{{Rsnum
|rsid=80356586
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OTOF
|position=26482441
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OTOF
}}{{omim
|id=603681
|rsnum=80356586
|variant=0011
}}{{ClinVar
|rsid=80356586
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=26705309
|CHROM=2
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=OTOF:9381
|GENE_NAME=OTOF
|GENE_ID=9381
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.26705309A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1251; 603681.0011
|CLNSIG=5
|CLNCUI=C1832828
|CLNDBN=Auditory neuropathy, autosomal recessive, 1; Deafness, autosomal recessive 9
|Disease=Auditory neuropathy; Deafness
|CLNACC=RCV000006517.1; RCV000021035.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C1832829; NBK1251:NBK1434:C1832828:601071:90636
}}{{PMID|9657592}} Transient deafness due to temperature-sensitive auditory neuropathy.

{{PMID|12127154}} Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness.

{{PMID|16371502|OA=1
}} OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele.