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FLASH GENE
Symbol GSN contributors: mct/npt/pgu - updated : 06-05-2014
HGNC name gelsolin (amyloidosis, Finnish type)
HGNC id 4620
ASSOCIATED DISORDERS
corresponding disease(s) CAAG
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional     --over  
is highly expressed in murine and human hearts after myocardial infarction and is associated with progression of heart failure
tumoral     --low  
in pancreatic cancer and enhanced targeting of gelsolin to the ubiquitin-proteasome pathway is an important contributing factor for this effect
tumoral     --low  
in breast cancer tissues and is linked with metastasis development and death in patients
constitutional       loss of function
inactivation of gelsolin during sperm capacitation occurs by its binding to PIP(2) and tyrosine phosphorylation by SRC
Susceptibility
Variant & Polymorphism
Candidate gene for malignant pleural mesothelioma
Marker
  • CSF-gelsolin level might reflect the alteration of gelsolin in brain tissue of epileptic patients and CSF-gelsolin seems to be a potential biomarker for epilepsy
  • Therapy target
    SystemTypeDisorderPubmed
    cardiovascularaquiredheart failure
    inhibition of GSN may form a novel target for heart failure therapy
    ANIMAL & CELL MODELS
  • GSN(-/-) mice have a surprisingly lower mortality, markedly reduced hypertrophy, smaller late infarct size, less interstitial fibrosis, and improved cardiac function when compared with GSN(+/+) mice
  • in Gsn(-/-) mice, emigration of newly generated cells from the subventricular zone into the olfactory bulb was slowed