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Slc12a2sy-ns
Spontaneous Allele Detail
Nomenclature
Symbol: Slc12a2sy-ns
Name: solute carrier family 12, member 2; no syndactylism
MGI ID: MGI:1857838
Synonyms: sy-ns
Gene: Slc12a2  Location: Chr18:57878678-57946821 bp, + strand  Genetic Position: Chr18, 32.15 cM
Mutation
origin
Strain of Origin:  MK/ReJ x C57BL/6J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Insertion
 
Mutation details
Inheritance:    Recessive
Phenotypes
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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 Slc12a2 Mutation:  5 strains or lines available
Notes
This allele fails to complement the sy locus but does complement the fused plalanges alleles. Therefore, the original sy deletion includes both the gene responsible for deafness (Slc12a2) and the gene responsible for abnormal foot morphology.

References
Original:  J:50578 Johnson KR, et al., The original shaker-with-syndactylism mutation (sy) is a contiguous gene deletion syndrome. Mamm Genome. 1998 Nov;9(11):889-92
All:  2 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
04/08/2014
MGI 5.17
The Jackson Laboratory