Gene Gene information from NCBI Gene database.
Entrez ID 348110
Gene name Actin related protein 2/3 complex inhibitor
Gene symbol ARPIN
Synonyms (NCBI Gene)
C15orf38
Chromosome 15
Chromosome location 15q26.1
miRNA miRNA information provided by mirtarbase database.
246
miRTarBase ID miRNA Experiments Reference
MIRT728134 hsa-miR-19a-3p HITS-CLIP 22473208
MIRT728132 hsa-miR-19b-3p HITS-CLIP 22473208
MIRT741273 hsa-miR-1247-3p PAR-CLIP 26701625
MIRT741273 hsa-miR-1247-3p PAR-CLIP 26701625
MIRT741274 hsa-miR-1827 PAR-CLIP 26701625
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 24132237, 25416956, 26774128, 32296183
GO:0030027 Component Lamellipodium IEA
GO:0030027 Component Lamellipodium ISS
GO:0030336 Process Negative regulation of cell migration IMP 24132237
GO:0033058 Process Directional locomotion IMP 24132237
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
615543 28782 ENSG00000242498
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q7Z6K5
Protein name Arpin (Arp2/3 inhibition protein)
Protein function Regulates actin polymerization by inhibiting the actin-nucleating activity of the Arp2/3 complex; the function is competitive with nucleation promoting factors. Participates in an incoherent feedforward loop at the lamellipodium tip where it inh
PDB 4Z68 , 7JPN
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10574 UPF0552 1 224 Arp2/3-interacting proteins Arpin Family
Sequence
Sequence length 226
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
DIABETIC NEUROPATHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OLIGODENDROGLIOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations