SCUBA

HSPA9 — Heat shock protein family A (Hsp70) member 9

HSPA9 belongs to a gene co-expression module in 6 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

HSPA9's module in each cell type

Cell typeModuleShares the module with
CD19⁺ B cellsHeat shock chaperones
Stress
AHSA1, CACYBP, FKBP4, HSP90AB1, HSPA8, HSPD1, HSPE1, STIP1 +1 moreView in SCUBA
CD8⁺ T cellsPre-mRNA Splicing
RNA processing & translation
BRD2, EIF3A, FUS, HNRNPU, NCL, PNN, RBM25, RBM39 +5 moreView in SCUBA
Gamma-delta T cellshnRNP Splicing Complex
RNA processing & translation
ASXL1, DDX21, HNRNPA1, HNRNPC, HNRNPH3, NOP58, PABPC1, PAPOLA +5 more
Innate lymphoid cellsmRNA Stability & Splicing
RNA processing & translation
BUD31, EIF4G2, GNAI3, PABPC1, PABPC4, PAIP2, PAPOLA, PRKAR1A +6 moreView in SCUBA
MacrophagesUbiquitin-ERAD Proteostasis
Housekeeping
GSPT1, ITCH, MAPK1IP1L, PANK3, PJA2, SEL1L, TOR1AIP2, USP39 +1 moreView in SCUBA
Mucosal-associated invariant T cellTranscription Factor Activity
DNA/chromatin regulation
AKAP17A, BTAF1, HNRNPH1, IKZF5, LCOR, NDEL1, POLR2M, SDE2 +3 more

About the gene

SynonymsGRP75, HSPA9B, mot-2, mthsp75, PBP74
Chromosome5: 138553756-138575675
Predicted locationIntracellular
Essential geneYes
Protein classDisease related genes, Essential proteins, Human disease related genes, Plasma proteins, Predicted intracellular proteins
Molecular functionChaperone, Hydrolase

Function

Mitochondrial chaperone that plays a key role in mitochondrial protein import, folding, and assembly. Plays an essential role in the protein quality control system, the correct folding of proteins, the re-folding of misfolded proteins, and the targeting of proteins for subsequent degradation. These processes are achieved through cycles of ATP binding, ATP hydrolysis, and ADP release, mediated by co-chaperones. In mitochondria, it associates with the TIM (translocase of the inner membrane) protein complex to assist in the import and folding of mitochondrial proteins (By similarity). Plays an important role in mitochondrial iron-sulfur cluster (ISC) biogenesis, interacts with and stabilizes ISC cluster assembly proteins FXN, NFU1, NFS1 and ISCU. Regulates erythropoiesis via stabilization of ISC assembly. Regulates mitochondrial calcium-dependent apoptosis by coupling two calcium channels, ITPR1 and VDAC1, at the mitochondria- associated endoplasmic reticulum (ER) membrane to facilitate calcium transport from the ER lumen to the mitochondria intermembrane space, providing calcium for the downstream calcium channel MCU, which releases it into the mitochondrial matrix (By similarity). Although primarily located in the mitochondria, it is also found in other cellular compartments. In the cytosol, it associates with proteins involved in signaling, apoptosis, or senescence. It may play a role in cell cycle regulation via its interaction with and promotion of degradation of TP53. May play a role in the control of cell proliferation and cellular aging (By similarity). Protects against reactive oxygen species (ROS) (By similarity). Extracellular HSPA9 plays a cytoprotective role by preventing cell lysis following immune attack by the membrane attack complex by disrupting formation of the complex.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.