ARL14
ADP-ribosylation factor-like protein 14
Also known as: ARF7, ARL14_HUMAN, FLJ22595
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N4G2
- Gene
- ARL14
- Ensembl
- ENSG00000179674
- Chromosome
- 3
- Canonical length
- 192 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable GTP binding activity. Predicted to be involved in intracellular protein transport and vesicle-mediated transport. Predicted to be located in cytoplasmic vesicle. Predicted to be active in cytoplasm and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
192 residues, UniProt reviewed canonical sequence.
>Q8N4G2|ARL14
1 MGSLGSKNPQ TKQAQVLLLG LDSAGKSTLL YKLKLAKDIT TIPTIGFNVE MIELERNLSL
61 TVWDVGGQEK MRTVWGCYCE NTDGLVYVVD STDKQRLEES QRQFEHILKN EHIKNVPVVL
121 LANKQDMPGA LTAEDITRMF KVKKLCSDRN WYVQPCCALT GEGLAQGFRK LTGFVKSHMK
181 SRGDTLAFFK QNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARL14 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
- 0
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 121 nTPM
Expression across tissuesHPA
Tissue
- gallbladder: 121 nTPM
- stomach: 73 nTPM
- duodenum: 48 nTPM
- colon: 40 nTPM
- rectum: 34 nTPM
- small intestine: 32 nTPM
Single-cell type
- colonocytes: 353 nCPM
- urothelial cells: 274 nCPM
- foveolar cells: 262 nCPM
- enterocytes: 166 nCPM
- goblet cells: 147 nCPM
- enteric transient amplifying cells: 84 nCPM
Immune cell
- memory B-cell: 1.8 nTPM
- naive B-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- amygdala: 0.1 nTPM
- cerebral cortex: 0.1 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 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)
- 1.89
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.11
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% 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 ARL14 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 ARL14 as an antibody target. Whether an autoantibody or antibody against ARL14 could matter depends on whether native ARL14 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARL14 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 ARL14 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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