About   Help   FAQ
C3H101H-Col3a1Tsk2/H Strain Detail
Summary
  • Strain Name
    C3H101H-Col3a1Tsk2/H
  • Attributes
    chemically induced mutation, mutant stock
  • MGI ID
    MGI:3579305
  • Synonyms
    C3H101H-Tsk2/H
  • Other IDs
    EM:02195, FESA:000067
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Col3a1Tsk2 Col3a1
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
systemic scleroderma √
Key √ disease model expected model not found
Find Mice (IMSR)
2 associated strain records at IMSR
IMSR Repository IMSR Strain Why Matched
EM:02195 EMMA C3H101H-Col3a1Tsk2/H exact match to ID
HAR:67 HAR C3H101H-Col3a1Tsk2/H exact match to name
References
  • Earliest
    J:215227 Long KB, et al., The Tsk2/+ mouse fibrotic phenotype is due to a gain-of-function mutation in the PIIINP segment of the Col3a1 gene. J Invest Dermatol. 2014 Oct 20;
  • 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
12/10/2024
MGI 6.24 		The Jackson Laboratory