SLC66A1
Lysosomal amino acid transporter 1 homolog
Also known as: FLJ20320, LAAT-1, LAAT1, LAAT1_HUMAN, PQLC2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6ZP29
- Gene
- SLC66A1
- Ensembl
- ENSG00000040487
- Chromosome
- 1
- Canonical length
- 291 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Vesicles
OverviewNCBI Gene
Enables L-arginine transmembrane transporter activity; L-histidine transmembrane transporter activity; and L-lysine transmembrane transporter activity. Involved in L-amino acid transport and intracellular amino acid homeostasis. Located in lysosomal membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
291 residues, UniProt reviewed canonical sequence.
>Q6ZP29|SLC66A1
1 MVWKKLGSRN FSSCPSGSIQ WIWDVLGECA QDGWDEASVG LGLISILCFA ASTFPQFIKA
61 YKTGNMDQAL SLWFLLGWIG GDSCNLIGSF LADQLPLQTY TAVYYVLADL VMLTLYFYYK
121 FRTRPSLLSA PINSVLLFLM GMACATPLLS AAGPVAAPRE AFRGRALLSV ESGSKPFTRQ
181 EVIGFVIGSI SSVLYLLSRL PQIRTNFLRK STQGISYSLF ALVMLGNTLY GLSVLLKNPE
241 EGQSEGSYLL HHLPWLVGSL GVLLLDTIIS IQFLVYRRST AASELEPLLP SLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC66A1 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 7
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 31 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 31 nTPM
- liver: 26 nTPM
- adrenal gland: 24 nTPM
- pituitary gland: 23 nTPM
- testis: 18 nTPM
- pancreas: 17 nTPM
Single-cell type
- syncytiotrophoblasts: 83 nCPM
- hofbauer cells: 61 nCPM
- cytotrophoblasts: 31 nCPM
- migrating cytotrophoblasts: 24 nCPM
- extravillous trophoblasts: 20 nCPM
- megakaryocytes: 19 nCPM
Immune cell
- plasmacytoid DC: 21 nTPM
- non-classical monocyte: 14 nTPM
- myeloid DC: 14 nTPM
- classical monocyte: 11 nTPM
- eosinophil: 10 nTPM
- intermediate monocyte: 9.1 nTPM
Brain region
- cerebellum: 32 nTPM
- cerebral cortex: 28 nTPM
- medulla oblongata: 28 nTPM
- pons: 26 nTPM
- white matter: 26 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)
- 1
- gnomAD pLI
- 0
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- none
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
- intracellular amino acid homeostasis
- L-arginine transmembrane transport
- L-histidine transmembrane transport
- L-lysine transmembrane transport
- lysine transport
- transmembrane transport
Molecular functions
- basic amino acid transmembrane transporter activity
- L-arginine transmembrane transporter activity
- L-histidine transmembrane transporter activity
- L-lysine transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC66A1 as an antibody target. Whether an autoantibody or antibody against SLC66A1 could matter depends on whether native SLC66A1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC66A1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SLC66A1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...