| Type | Description |
|---|---|
| Definition | troponin T1, slow skeletal type |
| Date | Results | Publications |
|---|---|---|
| 2021-02-13 13:23:00 | Troponin T but not C reactive protein is associated with future surgery for aortic stenosis: a population-based nested case-referent study. | 33051334 |
| 2020-08-01 15:05:00 | Three adults and 1 child shared a novel missense homozygous variant in the TNNT1 gene (NM_003283.6: c.287T > C; p.Leu96Pro). This study expands the phenotypic spectrum of TNNT1 myopathy. | 31970803 |
| 2020-01-18 12:38:00 | These findings indicated that TNNT1 may promote the progression of colon adenocarcinoma, mediating epithelial-mesenchymal transition process, and thus shed a novel light on colon adenocarcinoma therapeutic treatments. | 31512553 |
| 2019-08-17 10:14:00 | In a nationwide cohort in Sweden, patients with a first myocardial infarction had increased levels of Troponin T. | 29880121 |
| 2019-03-16 10:16:00 | Similar functional and histological phenotypes were observed in other human cohorts and two transgenic murine models (Tnnt1-/- and Tnnt1 c.505G>T). These findings have implications for emerging molecular therapies, including the suitably of TNNT1 gene replacement for newborns with 'Amish' nemaline myopathy or other TNNT1-associated myopathies. | 29931346 |
| Type | IDs |
|---|---|
| Synonymous | ANM, NEM5, STNT, TNT, TNTS |
| Gene |
UniProtKB-ID:
TNNT1_HUMAN
UniprotKB:
P13805
UniParc:
UPI000016A37B,
UPI0000000CAF,
UPI0000072B0F
EMBL:
S66057,
AJ011713,
BC010963,
S66170,
BC034143,
S69209,
AJ011712,
M19309,
BC022086,
M19308,
BT019630,
S69208
Ensembl:
ENSG00000105048
KO:
hsa:7138
|
| Nucleutide sequences |
EMBL-CDS:
AAH22086.2,
AAH34143.1,
AAD13978.1,
CAA09751.1,
AAB30272.1,
CAA09750.1,
AAB30273.1,
AAH10963.1,
CAA09752.1,
AAV38436.1,
AAA61204.1,
AAA61205.1
Ensembl_TRS:
ENST00000356783,
ENST00000588981,
ENST00000291901,
ENST00000587758
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000467789,
ENSP00000349233,
ENSP00000467176,
ENSP00000291901
RefSeq:
XP_016882675.1,
XP_011525548.1,
XP_016882676.1,
NP_003274.3,
NP_001119604.1,
NP_001278703.1,
NP_001119605.1
|
| Others |
UniRef100:
UniRef100_P13805
UniRef90:
UniRef90_P13805
UniRef50:
UniRef50_P13805
UniGene:
Hs.631558
CCDS:
CCDS46185.1,
CCDS12917.1,
CCDS59421.1
|
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|---|---|---|---|---|---|---|---|---|
| Refseq |
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