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MGI:Dfnb59
Contents |
| Species (Taxon ID) | Mus musculus (house mouse) (taxon:10090) | |
| Gene Name(s) | Dfnb59 ( synonyms: LOC381375, pejvakin ) | |
| Protein Name(s) | deafness, autosomal recessive 59 (human), | |
| External Links | ||
| MGI | MGI:2685847 | |
Annotations
| Qualifier | GO ID | GO term name | Reference | Evidence Code | with/from | Aspect | Notes | Status |
|---|---|---|---|---|---|---|---|---|
| GO:0003674 |
molecular function |
MGI:MGI:2156816 |
ND: No biological Data available |
F |
From MGI |
|||
| GO:0007605 |
sensory perception of sound |
MGI:MGI:3653531 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3654320 |
P |
From MGI |
||
| GO:0007605 |
sensory perception of sound |
MGI:MGI:3703302 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3708376 |
P |
From MGI |
||
| GO:0043025 |
neuronal cell body |
MGI:MGI:3653531 |
IDA: Inferred from Direct Assay |
C |
From MGI |
| ||
| edit table |
Notes
References
See Help:References for how to manage references in GONUTS.
- ↑ 1.0 1.1 Delmaghani S et al. (2006) Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Nat Genet 38: 770-8 PubMed GONUTS page
- ↑ Schwander M et al. (2007) A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. J Neurosci 27: 2163-75 PubMed GONUTS page
