Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
403
Gene name Gene Name - the full gene name approved by the HGNC.
ARF like GTPase 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ARL3
Synonyms (NCBI Gene) Gene synonyms aliases
ARFL3, JBTS35, RP83
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q24.32
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604695 694 ENSG00000138175
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Joubert Syndrome joubert syndrome 35 rs776901858 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Prostate cancer Prostate cancer N/A N/A GWAS
Retinitis Pigmentosa retinitis pigmentosa 83, retinitis pigmentosa N/A N/A ClinVar, GenCC
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease 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