dynol | Llygoden | |||||||||||||||
Entrez |
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Ensembl |
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UniProt |
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RefSeq (mRNA) |
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RefSeq (protein) |
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Lleoliad (UCSC) | n/a | n/a | |||||||||||||||
PubMed search | [1] | n/a | |||||||||||||||
Wicidata | |||||||||||||||||
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Cyfystyron golygu
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 PAPSS2.
- SK2
- BCYM4
- ATPSK2
Llyfryddiaeth golygu
- "PAPSS2 mutations cause autosomal recessive brachyolmia. ". J Med Genet. 2012. PMID 22791835.
- "Altered responsiveness to TGF-β results in reduced Papss2 expression and alterations in the biomechanical properties of mouse articular cartilage. ". Arthritis Res Ther. 2012. PMID 22394585.
- "Gene Expression Differences Between Offspring of Long-Lived Individuals and Controls in Candidate Longevity Regions: Evidence for PAPSS2 as a Longevity Gene. ". J Gerontol A Biol Sci Med Sci. 2016. PMID 26896383.
- "PAPSS2 deficiency causes androgen excess via impaired DHEA sulfation--in vitro and in vivo studies in a family harboring two novel PAPSS2 mutations. ". J Clin Endocrinol Metab. 2015. PMID 25594860.
- "Clinical and radiographic features of the autosomal recessive form of brachyolmia caused by PAPSS2 mutations.". Hum Mutat. 2013. PMID 23824674.