Symbol
Name
ID
|
|
|
Synonyms
|
DFNB16
|
|
Genetic Map
|
|
Chromosome 2
|
Syntenic
|
|
|
|
Mapping data(
1)
|
|
|
|
Sequence Map
|
|
Mammalian
homology
|
|
|
Sequences
|
All sequences(13)
|
Alleles
and
phenotypes
|
All alleles(1) :
Targeted, knock-out(1)
| Mice homozygous for a null allele exhibit progressive hearing loss from P15 with abnormal cochlear outer hair cell stereociliary bundle morphology. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (1)
|
|
Polymorphisms
|
SNPs within 2kb(102 from dbSNP Build 128)
|
Gene Ontology
(GO)
classifications
|
|
|
Expression
|
cDNA source data(2)
External Resources:
Allen Brain Atlas
GEO
|
Molecular
reagents
|
All nucleic(2)
cDNA(2)
Microarray probesets(2)
|
Other database
links
|
|
|
References
|
(Earliest)
J:72411
Verpy E et al.,
"Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus."
Nat Genet 2001 Nov;29(3):345-9
(Latest)
J:141421
Verpy E et al.,
"Stereocilin-deficient mice reveal the origin of cochlear waveform distortions."
Nature 2008 Nov 13;456(7219):255-8
|
All references(3)
|
