- persistence of hyaloid vascular system / IMPC
- fused cornea and lens / IMPC
- abnormal cornea morphology / IMPC
- corneal opacity / IMPC
- decreased caudal vertebrae number / IMPC
- abnormal coat/hair pigmentation / IMPC
- abnormal digit morphology / IMPC
- decreased circulating iron level / IMPC
- decreased circulating creatinine level / IMPC
- impaired pupillary reflex / IMPC
- fused phalanges / IMPC
- increased or absent threshold for auditory brainstem response / IMPC
C57BL/6N-Atm1Brd Myo10tm2(KOMP)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:08386 |
International strain name | C57BL/6N-Atm1Brd Myo10tm2(KOMP)Wtsi/WtsiOrl |
Alternative name | EPD0272_4_F10 |
Strain type | |
Allele/Transgene symbol | Myo10tm2(KOMP)Wtsi, |
Gene/Transgene symbol | Myo10 |
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 | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0272_4_F10. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac |
Disease and phenotype information
IMPC phenotypes (allele matching)
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