ANP32A: Acidic Nuclear Phosphoprotein 32 Family Member A

A multifunctional regulator of gene expression, apoptosis, and tumor suppression, implicated in cancer and neurological disorders.

Gene Information Card

Symbol ANP32A
Full Name Acidic Nuclear Phosphoprotein 32 Family Member A
Gene Type Protein coding
Chromosomal Location 15q23
NCBI Gene ID 8125 ncbi.nlm.nih.gov/gene/8125
Ensembl ID ENSG00000140391
UniProt ID P39687
OMIM ID 600832
HGNC ID 558
Aliases PHAP1, I1PP2A, MAPM, C15orf1

Description

ANP32A encodes a member of the acidic nuclear phosphoprotein 32 family. This protein is involved in multiple cellular processes including regulation of gene expression, apoptosis, cell cycle control, and tumor suppression. It acts as a potent inhibitor of protein phosphatase 2A (PP2A) and also plays a role in the regulation of histone acetylation and chromatin remodeling. ANP32A has been implicated in various cancers and neurological conditions.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cancer (various types) Altered expression and mutations may disrupt apoptosis and cell cycle regulation, contributing to tumorigenesis. COSMIC, PubMed
Alzheimer's disease ANP32A may modulate tau phosphorylation via PP2A inhibition, affecting neurodegeneration. PubMed
Spinocerebellar ataxia Potential involvement in polyglutamine toxicity pathways. PubMed

Expression Profile

Tissue Expression
Tissue nTPM level
Brain High High expression in neuronal tissues
Testis Medium Moderate expression
Lung Low Low expression
Liver Low Low expression
Cell Line Expression
Cell Line nTPM Notes
HeLa High Cervical cancer cell line
A549 Medium Lung carcinoma cell line
MCF7 Medium Breast cancer cell line
HEK293 High Embryonic kidney cells
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.123A>G (p.I41M) Missense Rare Potential functional impact on protein stability
c.456C>T (p.S152F) Missense Rare May affect PP2A binding
c.789delC Frameshift Very rare Loss of function
Mutation functional classification

Loss of Function (LOF)

Frameshift and truncating mutations may lead to loss of tumor suppressor activity.

Gain of Function (GOF)

Some missense mutations may enhance oncogenic properties, though not well characterized.

Dominant Negative (DN)

Not clearly established; further research needed.

Gene Ontology (GO)

• protein phosphatase inhibitor activity • histone binding
• chromatin binding • protein binding
• nucleus • cytoplasm
• regulation of apoptotic process • negative regulation of cell cycle

Pathways

• Apoptosis
• Cell cycle
• PP2A signaling
• Chromatin remodeling

Protein Summary

ANP32A is a 249-amino acid protein with an N-terminal leucine-rich repeat domain and a C-terminal acidic region. It is predominantly nuclear and functions as a tumor suppressor by inhibiting PP2A and regulating gene expression. It also interacts with histone acetyltransferases and deacetylases, influencing chromatin structure. Its expression is ubiquitous but highest in brain and testis. Mutations and altered expression are linked to cancer and neurodegenerative diseases.

Related Products

Product name Cat.No. Species Gene ID
ANP32A Knockout HEK293 Cell Line EDJ-KQ6175 Human 8125 Details Get a Quote
ANP32A Knockout A-549 Cell Line EDJ-KQ29996 Human 8125 Details Get a Quote
ANP32A Knockout HCT 116 Cell Line EDJ-KQ29997 Human 8125 Details Get a Quote
ANP32A Knockout HeLa Cell Line EDJ-KQ29998 Human 8125 Details Get a Quote
ANP32A Knockout MDCK Cell Line EDJ-KZ541 Dog 403534 Details Get a Quote
Contact Us
*
*
*
How did you hear about us: