Type | Description |
---|---|
Definition | troponin T2, cardiac |
Date | Results | Publications |
---|---|---|
2020-11-21 13:11:00 | Dystrophin and calcium current are decreased in cardiomyocytes expressing Cre enzyme driven by alphaMHC but not TNT promoter. | 31857666 |
2018-06-09 11:21:00 | Cardiac troponin T at the NMJ region contributes to NMJ functional decline with ageing mainly in the fast-twitch skeletal muscle through interfering with signalling. | 28419739 |
2018-05-05 10:07:00 | Hypertrophic cardiomyopathy pathophysiology is "mutation specific" in mice models carrying TNNT2 E163R and R92Q mutations. | 28735292 |
2017-07-01 11:58:00 | TnTA30V mutation attenuated Ca(2+)-activated maximal tension and length-mediated cross-bridge recruitment against alpha-myosin heavy chain but augmented these parameters against beta-myosin heavy chain, suggesting divergent contractile phenotypes. | 27769999 |
2017-06-24 12:02:00 | The shift from cTnT exon 5 inclusion to exclusion during development was delayed in the heart of Ts65Dn mice due to Dyrk1A overexpression. | 27049307 |
Type | IDs |
---|---|
Synonymous | Tnt, cTnT |
Gene |
UniProtKB-ID:
TNNT2_MOUSE,
Q6P3Z7_MOUSE,
Q3TQ90_MOUSE,
Q54AB6_MOUSE,
Q3TH80_MOUSE
UniprotKB:
P50752,
Q6P3Z7,
Q3TQ90,
Q54AB6,
Q3TH80
UniParc:
UPI00005B1FD0,
UPI00000E8954,
UPI00000E8AC3,
UPI0000000A3F,
UPI0000227C62,
UPI00005B24AE,
UPI000016388E
EMBL:
L47600,
L47552,
L47599,
L47551,
AB052890,
AC162441,
L47550,
L47553,
L47549,
L47570,
AK163786,
AK146945,
BC063753,
AK168393
Ensembl:
ENSMUSG00000026414
KO:
mmu:21956
|
Nucleutide sequences |
EMBL-CDS:
AAA85350.1,
AAA85349.1,
AAA85351.1,
AAA85347.1,
AAA85352.1,
AAA85345.1,
AAA85348.1,
AAA85346.1,
BAE27554.1,
AAH63753.1,
BAE37494.1,
BAB19881.1,
BAE40318.1
Ensembl_TRS:
ENSMUST00000027671,
ENSMUST00000189732,
ENSMUST00000178854,
ENSMUST00000112087,
ENSMUST00000189355,
ENSMUST00000188028,
ENSMUST00000179863
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000139919,
ENSMUSP00000107717,
ENSMUSP00000136265,
ENSMUSP00000139669,
ENSMUSP00000027671,
ENSMUSP00000137093,
ENSMUSP00000140941
RefSeq:
NP_001123647.4,
XP_006529458.1,
XP_006529455.1,
NP_001123646.1,
XP_006529451.2,
XP_006529457.1,
NP_035749.1,
NP_001123650.1,
NP_001123653.4,
XP_006529456.1,
NP_001123652.1,
XP_006529448.2,
XP_006529454.1,
NP_001123649.1,
XP_006529446.2,
NP_001123651.4,
NP_001123648.1,
XP_006529453.2
|
Others |
UniRef100:
UniRef100_Q3TQ90,
UniRef100_P50752,
UniRef100_Q6P3Z7,
UniRef100_Q3TH80
UniRef90:
UniRef90_P50752
UniRef50:
UniRef50_P45379
UniGene:
Mm.247470
CCDS:
CCDS48378.1,
CCDS48376.1,
CCDS48377.1
|
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