MYBPC1

Protein sy'n cael ei godio yn y corff dynol gan y genyn MYBPC1 yw MYBPC1 a elwir hefyd yn Myosin binding protein C, slow type (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 12, band 12q23.2.

MYBPC1
Strwythurau PDB Human UniProt search: PDBe RCSB Rhestr o ddynodwyr PDB 1X44, 2DAV, 2YUV, 2YUW, 2YUX, 2YUZ, 2YXM
Dynodwyr
Cyfenwau	MYBPC1, LCCS4, MYBPCC, MYBPCS, myosin binding protein C, slow type, ssMyBP-C, MYOTREM, myosin binding protein C1
Dynodwyr allanol	OMIM: 160794 HomoloGene: 1846 GeneCards: MYBPC1
Patrwm RNA pattern Rhagor o gyfeiriadau
Ontoleg y genyn Gweithrediad moleciwlaidd • actin binding • structural constituent of muscle • GO:0001948, GO:0016582 protein binding • titin binding • actin filament binding • muscle alpha-actinin binding • structural molecule activity conferring elasticity Cydrannau o'r gell • myosin filament • cytosol • Myoffibril • muscle myosin complex • Z disc • M band • striated muscle thin filament • sarcomere Prosesau biolegol • cell adhesion • muscle contraction • muscle filament sliding • striated muscle contraction • actin filament organization • sarcomere organization • striated muscle myosin thick filament assembly • skeletal muscle thin filament assembly • skeletal muscle myosin thick filament assembly • cardiac myofibril assembly • cardiac muscle tissue morphogenesis Sources:Amigo / QuickGO
Orthologau
Species	Bod dynol	Llygoden
Entrez	4604	n/a
Ensembl	ENSG00000196091	n/a
UniProt	Q00872	n/a
RefSeq (mRNA)	NM_001254718 NM_001254719 NM_001254720 NM_001254721 NM_001254722 NM_001254723 NM_002465 NM_206819 NM_206820 NM_206821 NM_001404675 NM_001404676 NM_001404677 NM_001404678 NM_001404679 NM_001404680 NM_001404681	n/a
RefSeq (protein)	NP_001241647 NP_001241648 NP_001241649 NP_001241650 NP_001241651 NP_001241652 NP_002456 NP_996555 NP_996556 NP_996557	n/a
Lleoliad (UCSC)	n/a	n/a
PubMed search		n/a
Wicidata
Gweld/Golygu Bod dynol

Cyfystyron

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 MYBPC1.

• LCCS4
• MYBPCC
• MYBPCS

Llyfryddiaeth

• "C0 and C1 N-terminal Ig domains of myosin binding protein C exert different effects on thin filament activation. ". Proc Natl Acad Sci U S A. 2016. PMID 26831109.
• "Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita. ". Clin Genet. 2016. PMID 26661508.
• "Two novel mutations in myosin binding protein C slow causing distal arthrogryposis type 2 in two large Han Chinese families may suggest important functional role of immunoglobulin domain C2. ". PLoS One. 2015. PMID 25679999.
• "Autosomal recessive lethal congenital contractural syndrome type 4 (LCCS4) caused by a mutation in MYBPC1. ". Hum Mutat. 2012. PMID 22610851.
• "MYBPC1 computational phosphoprotein network construction and analysis between frontal cortex of HIV encephalitis (HIVE) and HIVE-control patients.". Cell Mol Neurobiol. 2011. PMID 21061152.