Entity Details

Primary name CASQ1
Entity type gene
Source Source Link

Details

PrimaryID844
RefseqGeneNG_042040
SymbolCASQ1
Namecalsequestrin 1
Chromosome1
Location1q23.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-02-20
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCASQ1_HUMAN

GO terms

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GOName
GO:0005509 calcium ion binding
GO:0005739 mitochondrion
GO:0005759 mitochondrial matrix
GO:0005783 endoplasmic reticulum
GO:0005790 smooth endoplasmic reticulum
GO:0005794 Golgi apparatus
GO:0007029 endoplasmic reticulum organization
GO:0007519 skeletal muscle tissue development
GO:0009408 response to heat
GO:0010033 response to organic substance
GO:0014804 terminal cisterna lumen
GO:0014809 regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion
GO:0014894 response to denervation involved in regulation of muscle adaptation
GO:0016529 sarcoplasmic reticulum
GO:0030018 Z disc
GO:0030315 T-tubule
GO:0033017 sarcoplasmic reticulum membrane
GO:0033018 sarcoplasmic reticulum lumen
GO:0034220 ion transmembrane transport
GO:0042802 identical protein binding
GO:0045214 sarcomere organization
GO:0051258 protein polymerization
GO:0051279 regulation of release of sequestered calcium ion into cytosol
GO:0051281 positive regulation of release of sequestered calcium ion into cytosol
GO:1901341 positive regulation of store-operated calcium channel activity
GO:1903779 regulation of cardiac conduction
GO:2001256 regulation of store-operated calcium entry

Diseases

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Disease IDSourceNameDescription
160565 OMIMMyopathy, tubular aggregate, 1 (TAM1)A rare congenital myopathy characterized by regular arrays of membrane tubules on muscle biopsies without additional histopathological hallmarks. Tubular aggregates in muscle are structures of variable appearance consisting of an outer tubule containing either one or more microtubule-like structures or amorphous material. They may occur in a variety of circumstances, including inherited myopathies, alcohol- and drug-induced myopathies, exercise-induced cramps or muscle weakness. The disease is caused by variants affecting the gene represented in this entry.
616231 OMIMMyopathy, vacuolar, with CASQ1 aggregates (VMCQA)An autosomal dominant mild muscle disorder characterized by adult onset of muscle cramping and weakness as well as increased levels of serum creatine kinase. The disorder is not progressive, and some patients may be asymptomatic. The disease is caused by variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
CASQ1GAS2L2IntAct32296183 details
CASQ1PCNAUniProt26030842 details
CASQ1TRDNBioGRID24325401 details
CASQ1ILKAPBioGRID, IntAct28330616 details