TNNT3 (troponin T3, fast skeletal type)

2003-05-01  

Identity

HGNC
LOCATION
11p15.5
LOCUSID
ALIAS
DA2B2,TNTF,beta-TnTF
FUSION GENES

Other Information

Locus ID:

NCBI: 7140
MIM: 600692
HGNC: 11950
Ensembl: ENSG00000130595

Variants:

dbSNP: 7140
ClinVar: 7140
TCGA: ENSG00000130595
COSMIC: TNNT3

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000130595ENST00000278317P45378
ENSG00000130595ENST00000344578P45378
ENSG00000130595ENST00000381557F8WA37
ENSG00000130595ENST00000381558P45378
ENSG00000130595ENST00000381563P45378
ENSG00000130595ENST00000381579P45378
ENSG00000130595ENST00000381589P45378
ENSG00000130595ENST00000397301P45378
ENSG00000130595ENST00000397304H9KVA2
ENSG00000130595ENST00000446240C9JZN9
ENSG00000130595ENST00000453458C9JCA5
ENSG00000130595ENST00000641119P45378
ENSG00000130595ENST00000641225A0A286YFB1
ENSG00000130595ENST00000641787P45378

Expression (GTEx)

0
500
1000
1500
2000
2500

Pathways

PathwaySourceExternal ID
Muscle contractionREACTOMER-HSA-397014
Striated Muscle ContractionREACTOMER-HSA-390522

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
347663722021The distal arthrogryposis-linked p.R63C variant promotes the stability and nuclear accumulation of TNNT3.1
347663722021The distal arthrogryposis-linked p.R63C variant promotes the stability and nuclear accumulation of TNNT3.1
295968682018Troponin T3 associates with DNA consensus sequence that overlaps with p53 binding motifs.5
295968682018Troponin T3 associates with DNA consensus sequence that overlaps with p53 binding motifs.5
267747982016TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.93
269159362016Digitotalar dysmorphism: Molecular elucidation.0
267747982016TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.93
269159362016Digitotalar dysmorphism: Molecular elucidation.0
214021852011A novel mutation in TNNT3 associated with Sheldon-Hall syndrome in a Chinese family with vertical talus.14
214021852011A novel mutation in TNNT3 associated with Sheldon-Hall syndrome in a Chinese family with vertical talus.14
200664282010Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2.29
206280862010Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.15
206348912010Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.28
200664282010Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2.29
206280862010Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.15

Citation

Dessen P

TNNT3 (troponin T3, fast skeletal type)

Atlas Genet Cytogenet Oncol Haematol. 2003-05-01

Online version: http://atlasgeneticsoncology.org/gene/42646/cancer-prone-explorer/teaching-explorer/