MIP
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn MIP yw MIP a elwir hefyd yn Major intrinsic protein of lens fiber (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 12, band 12q13.3.[2]
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Dynodwyr | |||||||||||||||||
Cyfenwau | MIP, AQP0, CTRCT15, LIM1, MIP26, MP26, major intrinsic protein of lens fiber | ||||||||||||||||
Dynodwyr allanol | OMIM: 154050 HomoloGene: 40627 GeneCards: MIP | ||||||||||||||||
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Species | Bod dynol | Llygoden | |||||||||||||||
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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 MIP.
- AQP0
- LIM1
- MP26
- MIP26
- CTRCT15
Llyfryddiaeth
golygu- "A novel MIP mutation in familial congenital nuclear cataracts. ". Eur J Med Genet. 2016. PMID 27456987.
- "A decrease in the permeability of aquaporin zero as a possible cause for presbyopia. ". Med Hypotheses. 2016. PMID 26615967.
- "Identification and Functional Analysis of a Novel MIP Gene Mutation Associated with Congenital Cataract in a Chinese Family. ". PLoS One. 2015. PMID 25946197.
- "A novel nonsense mutation in the MIP gene linked to congenital posterior polar cataracts in a Chinese family. ". PLoS One. 2015. PMID 25803033.
- "A novel MIP gene mutation analysis in a Chinese family affected with congenital progressive punctate cataract.". PLoS One. 2014. PMID 25033405.