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sy
Radiation induced Allele Detail
Nomenclature
Symbol: sy
Name: shaker-with-syndactylism deletion region; shaker with syndactylism
MGI ID: MGI:1856182
Gene: sy  Location: unknown  Genetic Position: Chr18, Syntenic
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Radiation induced
Mutation:    Intergenic deletion
  sy involves 20 genes/genome features (4930511M06Rik, Ctxn3, 1700066O22Rik ...) View all
 
Mutation detailsThis deletion has been approximated to 1 cM region and consists of at least two genes. The gene responsible for deafness in the original sy mutant mouse and the ns allele has been identifed as Slc12a2. The gene responsible for the abnormal foot morphology seen in the fused phalanges alleles and the original sy mutant has been identified as Fbn2. (J:50578)
Inheritance:    Recessive
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 8 assay results
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 sy Mutation:  1 strain or line available
References
Original:  J:208 Hertwig P, Neue Mutationen und Koppelungsgruppen bei der Hausmaus. Z Indukt Abstamm Vererbungsl. 1942;80:220-246
All:  7 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/17/2015
MGI 5.21
The Jackson Laboratory