The CACNA1B gene homepage

General information
Gene symbol CACNA1B
Gene name calcium channel, voltage-dependent, N type, alpha 1B subunit
Chromosome 9
Chromosomal band q34
Imprinted Unknown
Genomic reference NC_000009.11
Transcript reference NM_000718.3
Exon/intron information NM_000718.3 exon/intron table
Associated with diseases DYT23, NEDNEH
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 125
Unique public DNA variants reported 111
Individuals with public variants 16
Hidden variants 3
Download all this gene's data Download all data
Date created September 13, 2012
Date last updated April 19, 2024
Version CACNA1B:240419

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_000718.3.
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 http://www.LOVD.nl/CACNA1B
HGNC 1389
Entrez Gene 774
PubMed articles CACNA1B
OMIM - Gene 601012
OMIM - Diseases DYT23 (dystonia?, type 23 (DYT-23))
NEDNEH (Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements)
HGMD CACNA1B
GeneCards CACNA1B
GeneTests CACNA1B
Orphanet CACNA1B


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001375 9 transcript variant 1 NM_000718.3 NP_000709.1 125


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