Symbol
| TNFRSF1B
| contributors: mct/npt - updated : 15-04-2014
|
HGNC name
| tumor necrosis factor receptor superfamily, member 1B
|
HGNC id
| 11917
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
tumoral
|  
| deletion
|  
|  
|
in neuroblastoma | |
Susceptibility
|
to familial combined hyperlipidemia to systemic lupus erythematosis and to narcolepsy to coronary artery disease and to osteoporosis to Mycobacterium tuberculosis infection |
Variant & Polymorphism
other
| A593 - T598 - C620 haplotype decreased bone mineral density |
|
functional haplotype in the 3 prime untranslated region of TNFRSF1B is associated with tuberculosis |
|
|
Candidate gene
Marker
Therapy target
|
System | Type | Disorder | Pubmed |
neurology | neurodegenerative | | |
activation of TNFSF1B signaling by TNC-scTNFSF1B appears a promising strategy to ameliorate neurodegenerative processes. |
| | | |