- persistence of hyaloid vascular system / IMPC
- abnormal lens morphology / IMPC
- cataract / IMPC
- fused cornea and lens / IMPC
- abnormal cornea morphology / IMPC
- corneal opacity / IMPC
- abnormal iris morphology / IMPC
- abnormal retina morphology / IMPC
- abnormal response to new environment / IMPC
- abnormal coat/hair pigmentation / IMPC
- abnormal digit morphology / IMPC
- abnormal tail morphology / IMPC
- decreased circulating creatinine level / IMPC
- impaired pupillary reflex / IMPC
- fused phalanges / 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)
IMPC phenotypes (gene matching)
- abnormal retina morphology / IMPC
- abnormal lens morphology / IMPC
- abnormal coat/hair pigmentation / IMPC
- abnormal digit morphology / IMPC
- fused phalanges / IMPC
- cataract / IMPC
- fused cornea and lens / IMPC
- abnormal cornea morphology / IMPC
- corneal opacity / IMPC
- abnormal tail morphology / IMPC
- abnormal response to new environment / IMPC
- persistence of hyaloid vascular system / IMPC
- decreased circulating creatinine level / IMPC
- abnormal iris morphology / IMPC
- impaired pupillary reflex / IMPC
MGI phenotypes (gene matching)
- belly spot / MGI
- syndactyly / MGI
- kinked tail / MGI
- exencephaly / MGI
- decreased body weight / MGI
- decreased body size / MGI
- persistence of hyaloid vascular system / MGI
- anophthalmia / MGI
- microphthalmia / MGI
- corneal opacity / MGI
- abnormal retina morphology / MGI
- decreased embryo size / MGI
- hemorrhage / MGI
- abnormal eye morphology / MGI
- abnormal brain morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal retinal vasculature morphology / MGI
- white spotting / MGI
- acrania / MGI
- abnormal vascular branching morphogenesis / MGI
- abnormal tail pigmentation / MGI
- behavior/neurological phenotype / MGI
- abnormal lens development / MGI
- fused phalanges / MGI
- decreased survivor rate / MGI
- craniorachischisis / MGI
- failure of eyelid fusion / MGI
- iris coloboma / MGI
- lethality during fetal growth through weaning, incomplete penetrance / MGI
- decreased tail pigmentation / MGI
- absent liver / MGI
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