- 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 |
Citation information | RRID:IMSR_EM:14543 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
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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