LMO2
Rhombotin-2
Also known as: RBTN2, RBTN2_HUMAN, RBTNL1, RHOM2, TTG2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P25791
- Gene
- LMO2
- Ensembl
- ENSG00000135363
- Chromosome
- 11
- Canonical length
- 158 aa
- Protein class
- Cancer-related genes, Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
LMO2 encodes a cysteine-rich, two LIM-domain protein that is required for yolk sac erythropoiesis. The LMO2 protein has a central and crucial role in hematopoietic development and is highly conserved. The LMO2 transcription start site is located approximately 25 kb downstream from the 11p13 T-cell translocation cluster (11p13 ttc), where a number T-cell acute lymphoblastic leukemia-specific translocations occur. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Nov 2008]
Canonical amino-acid sequenceUniProt
158 residues, UniProt reviewed canonical sequence.
>P25791|LMO2
1 MSSAIERKSL DPSEEPVDEV LQIPPSLLTC GGCQQNIGDR YFLKAIDQYW HEDCLSCDLC
61 GCRLGEVGRR LYYKLGRKLC RRDYLRLFGQ DGLCASCDKR IRAYEMTMRV KDKVYHLECF
121 KCAACQKHFC VGDRYLLINS DIVCEQDIYE WTKINGMILocalizationUniProt · AlphaFold · HPA
Whether an antibody against LMO2 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)
- 0.41
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 26 nTPM
- skeletal muscle: 22 nTPM
- lymph node: 18 nTPM
- spleen: 18 nTPM
- basal ganglia: 18 nTPM
- hippocampal formation: 17 nTPM
Single-cell type
- erythrocyte progenitors: 409 nCPM
- megakaryocyte-erythroid progenitors: 385 nCPM
- lymphatic endothelial cells: 262 nCPM
- thymic myoid cells: 237 nCPM
- ependymal cells: 222 nCPM
- megakaryocyte progenitors: 214 nCPM
Immune cell
- myeloid DC: 1.9 nTPM
- non-classical monocyte: 1.7 nTPM
- eosinophil: 1.5 nTPM
- intermediate monocyte: 1.4 nTPM
- neutrophil: 0.7 nTPM
- basophil: 0.6 nTPM
Brain region
- medulla oblongata: 37 nTPM
- thalamus: 36 nTPM
- spinal cord: 35 nTPM
- pons: 34 nTPM
- midbrain: 29 nTPM
- hypothalamus: 29 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)
- 1.03
- gnomAD pLI
- 0.16
- gnomAD missense Z
- 1.34
- DepMap mean gene effect
- 0
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- bHLH transcription factor binding
- DNA-binding transcription factor binding
- identical protein binding
- metal ion binding
- RNA polymerase II-specific DNA-binding transcription factor binding
- transcription coactivator activity
- transcription coregulator binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LMO2 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 LMO2 as an antibody target. Whether an autoantibody or antibody against LMO2 could matter depends on whether native LMO2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LMO2 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 LMO2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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