Entity Details

Primary name KIF3B
Entity type gene
Source Source Link

Details

PrimaryID9371
RefseqGene
SymbolKIF3B
Namekinesin family member 3B
Chromosome20
Location20q11.21
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1999-07-01
ModificationDate2021-06-22

Ontological Relatives

UniProt IDsKIF3B_HUMAN

GO terms

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GOName
GO:0003777 microtubule motor activity
GO:0005524 ATP binding
GO:0005813 centrosome
GO:0005819 spindle
GO:0005829 cytosol
GO:0005871 kinesin complex
GO:0005873 plus-end kinesin complex
GO:0005874 microtubule
GO:0005929 cilium
GO:0006890 retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum
GO:0007018 microtubule-based movement
GO:0007052 mitotic spindle organization
GO:0007100 mitotic centrosome separation
GO:0007368 determination of left/right symmetry
GO:0008017 microtubule binding
GO:0008089 anterograde axonal transport
GO:0008574 plus-end-directed microtubule motor activity
GO:0015630 microtubule cytoskeleton
GO:0016020 membrane
GO:0016887 ATP hydrolysis activity
GO:0016939 kinesin II complex
GO:0019886 antigen processing and presentation of exogenous peptide antigen via MHC class II
GO:0030496 midbody
GO:0031267 small GTPase binding
GO:0032467 positive regulation of cytokinesis
GO:0035735 intraciliary transport involved in cilium assembly
GO:0070062 extracellular exosome
GO:0072383 plus-end-directed vesicle transport along microtubule
GO:0090307 mitotic spindle assembly
GO:0097542 ciliary tip
GO:0120170 intraciliary transport particle B binding
GO:1904115 axon cytoplasm

Diseases

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Disease IDSourceNameDescription
618955 OMIMRetinitis pigmentosa 89 (RP89)A form of retinitis pigmentosa, a retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. RP89 is an autosomal dominant form associated with features of ciliopathy, including postaxial polydactyly, and renal and hepatic disease. The gene represented in this entry may be involved in disease pathogenesis.

Interactions

37 interactions

InteractorPartnerSourcesPublicationsLink
KIF3BLMO4BioGRID, HPRD, MINT15231748 details
KIF3BLMO2BioGRID, IntAct21988832 details
KIF3BARHGEF10bhf-ucl19635168 details
KIF3BKIFAP3bhf-ucl, BioGRID, HPRD, IntAct16298999 26496610 27173435 28514442 9506951 unassigned1312 details
KIF3BCLCN5IntAct19940036 details
KIF3BRAB4ABioGRID, HPRD12832475 details
KIF3BMAP3K11BioGRID9427749 details
KIF3BNEDD4LBioGRID19664597 details
KIF3BAPPBioGRID21244100 21832049 details
KIF3BPRC1BioGRID30217970 details
KIF3BSASH1BioGRID30480076 details
KIF3BMAP3K10HPRD9427749 details
KIF3BKIF3ABioGRID, HPRD, IntAct17825299 26496610 27173435 28514442 7559760 unassigned1312 details
KIF3BPSMC5BioGRID, IntAct27173435 unassigned1312 details
KIF3BSAV1BioGRID, IntAct27173435 unassigned1312 details
KIF3BDYRK2BioGRID, IntAct27173435 unassigned1312 details
KIF3BSTK3BioGRID, IntAct27173435 unassigned1312 details
KIF3BSTK4BioGRID, IntAct27173435 unassigned1312 details
KIF3BAKAP12BioGRID, IntAct27173435 unassigned1312 details
KIF3BKIF3CBioGRID, IntAct27173435 unassigned1312 details
KIF3BSLC9A3R2BioGRID, IntAct27173435 unassigned1312 details
KIF3BEXOC1IntAct31413325 details
KIF3BFMR1IntAct31413325 details
KIF3BRAB5ABioGRID12832475 details
KIF3BVHLBioGRID17825299 details
KIF3BRANBP2BioGRID9733766 details
KIF3BMEX3BBioGRID29395067 details
KIF3BIFT20HPRD12821668 details
KIF3BKIFBPBioGRID, IntAct28514442 details
KIF3BPLOD1BioGRID, IntAct30021884 details
KIF3BRAD21BioGRID22145905 details
KIF3BNTRK1BioGRID25921289 details
KIF3BRGS20BioGRID28514442 details
KIF3BPLEKHA4BioGRID31091453 details
KIF3BMOV10BioGRID22658674 details
KIF3BNXF1BioGRID22658674 details
KIF3BVIRMABioGRID29507755 details