SLC2A13
Proton myo-inositol cotransporter
Also known as: HMIT, MYCT_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96QE2
- Gene
- SLC2A13
- Ensembl
- ENSG00000151229
- Chromosome
- 12
- Canonical length
- 648 aa
- Protein class
- Metabolic proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Nuclear membrane
OverviewNCBI Gene
Enables ATPase binding activity; myo-inositol:proton symporter activity; and protease binding activity. Involved in myo-inositol transport and positive regulation of amyloid-beta formation. Located in cell body; cell projection; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
648 residues, UniProt reviewed canonical sequence.
>Q96QE2|SLC2A13
1 MSRKASENVE YTLRSLSSLM GERRRKQPEP DAASAAGECS LLAAAESSTS LQSAGAGGGG
61 VGDLERAARR QFQQDETPAF VYVVAVFSAL GGFLFGYDTG VVSGAMLLLK RQLSLDALWQ
121 ELLVSSTVGA AAVSALAGGA LNGVFGRRAA ILLASALFTA GSAVLAAANN KETLLAGRLV
181 VGLGIGIASM TVPVYIAEVS PPNLRGRLVT INTLFITGGQ FFASVVDGAF SYLQKDGWRY
241 MLGLAAVPAV IQFFGFLFLP ESPRWLIQKG QTQKARRILS QMRGNQTIDE EYDSIKNNIE
301 EEEKEVGSAG PVICRMLSYP PTRRALIVGC GLQMFQQLSG INTIMYYSAT ILQMSGVEDD
361 RLAIWLASVT AFTNFIFTLV GVWLVEKVGR RKLTFGSLAG TTVALIILAL GFVLSAQVSP
421 RITFKPIAPS GQNATCTRYS YCNECMLDPD CGFCYKMNKS TVIDSSCVPV NKASTNEAAW
481 GRCENETKFK TEDIFWAYNF CPTPYSWTAL LGLILYLVFF APGMGPMPWT VNSEIYPLWA
541 RSTGNACSSG INWIFNVLVS LTFLHTAEYL TYYGAFFLYA GFAAVGLLFI YGCLPETKGK
601 KLEEIESLFD NRLCTCGTSD SDEGRYIEYI RVKGSNYHLS DNDASDVELocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC2A13 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
- 12
- Mean surface accessibility (rSASA)
- 0.3
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 27 nTPM
- parathyroid gland: 21 nTPM
- cervix: 12 nTPM
- kidney: 10 nTPM
- basal ganglia: 9.6 nTPM
- hypothalamus: 8.9 nTPM
Single-cell type
- choroid plexus epithelial cells: 905 nCPM
- retinal horizontal cells: 561 nCPM
- brain inhibitory neurons: 506 nCPM
- other brain neurons: 469 nCPM
- lactotrophs: 443 nCPM
- oligodendrocyte progenitor cells: 411 nCPM
Immune cell
- naive B-cell: 0.5 nTPM
- eosinophil: 0.2 nTPM
- memory CD8 T-cell: 0.1 nTPM
- neutrophil: 0.1 nTPM
- NK-cell: 0.1 nTPM
- basophil: 0 nTPM
Brain region
- choroid plexus: 57 nTPM
- cerebral cortex: 52 nTPM
- midbrain: 48 nTPM
- hypothalamus: 45 nTPM
- thalamus: 43 nTPM
- basal ganglia: 42 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SLC2A13.
Disease | ImmuneIEDB
Conditions an epitope on SLC2A13 was assayed in.
- skin melanoma T cell
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)
- 0.38
- gnomAD pLI
- 0.83
- gnomAD missense Z
- 1.48
- DepMap mean gene effect
- -0.09
- 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
- myo-inositol transport
- positive regulation of amyloid-beta formation
- transmembrane transport
- transport across blood-brain barrier
Molecular functions
- ATPase binding
- myo-inositol transmembrane transporter activity
- protease binding
- myo-inositol:proton symporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC2A13 as an antibody target. Whether an autoantibody or antibody against SLC2A13 could matter depends on whether native SLC2A13 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC2A13 is annotated at the cell surface, where native SLC2A13 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 SLC2A13 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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