TSPAN32

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Tetraspanin-32 is a protein that in humans is encoded by the TSPAN32 gene.[5][6][7]

AliasesTSPAN32, ART1, PHEMX, PHMX, TSSC6, tetraspanin 32
End2,318,204 bp[1]
Quick facts Identifiers, Aliases ...
TSPAN32
Identifiers
AliasesTSPAN32, ART1, PHEMX, PHMX, TSSC6, tetraspanin 32
External IDsOMIM: 603853; MGI: 1350360; HomoloGene: 10650; GeneCards: TSPAN32; OMA:TSPAN32 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005705
NM_139022
NM_139024

NM_001128080
NM_001128081
NM_001128082
NM_020286

RefSeq (protein)

NP_620591

NP_001121552
NP_001121553
NP_001121554
NP_064682

Location (UCSC)Chr 11: 2.3 – 2.32 MbChr 7: 142.56 – 142.57 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Close

Function

This gene is described as a member of the tetraspanin superfamily whose expression is confined to hematopoietic tissues.[7]

Clinical significance

This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is located among several imprinted genes; however, this gene, as well as the tumor-suppressing subchromosomal transferable fragment 4 (TSSC4), escapes imprinting. This gene may play a role in malignancies and disease that involve this region as well as hematopoietic cell function.[7]

References

Further reading

Related Articles

Wikiwand AI