KCTD12

BTB/POZ domain-containing protein KCTD12 is a protein that in humans is encoded by the KCTD12 gene.^[5][6]

KCTD12
Identifiers
Aliases	KCTD12, C13orf2, PFET1, PFETIN, potassium channel tetramerization domain containing 12
External IDs	OMIM: 610521; MGI: 2145823; HomoloGene: 16316; GeneCards: KCTD12; OMA:KCTD12 - orthologs
Gene location (Human) Chr. Chromosome 13 (human)[1] Band 13q22.3 Start 76,880,175 bp[1] End 76,886,405 bp[1]
Gene location (Mouse) Chr. Chromosome 14 (mouse)[2] Band 14|14 E2.3 Start 103,214,017 bp[2] End 103,220,073 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in trigeminal ganglion urethra bronchial epithelial cell lactiferous duct synovial joint mucosa of paranasal sinus superficial temporal artery lower lobe of lung pericardium parietal pleura Top expressed in molar vestibular sensory epithelium granulocyte pineal gland dermis body of femur human fetus lobe of cerebellum skin of external ear cerebellar vermis More reference expression data BioGPS More reference expression data
Gene ontology Molecular function RNA binding identical protein binding Cellular component cell junction postsynaptic membrane plasma membrane synapse extracellular exosome presynaptic membrane membrane Biological process protein homooligomerization Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 115207 239217 Ensembl ENSG00000178695 ENSMUSG00000098557 UniProt Q96CX2 Q6WVG3 RefSeq (mRNA) NM_138444 NM_177715 RefSeq (protein) NP_612453 NP_808383 Location (UCSC) Chr 13: 76.88 – 76.89 Mb Chr 14: 103.21 – 103.22 Mb PubMed search [3] [4]
Wikidata
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It may be associated with rumination^[7] and Bipolar Disorder.^[8]