- decreased exploration in new environment / IMPC
- increased heart weight / IMPC
- decreased bone mineral density / IMPC
- decreased bone mineral content / IMPC
- abnormal head size / IMPC
- increased circulating amylase level / IMPC
- increased lean body mass / IMPC
- enlarged kidney / IMPC
- abnormal tooth morphology / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- abnormal startle reflex / IMPC
- tremors / IMPC
- decreased fasting circulating glucose level / IMPC
- abnormal bone structure / IMPC
- increased circulating total protein level / IMPC
- enlarged spleen / IMPC
- increased mean corpuscular volume / IMPC
- increased circulating phosphate level / IMPC
- increased blood urea nitrogen level / IMPC
- enlarged gallbladder / IMPC
- increased spleen weight / IMPC
- decreased total body fat amount / IMPC
- increased circulating calcium level / IMPC
- abnormal esophagus morphology / IMPC
- increased circulating aspartate transaminase level / IMPC
- decreased circulating glucose level / IMPC
- decreased circulating fructosamine level / IMPC
C57BL/6N-Itchtm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:09007 |
Citation information | RRID:IMSR_EM:09007 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-Itchtm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0706_7_E10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Itchtm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Itch |
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 HEPD0706_7_E10. 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
- Syndromic multisystem autoimmune disease due to Itch deficiency / Orphanet_228426
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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