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7139 TNNT2

7139

TNNT2

troponin T2, cardiac type

protein-coding

Homo sapiens

基因描述

Type Description
Definition troponin T2, cardiac type

研究结论

Date Results Publications
2021-03-27 14:42:00 Application of the fourth universal definition of myocardial infarction in clinical practice. 32362195
2021-03-20 13:34:00 High-sensitivity cardiac troponin T and the risk of heart failure in postmenopausal women of the ARIC Study. 33399316
2021-03-20 13:24:00 Variant R94C in TNNT2-Encoded Troponin T Predisposes to Pediatric Restrictive Cardiomyopathy and Sudden Death Through Impaired Relaxation Resulting in Myocardial Diastolic Dysfunction. 32098556
2021-03-13 13:27:00 Increased Myocardial Oxygen Consumption Precedes Contractile Dysfunction in Hypertrophic Cardiomyopathy Caused by Pathogenic TNNT2 Gene Variants. 32290750
2021-01-02 12:52:00 High sensitivity Troponin-T for prediction of adverse events in patients with COVID-19. 32981387

名称对应

Type IDs
Synonymous CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC, cTnT
Gene
UniProtKB-ID: TNNT2_HUMAN, A0A0A0MRJ5_HUMAN, Q15607_HUMAN
UniprotKB: P45379, A0A0A0MRJ5, Q15607
UniParc: UPI0000ED904C, UPI0000D62078, UPI0000ED904F, UPI0000ED904D, UPI000006DA90, UPI0000186843, UPI0000071647, UPI0000ED9052, UPI0000378488, UPI000014A55F, UPI0000ED9051, UPI0000ED904E, UPI000016B0F6, UPI0000378487
EMBL: X74819, AF004414, AC119427, AF004409, AK290621, AF004416, AF004411, AF004419, S64668, S71128, AF004422, AF004417, X79861, AF004415, S71126, AF004420, Y09628, AF004418, AY044273, AF004421, AF004410, X79855, Y09627, X79856, X79858, Y09626, AF004413, S71127, L40162, AF004412, EF179183, BC002653, X79857
Ensembl: ENSG00000118194
KO: hsa:7139
Nucleutide sequences
EMBL-CDS: CAA52818.1, CAA56235.1, AAA67422.1, CAA70841.1, AAB27731.1, AAK92231.1, AAC39590.1, CAA70839.1, CAA56237.1, CAA56236.1, AAH02653.1, BAF83310.1, AAB30957.1, CAA56238.1, CAA70840.1, ABN05286.1, AAB30956.1, CAA56240.1
Ensembl_TRS: ENST00000412633, ENST00000509001, ENST00000660295, ENST00000236918, ENST00000360372, ENST00000422165, ENST00000656932, ENST00000367320, ENST00000367318, ENST00000367317
Protein sequencees
Ensembl_PRO: ENSP00000499593, ENSP00000356289, ENSP00000353535, ENSP00000356287, ENSP00000499418, ENSP00000395163, ENSP00000236918, ENSP00000408731, ENSP00000422031, ENSP00000356286
RefSeq: NP_001263274.1, XP_024305222.1, XP_024305223.1, NP_000355.2, XP_011508245.1, NP_001263275.1, XP_011508244.1, XP_024305218.1, XP_011508243.1, XP_006711572.1, NP_001001431.1, XP_011508246.1, XP_016857706.1, XP_016857705.1, NP_001001432.1, XP_006711571.1, XP_011508242.1, XP_011508241.1, NP_001263276.1, XP_011508240.1, XP_011508248.1, NP_001001430.1
Others
UniRef100: UniRef100_P45379, UniRef100_A0A0A0MRJ5
UniRef90: UniRef90_P45379-5, UniRef90_P45379
UniRef50: UniRef50_P45379-5, UniRef50_P45379
UniGene: Hs.533613
CCDS: CCDS73003.1, CCDS60390.1, CCDS30969.1, CCDS30968.1

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