SLC6A7
Sodium-dependent proline transporter
Also known as: PROT, SC6A7_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99884
- Gene
- SLC6A7
- Ensembl
- ENSG00000011083
- Chromosome
- 5
- Canonical length
- 636 aa
- Protein class
- Metabolic proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
This gene is a member of the gamma-aminobutyric acid (GABA) neurotransmitter gene family and encodes a high-affinity mammalian brain L-proline transporter protein. This transporter protein differs from other sodium-dependent plasma membrane carriers by its pharmacological specificity, kinetic properties, and ionic requirements. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
636 residues, UniProt reviewed canonical sequence.
>Q99884|SLC6A7
1 MKKLQGAHLR KPVTPDLLMT PSDQGDVDLD VDFAAHRGNW TGKLDFLLSC IGYCVGLGNV
61 WRFPYRAYTN GGGAFLVPYF LMLAICGIPL FFLELSLGQF SSLGPLAVWK ISPLFKGAGA
121 AMLLIVGLVA IYYNMIIAYV LFYLFASLTS DLPWEHCGNW WNTELCLEHR VSKDGNGALP
181 LNLTCTVSPS EEYWSRYVLH IQGSQGIGSP GEIRWNLCLC LLLAWVIVFL CILKGVKSSG
241 KVVYFTATFP YLILLMLLVR GVTLPGAWKG IQFYLTPQFH HLLSSKVWIE AALQIFYSLG
301 VGFGGLLTFA SYNTFHQNIY RDTFIVTLGN AITSILAGFA IFSVLGYMSQ ELGVPVDQVA
361 KAGPGLAFVV YPQAMTMLPL SPFWSFLFFF MLLTLGLDSQ FAFLETIVTA VTDEFPYYLR
421 PKKAVFSGLI CVAMYLMGLI LTTDGGMYWL VLLDDYSASF GLMVVVITTC LAVTRVYGIQ
481 RFCRDIHMML GFKPGLYFRA CWLFLSPATL LALMVYSIVK YQPSEYGSYR FPPWAELLGI
541 LMGLLSCLMI PAGMLVAVLR EEGSLWERLQ QASRPAMDWG PSLEENRTGM YVATLAGSQS
601 PKPLMVHMRK YGGITSFENT AIEVDREIAE EEESMMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC6A7 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)
- 0.25
- Highest tissue expression
- 68 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 68 nTPM
- cerebral cortex: 30 nTPM
- hippocampal formation: 6.6 nTPM
- hypothalamus: 5.9 nTPM
- colon: 5.4 nTPM
- amygdala: 4.1 nTPM
Single-cell type
- brain excitatory neurons: 52 nCPM
- colonocytes: 32 nCPM
- goblet cells: 27 nCPM
- thymic myoid cells: 22 nCPM
- enteric stem cells: 22 nCPM
- cardiomyocytes: 21 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
- cerebral cortex: 53 nTPM
- cerebellum: 37 nTPM
- basal ganglia: 29 nTPM
- thalamus: 28 nTPM
- white matter: 27 nTPM
- hippocampal formation: 16 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)
- 0.88
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.52
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- glycine import across plasma membrane
- neurotransmitter transport
- proline transport
- protein catabolic process
- sodium ion transmembrane transport
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC6A7 as an antibody target. Whether an autoantibody or antibody against SLC6A7 could matter depends on whether native SLC6A7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC6A7 is annotated at the cell surface, where native SLC6A7 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 SLC6A7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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