C57BL/6N-Atm1Brd Myh14tm1a(EUCOMM)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:06262 |
International strain name | C57BL/6N-Atm1Brd Myh14tm1a(EUCOMM)Wtsi/WtsiCnbc |
Alternative name | EPD0373_3_A09 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Myh14tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Myh14 |
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 EPD0373_3_A09. 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 | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous C57BL/6NTac, wild-type C57BL/6NCrl |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Left ventricular noncompaction / Orphanet_54260
- Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome / Orphanet_397744
- Autosomal dominant non-syndromic sensorineural deafness type DFNA / Orphanet_90635
- Low isolated anorectal malformation / Orphanet_171215
MGI phenotypes (gene matching)
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