Symbol
| NMNAT3
| contributors: SGE/npt - updated : 05-10-2016
|
HGNC name
| nicotinamide nucleotide adenylyltransferase 3
|
HGNC id
| 20989
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
|  
| --over
|  
|
can delay axon degeneration | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| deficiency of Nmnat3 in mice caused splenomegaly and hemolytic anemia, which was associated with the findings that Nmnat3-deficient erythrocytes had markedly lower ATP levels and shortened lifespans |