BOP1 - BOP1 ribosomal biogenesis factor Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 23246

About BOP1

Cytogenetic location: 8q24.3 Genomic coordinates (GRCh38): 8:144,262,045-144,291,438 (from NCBI)

This gene has 6 transcripts (splice variants), 1 gene allele and 182 orthologues. Ubiquitous expression in testis (RPKM 10.2), appendix (RPKM 9.2) and 25 other tissues.

Summary

Enables RNA binding activity. Involved in regulation of cell cycle; regulation of signal transduction by p53 class mediator; and ribosomal large subunit biogenesis. Located in chromosome; nucleolus; and nucleoplasm. Part of PeBoW complex. [provided by Alliance of Genome Resources, Apr 2022]

BOP1 Products (1)

mRNA Protein Name
NM_015201.5 NP_056016.1 ribosome biogenesis protein BOP1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
16043514 GOA
Biological Process GO Annotation Evidence References Source
involved in maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) IMP
IMP: Inferred from mutant phenotype
17353269 GOA
involved in regulation of cell cycle IMP
IMP: Inferred from mutant phenotype
16043514 GOA
involved in regulation of signal transduction by p53 class mediator IMP
IMP: Inferred from mutant phenotype
24120868 GOA
involved in ribosomal large subunit assembly IMP
IMP: Inferred from mutant phenotype
24120868 GOA
Cellular Component GO Annotation Evidence References Source
part of PeBoW complex IDA
IDA: Inferred from direct assay
16043514 GOA
part of ribonucleoprotein complex IDA
IDA: Inferred from direct assay
18809582 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

BOP1 Protein Structure

BOP1NT

BOP1NT: BOP1NT (NUC169) domain (144 - 402)

WD40

WD40: WD domain, G-beta repeat (408 - 441)

WD40

WD40: WD domain, G-beta repeat (655 - 689)

WD40

WD40: WD domain, G-beta repeat (720 - 745)

  • 0
  • 200
  • 400
  • 600
  • 746 a.a.
Protein Preferred Names Protein Names

ribosome biogenesis protein BOP1

  • block of proliferation 1

BOP1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
BOP1 Q14137 PES1 Homo sapiens O00541 16043514
Intra
BOP1 Q14137 PES1 Homo sapiens O00541 16043514
Intra
BOP1 Q14137 WDR12 Homo sapiens Q9GZL7 16043514
Intra
BOP1 Q14137 WDR12 Homo sapiens Q9GZL7 16043514
Cross: Cross-species interaction Intra: Intraspecies interaction

BOP1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P89786 BOP1 Antibody (YA9130) WB, ICC/IF, IF-Tissue, IP, ELISA human

Related Diseases

Diseases Alias
Diamond-Blackfan Anemia
  • Congenital Pure Red Cell Aplasia

  • Aase Syndrome

  • Erythrogenesis Imperfecta

  • Anemia, Diamond-Blackfan

  • Congenital Hypoplastic Anemia

  • Aase-Smith Ii Syndrome

  • Bds

  • Blackfan-Diamond Anemia

  • Congenital Prca

  • Congenital Hypoplastic Anemia, Blackfan-Diamond Type

  • Dba

  • Blackfan - Diamond Syndrome

  • Chronic Constitutional Pure Red Cell Anaemia

  • Anemia Diamond Blackfan Type

  • Anemia Congenital Erythroid Hypoplastic

  • Aregenerative Anemia Chronic Congenital

  • Blackfan Diamond Syndrome

  • Red Cell Aplasia, Pure Hereditary

  • Aase-Smith Syndrome Ii

  • Bda

  • Blackfan Diamond Anemia

  • Blackfan-Diamond Disease

  • Blackfan-Diamond Syndrome

  • Chronic Congenital Agenerative Anemia

  • Congenital Erythroid Hypoplastic Anemia

  • Congenital Hypoplastic Anemia Of Blackfan And Diamond

  • Congenital Pure Red Cell Anemia

  • Hypoplastic Congenital Anemia

  • Inherited Erythroblastopenia

  • Pure Hereditary Red Cell Aplasia

  • Anemia, Hypoplastic, Congenital

  • Anemia Hypoplastic Congenital

  • Fanconi Anemia

  • Constitutional Aplastic Anemia

  • Diamond-Blackfan Anemia 1

  • Aase Smith Syndrome 2

  • Congenital Red Cell Aplasia

  • Red Cell Aplasia Of Infants

  • Pure Red Cell Aplasia Of Infants

  • Congenital Red Cell Aplastic Anaemia

  • Congenital Pure Red Cell Anaemia

  • Congenital Erythroid Hypoplasia

  • Pearson Marrow-Pancreas Syndrome

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
Macaca mulatta BOP1 VGNC VGNC:70315
Felis catus BOP1 VGNC VGNC:60149
Canis familiaris BOP1 VGNC VGNC:38498
Mus musculus BOP1 MGD MGI:1334460
Bos taurus BOP1 VGNC VGNC:26540
Rattus norvegicus BOP1 RGD RGD:1310589
Others BOP1 NCBI