BAIT

WNT3A

wingless-type MMTV integration site family, member 3A
GO Process (22)
GO Function (4)
GO Component (6)
Homo sapiens
PREY

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

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 Wnt-3a not clear

Curated By

  • BioGRID