SNX32
Sorting nexin-32
Also known as: FLJ30934, SNX32_HUMAN, SNX6B
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86XE0
- Gene
- SNX32
- Ensembl
- ENSG00000172803
- Chromosome
- 11
- Canonical length
- 403 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Focal adhesion sites,Cytosol
OverviewNCBI Gene
Predicted to enable phosphatidylinositol binding activity. Predicted to be involved in retrograde transport, endosome to Golgi. Predicted to be located in cytoplasmic vesicle and cytosol. Predicted to be active in endosome. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
403 residues, UniProt reviewed canonical sequence.
>Q86XE0|SNX32
1 METYAEVGKE GKPSCASVDL QGDSSLQVEI SDAVSERDKV KFTVQTKSCL PHFAQTEFSV
61 VRQHEEFIWL HDAYVENEEY AGLIIPPAPP RPDFEASREK LQKLGEGDSS VTREEFAKMK
121 QELEAEYLAI FKKTVAMHEV FLQRLAAHPT LRRDHNFFVF LEYGQDLSVR GKNRKELLGG
181 FLRNIVKSAD EALITGMSGL KEVDDFFEHE RTFLLEYHTR IRDACLRADR VMRAHKCLAD
241 DYIPISAALS SLGTQEVNQL RTSFLKLAEL FERLRKLEGR VASDEDLKLS DMLRYYMRDS
301 QAAKDLLYRR LRALADYENA NKALDKARTR NREVRPAESH QQLCCQRFER LSDSAKQELM
361 DFKSRRVSSF RKNLIELAEL ELKHAKASTL ILRNTLVALK GEPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SNX32 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
- 0
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 27 nTPM
- basal ganglia: 26 nTPM
- hippocampal formation: 18 nTPM
- amygdala: 15 nTPM
- hypothalamus: 8.1 nTPM
- cerebellum: 5.3 nTPM
Single-cell type
- epicardial cells: 212 nCPM
- cardiomyocytes: 108 nCPM
- thymocytes: 85 nCPM
- brain inhibitory neurons: 82 nCPM
- plasma cells: 73 nCPM
- paneth cells: 70 nCPM
Immune cell
- MAIT T-cell: 0.7 nTPM
- gdT-cell: 0.3 nTPM
- memory CD4 T-cell: 0.3 nTPM
- myeloid DC: 0.3 nTPM
- naive CD4 T-cell: 0.3 nTPM
- T-reg: 0.3 nTPM
Brain region
- cerebral cortex: 24 nTPM
- hippocampal formation: 19 nTPM
- basal ganglia: 18 nTPM
- white matter: 18 nTPM
- amygdala: 16 nTPM
- thalamus: 8.9 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)
- 1.4
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.26
- DepMap mean gene effect
- -0.19
- DepMap dependency class
- selective
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).
OntologyGO
Biological processes
- endosomal transport
- endosome to lysosome transport via multivesicular body sorting pathway
- neuron projection extension
- protein transport
- regulation of macroautophagy
- retrograde transport, endosome to Golgi
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SNX32 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SNX32 as an antibody target. Whether an autoantibody or antibody against SNX32 could matter depends on whether native SNX32 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SNX32 is annotated at the cell surface, where native SNX32 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 SNX32 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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