Seroatlas · Human Serome Atlas

ARL15

ADP-ribosylation factor-like protein 15

Also known as: ARFRP2, ARL15_HUMAN, FLJ20051

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

Protein identityUniProt · HPA

UniProt accession
Q9NXU5
Gene
ARL15
Ensembl
ENSG00000185305
Chromosome
5
Canonical length
204 aa
Protein class
Predicted intracellular proteins
Subcellular location
Microtubules,Cytokinetic bridge,Mitotic spindle,Primary cilium,Basal body

OverviewNCBI Gene

Predicted to enable GTP binding activity and GTPase activity. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

204 residues, UniProt reviewed canonical sequence.

>Q9NXU5|ARL15
     1  MSDLRITEAF LYMDYLCFRA LCCKGPPPAR PEYDLVCIGL TGSGKTSLLS KLCSESPDNV
    61  VSTTGFSIKA VPFQNAILNV KELGGADNIR KYWSRYYQGS QGVIFVLDSA SSEDDLEAAR
   121  NELHSALQHP QLCTLPFLIL ANHQDKPAAR SVQEIKKYFE LEPLARGKRW ILQPCSLDDM
   181  DALKDSFSQL INLLEEKDHE AVRM

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against ARL15 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
Unknown
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.32
Highest tissue expression
21 nTPM

Expression across tissuesHPA

Tissue

  • placenta: 21 nTPM
  • kidney: 17 nTPM
  • cervix: 16 nTPM
  • smooth muscle: 16 nTPM
  • endometrium: 15 nTPM
  • gallbladder: 13 nTPM

Single-cell type

  • renal connecting tubule cells: 3,280 nCPM
  • sertoli cells: 2,305 nCPM
  • renal collecting duct intercalated cells: 2,220 nCPM
  • cytotrophoblasts: 1,519 nCPM
  • vascular endothelial cells: 1,394 nCPM
  • pituitary stem cells: 1,168 nCPM

Immune cell

  • neutrophil: 3.7 nTPM
  • T-reg: 2.6 nTPM
  • myeloid DC: 2.5 nTPM
  • eosinophil: 2.4 nTPM
  • classical monocyte: 1.8 nTPM
  • intermediate monocyte: 1.5 nTPM

Brain region

  • hippocampal formation: 12 nTPM
  • cerebral cortex: 12 nTPM
  • basal ganglia: 9.8 nTPM
  • choroid plexus: 9.6 nTPM
  • hypothalamus: 9.2 nTPM
  • thalamus: 8.6 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)
1.2
gnomAD pLI
0
gnomAD missense Z
0.71
DepMap mean gene effect
-0.02
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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of ARL15 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 ARL15 as an antibody target. Whether an autoantibody or antibody against ARL15 could matter depends on whether native ARL15 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

ARL15 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 ARL15 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/ARL15. 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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