Entity Details

Primary name SKIV2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ15477
EntryNameSKIV2_HUMAN
FullNameHelicase SKI2W
TaxID9606
Evidenceevidence at protein level
Length1246
SequenceStatuscomplete
DateCreated1997-11-01
DateModified2021-06-02

Ontological Relatives

GenesSKIV2L

GO terms

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GOName
GO:0003723 RNA binding
GO:0003724 RNA helicase activity
GO:0005524 ATP binding
GO:0005634 nucleus
GO:0005829 cytosol
GO:0006401 RNA catabolic process
GO:0043928 exonucleolytic catabolism of deadenylated mRNA
GO:0055087 Ski complex
GO:0070478 nuclear-transcribed mRNA catabolic process, 3'-5' exonucleolytic nonsense-mediated decay

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus

Domains

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DomainNameCategoryType
IPR001650 Helicase, C-terminalDomainDomain
IPR011545 DEAD/DEAH box helicase domainDomainDomain
IPR012961 ATP-dependent RNA helicase Ski2, C-terminalDomainDomain
IPR014001 Helicase superfamily 1/2, ATP-binding domainDomainDomain
IPR016438 ATP-dependent RNA helicase Ski2-likeFamilyFamily
IPR025696 rRNA-processing arch domainDomainDomain
IPR027417 P-loop containing nucleoside triphosphate hydrolaseFamilyHomologous superfamily
IPR040801 Ski2, N-terminal domainDomainDomain

Diseases

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Disease IDSourceNameDescription
614602 OMIMTrichohepatoenteric syndrome 2 (THES2)A syndrome characterized by intrauterine growth retardation, severe diarrhea in infancy requiring total parenteral nutrition, facial dysmorphism, immunodeficiency, and hair abnormalities, mostly trichorrhexis nodosa. Hepatic involvement contributes to the poor prognosis of affected patients. The disease is caused by variants affecting the gene represented in this entry.