TNNI3

GENERAL INFORMATION

? »

Gene name

TNNI3

Gene description

Troponin I type 3 (cardiac)

Protein class

Candidate cardiovascular disease genes
Disease related genes
Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

3
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Tissue enriched (heart muscle)
GTEx:Group enriched (heart muscle)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in cardiac myocytes.

ANTIBODY RELIABILITY

? »

Data reliability
description

Antibody staining consistent with RNA expression data.

Data reliability

Supportive based on 2 antibodies.
HPA046428 , CAB009349
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Nasopharynx
N/A
N/A
Bronchus
N/A
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Heart muscle

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Tissue enriched (heart muscle)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (heart muscle)

Organ

Expression



GENE INFORMATION

? »

Gene name

TNNI3 (HGNC Symbol)

Synonyms

CMD2A, CMH7, TNNC1

Description

Troponin I type 3 (cardiac) (HGNC Symbol)

Entrez gene summary

Troponin I (TnI), along with troponin T (TnT) and troponin C (TnC), is one of 3 subunits that form the troponin complex of the thin filaments of striated muscle. TnI is the inhibitory subunit; blocking actin-myosin interactions and thereby mediating striated muscle relaxation. The TnI subfamily contains three genes: TnI-skeletal-fast-twitch, TnI-skeletal-slow-twitch, and TnI-cardiac. This gene encodes the TnI-cardiac protein and is exclusively expressed in cardiac muscle tissues. Mutations in this gene cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM). [provided by RefSeq, Jul 2008]

Chromosome

19

Cytoband

q13.42

Chromosome location (bp)

55151767 - 55157773

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000129991 (version 78.38)

Entrez gene

7137

UniProt

P19429 (UniProt - Evidence at protein level)

neXtProt

NX_P19429

Antibodypedia

TNNI3 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000344887
 
ENST00000586858
 
ENST00000588882
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

TNNI3-001 ENSP00000341838
ENST00000344887
P19429
Show all »
Show » Show » 210 24 No 0
TNNI3-005 ENSP00000465258
ENST00000586858
K7EJP0
Show all »
Show » 57 6.4 No 0
TNNI3-006 ENSP00000466729
ENST00000588882
K7EN02
Show all »
Show » Show » 185 21.3 No 0