Entity Details

Primary name FPGT-TNNI3K
Entity type gene
Source Source Link

Details

PrimaryID100526835
RefseqGeneNG_032939
SymbolFPGT-TNNI3K
NameFPGT-TNNI3K readthrough
Chromosome1
Location1p31.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2010-12-02
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTNI3K_HUMAN

GO terms

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GOName
GO:0002027 regulation of heart rate
GO:0004672 protein kinase activity
GO:0005524 ATP binding
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0006468 protein phosphorylation
GO:0008022 protein C-terminus binding
GO:0031013 troponin I binding
GO:0046872 metal ion binding
GO:0055117 regulation of cardiac muscle contraction
GO:0086069 bundle of His cell to Purkinje myocyte communication
GO:0106310 protein serine kinase activity
GO:0106311 protein threonine kinase activity
GO:1903779 regulation of cardiac conduction

Diseases

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Disease IDSourceNameDescription
616117 OMIMCardiac conduction disease with or without dilated cardiomyopathy (CCDD)A cardiac disorder characterized by atrial tachyarrhythmia and conduction system disease. Some patients have dilated cardiomyopathy. The disease is caused by variants affecting the gene represented in this entry.