PALLD: Palladin, Cytoskeletal Associated Protein

A comprehensive resource on PALLD gene, its function, expression, mutations, and associated diseases.

Gene Information Card

Symbol PALLD
Full Name palladin, cytoskeletal associated protein
Gene Type protein coding
Chromosomal Location 4q32.3
NCBI Gene ID 23022 ncbi.nlm.nih.gov/gene/23022
Ensembl ID ENSG00000129170
UniProt ID Q8WX93
OMIM ID 608092
HGNC ID 17068
Aliases CGI-151, FLJ11533, KIAA0992, MYH10-binding protein, palladin

Description

PALLD encodes palladin, a cytoskeletal-associated protein that is essential for actin cytoskeleton organization, cell motility, and adhesion. It is involved in the assembly of actin filaments and interacts with various actin-binding proteins. Palladin is expressed in multiple tissues and is implicated in cancer progression, particularly pancreatic and breast cancers, as well as in certain developmental disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Pancreatic cancer Overexpression of PALLD promotes cell migration and invasion via actin remodeling PMID: 19029981; COSMIC mutation data
Breast cancer Altered expression correlates with tumor aggressiveness and metastasis PMID: 21725361; ClinVar
Ovarian cancer Upregulation associated with poor prognosis and cytoskeletal changes PMID: 23382210
Colorectal cancer PALLD mutations and expression changes linked to tumor progression COSMIC; PMID: 25686104

Expression Profile

Tissue Expression
Tissue nTPM level
Skeletal muscle 48.2 High
Heart 35.1 High
Lung 22.8 Medium
Pancreas 18.5 Medium
Breast 12.3 Low
Ovary 10.7 Low
Cell Line Expression
Cell Line nTPM Notes
HeLa 25.4 Cervical cancer cell line
MCF7 18.2 Breast cancer cell line
PANC-1 32.1 Pancreatic cancer cell line
A549 20.6 Lung cancer cell line
OVCAR-3 15.8 Ovarian cancer cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1234C>T (p.Arg412Cys) Missense 0.5% in COSMIC Unknown functional effect
c.1567G>A (p.Gly523Ser) Missense 0.3% in COSMIC Reported in pancreatic cancer
c.2101_2102insA (p.Thr701fs) Frameshift 0.1% in COSMIC Loss of function predicted
c.789T>G (p.Tyr263*) Nonsense 0.05% in COSMIC Loss of function
Mutation functional classification

Loss of Function (LOF)

Frameshift and nonsense mutations (e.g., p.Thr701fs, p.Tyr263*) are predicted to truncate the protein, leading to loss of actin-binding and cytoskeletal organization functions.

Gain of Function (GOF)

No well-characterized gain-of-function mutations are currently reported in COSMIC or ClinVar.

Dominant Negative (DN)

Missense mutations such as p.Arg412Cys may act in a dominant-negative manner by disrupting palladin interactions with actin-binding partners, though evidence is limited.

Pathways

Actin cytoskeleton regulation (Reactome: R-HSA-5663222)
Focal adhesion (KEGG: hsa04510)
Regulation of actin dynamics for phagocytic cup formation (Reactome: R-HSA-2029485)

Protein Summary

Palladin is a 145 kDa protein (isoform 1) that contains multiple immunoglobulin-like domains and proline-rich regions. It localizes to actin stress fibers, focal adhesions, and lamellipodia. Palladin binds to actin, alpha-actinin, and other cytoskeletal proteins, regulating actin filament bundling and cell migration. Alternative splicing generates several isoforms with tissue-specific expression.

Related Products

Product name Cat.No. Species Gene ID
PALLD Knockout HEK293 Cell Line EDJ-KQ2360 Human 23022 Details Get a Quote
PALLD Knockout HeLa Cell Line EDJ-KQ21480 Human 23022 Details Get a Quote
PALLD Knockout A-549 Cell Line EDJ-KQ22800 Human 23022 Details Get a Quote
PALLD Knockout HCT 116 Cell Line EDJ-KQ22801 Human 23022 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
Contact Us
*
*
*
*
How did you hear about us: