B6NCrl;B6N-Atm1Brd Nrp1tm1a(EUCOMM)Hmgu/CipheOrl
Status | Available to order |
EMMA ID | EM:09943 |
Citation information | RRID:IMSR_EM:09943 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 | B6NCrl;B6N-Atm1Brd Nrp1tm1a(EUCOMM)Hmgu/CipheOrl |
Alternative name | HEPD0725_5_F02 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Nrp1tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Nrp1 |
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 | Centre d'ImmunoPhenomique - Ciphe |
Provider affiliation | Centre d |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0725_5_F02. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NCrl males |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal vascular development / MGI
- abnormal pulmonary artery morphology / MGI
- abnormal corpus callosum morphology / MGI
- abnormal hippocampus morphology / MGI
- abnormal facial motor nucleus morphology / MGI
- abnormal dorsal root ganglion morphology / MGI
- abnormal cranial nerve morphology / MGI
- abnormal trigeminal nerve morphology / MGI
- abnormal facial nerve morphology / MGI
- abnormal vestibulocochlear nerve morphology / MGI
- abnormal spinal nerve morphology / MGI
- decreased body size / MGI
- disorganized yolk sac vascular plexus / MGI
- postnatal growth retardation / MGI
- postnatal lethality / MGI
- premature death / MGI
- abnormal dendritic cell physiology / MGI
- abnormal T cell physiology / MGI
- persistent truncus arteriosis / MGI
- abnormal pharyngeal arch artery morphology / MGI
- abnormal retinal vasculature morphology / MGI
- abnormal axon guidance / MGI
- dilated heart atrium / MGI
- decreased tumor growth/size / MGI
- nervous system phenotype / MGI
- vascular smooth muscle hypoplasia / MGI
- transposition of great arteries / MGI
- abnormal coronary artery morphology / MGI
- right aortic arch / MGI
- double aortic arch / MGI
- abnormal dorsal aorta morphology / MGI
- abnormal brain vasculature morphology / MGI
- cardiovascular system phenotype / MGI
- vision/eye phenotype / MGI
- decreased angiogenesis / MGI
- abnormal neuronal migration / MGI
- abnormal fourth pharyngeal arch artery morphology / MGI
- abnormal sixth pharyngeal arch artery morphology / MGI
- abnormal third pharyngeal arch artery morphology / MGI
- abnormal induced retinal neovascularization / MGI
- abnormal retinal blood vessel morphology / MGI
- abnormal retinal blood vessel pattern / MGI
- abnormal first pharyngeal arch artery morphology / MGI
- abnormal second pharyngeal arch artery morphology / MGI
- abnormal aortic arch and aortic arch branch attachment / MGI
- abnormal coronary vessel morphology / MGI
- postnatal lethality, incomplete penetrance / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
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