- increased circulating cholesterol level / IMPC
- decreased circulating serum albumin level / IMPC
- increased circulating iron level / IMPC
- increased circulating alanine transaminase level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased leukocyte cell number / IMPC
- increased circulating aspartate transaminase level / IMPC
- increased hematocrit / IMPC
C57BL/6N-Atm1Brd Ap4m1tm1a(EUCOMM)Wtsi/WtsiPh
Status | Available to order |
EMMA ID | EM:08226 |
International strain name | C57BL/6N-Atm1Brd Ap4m1tm1a(EUCOMM)Wtsi/WtsiPh |
Alternative name | EPD0808_1_D06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ap4m1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Ap4m1 |
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 EPD0808_1_D06. 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
- Severe intellectual disability and progressive spastic paraplegia / Orphanet_280763
IMPC phenotypes (gene matching)
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