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7140 TNNT3

7140

TNNT3

troponin T3, fast skeletal type

protein-coding

Homo sapiens

基因描述

Type Description
Definition troponin T3, fast skeletal type

研究结论

Date Results Publications
2019-05-04 11:36:00 The TnT3 appears to contribute to age-related sarcopenia and possibly other age-related deficiencies such as muscle insulin resistance and beta cell dysfunction by interacting with TnT3-binding sequences in the promoter area of p53-related genes, among others, and consequently modulating the transcriptional regulation of these target genes. 29596868
2016-08-06 11:12:00 Three homologous genes have evolved in vertebrates to encode three muscle type-specific TnT isoforms: TNNT1 for slow skeletal muscle TnT, TNNT2 for cardiac muscle TnT, and TNNT3 for fast skeletal muscle TnT. 26774798
2016-07-16 11:29:00 The presence of the p.(Arg63His) missense mutation at position 63 of TNNT3 was confirmed through direct cycle sequencing of genomic DNA in six affected South African family members for whom DNA had been archived. 26915936
2011-10-01 10:56:00 Data show that a missense mutation at nucleotide position 187 in exon 9 of the TNNT3 gene was identified in all affected individuals in the family. 21402185
2010-09-15 22:06:00 Observational study of gene-disease association. (HuGE Navigator) 20634891

名称对应

Type IDs
Synonymous TNTF, beta-TnTF
Gene
UniProtKB-ID: TNNT3_HUMAN, H9KVA2_HUMAN
UniprotKB: P45378, H9KVA2
UniParc: UPI000066D8D2, UPI00003B5D08, UPI0000141B37, UPI0000049C92, UPI000198C548, UPI0000ED9058, UPI0000049C94, UPI000013DB6C
EMBL: BX640689, KF455299, CR541927, AF026276, BC117327, BT019997, BC171727, AK056968, U14641, DQ778624, M21984, U14643, BC050446, AC051649, U14642, U14644, BC143537
Ensembl: ENSG00000288250, ENSG00000130595
KO: hsa:7140
Nucleutide sequences
EMBL-CDS: AAH50446.1, AAI43538.1, AAI71727.1, AAA50360.1, AAA50359.1, AAF21629.1, CAG46725.1, CAE45814.1, AAA36777.1, AAV38800.1, ABG77458.1, AAA50361.1, AAA50362.1, BAG51835.1, AAI17328.1
Ensembl_TRS: ENST00000381589, ENST00000673503, ENST00000673572, ENST00000381579, ENST00000381563, ENST00000641119, ENST00000397301, ENST00000381558, ENST00000673174, ENST00000278317, ENST00000672214, ENST00000673082, ENST00000671850, ENST00000641787, ENST00000672629, ENST00000673157, ENST00000344578, ENST00000672659, ENST00000397304
Protein sequencees
Ensembl_PRO: ENSP00000500846, ENSP00000344870, ENSP00000500606, ENSP00000500796, ENSP00000499917, ENSP00000278317, ENSP00000380468, ENSP00000493331, ENSP00000500705, ENSP00000371001, ENSP00000500263, ENSP00000370975, ENSP00000492914, ENSP00000370970, ENSP00000500437, ENSP00000500081, ENSP00000500156, ENSP00000370991, ENSP00000380471
RefSeq: XP_016873703.1, NP_001036245.1, XP_016873706.1, NP_001354772.1, NP_001036246.1, NP_001350490.1, XP_016873698.1, NP_006748.1, XP_006718363.1, NP_001354773.1, XP_006718357.1, XP_024304438.1, XP_016873702.1, NP_001284575.1, NP_001354771.1, XP_016873705.1, XP_016873699.1, NP_001354780.1, XP_016873697.1, XP_006718351.1, XP_006718362.1, NP_001354774.1, XP_011518645.1, XP_016873701.1, XP_024304440.1, XP_016873700.1, XP_016873704.1, XP_016873707.1, XP_016873694.1, XP_016873696.1, NP_001354777.1, XP_016873708.1, NP_001036247.1, XP_016873695.1, XP_024304439.1, NP_001354778.1, NP_001354776.1, NP_001354775.1, NP_001354781.1, NP_001354779.1, XP_024304437.1
Others
UniRef100: UniRef100_H9KVA2, UniRef100_P45378
UniRef90: UniRef90_P45378-7, UniRef90_P45378
UniRef50: UniRef50_P13805, UniRef50_P45378
UniGene: Hs.73454
CCDS: CCDS41596.1, CCDS41594.1, CCDS86164.1, CCDS41595.1, CCDS7727.1

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