IMPC phenotypes (gene matching)
C57BL/6N-Atm1Brd Smg9tm1a(EUCOMM)Wtsi/WtsiCnrm
| Status | Available to order |
| EMMA ID | EM:10195 |
| Citation information | RRID:IMSR_EM:10195 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/6N-Atm1Brd Smg9tm1a(EUCOMM)Wtsi/WtsiCnrm |
| Alternative name | EPD0428_2_D07 |
| Strain type | Targeted Mutant Strains |
| Allele/Transgene symbol | Smg9tm1a(EUCOMM)Wtsi |
| Gene/Transgene symbol | Smg9 |
| 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 EPD0428_2_D07. 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 | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
MGI phenotypes (gene matching)
- lordosis / MGI
- abnormal interatrial septum morphology / MGI
- double outlet right ventricle / MGI
- abnormal atrioventricular cushion morphology / MGI
- absent kidney / MGI
- polydactyly / MGI
- enlarged liver sinusoidal spaces / MGI
- abnormal pineal gland morphology / MGI
- exencephaly / MGI
- absent superior cervical ganglion / MGI
- small superior cervical ganglion / MGI
- anophthalmia / MGI
- microphthalmia / MGI
- abnormal lens morphology / MGI
- edema / MGI
- hemorrhage / MGI
- abnormal nasal cavity morphology / MGI
- thin myocardium / MGI
- abnormal vein morphology / MGI
- aphakia / MGI
- liver cysts / MGI
- aorta coarctation / MGI
- abnormal eye muscle morphology / MGI
- atrium hypoplasia / MGI
- abnormal neurohypophysis morphology / MGI
- decreased fetal size / MGI
- fetal growth retardation / MGI
- abnormal optic cup morphology / MGI
- basisphenoid bone foramen / MGI
- fusion of vertebral bodies / MGI
- abnormal middle ear ossicle morphology / MGI
- coloboma / MGI
- abnormal endolymphatic duct morphology / MGI
- abnormal inferior vena cava morphology / MGI
- abnormal heart position or orientation / MGI
- abnormal cervical rib / MGI
- thoracoschisis / MGI
- preaxial polydactyly / MGI
- abnormal optic chiasm morphology / MGI
- absent optic chiasm / MGI
- atrioventricular septal defect / MGI
- perimembraneous ventricular septal defect / MGI
- muscular ventricular septal defect / MGI
- abnormal inferior vena cava valve morphology / MGI
- persistent right dorsal aorta / MGI
- left atrium hypoplasia / MGI
- postnatal lethality, complete penetrance / MGI
- lethality throughout fetal growth and development, incomplete penetrance / MGI
- double ureter / MGI
- interrupted aortic arch, type b / MGI
- decreased midbrain size / MGI
- decreased hindbrain size / MGI
- abnormal hypoglossal nerve topology / MGI
- absent segment of posterior cerebral artery / MGI
- subcutaneous edema / MGI
- absent ductus venosus valve / MGI
- abnormal ductus venosus valve morphology / MGI
- duplication of ductus venosus / MGI
- persistent right 6th pharyngeal arch artery / MGI
- reduced sympathetic cervical ganglion size / MGI
- absent connection between subcutaneous lymph vessels and lymph sac / MGI
- blood in lymph vessels / MGI
- heterochrony / MGI
- abnormal lens topology / MGI
- persistent trigeminal artery / MGI