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6932 TCF7

6932

TCF7

transcription factor 7

protein-coding

Homo sapiens

基因描述

Type Description
Definition transcription factor 7

研究结论

Date Results Publications
2020-01-11 10:41:00 Postoperative detection of TCF7, c-Myc, and FOSL1 may be useful for stratifying patients with a high risk of unfavorable prognosis, and suppressing TCF7 or its downstream effectors may be a promising strategy for the treatment of Perihilar cholangiocarcinoma (PHCC) 31248836
2019-12-07 11:04:00 The mRNA levels of TCF7 in GC tissues were significantly higher than in corresponding tumor adjacent tissues. The patients of low TCF7 expression and high TCF7 expression accounted for 76.79% (129/168) and 23.21% (39/168), respectively. 31133633
2019-06-01 10:45:00 The expression of LEF1 associated positively with TCF1 (TCF7) and clinical progression of nasopharyngeal carcinoma, predicting poor prognosis. 30918012
2019-06-01 10:08:00 High TCF7 expression associated with poor prognosis in Chinese glioblastoma multiforme patients. 29642232
2019-04-13 11:24:00 sSudy described a TCF7-dependent feedback control of the osteocalcin-GPRC6A axis in brown adipocyte physiologies. 29358218

名称对应

Type IDs
Synonymous TCF-1
Gene
UniProtKB-ID: TCF7_HUMAN, B3KQ75_HUMAN
UniprotKB: P36402, B3KQ75
UniParc: UPI000002B4F3, UPI00018132BC, UPI000002B4EF, UPI00018132BD, UPI000006230C, UPI00001A8434, UPI000020C5CA, UPI00018132BB, UPI000002B4F1, UPI00001AF318, UPI0000470EE1, UPI00018132BA, UPI0000470EDF, UPI000002B4F5, UPI0000470EE3, UPI0000118440, UPI000020C5C7
EMBL: BC048769, AK093530, X63901, Z47363, AK057580, X59869, Z47362, X59871, CH471062, X59870, Z47364, AF163776, BC072023, Z47361
Ensembl: ENSG00000081059
KO: hsa:6932
Nucleutide sequences
EMBL-CDS: CAA42526.1, EAW62277.1, AAH48769.1, AAF00616.1, CAA87442.1, CAA42528.1, CAA87441.1, CAA42527.1, CAB56795.1, CAA87440.1, CAA87439.1, BAG52735.1, AAH72023.1, BAG51937.1
Ensembl_TRS: ENST00000520958, ENST00000395023, ENST00000518915, ENST00000378560, ENST00000342854
Protein sequencees
Ensembl_PRO: ENSP00000367822, ENSP00000430179, ENSP00000429547, ENSP00000378469, ENSP00000340347
RefSeq: NP_998813.1, NP_001333379.1, XP_011541908.1, NP_001333354.1, NP_963963.1, XP_011541915.1, NP_001128323.2, XP_006714745.1, XP_006714748.1, NP_003193.2, XP_011541906.1, NP_001353431.1, NP_963965.1, XP_011541909.1, XP_006714741.1, XP_011541911.1, XP_016865279.1, XP_006714749.1, XP_006714742.1, XP_011541910.1, XP_006714747.1
Others
UniRef100: UniRef100_A0A2J8VQD1, UniRef100_P36402
UniRef90: UniRef90_A0A2J8VQD9, UniRef90_P36402
UniRef50: UniRef50_P36402
UniGene: Hs.573153
CCDS: CCDS43362.1, CCDS4170.1, CCDS47263.2, CCDS4169.1

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