Seroatlas · Human Serome Atlas

LYSMD2

LysM and putative peptidoglycan-binding domain-containing protein 2

Also known as: LYSM2_HUMAN, MGC35274

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

Protein identityUniProt · HPA

UniProt accession
Q8IV50
Gene
LYSMD2
Ensembl
ENSG00000140280
Chromosome
15
Canonical length
215 aa
Protein class
Predicted intracellular proteins
Subcellular location
Nuclear bodies,Mitochondria

OverviewNCBI Gene

No narrative summary is available for LYSMD2 in this catalog release; identity and structured annotations are shown without generated factual claims.

Canonical amino-acid sequenceUniProt

215 residues, UniProt reviewed canonical sequence.

>Q8IV50|LYSMD2
     1  MADSSPALSL REGGPRAPRP SAPSPPPRSR SGSESEEAEL SLSLARTKTR SYGSTASVRA
    61  PLGAGVIERH VEHRVRAGDT LQGIALKYGV TMEQIKRANK LFTNDCIFLK KTLNIPVISE
   121  KPLLFNGLNS IDSPENETAD NSFSQEEEPV VAGEDLPPPS PQESDVQPVQ PEEVSARDFL
   181  QRLDLQIKLS TQAAKKLKEE SRDEESPYAT SLYHS

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against LYSMD2 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
Unknown
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.57
Highest tissue expression
44 nTPM

Expression across tissuesHPA

Tissue

  • cerebral cortex: 44 nTPM
  • cerebellum: 37 nTPM
  • hypothalamus: 35 nTPM
  • basal ganglia: 34 nTPM
  • hippocampal formation: 31 nTPM
  • amygdala: 31 nTPM

Single-cell type

  • early spermatids: 174 nCPM
  • late spermatids: 134 nCPM
  • pdcs: 98 nCPM
  • neuroendocrine cells: 80 nCPM
  • late primary spermatocytes: 76 nCPM
  • kupffer cells: 63 nCPM

Immune cell

  • neutrophil: 113 nTPM
  • eosinophil: 77 nTPM
  • non-classical monocyte: 62 nTPM
  • plasmacytoid DC: 55 nTPM
  • naive B-cell: 50 nTPM
  • intermediate monocyte: 49 nTPM

Brain region

  • hypothalamus: 50 nTPM
  • pons: 50 nTPM
  • cerebral cortex: 47 nTPM
  • thalamus: 40 nTPM
  • medulla oblongata: 37 nTPM
  • basal ganglia: 37 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)
0.91
gnomAD pLI
0.42
gnomAD missense Z
0.21
DepMap mean gene effect
0.08
DepMap dependency class
none

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).

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads LYSMD2 as an antibody target. Whether an autoantibody or antibody against LYSMD2 could matter depends on whether native LYSMD2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

LYSMD2 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 LYSMD2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/LYSMD2. 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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