About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nrp1tm1Hfu
targeted mutation 1, Hajime Fujisawa
MGI:1857853
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nrp1tm1Hfu/Nrp1tm1Hfu involves: C57BL/6 * CBA MGI:3579403
hm2
Nrp1tm1Hfu/Nrp1tm1Hfu involves: C57BL/6 * CBA * ICR MGI:3036465
hm3
Nrp1tm1Hfu/Nrp1tm1Hfu involves: C57BL/6NCrlj * CBA/JNCrlj MGI:5432162
hm4
Nrp1tm1Hfu/Nrp1tm1Hfu involves: CD-1 * JF1 MGI:3512162
cn5
Nrp1tm1Hfu/Nrp1tm2Ddg
Tg(Tek-cre)1Ywa/0
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL MGI:5432163
cx6
Nrp1tm1Hfu/Nrp1tm1Hfu
Nrp2tm1Mkl/Nrp2+
involves: BALB/c * C57BL/6 * CBA MGI:3712945
cx7
Nrp1tm1Hfu/Nrp1+
Nrp2tm1Mkl/Nrp2tm1Mkl
involves: BALB/c * C57BL/6 * CBA MGI:3712946


Genotype
MGI:3579403
hm1
Allelic
Composition
Nrp1tm1Hfu/Nrp1tm1Hfu
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm1Hfu mutation (2 available); any Nrp1 mutation (81 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• defects as previously reported for mutations of this locus are observed
• however, mostly normal blood vessel network formation occurs in both yolk sac and embryo at E10

nervous system
• growth cone collapse of dorsal root ganglion and sympathetic ganglion axons in response to Sema3A was completely abolished
• ophthalmic nerve fibers overshot their peripheral target fields
• spinal nerve fibers overshot toward the opposite side of embryos after crossing the dorsal midline

cellular
• growth cone collapse of dorsal root ganglion and sympathetic ganglion axons in response to Sema3A was completely abolished




Genotype
MGI:3036465
hm2
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 (81 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




Genotype
MGI:5432162
hm3
Allelic
Composition
Nrp1tm1Hfu/Nrp1tm1Hfu
Genetic
Background
involves: C57BL/6NCrlj * CBA/JNCrlj
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm1Hfu mutation (2 available); any Nrp1 mutation (81 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• normal numbers of gonadotropin-releasing hormone neurons




Genotype
MGI:3512162
hm4
Allelic
Composition
Nrp1tm1Hfu/Nrp1tm1Hfu
Genetic
Background
involves: CD-1 * JF1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm1Hfu mutation (2 available); any Nrp1 mutation (81 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• delayed tangential somata migration of facial branchiomotor neurons that resulted in the separation of the migratory stream into several distinct streams on the ventricular side of the hindbrain
• facial branchiomotor neuron somata emerged on the pial side in an ectopic anterior location during radial migration
• migration defects are not due to abnormal hindbrain segmentation, vascular defects in the hindbrain or axon guidance defects in the periphery
• nuclei on the pial side were elongated or dumbbell-shaped and in severe cases, the entire nucleus was shifted anteriorly
• defasciculated facial nerve
• defasciculated trigeminal nerve branches

cellular
• delayed tangential somata migration of facial branchiomotor neurons that resulted in the separation of the migratory stream into several distinct streams on the ventricular side of the hindbrain
• facial branchiomotor neuron somata emerged on the pial side in an ectopic anterior location during radial migration
• migration defects are not due to abnormal hindbrain segmentation, vascular defects in the hindbrain or axon guidance defects in the periphery




Genotype
MGI:5432163
cn5
Allelic
Composition
Nrp1tm1Hfu/Nrp1tm2Ddg
Tg(Tek-cre)1Ywa/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm1Hfu mutation (2 available); any Nrp1 mutation (81 available)
Nrp1tm2Ddg mutation (1 available); any Nrp1 mutation (81 available)
Tg(Tek-cre)1Ywa mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• reduced gonadotropin-releasing hormone neurons

cardiovascular system




Genotype
MGI:3712945
cx6
Allelic
Composition
Nrp1tm1Hfu/Nrp1tm1Hfu
Nrp2tm1Mkl/Nrp2+
Genetic
Background
involves: BALB/c * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm1Hfu mutation (2 available); any Nrp1 mutation (81 available)
Nrp2tm1Mkl mutation (1 available); any Nrp2 mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos die at E10-10.5, showing longer survival thah double homozygous embryos

embryo
• yolk sacs are of normal size, but lack larger collecting vessels and contain irregular and less dense capillary networks
• vasulature of yolk sac at E10 is characterized by vessel heterogeneity, disorganization, and immaturity
• arterial and venous branching is not seen in yolk sacs at E10
• thickened blood vessels, lack of capillaries, and large avascular spaces between blood vessels are observed, with occasional dead-ended sprouts not connected to other sprouts
• much smaller than littermates; length of embryo in yolk sac is ~50% of control embryo length

growth/size/body
• much smaller than littermates; length of embryo in yolk sac is ~50% of control embryo length

cardiovascular system
• avascular regions, vessel size heterogeneity, and thickened blood vessels are observed
• outflow tract formation is abnormal
• blood vessel density in head region is slightly higher than in Npr1tm1Hfu/Npr1+; Npr2tm1Mkl /Npr2tm1Mkl embryos
• abnormal formation of dorsal aorta is observed
• yolk sacs are of normal size, but lack larger collecting vessels and contain irregular and less dense capillary networks
• vasulature of yolk sac at E10 is characterized by vessel heterogeneity, disorganization, and immaturity
• arterial and venous branching is not seen in yolk sacs at E10
• thickened blood vessels, lack of capillaries, and large avascular spaces between blood vessels are observed, with occasional dead-ended sprouts not connected to other sprouts
• multiple hemorrhages are observed in embryos at E10




Genotype
MGI:3712946
cx7
Allelic
Composition
Nrp1tm1Hfu/Nrp1+
Nrp2tm1Mkl/Nrp2tm1Mkl
Genetic
Background
involves: BALB/c * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm1Hfu mutation (2 available); any Nrp1 mutation (81 available)
Nrp2tm1Mkl mutation (1 available); any Nrp2 mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos die at E10-10.5, showing longer survival thah double homozygous embryos

embryo
• yolk sacs are of normal size, but lack larger collecting vessels and contain irregular and less dense capillary networks
• vasulature of yolk sac at E10 is characterized by vessel heterogeneity, disorganization, and immaturity
• thickened blood vessels, lack of capillaries, and large avascular spaces between blood vessels are observed, with occasional dead-ended sprouts not connected to other sprouts
• arterial and venous branching is not seen in yolk sacs at E10

cardiovascular system
• embryos show severe vascular impairment at E10
• blood vessels are disorganized, heterogeneous in size, and some show thickening
• blood vessel density is low in the head region, with avascular regions in head and trunk
• small vessel sprouting is seen, but is unconnected to other sprouts and no capillary plexus is formed
• dorsal aorta is poorly formed, and outflow tract is undetectable
• yolk sacs are of normal size, but lack larger collecting vessels and contain irregular and less dense capillary networks
• vasulature of yolk sac at E10 is characterized by vessel heterogeneity, disorganization, and immaturity
• thickened blood vessels, lack of capillaries, and large avascular spaces between blood vessels are observed, with occasional dead-ended sprouts not connected to other sprouts
• arterial and venous branching is not seen in yolk sacs at E10
• multiple hemorrhages are observed in embryos at E10





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory