- preweaning lethality, complete penetrance / IMPC
C57BL/6N-Atm1Brd Cmiptm1a(EUCOMM)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:08146 |
International strain name | C57BL/6N-Atm1Brd Cmiptm1a(EUCOMM)Wtsi/WtsiH |
Alternative name | EPD0844_1_B08 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cmiptm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Cmip |
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 EPD0844_1_B08. 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 |
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Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- preweaning lethality, complete penetrance / IMPC
MGI phenotypes (allele matching)
- abnormal large intestine morphology / MGI
- abnormal small intestine morphology / MGI
- abnormal lymphatic vessel morphology / MGI
- small thyroid gland / MGI
- intestinal/bowel diverticulum / MGI
- abnormal Mullerian duct morphology / MGI
- retroesophageal right subclavian artery / MGI
- abnormal liver vasculature morphology / MGI
- muscular ventricular septal defect / MGI
- dual inferior vena cava / MGI
- thin hypoglossal nerve / MGI
- absent hypoglossal nerve / MGI
- absent segment of posterior cerebral artery / MGI
- jugular vein stenosis / MGI
- multiple persisting craniopharyngeal ducts / MGI
- abnormal coronary sinus connection / MGI
- abnormal vitelline vein topology / MGI
- abnormal vertebral artery topology / MGI
- embryo tumor / MGI
- embryo cyst / MGI
MGI phenotypes (gene matching)
- abnormal large intestine morphology / MGI
- abnormal small intestine morphology / MGI
- abnormal lymphatic vessel morphology / MGI
- no abnormal phenotype detected / MGI
- small thyroid gland / MGI
- intestinal/bowel diverticulum / MGI
- abnormal Mullerian duct morphology / MGI
- retroesophageal right subclavian artery / MGI
- abnormal liver vasculature morphology / MGI
- muscular ventricular septal defect / MGI
- dual inferior vena cava / MGI
- thin hypoglossal nerve / MGI
- absent hypoglossal nerve / MGI
- absent segment of posterior cerebral artery / MGI
- jugular vein stenosis / MGI
- multiple persisting craniopharyngeal ducts / MGI
- abnormal coronary sinus connection / MGI
- abnormal vitelline vein topology / MGI
- abnormal vertebral artery topology / MGI
- embryo tumor / MGI
- embryo cyst / MGI
- persistent trigeminal artery / MGI
Literature references
- Functional analysis of candidate genes from genome-wide association studies of hearing.;Ingham Neil J, Rook Victoria, Di Domenico Francesca, James Elysia, Lewis Morag A, Girotto Giorgia, Buniello Annalisa, Steel Karen P, ;2020;Hearing research;387;107879; 31927188
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