View KCNJ10 gene homepage

General information
Gene symbol KCNJ10
Gene name potassium inwardly-rectifying channel, subfamily J, member 10
Chromosome 1
Chromosomal band q23.2
Imprinted Unknown
Genomic reference NG_016411.1
Transcript reference NM_002241.4
Associated with diseases DFNB-4, ID, PDS, SESAME syndrome
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 1
Unique public DNA variants reported 1
Individuals with public variants 1
Hidden variants 0
Date created May 03, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
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
HGNC 6256
Entrez Gene 3766
PubMed articles KCNJ10
OMIM - Gene 602208
OMIM - Diseases DFNB-4 (deafness, autosomal recessive, type 4 (DFNB-4), with enlarged vestibular aqueduct)
PDS (Pendred syndrome (PDS))
SESAME syndrome

Active transcripts




NCBI ID     

NCBI Protein ID     

00010379 1 potassium inwardly-rectifying channel, subfamily J, member 10 NM_002241.4 NP_002232.2 1