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 CMD1Z, CMH13
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 101
Unique public DNA variants reported 71
Individuals with public variants 37
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 November 27, 2023
Version TNNC1:231127

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
HGNC 11943
Entrez Gene 7134
PubMed articles TNNC1
OMIM - Gene 191040
OMIM - Diseases CMD1Z (cardiomyopathy, dilated, type 1Z (CMD-1Z))
CMH13 (cardiomyopathy, hypertrophic, familial, type 13 (CMH-13))
GeneCards TNNC1
GeneTests TNNC1
Orphanet TNNC1

Active transcripts




NCBI ID     

NCBI Protein ID     

00021591 3 troponin C type 1 (slow) NM_003280.2 NP_003271.1 101

Copyright & disclaimer
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