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FLASH GENE
Symbol VCP contributors: mct/npt/pgu - updated : 28-06-2020
HGNC name valosin-containing protein
HGNC id 12666
ASSOCIATED DISORDERS
corresponding disease(s) IBMPFD , ALS14 , CMT2Y , DDHDM
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional       loss of function
functional defect of VCP in DNA double-stranded break repair is critical for the pathology of neurons in which VCP is located dominantly in the nucleus
constitutional       loss of function
causes profound mitochondrial uncoupling leading to decreased mitochondrial membrane potential and increased mitochondrial oxygen consumption, resulting in a significant reduction of cellular ATP production
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS