Gene: TNFSF13B (tumor necrosis factor (ligand) superfamily, member 13b)  Homo sapiens

Symbol: TNFSF13B
Name: tumor necrosis factor (ligand) superfamily, member 13b
Description: The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This cytokine is a ligand for receptors TNFRSF13B/TACI, TNFRSF17/BCMA, and TNFRSF13C/BAFFR. This cytokine is expressed in B cell lineage cells, and acts as a potent B cell activator. It has been also shown to play an important role in the proliferation and differentiation of B cells. Alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2011]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: ApoL related ligand TALL-1; b lymphocyte stimulator; B-cell activating factor; B-cell-activating factor; B-lymphocyte stimulator; BAFF; BLYS; CD257; delta BAFF; Delta4 BAFF; dendritic cell-derived TNF-like molecule; DTL; OTTHUMP00000018691; TALL-1; TALL1; THANK; TNF and ApoL-related leukocyte expressed ligand 1; TNF homolog that activates apoptosis; TNF- and APOL-related leukocyte expressed ligand 1; TNFSF20; tumor necrosis factor (ligand) superfamily, member 20; tumor necrosis factor ligand superfamily member 13B; tumor necrosis factor superfamily, member 13b; tumor necrosis factor-like protein ZTNF4; ZTNF4
Orthologs: Mus musculus : Tnfsf13b (tumor necrosis factor (ligand) superfamily, member 13b)  MGI
Rattus norvegicus : Tnfsf13b (tumor necrosis factor (ligand) superfamily, member 13b)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_11389,850,057 - 89,884,156+NCBI
Human Genome Assembly HuRef1389,512,942 - 89,552,797+NCBI
Human Genome Assembly GRCh3713108,921,977 - 108,960,832+NCBI
Human Genome Assembly Build 3613107,719,978 - 107,757,366+NCBI
Human Cytogenetic Map13q32-q34 NCBI
Human Genome Assembly13107,719,977 - 107,757,366 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on TNFSF13B
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 1345205
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2013-05-14
Status: ACTIVE