SLK (STE20 Like Kinase)

A serine/threonine kinase involved in cell migration, cytoskeletal reorganization, and apoptosis.

Gene Information Card

Symbol SLK
Full Name STE20 Like Kinase
Gene Type Protein coding
Chromosomal Location 10q25.1
NCBI Gene ID 9748 ncbi.nlm.nih.gov/gene/9748
Ensembl ID ENSG00000165655
UniProt ID Q9H2G2
OMIM ID 608479
HGNC ID 11088
Aliases STK2, KIAA0204, LOSK, bA16H23.1

Description

SLK (STE20 Like Kinase) is a protein-coding gene that encodes a serine/threonine kinase belonging to the STE20 family. The protein is involved in the regulation of cell migration, cytoskeletal dynamics, and apoptosis. It acts as a downstream effector of Rho family GTPases and plays a role in stress fiber formation and focal adhesion turnover. SLK is widely expressed in various tissues and has been implicated in cancer progression and neurodegenerative disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer Overexpression of SLK promotes cell migration and invasion through cytoskeletal remodeling. NCBI Gene, PubMed
Prostate cancer SLK expression correlates with tumor aggressiveness and metastasis. NCBI Gene, PubMed
Neurodegenerative diseases SLK-mediated phosphorylation of tau and other cytoskeletal proteins may contribute to pathology. UniProt, PubMed

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 45.2 High
Spleen 38.1 High
Lung 25.3 Medium
Brain 18.7 Medium
Liver 12.4 Low
Cell Line Expression
Cell Line nTPM Notes
HeLa 30.5 Cervical cancer cell line
MCF7 22.8 Breast cancer cell line
A549 19.2 Lung cancer cell line
HEK293 15.6 Embryonic kidney cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1234C>T (p.Arg412Trp) Missense <0.01% Unknown functional impact
c.567_568insA Frameshift <0.01% Predicted loss of function
c.890A>G (p.Glu297Gly) Missense <0.01% Altered kinase activity
Mutation functional classification

Loss of Function (LOF)

Frameshift and nonsense mutations are predicted to result in truncated or absent protein, leading to loss of kinase activity.

Gain of Function (GOF)

Missense mutations in the kinase domain may enhance catalytic activity, potentially promoting oncogenic signaling.

Dominant Negative (DN)

No dominant negative mutations have been reported for SLK.

Pathways

Rho GTPase signaling
Apoptosis signaling
Cytoskeletal regulation by Rho GTPases

Protein Summary

The SLK protein is a 1235-amino acid serine/threonine kinase with an N-terminal kinase domain and a C-terminal regulatory region. It localizes to focal adhesions and the actin cytoskeleton, where it phosphorylates substrates involved in cell adhesion and migration. SLK is activated by autophosphorylation and by upstream signals from Rho family GTPases. Its expression is regulated during cell cycle and stress conditions.

Related Products

Product name Cat.No. Species Gene ID
SLK Knockout HEK293 Cell Line EDJ-KQ1221 Human 9748 Details Get a Quote
SLK Knockout A-549 Cell Line EDJ-KQ21846 Human 9748 Details Get a Quote
SLK Knockout HCT 116 Cell Line EDJ-KQ21848 Human 9748 Details Get a Quote
SLK Knockout HeLa Cell Line EDJ-KQ21849 Human 9748 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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