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Vsx2or
Spontaneous Allele Detail
Nomenclature
Symbol: Vsx2or
Name: visual system homeobox 2; ocular retardation
MGI ID: MGI:1856111
Gene: Vsx2  Location: Chr12:84569828-84595457 bp, + strand  Genetic Position: Chr12, 39.28 cM
Mutation
origin
Strain of Origin:  STOCK Ph
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 7 anatomical structures
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:  22 strains or lines available
References
Original:  J:307 TRUSLOVE GM, A gene causing ocular retardation in the mouse. J Embryol Exp Morphol. 1962 Dec;10:652-60
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)
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last database update
11/26/2019
MGI 6.14
The Jackson Laboratory