Type | Description |
---|---|
Definition | dual oxidase 2 |
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 |
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
|
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