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CHMU/Le Strain Detail
Summary
  • Strain Name
    CHMU/Le
  • Attributes
    inbred strain, segregating inbred, spontaneous mutation
  • MGI ID
    MGI:3795780
Associated
Mutations,
Markers,
and QTL
2 associated mutations
Mutation Carried Marker
Bloc1s5mu Bloc1s5
Foxc1ch Foxc1
Associated
Phenotypes
and
Diseases
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.
Human Diseases

model 1
Hermansky-Pudlak syndrome √
platelet storage pool deficiency √
Key √ disease model expected model not found
References
  • Earliest
    J:98808 Rice R, et al., Foxc1 integrates Fgf and Bmp signalling independently of twist or noggin during calvarial bone development. Dev Dyn. 2005 May 19;233(3):847-852
  • 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
05/07/2024
MGI 6.23 		The Jackson Laboratory