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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Plxnd1tm1.1Tmj
targeted mutation 1.1, Thomas M Jessell
MGI:3848812
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj
Tg(CAG-cre/Esr1*)5Amc/0
involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * CBA MGI:3848824
cn2
Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * CBA/J MGI:3848822
cn3
Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj
Tg(Tek-cre)1Ywa/0
involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL MGI:3848821
cn4
Plxnd1tm1Ddg/Plxnd1tm1.1Tmj
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S/SvEv * C57BL/6 * C57BL/6J * CBA/J MGI:3848832
cn5
Plxnd1tm1Ddg/Plxnd1tm1.1Tmj
Tg(CAG-cre/Esr1*)1Egwa/0
involves: 129S/SvEv * C57BL/6 * DBA/2 MGI:5052373
cn6
Plxnd1tm1Ddg/Plxnd1tm1.1Tmj
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S/SvEv * C57BL/6J * CBA/J MGI:5550533
cn7
Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj
Tg(Nes-cre)1Atp/0
involves: 129S/SvEv * FVB/N MGI:5007643


Genotype
MGI:3848824
cn1
Allelic
Composition
Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj
Tg(CAG-cre/Esr1*)5Amc/0
Genetic
Background
involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxnd1tm1.1Tmj mutation (1 available); any Plxnd1 mutation (86 available)
Tg(CAG-cre/Esr1*)5Amc mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• tamoxifen-treated retinas exhibit reduced angiogenesis and hemorrhages compared to in wild-type mice
• tamoxifen-treated retinas exhibit reduced angiogenesis compared to in wild-type mice
• vascular invasion of tamoxifen-treated endothelial cells into matrigel plugs treated with endothelial cell growth factor is deficient compared to that of wild-type cells
• tamoxifen-treated retinas exhibit hemorrhages unlike wild-type retinas

vision/eye
• tamoxifen-treated retinas exhibit reduced angiogenesis and hemorrhages compared to in wild-type mice

cellular
• vascular invasion of tamoxifen-treated endothelial cells into matrigel plugs treated with endothelial cell growth factor is deficient compared to that of wild-type cells




Genotype
MGI:3848822
cn2
Allelic
Composition
Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (26 available)
Plxnd1tm1.1Tmj mutation (1 available); any Plxnd1 mutation (86 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• normal numbers of mice are born

cardiovascular system
N
• mice exhibit normal cardiac development with normal outflow tract septation




Genotype
MGI:3848821
cn3
Allelic
Composition
Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj
Tg(Tek-cre)1Ywa/0
Genetic
Background
involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxnd1tm1.1Tmj mutation (1 available); any Plxnd1 mutation (86 available)
Tg(Tek-cre)1Ywa mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all but 1 mouse died by P2

cardiovascular system
• mice exhibit abnormal microvasculature within bones
• however, large vessels attached to the long bones appear intact
• the root of the aorta is located more distally from the ascending portion of the truncus arteriosis or from the ascending aorta than in wild-type mice
• in most mice
• at E11.5, mice exhibit poor remodeling of the vascular plexus of the immature intersomitic vessels unlike in wild-type mice
• mice exhibit abnormally condensed discontinuous atrial myocardial architecture unlike in wild-type mice
• the atrial myocardium is separated from the epicardium unlike in wild-type mice
• the ventricular myocardial wall is abnormal and unusual epicardial blood islands unlike in wild-type mice
• the outflow tract is malrotated compared to in wild-type mice
• at E12.5, mice exhibit coronary vessel defects
• originate more distally from the ascending portion of the truncus arteriosus, or from the ascending aorta (when partial or compete septation was present) in all mutant hearts examined (N=5)
• the atria appear raspberry-like
• mice exhibit abnormally condensed discontinuous atrial myocardial architecture unlike in wild-type mice
• the atrial myocardium is separated from the epicardium unlike in wild-type mice
• the ventricular myocardial wall is abnormal and unusual epicardial blood islands are present unlike in wild-type mice
• mice exhibit subcutaneous hemorrhage, especially in the head, unlike in wild-type mice
• small hemorrhages are observed in the ventricular walls unlike in wild-type mice

skeleton
• at E15.5
• poorly formed and frequently fused or split in the lumbar and thoracic regions
• frequently fused in the lumbar and thoracic regions
• in the one mouse that survives into adulthood, vertebral bodies are fused along the entire anterior-posterior axis

nervous system

homeostasis/metabolism
• at birth

growth/size/body

limbs/digits/tail

muscle
• mice exhibit abnormally condensed discontinuous atrial myocardial architecture unlike in wild-type mice
• the atrial myocardium is separated from the epicardium unlike in wild-type mice
• the ventricular myocardial wall is abnormal and unusual epicardial blood islands unlike in wild-type mice




Genotype
MGI:3848832
cn4
Allelic
Composition
Plxnd1tm1Ddg/Plxnd1tm1.1Tmj
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
involves: 129S/SvEv * C57BL/6 * C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (26 available)
Plxnd1tm1.1Tmj mutation (1 available); any Plxnd1 mutation (86 available)
Plxnd1tm1Ddg mutation (0 available); any Plxnd1 mutation (86 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mice exhibit a 3-fold increase in the number of proprioceptive synaptic contacts with identified cutaneous maximus motor neurons compared to in wild-type mice
• 43% of cutaneous motor neurons receive monosynaptic input after stimulation of cutaneous maximus afferents unlike wild-type motor neurons
• however, monosynaptic specificity from the tricep is normal

behavior/neurological
N
• mice exhibit no behavior deficits




Genotype
MGI:5052373
cn5
Allelic
Composition
Plxnd1tm1Ddg/Plxnd1tm1.1Tmj
Tg(CAG-cre/Esr1*)1Egwa/0
Genetic
Background
involves: 129S/SvEv * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxnd1tm1.1Tmj mutation (1 available); any Plxnd1 mutation (86 available)
Plxnd1tm1Ddg mutation (0 available); any Plxnd1 mutation (86 available)
Tg(CAG-cre/Esr1*)1Egwa mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Increase in extraretinal vascular outgrowth in ischemic Plxnd1tm1.1Tmj/Plxnd1tm1Ddg Tg(CAG-cre/Esr1*)1Egwa/0 retinas

vision/eye
• tamoxifen-treated mice exhibit increased extraretinal vascular outgrowth in ischemic retinas compared with control mice

cardiovascular system
• tamoxifen-treated mice exhibit increased extraretinal vascular outgrowth in ischemic retinas compared with control mice




Genotype
MGI:5550533
cn6
Allelic
Composition
Plxnd1tm1Ddg/Plxnd1tm1.1Tmj
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
involves: 129S/SvEv * C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (26 available)
Plxnd1tm1.1Tmj mutation (1 available); any Plxnd1 mutation (86 available)
Plxnd1tm1Ddg mutation (0 available); any Plxnd1 mutation (86 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• the patterns of hamstring knee flexor muscle and gluteus homonymous monosynaptic sensory-motor connections are similar to controls
• a large amplitude of monosynaptic EPSP is seen in 45% of gluteus motor neurons unlike in controls




Genotype
MGI:5007643
cn7
Allelic
Composition
Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj
Tg(Nes-cre)1Atp/0
Genetic
Background
involves: 129S/SvEv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plxnd1tm1.1Tmj mutation (1 available); any Plxnd1 mutation (86 available)
Tg(Nes-cre)1Atp mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
N
• mice exhibit normal retinal stratification





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory