About   Help   FAQ
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 (223 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





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory