WDR47

WD repeat domain 47 is a protein that in humans is encoded by the WDR47 gene.[5]

WDR47
Identifiers
AliasesWDR47, WD repeat domain 47
External IDsOMIM: 615734 MGI: 2139593 HomoloGene: 8984 GeneCards: WDR47
Gene location (Human)
Chr.Chromosome 1 (human)[1]
Band1p13.3Start108,970,214 bp[1]
End109,042,113 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

22911

99512

Ensembl

ENSG00000085433

ENSMUSG00000040389

UniProt

O94967

Q8CGF6

RefSeq (mRNA)

NM_001142550
NM_001142551
NM_014969

NM_181400
NM_001358053
NM_001358054
NM_001358055

RefSeq (protein)

NP_001136022
NP_001136023
NP_055784

NP_852065
NP_001344982
NP_001344983
NP_001344984

Location (UCSC)Chr 1: 108.97 – 109.04 MbChr 3: 108.59 – 108.65 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Model organisms

Model organisms have been used in the study of WDR47 function. A conditional knockout mouse line, called Wdr47tm1a(EUCOMM)Wtsi[11][12] 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.[13][14][15]

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[9][16] Twenty-six tests were carried out on mutant mice and three significant abnormalities were observed.[9] Homozygous mutant animals had an absence of corpus callosum and increased circulating alkaline phosphatase levels. Male homozygous mice also had abnormal indirect calorimetry measures.[9]

See also

References

  1. GRCh38: Ensembl release 89: ENSG00000085433 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000040389 - 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. "Entrez Gene: WD repeat domain 47". Retrieved 2011-08-30.
  6. "Indirect calorimetry data for Wdr47". Wellcome Trust Sanger Institute.
  7. "Clinical chemistry data for Wdr47". Wellcome Trust Sanger Institute.
  8. "Citrobacter infection data for Wdr47". Wellcome Trust Sanger Institute.
  9. Gerdin AK (2010). "The Sanger Mouse Genetics Programme: High throughput characterisation of knockout mice". Acta Ophthalmologica. 88: 925–7. doi:10.1111/j.1755-3768.2010.4142.x. S2CID 85911512.
  10. Mouse Resources Portal, Wellcome Trust Sanger Institute.
  11. "International Knockout Mouse Consortium".
  12. "Mouse Genome Informatics".
  13. Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF, Bradley A (Jun 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.
  14. Dolgin E (Jun 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718.
  15. Collins FS, Rossant J, Wurst W (Jan 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247. S2CID 18872015.
  16. van der Weyden L, White JK, Adams DJ, Logan DW (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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