SFTPC
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn SFTPC yw SFTPC a elwir hefyd yn Pulmonary surfactant-associated protein C (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 8, band 8p21.3.[2]
SFTPC | |||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
![]() | |||||||||||||||||
| |||||||||||||||||
Dynodwyr | |||||||||||||||||
Cyfenwau | SFTPC, BRICD6, PSP-C, SFTP2, SMDP2, SP-C, surfactant protein C, SP5 | ||||||||||||||||
Dynodwyr allanol | OMIM: 178620 HomoloGene: 2271 GeneCards: SFTPC | ||||||||||||||||
| |||||||||||||||||
| |||||||||||||||||
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
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 SFTPC.
- SP-C
- PSP-C
- SFTP2
- SMDP2
- BRICD6
Llyfryddiaeth
golygu- "Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype. ". Eur J Hum Genet. 2017. PMID 28295039.
- "A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancy. ". Pediatr Pulmonol. 2017. PMID 27362365.
- "A novel surfactant protein C L55F mutation associated with interstitial lung disease alters subcellular localization of proSP-C in A549 cells. ". Pediatr Res. 2016. PMID 26375473.
- "Folding and Intramembraneous BRICHOS Binding of the Prosurfactant Protein C Transmembrane Segment. ". J Biol Chem. 2015. PMID 26041777.
- "Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations.". Eur J Hum Genet. 2015. PMID 25782673.