CYB561

CYB561
Identifiers
Aliases CYB561, cytochrome b561, CYB561A1, FRRS2
External IDs MGI: 103253 HomoloGene: 37552 GeneCards: CYB561
RNA expression pattern




More reference expression data
Orthologs
Species Human Mouse
Entrez

1534

13056

Ensembl

ENSG00000008283

ENSMUSG00000019590

UniProt

P49447

Q60720

RefSeq (mRNA)

NM_001017916
NM_001017917
NM_001017918
NM_001915

NM_007805

RefSeq (protein)

NP_001017916.1
NP_001017917.1
NP_001906.3

NP_031831.2

Location (UCSC) Chr 17: 63.43 – 63.45 Mb Chr 11: 105.93 – 105.95 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

Cytochrome b561 is a protein that in humans is encoded by the CYB561 gene.[3][4]

Model organisms

Model organisms have been used in the study of CYB561 function. A conditional knockout mouse line, called Cyb561tm1a(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 three tests were carried out on mutant mice and one significant abnormality was observed: female homozygotes displayed a decreased circulating glucose level after a glucose tolerance test.[9]

References

  1. ↑ "Human PubMed Reference:".
  2. ↑ "Mouse PubMed Reference:".
  3. ↑ McBride OW, Yi HF, Srivastava M (Nov 1994). "The human cytochrome b561 gene (CYB561) is located at 17q11-qter". Genomics. 21 (3): 662–3. doi:10.1006/geno.1994.1332. PMID 7959749.
  4. ↑ "Entrez Gene: CYB561 cytochrome b-561".
  5. ↑ "Dysmorphology data for Cyb561". Wellcome Trust Sanger Institute.
  6. ↑ "Glucose tolerance test data for Cyb561". Wellcome Trust Sanger Institute.
  7. ↑ "Salmonella infection data for Cyb561". Wellcome Trust Sanger Institute.
  8. ↑ "Citrobacter infection data for Cyb561". Wellcome Trust Sanger Institute.
  9. 1 2 3 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.
  10. ↑ Mouse Resources Portal, Wellcome Trust Sanger Institute.
  11. ↑ "International Knockout Mouse Consortium".
  12. ↑ "Mouse Genome Informatics".
  13. ↑ Skarnes, W. C.; Rosen, B.; West, A. P.; Koutsourakis, M.; Bushell, W.; Iyer, V.; Mujica, A. O.; Thomas, M.; Harrow, J.; Cox, T.; Jackson, D.; Severin, J.; Biggs, P.; Fu, J.; Nefedov, M.; De Jong, P. J.; Stewart, A. F.; Bradley, A. (2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–342. doi:10.1038/nature10163. PMC 3572410Freely accessible. PMID 21677750.
  14. ↑ Dolgin E (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 (2007). "A Mouse for All Reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247.
  16. ↑ van der Weyden L, White JK, Adams DJ, Logan DW (2011). "The mouse genetics toolkit: revealing function and mechanism.". Genome Biol. 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMC 3218837Freely accessible. PMID 21722353.

Further reading


This article is issued from Wikipedia - version of the 5/22/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.