About   Help   FAQ
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
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