KCTD13

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

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

PDBOrtholog search: PDBe RCSB
AliasesKCTD13, BACURD1, PDIP1, POLDIP1, hBACURD1, FKSG86, potassium channel tetramerization domain containing 13
Quick facts Available structures, PDB ...
KCTD13
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKCTD13, BACURD1, PDIP1, POLDIP1, hBACURD1, FKSG86, potassium channel tetramerization domain containing 13
External IDsOMIM: 608947; MGI: 1923739; HomoloGene: 27800; GeneCards: KCTD13; OMA:KCTD13 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_178863

NM_172747

RefSeq (protein)

NP_849194

NP_766335

Location (UCSC)Chr 16: 29.91 – 29.93 MbChr 7: 126.53 – 126.54 Mb
PubMed search[3][4]
Wikidata
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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

Further reading

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