PLAC1
Placenta-specific protein 1
Also known as: CT92, OOSP2B, OOSP2L, PLAC1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9HBJ0
- Gene
- PLAC1
- Ensembl
- ENSG00000170965
- Chromosome
- X
- Canonical length
- 212 aa
- Protein class
- Predicted secreted proteins
- Subcellular location
- Vesicles,Cytosol
- Secretome location
- Secreted in female reproductive system
OverviewNCBI Gene
Involved in placenta development. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
212 residues, UniProt reviewed canonical sequence.
>Q9HBJ0|PLAC1
1 MKVFKFIGLM ILLTSAFSAG SGQSPMTVLC SIDWFMVTVH PFMLNNDVCV HFHELHLGLG
61 CPPNHVQPHA YQFTYRVTEC GIRAKAVSQD MVIYSTEIHY SSKGTPSKFV IPVSCAAPQK
121 SPWLTKPCSM RVASKSRATA QKDEKCYEVF SLSQSSQRPN CDCPPCVFSE EEHTQVPCHQ
181 AGAQEAQPLQ PSHFLDISED WSLHTDDMIG SMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLAC1 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.51
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- placenta: 26 nTPM
- testis: 0.9 nTPM
- ovary: 0.3 nTPM
- fallopian tube: 0.2 nTPM
- skin: 0.2 nTPM
- breast: 0.1 nTPM
Single-cell type
- fibroblasts: 25 nCPM
- early primary spermatocytes: 23 nCPM
- syncytiotrophoblasts: 18 nCPM
- differentiating spermatogonia: 13 nCPM
- peritubular myoid cells: 13 nCPM
- adrenal medulla cells: 11 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 0.3 nTPM
- cerebral cortex: 0.2 nTPM
- amygdala: 0.1 nTPM
- basal ganglia: 0.1 nTPM
- cerebellum: 0.1 nTPM
- hippocampal formation: 0.1 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PLAC1.
Disease | ImmuneIEDB
Conditions an epitope on PLAC1 was assayed in.
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 missense Z
- 0.26
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PLAC1 as an antibody target. Whether an autoantibody or antibody against PLAC1 could matter depends on whether native PLAC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLAC1 is annotated as secreted, so native PLAC1 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label PLAC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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