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Isl1Drsh
Chemically induced Allele Detail
Summary
Symbol: Isl1Drsh
Name: ISL1 transcription factor, LIM/homeodomain; dearisch
MGI ID: MGI:5523699
Synonyms: Dea2
Gene: Isl1  Location: Chr13:116434817-116446225 bp, - strand  Genetic Position: Chr13, 64.87 cM, cytoband D2.3
Alliance: Isl1Drsh page
Mutation
origin
Strain of Origin:  C3HeB/FeJ
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to C transition that results in the amino acid substitution of cysteine for a tyrosine at position 71 (Y71C). (J:202214)
Inheritance:    Dominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 5 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 Isl1 Mutation:  33 strains or lines available
Notes
Additional mutations found in this mouse line are listed in J:202214.
References
Original:  J:202214 Hilton JM, et al., Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice. Genome Biol. 2011;12(9):R90
All:  2 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
04/09/2024
MGI 6.23
The Jackson Laboratory