- dilated lateral ventricles / MGI
- abnormal third ventricle morphology / MGI
- obstructive hydrocephaly / MGI
- small superior cervical ganglion / MGI
- abnormal gait / MGI
- postnatal growth retardation / MGI
- bifid ureter / MGI
- nervous system phenotype / MGI
- abnormal Mullerian duct morphology / MGI
- abnormal Wolffian duct morphology / MGI
- retroesophageal right subclavian artery / MGI
- fusion of vertebral arches / MGI
- abnormal cerebral aqueduct morphology / MGI
- arteriovenous malformation / MGI
- enlarged third ventricle / MGI
- abnormal neural tube ventricular layer morphology / MGI
- brain ventricle stenosis / MGI
- subcutaneous edema / MGI
- reduced sympathetic cervical ganglion size / MGI
- blood in lymph vessels / MGI
C57BL/6NTac-Myo9atm1a(EUCOMM)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:06322 |
Citation information | RRID:IMSR_EM:06322 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | C57BL/6NTac-Myo9atm1a(EUCOMM)Wtsi/WtsiCnbc |
Alternative name | EPD0188_3_A12 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Myo9atm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Myo9a |
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 EPD0188_3_A12. 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 males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Presynaptic congenital myasthenic syndromes / Orphanet_98914
MGI phenotypes (gene matching)
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).