LUC7L3
Luc7-like protein 3
Also known as: CRA, CREAP-1, CROP, FLJ11063, hLuc7A, LC7L3_HUMAN, LUC7A, OA48-18
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95232
- Gene
- LUC7L3
- Ensembl
- ENSG00000108848
- Chromosome
- 17
- Canonical length
- 432 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nuclear speckles
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a protein with an N-terminal half that contains cysteine/histidine motifs and leucine zipper-like repeats, and the C-terminal half is rich in arginine and glutamate residues (RE domain) and arginine and serine residues (RS domain). This protein localizes with a speckled pattern in the nucleus, and could be involved in the formation of splicesome via the RE and RS domains. Two alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2009]
Canonical amino-acid sequenceUniProt
432 residues, UniProt reviewed canonical sequence.
>O95232|LUC7L3
1 MISAAQLLDE LMGRDRNLAP DEKRSNVRWD HESVCKYYLC GFCPAELFTN TRSDLGPCEK
61 IHDENLRKQY EKSSRFMKVG YERDFLRYLQ SLLAEVERRI RRGHARLALS QNQQSSGAAG
121 PTGKNEEKIQ VLTDKIDVLL QQIEELGSEG KVEEAQGMMK LVEQLKEERE LLRSTTSTIE
181 SFAAQEKQME VCEVCGAFLI VGDAQSRVDD HLMGKQHMGY AKIKATVEEL KEKLRKRTEE
241 PDRDERLKKE KQEREEREKE REREREERER KRRREEEERE KERARDRERR KRSRSRSRHS
301 SRTSDRRCSR SRDHKRSRSR ERRRSRSRDR RRSRSHDRSE RKHRSRSRDR RRSKSRDRKS
361 YKHRSKSRDR EQDRKSKEKE KRGSDDKKSS VKSGSREKQS EDTNTESKES DTKNEVNGTS
421 EDIKSEGDTQ SNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LUC7L3 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.49
- Highest tissue expression
- 295 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 295 nTPM
- ovary: 213 nTPM
- cervix: 168 nTPM
- retina: 163 nTPM
- pituitary gland: 163 nTPM
- fallopian tube: 158 nTPM
Single-cell type
- sertoli cells: 824 nCPM
- leydig cells: 674 nCPM
- tuft cells: 542 nCPM
- myonuclei: 488 nCPM
- peritubular myoid cells: 478 nCPM
- lactotrophs: 475 nCPM
Immune cell
- memory B-cell: 68 nTPM
- plasmacytoid DC: 65 nTPM
- naive B-cell: 56 nTPM
- basophil: 50 nTPM
- neutrophil: 49 nTPM
- naive CD4 T-cell: 38 nTPM
Brain region
- cerebellum: 175 nTPM
- white matter: 138 nTPM
- hypothalamus: 119 nTPM
- thalamus: 109 nTPM
- cerebral cortex: 109 nTPM
- basal ganglia: 109 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)
- 0.09
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.58
- DepMap mean gene effect
- -1.66
- DepMap dependency class
- pan
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
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LUC7L3 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 LUC7L3 as an antibody target. Whether an autoantibody or antibody against LUC7L3 could matter depends on whether native LUC7L3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LUC7L3 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label LUC7L3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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