- decreased food intake / IMPC
C57BL/6N-Myo9atm1b(EUCOMM)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:14487 |
International strain name | C57BL/6N-Myo9atm1b(EUCOMM)Wtsi/WtsiCnbc |
Alternative name | EPD0188_3_A12 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Myo9atm1b(EUCOMM)Wtsi, |
Gene/Transgene symbol | Myo9a |
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 EPD0188_3_A12. 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 a cell permeable HTN-Cre as described in doi:10.1007/s11248-013-9764-x. 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 | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous C57BL/6N |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Presynaptic congenital myasthenic syndromes / Orphanet_98914
IMPC phenotypes (allele matching)
MGI phenotypes (allele matching)
- small superior cervical ganglion / MGI
- bifid ureter / MGI
- abnormal Mullerian duct morphology / MGI
- abnormal Wolffian duct morphology / MGI
- retroesophageal right subclavian artery / MGI
- fusion of vertebral arches / MGI
- arteriovenous malformation / MGI
- subcutaneous edema / MGI
- reduced sympathetic cervical ganglion size / MGI
- blood in lymph vessels / MGI
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