PLEKHB2
Pleckstrin homology domain-containing family B member 2
Also known as: EVT2, FLJ20783, PKHB2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96CS7
- Gene
- PLEKHB2
- Ensembl
- ENSG00000115762
- Chromosome
- 2
- Canonical length
- 222 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Enables phosphatidylinositol-3,4,5-trisphosphate binding activity. Predicted to be involved in regulation of cell differentiation. Predicted to be located in recycling endosome membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
222 residues, UniProt reviewed canonical sequence.
>Q96CS7|PLEKHB2
1 MAFVKSGWLL RQSTILKRWK KNWFDLWSDG HLIYYDDQTR QNIEDKVHMP MDCINIRTGQ
61 ECRDTQPPDG KSKDCMLQIV CRDGKTISLC AESTDDCLAW KFTLQDSRTN TAYVGSAVMT
121 DETSVVSSPP PYTAYAAPAP EQAYGYGPYG GAYPPGTQVV YAANGQAYAV PYQYPYAGLY
181 GQQPANQVII RERYRDNDSD LALGMLAGAA TGMALGSLFW VFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLEKHB2 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.49
- Highest tissue expression
- 114 nTPM
Expression across tissuesHPA
Tissue
- kidney: 114 nTPM
- parathyroid gland: 87 nTPM
- retina: 82 nTPM
- cerebral cortex: 76 nTPM
- bone marrow: 65 nTPM
- rectum: 62 nTPM
Single-cell type
- parietal cells: 347 nCPM
- endometrial glandular cells: 331 nCPM
- endometrial luminal cells: 304 nCPM
- neutrophils: 242 nCPM
- epididymal clear cells: 235 nCPM
- monocytes: 219 nCPM
Immune cell
- non-classical monocyte: 79 nTPM
- intermediate monocyte: 71 nTPM
- classical monocyte: 56 nTPM
- myeloid DC: 54 nTPM
- total PBMC: 49 nTPM
- neutrophil: 34 nTPM
Brain region
- pons: 157 nTPM
- hypothalamus: 139 nTPM
- midbrain: 136 nTPM
- medulla oblongata: 122 nTPM
- white matter: 116 nTPM
- cerebellum: 112 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)
- 1.46
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.1
- DepMap mean gene effect
- 0
- 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
Molecular functions
- 5-trisphosphate binding
- phosphatidylinositol-3
- 4
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PLEKHB2 as an antibody target. Whether an autoantibody or antibody against PLEKHB2 could matter depends on whether native PLEKHB2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLEKHB2 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 PLEKHB2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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