- abnormal retina morphology / IMPC
- decreased lean body mass / IMPC
- cataract / IMPC
- increased circulating alanine transaminase level / IMPC
- decreased circulating total protein level / IMPC
- abnormal auditory brainstem response / IMPC
- decreased circulating cholesterol level / IMPC
- limb grasping / IMPC
- decreased prepulse inhibition / IMPC
- decreased blood urea nitrogen level / IMPC
- increased basophil cell number / IMPC
- increased circulating alkaline phosphatase level / IMPC
- abnormal tooth morphology / IMPC
- increased fasting circulating glucose level / IMPC
- decreased circulating serum albumin level / IMPC
- decreased circulating HDL cholesterol level / IMPC
- short tibia / IMPC
C57BL/6N-Atg4btm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:11966 |
Citation information | RRID:IMSR_EM:11966 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-Atg4btm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0752_1_B03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Atg4btm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Atg4b |
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 HEPD0752_1_B03. 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
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- circling / MGI
- impaired coordination / MGI
- impaired swimming / MGI
- abnormal lipid homeostasis / MGI
- abnormal motor learning / MGI
- abnormal otolith morphology / MGI
- absent otoliths / MGI
- enlarged otoliths / MGI
- nervous system phenotype / MGI
- abnormal vestibular saccular macula morphology / MGI
- head tilt / MGI
- abnormal utricle morphology / MGI
- abnormal autophagy / MGI
- abnormal cerebellum deep nucleus morphology / MGI
- preweaning lethality, incomplete penetrance / MGI
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