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3431 SP110

3431

SP110

SP110 nuclear body protein

protein-coding

Homo sapiens

基因描述

Type Description
Definition SP110 nuclear body protein

研究结论

Date Results Publications
2021-02-13 13:29:00 Novel Missense Mutation inSP110Associated with Combined Immunodeficiency and Advanced Liver Disease Without VOD. 31721003
2019-04-27 11:01:00 Results suggest that the SP110 variants have a role in controlling genetic susceptibility to latent and active tuberculosis (TB) infection in Taiwan. Additionally, the SP110 rs9061 SNP is shown to be associated with plasma TNFalpha levels in LTBI individuals. These data suggest that the identified SP110 SNPs may serve as a biomarker for latent and active TB infection in Taiwan. 30627224
2018-08-18 11:22:00 TNF-alpha -308G>A (rs1800629) showed no association with susceptibility to pulmonary tuberculosis and spinal tuberculosis patients in southern China. 29430075
2018-02-17 10:34:00 SP110 polymorphism is associated with tuberculosis. 27623071
2018-01-27 10:20:00 Data suggest that Sp110 is sumoylated, de-sumoylated, and then released from the promyelocytic leukemia nuclear bodies in hepatocytes infected with HBV (hepatitis B virus); Sp110 differentially regulates several direct target genes of HBx, a viral co-factor; these mechanisms may be involved in evasion of host immune response by HBV. (Sp110 = Speckled 110 kDa; HBx = hepatitis B virus protein X) 29046350

名称对应

Type IDs
Synonymous IFI41, IFI75, IPR1, VODI
Gene
UniProtKB-ID: SP110_HUMAN
UniprotKB: Q9HB58
UniParc: UPI0001E88EDB, UPI000013CFC9, UPI000013CFCA, UPI0001E88EDA, UPI0001D411CC, UPI000013D98F, UPI0001E88EDC
EMBL: AF280094, BC019059, L22343, AC009950, L22342, AK026488, CH471063, AK301097, AF280095
Ensembl: ENSG00000135899
KO: hsa:3431
Nucleutide sequences
EMBL-CDS: AAF99318.1, AAD13402.1, EAW70915.1, AAX93281.1, AAA18806.1, AAH19059.1, BAG62696.1, AAG09826.1
Ensembl_TRS: ENST00000540870, ENST00000258382, ENST00000358662, ENST00000258381
Protein sequencees
Ensembl_PRO: ENSP00000258381, ENSP00000351488, ENSP00000258382, ENSP00000439558
RefSeq: NP_001365373.1, XP_016859457.1, NP_004501.4, XP_011509394.1, NP_001365374.1, NP_536349.3, NP_001365376.1, NP_001365371.1, XP_016859458.1, NP_001365375.1, NP_001365372.1, NP_001171944.1, XP_011509392.1, XP_011509393.1, NP_004500.4, XP_024308618.1
Others
UniRef100: UniRef100_Q9HB58
UniRef90: UniRef90_Q9HB58
UniRef50: UniRef50_Q9HB58
UniGene: Hs.145150
CCDS: CCDS2474.1, CCDS2476.1, CCDS2475.1, CCDS54435.1

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