B6NTac;B6N-Atm1Brd Il31ratm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:09660 |
International strain name | B6NTac;B6N-Atm1Brd Il31ratm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0673_5_F03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Il31ratm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Il31ra |
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 HEPD0673_5_F03. 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
- Familial primary localized cutaneous amyloidosis / Orphanet_353220
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased bone marrow cell number / MGI
- spleen hypoplasia / MGI
- abnormal bone marrow cell morphology/development / MGI
- abnormal macrophage physiology / MGI
- increased IgE level / MGI
- granulomatous inflammation / MGI
- increased susceptibility to parasitic infection / MGI
- increased T cell proliferation / MGI
- immune system phenotype / MGI
- abnormal common myeloid progenitor cell morphology / MGI
- abnormal interleukin level / MGI
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