- decreased eosinophil cell number / IMPC
- increased Ly6C low monocyte number / IMPC
- increased circulating alkaline phosphatase level / IMPC
- abnormal cranium morphology / IMPC
- decreased circulating triglyceride level / IMPC
- fusion of vertebral arches / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased circulating amylase level / IMPC
- increased monocyte cell number / IMPC
- increased mean platelet volume / IMPC
C57BL/6N-Atm1Brd Wactm2a(EUCOMM)Wtsi/WtsiPh
Status | Available to order |
EMMA ID | EM:09280 |
International strain name | C57BL/6N-Atm1Brd Wactm2a(EUCOMM)Wtsi/WtsiPh |
Alternative name | MEPD0997_2_D04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Wactm2a(EUCOMM)Wtsi |
Gene/Transgene symbol | Wac |
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 | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from EUCOMM ES clone MEPD0997_2_D04. 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 | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation / Orphanet_466950
IMPC phenotypes (gene matching)
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