Seroatlas · Human Serome Atlas

MOBP

Myelin-associated oligodendrocyte basic protein

Also known as: MOBP_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q13875
Gene
MOBP
Ensembl
ENSG00000168314
Chromosome
3
Canonical length
183 aa
Protein class
Predicted intracellular proteins
Subcellular location
Cytoplasmic bodies

OverviewNCBI Gene

Predicted to be a structural constituent of myelin sheath. Predicted to be involved in nervous system development. Predicted to be located in mitochondrion and perinuclear region of cytoplasm. Implicated in frontotemporal dementia. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

183 residues, UniProt reviewed canonical sequence.

>Q13875|MOBP
     1  MSQKPAKEGP RLSKNQKYSE HFSIHCCPPF TFLNSKKEIV DRKYSICKSG CFYQKKEEDW
    61  ICCACQKTRT SRRAKSPQRP KQQPAAPPAV VRAPAKPRSP PRSERQPRSP PRSERQPRSP
   121  PRSERQPRSP PRSERQPRPR PEVRPPPAKQ RPPQKSKQQP RSSPLRGPGA SRGGSPVKAS
   181  RFW

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against MOBP 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)
0.68
Highest tissue expression
874 nTPM

Expression across tissuesHPA

Tissue

  • spinal cord: 874 nTPM
  • midbrain: 336 nTPM
  • hippocampal formation: 202 nTPM
  • hypothalamus: 139 nTPM
  • amygdala: 136 nTPM
  • basal ganglia: 105 nTPM

Single-cell type

  • oligodendrocytes: 1,900 nCPM
  • late spermatids: 153 nCPM
  • early spermatids: 110 nCPM
  • late primary spermatocytes: 109 nCPM
  • granulosa cells: 58 nCPM
  • platelets: 14 nCPM

Immune cell

  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM
  • intermediate monocyte: 0 nTPM
  • MAIT T-cell: 0 nTPM

Brain region

  • white matter: 1,773 nTPM
  • medulla oblongata: 1,626 nTPM
  • pons: 1,277 nTPM
  • spinal cord: 1,048 nTPM
  • basal ganglia: 954 nTPM
  • thalamus: 931 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about MOBP.

Disease | ImmuneIEDB

Conditions an epitope on MOBP 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)
1.2
gnomAD pLI
0.55
gnomAD missense Z
0.97
DepMap mean gene effect
0.02
DepMap dependency class
none

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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

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

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

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