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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fgfr1tm6.1Jrt
targeted mutation 6.1, Janet Rossant
MGI:2153352
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fgfr1tm6.1Jrt/Fgfr1tm6.1Jrt involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:2181574
ht2
Fgfr1tm1Jrt/Fgfr1tm6.1Jrt involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:2181575
cn3
Fgfr2tm1Dor/Fgfr2tm1Dor
Fgfr3tm6.1Cxd/Fgfr3tm6.1Cxd
Foxg1tm1(cre)Skm/Foxg1+
Fgfr1tm6.1Jrt/Fgfr1tm1Jpa
involves: 129 MGI:6116894


Genotype
MGI:2181574
hm1
Allelic
Composition
Fgfr1tm6.1Jrt/Fgfr1tm6.1Jrt
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgfr1tm6.1Jrt mutation (0 available); any Fgfr1 mutation (223 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• R7 (45%) is not attached to the sternum of newborn mice
• rib fusion (21%) occurs in newborn mice
• vertebral transformations to posterior direction
• however, the number of caudal vertebrae is not reduced
• transformations of T1 to T2 (9.1%), T12 to L1 (4.5%), and T13 to L1 (55%)
• transformations of C5 to C6 (9.1%), C6 to C7 (13.6%), and C7 to T1 (59%)
• transformation of L5 to S1 (4.5%) and L6 to S1 (73%)
• transformation of S1 to S2 (59%) and S3 to S4 (23%)




Genotype
MGI:2181575
ht2
Allelic
Composition
Fgfr1tm1Jrt/Fgfr1tm6.1Jrt
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgfr1tm1Jrt mutation (0 available); any Fgfr1 mutation (223 available)
Fgfr1tm6.1Jrt mutation (0 available); any Fgfr1 mutation (223 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• rib (27%) fusion occurs in newborn mice
• vertebral transformations to posterior direction
• however, the number of caudal vertebrae is not reduced
• transformations of T1 to T2 (11%), T12 to L1 (44%), and T13 to L1 (11%)
• transformations of C5 to C6 (22%), C6 to C7 (11%), and C7 to T1 (44%)
• transformations of L5 to S1 (11%) and L6 to S1 (55%)
• transformations of S1 to S2 (44%) and S3 to S4 (28%)




Genotype
MGI:6116894
cn3
Allelic
Composition
Fgfr2tm1Dor/Fgfr2tm1Dor
Fgfr3tm6.1Cxd/Fgfr3tm6.1Cxd
Foxg1tm1(cre)Skm/Foxg1+
Fgfr1tm6.1Jrt/Fgfr1tm1Jpa
Genetic
Background
involves: 129
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgfr1tm1Jpa mutation (0 available); any Fgfr1 mutation (223 available)
Fgfr1tm6.1Jrt mutation (0 available); any Fgfr1 mutation (223 available)
Fgfr2tm1Dor mutation (3 available); any Fgfr2 mutation (90 available)
Fgfr3tm6.1Cxd mutation (0 available); any Fgfr3 mutation (54 available)
Foxg1tm1(cre)Skm mutation (2 available); any Foxg1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• brain morphology at E12.5





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory