LCOR
Ligand-dependent corepressor
Also known as: C10orf12, DKFZP564P1916, FLJ13022, FLJ38026, KIAA1795, LCOR_HUMAN, MLR2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96JN0
- Gene
- LCOR
- Ensembl
- ENSG00000196233
- Chromosome
- 10
- Canonical length
- 433 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
LCOR is a transcriptional corepressor widely expressed in fetal and adult tissues that is recruited to agonist-bound nuclear receptors through a single LxxLL motif, also referred to as a nuclear receptor (NR) box (Fernandes et al., 2003 [PubMed 12535528]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
433 residues, UniProt reviewed canonical sequence.
>Q96JN0|LCOR
1 MQRMIQQFAA EYTSKNSSTQ DPSQPNSTKN QSLPKASPVT TSPTAATTQN PVLSKLLMAD
61 QDSPLDLTVR KSQSEPSEQD GVLDLSTKKS PCAGSTSLSH SPGCSSTQGN GRPGRPSQYR
121 PDGLRSGDGV PPRSLQDGTR EGFGHSTSLK VPLARSLQIS EELLSRNQLS TAASLGPSGL
181 QNHGQHLILS REASWAKPHY EFNLSRMKFR GNGALSNISD LPFLAENSAF PKMALQAKQD
241 GKKDVSHSSP VDLKIPQVRG MDLSWESRTG DQYSYSSLVM GSQTESALSK KLRAILPKQS
301 RKSMLDAGPD SWGSDAEQST SGQPYPTSDQ EGDPGSKQPR KKRGRYRQYN SEILEEAISV
361 VMSGKMSVSK AQSIYGIPHS TLEYKVKERL GTLKNPPKKK MKLMRSEGPD VSVKIELDPQ
421 GEAAQSANES KNELocalizationUniProt · AlphaFold · HPA
Whether an antibody against LCOR 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)
- 0.68
- Highest tissue expression
- 24 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 24 nTPM
- retina: 15 nTPM
- duodenum: 11 nTPM
- small intestine: 10 nTPM
- skeletal muscle: 8.6 nTPM
- colon: 8.1 nTPM
Single-cell type
- neutrophils: 650 nCPM
- myonuclei: 536 nCPM
- neutrophil progenitors: 459 nCPM
- urothelial cells: 364 nCPM
- oligodendrocytes: 327 nCPM
- microglia: 310 nCPM
Immune cell
- neutrophil: 17 nTPM
- naive B-cell: 8.7 nTPM
- eosinophil: 8.1 nTPM
- gdT-cell: 5.9 nTPM
- plasmacytoid DC: 5.4 nTPM
- memory CD8 T-cell: 5.3 nTPM
Brain region
- cerebellum: 78 nTPM
- hypothalamus: 59 nTPM
- white matter: 58 nTPM
- thalamus: 43 nTPM
- medulla oblongata: 42 nTPM
- pons: 41 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)
- 0.35
- gnomAD pLI
- 0.95
- gnomAD missense Z
- 1.12
- DepMap mean gene effect
- -0.04
- 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
- cellular response to estradiol stimulus
- negative regulation of transcription by RNA polymerase II
- regulation of transcription by RNA polymerase II
Molecular functions
- DNA binding
- histone deacetylase binding
- histone methyltransferase binding
- nuclear estrogen receptor binding
- transcription corepressor activity
- transcription corepressor binding
- ubiquitin-specific protease binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LCOR 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 LCOR as an antibody target. Whether an autoantibody or antibody against LCOR could matter depends on whether native LCOR is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LCOR 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 LCOR as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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