C57BL/6N-Pdgfrbtm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:08382 |
International strain name | C57BL/6N-Pdgfrbtm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0676_4_F11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Pdgfrbtm1a(EUCOMM)Hmgu, |
Gene/Transgene symbol | Pdgfrb |
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 | Mammalian Genetics Unit, Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0676_4_F11. 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
- Acroosteolysis-keloid-like lesions-premature aging syndrome / Orphanet_363665
- Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome / Orphanet_477831
- Infantile myofibromatosis / Orphanet_2591
- Bilateral striopallidodentate calcinosis / Orphanet_1980
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