Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol: Vsx2or-J Name: visual system homeobox 2; ocular retardation Jackson MGI ID: MGI:1856112 Synonyms: Chx10-, orJ Gene: Vsx2  Location: Chr12:84616602-84642231 bp, + strand  Genetic Position: Chr12, 39.28 cM Alliance: Vsx2or-J page

Vsx2or-J/Vsx2or-J and control Show the 7 phenotype image(s) involving this allele.

Strain of Origin:

129S1/Sv-Oca2+ Tyr+ KitlSl

Allele Type:    Spontaneous Mutation:    Nucleotide substitutions   Mutation details: The molecular mutation is a premature stop codon in exon 3, corresponding to the homeobox domain of the encoded protein. (J:30800, J:32083) Inheritance:    Recessive

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

In Mice Carrying this Mutation:	183 assay results 2 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation:	11 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Vsx2 Mutation:	23 strains or lines available

Original:	J:5767 Theiler K, et al., A new allele of ocular retardation: early development and morphogenetic cell death. Anat Embryol (Berl). 1976 Dec 22;150(1):85-97
All:	39 reference(s)