HomeAboutRankingsData Sources
© 2026 GeneE
🧬
GeneE
10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
ⓘGeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
ARPC5L
actin related protein 2/3 complex subunit 5 like
Chromosome 9 · 9q33.3
NCBI Gene: 81873Ensembl: ENSG00000136950.14HGNC: HGNC:23366UniProt: A0A024R897
82PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
focal adhesionextracellular exosomeArp2/3 complex-mediated actin nucleationprotein bindingneurodegenerative diseaseAlzheimer diseasemultiple sclerosisParkinson disease
✦AI Summary

ARPC5L is a subunit of the Arp2/3 complex, a seven-protein assembly that nucleates branched actin filament networks 1. As a component of this complex, ARPC5L participates in actin polymerization regulation essential for cellular processes including cell migration, immune responses, and mechanotransduction. ARPC5L exists as an isoform of ARPC5 (67% identical) 2, and these paralogs have distinct functional roles. ARPC5L-containing complexes demonstrate superior actin assembly kinetics and slower filament disassembly compared to ARPC5-containing complexes 1, with structural differences in the N-terminal region contributing to this enhanced activity 3. In CD4 T cells, ARPC5L specifically drives nuclear actin polymerization upon T cell receptor activation 4. ARPC5L functions in macrophage migration and bacterial restriction 5, and its expression promotes single-cell migration in breast cancer models when combined with PI 3-kinase activation 6. ARPC5L also mediates cellular stiffness sensing through talin 1 interactions, contributing to tissue mechanical homeostasis 7. Unlike ARPC5, which shows non-redundant roles in development and immune function 2, ARPC5L functions as a specialized isoform for specific physiological contexts requiring enhanced actin nucleation capacity.

Sources cited
1
ARPC5L is an isoform of ARPC5 in mammalian Arp2/3 complexes; ARPC5L-containing complexes promote actin assembly better and have slower filament disassembly
PMID: 26655834
2
ARPC5 and ARPC5L are two paralogous genes with 67% identity encoding Arp2/3 complex subunits; ARPC5 but not ARPC5L has non-redundant roles in development and immunity
PMID: 37382373
3
ARPC5L-containing Arp2/3 complexes have a partially disordered N-terminal region contributing to higher nucleation activity compared to ARPC5-containing complexes
PMID: 32661131
4
ARPC5L specifically drives nuclear actin polymerization in CD4 T cells upon T cell receptor activation
PMID: 37162507
5
ARPC5L-containing Arp2/3 complexes are not essential for macrophage-dependent immune homeostasis, unlike ARPC5-containing complexes
PMID: 41231985
6
ARPC5L expression is induced by combined PI 3-kinase activation and KMT2D inactivation and promotes Arp2/3-dependent single-cell migration
PMID: 38786098
7
ARPC5L mediates cellular stiffness sensing through talin 1 interactions and contributes to tissue mechanical homeostasis
PMID: 39167642
8
ARPC5L is a subunit of the actin-related Arp2/3 complex involved in cell migration and adhesion
PMID: 24615350
Disease Associationsⓘ20
neurodegenerative diseaseOpen Targets
0.51Moderate
Alzheimer diseaseOpen Targets
0.35Weak
lysosomal storage diseaseOpen Targets
0.35Weak
multiple sclerosisOpen Targets
0.35Weak
Parkinson diseaseOpen Targets
0.35Weak
PainOpen Targets
0.22Weak
Chest painOpen Targets
0.21Weak
celiac diseaseOpen Targets
0.10Suggestive
Griscelli diseaseOpen Targets
0.07Suggestive
Griscelli disease type 3Open Targets
0.06Suggestive
Griscelli syndrome type 3Open Targets
0.06Suggestive
Ataxia - oculomotor apraxia type 1Open Targets
0.06Suggestive
Piebald trait - neurologic defectsOpen Targets
0.05Suggestive
piebald trait-neurologic defects syndromeOpen Targets
0.05Suggestive
uncombable hair syndromeOpen Targets
0.05Suggestive
Benign familial choreaOpen Targets
0.05Suggestive
oculocutaneous albinism type 3Open Targets
0.05Suggestive
Ascher syndromeOpen Targets
0.04Suggestive
Griscelli disease type 1Open Targets
0.04Suggestive
Griscelli syndrome type 1Open Targets
0.04Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
ACTBProtein interaction98%ACTR3CProtein interaction97%ACTG1Protein interaction96%HCLS1Protein interaction96%WASProtein interaction96%WASF1Protein interaction96%
Tissue Expression6 tissues
Bone Marrow
100%
Brain
57%
Liver
48%
Lung
46%
Heart
39%
Ovary
15%
Gene Interaction Network
Click a node to explore
ARPC5LACTBACTR3CACTG1HCLS1WASWASF1
PROTEIN STRUCTURE
Preparing viewer…
PDB9I2B · 3.00 Å · EM
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
0.61LoF Tolerant
pLIⓘ
0.87Intermediate
Observed/Expected LoF0.27 [0.13–0.61]
RankingsWhere ARPC5L stands among ~20K protein-coding genes
  • #5,773of 20,598
    Most Researched82
  • #4,211of 17,882
    Most Constrained (LOEUF)0.61 · top quartile
Genes detectedARPC5L
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Branched actin networks mediate macrophage-dependent host-microbiota homeostasis.
PMID: 41231985
Science · 2025
1.00
2
ARPC5 deficiency leads to severe early-onset systemic inflammation and mortality.
PMID: 37382373
Dis Model Mech · 2023
0.90
3
ARPC5 isoforms and their regulation by calcium-calmodulin-N-WASP drive distinct Arp2/3-dependent actin remodeling events in CD4 T cells.
PMID: 37162507
Elife · 2023
0.80
4
Isoform diversity in the Arp2/3 complex determines actin filament dynamics.
PMID: 26655834
Nat Cell Biol · 2016
0.70
5
Cryo-EM of human Arp2/3 complexes provides structural insights into actin nucleation modulation by ARPC5 isoforms.
PMID: 32661131
Biol Open · 2020
0.60