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26064 RAI14

26064

RAI14

retinoic acid induced 14

protein-coding

Homo sapiens

基因描述

Type Description
Definition retinoic acid induced 14

研究结论

Date Results Publications
2019-05-04 10:50:00 These findings provide significant insight into the role of RAI14 in mTOR-induced glial inflammation, which is closely associated with infection and ischemia stimuli. 30554401
2018-09-15 11:14:00 TCGA database and Kaplan-Meier Plotter mining results showed that compared to those with RAI14 low mRNA expression levels, Gastric Cancer patients with RAI14 high mRNA expression levels had remarkably lower time of both overall survival and disease-free survival. Cox multivariate survival analyses shows high expression of RAI14 was the only independent predictor of unfavorable prognosis in patients with gastric cancer. 29654694
2010-06-30 22:06:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614
2010-01-21 00:00:00 Subcellular localization of NORPEG in retinal pigment epithelial cells varies with cell density, with predominantly nuclear localization in nonconfluent cells, but a cytoplasmic localization in confluent cultures. 16729964

名称对应

Type IDs
Synonymous NORPEG, RAI13
Gene
UniProtKB-ID: RAI14_HUMAN
UniprotKB: Q9P0K7
UniParc: UPI0000D7E61F, UPI0001963764, UPI000013F319, UPI00001B296B
EMBL: AY354204, AY317139, BC052988, AF155135, AB037755, AC026801, AL050011, AC016602, AK314379, AC025754
Ensembl: ENSG00000039560
KO: hsa:26064
Nucleutide sequences
EMBL-CDS: CAB43236.2, AAQ63889.2, AAF44722.1, BAA92572.1, AAH52988.1, AAP84319.1
Ensembl_TRS: ENST00000265109, ENST00000503673, ENST00000515799, ENST00000512629, ENST00000428746, ENST00000506376
Protein sequencees
Ensembl_PRO: ENSP00000388725, ENSP00000423854, ENSP00000422377, ENSP00000265109, ENSP00000427123, ENSP00000422942
RefSeq: NP_001138992.1, XP_016864823.1, XP_006714532.1, XP_011512320.1, XP_011512325.1, XP_011512321.1, XP_011512318.2, XP_011512327.2, XP_011512322.1, NP_001138995.1, NP_001138997.1, XP_011512319.1, XP_024301785.1, NP_001138993.1, NP_056392.2, XP_011512326.1, XP_016864825.1, XP_011512323.1, XP_011512324.1, NP_001138994.1, XP_016864824.1
Others
UniRef100: UniRef100_Q9P0K7
UniRef90: UniRef90_Q9P0K7
UniRef50: UniRef50_Q9P0K7
UniGene: Hs.431400
CCDS: CCDS54838.1, CCDS54837.1, CCDS34142.1, CCDS54839.1

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