KIF3A

gene
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Also known as FLA10KLP-20

Summary

KIF3A (kinesin family member 3A, HGNC:6319) is a protein-coding gene on chromosome 5q31.1, encoding Kinesin-like protein KIF3A (Q9Y496). Microtubule-based anterograde translocator for membranous organelles.

Enables protein phosphatase binding activity; small GTPase binding activity; and spectrin binding activity. Involved in protein localization to cell junction and protein transport. Located in centriole; centrosome; and spindle microtubule. Part of kinesin II complex. Biomarker of silicosis.

Source: NCBI Gene 11127 — RefSeq curated summary.

At a glance

  • GWAS associations: 20
  • Clinical variants (ClinVar): 73 total
  • Druggable target: yes
  • MANE Select transcript: NM_001300791

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:6319
Approved symbolKIF3A
Namekinesin family member 3A
Location5q31.1
Locus typegene with protein product
StatusApproved
AliasesFLA10, KLP-20
Ensembl geneENSG00000131437
Ensembl biotypeprotein_coding
OMIM604683
Entrez11127

Gene structure

Transcript identifiers

Ensembl transcripts: 11 — 9 protein_coding, 2 protein_coding_CDS_not_defined

ENST00000378735, ENST00000378746, ENST00000403231, ENST00000428744, ENST00000450441, ENST00000487055, ENST00000488471, ENST00000618515, ENST00000875777, ENST00000928467, ENST00000928468

RefSeq mRNA: 3 — MANE Select: NM_001300791 NM_001300791, NM_001300792, NM_007054

CCDS: CCDS34235, CCDS75295, CCDS75296

Canonical transcript exons

ENST00000403231 — 19 exons

ExonStartEnd
ENSE00000899329132699171132699295
ENSE00000899330132700216132700284
ENSE00000899332132700647132700700
ENSE00000899340132703463132703619
ENSE00000899341132710959132711057
ENSE00000899342132715757132715931
ENSE00000899343132716245132716442
ENSE00000899344132716845132716984
ENSE00000899345132720609132720714
ENSE00000899347132726354132726498
ENSE00001551763132692631132696682
ENSE00001562378132708907132708978
ENSE00002445575132706451132706459
ENSE00002445604132734205132734478
ENSE00002500727132737414132737546
ENSE00003586161132702558132702668
ENSE00003587109132702087132702212
ENSE00003678716132702885132703065
ENSE00003789387132726128132726212

Expression profiles

Bgee: expression breadth ubiquitous, 264 present calls, max score 99.17.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 27.6893 / max 2009.5060, expressed in 1746 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
6334923.99431729
633483.63151157
633470.063521

Top tissues by expression

287 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
Brodmann (1909) area 23UBERON:001355499.17gold quality
endothelial cellCL:000011597.72gold quality
middle temporal gyrusUBERON:000277197.42gold quality
secondary oocyteCL:000065596.10gold quality
ponsUBERON:000098896.09gold quality
buccal mucosa cellCL:000233695.61gold quality
entorhinal cortexUBERON:000272895.45gold quality
postcentral gyrusUBERON:000258195.13gold quality
superior vestibular nucleusUBERON:000722795.02gold quality
parietal lobeUBERON:000187295.01gold quality
sural nerveUBERON:001548894.74gold quality
cortical plateUBERON:000534394.73gold quality
primary visual cortexUBERON:000243694.72gold quality
superior frontal gyrusUBERON:000266194.68gold quality
lateral nuclear group of thalamusUBERON:000273694.55gold quality
substantia nigra pars compactaUBERON:000196593.78gold quality
occipital lobeUBERON:000202193.69gold quality
substantia nigra pars reticulataUBERON:000196693.07gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047392.63gold quality
prefrontal cortexUBERON:000045192.57gold quality
dorsal root ganglionUBERON:000004492.54gold quality
bronchial epithelial cellCL:000232892.15gold quality
oocyteCL:000002391.90gold quality
corpus callosumUBERON:000233691.39gold quality
calcaneal tendonUBERON:000370191.06gold quality
dorsolateral prefrontal cortexUBERON:000983490.62gold quality
frontal cortexUBERON:000187090.46gold quality
cerebral cortexUBERON:000095690.40gold quality
neocortexUBERON:000195090.18gold quality
ventral tegmental areaUBERON:000269190.13gold quality

Single-cell (SCXA)

Detected in 3 experiment(s), a significant marker in 3.

ExperimentMarker?Max mean expression
E-HCAD-5yes46.27
E-GEOD-134144yes27.96
E-ANND-3yes11.12

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

204 targeting KIF3A, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-3613-3P100.0076.367965
HSA-MIR-4262100.0073.263931
HSA-MIR-4673100.0066.641490
HSA-MIR-5011-5P100.0083.465820
HSA-MIR-5692A100.0074.406850
HSA-LET-7A-3P100.0074.033932
HSA-LET-7B-3P100.0074.083913
HSA-LET-7F-1-3P100.0074.023928
HSA-MIR-98-3P100.0074.083907
HSA-MIR-3924100.0072.092394
HSA-MIR-190A-3P100.0080.355520
HSA-MIR-4747-5P100.0067.902681
HSA-MIR-5196-5P100.0067.982761
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-1277-5P100.0073.955056
HSA-MIR-3646100.0073.565283
HSA-MIR-3163100.0077.238605
HSA-MIR-4455100.0065.481587
HSA-MIR-6748-5P100.0065.811057
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-181A-5P99.9972.962995
HSA-MIR-181B-5P99.9972.972996
HSA-MIR-181C-5P99.9972.952996
HSA-MIR-181D-5P99.9973.042997
HSA-MIR-196A-1-3P99.9972.152772
HSA-MIR-366299.9973.825684
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775
HSA-MIR-4645-5P99.9865.811284
HSA-MIR-19A-3P99.9875.332762

Literature-anchored findings (GeneRIF, showing 36)

  • both motor domains of KIF3A/B coordinate for processive motility and move at different speeds (PMID:15345558)
  • Required for the normal steady-state localization of late endosomes/lysosomes but not early endosomes or recycling endosomes. (PMID:16262723)
  • Interaction of KIF3A/3B with KAP3 may be important for the proper progression of mitosis. (PMID:16298999)
  • We detected ALS-specific down-regulation of KIF1Bbeta and novel KIF3Abeta, two isoforms we show to be enriched in the brain, and also of SOD1, a key enzyme linked to familial ALS (PMID:17418584)
  • Rip11/FIP5-kinesin-II complex plays a key role in the routing of internalized receptors through the perinuclear recycling endosomes. (PMID:18957512)
  • Protein phosphatase Dusp26 associates with KIF3 motor and promotes N-cadherin-mediated cell-cell adhesion. (PMID:19043453)
  • This study thus reports on transportation of KSHV viral complexes on microtubules by KIF3A (PMID:19282970)
  • KIF3, cilia, and nodal flow have roles in left-right determination [review] (PMID:20066075)
  • Variants carried by the haplotypes of SLC22A4, SLC22A5 and KIF3A region potentially contribute to tuberculosis susceptibility among the Thai population. (PMID:20485362)
  • Our findings suggest that the KIF3A gene and/or its polymorphisms might have a susceptibility effect on aspirin-intolerant asthma (AIA). (PMID:20922562)
  • KIF3A is a novel candidate gene for childhood asthma (PMID:21912604)
  • Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patients (PMID:23278845)
  • in addition to its ciliogenic roles, Kif3a recruits p150(Glued) to the subdistal appendages of mother centrioles, critical for centrosomes to function as microtubule-organizing centres. (PMID:23386061)
  • POPX2 affects trafficking by determining the phosphorylation status of KIF3A at serine 690. (PMID:24338362)
  • Findings support the notion that upregulation of KIF3a is causal of aberrant activation of Wnt signaling in advanced prostate cancer through the KIF3a-DVL2-beta-catenin axis. (PMID:24413182)
  • These data suggest that GLI interactions with KIF3A-KIF3B-KAP3 complexes are essential for proper GLI transcriptional activity. (PMID:25588831)
  • Ablation of this phosphorylation abolished herpes simplex virus 1 US3-mediated downregulation of CD1d expression, suggesting that phosphorylation of KIF3A is the primary mechanism of viral suppression of CD1d expression. (PMID:25878107)
  • KIF3A and OVOL1 are involved in the development of Atopic dermatitis in the Chinese pediatric population. (PMID:26127003)
  • High KIF3A expression is associated with glioblastoma. (PMID:26760767)
  • Inhibition of kif3a in the human dental follicle cells (hDFCs) and human dental pulp cells (hDPCs) is disrupted primary cilia formation and/or function, and it was shown that kif3a is important in the differentiation of hDFCs and hDPCs through the Wnt pathway. (PMID:27432616)
  • A correlation between KIF3A loss and a poorer NSCLC prognosis as well as beta-catenin and cyclin D1 upregulation further suggests that KIF3A suppresses Wnt/beta-catenin signalling and tumourigenesis in NSCLC (PMID:27596264)
  • the association of KIF3A is with asthma + eczema. The presence of AR comorbidity did not increase the genetic association of KIF3A with asthma or even with asthma + eczema. Thus, asthma + eczema constitutes a distinct asthmatic phenotype characterized by an association with KIF3A SNPs, which is not strengthened by AR. (PMID:28238750)
  • PLCD1 acts as a tumour suppressor, by KIF3A-mediated suppression of ERK1/2/beta-catenin/MMP7 signalling, at least in part, in breast cancer. (PMID:28423710)
  • The rate of transport is set by an equilibrium between a faster state, where only kinesin family member 17 protein (KIF17) motors move the train, and a slower state, where at least one kinesin family member 3A/B protein (KIF3AB) motor on the train remains active in transport. (PMID:28761002)
  • p0071 is required for directional vesicle movement and secretion of different KIF3-transported carriers, thereby regulating the transport of intracellular membrane vesicles along microtubules. (PMID:28808088)
  • KIF3A plays an important role in epithelium apoptosis and bronchial inflammation in asthma (PMID:29156524)
  • Study demonstrates that human ICK (intestinal cell kinase) that authors herein call CAPK (ciliopathy-associated protein kinase) interacts with human KIF3A and phosphorylates a conserved site Thr672 both in vitro and in vivo. Long, unstructured, non-catalytic carboxyl-terminal domain (CTD) of CAPK is required for this interaction with and phosphorylation of KIF3A (PMID:31277411)
  • Silencing of KIF3A suppressed TNBC cell proliferation by repressing the Rb-E2F signaling pathway and inhibited migration and invasion by repressing epithelial-mesenchymal transition. The tumor size was smaller and the number of lung metastatic nodules was lower in KIF3A depletion MDA-MB-231 cell xenograft mice than in the negative control group. In addition, KIF3A overexpression correlated with chemoresistance. (PMID:32011034)
  • Disease-associated KIF3A variants alter gene methylation and expression impacting skin barrier and atopic dermatitis risk. (PMID:32796837)
  • Skin depletion of Kif3a resembles the pediatric atopic dermatitis transcriptome profile. (PMID:34964466)
  • Coordination of two kinesin superfamily motor proteins, KIF3A and KIF13A, is essential for pericellular matrix degradation by membrane-type 1 matrix metalloproteinase (MT1-MMP) in cancer cells. (PMID:35122963)
  • lncRNA MIR600HG induces the proliferation and invasion of colorectal cancer cells via regulating miR-144-3p/KIF3A. (PMID:35378445)
  • Kinesin family member 3A induces related diseases via wingless-related integration site/beta-catenin signaling pathway. (PMID:36594221)
  • Inhibitory mechanism of KIF3A gene on nasopharyngeal carcinoma stem cells. (PMID:37715417)
  • CircRAPGEF5 sponges miR-582-3p and targets KIF3A to regulate bladder cancer cell proliferation, migration and invasion. (PMID:38489970)
  • The heterotrimeric kinesin-2 family member KIF3A directly binds to disabled-1 (Dab1). (PMID:38919020)

Cross-species orthologs

5 orthologs

OrganismSymbolGene ID
danio_reriokif3aENSDARG00000087538
mus_musculusKif3aENSMUSG00000018395
rattus_norvegicusKif3aENSRNOG00000007515
drosophila_melanogasterKlp64DFBGN0004380
caenorhabditis_elegansWBGENE00002230

Paralogs (41): KIF1B (ENSG00000054523), KIF26A (ENSG00000066735), KIF2A (ENSG00000068796), KIF22 (ENSG00000079616), KIF3C (ENSG00000084731), KIF9 (ENSG00000088727), KIF16B (ENSG00000089177), KIF4A (ENSG00000090889), KIF3B (ENSG00000101350), KIF20A (ENSG00000112984), KIF21B (ENSG00000116852), KIF17 (ENSG00000117245), KIF14 (ENSG00000118193), KIF18A (ENSG00000121621), KIF25 (ENSG00000125337), KIF1C (ENSG00000129250), KIF1A (ENSG00000130294), KIF12 (ENSG00000136883), KIF13A (ENSG00000137177), KIF23 (ENSG00000137807), KIF11 (ENSG00000138160), CENPE (ENSG00000138778), KIF21A (ENSG00000139116), KIFC3 (ENSG00000140859), KIF2B (ENSG00000141200), KIF2C (ENSG00000142945), KIF5A (ENSG00000155980), KIF26B (ENSG00000162849), KIF15 (ENSG00000163808), KIF6 (ENSG00000164627), KIF27 (ENSG00000165115), KIF7 (ENSG00000166813), KIFC2 (ENSG00000167702), KIF5C (ENSG00000168280), KIF5B (ENSG00000170759), KIF18B (ENSG00000186185), KIF24 (ENSG00000186638), KIF19 (ENSG00000196169), KIF13B (ENSG00000197892), KIF4B (ENSG00000226650)

Protein

Protein identifiers

Kinesin-like protein KIF3AQ9Y496 (reviewed: Q9Y496)

Alternative names: Microtubule plus end-directed kinesin motor 3A

All UniProt accessions (6): A0A087X011, C9J9X2, E9PES4, Q9Y496, H7C2F6, J3KPF9

UniProt curated annotations — full annotation on UniProt →

Function. Microtubule-based anterograde translocator for membranous organelles. Plus end-directed microtubule sliding activity in vitro. Plays a role in primary cilia formation. Plays a role in centriole cohesion and subdistal appendage organization and function. Regulates the formation of the subdistal appendage via recruitment of DCTN1 to the centriole. Also required for ciliary basal feet formation and microtubule anchoring to mother centriole.

Subunit / interactions. Heterodimer of KIF3A and KIF3B. Interacts with CIMAP3. Interacts with CLN3. Interacts with DCTN1. Interacts with FLCN. Interacts with AP3B1.

Subcellular location. Cytoplasm. Cytoskeleton. Cell projection. Cilium. Microtubule organizing center. Centrosome. Centriole.

Similarity. Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. Kinesin II subfamily.

RefSeq proteins (3): NP_001287720, NP_001287721, NP_008985 (=MANE)

Domains & families (InterPro)

IDNameType
IPR001752Kinesin_motor_domDomain
IPR019821Kinesin_motor_CSConserved_site
IPR027417P-loop_NTPaseHomologous_superfamily
IPR027640Kinesin-like_famFamily
IPR036961Kinesin_motor_dom_sfHomologous_superfamily

Pfam: PF00225

UniProt features (16 total): sequence conflict 5, region of interest 3, compositionally biased region 2, chain 1, domain 1, sequence variant 1, coiled-coil region 1, binding site 1, modified residue 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9Y496-F175.650.20

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Ligand- & substrate-binding residues (1): 100–107

Post-translational modifications (1): 687

Function

Pathways and Gene Ontology

Reactome pathways

20 pathways

IDPathway
R-HSA-1445148Translocation of SLC2A4 (GLUT4) to the plasma membrane
R-HSA-2132295MHC class II antigen presentation
R-HSA-5610787Hedgehog ‘off’ state
R-HSA-5620924Intraflagellar transport
R-HSA-5635838Activation of SMO
R-HSA-6811434COPI-dependent Golgi-to-ER retrograde traffic
R-HSA-983189Kinesins
R-HSA-109582Hemostasis
R-HSA-1280218Adaptive Immune System
R-HSA-162582Signal Transduction
R-HSA-168256Immune System
R-HSA-1852241Organelle biogenesis and maintenance
R-HSA-199991Membrane Trafficking
R-HSA-5358351Signaling by Hedgehog
R-HSA-5617833Cilium Assembly
R-HSA-5632684Hedgehog ‘on’ state
R-HSA-5653656Vesicle-mediated transport
R-HSA-6811442Intra-Golgi and retrograde Golgi-to-ER traffic
R-HSA-8856688Golgi-to-ER retrograde transport
R-HSA-983231Factors involved in megakaryocyte development and platelet production

MSigDB gene sets: 294 (showing top): MULLIGHAN_NPM1_SIGNATURE_3_UP, GOBP_AXO_DENDRITIC_TRANSPORT, TGCGCANK_UNKNOWN, GOBP_VESICLE_LOCALIZATION, REACTOME_ADAPTIVE_IMMUNE_SYSTEM, GOBP_MICROTUBULE_ANCHORING, GOCC_KINESIN_COMPLEX, REACTOME_MEMBRANE_TRAFFICKING, GOBP_ORGANELLE_TRANSPORT_ALONG_MICROTUBULE, GOMF_GTPASE_BINDING, GOCC_MICROTUBULE_ORGANIZING_CENTER, MODULE_66, GTGCCTT_MIR506, GOBP_VESICLE_CYTOSKELETAL_TRAFFICKING, GOBP_CILIUM_ORGANIZATION

GO Biological Process (16): organelle organization (GO:0006996), anterograde axonal transport (GO:0008089), centriole-centriole cohesion (GO:0010457), protein transport (GO:0015031), microtubule anchoring at centrosome (GO:0034454), cilium assembly (GO:0060271), plus-end-directed vesicle transport along microtubule (GO:0072383), protein localization to cell junction (GO:1902414), microtubule-based movement (GO:0007018), transport along microtubule (GO:0010970), cell projection organization (GO:0030030), response to silicon dioxide (GO:0034021), positive regulation of receptor-mediated endocytosis (GO:0048260), positive regulation of intracellular protein transport (GO:0090316), positive regulation of axo-dendritic protein transport (GO:1905128), positive regulation of establishment or maintenance of cell polarity regulating cell shape (GO:2000771)

GO Molecular Function (14): microtubule motor activity (GO:0003777), ATP binding (GO:0005524), microtubule binding (GO:0008017), plus-end-directed microtubule motor activity (GO:0008574), ATP hydrolysis activity (GO:0016887), protein phosphatase binding (GO:0019903), spectrin binding (GO:0030507), small GTPase binding (GO:0031267), nucleotide binding (GO:0000166), cytoskeletal motor activity (GO:0003774), protein binding (GO:0005515), cytoskeletal protein binding (GO:0008092), kinesin binding (GO:0019894), protein-containing complex binding (GO:0044877)

GO Cellular Component (18): cytoplasm (GO:0005737), centrosome (GO:0005813), centriole (GO:0005814), cytosol (GO:0005829), kinesin complex (GO:0005871), microtubule (GO:0005874), cilium (GO:0005929), microtubule cytoskeleton (GO:0015630), kinesin II complex (GO:0016939), extracellular exosome (GO:0070062), ciliary tip (GO:0097542), axon cytoplasm (GO:1904115), cytoskeleton (GO:0005856), spindle microtubule (GO:0005876), axoneme (GO:0005930), cell projection (GO:0042995), neuronal cell body (GO:0043025), ribbon synapse (GO:0097470)

Reactome top-level categories

Rollup of top-13 pathways:

CategoryPathways
Membrane Trafficking2
Signaling by Hedgehog2
Adaptive Immune System1
Assembly of the 9+0 primary cilium1
Hedgehog ‘on’ state1
Golgi-to-ER retrograde transport1
Factors involved in megakaryocyte development and platelet production1
Immune System1
Vesicle-mediated transport1
Signal Transduction1
Organelle biogenesis and maintenance1
Intra-Golgi and retrograde Golgi-to-ER traffic1
Hemostasis1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure5
cellular component organization2
intracellular protein localization2
ATP-dependent activity2
cytoskeletal protein binding2
binding2
microtubule organizing center2
intracellular membraneless organelle2
cytoskeleton2
microtubule2
axonal transport1
axon cytoplasm1
centrosome cycle1
cell cycle process1
transport1
establishment of protein localization1
microtubule anchoring at microtubule organizing center1
axoneme assembly1
intraciliary transport involved in cilium assembly1
cilium organization1
protein localization to cilium1
organelle assembly1
trans-Golgi to periciliary membrane compartment transport1
plasma membrane bounded cell projection assembly1
ciliary transition zone assembly1
vesicle transport along microtubule1
plus-end-directed organelle transport along microtubule1
microtubule-based process1
microtubule-based movement1
cytoskeleton-dependent intracellular transport1
microtubule-based transport1
response to oxygen-containing compound1
receptor-mediated endocytosis1
positive regulation of endocytosis1
regulation of receptor-mediated endocytosis1
intracellular protein transport1
positive regulation of intracellular transport1
regulation of intracellular protein transport1
positive regulation of protein transport1
positive regulation of intracellular protein transport1

Protein interactions and networks

STRING

2324 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
KIF3AKIFAP3Q92845998
KIF3AKIF3BO15066984
KIF3ASMOQ99835983
KIF3AIFT88Q13099978
KIF3AKIF3CO14782907
KIF3AARRB1P49407903
KIF3AIFT172Q9UG01900
KIF3AARRB2P32121892
KIF3ASAGP10523867
KIF3APKD2Q13563858
KIF3ATTC21BQ7Z4L5829
KIF3AMAP3K10Q02779826
KIF3ASUFUQ9UMX1802
KIF3ASHHQ15465786
KIF3AARL13BQ3SXY8773

IntAct

121 interactions, top by confidence:

ABTypeScore
KIF3AKIFAP3psi-mi:“MI:0403”(colocalization)0.910
KIFAP3KIF3Apsi-mi:“MI:0915”(physical association)0.910
KIFAP3KIF3Bpsi-mi:“MI:0914”(association)0.900
MED4MED19psi-mi:“MI:2364”(proximity)0.900
KIF3BKIFAP3psi-mi:“MI:0914”(association)0.900
KIFAP3KIF3Bpsi-mi:“MI:0915”(physical association)0.900
KIF3AKIF3Bpsi-mi:“MI:0914”(association)0.840
EXOC3EXOC5psi-mi:“MI:0914”(association)0.790
KIF3AKIF3Cpsi-mi:“MI:0914”(association)0.730
KIFAP3KIF3Cpsi-mi:“MI:0914”(association)0.640
AP3B1KIF3Apsi-mi:“MI:0407”(direct interaction)0.600
KIF3AAP3B1psi-mi:“MI:0407”(direct interaction)0.600
KIF3AAP3B1psi-mi:“MI:0915”(physical association)0.600
AP3B1KIF3Apsi-mi:“MI:0915”(physical association)0.600
NUF2SPC24psi-mi:“MI:0914”(association)0.530
STN1SMCO3psi-mi:“MI:0914”(association)0.530
KIFBPKIF3Cpsi-mi:“MI:0914”(association)0.530
TNFRSF8DAPK3psi-mi:“MI:0914”(association)0.530
HENMT1SNX2psi-mi:“MI:0914”(association)0.530
KIF3BPSMC5psi-mi:“MI:0914”(association)0.510

BioGRID (199): KIF3A (Affinity Capture-MS), KIF3A (Affinity Capture-MS), KIF3A (Affinity Capture-MS), KIF3A (Affinity Capture-MS), KIF3A (Co-fractionation), KIF3A (Affinity Capture-MS), KIF3A (Reconstituted Complex), KIF3A (Proximity Label-MS), KIF3A (Proximity Label-MS), RAN (Affinity Capture-MS), KIF3B (Affinity Capture-MS), DHX34 (Affinity Capture-MS), KIF3A (Affinity Capture-MS), KIF3A (Affinity Capture-MS), KIF3A (Affinity Capture-MS)

ESM2 similar proteins: A0JN40, A8BB91, A8BKD1, B1AVY7, B9F2Y7, F1M4A4, F1M5N7, F1QN54, F4K0J3, G5EGS3, O14782, O15066, O35066, O55165, O60333, O75037, O88658, P28741, P33173, P33176, P34540, P35978, P46867, P46871, P46872, P46873, Q10E64, Q12756, Q29DY1, Q2PQA9, Q4R628, Q5JKW1, Q5R4H3, Q5R706, Q60575, Q61768, Q61771, Q6YUL8, Q7Z4S6, Q86Z98

Diamond homologs: A0A068FIK2, A0JN40, A1ZAJ2, A8BB91, A8BKD1, B1AVY7, B7EJ91, B7ZNG0, B9F2Y7, B9GE13, F1M4A4, F1M5N7, F1QN54, F4IIS5, F4J1U4, F4K0J3, G5EGS3, O14343, O14782, O15066, O23826, O35066, O35071, O35787, O43896, O45935, O55165, O60282, O60333, O75037, O88658, O95239, P17210, P21613, P23678, P28738, P28741, P33173, P33174, P33175

SIGNOR signaling

6 interactions.

AEffectBMechanism
ARRB2up-regulatesKIF3Abinding
ARRB1up-regulatesKIF3Abinding
KIF3Aup-regulates“Plus-end directed sliding movement”
KIF3Aup-regulates“Minus-end directed microtubule movement”
AP3B1“up-regulates activity”KIF3Abinding

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 121 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.

GO biological processes:

GO termPartnersFoldFDR
microtubule-based movement513.4×9e-03
non-motile cilium assembly513.2×9e-03
mitotic spindle organization512.3×1e-02
cilium assembly96.0×9e-03

Disease & clinical

Clinical variants and AI predictions

ClinVar

73 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance45
Likely benign5
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

2744 predictions. Top by Δscore:

VariantEffectΔscore
5:132699167:TTACC:Tdonor_loss1.0000
5:132699169:A:ACdonor_gain1.0000
5:132699169:A:AGdonor_loss1.0000
5:132699170:C:CCdonor_gain1.0000
5:132699170:CCTT:Cdonor_gain1.0000
5:132699170:CCTTC:Cdonor_loss1.0000
5:132699292:AGGG:Aacceptor_gain1.0000
5:132699293:GGG:Gacceptor_gain1.0000
5:132699294:GG:Gacceptor_gain1.0000
5:132699295:GCT:Gacceptor_loss1.0000
5:132699296:C:CCacceptor_gain1.0000
5:132699297:T:Aacceptor_loss1.0000
5:132699300:G:Cacceptor_gain1.0000
5:132699300:G:GCacceptor_gain1.0000
5:132700215:CAT:Cdonor_gain1.0000
5:132700645:A:ACdonor_gain1.0000
5:132700646:C:CTdonor_gain1.0000
5:132700646:CTAG:Cdonor_gain1.0000
5:132702077:T:TAdonor_gain1.0000
5:132702081:TTTTA:Tdonor_loss1.0000
5:132702082:TTTAC:Tdonor_loss1.0000
5:132702083:TTACC:Tdonor_loss1.0000
5:132702084:TAC:Tdonor_loss1.0000
5:132702085:ACCT:Adonor_loss1.0000
5:132702086:CCTGA:Cdonor_loss1.0000
5:132702208:GCCAT:Gacceptor_gain1.0000
5:132702209:CCAT:Cacceptor_gain1.0000
5:132702209:CCATC:Cacceptor_gain1.0000
5:132702210:CAT:Cacceptor_gain1.0000
5:132702210:CATC:Cacceptor_gain1.0000

AlphaMissense

4817 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
5:132700265:C:TG626E1.000
5:132700655:A:GW617R1.000
5:132700655:A:TW617R1.000
5:132702569:C:GA556P1.000
5:132702577:A:GL553P1.000
5:132702620:C:GA539P1.000
5:132702953:A:GS500P1.000
5:132715852:A:CI345S1.000
5:132715852:A:TI345N1.000
5:132715857:C:AK343N1.000
5:132715857:C:GK343N1.000
5:132715859:T:CK343E1.000
5:132715861:G:TA342D1.000
5:132715862:C:GA342P1.000
5:132715864:C:GR341P1.000
5:132715865:G:TR341S1.000
5:132715870:G:TA339D1.000
5:132715871:C:GA339P1.000
5:132715873:T:CY338C1.000
5:132715874:A:GY338H1.000
5:132715876:C:GR337P1.000
5:132715879:A:GL336S1.000
5:132715882:G:TT335K1.000
5:132715927:G:TA320E1.000
5:132716259:A:GS314P1.000
5:132716264:C:AG312V1.000
5:132716264:C:TG312E1.000
5:132716265:C:GG312R1.000
5:132716265:C:TG312R1.000
5:132716267:C:AG311V1.000

dbSNP variants (sampled 300 via entrez): RS1000050397 (5:132691484 T>C), RS1000067175 (5:132718122 T>C), RS1000072739 (5:132710814 A>C,G), RS1000088881 (5:132699178 C>T), RS1000144320 (5:132698824 G>A,C), RS1000258761 (5:132733713 T>C), RS1000265307 (5:132726280 A>C,G), RS1000339311 (5:132726065 C>T), RS1000352929 (5:132703826 G>A), RS1000417025 (5:132717691 T>C,G), RS1000477622 (5:132722192 T>C), RS1000565886 (5:132689968 C>T), RS1000601136 (5:132727838 A>G), RS1000674505 (5:132727635 G>A), RS1000718011 (5:132727876 C>A)

Disease associations

OMIM: gene MIM:604683 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

20 associations (top):

StudyTraitp-value
GCST001363_3Atopic dermatitis4.000000e-08
GCST001709_5Atopic dermatitis2.000000e-06
GCST002737_2Atopic dermatitis5.000000e-09
GCST003180_4Atopic march5.000000e-08
GCST003184_27Atopic dermatitis1.000000e-10
GCST004862_229Itch intensity from mosquito bite adjusted by bite size1.000000e-08
GCST004863_107Mosquito bite size3.000000e-07
GCST007564_19Asthma or allergic disease (pleiotropy)2.000000e-10
GCST007995_20Asthma (childhood onset)3.000000e-22
GCST008916_112Asthma2.000000e-11
GCST008916_34Asthma2.000000e-09
GCST008916_48Asthma1.000000e-11
GCST008916_99Asthma6.000000e-32
GCST009798_39Asthma5.000000e-29
GCST009798_75Asthma9.000000e-24
GCST010002_38Refractive error3.000000e-10
GCST010984_17Allergic disease (asthma, hay fever and/or eczema) (multivariate analysis)2.000000e-10
GCST010985_4Allergic disease (asthma, hay fever and/or eczema) (age of onset)2.000000e-10
GCST90002381_389Eosinophil count1.000000e-18
GCST90002382_122Eosinophil percentage of white cells1.000000e-10

EFO canonical traits (6, from GWAS)

EFO IDTrait name
EFO:0007755atopic march
EFO:0008377mosquito bite reaction itch intensity measurement
EFO:0008378mosquito bite reaction size measurement
EFO:0004847age at onset
EFO:0004842eosinophil count
EFO:0007991eosinophil percentage of leukocytes

Drugs & pharmacology

Drug and pharmacology data

Is drug target: yes

ChEMBL targets (1): CHEMBL5544 (SINGLE PROTEIN)

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

34 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
trichostatin Aincreases expression, affects expression2
Hydrogen Peroxideincreases expression, affects expression2
Valproic Acidincreases expression2
triphenyl phosphateaffects expression1
bisphenol Aincreases methylation1
arsenic disulfidedecreases expression1
CD 437decreases expression1
3-(4’-hydroxy-3’-adamantylbiphenyl-4-yl)acrylic aciddecreases expression1
abrinedecreases expression1
(+)-JQ1 compoundincreases expression1
Sunitinibincreases expression1
Arsenic Trioxideincreases expression1
Vorinostatdecreases expression1
Acetaminophenincreases expression1
Air Pollutantsdecreases expression, increases abundance1
Aspirinincreases expression, affects response to substance1
Benzo(a)pyreneaffects methylation1
Cyclophosphamideaffects cotreatment, affects response to substance1
Demecolcineincreases expression1
Dimethyl Sulfoxidedecreases expression1
Doxorubicinaffects cotreatment, affects response to substance1
Fluorouracilaffects cotreatment, affects response to substance1
Mercuric Chloridedecreases expression1
Polychlorinated Biphenylsaffects expression1
Quercetindecreases expression1
Rotenonedecreases expression1
Urethaneincreases expression1
Vanadatesdecreases expression1
Cyclosporineincreases expression1
Aflatoxin M1decreases expression1

ChEMBL screening assays

1 unique, capped per target: 1 binding

Representative assays (with source publication via chembl_document):

Assay IDTypeDescriptionSource paper
CHEMBL1020051BindingInhibition of cloned human Kif3AKinesin spindle protein (KSP) inhibitors. 9. Discovery of (2S)-4-(2,5-difluorophenyl)-n-[(3R,4S)-3-fluoro-1-methylpiperidin-4-yl]-2-(hydroxymethyl)-N-methyl-2-phenyl-2,5-dihydro-1H-pyrrole-1-carboxamide (MK-0731) for the treatment of taxane-refractory cancer. — J Med Chem

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.