Gene Gene information from NCBI Gene database.
Entrez ID 403
Gene name ARF like GTPase 3
Gene symbol ARL3
Synonyms (NCBI Gene)
ARFL3JBTS35RP83
Chromosome 10
Chromosome location 10q24.32
Summary ADP-ribosylation factor-like 3 is a member of the ADP-ribosylation factor family of GTP-binding proteins. ARL3 binds guanine nucleotides but lacks ADP-ribosylation factor activity. [provided by RefSeq, Jul 2008]
SNPs SNP information provided by dbSNP.
3
SNP ID Visualize variation Clinical significance Consequence
rs770782663 C>T Uncertain-significance, pathogenic Coding sequence variant, missense variant
rs776901858 G>A Pathogenic Coding sequence variant, missense variant
rs1590122229 C>A Pathogenic Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
161
miRTarBase ID miRNA Experiments Reference
MIRT027108 hsa-miR-103a-3p Sequencing 20371350
MIRT031723 hsa-miR-16-5p Sequencing 20371350
MIRT719652 hsa-miR-6736-3p HITS-CLIP 19536157
MIRT719651 hsa-miR-1976 HITS-CLIP 19536157
MIRT719650 hsa-miR-4660 HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
54
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0000166 Function Nucleotide binding IEA
GO:0000281 Process Mitotic cytokinesis IMP 16525022
GO:0000287 Function Magnesium ion binding IEA
GO:0001822 Process Kidney development IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604695 694 ENSG00000138175
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P36405
Protein name ADP-ribosylation factor-like protein 3
Protein function Small GTP-binding protein which cycles between an inactive GDP-bound and an active GTP-bound form, and the rate of cycling is regulated by guanine nucleotide exchange factors (GEF) and GTPase-activating proteins (GAP) (PubMed:16525022, PubMed:18
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00025 Arf 3 177 ADP-ribosylation factor family Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in the retina. Strongly expressed in connecting cilium, the myoid region of the inner segments (IS) and in cone photoreceptors (at protein level). {ECO:0000269|PubMed:12417528}.
Sequence
Sequence length 182
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Trafficking of myristoylated proteins to the cilium
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
27
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Joubert syndrome 35 Pathogenic rs776901858 RCV000714511
Progressive cone degeneration Pathogenic rs1590122229 RCV000791321
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
ARL3-related disorder Likely benign rs770491993, rs1477501222 RCV003938871
RCV003971396
Hepatocellular carcinoma Uncertain significance rs763678922 RCV005909093
Retinal dystrophy Uncertain significance; Benign; Likely benign; Conflicting classifications of pathogenicity rs1249451954, rs148260445, rs746743719, rs370505468, rs201771386, rs763678922, rs551366324 RCV004815377
RCV003888125
RCV003888137
RCV003888998
RCV003889015
RCV003889568
RCV003887991
Retinitis pigmentosa Conflicting classifications of pathogenicity rs551366324, rs2064304102 RCV001293654
RCV001293655
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Agenesis of Cerebellar Vermis Associate 30269812, 33297941
Ciliopathies Associate 33297941
Disease Associate 31234870
Genetic Diseases Inborn Associate 26964041
Glioma Inhibit 31234870
Retinal Degeneration Associate 28444310
Retinitis Pigmentosa Associate 26964041, 30280194
Retinitis Pigmentosa 2 Associate 18588884