TNFRSF13B

GENERAL INFORMATION

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Gene name

TNFRSF13B

Gene description

Tumor necrosis factor receptor superfamily, member 13B

Protein class

CD markers
Disease related genes
Predicted intracellular proteins
Predicted membrane proteins

Predicted localization

Intracellular,Membrane

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (lymph node, spleen, tonsil)
GTEx:Group enriched (small intestine, spleen)

Protein evidence

Evidence at protein level

Protein localization

Normal tissues showed moderate to strong cytoplasmic positivity with a granular pattern. Renal glomeruli, alveolar cells, glial cells and smooth muscle were weakly stained or negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA030453
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Small intestine

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (lymph node, spleen, tonsil)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (small intestine, spleen)

Organ

Expression



GENE INFORMATION

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Gene name

TNFRSF13B (HGNC Symbol)

Synonyms

CD267, TACI

Description

Tumor necrosis factor receptor superfamily, member 13B (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is a lymphocyte-specific member of the tumor necrosis factor (TNF) receptor superfamily. It interacts with calcium-modulator and cyclophilin ligand (CAML). The protein induces activation of the transcription factors NFAT, AP1, and NF-kappa-B and plays a crucial role in humoral immunity by interacting with a TNF ligand. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]

Chromosome

17

Cytoband

p11.2

Chromosome location (bp)

16929816 - 16972118

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000240505 (version 78.38)

Entrez gene

23495

UniProt

O14836 (UniProt - Evidence at protein level)

neXtProt

NX_O14836

Antibodypedia

TNFRSF13B antibodies


PROTEIN BROWSER

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ENST00000261652
 
ENST00000579315
 
ENST00000583789
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

TNFRSF13B-001 ENSP00000261652
ENST00000261652
O14836
Show all »
Show » Show » 293 31.8 No 1
TNFRSF13B-002 ENSP00000462952
ENST00000583789
O14836
Show all »
Show » Show » 247 26.7 No 1
TNFRSF13B-006 ENSP00000464069
ENST00000579315
J3QR67
Show all »
Show » Show » 156 17.7 No 0