Gene Gene information from NCBI Gene database.
Entrez ID 339231
Gene name ARF like GTPase 16
Gene symbol ARL16
Synonyms (NCBI Gene)
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Chromosome 17
Chromosome location 17q25.3
Summary The protein encoded by this gene belongs to the ARL (ADP-ribosylation factor-like) family of proteins, which are structurally related to ADP-ribosylation factors (ARFs). This protein has been shown to have an inhibitory role in the cellular antiviral resp
miRNA miRNA information provided by mirtarbase database.
156
miRTarBase ID miRNA Experiments Reference
MIRT045382 hsa-miR-185-5p CLASH 23622248
MIRT797570 hsa-miR-136 CLIP-seq
MIRT797571 hsa-miR-1915 CLIP-seq
MIRT797572 hsa-miR-1976 CLIP-seq
MIRT797573 hsa-miR-3149 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0003924 Function GTPase activity IEA
GO:0005515 Function Protein binding IPI 21233210, 25416956, 31515488, 32296183, 32814053
GO:0005525 Function GTP binding IEA
GO:0005737 Component Cytoplasm IDA 21233210
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619117 27902 ENSG00000214087
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q0P5N6
Protein name ADP-ribosylation factor-like protein 16
Protein function May suppress the RNA sensing activity of RIGI in a GTP-dependent.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00025 Arf 14 193 ADP-ribosylation factor family Domain
Sequence
Sequence length 197
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Childhood-onset schizophrenia Likely pathogenic rs863223352 RCV000202347