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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
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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory