PLEKHO1
Pleckstrin homology domain-containing family O member 1
Also known as: CKIP-1, OC120, PKHO1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q53GL0
- Gene
- PLEKHO1
- Ensembl
- ENSG00000023902
- Chromosome
- 1
- Canonical length
- 409 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Mitochondria
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Predicted to be involved in regulation of myoblast fusion. Predicted to act upstream of or within several processes, including lamellipodium morphogenesis; myoblast fusion; and myoblast migration. Predicted to be located in cytoplasm; nucleus; and plasma membrane. Predicted to be active in muscle cell projection membrane and ruffle membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
409 residues, UniProt reviewed canonical sequence.
>Q53GL0|PLEKHO1
1 MMKKNNSAKR GPQDGNQQPA PPEKVGWVRK FCGKGIFREI WKNRYVVLKG DQLYISEKEV
61 KDEKNIQEVF DLSDYEKCEE LRKSKSRSKK NHSKFTLAHS KQPGNTAPNL IFLAVSPEEK
121 ESWINALNSA ITRAKNRILD EVTVEEDSYL AHPTRDRAKI QHSRRPPTRG HLMAVASTST
181 SDGMLTLDLI QEEDPSPEEP TSCAESFRVD LDKSVAQLAG SRRRADSDRI QPSADRASSL
241 SRPWEKTDKG ATYTPQAPKK LTPTEKGRCA SLEEILSQRD AASARTLQLR AEEPPTPALP
301 NPGQLSRIQD LVARKLEETQ ELLAEVQGLG DGKRKAKDPP RSPPDSESEQ LLLETERLLG
361 EASSNWSQAK RVLQEVRELR DLYRQMDLQT PDSHLRQTTP HSQYRKSLMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLEKHO1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.55
- Highest tissue expression
- 189 nTPM
Expression across tissuesHPA
Tissue
- colon: 189 nTPM
- blood vessel: 98 nTPM
- urinary bladder: 92 nTPM
- testis: 77 nTPM
- spleen: 56 nTPM
- small intestine: 54 nTPM
Single-cell type
- platelets: 1,195 nCPM
- late spermatids: 526 nCPM
- smooth muscle cells: 349 nCPM
- late primary spermatocytes: 292 nCPM
- early spermatids: 256 nCPM
- cdc: 226 nCPM
Immune cell
- neutrophil: 31 nTPM
- plasmacytoid DC: 27 nTPM
- classical monocyte: 26 nTPM
- intermediate monocyte: 25 nTPM
- non-classical monocyte: 24 nTPM
- memory B-cell: 20 nTPM
Brain region
- cerebral cortex: 29 nTPM
- cerebellum: 26 nTPM
- basal ganglia: 21 nTPM
- medulla oblongata: 21 nTPM
- amygdala: 20 nTPM
- hippocampal formation: 20 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)
- 0.48
- gnomAD pLI
- 0.48
- gnomAD missense Z
- 0.07
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- lamellipodium morphogenesis
- myoblast fusion
- myoblast migration
- regulation of cell shape
- regulation of myoblast fusion
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PLEKHO1 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 PLEKHO1 as an antibody target. Whether an autoantibody or antibody against PLEKHO1 could matter depends on whether native PLEKHO1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLEKHO1 is annotated at the cell surface, where native PLEKHO1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label PLEKHO1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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