KCTD12
Sign in to saveAlso known as C13orf2, PFET1, PFETIN, potassium channel tetramerization domain containing 12
BTB/POZ domain-containing protein KCTD12 is a protein that in humans is encoded by the KCTD12 gene.
Gene data
KCTD12- Name
- potassium channel tetramerization domain containing 12
- Type
- protein-coding
- Position
- 76,880,175–76,886,405 (−)
- Aliases
- C13orf2, PFET1, PFETIN
- Ensembl
- ENSG00000178695
- RefSeq RNA
- NM_138444.4
- RefSeq protein
- NP_612453.1
Enables identical protein binding activity. Predicted to be involved in protein homooligomerization. Predicted to act upstream of or within regulation of G protein-coupled receptor signaling pathway. Predicted to be located in cell projection. Predicted to be part of receptor complex. Predicted to be active in postsynaptic membrane and presynaptic membrane. [provided by Alliance of Genome Resources, Apr 2022]
Gene Ontology
Biological process
Molecular function
via MyGene.info
Gene · Ensembl
potassium channel tetramerization domain containing 12
- Symbol
- KCTD12
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 13:76,880,175-76,886,405
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 16316
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/115207
- chromosome
- human chromosome 13
- genomic start
- 76880175
- genomic end
- 76886405
- cytogenetic location
- 13q22.3
Sources (4)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- References
- Further reading
BTB/POZ domain-containing protein KCTD12 is a protein that in humans is encoded by the KCTD12 gene.
It may be associated with rumination and Bipolar Disorder.
Excerpted from Wikipedia’s “KCTD12” article, available under the CC BY-SA 4.0 licence.