Seroatlas · Human Serome Atlas

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 S

LocalizationUniProt · 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

Molecular functions

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.

Canonical record: https://seroatlas.com/gene/SLC66A1. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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