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50506 DUOX2

50506

DUOX2

dual oxidase 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition dual oxidase 2

研究结论

Date Results Publications
2021-01-23 12:57:00 Insilico study of genes involved in Congenital Hypothyroidism. 32207419
2020-10-24 13:56:00 Wide Spectrum of DUOX2 Deficiency: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism. 31030636
2020-10-03 12:54:00 DUOX2/DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom. 31044655
2020-06-20 12:47:00 H2O2 produced by the Duox2/DuoxA2 cell surface enzymatic complex could provoke potential mutagenic DNA damage. 31513783
2020-05-30 12:22:00 Patients with sporadic thyroid cancer homozygous for rs965513[A] demonstrated higher DUOX2 expression. 31501191

名称对应

Type IDs
Synonymous LNOX2, NOXEF2, P138-TOX, TDH6, THOX2
Gene
UniProtKB-ID: DUOX2_HUMAN
UniprotKB: Q9NRD8
UniParc: UPI000013D775
EMBL: AF181972, AF267981, GU174495, AC091117, AF230496
Ensembl: ENSG00000140279
KO: hsa:50506
Nucleutide sequences
EMBL-CDS: AAF73922.1, AAF20055.1, AAF78954.1, ADB22378.1
Ensembl_TRS: ENST00000603300
Protein sequencees
Ensembl_PRO: ENSP00000475084
RefSeq: NP_054799.4, NP_001350640.1
Others
UniRef100: UniRef100_Q9NRD8
UniRef90: UniRef90_Q9NRD8
UniRef50: UniRef50_Q9NRD8
UniGene: Hs.71377
CCDS: CCDS86454.1, CCDS10117.1

全选

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研究热度

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