- 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 |
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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