Seroatlas · Human Serome Atlas

LEPROTL1

Leptin receptor overlapping transcript-like 1

Also known as: LERL1_HUMAN, my047, Vps55

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
O95214
Gene
LEPROTL1
Ensembl
ENSG00000104660
Chromosome
8
Canonical length
131 aa
Protein class
Predicted membrane proteins

OverviewNCBI Gene

Enables identical protein binding activity. Predicted to be involved in late endosome to vacuole transport via multivesicular body sorting pathway and negative regulation of growth hormone receptor signaling pathway. Predicted to be located in membrane. Predicted to be active in endosome. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

131 residues, UniProt reviewed canonical sequence.

>O95214|LEPROTL1
     1  MAGIKALISL SFGGAIGLMF LMLGCALPIY NKYWPLFVLF FYILSPIPYC IARRLVDDTD
    61  AMSNACKELA IFLTTGIVVS AFGLPIVFAR AHLIEWGACA LVLTGNTVIF ATILGFFLVF
   121  GSNDDFSWQQ W

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against LEPROTL1 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
Intracellular
Secreted
No
Transmembrane segments
4
Mean surface accessibility (rSASA)
0.35
Highest tissue expression
71 nTPM

Expression across tissuesHPA

Tissue

  • placenta: 71 nTPM
  • thymus: 62 nTPM
  • bone marrow: 53 nTPM
  • adrenal gland: 44 nTPM
  • lymph node: 37 nTPM
  • liver: 35 nTPM

Single-cell type

  • t-cells: 518 nCPM
  • gastric progenitor cells: 296 nCPM
  • nk-cells: 268 nCPM
  • late primary spermatocytes: 258 nCPM
  • innate lymphoid cells: 242 nCPM
  • mast cells: 190 nCPM

Immune cell

  • naive CD4 T-cell: 350 nTPM
  • T-reg: 341 nTPM
  • total PBMC: 285 nTPM
  • naive CD8 T-cell: 262 nTPM
  • basophil: 255 nTPM
  • memory CD4 T-cell: 248 nTPM

Brain region

  • cerebellum: 44 nTPM
  • cerebral cortex: 43 nTPM
  • hippocampal formation: 43 nTPM
  • white matter: 41 nTPM
  • basal ganglia: 39 nTPM
  • hypothalamus: 38 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)
0.71
gnomAD pLI
0.72
gnomAD missense Z
0.94
DepMap mean gene effect
0.14
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

InteractionsUniProt · HPA

Protein binding partners of LEPROTL1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads LEPROTL1 as an antibody target. Whether an autoantibody or antibody against LEPROTL1 could matter depends on whether native LEPROTL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

LEPROTL1 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 LEPROTL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/LEPROTL1. 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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