About   Help   FAQ
B6(Cg)-Prrt2tm1d(KOMP)Wtsi Strain Detail
Summary
  • Strain Name
    B6(Cg)-Prrt2tm1d(KOMP)Wtsi
  • Attributes
    mutant strain, targeted mutation
  • MGI ID
    MGI:6502638
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Prrt2tm1d(KOMP)Wtsi Prrt2
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 model 2
episodic kinesigenic dyskinesia 1 √ √
Key √ disease model expected model not found
References
  • Earliest
    J:299667 Calame DJ, et al., Presynaptic PRRT2 Deficiency Causes Cerebellar Dysfunction and Paroxysmal Kinesigenic Dyskinesia. Neuroscience. 2020 Nov 10;448:272-286
  • 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
11/12/2024
MGI 6.24 		The Jackson Laboratory