PLEKHF2
Pleckstrin homology domain-containing family F member 2
Also known as: FLJ13187, PHAFIN2, PKHF2_HUMAN, ZFYVE18
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H8W4
- Gene
- PLEKHF2
- Ensembl
- ENSG00000175895
- Chromosome
- 8
- Canonical length
- 249 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable phosphatidylinositol binding activity. Predicted to be involved in endosome organization and endosome to lysosome transport. Located in transport vesicle. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
249 residues, UniProt reviewed canonical sequence.
>Q9H8W4|PLEKHF2
1 MVDRLANSEA NTRRISIVEN CFGAAGQPLT IPGRVLIGEG VLTKLCRKKP KARQFFLFND
61 ILVYGNIVIQ KKKYNKQHII PLENVTIDSI KDEGDLRNGW LIKTPTKSFA VYAATATEKS
121 EWMNHINKCV TDLLSKSGKT PSNEHAAVWV PDSEATVCMR CQKAKFTPVN RRHHCRKCGF
181 VVCGPCSEKR FLLPSQSSKP VRICDFCYDL LSAGDMATCQ PARSDSYSQS LKSPLNDMSD
241 DDDDDDSSDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLEKHF2 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)
- 0.35
- Highest tissue expression
- 97 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 97 nTPM
- tonsil: 67 nTPM
- lymph node: 59 nTPM
- thymus: 29 nTPM
- spleen: 25 nTPM
- appendix: 24 nTPM
Single-cell type
- neutrophils: 157 nCPM
- b-cells: 116 nCPM
- neutrophil progenitors: 116 nCPM
- breast hormone-responsive cells: 100 nCPM
- respiratory ionocytes: 99 nCPM
- endometrial luminal cells: 94 nCPM
Immune cell
- basophil: 124 nTPM
- naive B-cell: 87 nTPM
- memory B-cell: 78 nTPM
- eosinophil: 48 nTPM
- neutrophil: 33 nTPM
- myeloid DC: 27 nTPM
Brain region
- white matter: 16 nTPM
- choroid plexus: 14 nTPM
- spinal cord: 13 nTPM
- medulla oblongata: 12 nTPM
- cerebellum: 12 nTPM
- midbrain: 11 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)
- 0.45
- gnomAD pLI
- 0.87
- gnomAD missense Z
- 1.88
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 10% 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
- FYVE zinc finger
- Pleckstrin homology domain
- Zinc finger, FYVE/PHD-type
- PH-like domain superfamily
- Zinc finger, RING/FYVE/PHD-type
- Zinc finger, FYVE-related
- Phafin, PH domain
- Pleckstrin homology domain-containing family F
- PH domain
- FYVE zinc finger
- Pleckstrin homology domain-containing family F member 2, FYVE domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PLEKHF2 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 PLEKHF2 as an antibody target. Whether an autoantibody or antibody against PLEKHF2 could matter depends on whether native PLEKHF2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLEKHF2 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 PLEKHF2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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