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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

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
05/17/2022
MGI 6.19
The Jackson Laboratory