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Dstncorn1
Spontaneous Allele Detail
Nomenclature
Symbol: Dstncorn1
Name: destrin; corneal disease 1
MGI ID: MGI:1889311
Synonyms: corn1
Gene: Dstn  Location: Chr2:143915331-143943324 bp, + strand  Genetic Position: Chr2, 70.89 cM, cytoband H1
The Dstncorn1/Dstncorn1 mouse

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

Mutation
origin
Strain of Origin:  A.BY-H2bc H2-T18f/SnJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsThe mutation in the corn1 mouse was identified as a 35 kb deletion encompassing the entire coding region of the gene. (J:83125)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 4 assay results
In Structures Affected by this Mutation: 3 anatomical structures
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 Dstn Mutation:  19 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:  18 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
09/22/2020
MGI 6.16
The Jackson Laboratory