- 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 |
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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