LRRC26
Leucine-rich repeat-containing protein 26
Also known as: bA350O14.10, LRC26_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q2I0M4
- Gene
- LRRC26
- Ensembl
- ENSG00000184709
- Chromosome
- 9
- Canonical length
- 334 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoli fibrillar center,Plasma membrane
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. Located in plasma membrane. Part of voltage-gated potassium channel complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
334 residues, UniProt reviewed canonical sequence.
>Q2I0M4|LRRC26
1 MRGPSWSRPR PLLLLLLLLS PWPVWAQVSA TASPSGSLGA PDCPEVCTCV PGGLASCSAL
61 SLPAVPPGLS LRLRALLLDH NRVRALPPGA FAGAGALQRL DLRENGLHSV HVRAFWGLGA
121 LQLLDLSANQ LEALAPGTFA PLRALRNLSL AGNRLARLEP AALGALPLLR SLSLQDNELA
181 ALAPGLLGRL PALDALHLRG NPWGCGCALR PLCAWLRRHP LPASEAETVL CVWPGRLTLS
241 PLTAFSDAAF SHCAQPLALR DLAVVYTLGP ASFLVSLASC LALGSGLTAC RARRRRLRTA
301 ALRPPRPPDP NPDPDPHGCA SPADPGSPAA AAQALocalizationUniProt · AlphaFold · HPA
Whether an antibody against LRRC26 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)
- 0.41
- Highest tissue expression
- 286 nTPM
Expression across tissuesHPA
Tissue
- salivary gland: 286 nTPM
- prostate: 50 nTPM
- colon: 11 nTPM
- small intestine: 7 nTPM
- breast: 6.3 nTPM
- stomach: 4.9 nTPM
Single-cell type
- goblet cells: 583 nCPM
- lacrimal acinar cells: 318 nCPM
- salivary acinar cells: 259 nCPM
- prostatic glandular cells: 180 nCPM
- salivary duct cells: 159 nCPM
- gastric chief cells: 131 nCPM
Immune cell
- plasmacytoid DC: 118 nTPM
- total PBMC: 0.5 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- cerebellum: 6.5 nTPM
- hypothalamus: 2.1 nTPM
- cerebral cortex: 1.9 nTPM
- basal ganglia: 1.6 nTPM
- spinal cord: 1.3 nTPM
- midbrain: 1.2 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)
- 1.68
- gnomAD pLI
- 0.01
- gnomAD missense Z
- -0.55
- DepMap mean gene effect
- 0.1
- 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
- positive regulation of voltage-gated potassium channel activity
- potassium ion transmembrane transport
Molecular functions
- potassium channel activator activity
- potassium channel regulator activity
- transmembrane transporter binding
- voltage-gated potassium channel activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LRRC26 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 LRRC26 as an antibody target. Whether an autoantibody or antibody against LRRC26 could matter depends on whether native LRRC26 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LRRC26 is annotated at the cell surface, where native LRRC26 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 LRRC26 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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