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C3HeB/FeJ-Fgfr1Hspy Strain Detail
Summary
  • Strain Name
    C3HeB/FeJ-Fgfr1Hspy
  • Attributes
    chemically induced mutation, coisogenic, mutant strain
  • MGI ID
    MGI:5007771
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Fgfr1Hspy Fgfr1
Associated
Phenotypes
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
immune system
integument
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
neoplasm
nervous system
normal phenotype
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
vision/eye

Click cells to view annotations.
References
  • Earliest
    J:171915 Calvert JA, et al., A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice. Mamm Genome. 2011 Jun;22(5-6):290-305
  • All
    1
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
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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory