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B6.129P2-Hprt1b-m3 Strain Detail
Summary
  • Strain Name
    B6.129P2-Hprt1b-m3
  • Attributes
    congenic, mutant strain, spontaneous mutation
  • MGI ID
    MGI:3625515
  • Synonyms
    B6.129P2-Hprtb-m3
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Hprt1b-m3 Hprt1
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 model 2
Lesch-Nyhan syndrome
Key disease model expected model not found
Find Mice (IMSR)
1 associated strain record at IMSR
IMSR Repository IMSR Strain Why Matched
ORNL:B6.129P2-Hprtb-m3 ORNL B6.129P2-Hprtb-m3 exact match to synonym
References
  • Earliest
    J:59994 Stubdal H, et al., Targeted deletion of the tub mouse obesity gene reveals that tubby is a loss-of-function mutation. Mol Cell Biol. 2000 Feb;20(3):878-82
  • 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
03/19/2024
MGI 6.23
The Jackson Laboratory