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sy
Gene Detail
 Symbol
Name
ID
sy
shaker-with-syndactylism deletion region
MGI:98457
Feature Type heritable phenotypic marker
Genetic Map
Chromosome 18
Syntenic

Mapping data(22)
Mutations,
alleles, and
phenotypes
All mutations/alleles(1) : Radiation induced(1)
 
Mice homozygous for a radiation-induced deletion die within one month of birth exhibiting syndactylous feet and other skeletal malformations, inner ear dysmorphology, deafness, and abnormal behavior characteristic of vestibular dysfunction.
 
Other database
links
Entrez Gene20954
References (Earliest) J:208 Hertwig P, Neue Mutationen und Koppelungsgruppen bei der Hausmaus. Z Indukt Abstamm Vererbungsl. 1942;80:220-246
(Latest) J:68881 Chaudhry SS, et al., Mutation of the gene encoding fibrillin-2 results in syndactyly in mice. Hum Mol Genet. 2001 Apr 1;10(8):835-43
All references(17)
Other
accession IDs
MGD-MRK-14674

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
08/26/2014
MGI 5.19
The Jackson Laboratory