Seroatlas · Human Serome Atlas

MOSMO

Modulator of smoothened protein

Also known as: ATTHOG, BC030336, C16orf52, MOSMO_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q8NHV5
Gene
MOSMO
Ensembl
ENSG00000185716
Chromosome
16
Canonical length
167 aa
Protein class
Predicted membrane proteins

OverviewNCBI Gene

Predicted to be involved in negative regulation of smoothened signaling pathway; regulation of neuron differentiation; and regulation of protein stability. Predicted to act upstream of or within several processes, including chordate embryonic development; embryonic limb morphogenesis; and smoothened signaling pathway. Predicted to be located in plasma membrane. Predicted to be active in Golgi apparatus and ciliary membrane. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

167 residues, UniProt reviewed canonical sequence.

>Q8NHV5|MOSMO
     1  MDKLTIISGC LFLAADIFAI ASIANPDWIN TGESAGALTV GLVRQCQTIH GRDRTCIPPR
    61  LPPEWVTTLF FIIMGIISLT VTCGLLVASH WRREATKYAR WIAFTGMILF CMAALIFPIG
   121  FYINEVGGQP YKLPNNTVVG SSYVLFVLSI FFTIVGLLFA GKVCLPG

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against MOSMO 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
Cell surface
Secreted
No
Transmembrane segments
4
Mean surface accessibility (rSASA)
0.3
Highest tissue expression
20 nTPM

Expression across tissuesHPA

Tissue

  • adrenal gland: 20 nTPM
  • parathyroid gland: 17 nTPM
  • cerebral cortex: 14 nTPM
  • cerebellum: 13 nTPM
  • liver: 13 nTPM
  • retina: 12 nTPM

Single-cell type

  • brain excitatory neurons: 146 nCPM
  • brain inhibitory neurons: 140 nCPM
  • other brain neurons: 117 nCPM
  • choroid plexus epithelial cells: 114 nCPM
  • oligodendrocyte progenitor cells: 104 nCPM
  • podocytes: 95 nCPM

Immune cell

  • naive B-cell: 1 nTPM
  • T-reg: 0.6 nTPM
  • eosinophil: 0.4 nTPM
  • basophil: 0.3 nTPM
  • gdT-cell: 0.3 nTPM
  • intermediate monocyte: 0.3 nTPM

Brain region

  • cerebral cortex: 38 nTPM
  • cerebellum: 34 nTPM
  • white matter: 30 nTPM
  • basal ganglia: 25 nTPM
  • hippocampal formation: 24 nTPM
  • thalamus: 24 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)
0.82
gnomAD pLI
0.26
DepMap mean gene effect
0.06
DepMap dependency class
selective

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

Cellular components

Protein domainsUniProt · Pfam · InterPro

  • Modulator of smoothened protein
  • Attenuator of Hedgehog

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

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

MOSMO is annotated at the cell surface, where native MOSMO is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.

Annotation status

The present source text does not explicitly label MOSMO as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

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