- abnormal kidney morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal vitreous body morphology / IMPC
- abnormal skin morphology / IMPC
- embryonic growth retardation / IMPC
- abnormal placenta morphology / IMPC
- microphthalmia / IMPC
- abnormal retina morphology / IMPC
- small kidney / IMPC
C57BL/6J-Chrndem1H/H
Status | Available to order |
EMMA ID | EM:13032 |
International strain name | C57BL/6J-Chrndem1H/H |
Alternative name | Chrnd-R399H-EM1-B6 |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Chrndem1H |
Gene/Transgene symbol | Chrnd |
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. |
Phenotypic information | Homozygous:UnknownHeterozygous:None |
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
Orphanet associated rare diseases, based on orthologous gene matching
- Postsynaptic congenital myasthenic syndromes / Orphanet_98913
- Lethal multiple pterygium syndrome / Orphanet_33108
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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