Symbol
| P3H2
| contributors: mct - updated : 02-01-2019
|
HGNC name
| prolyl 3-hydroxylase 2
|
HGNC id
| 19317
|
corresponding disease(s)
|
MCVD
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
|  
|  
| loss of function
|
altered collagen prolyl 3-hydroxylation is caused by loss of P3H2 | tumoral
|  
|  
| --low
|  
|
in human hepatocellular carcinoma | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| P3h2-null mice are embryonic-lethal by embryonic day 8.5 |