Cox6b1 | cytochrome c oxidase, subunit 6B1

GeneMGI:107460Synonyms: 2010000G05Rik

Physiological systems

21 / 24 physiological systems tested

9 Significantly impacted by the knock-out

 Immune system Integument Endocrine/exocrine gland Embryo Growth/size/body region Vision/eye Hematopoietic system Cardiovascular system Mortality/aging

12 No significant impact

3 Not tested

Gene metrics:7Significant phenotypes
2Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues

Phenotypes

preweaning lethality, complete penetrance3 supporting datasetsCox6b1em1(IMPC)TcphomozygoteEarly adultN/A * 
abnormal embryo size1 supporting datasetCox6b1em1(IMPC)TcphomozygoteE12.5N/A * 
abnormal sinus arrhythmia1 supporting datasetCox6b1em1(IMPC)TcpheterozygoteEarly adult1.13x10-8 
absent adrenal gland1 supporting datasetCox6b1em1(IMPC)TcpheterozygoteEarly adultN/A * 
increased spleen weight1 supporting datasetCox6b1em1(IMPC)TcpheterozygoteEarly adult8.62x10-5 
abnormal skin morphology1 supporting datasetCox6b1em1(IMPC)TcpheterozygoteEarly adultN/A * 
microphthalmia1 supporting datasetCox6b1em1(IMPC)TcphomozygoteE12.5N/A * 
* Does not have a P-value assigned because it was manually marked as significant.
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* This parameter was manually assessed for significance.
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lacZ Expression

Human diseases caused by Cox6b1 mutations

The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.

Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.






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Histopathology

IMPC related publications

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Cox6b1em1(IMPC)TcpExon Deletionmouse
Cox6b1tm1a(EUCOMM)HmguKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
Cox6b1tm1e(EUCOMM)HmguTargeted, non-conditional alleleES Cell

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