Symbol
| SEPTIN5
| contributors: mct/ - updated : 28-08-2019
|
HGNC name
| septin 5
|
HGNC id
| 9164
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
| deletion
|  
|  
|
in DiGeorge syndrome and velocardiofacial syndromes | tumoral
| fusion
|  
|  
|  
|
fused with HRX (MLL)with t(11;22)(q23;q11.2)in adulte myeloid leukemia | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| both Sept4 and Sept5 null mice had similar auditory functions to their wild type littermates |