- decreased bone mineral density / IMPC
- decreased hemoglobin content / IMPC
- decreased erythrocyte cell number / IMPC
- abnormal bone mineralization / IMPC
- abnormal bone structure / IMPC
- abnormal behavior / IMPC
- increased B cell number / IMPC
- decreased T cell number / IMPC
- decreased CD4-positive, alpha-beta T cell number / IMPC
- decreased CD8-positive, alpha-beta T cell number / IMPC
- increased bone mineral content / IMPC
C57BL/6N-Acp2tm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:05128 |
International strain name | C57BL/6N-Acp2tm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0370_6_H05 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Acp2tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Acp2 |
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 EPD0370_6_H05. 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 |
Animals used for archiving | heterozygous C57BL/6NTac |
Breeding at archiving centre | Chimeras were mated to C57BL/6N Tac USA and maintained on this background thereafter. |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased B cell number / IMPC
- decreased erythrocyte cell number / IMPC
- decreased hemoglobin content / IMPC
- decreased CD4-positive, alpha-beta T cell number / IMPC
- decreased T cell number / IMPC
- decreased CD8-positive, alpha-beta T cell number / IMPC
- abnormal bone structure / IMPC
- abnormal bone mineralization / IMPC
- decreased bone mineral density / IMPC
- increased bone mineral content / IMPC
- abnormal behavior / IMPC
MGI phenotypes (gene matching)
- kyphoscoliosis / MGI
- abnormal microglial cell morphology / MGI
- abnormal vertebral body morphology / MGI
- kyphosis / MGI
- lordosis / MGI
- abnormal hair follicle morphology / MGI
- alopecia / MGI
- delayed hair appearance / MGI
- tremors / MGI
- abnormal cerebellum morphology / MGI
- small cerebellum / MGI
- thin external granule cell layer / MGI
- abnormal cerebellar Purkinje cell layer / MGI
- ectopic Purkinje cell / MGI
- absent cerebellar granule layer / MGI
- abnormal cerebellar molecular layer / MGI
- abnormal CNS glial cell morphology / MGI
- abnormal epidermis stratum basale morphology / MGI
- abnormal dermal layer morphology / MGI
- decreased body height / MGI
- decreased body weight / MGI
- ataxia / MGI
- postnatal growth retardation / MGI
- astrocytosis / MGI
- abnormal compact bone morphology / MGI
- tonic-clonic seizures / MGI
- abnormal vertebral pedicle morphology / MGI
- abnormal vertebral column morphology / MGI
- abnormal lysosome morphology / MGI
- accumulation of giant lysosomes in kidney/renal tubule cells / MGI
- behavior/neurological phenotype / MGI
- abnormal Purkinje cell dendrite morphology / MGI
- thin hair shaft / MGI
- increased trabecular bone connectivity density / MGI
- decreased bone mineralization / MGI
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