Seroatlas · Human Serome Atlas

MAFF

Transcription factor MafF

Also known as: hMafF, MAFF_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q9ULX9
Gene
MAFF
Ensembl
ENSG00000185022
Chromosome
22
Canonical length
164 aa
Protein class
Predicted intracellular proteins, Transcription factors
Subcellular location
Nucleoplasm,Mitochondria

OverviewNCBI Gene

The protein encoded by this gene is a basic leucine zipper (bZIP) transcription factor that lacks a transactivation domain. It is known to bind the US-2 DNA element in the promoter of the oxytocin receptor (OTR) gene and most likely heterodimerizes with other leucine zipper-containing proteins to enhance expression of the OTR gene during term pregnancy. The encoded protein can also form homodimers, and since it lacks a transactivation domain, the homodimer may act as a repressor of transcription. This gene may also be involved in the cellular stress response. Multiple transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]

Canonical amino-acid sequenceUniProt

164 residues, UniProt reviewed canonical sequence.

>Q9ULX9|MAFF
     1  MSVDPLSSKA LKIKRELSEN TPHLSDEALM GLSVRELNRH LRGLSAEEVT RLKQRRRTLK
    61  NRGYAASCRV KRVCQKEELQ KQKSELEREV DKLARENAAM RLELDALRGK CEALQGFARS
   121  VAAARGPATL VAPASVITIV KSTPGSGSGP AHGPDPAHGP ASCS

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against MAFF 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)
0.55
Highest tissue expression
101 nTPM

Expression across tissuesHPA

Tissue

  • adipose tissue: 101 nTPM
  • blood vessel: 81 nTPM
  • skeletal muscle: 74 nTPM
  • breast: 71 nTPM
  • lung: 58 nTPM
  • fallopian tube: 57 nTPM

Single-cell type

  • endometrial glandular cells: 819 nCPM
  • epididymal basal cells: 772 nCPM
  • esophageal apical cells: 771 nCPM
  • endometrial luminal cells: 688 nCPM
  • syncytiotrophoblasts: 607 nCPM
  • urothelial cells: 528 nCPM

Immune cell

  • basophil: 24 nTPM
  • NK-cell: 21 nTPM
  • neutrophil: 8.6 nTPM
  • non-classical monocyte: 3.6 nTPM
  • gdT-cell: 2.8 nTPM
  • MAIT T-cell: 2.8 nTPM

Brain region

  • white matter: 26 nTPM
  • medulla oblongata: 23 nTPM
  • thalamus: 23 nTPM
  • pons: 21 nTPM
  • hypothalamus: 18 nTPM
  • cerebral cortex: 16 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about MAFF.

Disease | ImmuneIEDB

Conditions an epitope on MAFF was assayed in.

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)
1.6
gnomAD pLI
0.02
gnomAD missense Z
1.7
DepMap mean gene effect
-0.19
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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

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

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

Canonical record: https://seroatlas.com/gene/MAFF. 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).

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