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RCBTB1, RCC1 and BTB domain containing protein 1

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RCBTB1, RCC1 and BTB domain containing protein 1

  • This gene encodes a protein with an N-terminal RCC1 domain and a C-terminal BTB (broad complex, tramtrack and bric-a-brac) domain. In rat, over-expression of this gene in vascular smooth muscle cells induced cellular hypertrophy. In rat, the C-terminus of RCBTB1 interacts with the angiotensin II receptor-1A. In humans, this gene maps to a region of chromosome 13q that is frequently deleted in B-cell chronic lymphocytic leukemia and other lymphoid malignancies. [provided by RefSeq, Jul 2008]

  • Gene Synonyms (CLLD7, CLLL7, GLP, RDEOA, RCC1 and BTB domain-containing protein 1, CLL deletion region gene 7 protein, GDP/GTP exchange factor (GEF)-like protein, chronic lymphocytic leukemia deletion region gene 7 protein, regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1, regulator of chromosome condensation and BTB domain-containing protein 1,)
  • NCBI Gene ID: 55213
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>B3KR20
    UNIPROT ID#>>Q8NDN9
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

RCC1 and BTB domain containing protein 1 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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