- abnormal blood vessel morphology / MGI
- absent vitelline blood vessels / MGI
- pale yolk sac / MGI
- no abnormal phenotype detected / MGI
- embryonic growth retardation / MGI
- abnormal dorsal aorta morphology / MGI
- pericardial effusion / MGI
- cardiovascular system phenotype / MGI
- abnormal vascular smooth muscle morphology / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- cardiac edema / MGI
C57BL/6J-Myocdem1H/H
Status | Available to order |
EMMA ID | EM:15114 |
International strain name | C57BL/6J-Myocdem1H/H |
Alternative name | MYOCD-FLOX-EM1-B6 |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Myocdem1H |
Gene/Transgene symbol | Myocd |
Information from provider
Provider | MRC-Harwell |
Provider affiliation | Mammalian Genetics Unit, Mary Lyon Centre at MRC Harwell |
Genetic information | For detailed information on the genetic description of this strain, please have a look at this report. |
Breeding history | Co-isogenic on original background |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | not known |
Immunocompromised | not known |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI phenotypes (gene matching)
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