KCTD13

From Wikipedia, the free encyclopedia
Jump to: navigation, search
KCTD13
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases KCTD13, BACURD1, PDIP1, POLDIP1, hBACURD1, FKSG86, potassium channel tetramerization domain containing 13
External IDs MGI: 1923739 HomoloGene: 27800 GeneCards: KCTD13
RNA expression pattern
PBB GE KCTD13 221889 at fs.png

PBB GE KCTD13 45653 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_178863

NM_172747

RefSeq (protein)

NP_849194

NP_766335.1
NP_766335

Location (UCSC) Chr 16: 29.91 – 29.93 Mb Chr 7: 126.93 – 126.95 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

BTB/POZ domain-containing protein KCTD13 is a protein that in humans is encoded by the KCTD13 gene.[3][4]


Interactions[edit]

KCTD13 has been shown to interact with PCNA.[3]

Clinical relevance[edit]

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

References[edit]

Further reading[edit]