LMO3
LIM domain only protein 3
Also known as: DAT1, LMO3_HUMAN, RBTNL2, Rhom-3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TAP4
- Gene
- LMO3
- Ensembl
- ENSG00000048540
- Chromosome
- 12
- Canonical length
- 145 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
The protein encoded by this gene belongs to the rhombotin family of cysteine-rich LIM domain oncogenes. This gene is predominantly expressed in the brain. Related family members, LMO1 and LMO2 on chromosome 11, have been reported to be involved in chromosomal translocations in T-cell leukemia. Many alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]
Canonical amino-acid sequenceUniProt
145 residues, UniProt reviewed canonical sequence.
>Q8TAP4|LMO3
1 MLSVQPDTKP KGCAGCNRKI KDRYLLKALD KYWHEDCLKC ACCDCRLGEV GSTLYTKANL
61 ILCRRDYLRL FGVTGNCAAC SKLIPAFEMV MRAKDNVYHL DCFACQLCNQ RFCVGDKFFL
121 KNNMILCQTD YEEGLMKEGY APQVRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LMO3 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)
- 0.4
- Highest tissue expression
- 110 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 110 nTPM
- amygdala: 97 nTPM
- cerebral cortex: 91 nTPM
- colon: 67 nTPM
- hippocampal formation: 54 nTPM
- urinary bladder: 42 nTPM
Single-cell type
- alveolar cells type 1: 645 nCPM
- alveolar cells type 2: 546 nCPM
- transitional alveolar cells: 473 nCPM
- medullary thymic epithelial cells: 413 nCPM
- astrocytes: 402 nCPM
- adipocytes: 388 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
- basal ganglia: 141 nTPM
- cerebral cortex: 139 nTPM
- hypothalamus: 95 nTPM
- amygdala: 90 nTPM
- hippocampal formation: 89 nTPM
- midbrain: 88 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)
- 0.57
- gnomAD pLI
- 0.71
- gnomAD missense Z
- 2.01
- DepMap mean gene effect
- 0.08
- 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
- negative regulation of ERK1 and ERK2 cascade
- positive regulation of fat cell differentiation
- positive regulation of nuclear receptor-mediated glucocorticoid signaling pathway
- positive regulation of peroxisome proliferator activated receptor signaling pathway
- positive regulation of transcription by RNA polymerase II
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LMO3 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 LMO3 as an antibody target. Whether an autoantibody or antibody against LMO3 could matter depends on whether native LMO3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LMO3 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 LMO3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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