Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgfr1tm1Jpa mutation
(0 available);
any
Fgfr1 mutation
(221 available)
Fgfr2tm1Dor mutation
(3 available);
any
Fgfr2 mutation
(87 available)
Fgfr3tm6.1Cxd mutation
(0 available);
any
Fgfr3 mutation
(52 available)
Foxg1tm1(cre)Skm mutation
(2 available);
any
Foxg1 mutation
(28 available)
Frs3tm1Jheb mutation
(0 available);
any
Frs3 mutation
(35 available)
|
|
|
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgfr1tm1Jpa mutation
(0 available);
any
Fgfr1 mutation
(221 available)
Fgfr2tm1Dor mutation
(3 available);
any
Fgfr2 mutation
(87 available)
Fgfr3tm6.1Cxd mutation
(0 available);
any
Fgfr3 mutation
(52 available)
Foxg1tm1(cre)Skm mutation
(2 available);
any
Foxg1 mutation
(28 available)
Frs3tm1Jheb mutation
(0 available);
any
Frs3 mutation
(35 available)
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cellular
N |
• cell survival and cell division at E8.75 according to mitotic marker p-HH3 immunoreactivity
|
nervous system
N |
• brain morphology at E12.5
|
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgfr1tm1Jpa mutation
(0 available);
any
Fgfr1 mutation
(221 available)
Fgfr1tm3.1Sor mutation
(0 available);
any
Fgfr1 mutation
(221 available)
Fgfr2tm1Dor mutation
(3 available);
any
Fgfr2 mutation
(87 available)
Fgfr3tm6.1Cxd mutation
(0 available);
any
Fgfr3 mutation
(52 available)
Foxg1tm1(cre)Skm mutation
(2 available);
any
Foxg1 mutation
(28 available)
Frs3tm1Jheb mutation
(0 available);
any
Frs3 mutation
(35 available)
|
|
|
cellular
N |
• cell division at E8.75 according to mitotic marker p-HH3 immunoreactivity
|
|
• according to TUNEL assay at E8.75
|
nervous system
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgfr1tm1Jpa mutation
(0 available);
any
Fgfr1 mutation
(221 available)
Fgfr1tm6.1Jrt mutation
(0 available);
any
Fgfr1 mutation
(221 available)
Fgfr2tm1Dor mutation
(3 available);
any
Fgfr2 mutation
(87 available)
Fgfr3tm6.1Cxd mutation
(0 available);
any
Fgfr3 mutation
(52 available)
Foxg1tm1(cre)Skm mutation
(2 available);
any
Foxg1 mutation
(28 available)
|
|
|
nervous system
N |
• brain morphology at E12.5
|