- abnormal testis morphology / IMPC
- abnormal lens morphology / IMPC
- decreased total retina thickness / IMPC
- decreased mean corpuscular hemoglobin concentration / IMPC
- abnormal spleen morphology / IMPC
- increased lean body mass / IMPC
- hyperactivity / IMPC
- decreased heart rate / IMPC
- increased startle reflex / IMPC
- decreased grip strength / IMPC
- abnormal vertebral arch morphology / IMPC
- increased grip strength / IMPC
- hyperplasia / IMPC
- increased circulating sodium level / IMPC
- decreased exploration in new environment / IMPC
- decreased total body fat amount / IMPC
- decreased circulating chloride level / IMPC
- decreased vertical activity / IMPC
- increased bone mineral content / IMPC
- abnormal cholesterol homeostasis / IMPC
- abnormal retina inner nuclear layer morphology / IMPC
- decreased circulating serum albumin level / IMPC
- decreased mean corpuscular volume / IMPC
- decreased circulating glucose level / IMPC
- increased prepulse inhibition / IMPC
- fibro-osseous lesion / IMPC
- increased lung compliance / IMPC
- decreased respiratory quotient / IMPC
- abnormal sleep behavior / IMPC
- unresponsive to tactile stimuli / IMPC
- increased cardiac muscle contractility / IMPC
- abnormal behavior / IMPC
- increased circulating creatine kinase level / IMPC
- limb grasping / IMPC
- increased circulating free fatty acids level / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- decreased thigmotaxis / IMPC
- hypoplasia / IMPC
- abnormal coat appearance / IMPC
- increased kidney weight / IMPC
- decreased circulating total protein level / IMPC
- increased erythrocyte cell number / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- abnormal inspiratory capacity / IMPC
- impaired glucose tolerance / IMPC
- small testis / IMPC
- increased circulating amylase level / IMPC
- decreased anxiety-related response / IMPC
- decreased circulating triglyceride level / IMPC
- abnormal vertebrae morphology / IMPC
- cardiovascular system phenotype / IMPC
- increased circulating alkaline phosphatase level / IMPC
- decreased cardiac output / IMPC
- decreased heart rate variability / IMPC
- increased bone mineral density / IMPC
- abnormal freezing behavior / IMPC
- abnormal sinus arrhythmia / IMPC
- decreased circulating alanine transaminase level / IMPC
- depletion / IMPC
- enlarged lymph nodes / IMPC
- increased hemoglobin content / IMPC
- enlarged spleen / IMPC
- process of degenerative change / IMPC
- increased red blood cell distribution width / IMPC
- decreased locomotor activity / IMPC
- increased circulating aspartate transaminase level / IMPC
- increased heart weight / IMPC
- increased hematocrit / IMPC
- impaired contextual conditioning behavior / IMPC
- decreased circulating creatinine level / IMPC
- decreased circulating free fatty acids level / IMPC
- abnormal kidney morphology / IMPC
- decreased hemoglobin content / IMPC
- increased exploration in new environment / IMPC
- increased fasting circulating glucose level / IMPC
C57BL/6N-Ap4e1tm1c(KOMP)Wtsi/H
Status | Available to order |
EMMA ID | EM:09035 |
Citation information | RRID:IMSR_EM:09035 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-Ap4e1tm1c(KOMP)Wtsi/H |
Alternative name | EPD0025_5_A08 |
Strain type | Targeted Mutant Strains : Targeted Conditional |
Allele/Transgene symbol | Ap4e1tm1c(KOMP)Wtsi |
Gene/Transgene symbol | Ap4e1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This line originates from KOMP ES clone EPD0025_5_A08, after breeding with a Flp recombinase deleter line to convert the original targeted allele tm1a (knock-out first allele) into a conditional allele tm1c. 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
- Severe intellectual disability and progressive spastic paraplegia / Orphanet_280763
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- increased bone mineral density / MGI
- abnormal femur morphology / MGI
- decreased corpus callosum size / MGI
- anemia / MGI
- decreased vertical activity / MGI
- decreased hemoglobin content / MGI
- increased lean body mass / MGI
- abnormal behavior / MGI
- decreased mean corpuscular hemoglobin / MGI
- enlarged lateral ventricles / MGI
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).