TSPAN32

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Tetraspanin 32
Identifiers
Symbols TSPAN32 ; ART1; PHEMX; PHMX; TSSC6
External IDs OMIM603853 MGI1350360 HomoloGene10650 GeneCards: TSPAN32 Gene
RNA expression pattern
PBB GE TSPAN32 220558 x at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 10077 27027
Ensembl ENSG00000064201 ENSMUSG00000000244
UniProt Q96QS1 Q9JHH2
RefSeq (mRNA) NM_005705 NM_001128080
RefSeq (protein) NP_620591 NP_001121552
Location (UCSC) Chr 11:
2.32 – 2.34 Mb
Chr 7:
143.01 – 143.02 Mb
PubMed search [1] [2]

Tetraspanin-32 is a protein that in humans is encoded by the TSPAN32 gene.[1][2][3]

Function[edit]

This gene is described as a member of the tetraspanin superfamily whose expression is confined to hematopoietic tissues.[3]

Clinical significance[edit]

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.[3]

References[edit]

  1. ^ Lee MP, Brandenburg S, Landes GM, Adams M, Miller G, Feinberg AP (Apr 1999). "Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting". Hum Mol Genet 8 (4): 683–90. doi:10.1093/hmg/8.4.683. PMID 10072438. 
  2. ^ Nicholson RH, Pantano S, Eliason JF, Galy A, Weiler S, Kaplan J, Hughes MR, Ko MS (Sep 2000). "Phemx, a novel mouse gene expressed in hematopoietic cells maps to the imprinted cluster on distal chromosome 7". Genomics 68 (1): 13–21. doi:10.1006/geno.2000.6277. PMID 10950922. 
  3. ^ a b c "Entrez Gene: TSPAN32 tetraspanin 32". 

Further reading[edit]

  • Koi M, Johnson LA, Kalikin LM, Little PF, Nakamura Y, Feinberg AP (1993). "Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11.". Science 260 (5106): 361–4. doi:10.1126/science.8469989. PMID 8469989. 
  • Hu RJ, Lee MP, Connors TD, Johnson LA, Burn TC, Su K, Landes GM, Feinberg AP (1998). "A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes.". Genomics 46 (1): 9–17. doi:10.1006/geno.1997.4981. PMID 9403053. 
  • Paulsen M, El-Maarri O, Engemann S, Strödicke M, Franck O, Davies K, Reinhardt R, Reik W, Walter J (2000). "Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse.". Hum. Mol. Genet. 9 (12): 1829–41. doi:10.1093/hmg/9.12.1829. PMID 10915772. 
  • Robb L, Tarrant J, Groom J, Ibrahim M, Li R, Borobakas B, Wright MD (2001). "Molecular characterisation of mouse and human TSSC6: evidence that TSSC6 is a genuine member of the tetraspanin superfamily and is expressed specifically in haematopoietic organs.". Biochim. Biophys. Acta 1522 (1): 31–41. doi:10.1016/s0167-4781(01)00306-2. PMID 11718897. 
  • Hillman RT, Green RE, Brenner SE (2005). "An unappreciated role for RNA surveillance.". Genome Biol. 5 (2): R8. doi:10.1186/gb-2004-5-2-r8. PMC 395752. PMID 14759258. 

External links[edit]