PLAGL2
Zinc finger protein PLAGL2
Also known as: PLAL2_HUMAN, ZNF900
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UPG8
- Gene
- PLAGL2
- Ensembl
- ENSG00000126003
- Chromosome
- 20
- Canonical length
- 496 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Pleiomorphic adenoma gene-like 2 is a zinc-finger protein that recognizes DNA and/or RNA. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
496 residues, UniProt reviewed canonical sequence.
>Q9UPG8|PLAGL2
1 MTTFFTSVPP WIQDAKQEEE VGWKLVPRPR GREAESQVKC QCEISGTPFS NGEKLRPHSL
61 PQPEQRPYSC PQLHCGKAFA SKYKLYRHMA THSAQKPHQC MYCDKMFHRK DHLRNHLQTH
121 DPNKEALHCS ECGKNYNTKL GYRRHLAMHA ASSGDLSCKV CLQTFESTQA LLEHLKAHSR
181 RVAGGAKEKK HPCDHCDRRF YTRKDVRRHL VVHTGRKDFL CQYCAQRFGR KDHLTRHVKK
241 SHSQELLKIK TEPVDMLGLL SCSSTVSVKE ELSPVLCMAS RDVMGTKAFP GMLPMGMYGA
301 HIPTMPSTGV PHSLVHNTLP MGMSYPLESS PISSPAQLPP KYQLGSTSYL PDKLPKVEVD
361 SFLAELPGSL SLSSAEPQPA SPQPAAAAAL LDEALLAKSP ANLSEALCAA NVDFSHLLGF
421 LPLNLPPCNP PGATGGLVMG YSQAEAQPLL TTLQAQPQDS PGAGGPLNFG PLHSLPPVFT
481 SGLSSTTLPR FHQAFQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLAGL2 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)
- 0.6
- Highest tissue expression
- 30 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 30 nTPM
- testis: 16 nTPM
- esophagus: 13 nTPM
- small intestine: 12 nTPM
- retina: 12 nTPM
- tonsil: 10 nTPM
Single-cell type
- late spermatids: 265 nCPM
- early spermatids: 62 nCPM
- endometrial glandular cells: 59 nCPM
- esophageal apical cells: 53 nCPM
- endometrial luminal cells: 53 nCPM
- neutrophil progenitors: 42 nCPM
Immune cell
- non-classical monocyte: 35 nTPM
- intermediate monocyte: 18 nTPM
- classical monocyte: 3.6 nTPM
- total PBMC: 2.5 nTPM
- basophil: 2.2 nTPM
- myeloid DC: 2.2 nTPM
Brain region
- choroid plexus: 15 nTPM
- basal ganglia: 10 nTPM
- hippocampal formation: 9.6 nTPM
- cerebellum: 9.5 nTPM
- cerebral cortex: 9 nTPM
- medulla oblongata: 8.4 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)
- 0.24
- gnomAD pLI
- 0.98
- gnomAD missense Z
- 2.11
- DepMap mean gene effect
- -0.17
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 13% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chylomicron assembly
- lipid metabolic process
- positive regulation of intrinsic apoptotic signaling pathway
- post-embryonic development
- regulation of transcription by RNA polymerase II
Molecular functions
- DNA-binding transcription activator activity, RNA polymerase II-specific
- DNA-binding transcription factor activity
- DNA-binding transcription factor activity, RNA polymerase II-specific
- sequence-specific DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PLAGL2 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 PLAGL2 as an antibody target. Whether an autoantibody or antibody against PLAGL2 could matter depends on whether native PLAGL2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLAGL2 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 PLAGL2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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