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FLASH GENE
Symbol MIA2 contributors: mct - updated : 05-12-2018
HGNC name melanoma inhibitory activity 2
HGNC id 18432
ASSOCIATED DISORDERS
corresponding disease(s)
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional     --over  
in liver damage, in chronic liver disease and correlates with the severity of fibrosis and inflammation in hepatitis C
constitutional germinal mutation      
in patients with Fahr disease
Susceptibility to Familial idiopathic basal ganglia calcification (IBGC)
Variant & Polymorphism other
  • P521A variation associated with the risk of familial idiopathic basal ganglia calcification
  • Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS