HAPSTR1
HUWE1-associated protein modifying stress responses 1
Also known as: C16orf72, FLJ41272, HAPR1_HUMAN, PRO0149, TAPR1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q14CZ0
- Gene
- HAPSTR1
- Ensembl
- ENSG00000182831
- Chromosome
- 16
- Canonical length
- 275 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
- Quaternary structure
- Homooligomer
OverviewNCBI Gene
Enables ubiquitin protein ligase binding activity. Involved in negative regulation of signal transduction by p53 class mediator and regulation of cellular response to stress. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
275 residues, UniProt reviewed canonical sequence.
>Q14CZ0|HAPSTR1
1 MEERKEEGEA EIQEHGPEHW FSKWERQCLA EAEQDEQLPP ELQEEAAAAA QPEHKQQKLW
61 HLFQNSATAV AQLYKDRVCQ QPGLSLWVPF QNAATAVTNL YKESVDTHQR SFDIGIQIGY
121 QRRNKDVLAW VKKRRRTIRR EDLISFLCGK VPPPRNSRAP PRLTVVSPNR ATSTETSSSV
181 ETDLQPFREA IALHGLSGAM ASISVRSSTP GSPTHVSSGS NASRRRNGLH DVDLNTFISE
241 EMALHLDNGG TRKRTSAQCG DVITDSPTHK RNRMILocalizationUniProt · AlphaFold · HPA
Whether an antibody against HAPSTR1 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)
- 0.55
- Highest tissue expression
- 100 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 100 nTPM
- skeletal muscle: 30 nTPM
- tongue: 26 nTPM
- liver: 25 nTPM
- blood vessel: 21 nTPM
- parathyroid gland: 21 nTPM
Single-cell type
- late spermatids: 1,081 nCPM
- neutrophils: 370 nCPM
- early spermatids: 258 nCPM
- neutrophil progenitors: 102 nCPM
- esophageal apical cells: 99 nCPM
- monocytes: 94 nCPM
Immune cell
- neutrophil: 11 nTPM
- basophil: 5 nTPM
- MAIT T-cell: 4.1 nTPM
- gdT-cell: 3.6 nTPM
- naive CD4 T-cell: 3.4 nTPM
- non-classical monocyte: 3.3 nTPM
Brain region
- cerebral cortex: 73 nTPM
- basal ganglia: 67 nTPM
- hippocampal formation: 67 nTPM
- hypothalamus: 66 nTPM
- thalamus: 66 nTPM
- midbrain: 66 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)
- 0.29
- gnomAD pLI
- 0.98
- DepMap mean gene effect
- -0.38
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of signal transduction by p53 class mediator
- regulation of cellular response to stress
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HAPSTR1 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 HAPSTR1 as an antibody target. Whether an autoantibody or antibody against HAPSTR1 could matter depends on whether native HAPSTR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HAPSTR1 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 HAPSTR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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