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 GKVCLPGLocalizationUniProt · 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
- cell differentiation
- embryonic limb morphogenesis
- embryonic skeletal system development
- gene expression
- heart development
- in utero embryonic development
- intracellular protein localization
- left/right pattern formation
- lung development
- negative regulation of smoothened signaling pathway
- regulation of neuron differentiation
- regulation of protein stability
- smoothened signaling pathway
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.
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