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83641 FAM107B

83641

FAM107B

family with sequence similarity 107 member B

protein-coding

Homo sapiens

基因描述

Type Description
Definition family with sequence similarity 107 member B

研究结论

Date Results Publications
2018-03-24 11:12:00 Authors first provide experimental evidence suggesting that FAM107B was downregulated by S100A4 in gastric cancer MGC803 cells. And FAM107B at least partially mediates the biological effect of S100A4 in the cells. 28675500
2014-01-04 10:18:00 These results show that loss of HITS (FAM107B) expression is a common phenomenon observed in cancers of distinct organs and involved in tumor development and proliferation. 22825356
2010-09-15 22:05:00 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) 20628086
2010-09-15 22:05:00 Observational study of gene-disease association. (HuGE Navigator) 19913121
2010-06-30 22:06:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614

名称对应

Type IDs
Synonymous C10orf45, HITS
Gene
UniProtKB-ID: F107B_HUMAN
UniprotKB: Q9H098
UniParc: UPI00000373D5, UPI00001C0E1E
EMBL: BC064407, AL158168, AK127413, AL157706, CR533466, BC072452, AK289959, BC004872, AL136885, CH471072, AC069544
Ensembl: ENSG00000065809
KO: hsa:83641
Nucleutide sequences
EMBL-CDS: BAC86966.1, CAB66819.1, EAW86270.1, AAH64407.1, EAW86269.1, AAH72452.1, BAF82648.1, EAW86268.1, CAG38497.1, AAH04872.1
Ensembl_TRS: ENST00000496330, ENST00000378467, ENST00000378465, ENST00000479731, ENST00000468747, ENST00000378462, ENST00000378470, ENST00000378458, ENST00000622567, ENST00000181796, ENST00000478076
Protein sequencees
Ensembl_PRO: ENSP00000367719, ENSP00000479842, ENSP00000367723, ENSP00000417782, ENSP00000367731, ENSP00000181796, ENSP00000367728, ENSP00000418330, ENSP00000367726, ENSP00000418120, ENSP00000419603
RefSeq: NP_001307668.1, NP_001269627.1, NP_001269625.1, NP_001307666.1, NP_001307669.1, NP_001269626.1, XP_016872238.1, NP_001269629.1, NP_001307664.1, NP_001269624.1, NP_001269628.1, NP_113641.2, NP_001307670.1, NP_001269631.1, NP_001269630.1, NP_001307667.1, XP_011518037.1, NP_001269632.1, NP_001307665.1, XP_005252673.1
Others
UniRef100: UniRef100_Q9H098
UniRef90: UniRef90_Q9H098
UniRef50: UniRef50_Q3TGF2
UniGene: Hs.446315
CCDS: CCDS60486.1, CCDS7102.1

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