C57BL/6N-Atm1Brd Myh3tm1a(EUCOMM)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:13942 |
International strain name | C57BL/6N-Atm1Brd Myh3tm1a(EUCOMM)Wtsi/WtsiH |
Alternative name | EPD0780_2_F11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Myh3tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Myh3 |
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 | 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. |
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
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