KIF18B

Kinesin Family Member 18B: A Mitotic Kinesin Involved in Chromosome Congression and Spindle Dynamics

Gene Information Card

Symbol KIF18B
Full Name kinesin family member 18B
Gene Type protein-coding
Chromosomal Location 17q21.31
NCBI Gene ID 146909 ncbi.nlm.nih.gov/gene/146909
Ensembl ID ENSG00000186185
UniProt ID Q8NI77
OMIM ID 615289
HGNC ID 29485
Aliases FLJ10769, MGC35010, KIF18B

Description

KIF18B (kinesin family member 18B) is a protein-coding gene that encodes a member of the kinesin-8 family of microtubule motor proteins. The protein plays a critical role in mitosis by regulating microtubule dynamics, chromosome congression, and spindle assembly. KIF18B localizes to kinetochores and spindle microtubules, where it modulates microtubule plus-end dynamics to ensure proper chromosome alignment and segregation. Dysregulation of KIF18B has been implicated in various cancers, including breast, lung, and colorectal cancers, where it may promote aneuploidy and tumor progression.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer Overexpression leads to mitotic defects and aneuploidy PMID: 25657329
Lung cancer Upregulation associated with poor prognosis and cell proliferation PMID: 30356099
Colorectal cancer High expression correlates with tumor stage and metastasis PMID: 31570863
Hepatocellular carcinoma KIF18B knockdown reduces cell growth and invasion PMID: 32561859

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 12.5 Medium
Bone marrow 8.3 Medium
Lymph node 6.1 Low
Brain 2.4 Low
Liver 1.8 Not detected
Cell Line Expression
Cell Line nTPM Notes
HeLa 15.2 Cervical cancer cell line
MCF7 10.8 Breast cancer cell line
A549 9.5 Lung cancer cell line
HCT116 11.3 Colorectal cancer cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1234G>A (p.Gly412Arg) Missense 0.02% (COSMIC) Unknown functional impact
c.567_568insA (p.Gln190Thrfs*5) Frameshift 0.01% (COSMIC) Predicted loss of function
c.890C>T (p.Thr297Met) Missense 0.03% (ClinVar) Uncertain significance
Mutation functional classification

Loss of Function (LOF)

Frameshift mutations (e.g., p.Gln190Thrfs*5) are predicted to truncate the protein, likely impairing microtubule binding and motor activity.

Gain of Function (GOF)

No well-characterized gain-of-function mutations reported in KIF18B.

Dominant Negative (DN)

Missense mutations in the motor domain may exert dominant-negative effects by interfering with wild-type KIF18B function, but evidence is limited.

Pathways

• Kinesin-mediated microtubule depolymerization (Reactome: R-HSA-983189)
• Mitotic prometaphase (Reactome: R-HSA-68877)
• Resolution of sister chromatid cohesion (Reactome: R-HSA-2500257)

Protein Summary

KIF18B is a 798-amino acid protein belonging to the kinesin-8 family. It contains an N-terminal motor domain with ATPase and microtubule-binding activities, a central coiled-coil region for dimerization, and a C-terminal tail domain involved in kinetochore localization. The protein functions as a microtubule depolymerase, regulating microtubule plus-end dynamics during mitosis. KIF18B is essential for proper chromosome alignment and spindle length control; its depletion leads to mitotic delay, chromosome misalignment, and aneuploidy.

Related Products

Product name Cat.No. Species Gene ID
KIF18B Knockout HEK293 Cell Line EDJ-KQ10518 Human 146909 Details Get a Quote
KIF18B Knockout A-549 Cell Line EDJ-KQ37926 Human 146909 Details Get a Quote
KIF18B Knockout HCT 116 Cell Line EDJ-KQ37927 Human 146909 Details Get a Quote
KIF18B Knockout HeLa Cell Line EDJ-KQ37928 Human 146909 Details Get a Quote
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