C57BL/6N-Myh3tm1b(EUCOMM)Wtsi/WtsiH
Status | Only small colony available |
EMMA ID | EM:14254 |
International strain name | C57BL/6N-Myh3tm1b(EUCOMM)Wtsi/WtsiH |
Alternative name | EPD0780_2_F11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Myh3tm1b(EUCOMM)Wtsi |
Gene/Transgene symbol | Myh3 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0780_2_F11. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele using an X-linked CMV-Cre driver (EM:05414; C57BL/6N-Hprttm1(CMV-cre)Wtsi/WtsiOulu) for this purpose. Click here for more information on EUCOMM final vectors. |
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
- Sheldon-Hall syndrome / Orphanet_1147
- Digitotalar dysmorphism / Orphanet_1146
- Freeman-Sheldon syndrome / Orphanet_2053
- Spondylocarpotarsal synostosis / Orphanet_3275
- Autosomal recessive multiple pterygium syndrome / Orphanet_2990
- Autosomal dominant multiple pterygium syndrome / Orphanet_65743
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).