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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nrp1tm2.1Ddg
targeted mutation 2.1, David D Ginty
MGI:3512103
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nrp1tm2.1Ddg/Nrp1tm2.1Ddg involves: 129 * C57BL/6 MGI:3512122
cn2
Nrp1tm2Ddg/Nrp1tm2.1Ddg
Tg(Tek-cre)1Ywa/0
involves: 129 * C57BL/6 MGI:3512130
cn3
Nrp1tm2Ddg/Nrp1tm2.1Ddg
Tg(Gucy2g-cre,-EGFP)52Irod/0
involves: 129P2/OlaHsd * C57BL/6 * SJL MGI:5431517


Genotype
MGI:3512122
hm1
Allelic
Composition
Nrp1tm2.1Ddg/Nrp1tm2.1Ddg
Genetic
Background
involves: 129 * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm2.1Ddg mutation (0 available); any Nrp1 mutation (84 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• distal axons of the ophthalmic nerve were more defasciculated and disorganized than those in Nrp1tm1Ddg
• spinal nerves were disorganized in E11.5 mutants




Genotype
MGI:3512130
cn2
Allelic
Composition
Nrp1tm2Ddg/Nrp1tm2.1Ddg
Tg(Tek-cre)1Ywa/0
Genetic
Background
involves: 129 * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm2.1Ddg mutation (0 available); any Nrp1 mutation (84 available)
Nrp1tm2Ddg mutation (1 available); any Nrp1 mutation (84 available)
Tg(Tek-cre)1Ywa mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mid-to-late embryonic lethality

cardiovascular system
• systemic vascular deficiencies at E12.5 such as distended vessels in the abdominal wall
• brain vessels were large and underdeveloped
• lack of medium and small-diameter branched vessels in the abdominal wall and brain vessels were not branched
• exhibited bilateral atrial enlargement




Genotype
MGI:5431517
cn3
Allelic
Composition
Nrp1tm2Ddg/Nrp1tm2.1Ddg
Tg(Gucy2g-cre,-EGFP)52Irod/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm2.1Ddg mutation (0 available); any Nrp1 mutation (84 available)
Nrp1tm2Ddg mutation (1 available); any Nrp1 mutation (84 available)
Tg(Gucy2g-cre,-EGFP)52Irod mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• in the olfactory bulb, Grueneberg glomeruli formation is not affected and their exclusion from guanylate cyclase G (GC-G) glomeruli is not affected
• numbers of Grueneberg axonal bundles consisting of multiple axons do not avoid the accessory olfactory bulb as seen in control animals; axonal fibers and microglomeruli cross bulb from medial to lateral side
• some Grueneberg fibers end deep into the vomeronasal glomeruli primarily in rostral part (not seen in controls)
• Grueneberg glomeruli form normally in mice with specific Nrp2 deletion and Grueneberg axons lacking Nrp2 do not cross the accessory olfactory bulb





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory