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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fgfr1tm8.1Sor
targeted mutation 8.1, Philippe Soriano
MGI:5828622
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fgfr1tm8.1Sor/Fgfr1tm8.1Sor 129S4/SvJaeSor-Fgfr1tm8.1Sor MGI:5882536


Genotype
MGI:5882536
hm1
Allelic
Composition
Fgfr1tm8.1Sor/Fgfr1tm8.1Sor
Genetic
Background
129S4/SvJaeSor-Fgfr1tm8.1Sor
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgfr1tm8.1Sor mutation (1 available); any Fgfr1 mutation (221 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• at P0, 2 of 15 homozygotes show axial skeleton defects
• 2 of 15 homozygotes show defects in the most posterior thoracic vertebrae and ribs
• one homozygote missing the 13th thoracic vertebra shows a rib rudiment on one side of the 12th thoracic vertebrae with a separated distal element of the rib present on the other side
• a second homozygote shows small rib rudiments present on the 13th thoracic vertebra
• 1 of 15 homozygotes shows bifurcation of the 4th rib
• 1 of 15 homozygotes is missing the 13th thoracic vertebra while the ossification center of the 4th thoracic vertebra is duplicated and the attached rib is bifurcated
• 1 of 15 homozygotes is missing the 13th thoracic vertebra
• 2 of 15 homozygotes have five lumbar vertebrae

growth/size/body
N
• homozygotes show normal postnatal growth relative to wild-type controls

homeostasis/metabolism
N
• complete blood count and serum chemistries are normal





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory