C57BL/6J-Pmp22<Tr-2J>/GrsrJ Strain Detail MGI Mouse MGI:5515891

C57BL/6J-Pmp22^Tr-2J/GrsrJ Strain Detail

Summary

1 associated mutation

Mutation Carried	Marker
Pmp22^Tr-2J	Pmp22

Phenotype Overview

Blue squares indicate phenotypes directly attributed to mutations/alleles in this strain.

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
Charcot-Marie-Tooth disease type 1A	√
Charcot-Marie-Tooth disease type 1E	√
Charcot-Marie-Tooth disease type 3	√
hereditary neuropathy with liability to pressure palsies	√

Key

√

disease model

expected model not found

1 associated strain record at IMSR

IMSR	Repository	IMSR Strain	Why Matched
JAX:021550	JAX	C57BL/6J-Pmp22^Tr-2J/GrsrJ	exact match to ID

Earliest

J:201866 Dionne L, et al., Trembler 2 Jackson, a spontaneous point mutation in Pmp22. MGI Direct Data Submission. 2013;
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)
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