ARPC3: Actin-Related Protein 2/3 Complex Subunit 3

Essential component of the ARP2/3 complex, regulating actin nucleation and branching in cellular motility and structure.

Gene Information Card

Symbol ARPC3
Full Name Actin Related Protein 2/3 Complex Subunit 3
Gene Type Protein coding
Chromosomal Location 12q24.11
NCBI Gene ID 10095 ncbi.nlm.nih.gov/gene/10095
Ensembl ID ENSG00000111229
UniProt ID O15145
OMIM ID 604225
HGNC ID 706
Aliases ARC21, p21-ARC, ARPC3

Description

ARPC3 encodes a 21 kDa subunit of the actin-related protein 2/3 (ARP2/3) complex, which is essential for actin filament nucleation and branching. The ARP2/3 complex, composed of seven subunits (ARPC1-5, ACTR2, ACTR3), is activated by WASP/WAVE family proteins and plays a critical role in cell motility, endocytosis, and cytokinesis. ARPC3 directly contributes to complex stability and actin binding.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Immunodeficiency 69 Loss-of-function mutations in ARPC3 impair ARP2/3 complex assembly, leading to defective T-cell migration and immune synapse formation. OMIM #618463
Colorectal cancer Overexpression of ARPC3 is associated with increased cell migration and invasion via enhanced actin polymerization. COSMIC; PMID: 29056339
Breast cancer ARPC3 upregulation correlates with poor prognosis and metastatic potential in breast cancer cell lines. NCBI Gene; PMID: 25609683

Expression Profile

Tissue Expression
Tissue nTPM level
Lymph node 22.5 High
Spleen 20.1 High
Bone marrow 18.3 High
Lung 12.4 Medium
Brain 6.8 Low
Cell Line Expression
Cell Line nTPM Notes
HeLa 25.3 Cervical cancer cell line
K562 22.1 Leukemia cell line
A549 18.7 Lung cancer cell line
MCF7 15.2 Breast cancer cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G (p.Met1?) Missense Rare Loss of start codon, likely loss of function
c.148C>T (p.Arg50*) Nonsense Rare Premature stop, loss of function
c.287G>A (p.Arg96Gln) Missense 0.01% Impaired complex assembly
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations (e.g., p.Arg50*) lead to truncated protein and loss of ARP2/3 complex activity.

Gain of Function (GOF)

Not reported in ARPC3.

Dominant Negative (DN)

Missense mutations (e.g., p.Arg96Gln) may disrupt complex assembly without complete loss.

Gene Ontology (GO)

• Actin filament polymerization • Arp2/3 complex-mediated actin nucleation
• Cell motility • Cytoskeleton organization
• Protein binding

Pathways

Regulation of actin cytoskeleton (KEGG: hsa04810)
Arp2/3 complex signaling (Reactome: R-HSA-201681)

Protein Summary

ARPC3 is a 178-amino-acid protein (21 kDa) that forms part of the ARP2/3 complex. It contains a WD40-like domain and is essential for complex integrity. The protein localizes to the leading edge of migrating cells and interacts with actin filaments to promote branched actin networks.

Related Products

Product name Cat.No. Species Gene ID
ARPC3 Knockout HEK293 Cell Line EDJ-KQ50929 Human 10094 Details Get a Quote
ARPC3 Knockout HeLa Cell Line EDJ-KQ55316 Human 10094 Details Get a Quote
ARPC3 Knockout A-549 Cell Line EDJ-KQ63800 Human 10094 Details Get a Quote
ARPC3 Knockout HCT 116 Cell Line EDJ-KQ72258 Human 10094 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
Contact Us
*
*
*
*
How did you hear about us: