LRRC24
Leucine-rich repeat-containing protein 24
Also known as: LRC24_HUMAN, LRRC14OS
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q50LG9
- Gene
- LRRC24
- Ensembl
- ENSG00000254402
- Chromosome
- 8
- Canonical length
- 513 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be located in membrane. Predicted to be active in external side of plasma membrane; extracellular matrix; and extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
513 residues, UniProt reviewed canonical sequence.
>Q50LG9|LRRC24
1 MALRAPALLP LLLLLLPLRA AGCPAACRCY SATVECGALR LRVVPLGIPP GTQTLFLQDN
61 NIARLEPGAL APLAALRRLY LHNNSLRALE AGAFRAQPRL LELALTSNRL RGLRSGAFVG
121 LAQLRVLYLA GNQLARLLDF TFLHLPRLQE LHLQENSIEL LEDQALAGLS SLALLDLSRN
181 QLGTISREAL QPLASLQVLR LTENPWRCDC ALHWLGAWIK EGGQRLLTSR DRKIMCAEPP
241 RLALQSLLDV SHSSLICIPP SVHVQPLELT ANLGEDLRVA CQASGYPQPL VTWRKVPQPR
301 EGRPRAQAQL EGGLLGLGGH SASDTGSGML FLSNITLAHA GKYECEASNA GGAARVPFRL
361 LVNASRQQPQ QPAQPPPPAA RPAGSEPRPE AGSMAFRALG VATQTAIAAA IALLALTALL
421 LVAMICRRRR RRKKARGPPG EGALFVNDYL DGPCTFAQLE ELRDERGHEM FVINRSKPLF
481 AEGPAEAPAD CGPEQGAGPG LRVPPPVAYE IHCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LRRC24 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
- 13 nTPM
Expression across tissuesHPA
Tissue
- pituitary gland: 13 nTPM
- hypothalamus: 12 nTPM
- cerebral cortex: 12 nTPM
- prostate: 11 nTPM
- cerebellum: 11 nTPM
- basal ganglia: 10 nTPM
Single-cell type
- late spermatids: 115 nCPM
- retinal bipolar cells: 61 nCPM
- rod photoreceptor cells: 36 nCPM
- cone photoreceptor cells: 35 nCPM
- pancreatic islet cells: 35 nCPM
- cardiomyocytes: 30 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
- medulla oblongata: 24 nTPM
- hypothalamus: 22 nTPM
- midbrain: 22 nTPM
- cerebral cortex: 19 nTPM
- pons: 17 nTPM
- basal ganglia: 16 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)
- 0.96
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.68
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% 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
- Leucine-rich repeat N-terminal domain
- Cysteine-rich flanking region, C-terminal
- Leucine-rich repeat
- Leucine-rich repeat, typical subtype
- Immunoglobulin subtype 2
- Immunoglobulin domain subtype
- Immunoglobulin-like domain
- Immunoglobulin-like fold
- Leucine-rich repeat domain superfamily
- Immunoglobulin-like domain superfamily
- Small Leucine-Rich Proteoglycans
- Leucine rich repeat
- Immunoglobulin domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LRRC24 as an antibody target. Whether an autoantibody or antibody against LRRC24 could matter depends on whether native LRRC24 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LRRC24 is annotated at the cell surface, where native LRRC24 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 LRRC24 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...