TNNC1 |
---|
|
Strwythurau |
---|
PDB | Human UniProt search: PDBe RCSB |
---|
Rhestr o ddynodwyr PDB |
---|
1AP4, 1IH0, 1J1D, 1J1E, 1LXF, 1MXL, 1OZS, 1SPY, 1WRK, 1WRL, 2JT0, 2JT3, 2JT8, 2JTZ, 2JXL, 2KDH, 2KFX, 2KGB, 2KRD, 2L1R, 2L98, 2MKP, 2MLE, 2MLF, 2MZP, 3RV5, 3SD6, 3SWB, 4GJE, 4GJF, 4GJG, 2N79, 4Y99 |
|
|
Dynodwyr |
---|
Cyfenwau | TNNC1, CMD1Z, CMH13, TN-C, TNC, TNNC, Troponin C type 1, troponin C1, slow skeletal and cardiac type |
---|
Dynodwyr allanol | OMIM: 191040 HomoloGene: 55728 GeneCards: TNNC1 |
---|
|
|
Orthologau |
---|
Species | Bod dynol | Llygoden |
---|
Entrez | | |
---|
Ensembl | | |
---|
UniProt | | |
---|
RefSeq (mRNA) | | |
---|
RefSeq (protein) | | |
---|
Lleoliad (UCSC) | n/a | n/a |
---|
PubMed search | [1] | n/a |
---|
Wicidata |
|
Protein sy'n cael ei godio yn y corff dynol gan y genyn TNNC1 yw TNNC1 a elwir hefyd yn Troponin C1, slow skeletal and cardiac type (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 3, band 3p21.1.[2]
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 TNNC1.
- TNC
- TN-C
- TNNC
- CMD1Z
- CMH13
- "The structural and functional effects of the familial hypertrophic cardiomyopathy-linked cardiac troponin C mutation, L29Q. ". J Mol Cell Cardiol. 2015. PMID 26341255.
- "In Vivo Analysis of Troponin C Knock-In (A8V) Mice: Evidence that TNNC1 Is a Hypertrophic Cardiomyopathy Susceptibility Gene. ". Circ Cardiovasc Genet. 2015. PMID 26304555.
- "Use of the HEART Pathway with high sensitivity cardiac troponins: A secondary analysis. ". Clin Biochem. 2017. PMID 28087371.
- "Evidence for troponin C (TNNC1) as a gene for autosomal recessive restrictive cardiomyopathy with fatal outcome in infancy. ". Am J Med Genet A. 2016. PMID 27604170.
- "Enhanced troponin I binding explains the functional changes produced by the hypertrophic cardiomyopathy mutation A8V of cardiac troponin C.". Arch Biochem Biophys. 2016. PMID 26976709.