LMO4
LIM domain transcription factor LMO4
Also known as: LMO4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P61968
- Gene
- LMO4
- Ensembl
- ENSG00000143013
- Chromosome
- 1
- Canonical length
- 165 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Midbody ring
OverviewNCBI Gene
This gene encodes a cysteine-rich protein that contains two LIM domains but lacks a DNA-binding homeodomain. The encoded protein may play a role as a transcriptional regulator or as an oncogene. [provided by RefSeq, Aug 2008]
Canonical amino-acid sequenceUniProt
165 residues, UniProt reviewed canonical sequence.
>P61968|LMO4
1 MVNPGSSSQP PPVTAGSLSW KRCAGCGGKI ADRFLLYAMD SYWHSRCLKC SCCQAQLGDI
61 GTSCYTKSGM ILCRNDYIRL FGNSGACSAC GQSIPASELV MRAQGNVYHL KCFTCSTCRN
121 RLVPGDRFHY INGSLFCEHD RPTALINGHL NSLQSNPLLP DQKVCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LMO4 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.42
- Highest tissue expression
- 240 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 240 nTPM
- hippocampal formation: 138 nTPM
- amygdala: 88 nTPM
- stomach: 86 nTPM
- salivary gland: 82 nTPM
- tonsil: 82 nTPM
Single-cell type
- lacrimal acinar cells: 1,217 nCPM
- extravillous trophoblasts: 458 nCPM
- esophageal apical cells: 399 nCPM
- respiratory ionocytes: 384 nCPM
- respiratory basal cells: 383 nCPM
- migrating cytotrophoblasts: 381 nCPM
Immune cell
- basophil: 31 nTPM
- NK-cell: 22 nTPM
- eosinophil: 20 nTPM
- neutrophil: 15 nTPM
- intermediate monocyte: 12 nTPM
- non-classical monocyte: 12 nTPM
Brain region
- cerebral cortex: 129 nTPM
- basal ganglia: 106 nTPM
- hippocampal formation: 104 nTPM
- white matter: 76 nTPM
- hypothalamus: 39 nTPM
- medulla oblongata: 38 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)
- 0.6
- gnomAD pLI
- 0.68
- gnomAD missense Z
- 2.1
- 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
- motor neuron axon guidance
- negative regulation of protein-containing complex assembly
- negative regulation of transcription by RNA polymerase II
- neural tube closure
- positive regulation of kinase activity
- positive regulation of transcription by RNA polymerase II
- regulation of cell fate specification
- regulation of cell migration
- spinal cord association neuron differentiation
- spinal cord motor neuron cell fate specification
- thymus development
- ventral spinal cord interneuron differentiation
- ventricular septum development
- regulation of cell activation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LMO4 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 LMO4 as an antibody target. Whether an autoantibody or antibody against LMO4 could matter depends on whether native LMO4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LMO4 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 LMO4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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