ARPC1B - actin related protein 2/3 complex subunit 1B Gene

Also Known as ARC41; IMD71; PLTEID; p40-ARC; p41-ARC

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10095

About ARPC1B

Cytogenetic location: 7q22.1 Genomic coordinates (GRCh38): 7:99,374,259-99,394,816 (from NCBI)

This gene has 25 transcripts (splice variants), 212 orthologues, 1 paralogue and is associated with 1 phenotype. Broad expression in spleen (RPKM 111.2), appendix (RPKM 92.6) and 24 other tissues.

Summary

This gene encodes one of seven subunits of the human Arp2/3 protein complex. This subunit is a member of the SOP2 family of proteins and is most similar to the protein encoded by gene ARPC1A. The similarity between these two proteins suggests that they both may function as p41 subunit of the human Arp2/3 complex that has been implicated in the control of actin polymerization in cells. It is possible that the p41 subunit is involved in assembling and maintaining the structure of the Arp2/3 complex. Multiple versions of the p41 subunit may adapt the functions of the complex to different cell types or developmental stages. This protein also has a role in centrosomal homeostasis by being an activator and substrate of the Aurora A kinase. [provided by RefSeq, Mar 2011]

ARPC1B Products (1)

mRNA Protein Name
NM_005720.4 NP_005711.1 actin-related protein 2月3日 complex subunit 1B
Molecular Function GO Annotation Evidence References Source
contributes to actin filament binding IDA
IDA: Inferred from direct assay
11741539 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25944859 GOA
enables structural constituent of cytoskeleton IDA
IDA: Inferred from direct assay
11741539 GOA
Biological Process GO Annotation Evidence References Source
involved in Arp2/3 complex-mediated actin nucleation IDA
IDA: Inferred from direct assay
11741539 GOA
Cellular Component GO Annotation Evidence References Source
part of Arp2/3 protein complex IDA
IDA: Inferred from direct assay
11741539 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ARPC1B Protein Structure

WD40

WD40: WD domain, G-beta repeat (42 - 79)

WD40

WD40: WD domain, G-beta repeat (98 - 121)

WD40

WD40: WD domain, G-beta repeat (132 - 170)

  • 0
  • 100
  • 200
  • 300
  • 372 a.a.
Protein Preferred Names Protein Names

actin-related protein 2/3 complex subunit 1B

  • ARP2/3 protein complex subunit p41

Related Diseases

Diseases Alias
Immunodeficiency 71 With Inflammatory Disease And Congenital Thrombocytopenia
  • Platelet Abnormalities With Eosinophilia And Immune-Mediated Inflammatory Disease

  • IMD71

  • Plteid

  • Immunodeficiency 71

Combined T And B Cell Immunodeficiency
Combined Immunodeficiency
  • Combined T Cell And B Cell Immunodeficiency

  • Congenital Combined Immunodeficiency

  • Syndrome With Combined Immunodeficiency

  • Combined T And B Cell Immunodeficiency

  • Combined Immunity Deficiency

  • Combined Immunodeficiency Syndrome

  • Combined T-Cell And B-Cell Immunodeficiency

  • Lymphopenic Agammaglobulinaemia

Immunodeficiency 63 With Lymphoproliferation And Autoimmunity
  • IMD63

  • Il2rb Deficiency

  • Cd122 Deficiency

  • Immunodeficiency 63

  • Interleukin 2 Receptor, Beta, Deficiency Of

  • Deficiency Of Interleukin 2 Receptor Beta

Wiskott-Aldrich Syndrome
  • WAS

  • Eczema-Thrombocytopenia-Immunodeficiency Syndrome

  • Immunodeficiency 2

  • Aldrich Syndrome

  • Imd2

  • Wiskott-Aldrich Syndrome 1

  • Was1

  • Wiskott Syndrome

  • Wiskott Aldrich Syndrome

  • Eczema Thrombocytopenia Immunodeficiency Syndrome

  • Imd 2

Cd3zeta Deficiency
Thrombocytopenia
  • Low Platelet Count

  • Low Platelets

  • Decreased Platelets

  • Platelet Dysfunction Nos

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus ARPC1B VGNC VGNC:68245
Bos taurus ARPC1B VGNC VGNC:26164
Mus musculus ARPC1B MGD MGI:1343142
Rattus norvegicus ARPC1B RGD RGD:2155
Canis familiaris ARPC1B VGNC VGNC:38131