C57BL/6N-Notch1tm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:09421 |
International strain name | C57BL/6N-Notch1tm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0627_7_B12 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Notch1tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Notch1 |
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 | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0627_7_B12. 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Adams-Oliver syndrome / Orphanet_974
- Familial bicuspid aortic valve / Orphanet_402075
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal vertebrae morphology / MGI
- abnormal vascular development / MGI
- abnormal heart development / MGI
- distended pericardium / MGI
- trabecula carnea hypoplasia / MGI
- abnormal cell death / MGI
- decreased thymocyte number / MGI
- abnormal trigeminal ganglion morphology / MGI
- anemia / MGI
- abnormal vasculogenesis / MGI
- abnormal somite development / MGI
- decreased embryo size / MGI
- absent vitelline blood vessels / MGI
- pale yolk sac / MGI
- embryonic growth arrest / MGI
- postnatal growth retardation / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal T cell differentiation / MGI
- no abnormal phenotype detected / MGI
- disorganized myocardium / MGI
- abnormal artery morphology / MGI
- abnormal placenta vasculature / MGI
- kinked neural tube / MGI
- delayed somite formation / MGI
- abnormal nervous system development / MGI
- embryonic growth retardation / MGI
- abnormal embryonic neuroepithelium morphology / MGI
- increased cochlear outer hair cell number / MGI
- notochord degeneration / MGI
- abnormal dorsal aorta morphology / MGI
- decreased T cell number / MGI
- decreased double-negative T cell number / MGI
- abnormal rostral-caudal axis patterning / MGI
- abnormal somite size / MGI
- abnormal left-right axis symmetry of the somites / MGI
- abnormal myocardium layer morphology / MGI
- decreased angiogenesis / MGI
- embryonic lethality during organogenesis / MGI
- small pharyngeal arch / MGI
- increased T cell apoptosis / MGI
- embryonic lethality / MGI
- abnormal cardiac epithelial to mesenchymal transition / MGI
- abnormal retinal blood vessel morphology / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
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