- head bobbing / IMPC
- decreased thigmotaxis / IMPC
- decreased bone mineral content / IMPC
- increased circulating triglyceride level / IMPC
- increased circulating phosphate level / IMPC
- decreased locomotor activity / IMPC
- impaired glucose tolerance / IMPC
- abnormal spine curvature / IMPC
- abnormal maxilla morphology / IMPC
- abnormal behavior / IMPC
- increased circulating cholesterol level / IMPC
- abnormal bone structure / IMPC
- abnormal cranium morphology / IMPC
- increased circulating HDL cholesterol level / IMPC
C57BL/6N-Nischtm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:08808 |
Citation information | RRID:IMSR_EM:08808 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-Nischtm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0811_2_A03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Nischtm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Nisch |
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 HEPD0811_2_A03. 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)
- short snout / MGI
- decreased body weight / MGI
- decreased body size / MGI
- postnatal growth retardation / MGI
- increased susceptibility to otitis media / MGI
- emphysema / MGI
- abnormal middle ear ossicle morphology / MGI
- hearing/vestibular/ear phenotype / MGI
- abnormal tympanic membrane morphology / MGI
- impaired hearing / MGI
- postnatal lethality, incomplete penetrance / MGI
- abnormal lung-associated mesenchyme development / MGI
- increased or absent threshold for auditory brainstem response / MGI
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