Dstn^corn1
Spontaneous Allele Detail

Summary

• Symbol: Dstn^corn1
• Name: destrin; corneal disease 1
• MGI ID: MGI:1889311
• Synonyms: corn1
• Gene: Dstn Location: Chr2:143757251-143785244 bp, + strand Genetic Position: Chr2, 70.89 cM, cytoband H1
• Alliance: Dstn^corn1 page

The Dstn^corn1/Dstn^corn1 mouse

Show the 1 phenotype image(s) involving this allele.

Mutation origin

• Strain of Origin: A.BY-H2^bc H2-T18^f/SnJ

Mutation description

• Allele Type: Spontaneous
• Mutation: Intragenic deletion
• Mutation details: The mutation in the corn1 mouse was identified as a 35 kb deletion encompassing the entire coding region of the gene. (J:83125)
• Inheritance: Recessive

Expression

In Mice Carrying this Mutation:	4 assay results 1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation:	3 anatomical structure(s)

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 Dstn Mutation: 43 strains or lines available

References

• Original: J:31798 Smith RS, et al., Corn1: a mouse model for corneal surface disease and neovascularization. Invest Ophthalmol Vis Sci. 1996 Feb;37(2):397-404
• All: 19 reference(s)