{{Rsnum
|rsid=80356591
|Chromosome=2
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=OTOF
|position=26477474
|Gene_s=OTOF
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356591
|Reversed=1
|FwdREF=G
|FwdALT=
|REF=GC
|ALT=G
|RSPOS=26700341
|CHROM=2
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=OTOF:9381
|GENE_NAME=OTOF
|GENE_ID=9381
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.26700342delC
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=601071
|CLNDBN=Deafness, autosomal recessive 9; Hereditary hearing loss and deafness
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000021046.1; RCV000041490.1
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1251:NBK1434:C1832828:601071:90636; NBK1434:C0236038:95827002
|CLNSRC=GeneReviews
|CLNSRCID=NBK1251
|Disease=Deafness; Hereditary hearing loss and deafness
}}{{PMID Auto
|PMID=12525542
|Title=Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene.
|OA=1
}}

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