C57BL/6N-Zfp106tm1c(KOMP)Wtsi/H
| Status | Available to order |
| EMMA ID | EM:09050 |
| Citation information | RRID:IMSR_EM:09050 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-Zfp106tm1c(KOMP)Wtsi/H |
| Alternative name | EPD0033_4_C03 |
| Strain type | Targeted Mutant Strains : Targeted Conditional |
| Allele/Transgene symbol | Zfp106tm1c(KOMP)Wtsi |
| Gene/Transgene symbol | Zfp106 |
| 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 line originates from KOMP ES clone EPD0033_4_C03, 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 IKMC page on 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)
- kyphosis / MGI
- increased circulating calcium level / MGI
- tremors / MGI
- abnormal skeletal muscle morphology / MGI
- motor neuron degeneration / MGI
- decreased motor neuron number / MGI
- abnormal spinal cord morphology / MGI
- small dorsal root ganglion / MGI
- small L4 dorsal root ganglion / MGI
- small L5 dorsal root ganglion / MGI
- weight loss / MGI
- hypoactivity / MGI
- impaired coordination / MGI
- abnormal gait / MGI
- limb grasping / MGI
- impaired limb coordination / MGI
- premature death / MGI
- abnormal muscle physiology / MGI
- gliosis / MGI
- neurodegeneration / MGI
- chromatolysis / MGI
- abnormal soleus morphology / MGI
- abnormal gastrocnemius morphology / MGI
- abnormal redox activity / MGI
- astrocytosis / MGI
- nervous system phenotype / MGI
- abnormal muscle electrophysiology / MGI
- abnormal physical strength / MGI
- cachexia / MGI
- positive geotaxis / MGI
- abnormal axon morphology / MGI
- axon degeneration / MGI
- abnormal mitochondrial physiology / MGI
- abnormal lumbar dorsal root ganglion morphology / MGI
- microgliosis / MGI
- abnormal external male genitalia morphology / MGI
- increased variability of skeletal muscle fiber size / MGI
- centrally nucleated skeletal muscle fibers / MGI
- decreased skeletal muscle fiber number / MGI
- abnormal skeletal muscle fiber type ratio / MGI
- skeletal muscle fiber degeneration / MGI
- skeletal muscle fiber atrophy / MGI
- skeletal muscle atrophy / MGI
- skeletal muscle fibrosis / MGI
- decreased gastrocnemius weight / MGI
- decreased soleus weight / MGI
- decreased tibialis anterior weight / MGI
- decreased grip strength / MGI
- abnormal mitochondrial ATP synthesis coupled electron transport / MGI
- increased spinal cord apoptosis / MGI
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