HSPA1B (Heat Shock Protein Family A (Hsp70) Member 1B)

A stress-inducible molecular chaperone involved in protein folding, cytoprotection, and immune modulation; implicated in autoimmune and neurodegenerative diseases.

Gene Information Card

Symbol HSPA1B
Full Name Heat Shock Protein Family A (Hsp70) Member 1B
Gene Type protein-coding
Chromosomal Location 6p21.33 (GRCh38)
NCBI Gene ID 3304 ncbi.nlm.nih.gov/gene/3304
Ensembl ID ENSG00000204388
UniProt ID P0DMV9
OMIM ID 603012
HGNC ID 5233
Aliases HSP70-2, HSP70.2, HSPA1A, HSP70-1B

Description

HSPA1B encodes a 70 kDa heat shock protein that is strongly induced by cellular stress (e.g., heat, oxidative stress, inflammation). As a molecular chaperone, it assists in protein folding, prevents aggregation of denatured proteins, and facilitates protein transport and degradation. It also plays roles in immune responses and cytoprotection. HSPA1B is part of the highly homologous HSPA1A/HSPA1B pair located in the major histocompatibility complex (MHC) class III region.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Rheumatoid Arthritis HSPA1B polymorphisms (e.g., +1267 A/G) may influence susceptibility and severity, possibly via altered chaperone function and immune modulation. Association studies; PMID: 10984555
Type 1 Diabetes Variants in HSPA1B have been linked to risk, potentially through effects on antigen presentation and autoimmune response. Genetic association; PMID: 15199473
Alzheimer's Disease HSPA1B expression is altered in affected brains; chaperone dysfunction may contribute to protein aggregation pathology. Expression studies; PMID: 16936722
Parkinson's Disease HSPA1B may modulate alpha-synuclein toxicity; polymorphisms could affect disease risk. Functional studies; PMID: 20624804

Expression Profile

Tissue Expression
Tissue nTPM level
Liver 12.3 Medium
Kidney 10.1 Medium
Heart 8.5 Low
Brain 6.2 Low
Testis 15.7 High
Cell Line Expression
Cell Line nTPM Notes
HeLa 18.4 High baseline; induced by heat shock
A549 12.0 Moderate; inducible
MCF7 9.8 Moderate
K562 7.5 Low
HepG2 14.2 High
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
rs1061581 (A/G) SNP ~40% (G allele) Associated with altered HSP70 expression and disease susceptibility
rs539689 (C/T) SNP ~30% (T allele) May affect promoter activity and stress response
rs2227956 (A/G) SNP ~20% (G allele) Coding variant (Met493Thr) with potential functional impact
Mutation functional classification

Loss of Function (LOF)

Rare loss-of-function mutations are not well documented; complete knockout in mice is viable but shows impaired stress tolerance.

Gain of Function (GOF)

No clear gain-of-function mutations reported; overexpression is generally protective.

Dominant Negative (DN)

No dominant-negative variants described in human disease.

Gene Ontology (GO)

• ATP binding • ATP hydrolysis activity
• chaperone binding • protein folding
• response to heat • cellular response to unfolded protein
• protein refolding • ubiquitin-dependent protein catabolic process

Pathways

• Protein processing in endoplasmic reticulum (KEGG hsa04141)
• Antigen processing and presentation (KEGG hsa04612)
• MAPK signaling pathway (KEGG hsa04010)
• Heat shock response (Reactome R-HSA-3371568)

Protein Summary

HSPA1B is a 70 kDa heat shock protein that functions as an ATP-dependent molecular chaperone. It binds to exposed hydrophobic patches of unfolded or misfolded proteins, promoting proper folding and preventing aggregation. It also participates in the degradation of irreversibly damaged proteins via the ubiquitin-proteasome system. In addition to its chaperone role, HSPA1B modulates immune responses by influencing antigen presentation and cytokine production. Its expression is low under normal conditions but rapidly induced upon stress, making it a key cytoprotective factor.

Related Products

Product name Cat.No. Species Gene ID
HSPA1B Knockout HEK293 Cell Line EDJ-KQ50367 Human 3304 Details Get a Quote
HSPA1B Knockout HeLa Cell Line EDJ-KQ53580 Human 3304 Details Get a Quote
HSPA1B Knockout A-549 Cell Line EDJ-KQ62047 Human 3304 Details Get a Quote
HSPA1B Knockout HCT 116 Cell Line EDJ-KQ70528 Human 3304 Details Get a Quote
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