ST5 (gene)

Suppression of tumorigenicity 5
Identifiers
Symbols ST5 ; DENND2B; HTS1; p126
External IDs OMIM: 140750 MGI: 108517 HomoloGene: 3951 GeneCards: ST5 Gene
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 6764 76954
Ensembl ENSG00000166444 ENSMUSG00000031024
UniProt P78524 Q924W7
RefSeq (mRNA) NM_005418 NM_001001326
RefSeq (protein) NP_005409 NP_001001326
Location (UCSC) Chr 11:
8.69 – 8.91 Mb
Chr 7:
109.52 – 109.62 Mb
PubMed search

Suppression of tumorigenicity 5 is a protein that in humans is encoded by the ST5 gene.[1][2] ST5 orthologs [3] have been identified in nearly all mammals for which complete genome data are available.

This gene was identified by its ability to suppress the tumorigenicity of Hela cells in nude mice. The protein encoded by this gene contains a C-terminal region that shares similarity with the Rab 3 family of small GTP binding proteins. This protein preferentially binds to the SH3 domain of c-Abl kinase, and acts as a regulator of MAPK1/ERK2 kinase, which may contribute to its ability to reduce the tumorigenic phenotype in cells. Three alternatively spliced transcript variants of this gene encoding distinct isoforms are identified.[2]

References

  1. Lichy JH, Modi WS, Seuanez HN, Howley PM (Nov 1992). "Identification of a human chromosome 11 gene which is differentially regulated in tumorigenic and nontumorigenic somatic cell hybrids of HeLa cells". Cell Growth Differ 3 (8): 541–8. PMID 1390339.
  2. 1 2 "Entrez Gene: ST5 suppression of tumorigenicity 5".
  3. "OrthoMaM phylogenetic marker: ST5 coding sequence".

Further reading

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