Seroatlas · Human Serome Atlas

MMD

Monocyte to macrophage differentiation factor

Also known as: MMA, PAQR11, PAQRB_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q15546
Gene
MMD
Ensembl
ENSG00000108960
Chromosome
17
Canonical length
238 aa
Protein class
Predicted membrane proteins, Transporters
Subcellular location
Vesicles

OverviewNCBI Gene

This protein is expressed by in vitro differentiated macrophages but not freshly isolated monocytes. Although sequence analysis identifies seven potential transmembrane domains, this protein has little homology to G-protein receptors and it has not been positively identified as a receptor. A suggested alternative function is that of an ion channel protein in maturing macrophages. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

238 residues, UniProt reviewed canonical sequence.

>Q15546|MMD
     1  MRFKNRFQRF MNHRAPANGR YKPTCYEHAA NCYTHAFLIV PAIVGSALLH RLSDDCWEKI
    61  TAWIYGMGLC ALFIVSTVFH IVSWKKSHLR TVEHCFHMCD RMVIYFFIAA SYAPWLNLRE
   121  LGPLASHMRW FIWLMAAGGT IYVFLYHEKY KVVELFFYLT MGFSPALVVT SMNNTDGLQE
   181  LACGGLIYCL GVVFFKSDGI IPFAHAIWHL FVATAAAVHY YAIWKYLYRS PTDFMRHL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against MMD 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
Other membrane
Secreted
No
Transmembrane segments
7
Mean surface accessibility (rSASA)
0.28
Highest tissue expression
143 nTPM

Expression across tissuesHPA

Tissue

  • adipose tissue: 143 nTPM
  • basal ganglia: 102 nTPM
  • amygdala: 85 nTPM
  • hippocampal formation: 73 nTPM
  • cerebral cortex: 58 nTPM
  • midbrain: 33 nTPM

Single-cell type

  • platelets: 2,538 nCPM
  • adipocytes: 216 nCPM
  • kupffer cells: 138 nCPM
  • early primary spermatocytes: 63 nCPM
  • megakaryocytes: 62 nCPM
  • microglia: 62 nCPM

Immune cell

  • total PBMC: 18 nTPM
  • basophil: 14 nTPM
  • naive B-cell: 5 nTPM
  • MAIT T-cell: 4.9 nTPM
  • neutrophil: 4.6 nTPM
  • memory B-cell: 4.5 nTPM

Brain region

  • hippocampal formation: 183 nTPM
  • cerebral cortex: 120 nTPM
  • basal ganglia: 116 nTPM
  • amygdala: 112 nTPM
  • midbrain: 62 nTPM
  • white matter: 56 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)
1.08
gnomAD pLI
0
gnomAD missense Z
1.69
DepMap mean gene effect
0
DepMap dependency class
none

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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

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

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

Canonical record: https://seroatlas.com/gene/MMD. 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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