TSPAN32

GENERAL INFORMATION

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Gene name

TSPAN32

Gene description

Tetraspanin 32

Protein class

Predicted membrane proteins

Predicted localization

Membrane

Number of transcripts

5
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (bone marrow, heart muscle, lung, lymph node, spleen)
GTEx:Tissue enhanced (spleen)

Protein evidence

Evidence at protein level

Protein localization

General cytoplasmic and nuclear expression.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly not consistent with RNA expression data. Pending external verification.

Data reliability

Uncertain based on 1 antibody.
HPA024135
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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

Bone marrow

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Group enriched (bone marrow, heart muscle, lung, lymph node, spleen)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (spleen)

Organ

Expression



GENE INFORMATION

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Gene name

TSPAN32 (HGNC Symbol)

Synonyms

PHEMX, TSSC6

Description

Tetraspanin 32 (HGNC Symbol)

Entrez gene summary

This gene, which is a member of the tetraspanin superfamily, is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of chromosome 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian and breast cancers. This gene is located among several imprinted genes; however, this gene, as well as the tumor-suppressing subchromosomal transferable fragment 4, escapes imprinting. This gene may play a role in malignancies and diseases that involve this region, and it is also involved in hematopoietic cell function. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]

Chromosome

11

Cytoband

p15.5

Chromosome location (bp)

2301997 - 2318200

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000064201 (version 78.38)

Entrez gene

10077

UniProt

Q96QS1 (UniProt - Evidence at transcript level)

neXtProt

NX_Q96QS1

Antibodypedia

TSPAN32 antibodies


PROTEIN BROWSER

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ENST00000182290
 
ENST00000381117
 
ENST00000381121
 
ENST00000451520
 
ENST00000612299
 
 
 
 


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)

TSPAN32-001 ENSP00000182290
ENST00000182290
Q96QS1
Show all »
Show » Show » 320 34.6 No 3
TSPAN32-003 ENSP00000405205
ENST00000451520
D3YTD1
Show all »
Show » Show » 309 33.3 No 4
TSPAN32-005 ENSP00000370513
ENST00000381121
Q96QS1
Show all »
Show » Show » 253 27.8 No 3
TSPAN32-014 ENSP00000370509
ENST00000381117
G3XAG6
Show all »
Show » Show » 265 28.4 No 1
TSPAN32-201 ENSP00000482901
ENST00000612299
G3XAG6
Show all »
Show » Show » 265 28.4 No 1