LRRC52
Leucine-rich repeat-containing protein 52
Also known as: FLJ25811, LRC52_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N7C0
- Gene
- LRRC52
- Ensembl
- ENSG00000162763
- Chromosome
- 1
- Canonical length
- 313 aa
- Protein class
- Predicted membrane proteins
OverviewNCBI Gene
Enables potassium channel activator activity; transmembrane transporter binding activity; and voltage-gated potassium channel activity. Involved in positive regulation of voltage-gated potassium channel activity and potassium ion transmembrane transport. Part of voltage-gated potassium channel complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
313 residues, UniProt reviewed canonical sequence.
>Q8N7C0|LRRC52
1 MSLASGPGPG WLLFSFGMGL VSGSKCPNNC LCQAQEVICT GKQLTEYPLD IPLNTRRLFL
61 NENRITSLPA MHLGLLSDLV YLDCQNNRIR EVMDYTFIGV FKLIYLDLSS NNLTSISPFT
121 FSVLSNLVQL NIANNPHLLS LHKFTFANTT SLRYLDLRNT GLQTLDSAAL YHLTTLETLF
181 LSGNPWKCNC SFLDFAIFLI VFHMDPSDDL NATCVEPTEL TGWPITRVGN PLRYMCITHL
241 DHKDYIFLLL IGFCIFAAGT VAAWLTGVCA VLYQNTRHKS SEEDEDEAGT RVEVSRRIFQ
301 TQTSSVQEFP QLILocalizationUniProt · AlphaFold · HPA
Whether an antibody against LRRC52 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
- 1
- Mean surface accessibility (rSASA)
- 0.35
- Highest tissue expression
- 16 nTPM
Expression across tissuesHPA
Tissue
- testis: 16 nTPM
- parathyroid gland: 3.8 nTPM
- choroid plexus: 2.9 nTPM
- skeletal muscle: 1.2 nTPM
- heart muscle: 0.4 nTPM
- kidney: 0.3 nTPM
Single-cell type
- early spermatids: 235 nCPM
- late primary spermatocytes: 96 nCPM
- late spermatids: 43 nCPM
- retinal ganglion cells: 16 nCPM
- myonuclei: 8.2 nCPM
- distal convoluted tubule cells: 6.5 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 2.7 nTPM
- midbrain: 0.9 nTPM
- medulla oblongata: 0.7 nTPM
- pons: 0.3 nTPM
- cerebellum: 0.1 nTPM
- hippocampal formation: 0.1 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)
- 1.66
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.04
- DepMap mean gene effect
- 0.18
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- establishment of localization in cell
- positive regulation of voltage-gated potassium channel activity
- potassium ion transmembrane transport
Molecular functions
- potassium channel activator activity
- transmembrane transporter binding
- voltage-gated potassium channel activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LRRC52 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 LRRC52 as an antibody target. Whether an autoantibody or antibody against LRRC52 could matter depends on whether native LRRC52 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LRRC52 is annotated at the cell surface, where native LRRC52 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 LRRC52 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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