SYN2
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn SYN2 yw SYN2 a elwir hefyd yn Synapsin II (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 3, band 3p25.2.[2]
SYN2 | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | SYN2, SYNII, Synapsin 2, synapsin II | ||||||||||||||||
Dynodwyr allanol | OMIM: 600755 HomoloGene: 49348 GeneCards: SYN2 | ||||||||||||||||
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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
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 SYN2.
- SYNII
Llyfryddiaeth
golygu- "Lack of association between synapsin II (SYN2) gene polymorphism and susceptibility epilepsy: a case-control study and meta-analysis. ". Synapse. 2011. PMID 21465568.
- "Association of intronic polymorphism rs3773364 A>G in synapsin-2 gene with idiopathic epilepsy. ". Synapse. 2010. PMID 20034013.
- "Identification of novel DNA-methylated genes that correlate with human prostate cancer and high-grade prostatic intraepithelial neoplasia. ". Prostate Cancer Prostatic Dis. 2013. PMID 23896626.
- "New methods for inducing the differentiation of amniotic-derived mesenchymal stem cells into motor neuron precursor cells. ". Tissue Cell. 2013. PMID 23806299.
- "Synapsin II is involved in the molecular pathway of lithium treatment in bipolar disorder.". PLoS One. 2012. PMID 22384280.