Gene Gene information from NCBI Gene database.
Entrez ID 10120
Gene name Actin related protein 1B
Gene symbol ACTR1B
Synonyms (NCBI Gene)
ARP1BCTRN2PC3
Chromosome 2
Chromosome location 2q11.2
Summary This gene encodes a 42.3 kD subunit of dynactin, a macromolecular complex consisting of 10 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein and is involved in a diverse array of cellular functions, inc
miRNA miRNA information provided by mirtarbase database.
342
miRTarBase ID miRNA Experiments Reference
MIRT026412 hsa-miR-192-5p Microarray 19074876
MIRT048557 hsa-miR-100-5p CLASH 23622248
MIRT044201 hsa-miR-99b-5p CLASH 23622248
MIRT764387 hsa-miR-1205 CLIP-seq
MIRT764388 hsa-miR-1224-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0005515 Function Protein binding IPI 12857853, 26638075, 32814053, 33961781
GO:0005524 Function ATP binding IEA
GO:0005576 Component Extracellular region TAS
GO:0005737 Component Cytoplasm IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605144 168 ENSG00000115073
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P42025
Protein name Beta-centractin (Actin-related protein 1B) (ARP1B)
Protein function Component of a multi-subunit complex involved in microtubule based vesicle motility. It is associated with the centrosome.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00022 Actin 7 376 Actin Family
Sequence
Sequence length 376
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Motor proteins
Amyotrophic lateral sclerosis
Huntington disease
Pathways of neurodegeneration - multiple diseases
Salmonella infection
  MHC class II antigen presentation
Neutrophil degranulation
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
19
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Likely benign rs142996046 RCV005929595
Cervical cancer Likely benign rs142996046 RCV005929598
Clear cell carcinoma of kidney Likely benign rs142996046 RCV005929599
Colon adenocarcinoma Likely benign rs142996046 RCV005929594