The OTOG gene homepage

General information
Gene symbol OTOG
Gene name otogelin
Chromosome 11
Chromosomal band p14.3
Imprinted Unknown
Genomic reference NG_033191.2
Transcript reference NM_001277269.1
Exon/intron information NM_001277269.1 exon/intron table
Associated with diseases DFN, DFNB, DFNB18B
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 172
Unique public DNA variants reported 148
Individuals with public variants 114
Hidden variants 2
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated September 15, 2020
Version OTOG:200915

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001277269.1.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/OTOG
HGNC 8516
Entrez Gene 340990
PubMed articles OTOG
OMIM - Gene 604487
OMIM - Diseases DFNB18B (deafness, autosomal recessive, type 18b (DFNB-18B))
HGMD OTOG
GeneCards OTOG
GeneTests OTOG


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024096 11 otogelin NM_001277269.1 NP_001264198.1 172


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