TNNI2
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn TNNI2 yw TNNI2 a elwir hefyd yn Troponin I2, fast skeletal type (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 11, band 11p15.5.[2]
TNNI2 | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | TNNI2, AMCD2B, DA2B, FSSV, fsTnI, troponin I2, fast skeletal type, DA2B1 | ||||||||||||||||
Dynodwyr allanol | OMIM: 191043 HomoloGene: 37752 GeneCards: TNNI2 | ||||||||||||||||
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Species | Bod dynol | Llygoden | |||||||||||||||
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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
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 TNNI2.
- DA2B
- FSSV
- fsTnI
- AMCD2B
Llyfryddiaeth
golygu- "A mutation in the fast skeletal muscle troponin I gene causes myopathy and distal arthrogryposis. ". Neurology. 2006. PMID 16924011.
- "A novel deletion in TNNI2 causes distal arthrogryposis in a large Chinese family with marked variability of expression. ". Hum Genet. 2006. PMID 16802141.
- "A novel missense mutation of TNNI2 in a Chinese family cause distal arthrogryposis type 1. ". Am J Med Genet A. 2016. PMID 26374086.
- "A novel TNNI2 mutation causes Freeman-Sheldon syndrome in a Chinese family with an affected adult with only facial contractures. ". Gene. 2013. PMID 23850728.
- "Expression of the human fast-twitch skeletal muscle troponin I cDNA in a human ovarian carcinoma suppresses tumor growth.". Sci China C Life Sci. 2007. PMID 17393089.