B6;C3Fe-Wnt7a<px-2J>/GrsrJ Strain Detail MGI Mouse MGI:5440882

B6;C3Fe-Wnt7a^px-2J/GrsrJ Strain Detail

Summary

1 associated mutation

Mutation Carried	Marker
Wnt7a^px-2J	Wnt7a

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
Fuhrmann syndrome	√

Key

√

disease model

expected model not found

1 associated strain record at IMSR

IMSR	Repository	IMSR Strain	Why Matched
JAX:018166	JAX	B6;C3Fe-Wnt7a^px-2J/GrsrJ	exact match to ID

Earliest

J:188478 Harris BS, et al., Postaxial hemimelia 2 Jackson: a new point mutation in Wnt7a and model of Fuhrmann syndrome. MGI Direct Data Submission. 2012;
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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