CBX7 (gene)

From Wikipedia, the free encyclopedia
CBX7
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCBX7, chromobox 7
External IDsOMIM: 608457 MGI: 1196439 HomoloGene: 65296 GeneCards: CBX7
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_175709
NM_001346743
NM_001346744

NM_144811

RefSeq (protein)

NP_001333672
NP_001333673
NP_783640
NP_783640.1

NP_659060

Location (UCSC)Chr 22: 39.12 – 39.15 MbChr 15: 79.8 – 79.86 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Chromobox homolog 7 is a protein that in humans is encoded by the CBX7 gene.[5] The loss of CBX7 gene expression has been shown to correlate with a malignant form of thyroid cancer.[6]

Model organisms[]

Model organisms have been used in the study of CBX7 function. A conditional knockout mouse line, called Cbx7tm1a(KOMP)Wtsi[13][14] was generated as part of the International Knockout Mouse Consortium program — a high-throughput mutagenesis project to generate and distribute animal models of disease to interested scientists — at the Wellcome Trust Sanger Institute.[15][16][17] Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[11][18] Twenty six tests were carried out and three significant phenotypes were reported. Homozygous mutant female adults showed a decreased response to stress-induced hyperthermia and had an increased red blood cell count. Animals of both sex had an integument phenotype when tail epidermis was examined.[11]

References[]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000100307 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000053411 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Chromobox homolog 7". Retrieved 2011-12-06.
  6. ^ Pallante P, Federico A, Berlingieri MT, Bianco M, Ferraro A, Forzati F, et al. (August 2008). "Loss of the CBX7 gene expression correlates with a highly malignant phenotype in thyroid cancer". Cancer Research. 68 (16): 6770–8. doi:10.1158/0008-5472.CAN-08-0695. PMID 18701502.
  7. ^ "Body temperature data for Cbx7". Wellcome Trust Sanger Institute.
  8. ^ "Haematology data for Cbx7". Wellcome Trust Sanger Institute.
  9. ^ "Salmonella infection data for Cbx7". Wellcome Trust Sanger Institute.
  10. ^ "Citrobacter infection data for Cbx7". Wellcome Trust Sanger Institute.
  11. ^ a b c Gerdin AK (2010). "The Sanger Mouse Genetics Programme: High throughput characterisation of knockout mice". Acta Ophthalmologica. 88 (S248). doi:10.1111/j.1755-3768.2010.4142.x. S2CID 85911512.
  12. ^ Mouse Resources Portal, Wellcome Trust Sanger Institute.
  13. ^ "International Knockout Mouse Consortium". Archived from the original on 2012-03-20. Retrieved 2012-01-05.
  14. ^ "Mouse Genome Informatics".
  15. ^ Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, et al. (June 2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–42. doi:10.1038/nature10163. PMC 3572410. PMID 21677750.
  16. ^ Dolgin E (June 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718.
  17. ^ Collins FS, Rossant J, Wurst W (January 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247. S2CID 18872015.
  18. ^ van der Weyden L, White JK, Adams DJ, Logan DW (June 2011). "The mouse genetics toolkit: revealing function and mechanism". Genome Biology. 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMC 3218837. PMID 21722353.

Further reading[]


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