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6697 SPR

6697

SPR

sepiapterin reductase

protein-coding

Homo sapiens

基因描述

Type Description
Definition sepiapterin reductase

研究结论

Date Results Publications
2017-05-20 15:04:00 The allele frequencies for the SPR c.596-2A > G (0.7%) polymorphism is not a major cause of Parkinson's disease in the Maltese. 27613114
2016-02-27 11:42:00 We earlier presented evidence for a physical interaction between ODC and SPR and we showed that knockdown of SPR expression significantly reduced native ODC enzyme activity and impeded Neuroblastoma cell proliferation. 26093909
2014-12-20 12:55:00 new homozygous mutation in the SPR gene was found in two sisters with dopa-responsive dystonia 24588500
2014-04-19 10:11:00 Authors identified SPR as a novel regulator of ODC enzyme activity and, based on clinical evidence, present a model in which SPR drives ODC-mediated malignant progression in neuroblastoma. 24096079
2013-09-14 10:42:00 SPR-mediated reduction of sepiapterin and redox cycling occur by distinct mechanisms 23640889

名称对应

Type IDs
Synonymous SDR38C1
Gene
UniProtKB-ID: SPRE_HUMAN
UniprotKB: P35270
UniParc: UPI000004C79D
EMBL: AK222942, AB017547, CH471053, BC017310, M76231, AK291856, AC092630
Ensembl: ENSG00000116096
KO: hsa:6697
Nucleutide sequences
EMBL-CDS: AAY15035.1, BAD96662.1, BAF84545.1, EAW99757.1, AAA60314.1, EAW99758.1, BAA34534.1, AAH17310.1
Ensembl_TRS: ENST00000234454
Protein sequencees
Ensembl_PRO: ENSP00000234454
RefSeq: NP_003115.1
Others
UniRef100: UniRef100_P35270
UniRef90: UniRef90_P35270
UniRef50: UniRef50_P35270
UniGene: Hs.301540
CCDS: CCDS1920.1

全选

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研究热度

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