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Dfnb59tm1Ugds
Targeted Allele Detail
Nomenclature
Symbol: Dfnb59tm1Ugds
Name: deafness, autosomal recessive 59 (human); targeted mutation 1, Unite de Genetique des Deficits Sensoriels
MGI ID: MGI:3654320
Gene: Dfnb59  Location: Chr2:76648476-76658556 bp, + strand  Genetic Position: Chr2, 45.08 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:111260
Parent Cell Line:  CK35 (ES Cell)
Strain of Origin:  129S2/SvPas
Mutation
description
Allele Type:    Targeted (knock-in)
Mutation:    Single point mutation
 
Mutation details
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Dfnb59 Mutation:  0 strains or lines available
References
Original:  J:111260 Delmaghani S, et al., Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Nat Genet. 2006 Jul;38(7):770-8
All:  1 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