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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Kdrtm1Jrt
targeted mutation 1, Janet Rossant
MGI:1857168
Summary 15 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Kdrtm1Jrt/Kdrtm1Jrt B6.129-Kdrtm1Jrt/J MGI:3531326
hm2
Kdrtm1Jrt/Kdrtm1Jrt involves: 129S1/Sv * 129X1/SvJ MGI:2167318
hm3
Kdrtm1Jrt/Kdrtm1Jrt Not Specified MGI:3527544
ht4
Kdrtm1Jrt/Kdr+ involves: 129S1/Sv * 129X1/SvJ MGI:2167319
ht5
Kdrtm1Jrt/Kdrtm1.1Msh involves: 129P2/OlaHsd * B6.129-Kdrtm1Jrt/J * C57BL/6J MGI:3531324
cn6
Kdrtm1Jrt/Kdr+
Ptentm1Hwu/Ptentm1Hwu
Twist2tm1.1(cre)Dor/Twist2+
B6.129-Twist2tm1.1(cre)Dor Kdrtm1Jrt Ptentm1Hwu MGI:5503216
cn7
Flt1tm1.1Fong/Flt1tm1.1Fong
Kdrtm1Jrt/Kdr+
Gt(ROSA)26Sortm1(cre/ERT2)Thl/Gt(ROSA)26Sor+
involves: 129 * C57BL/6NCr * CD-1 MGI:5523778
cn8
Kdrtm1Jrt/Kdrtm2Sato
Tg(Nes-cre)1Wmz/0
involves: 129S1/Sv * 129X1/SvJ MGI:5432161
cn9
Kdrtm1Jrt/Kdrtm1.1Jamb
Tg(CAG-cre/Esr1*)1Egwa/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 MGI:5052372
cx10
Kdrtm1Jrt/Kdr+
Prdm1tm2Rob/Prdm1tm2Rob
involves: 129 MGI:5439606
cx11
Kdrtm1Jrt/Kdr+
Tmem204tm1.1Ali/Tmem204tm1.1Ali
involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 MGI:4454673
cx12
Kdrtm1Jrt/Kdr+
Rasip1tm1.1Oncl/Rasip1tm1.1Oncl
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA MGI:5056105
cx13
Kdrtm1Jrt/Kdr+
Tg(tetO-Kdr*)4377.5Rwng/0
Tg(Cebpb-tTA)5Bjd/0
involves: 129S1/Sv * 129X1/SvJ * FVB/N * NMRI MGI:3810713
cx14
Flt1tm2Msh/Flt1tm2Msh
Kdrtm1Jrt/Kdrtm1Jrt
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:3527543
cx15
Flt1tm2Msh/Flt1tm2Msh
Kdrtm1Jrt/Kdr+
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:3527542


Genotype
MGI:3531326
hm1
Allelic
Composition
Kdrtm1Jrt/Kdrtm1Jrt
Genetic
Background
B6.129-Kdrtm1Jrt/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• at E8.5, dorsal aorta is absent
• at E8.5 vessels in the head as well as the dorsal aorta and vitelline artery are absent
• at E9.5 no blood vessels are seen

embryo
• at E7.5 the extraembryonic mesoderm consists of only a single cell layer

hematopoietic system
• the number of hematopoietic progenitors and the number of erythoid, granulocyte/macrophage and mixed colonies formed are severely reduced




Genotype
MGI:2167318
hm2
Allelic
Composition
Kdrtm1Jrt/Kdrtm1Jrt
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no embryos are recovered at E10.5 but are present at E9.5

embryo
• at E8.5, yolk sac lack blood vessels and consist of a single layer of mesothelium lining the yolk sac endothelium
• embryos exhibit necrosis likely from cardiac failure
• allantois explants fail to form any endothelial structures

cardiovascular system
• at E8.5, yolk sac lack blood vessels and consist of a single layer of mesothelium lining the yolk sac endothelium
• embryos exhibit necrosis likely from cardiac failure

hematopoietic system
• expression of markers for hematopiesis could not be detected at E8.5
• at E8.5 only very rare committed hematopoietic cells could be identified by methylcellulose colony assay

growth/size/body

cellular
• embryos exhibit necrosis likely from cardiac failure




Genotype
MGI:3527544
hm3
Allelic
Composition
Kdrtm1Jrt/Kdrtm1Jrt
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• Kdr+ cells (lacZ expressing) reach the anterior portion portion of the embryo but no blood vessels develop




Genotype
MGI:2167319
ht4
Allelic
Composition
Kdrtm1Jrt/Kdr+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype




Genotype
MGI:3531324
ht5
Allelic
Composition
Kdrtm1Jrt/Kdrtm1.1Msh
Genetic
Background
involves: 129P2/OlaHsd * B6.129-Kdrtm1Jrt/J * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1.1Msh mutation (1 available); any Kdr mutation (71 available)
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• at E8.5, dorsal aorta is absent
• at E8.5 vessels in the head as well as the dorsal aorta and vitelline artery are absent

embryo
• at E7.5 the extraembryonic mesoderm consists of only a single cell layer




Genotype
MGI:5503216
cn6
Allelic
Composition
Kdrtm1Jrt/Kdr+
Ptentm1Hwu/Ptentm1Hwu
Twist2tm1.1(cre)Dor/Twist2+
Genetic
Background
B6.129-Twist2tm1.1(cre)Dor Kdrtm1Jrt Ptentm1Hwu
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
Ptentm1Hwu mutation (16 available); any Pten mutation (81 available)
Twist2tm1.1(cre)Dor mutation (1 available); any Twist2 mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Defect in angioblast differentiation in Ptentm1Hwu/Ptentm1Hwu Kdrtm1Jrt/Kdr+ Twist2tm1.1(cre)Dor/Twist2+ mice

cardiovascular system
• vasculogenesis defect
• impaired differentiation of angioblasts into mature endothelial cells and blood vessels

respiratory system
• increase in angioblasts in E18.5 lungs




Genotype
MGI:5523778
cn7
Allelic
Composition
Flt1tm1.1Fong/Flt1tm1.1Fong
Kdrtm1Jrt/Kdr+
Gt(ROSA)26Sortm1(cre/ERT2)Thl/Gt(ROSA)26Sor+
Genetic
Background
involves: 129 * C57BL/6NCr * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Flt1tm1.1Fong mutation (1 available); any Flt1 mutation (73 available)
Gt(ROSA)26Sortm1(cre/ERT2)Thl mutation (0 available); any Gt(ROSA)26Sor mutation (942 available)
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• in the brain and liver of tamoxifen treated mice compared with control mice but not as severe as in mice also lacking the Kdr null allele
• some small focal areas in the retina in tamoxifen-treated mice relative to mice lacking the Kdr null allele
• however, angiogenesis in the heart is normal




Genotype
MGI:5432161
cn8
Allelic
Composition
Kdrtm1Jrt/Kdrtm2Sato
Tg(Nes-cre)1Wmz/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
Kdrtm2Sato mutation (1 available); any Kdr mutation (71 available)
Tg(Nes-cre)1Wmz mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• normal numbers of gonadotropin-releasing hormone neurons




Genotype
MGI:5052372
cn9
Allelic
Composition
Kdrtm1Jrt/Kdrtm1.1Jamb
Tg(CAG-cre/Esr1*)1Egwa/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1.1Jamb mutation (0 available); any Kdr mutation (71 available)
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
Tg(CAG-cre/Esr1*)1Egwa mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Suppression of of extraretinal vascular outgrowth in ischemic Kdrtm1.1Jamb/Kdrtm1Jrt Tg(CAG-cre/Esr1*)1Egwa/0 retinas

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

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




Genotype
MGI:5439606
cx10
Allelic
Composition
Kdrtm1Jrt/Kdr+
Prdm1tm2Rob/Prdm1tm2Rob
Genetic
Background
involves: 129
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
Prdm1tm2Rob mutation (0 available); any Prdm1 mutation (64 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• fetal capillaries fail to extend into the labyrinth tissue and instead are largely restricted to the base of the labyrinth

cardiovascular system
• fetal capillaries fail to extend into the labyrinth tissue and instead are largely restricted to the base of the labyrinth




Genotype
MGI:4454673
cx11
Allelic
Composition
Kdrtm1Jrt/Kdr+
Tmem204tm1.1Ali/Tmem204tm1.1Ali
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
Tmem204tm1.1Ali mutation (0 available); any Tmem204 mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• abnormal smooth muscle cell coating
• enlarged lymphatic vessels are even more dilated than in Tmem204tm1.1Ali single knock-outs

muscle
• abnormal smooth muscle cell coating




Genotype
MGI:5056105
cx12
Allelic
Composition
Kdrtm1Jrt/Kdr+
Rasip1tm1.1Oncl/Rasip1tm1.1Oncl
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
Rasip1tm1.1Oncl mutation (0 available); any Rasip1 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• at E9.5, mice fail to exhibit remodeling of the initial plexus in embryonic tissue unlike wild-type mice

embryo
• at E9.5, mice fail to exhibit remodeling of the initial plexus in the yolk sac unlike wild-type mice




Genotype
MGI:3810713
cx13
Allelic
Composition
Kdrtm1Jrt/Kdr+
Tg(tetO-Kdr*)4377.5Rwng/0
Tg(Cebpb-tTA)5Bjd/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * FVB/N * NMRI
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
Tg(Cebpb-tTA)5Bjd mutation (3 available)
Tg(tetO-Kdr*)4377.5Rwng mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
liver/biliary system
• at E12.5, liver vasculature is less organized and vessels are dilated
• at E13.5, microvascular network is more disorganized with fewer branches than in control livers; newborns have very little microvascular network is observed




Genotype
MGI:3527543
cx14
Allelic
Composition
Flt1tm2Msh/Flt1tm2Msh
Kdrtm1Jrt/Kdrtm1Jrt
Genetic
Background
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Flt1tm2Msh mutation (1 available); any Flt1 mutation (73 available)
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all of the double homozygotes die as embryos

cardiovascular system
• Kdr+ cells (lacZ expressing) abnormally accumulate in the posterior portion of the embryo

cellular
• Kdr+ cells (lacZ expressing) abnormally accumulate in the posterior portion of the embryo




Genotype
MGI:3527542
cx15
Allelic
Composition
Flt1tm2Msh/Flt1tm2Msh
Kdrtm1Jrt/Kdr+
Genetic
Background
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Flt1tm2Msh mutation (1 available); any Flt1 mutation (73 available)
Kdrtm1Jrt mutation (1 available); any Kdr mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• about 90% of mutants die as embryos

cardiovascular system
• differentiation of vascular endothelial cells is disturbed
• Kdr+ cells (lacZ expressing) abnormally accumulate in the middle to posterior portion of the embryo

cellular
• differentiation of vascular endothelial cells is disturbed
• Kdr+ cells (lacZ expressing) abnormally accumulate in the middle to posterior portion of the embryo





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory