- abnormal eye morphology / IMPC
- decreased mean corpuscular hemoglobin concentration / IMPC
- preweaning lethality, complete penetrance / IMPC
- increased grip strength / IMPC
- decreased red blood cell distribution width / IMPC
- embryonic lethality prior to organogenesis / IMPC
- abnormal embryo size / IMPC
- anophthalmia / IMPC
- embryonic lethality prior to tooth bud stage / IMPC
- abnormal tooth morphology / IMPC
- abnormal maxilla morphology / IMPC
C57BL/6N-Chd1em1(IMPC)Wtsi/WtsiPh
Status | Available to order |
EMMA ID | EM:14543 |
International strain name | C57BL/6N-Chd1em1(IMPC)Wtsi/WtsiPh |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Chd1em1(IMPC)Wtsi |
Gene/Transgene symbol | Chd1 |
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome / Orphanet_529965
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal embryo development / MGI
- abnormal mesoderm development / MGI
- failure to gastrulate / MGI
- decreased embryo size / MGI
- abnormal developmental patterning / MGI
- no abnormal phenotype detected / MGI
- absent extraembryonic ectoderm / MGI
- no phenotypic analysis / MGI
- abnormal cell cycle / MGI
- abnormal rostral-caudal axis patterning / MGI
- embryonic lethality, complete penetrance / MGI
- small embryonic epiblast / MGI
- increased embryonic epiblast cell apoptosis / MGI
- absent anterior visceral endoderm / MGI
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