Vsx2<or> Spontaneous Allele Detail MGI Mouse (MGI:1856111)

Vsx2^or
Spontaneous Allele Detail

Summary

Symbol:	Vsx2^or
Name:	visual system homeobox 2; ocular retardation
MGI ID:	MGI:1856111
Gene:	Vsx2 Location: Chr12:84616602-84642231 bp, + strand Genetic Position: Chr12, 39.28 cM
Alliance:	Vsx2^or page

Mutation
origin

Strain of Origin:

STOCK Ph

Mutation
description

Allele Type:		Spontaneous
Inheritance:		Recessive

Phenotypes

View phenotypes and curated references for all genotypes (concatenated display).

Expression

In Structures Affected by this Mutation:

Find Mice (IMSR)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 0 strains available Cell Lines: 0 lines available
Carrying any Vsx2 Mutation:	23 strains or lines available

References

Original:	J:307 TRUSLOVE GM, A gene causing ocular retardation in the mouse. J Embryol Exp Morphol. 1962 Dec;10(4):652-60
All:	8 reference(s)

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 11/19/2024 MGI 6.24