Vsx2<or-J> Spontaneous Allele Detail MGI Mouse (MGI:1856112)

Vsx2^or-J
Spontaneous Allele Detail

Summary

Symbol:	Vsx2^or-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:	Vsx2^or-J page

Vsx2^or-J/Vsx2^or-J and control

Show the 7 phenotype image(s) involving this allele.

Mutation
origin

Strain of Origin:

Mutation
description

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

Phenotypes

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

Expression

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)

Find Mice (IMSR)

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

References

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)

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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