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Je něco špatně v tomto záznamu ?
A mutation in CFTR produces different phenotypes depending on chromosomal background
S Kiesewetter, M Jr Macek, C Davis, SM Curristin, CS Chu, C Graham, AE Shrimpton, SM Cashman, LC Tsui, J Mickle
Jazyk angličtina Země Spojené státy americké
Typ dokumentu práce podpořená grantem, Research Support, U.S. Gov't, P.H.S.
Grantová podpora
PL215
MZ0
CEP - Centrální evidence projektů
PubMed
7506096
Knihovny.cz E-zdroje
- MeSH
- běloši genetika MeSH
- černoši genetika MeSH
- cystická fibróza etnologie genetika MeSH
- DNA MeSH
- etnicita genetika MeSH
- fenotyp MeSH
- genotyp MeSH
- introny MeSH
- lidé MeSH
- membránové proteiny * genetika MeSH
- molekulární sekvence - údaje MeSH
- mutace * MeSH
- protein CFTR MeSH
- sekvence nukleotidů MeSH
- sestřih RNA MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- práce podpořená grantem MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR) gene but the association between mutation (genotype) and disease presentation (phenotype) is not straightforward. We have been investigating whether variants in the CFTR gene that alter splicing efficiency of exon 9 can affect the phenotype produced by a mutation. A missense mutation, R117H, which has been observed in three phenotypes, was found to occur on two chromosome backgrounds with intron 8 variants that have profoundly different effects upon splicing efficiency. A close association is shown between chromosome background of the R117H mutation and phenotype. These findings demonstrate that the genetic context in which a mutation occurs can play a significant role in determining the type of illness produced.
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- $a Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR) gene but the association between mutation (genotype) and disease presentation (phenotype) is not straightforward. We have been investigating whether variants in the CFTR gene that alter splicing efficiency of exon 9 can affect the phenotype produced by a mutation. A missense mutation, R117H, which has been observed in three phenotypes, was found to occur on two chromosome backgrounds with intron 8 variants that have profoundly different effects upon splicing efficiency. A close association is shown between chromosome background of the R117H mutation and phenotype. These findings demonstrate that the genetic context in which a mutation occurs can play a significant role in determining the type of illness produced.
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