PLCXD2
PI-PLC X domain-containing protein 2
Also known as: FLJ31579, PLCX2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q0VAA5
- Gene
- PLCXD2
- Ensembl
- ENSG00000240891
- Chromosome
- 3
- Canonical length
- 305 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Predicted to enable phosphoric diester hydrolase activity. Predicted to be involved in lipid catabolic process and signal transduction. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
305 residues, UniProt reviewed canonical sequence.
>Q0VAA5|PLCXD2
1 MLAVRKARRK LRMGTICSPN PSGTKTSSEV CNADWMASLP PHLHNLPLSN LAIPGSHDSF
61 SYWVDEKSPV GPDQTQAIKR LARISLVKKL MKKWSVTQNL TFREQLEAGI RYFDLRVSSK
121 PGDADQEIYF IHGLFGIKVW DGLMEIDSFL TQHPQEIIFL DFNHFYAMDE THHKCLVLRI
181 QEAFGNKLCP ACSVESLTLR TLWEKNCQVL IFYHCPFYKQ YPFLWPGKKI PAPWANTTSV
241 RKLILFLETT LSERASRGSF HVSQAILTPR VKTIARGLVG GLKNTLVHSN RWNSHGPSLL
301 SQERSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLCXD2 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)
- 0.32
- Highest tissue expression
- 14 nTPM
Expression across tissuesHPA
Tissue
- retina: 14 nTPM
- bone marrow: 4.4 nTPM
- cerebral cortex: 3.6 nTPM
- lymph node: 2.7 nTPM
- cerebellum: 2.6 nTPM
- duodenum: 2.6 nTPM
Single-cell type
- hepatocytes: 160 nCPM
- parietal cells: 156 nCPM
- cone photoreceptor cells: 60 nCPM
- nk-cells: 55 nCPM
- rod photoreceptor cells: 54 nCPM
- epididymal clear cells: 53 nCPM
Immune cell
- plasmacytoid DC: 3.8 nTPM
- gdT-cell: 1.8 nTPM
- MAIT T-cell: 1.8 nTPM
- memory CD8 T-cell: 1.8 nTPM
- NK-cell: 1.1 nTPM
- memory CD4 T-cell: 0.9 nTPM
Brain region
- cerebral cortex: 22 nTPM
- midbrain: 14 nTPM
- pons: 14 nTPM
- thalamus: 12 nTPM
- basal ganglia: 11 nTPM
- medulla oblongata: 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)
- 1.45
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.34
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PLCXD2 as an antibody target. Whether an autoantibody or antibody against PLCXD2 could matter depends on whether native PLCXD2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLCXD2 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 PLCXD2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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