LYL1
Protein lyl-1
Also known as: bHLHa18, LYL1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P12980
- Gene
- LYL1
- Ensembl
- ENSG00000104903
- Chromosome
- 19
- Canonical length
- 280 aa
- Protein class
- Cancer-related genes, Disease related genes, Human disease related genes, Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene represents a basic helix-loop-helix transcription factor. The encoded protein may play roles in blood vessel maturation and hematopoeisis. A translocation between this locus and the T cell receptor beta locus (GeneID 6957) on chromosome 7 has been associated with acute lymphoblastic leukemia. [provided by RefSeq, Sep 2010]
Canonical amino-acid sequenceUniProt
280 residues, UniProt reviewed canonical sequence.
>P12980|LYL1
1 MCPPQAQAEV GPTMTEKAEM VCAPSPAPAP PPKPASPGPP QVEEVGHRGG SSPPRLPPGV
61 PVISLGHSRP PGVAMPTTEL GTLRPPLLQL STLGTAPPTL ALHYHPHPFL NSVYIGPAGP
121 FSIFPSSRLK RRPSHCELDL AEGHQPQKVA RRVFTNSRER WRQQNVNGAF AELRKLLPTH
181 PPDRKLSKNE VLRLAMKYIG FLVRLLRDQA AALAAGPTPP GPRKRPVHRV PDDGARRGSG
241 RRAEAAARSQ PAPPADPDGS PGGAARPIKM EQTALSPEVRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LYL1 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)
- 0.66
- Highest tissue expression
- 35 nTPM
Expression across tissuesHPA
Tissue
- spleen: 35 nTPM
- bone marrow: 34 nTPM
- testis: 20 nTPM
- small intestine: 13 nTPM
- lung: 12 nTPM
- lymph node: 12 nTPM
Single-cell type
- late spermatids: 1,265 nCPM
- platelets: 697 nCPM
- megakaryocytes: 501 nCPM
- early spermatids: 366 nCPM
- late primary spermatocytes: 299 nCPM
- hofbauer cells: 200 nCPM
Immune cell
- eosinophil: 6.4 nTPM
- naive B-cell: 3.7 nTPM
- non-classical monocyte: 2.8 nTPM
- basophil: 2.4 nTPM
- neutrophil: 2.4 nTPM
- memory B-cell: 2.1 nTPM
Brain region
- white matter: 16 nTPM
- spinal cord: 15 nTPM
- thalamus: 15 nTPM
- medulla oblongata: 15 nTPM
- pons: 13 nTPM
- cerebellum: 11 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)
- 0.61
- gnomAD pLI
- 0.77
- gnomAD missense Z
- 0.95
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- selective
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
- B cell differentiation
- blood vessel maturation
- definitive hemopoiesis
- positive regulation of DNA-templated transcription
- regulation of DNA-templated transcription
- regulation of transcription by RNA polymerase II
Molecular functions
- DNA binding
- DNA-binding transcription factor activity, RNA polymerase II-specific
- protein dimerization activity
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LYL1 as an antibody target. Whether an autoantibody or antibody against LYL1 could matter depends on whether native LYL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LYL1 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 LYL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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