Seroatlas · Human Serome Atlas

CEBPA

CCAAT/enhancer-binding protein alpha

Also known as: C/EBP-alpha, CEBP, CEBPA_HUMAN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
P49715
Gene
CEBPA
Ensembl
ENSG00000245848
Chromosome
19
Canonical length
358 aa
Protein class
Cancer-related genes, Disease related genes, Human disease related genes, Predicted intracellular proteins, Transcription factors
Subcellular location
Nucleoplasm,Vesicles
Quaternary structure
Homodimer

OverviewNCBI Gene

This intronless gene encodes a transcription factor that contains a basic leucine zipper (bZIP) domain and recognizes the CCAAT motif in the promoters of target genes. The encoded protein functions in homodimers and also heterodimers with CCAAT/enhancer-binding proteins beta and gamma. Activity of this protein can modulate the expression of genes involved in cell cycle regulation as well as in body weight homeostasis. Mutation of this gene is associated with acute myeloid leukemia. The use of alternative in-frame non-AUG (GUG) and AUG start codons results in protein isoforms with different lengths. Differential translation initiation is mediated by an out-of-frame, upstream open reading frame which is located between the GUG and the first AUG start codons. [provided by RefSeq, Dec 2013]

Canonical amino-acid sequenceUniProt

358 residues, UniProt reviewed canonical sequence.

>P49715|CEBPA
     1  MESADFYEAE PRPPMSSHLQ SPPHAPSSAA FGFPRGAGPA QPPAPPAAPE PLGGICEHET
    61  SIDISAYIDP AAFNDEFLAD LFQHSRQQEK AKAAVGPTGG GGGGDFDYPG APAGPGGAVM
   121  PGGAHGPPPG YGCAAAGYLD GRLEPLYERV GAPALRPLVI KQEPREEDEA KQLALAGLFP
   181  YQPPPPPPPS HPHPHPPPAH LAAPHLQFQI AHCGQTTMHL QPGHPTPPPT PVPSPHPAPA
   241  LGAAGLPGPG SALKGLGAAH PDLRASGGSG AGKAKKSVDK NSNEYRVRRE RNNIAVRKSR
   301  DKAKQRNVET QQKVLELTSD NDRLRKRVEQ LSRELDTLRG IFRQLPESSL VKAMGNCA

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CEBPA 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
198 nTPM

Expression across tissuesHPA

Tissue

  • liver: 198 nTPM
  • skin: 115 nTPM
  • adipose tissue: 93 nTPM
  • breast: 68 nTPM
  • parathyroid gland: 25 nTPM
  • lung: 24 nTPM

Single-cell type

  • syncytiotrophoblasts: 278 nCPM
  • suprabasal keratinocytes: 129 nCPM
  • hofbauer cells: 114 nCPM
  • hepatocytes: 111 nCPM
  • microglia: 87 nCPM
  • alveolar cells type 2: 84 nCPM

Immune cell

  • basophil: 16 nTPM
  • non-classical monocyte: 16 nTPM
  • intermediate monocyte: 12 nTPM
  • classical monocyte: 7.1 nTPM
  • myeloid DC: 5.1 nTPM
  • neutrophil: 2.5 nTPM

Brain region

  • white matter: 59 nTPM
  • medulla oblongata: 43 nTPM
  • spinal cord: 40 nTPM
  • thalamus: 37 nTPM
  • midbrain: 33 nTPM
  • pons: 29 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about CEBPA.

Disease | AllUniProt

Conditions CEBPA is implicated in, by any mechanism.

Disease | GeneticClinVar

66 pathogenic / likely-pathogenic of 1,280 ClinVar records.

Conditions with pathogenic or likely-pathogenic variants.

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)
1.18
gnomAD pLI
0.55
gnomAD missense Z
0.57
DepMap mean gene effect
-0.08
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of CEBPA 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 CEBPA as an antibody target. Whether an autoantibody or antibody against CEBPA could matter depends on whether native CEBPA is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CEBPA 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 CEBPA as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CEBPA. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

Loading the interactive Seroatlas protein explorer...