Entity Details

Primary name ACTG2
Entity type gene
Source Source Link

Details

PrimaryID72
RefseqGeneNG_034140
SymbolACTG2
Nameactin gamma 2, smooth muscle
Chromosome2
Location2p13.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1995-10-10
ModificationDate2021-06-13

Ontological Relatives

UniProt IDsACTH_HUMAN

GO terms

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GOName
GO:0005524 ATP binding
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005869 dynactin complex
GO:0006936 muscle contraction
GO:0010628 positive regulation of gene expression
GO:0030027 lamellipodium
GO:0030175 filopodium
GO:0032982 myosin filament
GO:0044297 cell body
GO:0070062 extracellular exosome
GO:0071944 cell periphery
GO:0072562 blood microparticle
GO:0090131 mesenchyme migration

Diseases

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Disease IDSourceNameDescription
155310 OMIMVisceral myopathy (VSCM)A rare inherited form of myopathic pseudo-obstruction characterized by impaired function of enteric smooth muscle cells, resulting in abnormal intestinal motility, severe abdominal pain, malnutrition, and even death. The disease shows inter- and intrafamilial variability. Most severely affected patients exhibit prenatal bladder enlargement, intestinal malrotation, neonatal functional gastrointestinal obstruction, and dependence on total parenteral nutrition and urinary catheterization. The disease is caused by variants affecting the gene represented in this entry.