MYCL
Protein L-Myc
Also known as: bHLHe38, LMYC, MYCL_HUMAN, MYCL1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P12524
- Gene
- MYCL
- Ensembl
- ENSG00000116990
- Chromosome
- 1
- Canonical length
- 364 aa
- Protein class
- Cancer-related genes, Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Mitotic chromosome
OverviewNCBI Gene
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within regulation of inner ear auditory receptor cell differentiation. Located in chromosome and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
364 residues, UniProt reviewed canonical sequence.
>P12524|MYCL
1 MDYDSYQHYF YDYDCGEDFY RSTAPSEDIW KKFELVPSPP TSPPWGLGPG AGDPAPGIGP
61 PEPWPGGCTG DEAESRGHSK GWGRNYASII RRDCMWSGFS ARERLERAVS DRLAPGAPRG
121 NPPKASAAPD CTPSLEAGNP APAAPCPLGE PKTQACSGSE SPSDSENEEI DVVTVEKRQS
181 LGIRKPVTIT VRADPLDPCM KHFHISIHQQ QHNYAARFPP ESCSQEEASE RGPQEEVLER
241 DAAGEKEDEE DEEIVSPPPV ESEAAQSCHP KPVSSDTEDV TKRKNHNFLE RKRRNDLRSR
301 FLALRDQVPT LASCSKAPKV VILSKALEYL QALVGAEKRM ATEKRQLRCR QQQLQKRIAY
361 LTGYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MYCL 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)
- 0.63
- Highest tissue expression
- 64 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 64 nTPM
- skin: 37 nTPM
- esophagus: 20 nTPM
- urinary bladder: 14 nTPM
- vagina: 11 nTPM
- liver: 11 nTPM
Single-cell type
- urothelial cells: 86 nCPM
- respiratory deuterosomal cells: 80 nCPM
- cytotrophoblasts: 44 nCPM
- prostatic hillock cells: 41 nCPM
- hepatocytes: 31 nCPM
- esophageal suprabasal cells: 31 nCPM
Immune cell
- plasmacytoid DC: 23 nTPM
- myeloid DC: 19 nTPM
- classical monocyte: 17 nTPM
- intermediate monocyte: 8.2 nTPM
- total PBMC: 6.7 nTPM
- non-classical monocyte: 3.5 nTPM
Brain region
- hippocampal formation: 3.6 nTPM
- hypothalamus: 3.3 nTPM
- basal ganglia: 3.1 nTPM
- cerebral cortex: 3.1 nTPM
- spinal cord: 3 nTPM
- choroid plexus: 2.9 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)
- 0.67
- gnomAD pLI
- 0.12
- gnomAD missense Z
- 1.05
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- regulation of inner ear auditory receptor cell differentiation
- 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 MYCL as an antibody target. Whether an autoantibody or antibody against MYCL could matter depends on whether native MYCL is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MYCL 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 MYCL as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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