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Phenotypes Associated with This Genotype
Genotype
MGI:3036465
Allelic
Composition
Nrp1tm1Hfu/Nrp1tm1Hfu
Genetic
Background
involves: C57BL/6 * CBA * ICR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm1Hfu mutation (2 available); any Nrp1 mutation (83 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• by 13.5 dpc, most mutant embryos had died, but a few embryos with severe edema were still alive

cardiovascular system
• at E10.5 segements of the dorsal aorta are regressed
• at E9.5 all embryos (N = 5) exhibited severe regression of the arch artery system (arch arteries 1 - 3 are normally bilaterally symmetrical at this time)
• at E10.5 the arch arteries 1 and 2 often persisted
• at E10.5, 15 out of 22 embryos lack the right and left arch arteries 4
• at E 12.5 the left arch artery 4, which normally forms the arch of the aorta is absent and the arch of the aorta forms on the right side (15 out of 21)
• at E10.5 the arch arteries 1 and 2 often persisted
• at E10.5, all embryos (N = 22) lack the right and left arch arteries 6
• at E12.5 all embryos (N = 21) lack the left arch artery 6
• at E10.5, some embryos missing arch artery 4 also lack the arch artery 3 on either side
• the distal end of the pulmonary channel merges with the aortic arch
• at E12.5 the left subclavian artery arises from the right sided arch of the aorta
• right arotic arch is observed in some mutants
• observed in some mutants
• capillary invasion is absent from the central nervous system of mutants at E10.5
• at E12.5 little vascularization is seen in the neocortex, dorsal part of the midbrain, spinal cord, and sensory ganglia
• at E12.5 abnormal capillaries, that are of large caliber, with few branches and often broken into small spherical segments, are present in the diencephalon, ventral midbrain, hindbrain, and ventral spinal cord
• at E12.5 the yolk sac of mutants is as well vascularized as that of wild-types however the vascular networks are abnormal
• the large vessels meander and are often divided into small vessels that anastomose
• capillary networks in the yolk sac are sparse
• at E12.5 seperation of the truncus arteriosus is incomplete (5 out of 6)

embryo
• at E9.5 all embryos (N = 5) exhibited severe regression of the arch artery system (arch arteries 1 - 3 are normally bilaterally symmetrical at this time)
• at E10.5 the arch arteries 1 and 2 often persisted
• at E10.5, 15 out of 22 embryos lack the right and left arch arteries 4
• at E 12.5 the left arch artery 4, which normally forms the arch of the aorta is absent and the arch of the aorta forms on the right side (15 out of 21)
• at E10.5 the arch arteries 1 and 2 often persisted
• at E10.5, all embryos (N = 22) lack the right and left arch arteries 6
• at E12.5 all embryos (N = 21) lack the left arch artery 6
• at E10.5, some embryos missing arch artery 4 also lack the arch artery 3 on either side
• at E12.5 the yolk sac of mutants is as well vascularized as that of wild-types however the vascular networks are abnormal
• the large vessels meander and are often divided into small vessels that anastomose
• capillary networks in the yolk sac are sparse

craniofacial
• at E9.5 all embryos (N = 5) exhibited severe regression of the arch artery system (arch arteries 1 - 3 are normally bilaterally symmetrical at this time)
• at E10.5 the arch arteries 1 and 2 often persisted
• at E10.5, 15 out of 22 embryos lack the right and left arch arteries 4
• at E 12.5 the left arch artery 4, which normally forms the arch of the aorta is absent and the arch of the aorta forms on the right side (15 out of 21)
• at E10.5 the arch arteries 1 and 2 often persisted
• at E10.5, all embryos (N = 22) lack the right and left arch arteries 6
• at E12.5 all embryos (N = 21) lack the left arch artery 6
• at E10.5, some embryos missing arch artery 4 also lack the arch artery 3 on either side


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
09/17/2024
MGI 6.24
The Jackson Laboratory