Entity Details

Primary name REN3B_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9BZI7
EntryNameREN3B_HUMAN
FullNameRegulator of nonsense transcripts 3B
TaxID9606
Evidenceevidence at protein level
Length483
SequenceStatuscomplete
DateCreated2005-03-01
DateModified2021-06-02

Ontological Relatives

GenesUPF3B

GO terms

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GOName
GO:0000184 nuclear-transcribed mRNA catabolic process, nonsense-mediated decay
GO:0000398 mRNA splicing, via spliceosome
GO:0003723 RNA binding
GO:0003729 mRNA binding
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005730 nucleolus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0006405 RNA export from nucleus
GO:0006406 mRNA export from nucleus
GO:0017056 structural constituent of nuclear pore
GO:0031124 mRNA 3'-end processing
GO:0034451 centriolar satellite
GO:0035145 exon-exon junction complex
GO:0045727 positive regulation of translation

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus

Domains

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DomainNameCategoryType
IPR005120 UPF3 domainDomainDomain
IPR012677 Nucleotide-binding alpha-beta plait domain superfamilyFamilyHomologous superfamily
IPR034979 UPF3B, RNA recognition motif-like domainDomainDomain
IPR035979 RNA-binding domain superfamilyFamilyHomologous superfamily
IPR039722 Nonsense-mediated mRNA decay protein 3FamilyFamily

Diseases

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Disease IDSourceNameDescription
300676 OMIMMental retardation, X-linked, syndromic, 14 (MRXS14)A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. MRXS14 patients manifest mental retardation associated with other variable signs such as autistic features, slender build, poor musculature, long, thin face, high-arched palate, high nasal bridge, and pectus deformities. The disease is caused by variants affecting the gene represented in this entry.

Interactions

21 interactions

InteractorPartnerSourcesPublicationsLink
REN3B_HUMANRBM8A_HUMANBioGRID, HPRD, IntAct, MINT, UniProt11546873 11546874 12718880 16209946 16452507 16601204 20371770 22961380 23084401 details
REN3B_HUMANRENT2_HUMANBioGRID, DIP, HPRD, IntAct, MINT, UniProt11163187 12417715 12718880 14527413 15231747 16452507 16601204 18066079 19503078 20479275 22522823 26344197 26496610 details
REN3B_HUMANMCRS1_HUMANBioGRID, HPRD, IntAct15231747 details
REN3B_HUMANTTC19_HUMANBioGRID, HPRD, IntAct15231747 details
REN3B_HUMANIF4A3_HUMANBioGRID, DIP, IntAct, UniProt15361857 16209946 16601204 18066079 19410547 19478851 19884259 22961380 23084401 details
REN3B_HUMANMGN_HUMANBioGRID, DIP, IntAct, UniProt16209946 16601204 18066079 19410547 19478851 22961380 details
REN3B_HUMANCASC3_HUMANBioGRID, DIP, IntAct, UniProt16601204 18066079 19478851 20479275 22522823 22961380 26496610 details
REN3B_HUMANREN3A_HUMANBioGRID, DIP14527413 19503078 details
REN3B_HUMANIF6_HUMANBioGRID, HPRD16169070 34079125 details
REN3B_HUMANSRPK2_HUMANBioGRID26167880 details
REN3B_HUMANOGT1_HUMANBioGRID32994395 details
REN3B_HUMANRBBP6_HUMANHPRD18851979 details
REN3B_HUMANRENT1_HUMANBioGRID, DIP, HPRD, IntAct, UniProt11163187 12417715 12723973 14527413 15680326 16601204 18066079 19417104 19478851 20371770 21145460 22522823 24778252 26496610 details
REN3B_HUMANCENPR_HUMANIntAct16169070 details
REN3B_HUMANSMG1_HUMANBioGRID, UniProt16452507 18256688 details
REN3B_HUMANTR150_HUMANUniProt20123736 details
REN3B_HUMANSTAU1_HUMANBioGRID23125841 30948266 details
REN3B_HUMANEST1A_HUMANBioGRID20930030 details
REN3B_HUMANREN3B_HUMANHPRD12093754 details
REN3B_HUMANXRN1_HUMANHPRD14527413 details
REN3B_HUMANEXOS4_HUMANHPRD14527413 details