PIERCE1
Piercer of microtubule wall 1 protein
Also known as: C9orf116, MGC29761, PIRC1_HUMAN, RbEST47
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5BN46
- Gene
- PIERCE1
- Ensembl
- ENSG00000160345
- Chromosome
- 9
- Canonical length
- 136 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol,Mid piece
OverviewNCBI Gene
Predicted to be involved in axoneme assembly; establishment of left/right asymmetry; and flagellated sperm motility. Predicted to act upstream of or within DNA damage response; cellular response to UV-C; and regulation of gene expression. Located in axonemal microtubule. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
136 residues, UniProt reviewed canonical sequence.
>Q5BN46|PIERCE1
1 MAEECPRACA EPVAPKATAP PERTSDYYRV SADLPGRFNN PGWFRGYRTQ KAVSVYRTSN
61 QAYGSRAPTV HEMPKVFYPN SNKFSQQLAA GGMFRNNTLN VYLEKSIVTG PDNCITSCDR
121 LNFHPSYNIN RPSICDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PIERCE1 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)
- 0.57
- Highest tissue expression
- 91 nTPM
Expression across tissuesHPA
Tissue
- fallopian tube: 91 nTPM
- testis: 60 nTPM
- choroid plexus: 58 nTPM
- epididymis: 24 nTPM
- hippocampal formation: 20 nTPM
- hypothalamus: 20 nTPM
Single-cell type
- fallopian tube ciliated cells: 828 nCPM
- epididymal efferent duct ciliated cells: 811 nCPM
- respiratory ciliated cells: 792 nCPM
- late spermatids: 686 nCPM
- late primary spermatocytes: 533 nCPM
- endometrial ciliated cells: 451 nCPM
Immune cell
- MAIT T-cell: 1.2 nTPM
- classical monocyte: 0.8 nTPM
- naive CD4 T-cell: 0.7 nTPM
- NK-cell: 0.6 nTPM
- gdT-cell: 0.5 nTPM
- intermediate monocyte: 0.5 nTPM
Brain region
- choroid plexus: 37 nTPM
- midbrain: 27 nTPM
- medulla oblongata: 19 nTPM
- spinal cord: 18 nTPM
- hypothalamus: 15 nTPM
- hippocampal formation: 15 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)
- 1.93
- gnomAD pLI
- 0
- DepMap mean gene effect
- 0.1
- 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
- axoneme assembly
- cellular response to UV-C
- cilium movement
- determination of left/right symmetry
- DNA damage response
- establishment of left/right asymmetry
- flagellated sperm motility
- regulation of gene expression
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PIERCE1 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 PIERCE1 as an antibody target. Whether an autoantibody or antibody against PIERCE1 could matter depends on whether native PIERCE1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PIERCE1 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 PIERCE1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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