Protein-coding gene in the species Homo sapiens
BTB/POZ domain-containing protein KCTD12 is a protein that in humans is encoded by the KCTD12 gene.[5][6]
It may be associated with rumination[7] and Bipolar Disorder.[8]
- ^ a b c GRCh38: Ensembl release 89: ENSG00000178695 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000098557 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Resendes BL, Kuo SF, Robertson NG, Giersch AB, Honrubia D, Ohara O, Adams JC, Morton CC (Sep 2004). "Isolation from cochlea of a novel human intronless gene with predominant fetal expression". J Assoc Res Otolaryngol. 5 (2): 185–202. doi:10.1007/s10162-003-4042-x. PMC 2538407. PMID 15357420.
- ^ "Entrez Gene: KCTD12 potassium channel tetramerisation domain containing 12".
- ^ Eszlari, Nora; Millinghoffer, Andras; Petschner, Peter; Gonda, Xenia; Baksa, Daniel; Pulay, Attila J.; Réthelyi, János M.; Breen, Gerome; Deakin, John Francis William; Antal, Peter; Bagdy, Gyorgy; Juhasz, Gabriella (2019). "Genome-wide association analysis reveals KCTD12 and miR-383-binding genes in the background of rumination". Translational Psychiatry. 9 (1): 119. doi:10.1038/s41398-019-0454-1. PMC 6423133. PMID 30886212.
- ^ "KCTD12 Gene - GeneCards | KCD12 Protein | KCD12 Antibody".