KCTD13

KCTD13

KCTD13

Protein-coding gene in the species Homo sapiens

BTB/POZ domain-containing protein KCTD13 is a protein that in humans is encoded by the KCTD13 gene.[5][6]

Quick Facts Available structures, PDB ...

Interactions

KCTD13 has been shown to interact with PCNA.[5]

Clinical relevance

Mutations in this gene have been associated to abnormalities in brain growth and behaviour.[7]

References

  1. [1]
    GRCh38: Ensembl release 89: ENSG00000174943 – Ensembl, May 2017
  2. [2]
    GRCm38: Ensembl release 89: ENSMUSG00000030685 – Ensembl, May 2017
  3. [3]
    "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. [4]
    "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. [5]
    He H, Tan CK, Downey KM, So AG (October 2001). "A tumor necrosis factor alpha- and interleukin 6-inducible protein that interacts with the small subunit of DNA polymerase delta and proliferating cell nuclear antigen". Proceedings of the National Academy of Sciences of the United States of America. 98 (21): 11979–84. Bibcode:2001PNAS...9811979H. doi:10.1073/pnas.221452098. PMC 59753. PMID 11593007.
  6. [6]
    "Entrez Gene: KCTD13 potassium channel tetramerisation domain containing 13".
  7. [7]
    Arbogast T, Razaz P, Ellegood J, McKinstry SU, Erdin S, Currall B, et al. (May 2019). "Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions". Human Molecular Genetics. 28 (9): 1474–1486. doi:10.1093/hmg/ddy436. PMC 6489413. PMID 30590535.

Further reading

  • PDBe-KB provides an overview of all the structure information available in the PDB for Human KCTD13


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