Symbol
| FURIN
| contributors: mct - updated : 29-11-2014
|
HGNC name
| furin (paired basic amino acid cleaving enzyme)
|
HGNC id
| 8568
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
tumoral
|  
|  
|  
|  
|
no expression in small cell lung cancers | tumoral
|  
|  
| --over
|  
|
overexpressed in non small cell lung cancers | constitutional
|  
|  
| --low
|  
|
decreased hypothalamic PCSK1, PCSK2, FURIN in huntington disease patients | constitutional
|  
|  
| --low
|  
|
in the syncytiotrophoblast is significantly lower in the placentas from pre-eclamptic patients as compared with their gestational age-matched control placentas | |
Susceptibility
|
to (PACE) insulin-resistent diabetes (INSR), hemophilia B (F9) and Marfan syndrome (FBN1) |
Variant & Polymorphism
SNP
| SNP in the P1 promoter of FURIN affects furin transcription activity and hepatitis B virus infection outcome |
|
|
Candidate gene
Marker
Therapy target
| | | |
| mutant-/- embryomic lethal,failing to undergo looping and embryonic turning |