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B6.129P2-Msx1tm1Bero Strain Detail
Summary
  • Strain Name
    B6.129P2-Msx1tm1Bero
  • Attributes
    congenic, mutant strain, targeted mutation
  • MGI ID
    MGI:3702864
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Msx1tm1Bero Msx1
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
tooth agenesis
Key disease model expected model not found
References
  • Earliest
    J:42035 Houzelstein D, et al., Insertional mutation of the mouse Msx1 homeobox gene by an nlacZ reporter gene. Mech Dev. 1997 Jul;65(1-2):123-33
  • All

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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last database update
07/02/2024
MGI 6.13
The Jackson Laboratory