BAIT

KCTD1

C18orf5, SENS, hCG_38480
potassium channel tetramerization domain containing 1
GO Process (1)
GO Function (2)
GO Component (1)

Gene Ontology Cellular Component

Homo sapiens
PREY

APC

BTPS2, DP2, DP2.5, DP3, GS, PPP1R46
adenomatous polyposis coli
GO Process (21)
GO Function (8)
GO Component (12)
Homo sapiens

Phenotypic Suppression

A genetic interaction is inferred when mutation or over expression of one gene results in suppression of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene.

Publication

KCTD1 Suppresses Canonical Wnt Signaling Pathway by Enhancing β-catenin Degradation.

Li X, Chen C, Wang F, Huang W, Liang Z, Xiao Y, Wei K, Wan Z, Hu X, Xiang S, Ding X, Zhang J

The canonical Wnt signaling pathway controls normal embryonic development, cellular proliferation and growth, and its aberrant activity results in human carcinogenesis. The core component in regulation of this pathway is β-catenin, but molecular regulation mechanisms of β-catenin stability are not completely known. Here, our recent studies have shown that KCTD1 strongly inhibits TCF/LEF reporter activity. Moreover, KCTD1 interacted with β-catenin ... [more]

PLoS ONE Apr. 17, 2014; 9(4);e94343 [Pubmed: 24736394]

Throughput

  • Low Throughput

Additional Notes

  • source of APC not clear

Curated By

  • BioGRID