HSPA12B
Heat shock 70 kDa protein 12B
Also known as: C20orf60, dJ1009E24.2, HS12B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96MM6
- Gene
- HSPA12B
- Ensembl
- ENSG00000132622
- Chromosome
- 20
- Canonical length
- 686 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
The protein encoded by this gene contains an atypical heat shock protein 70 (Hsp70) ATPase domain and is therefore a distant member of the mammalian Hsp70 family. This gene may be involved in susceptibility to atherosclerosis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]
Canonical amino-acid sequenceUniProt
686 residues, UniProt reviewed canonical sequence.
>Q96MM6|HSPA12B
1 MLAVPEMGLQ GLYIGSSPER SPVPSPPGSP RTQESCGIAP LTPSQSPKPE VRAPQQASFS
61 VVVAIDFGTT SSGYAFSFAS DPEAIHMMRK WEGGDPGVAH QKTPTCLLLT PEGAFHSFGY
121 TARDYYHDLD PEEARDWLYF EKFKMKIHSA TDLTLKTQLE AVNGKTMPAL EVFAHALRFF
181 REHALQELRE QSPSLPEKDT VRWVLTVPAI WKQPAKQFMR EAAYLAGLVS RENAEQLLIA
241 LEPEAASVYC RKLRLHQLLD LSGRAPGGGR LGERRSIDSS FRQAREQLRR SRHSRTFLVE
301 SGVGELWAEM QAGDRYVVAD CGGGTVDLTV HQLEQPHGTL KELYKASGGP YGAVGVDLAF
361 EQLLCRIFGE DFIATFKRQR PAAWVDLTIA FEARKRTAGP HRAGALNISL PFSFIDFYRK
421 QRGHNVETAL RRSSVNFVKW SSQGMLRMSC EAMNELFQPT VSGIIQHIEA LLARPEVQGV
481 KLLFLVGGFA ESAVLQHAVQ AALGARGLRV VVPHDVGLTI LKGAVLFGQA PGVVRVRRSP
541 LTYGVGVLNR FVPGRHPPEK LLVRDGRRWC TDVFERFVAA EQSVALGEEV RRSYCPARPG
601 QRRVLINLYC CAAEDARFIT DPGVRKCGAL SLELEPADCG QDTAGAPPGR REIRAAMQFG
661 DTEIKVTAVD VSTNRSVRAS IDFLSNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HSPA12B 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 29 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 29 nTPM
- spleen: 24 nTPM
- adipose tissue: 22 nTPM
- breast: 22 nTPM
- lung: 20 nTPM
- cervix: 15 nTPM
Single-cell type
- vascular endothelial cells: 49 nCPM
- lymphatic endothelial cells: 37 nCPM
- late spermatids: 32 nCPM
- fibro-adipogenic progenitors: 15 nCPM
- peritubular myoid cells: 14 nCPM
- late primary spermatocytes: 11 nCPM
Immune cell
- non-classical monocyte: 0.8 nTPM
- intermediate monocyte: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- thalamus: 16 nTPM
- amygdala: 13 nTPM
- basal ganglia: 13 nTPM
- pons: 11 nTPM
- medulla oblongata: 10 nTPM
- midbrain: 10 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)
- 0.62
- gnomAD pLI
- 0
- gnomAD missense Z
- 2.27
- DepMap mean gene effect
- -0.04
- 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
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HSPA12B 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 HSPA12B as an antibody target. Whether an autoantibody or antibody against HSPA12B could matter depends on whether native HSPA12B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HSPA12B 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 HSPA12B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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