- increased red blood cell distribution width / IMPC
- decreased locomotor activity / IMPC
- decreased hemoglobin content / IMPC
- decreased erythrocyte cell number / IMPC
- decreased circulating fructosamine level / IMPC
- decreased circulating serum albumin level / IMPC
- decreased lymphocyte cell number / IMPC
- preweaning lethality, complete penetrance / IMPC
- increased neutrophil cell number / IMPC
- impaired glucose tolerance / IMPC
C57BL/6NTac-Commd9tm1a(KOMP)Wtsi/H
Status | Available to order |
EMMA ID | EM:09482 |
International strain name | C57BL/6NTac-Commd9tm1a(KOMP)Wtsi/H |
Alternative name | EPD0136_6_D11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Commd9tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Commd9 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from KOMP ES clone EPD0136_6_D11. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal cardiovascular system physiology / MGI
- edema / MGI
- hemorrhage / MGI
- intracranial hemorrhage / MGI
- intracerebral hemorrhage / MGI
- abnormal neural tube morphology / MGI
- abnormal vein morphology / MGI
- heart hypoplasia / MGI
- abnormal dorsal aorta morphology / MGI
- dilated vasculature / MGI
- hemopericardium / MGI
- myocardial necrosis / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal cranial blood vasculature morphology / MGI
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