Type | Description |
---|---|
Definition | troponin T1, skeletal, slow |
Date | Results | Publications |
---|---|---|
2020-08-22 15:30:00 | The loss of slow skeletal muscle isoform of troponin T in spindle intrafusal fibres explains the pathophysiology of Amish nemaline myopathy. | 31148174 |
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 |
2015-04-04 10:51:00 | Mouse tumor endothelial cells express troponin T. | 24810801 |
2015-02-21 13:12:00 | demonstrated that ssTnT deficiency resulted in significantly decreased levels of other slow fibre-specific myofilament proteins whereas fast fibre-specific myofilament proteins were increased correspondingly | 24445317 |
2010-01-21 00:00:00 | the induction of Tnnt1 gene expression in adult mouse brains by ketamine may illustrate the genes involved in the metabolic syndromes observed in neuropsychiatric disorders | 17850769 |
Type | IDs |
---|---|
Synonymous | AW146156, Tnt, sTnT, ssTnT |
Gene |
UniProtKB-ID:
TNNT1_MOUSE,
Q3TVB8_MOUSE
UniprotKB:
O88346,
Q3TVB8
UniParc:
UPI0000029652,
UPI00000E8AB7,
UPI00000E75CC
EMBL:
BC141142,
BC145451,
U92882,
U92884,
AF020946,
U92883,
BC145450,
AJ131711,
AK160226,
BC138871
Ensembl:
ENSMUSG00000064179
KO:
mmu:21955
|
Nucleutide sequences |
EMBL-CDS:
AAC32541.1,
CAB38082.1,
AAC32540.1,
AAI45452.1,
AAI45451.1,
AAC32546.1,
AAD00730.1,
AAI41143.1,
AAI38872.1,
BAE35701.1
Ensembl_TRS:
ENSMUST00000071798,
ENSMUST00000163710,
ENSMUST00000108587
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000104228,
ENSMUSP00000071704,
ENSMUSP00000129626
RefSeq:
XP_017177601.1,
NP_001264833.1,
XP_017177602.1,
NP_001347083.1,
XP_011248779.1,
XP_017177603.1,
NP_001264832.1,
XP_017177600.1,
XP_011248780.1,
NP_035748.1
|
Others |
UniRef100:
UniRef100_O88346,
UniRef100_Q3TVB8
UniRef90:
UniRef90_J3QPC8,
UniRef90_Q7TNB2
UniRef50:
UniRef50_Q7TNB2
UniGene:
Mm.358643
CCDS:
CCDS71880.1,
CCDS71879.1,
CCDS51973.1
|
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Refseq |
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