SLC7A10
Asc-type amino acid transporter 1
Also known as: AAA1_HUMAN, asc-1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NS82
- Gene
- SLC7A10
- Ensembl
- ENSG00000130876
- Chromosome
- 19
- Canonical length
- 523 aa
- Protein class
- Metabolic proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoplasm,Nucleoli
OverviewNCBI Gene
SLC7A10, in association with 4F2HC (SLC3A2; MIM 158070), mediates high-affinity transport of D-serine and several other neutral amino acids (Nakauchi et al., 2000 [PubMed 10863037]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
523 residues, UniProt reviewed canonical sequence.
>Q9NS82|SLC7A10
1 MAGHTQQPSG RGNPRPAPSP SPVPGTVPGA SERVALKKEI GLLSACTIII GNIIGSGIFI
61 SPKGVLEHSG SVGLALFVWV LGGGVTALGS LCYAELGVAI PKSGGDYAYV TEIFGGLAGF
121 LLLWSAVLIM YPTSLAVISM TFSNYVLQPV FPNCIPPTTA SRVLSMACLM LLTWVNSSSV
181 RWATRIQDMF TGGKLLALSL IIGVGLLQIF QGHFEELRPS NAFAFWMTPS VGHLALAFLQ
241 GSFAFSGWNF LNYVTEEMVD ARKNLPRAIF ISIPLVTFVY TFTNIAYFTA MSPQELLSSN
301 AVAVTFGEKL LGYFSWVMPV SVALSTFGGI NGYLFTYSRL CFSGAREGHL PSLLAMIHVR
361 HCTPIPALLV CCGATAVIML VGDTYTLINY VSFINYLCYG VTILGLLLLR WRRPALHRPI
421 KVNLLIPVAY LVFWAFLLVF SFISEPMVCG VGVIIILTGV PIFFLGVFWR SKPKCVHRLT
481 ESMTHWGQEL CFVVYPQDAP EEEENGPCPP SLLPATDKPS KPQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC7A10 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
- 9
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 30 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 30 nTPM
- basal ganglia: 20 nTPM
- amygdala: 14 nTPM
- cerebral cortex: 13 nTPM
- breast: 13 nTPM
- midbrain: 11 nTPM
Single-cell type
- astrocytes: 59 nCPM
- adipocytes: 47 nCPM
- retinal pigment epithelial cells: 43 nCPM
- bergmann glia: 29 nCPM
- oligodendrocyte progenitor cells: 20 nCPM
- undifferentiated spermatogonia: 9.1 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- thalamus: 22 nTPM
- midbrain: 21 nTPM
- cerebellum: 16 nTPM
- basal ganglia: 15 nTPM
- hypothalamus: 14 nTPM
- pons: 13 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)
- 0.77
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.11
- DepMap mean gene effect
- -0.05
- 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).
OntologyGO
Biological processes
- amino acid transport
- glycine transport
- negative regulation of brown fat cell differentiation
- neutral amino acid transport
- D-alanine transmembrane transport
- D-serine transmembrane transport
- positive regulation of synaptic transmission, glycinergic
Molecular functions
- L-amino acid transmembrane transporter activity
- L-serine transmembrane transporter activity
- neutral L-amino acid transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC7A10 as an antibody target. Whether an autoantibody or antibody against SLC7A10 could matter depends on whether native SLC7A10 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC7A10 is annotated at the cell surface, where native SLC7A10 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 SLC7A10 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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