PRPF3
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn PRPF3 yw PRPF3 a elwir hefyd yn Pre-mRNA processing factor 3 (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 1, band 1q21.2.[2]
PRPF3 | |||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| |||||||||||||||||
Dynodwyr | |||||||||||||||||
Cyfenwau | PRPF3, pre-mRNA processing factor 3, HPRP3, HPRP3P, PRP3, Prp3p, RP18, SNRNP90 | ||||||||||||||||
Dynodwyr allanol | OMIM: 607301 HomoloGene: 3447 GeneCards: PRPF3 | ||||||||||||||||
| |||||||||||||||||
| |||||||||||||||||
Orthologau | |||||||||||||||||
Species | Bod dynol | Llygoden | |||||||||||||||
Entrez |
| ||||||||||||||||
Ensembl |
| ||||||||||||||||
UniProt |
| ||||||||||||||||
RefSeq (mRNA) |
| ||||||||||||||||
RefSeq (protein) |
| ||||||||||||||||
Lleoliad (UCSC) | n/a | n/a | |||||||||||||||
PubMed search | [1] | n/a | |||||||||||||||
Wicidata | |||||||||||||||||
|
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 PRPF3.
- PRP3
- RP18
- HPRP3
- Prp3p
- HPRP3P
- SNRNP90
Llyfryddiaeth golygu
- "SUMO conjugation to spliceosomal proteins is required for efficient pre-mRNA splicing. ". Nucleic Acids Res. 2017. PMID 28379520.
- "Variable phenotypic expressivity in a Swiss family with autosomal dominant retinitis pigmentosa due to a T494M mutation in the PRPF3 gene. ". Mol Vis. 2010. PMID 20309403.
- "Contribution of the individual subunits of protein kinase CK2 and of hPrp3p to the splicing process. ". Mol Cell Biochem. 2008. PMID 18553058.
- "Mutation in the splicing factor Hprp3p linked to retinitis pigmentosa impairs interactions within the U4/U6 snRNP complex. ". Hum Mol Genet. 2008. PMID 17932117.
- "Mutations in splicing factor PRPF3, causing retinal degeneration, form detrimental aggregates in photoreceptor cells.". Hum Mol Genet. 2007. PMID 17517693.