About   Help   FAQ
C57BL/6N-Hbs1ltm1a(KOMP)Wtsi/Wtsi Strain Detail
Summary
  • Strain Name
    C57BL/6N-Hbs1ltm1a(KOMP)Wtsi/Wtsi
  • Attributes
    coisogenic, targeted mutation
  • MGI ID
    MGI:5700647
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Hbs1ltm1a(KOMP)Wtsi Hbs1l
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:272028 O'Connell AE, et al., Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation. PLoS Genet. 2019 Feb;15(2):e1007917
  • 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
04/16/2024
MGI 6.23 		The Jackson Laboratory