Rb1

                                                   (retinoblastoma 1 (including osteosarcoma))

  • Alias                                 (According to NCBI)

 

 
  • RB
  • Retinoblastoma-1
  • retinoblastoma 1 (including osteosarcoma) 
  • Retinoblastoma-associated protein (PP110) (P105-RB) (RB)
  • Retinoblastoma (RB) is an embryonic malignant neoplasm of retinal origin. It almost always presents in early childhood and is often bilateral. Probably acts as a regulator of other genes. Forms a complex with adenovirus E1A and with SV40 large T antigen. Acts as a tumor suppressor. May bind and modulate functionally certain cellular proteins with which T and E1A compete for pocket binding. Potent inhibitor of E2F-mediated trans-activation. Recruits and targets histone methyltransferase SUV39H1 leading to epigenetic transcriptional repression. Inhibits the intrinsic kinase activity of TAF1.

  • Location:13q 14.2
  • Orientation: Plus strand
  • Size: 178,211 bases
  • 27 Exons
  • DNA Sequence:NT_024524

                                 

  • CGH (13q14.2):  Losses (%) - 11.2   Gain (%)  2.8  
  • Mutations and SNPs (According to HGMD and SNP)
  • m-RNA                       (According to NCBI and CGAP)

 

  • m-RNA sequence: NM_000321
  • Size:4740 bp
  • c-DNA Libraries: Rb1
  • Size: 928 amino acids; 106159 Da
  • Protein domains:

                                    

  • Sub cellular location: Nuclear
  • Protein sequence:P06400
  • Homologous genes: Rb1
  • 3D Structure:1GH6
  • PTM: RB

 

  • Pathways and interactions (According to BioCarta, DIP)
    

 

  • Protein Interactions: 582N

  • Clinical                            (According to OMIM, PubMed)