HSPA12A
Heat shock 70 kDa protein 12A
Also known as: FLJ13874, HS12A_HUMAN, KIAA0417
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43301
- Gene
- HSPA12A
- Ensembl
- ENSG00000165868
- Chromosome
- 10
- Canonical length
- 675 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Golgi apparatus,Cytosol
OverviewNCBI Gene
Predicted to enable ATP binding activity. Predicted to act upstream of or within several processes, including import into nucleus; liver development; and macrophage activation. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
675 residues, UniProt reviewed canonical sequence.
>O43301|HSPA12A
1 MADKEAGGSD GPRETAPTSA YSSPARSLGD TGITPLSPSH IVNDTDSNVS EQQSFLVVVA
61 VDFGTTSSGY AYSFTKEPEC IHVMRRWEGG DPGVSNQKTP TTILLTPERK FHSFGYAARD
121 FYHDLDPNEA KQWLYLEKFK MKLHTTGDLT MDTDLTAANG KKVKALEIFA YALQYFKEQA
181 LKELSDQAGS EFENSDVRWV ITVPAIWKQP AKQFMRQAAY QAGLASPENS EQLIIALEPE
241 AASIYCRKLR LHQMIELSSK AAVNGYSGSD TVGAGFTQAK EHIRRNRQSR TFLVENVIGE
301 IWSELEEGDK YVVVDSGGGT VDLTVHQIRL PEGHLKELYK ATGGPYGSLG VDYEFEKLLY
361 KIFGEDFIEQ FKIKRPAAWV DLMIAFESRK RAAAPDRTNP LNITLPFSFI DYYKKFRGHS
421 VEHALRKSNV DFVKWSSQGM LRMSPDAMNA LFKPTIDSII EHLRDLFQKP EVSTVKFLFL
481 VGGFAEAPLL QQAVQAAFGD QCRIIIPQDV GLTILKGAVL FGLDPAVIKV RRSPLTYGVG
541 VLNRYVEGKH PPEKLLVKDG TRWCTDVFDK FISADQSVAL GELVKRSYTP AKPSQLVIVI
601 NIYSSEHDNV SFITDPGVKK CGTLRLDLTG TSGTAVPARR EIQTLMQFGD TEIKATAIDI
661 ATSKSVKVGI DFLNYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HSPA12A can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.26
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 27 nTPM
- parathyroid gland: 19 nTPM
- epididymis: 12 nTPM
- adipose tissue: 11 nTPM
- retina: 10 nTPM
- ovary: 9.7 nTPM
Single-cell type
- choroid plexus epithelial cells: 370 nCPM
- podocytes: 323 nCPM
- schwann cells: 318 nCPM
- retinal ganglion cells: 313 nCPM
- brain excitatory neurons: 240 nCPM
- brain inhibitory neurons: 225 nCPM
Immune cell
- naive B-cell: 1.8 nTPM
- memory B-cell: 1.4 nTPM
- T-reg: 1 nTPM
- total PBMC: 0.2 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
Brain region
- cerebral cortex: 96 nTPM
- thalamus: 89 nTPM
- medulla oblongata: 75 nTPM
- pons: 71 nTPM
- white matter: 67 nTPM
- hippocampal formation: 67 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.3
- gnomAD pLI
- 0.98
- gnomAD missense Z
- 2.12
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- ATPase, nucleotide binding domain
- Heat shock 70kDa protein 12A, nucleotide-binding domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HSPA12A in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HSPA12A as an antibody target. Whether an autoantibody or antibody against HSPA12A could matter depends on whether native HSPA12A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HSPA12A is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label HSPA12A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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