HCSGD entry for KIF20A


1. General information

Official gene symbolKIF20A
Entrez ID10112
Gene full namekinesin family member 20A
Other gene symbolsMKLP2 RAB6KIFL
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar
This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0000278Mitotic cell cycleTASbiological_process
GO:0000910CytokinesisIDA IEAbiological_process
GO:0001578Microtubule bundle formationIDAbiological_process
GO:0003777Microtubule motor activityIEAmolecular_function
GO:0005215Transporter activityTASmolecular_function
GO:0005524ATP bindingIEAmolecular_function
GO:0005654NucleoplasmTAScellular_component
GO:0005794Golgi apparatusIEAcellular_component
GO:0005819SpindleIDAcellular_component
GO:0005871Kinesin complexIEAcellular_component
GO:0005874MicrotubuleIEAcellular_component
GO:0007018Microtubule-based movementIEAbiological_process
GO:0008017Microtubule bindingIEAmolecular_function
GO:0015031Protein transportIEAbiological_process
GO:0016192Vesicle-mediated transportTASbiological_process
GO:0019901Protein kinase bindingIPImolecular_function
Entries Per Page
Displaying Page of

4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.93211711560.00000490100.99999024730.0069833333

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Down-2.1872242377
GSE13712_SHEARDown-0.7287679201
GSE13712_STATICDown-0.9339266992
GSE19018Up0.4884098307
GSE19899_A1Down-2.7109716102
GSE19899_A2Down-5.4915611069
PubMed_21979375_A1Down-5.6286218288
PubMed_21979375_A2Down-7.4121682248
GSE35957Down-5.2234045140
GSE36640Down-6.4183302433
GSE54402Down-2.3569776008
GSE9593Down-2.1849313794
GSE43922Down-4.0173181673
GSE24585Up0.1178439956
GSE37065Down-1.6686852616
GSE28863_A1Down-0.4499554014
GSE28863_A2Up1.3980422838
GSE28863_A3Down-0.6592541922
GSE28863_A4Up0.0009588614
GSE48662Down-1.9683395015

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

  • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-124-3pMIMAT0000422MIRT023002ProteomicsFunctional MTI (Weak)18668037
hsa-miR-215-5pMIMAT0000272MIRT024718MicroarrayFunctional MTI (Weak)19074876
hsa-miR-192-5pMIMAT0000222MIRT026859MicroarrayFunctional MTI (Weak)19074876
hsa-miR-92a-3pMIMAT0000092MIRT049540CLASHFunctional MTI (Weak)23622248
hsa-miR-23a-3pMIMAT0000078MIRT050411CLASHFunctional MTI (Weak)23622248
Entries Per Page
Displaying Page of
  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 1 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25961928Paclitaxel targets FOXM1 to regulate KIF20A in mitotic catastrophe and breast cancer paclitaxel resistance
25961928We also demonstrate that FOXM1 regulates the expression of the microtubulin-associated kinesin KIF20A at the transcriptional level directly through a Forkhead response element (FHRE) in its promoter
25961928Similar to FOXM1, KIF20A expression is downregulated by paclitaxel in the sensitive MCF-7 breast cancer cells and deregulated in the paclitaxel-resistant MCF-7Tax(R) cells
25961928KIF20A depletion also renders MCF-7 and MCF-7Tax(R) cells more sensitive to paclitaxel-induced cellular senescence
25961928Crucially, resembling paclitaxel treatment, silencing of FOXM1 and KIF20A similarly promotes abnormal mitotic spindle morphology and chromosome alignment, which have been shown to induce mitotic catastrophe-dependent senescence
25961928The physiological relevance of the regulation of KIF20A by FOXM1 is further highlighted by the strong and significant correlations between FOXM1 and KIF20A expression in breast cancer patient samples
25961928Statistical analysis reveals that both FOXM1 and KIF20A protein and mRNA expression significantly associates with poor survival, consistent with a role of FOXM1 and KIF20A in paclitaxel action and resistance
25961928Collectively, our findings suggest that paclitaxel targets the FOXM1-KIF20A axis to drive abnormal mitotic spindle formation and mitotic catastrophe and that deregulated FOXM1 and KIF20A expression may confer paclitaxel resistance
Entries Per Page
Displaying Page of