View HCN4 gene homepage

General information
Gene symbol HCN4
Gene name hyperpolarization activated cyclic nucleotide-gated potassium channel 4
Chromosome 15
Chromosomal band q24.1
Imprinted Unknown
Genomic reference NG_009063.1
Transcript reference NM_005477.2
Exon/intron information NM_005477.2
Associated with diseases BRGDA-8, SSS-2
Citation reference(s) -
Refseq URL Genomic reference sequence
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
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 January 27, 2016
Version HCN4:160127

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
Homepage URL
HGNC 16882
Entrez Gene 10021
PubMed articles HCN4
OMIM - Gene 605206
OMIM - Diseases BRGDA-8 (Brugada syndrome, type 8 (BRGDA-8))
SSS-2 (sinus, sick, syndrome, type 2, autosomal dominant (SSS-2))
GeneCards HCN4
GeneTests HCN4

Active transcripts




NCBI ID     

NCBI Protein ID     

00009206 15 hyperpolarization activated cyclic nucleotide-gated potassium channel 4 NM_005477.2 NP_005468.1 1

Copyright & disclaimer
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