PDLIM3
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn PDLIM3 yw PDLIM3 a elwir hefyd yn PDZ and LIM domain 3 (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 dynol 4, band 4q35.1.[2]
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Dynodwyr | |||||||||||||||||
Cyfenwau | PDLIM3, ALP, PDZ and LIM domain 3 | ||||||||||||||||
Dynodwyr allanol | OMIM: 605889 HomoloGene: 8710 GeneCards: PDLIM3 | ||||||||||||||||
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Species | Bod dynol | Llygoden | |||||||||||||||
Entrez |
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Ensembl |
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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 | |||||||||||||||
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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 PDLIM3.
- ALP
Llyfryddiaeth golygu
- "Analysis of the Z-disc genes PDLIM3 and MYPN in patients with hypertrophic cardiomyopathy. ". Int J Cardiol. 2010. PMID 20801532.
- "Mutations in PDLIM3 and MYOZ1 encoding myocyte Z line proteins are infrequently found in idiopathic dilated cardiomyopathy. ". Mol Genet Metab. 2007. PMID 17254821.
- "Alternative splicing of PDLIM3/ALP, for α-actinin-associated LIM protein 3, is aberrant in persons with myotonic dystrophy. ". Biochem Biophys Res Commun. 2011. PMID 21549096.
- "Characterization of lobulated fibers in limb girdle muscular dystrophy type 2A by gene expression profiling. ". Neurosci Res. 2007. PMID 17258832.
- "Exclusion of muscle specific actinin-associated LIM protein (ALP) gene from 4q35 facioscapulohumeral muscular dystrophy (FSHD) candidate genes.". Neuromuscul Disord. 1999. PMID 10063829.