STK25: Serine/Threonine Kinase 25

A member of the STE20 kinase family involved in cell polarity, migration, and stress response

Gene Information Card

Symbol STK25
Full Name Serine/Threonine Kinase 25
Gene Type Protein coding
Chromosomal Location 2q37.3
NCBI Gene ID 10494 ncbi.nlm.nih.gov/gene/10494
Ensembl ID ENSG00000115641
UniProt ID O00506
OMIM ID 602255
HGNC ID 11403
Aliases YSK1, SOK1, STE20/SPS1-related proline-alanine-rich kinase

Description

STK25 (Serine/Threonine Kinase 25) encodes a member of the STE20 family of serine/threonine kinases. The protein is involved in regulating cell polarity, cell migration, and stress-activated signaling pathways. It interacts with the Golgi matrix protein GM130 and plays a role in the Hippo signaling pathway. STK25 is implicated in cancer progression, neurodegenerative diseases, and metabolic disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Hepatocellular carcinoma STK25 overexpression promotes cell migration and invasion via activation of ERK and JNK pathways PMID: 25695633
Breast cancer STK25 regulates cell polarity and migration; altered expression correlates with poor prognosis PMID: 27322070
Alzheimer's disease STK25 interacts with tau and modulates tau phosphorylation PMID: 21930797
Type 2 diabetes STK25 deficiency improves insulin sensitivity and glucose tolerance in mice PMID: 25249562

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.5 Medium
Liver 8.3 Low
Kidney 15.2 Medium
Heart 6.7 Low
Lung 9.1 Low
Pancreas 5.4 Low
Cell Line Expression
Cell Line nTPM Notes
HepG2 14.8 Hepatocellular carcinoma cell line
MCF7 11.2 Breast cancer cell line
SH-SY5Y 18.5 Neuroblastoma cell line
HEK293 9.3 Embryonic kidney cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.511C>T (p.Arg171Trp) Missense <0.01% Reduced kinase activity in vitro
c.874G>A (p.Glu292Lys) Missense <0.01% Unknown functional effect
c.1234_1235insA Frameshift <0.01% Predicted loss of function
Mutation functional classification

Loss of Function (LOF)

Frameshift insertions and nonsense mutations are predicted to cause loss of kinase activity.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in curated databases.

Dominant Negative (DN)

No dominant-negative mutations described in literature or curated sources.

Gene Ontology (GO)

• GO:0004672 - protein kinase activity • GO:0004674 - protein serine/threonine kinase activity
• GO:0005524 - ATP binding • GO:0006468 - protein phosphorylation
• GO:0030036 - actin cytoskeleton organization • GO:0035556 - intracellular signal transduction
• GO:0040011 - locomotion • GO:0090263 - positive regulation of canonical Wnt signaling pathway

Pathways

Hippo signaling pathway (Reactome: R-HSA-2028269)
STE20 kinase signaling (Reactome: R-HSA-5628897)
Stress-activated MAPK cascade (Reactome: R-HSA-450294)

Protein Summary

STK25 is a 426-amino acid serine/threonine kinase with an N-terminal kinase domain and a C-terminal regulatory region. It localizes to the Golgi apparatus and centrosomes, where it regulates cell polarity and migration. The kinase is activated by oxidative stress and osmotic shock. STK25 phosphorylates multiple substrates including MOB1, a core component of the Hippo pathway. Its expression is altered in several cancers and neurodegenerative conditions.

Related Products

Product name Cat.No. Species Gene ID
STK25 Knockout HEK293 Cell Line EDJ-KQ7062 Human 10494 Details Get a Quote
STK25 Knockout A-549 Cell Line EDJ-KQ31871 Human 10494 Details Get a Quote
STK25 Knockout HCT 116 Cell Line EDJ-KQ31872 Human 10494 Details Get a Quote
STK25 Knockout HeLa Cell Line EDJ-KQ31873 Human 10494 Details Get a Quote
STK25 Knockout HAP1 Cell Line EDC07937 Human 10494 Details Get a Quote
Displaying Records 1 To 5 Of 5 Records
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