Details for: USP18
Associated with
Other Information
Genular Protein ID: 922462178
Symbol: UBP18_HUMAN
Name: Ubl carboxyl-terminal hydrolase 18
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 10777664
Title: Cloning and characterization of a novel human ubiquitin-specific protease, a homologue of murine UBP43 (Usp18).
PubMed ID: 10777664
PubMed ID: 11230166
Title: Towards a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.
PubMed ID: 11230166
DOI: 10.1101/gr.gr1547r
PubMed ID: 15461802
Title: A genome annotation-driven approach to cloning the human ORFeome.
PubMed ID: 15461802
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 11313150
Title: Cloning and characterization of human ubiquitin-processing protease-43 from terminally differentiated human melanoma cells using a rapid subtraction hybridization protocol RaSH.
PubMed ID: 11313150
PubMed ID: 11788588
Title: UBP43 (USP18) specifically removes ISG15 from conjugated proteins.
PubMed ID: 11788588
PubMed ID: 22170061
Title: Two independent mechanisms promote expression of an N-terminal truncated USP18 isoform with higher DeISGylation activity in the nucleus.
PubMed ID: 22170061
PubMed ID: 23825189
Title: USP18 inhibits NF-kappaB and NFAT activation during Th17 differentiation by deubiquitinating the TAK1-TAB1 complex.
PubMed ID: 23825189
DOI: 10.1084/jem.20122327
PubMed ID: 27325888
Title: Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome.
PubMed ID: 27325888
DOI: 10.1084/jem.20151529
PubMed ID: 27801882
Title: USP18 recruits USP20 to promote innate antiviral response through deubiquitinating STING/MITA.
PubMed ID: 27801882
DOI: 10.1038/cr.2016.125
PubMed ID: 28165510
Title: STAT2 is an essential adaptor in USP18-mediated suppression of type I interferon signaling.
PubMed ID: 28165510
DOI: 10.1038/nsmb.3378
PubMed ID: 31836668
Title: Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2.
PubMed ID: 31836668
PubMed ID: 32092142
Title: Homozygous STAT2 gain-of-function mutation by loss of USP18 activity in a patient with type I interferonopathy.
PubMed ID: 32092142
DOI: 10.1084/jem.20192319
Sequence Information:
- Length: 372
- Mass: 43011
- Checksum: 60248E8D4CC42BF0
- Sequence:
MSKAFGLLRQ ICQSILAESS QSPADLEEKK EEDSNMKREQ PRERPRAWDY PHGLVGLHNI GQTCCLNSLI QVFVMNVDFT RILKRITVPR GADEQRRSVP FQMLLLLEKM QDSRQKAVRP LELAYCLQKC NVPLFVQHDA AQLYLKLWNL IKDQITDVHL VERLQALYTI RVKDSLICVD CAMESSRNSS MLTLPLSLFD VDSKPLKTLE DALHCFFQPR ELSSKSKCFC ENCGKKTRGK QVLKLTHLPQ TLTIHLMRFS IRNSQTRKIC HSLYFPQSLD FSQILPMKRE SCDAEEQSGG QYELFAVIAH VGMADSGHYC VYIRNAVDGK WFCFNDSNIC LVSWEDIQCT YGNPNYHWQE TAYLLVYMKM EC
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.