Seroatlas · Human Serome Atlas

PLGRKT

Plasminogen receptor (KT)

Also known as: AD025, C9orf46, FLJ14688, MDS030, Plg-RKT, PLRKT_HUMAN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q9HBL7
Gene
PLGRKT
Ensembl
ENSG00000107020
Chromosome
9
Canonical length
147 aa
Protein class
Predicted membrane proteins
Subcellular location
Mitochondria

OverviewNCBI Gene

Predicted to be involved in positive regulation of plasminogen activation. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

147 residues, UniProt reviewed canonical sequence.

>Q9HBL7|PLGRKT
     1  MGFIFSKSMN ESMKNQKEFM LMNARLQLER QLIMQSEMRE RQMAMQIAWS REFLKYFGTF
    61  FGLAAISLTA GAIKKKKPAF LVPIVPLSFI LTYQYDLGYG TLLERMKGEA EDILETEKSK
   121  LQLPRGMITF ESIEKARKEQ SRFFIDK

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against PLGRKT 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
2
Mean surface accessibility (rSASA)
0.45
Highest tissue expression
55 nTPM

Expression across tissuesHPA

Tissue

  • skeletal muscle: 55 nTPM
  • rectum: 44 nTPM
  • duodenum: 42 nTPM
  • colon: 39 nTPM
  • choroid plexus: 35 nTPM
  • tongue: 35 nTPM

Single-cell type

  • enterocytes: 178 nCPM
  • colonocytes: 164 nCPM
  • extravillous trophoblasts: 146 nCPM
  • enteric transient amplifying cells: 132 nCPM
  • gastric progenitor cells: 129 nCPM
  • mast cells: 125 nCPM

Immune cell

  • basophil: 246 nTPM
  • T-reg: 75 nTPM
  • memory CD8 T-cell: 57 nTPM
  • MAIT T-cell: 54 nTPM
  • memory CD4 T-cell: 54 nTPM
  • NK-cell: 53 nTPM

Brain region

  • choroid plexus: 20 nTPM
  • white matter: 10 nTPM
  • medulla oblongata: 9.8 nTPM
  • spinal cord: 9.7 nTPM
  • basal ganglia: 9.1 nTPM
  • cerebellum: 9.1 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)
1.87
gnomAD pLI
0
gnomAD missense Z
-1.09
DepMap mean gene effect
0.28
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

Cellular components

Protein domainsUniProt · Pfam · InterPro

  • Plasminogen receptor (KT)
  • Uncharacterised conserved protein (DUF2368)

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of PLGRKT 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 PLGRKT as an antibody target. Whether an autoantibody or antibody against PLGRKT could matter depends on whether native PLGRKT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

PLGRKT is annotated at the cell surface, where native PLGRKT 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 PLGRKT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/PLGRKT. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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