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B6.B10Sn-Mctp1dwnd/Kjn Strain Detail
Summary
  • Strain Name
    B6.B10Sn-Mctp1dwnd/Kjn
  • Attributes
    congenic, mutant strain, spontaneous mutation
  • MGI ID
    MGI:6197506
  • Other IDs
    JAX:009690
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Mctp1dwnd Mctp1
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.
Find Mice (IMSR)
1 associated strain record at IMSR
IMSR Repository IMSR Strain Why Matched
JAX:009690 JAX B6.B10Sn-Mctp1dwnd/Kjn exact match to ID
References
  • Earliest
    J:264553 Tarchini B, et al., A spontaneous mouse deletion in Mctp1 uncovers a long-range cis-regulatory region crucial for NR2F1 function during inner ear development. Dev Biol. 2018 Nov 15;443(2):153-164
  • 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
04/23/2024
MGI 6.23
The Jackson Laboratory