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Whrnwi
Spontaneous Allele Detail
Nomenclature
Symbol: Whrnwi
Name: whirlin; whirler
MGI ID: MGI:1857090
Synonyms: wi
Gene: Whrn  Location: Chr4:63414910-63495991 bp, - strand  Genetic Position: Chr4, 33.97 cM, cytoband C1
Mutation
origin
Strain of Origin:  STOCK a Tyrp1b Myo5ad Oca2p Ednrbs
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation details
Inheritance:    Recessive
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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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: 2 strains available      Cell Lines: 0 lines available
Carrying any Whrn Mutation:  11 strains or lines available
Notes
They have defects of the membranous labyrinth similar to those of Myo15 (M.S. Deol, personal communication).

References
Original:  J:269 Lane PW, Whirler mice, a recessive behavior mutation in linkage group VIII. J Hered. 1963 Nov-Dec;54:263-6
All:  20 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
12/16/2014
MGI 5.20
The Jackson Laboratory