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FLASH GENE
Symbol P3H2 contributors: mct - updated : 02-01-2019
HGNC name prolyl 3-hydroxylase 2
HGNC id 19317
ASSOCIATED DISORDERS
corresponding disease(s) MCVD
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional       loss of function
altered collagen prolyl 3-hydroxylation is caused by loss of P3H2
tumoral     --low  
in human hepatocellular carcinoma
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS
  • P3h2-null mice are embryonic-lethal by embryonic day 8.5