- decreased circulating serum albumin level / IMPC
- preweaning lethality, complete penetrance / IMPC
- embryonic lethality prior to organogenesis / IMPC
- enlarged kidney / IMPC
- embryonic lethality prior to tooth bud stage / IMPC
- increased circulating cholesterol level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased circulating HDL cholesterol level / IMPC
- corneal opacity / IMPC
- abnormal cranium morphology / IMPC
- abnormal retina morphology / IMPC
- increased circulating aspartate transaminase level / IMPC
C57BL/6N-Cdc42tm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:08276 |
Citation information | RRID:IMSR_EM:08276 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-Cdc42tm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0727_4_A06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cdc42tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Cdc42 |
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 | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0727_4_A06. 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome / Orphanet_487796
- Neonatal-onset severe multisystemic autoinflammatory disease with increased IL18 / Orphanet_619363
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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