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11262 SP140

11262

SP140

SP140 nuclear body protein

protein-coding

Homo sapiens

基因描述

Type Description
Definition SP140 nuclear body protein

研究结论

Date Results Publications
2019-10-05 11:14:00 The Sp140 is multi-SUMOylated and its PHD finger works as versatile protein-protein interaction platform promoting intramolecular SUMOylation of the adjacent BRD. 30465816
2019-05-18 11:50:00 Our findings showed that SP140 is an important repressor of genes implicated in inflammation, suggesting that decreased expression of SP140, promoted by the rs28445040-T risk variant, may lead to up-regulation of these genes by means of NF-kappaB inhibition in B cells. 30102396
2016-12-17 11:25:00 IL1R2 hypomethylation and androgen receptor hypermethylation may constitute an important determinant of disease severity, whereas NPR2 hypomethylation and SP140 hypermethylation may provide a biomarker for vulnerability to excessive daytime sleepiness in Obstructive Sleep Apnea 26888452
2016-07-16 11:36:00 Data identified rs28445040 variant in SP140 gene as the causal factor for skipping of exon 7 and the most associated with multiple sclerosis. 26152201
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 20731705

名称对应

Type IDs
Synonymous LYSP100, LYSP100-A, LYSP100-B
Gene
UniProtKB-ID: SP140_HUMAN, B4DVW8_HUMAN, Q8IWJ1_HUMAN, Q0VGE4_HUMAN
UniprotKB: Q13342, B4DVW8, Q8IWJ1, Q0VGE4
UniParc: UPI0000E07F02, UPI00000744D4, UPI000035ECB1, UPI00015E0ACB, UPI0000DBE1A1, UPI000185D560, UPI0000EE3852, UPI0000209746, UPI00017A7DFC
EMBL: BC070160, BC038091, CH471063, BC105744, BC105743, AK301267, BC105960, U63420, U36500, AC009950, AC009949, U36499
Ensembl: ENSG00000079263
KO: hsa:11262
Nucleutide sequences
EMBL-CDS: AAI05961.1, AAX93282.1, EAW70922.1, AAH70160.1, AAC50817.1, AAI05744.1, AAB18617.1, AAX88868.1, AAB18616.1, BAG62830.1, AAH38091.1, AAI05745.1
Ensembl_TRS: ENST00000420434, ENST00000392045, ENST00000373645, ENST00000343805, ENST00000417495
Protein sequencees
Ensembl_PRO: ENSP00000398210, ENSP00000393618, ENSP00000375899, ENSP00000342096, ENSP00000362749
RefSeq: XP_005246313.1, XP_016858733.1, NP_001265381.1, XP_016858741.1, XP_005246310.1, NP_001265382.1, XP_016858729.1, XP_016858739.1, XP_016858738.1, XP_011508818.1, XP_005246312.1, XP_011508819.1, XP_011508822.1, NP_009168.4, XP_005246309.1, XP_016858730.1, XP_011508820.1, NP_001005176.1, XP_011508821.1, XP_016858740.1, XP_016858728.1, NP_001265380.1, XP_016858734.1, XP_016858736.1, XP_016858735.1, XP_005246311.1, XP_011508817.1, XP_016858731.1, XP_016858737.1, XP_016858742.1, XP_016858732.1, XP_006712286.1
Others
UniRef100: UniRef100_Q8IWJ1, UniRef100_Q13342, UniRef100_Q0VGE4, UniRef100_B4DVW8
UniRef90: UniRef90_Q8IWJ1, UniRef90_Q13342
UniRef50: UniRef50_Q13342, UniRef50_Q8IWJ1
UniGene: Hs.632549
CCDS: CCDS33392.1, CCDS63150.1, CCDS63151.1, CCDS42831.1, CCDS63149.1

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