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81846 SBF2

81846

SBF2

SET binding factor 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition SET binding factor 2

研究结论

Date Results Publications
2018-02-24 10:15:00 Rare variants in SBF2 predict an increased risk of taxane-induced peripheral neuropathy in African American breast cancer patients receiving paclitaxel. 27732968
2015-12-12 10:55:00 Starvation-induced MTMR13 and RAB21 activity regulates VAMP8 to promote autophagosome-lysosome fusion. 25648148
2015-05-16 10:32:00 SBF2 frameshift mutation is associated with charcot-marie-tooth disease type 4B2. 25462154
2014-06-28 12:03:00 Identification of a novel SBF2 missense mutation associated with a rare case of thrombocytopenia using whole-exome sequencing. 23334996
2014-02-15 10:42:00 Germline genetic variation in the SBF2 locus was associated with overall survival in patients with pancreatic adenocarcinoma of European and Asian ancestry. 23180869

名称对应

Type IDs
Synonymous CMT4B2, DENND7B, MTMR13
Gene
UniProtKB-ID: MTMRD_HUMAN
UniprotKB: Q86WG5
UniParc: UPI0000160A78, UPI00000622D5
EMBL: BC063656, BC053867, BC011143, AB051553, BC101466, CR749312, AY234241, BC043389, BX538184
Ensembl: ENSG00000133812
KO: hsa:81846
Nucleutide sequences
EMBL-CDS: AAI01467.1, CAD98056.1, AAH53867.1, BAB21857.1, AAH63656.1, AAO62733.1, AAH43389.1, CAH18167.1, AAH11143.1
Ensembl_TRS: ENST00000256190
Protein sequencees
Ensembl_PRO: ENSP00000256190
RefSeq: XP_011518696.1, NP_112224.1, XP_011518698.1, XP_016873862.1, XP_016873866.1, XP_016873865.1, NP_001373268.1, XP_016873861.1, XP_011518697.1, XP_005253212.1, XP_016873864.1, NP_001373271.1
Others
UniRef100: UniRef100_Q86WG5
UniRef90: UniRef90_Q86WG5
UniRef50: UniRef50_Q86WG5
UniGene: Hs.577252
CCDS: CCDS31427.1

全选

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