FHL1 |
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Dynodwyr |
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Cyfenwau | FHL1, FHL-1, FHL1A, FHL1B, FLH1A, KYOT, SLIM, SLIM-1, SLIM1, SLIMMER, XMPMA, RBMX1A, RBMX1B, four and a half LIM domains 1, FCMSU |
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Dynodwyr allanol | OMIM: 300163 HomoloGene: 31038 GeneCards: FHL1 |
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Orthologau |
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Species | Bod dynol | Llygoden |
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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 |
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PubMed search | [1] | n/a |
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Wicidata |
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Protein sy'n cael ei godio yn y corff dynol gan y genyn FHL1 yw FHL1 a elwir hefyd yn Four and a half LIM domains protein 1 (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 X dynol, band Xq26.3.[2]
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 FHL1.
- KYOT
- SLIM
- FCMSU
- FHL-1
- FHL1A
- FHL1B
- FLH1A
- SLIM1
- XMPMA
- RBMX1A
- RBMX1B
- SLIM-1
- SLIMMER
- "Exome Sequencing Identified a Splice Site Mutation in FHL1 that Causes Uruguay Syndrome, an X-Linked Disorder With Skeletal Muscle Hypertrophy and Premature Cardiac Death. ". Circ Cardiovasc Genet. 2016. PMID 26933038.
- "X-linked FHL1 as a novel therapeutic target for head and neck squamous cell carcinoma. ". Oncotarget. 2016. PMID 26908444.
- "Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1. ". Clin Genet. 2016. PMID 26857240.
- "Development of autoantibodies against muscle-specific FHL1 in severe inflammatory myopathies. ". J Clin Invest. 2015. PMID 26551678.
- "[FHL1 knockdown mediated by lentiviral shRNA promotes the growth of HeLa and HepG2 cells].". Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2015. PMID 26146054.