The TNNC1 gene homepage

General information
Gene symbol TNNC1
Gene name troponin C type 1 (slow)
Chromosome 3
Chromosomal band p21.1
Imprinted Unknown
Genomic reference LRG_378
Transcript reference NM_003280.2
Exon/intron information NM_003280.2 exon/intron table
Associated with diseases CMD-1Z, CMH-13
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 87
Unique public DNA variants reported 64
Individuals with public variants 36
Hidden variants 1
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 17, 2021
Version TNNC1:210917

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_003280.2.
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/TNNC1
HGNC 11943
Entrez Gene 7134
PubMed articles TNNC1
OMIM - Gene 191040
OMIM - Diseases CMD-1Z (cardiomyopathy, dilated, type 1Z (CMD-1Z))
CMH-13 (cardiomyopathy, hypertrophic, familial, type 13 (CMH-13))
HGMD TNNC1
GeneCards TNNC1
GeneTests TNNC1
Orphanet TNNC1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00021591 3 troponin C type 1 (slow) NM_003280.2 NP_003271.1 87


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