BAIT

NF1

NFNS, VRNF, WSS
neurofibromin 1
GO Process (49)
GO Function (4)
GO Component (6)

Gene Ontology Biological Process

Homo sapiens
PREY

PML

MYL, PP8675, RNF71, TRIM19
promyelocytic leukemia
GO Process (39)
GO Function (8)
GO Component (9)

Gene Ontology Biological Process

Homo sapiens

Co-localization

Interaction inferred from two proteins that co-localize in the cell by indirect immunofluorescence only when in addition, if one gene is deleted, the other protein becomes mis-localized. Also includes co-dependent association of proteins with promoter DNA in chromatin immunoprecipitation experiments.

Publication

A fraction of neurofibromin interacts with PML bodies in the nucleus of the CCF astrocytoma cell line.

Godin F, Villette S, Vallee B, Doudeau M, Morisset-Lopez S, Ardourel M, Hevor T, Pichon C, Benedetti H

Neurofibromatosis type 1 is a common genetic disease that causes nervous system tumors, and cognitive deficits. It is due to mutations within the NF1 gene, which encodes the Nf1 protein. Nf1 has been shown to be involved in the regulation of Ras, cAMP and actin cytoskeleton dynamics. In this study, using immunofluorescence experiments, we have shown a partial nuclear localization ... [more]

Biochem. Biophys. Res. Commun. Feb. 24, 2012; 418(4);689-94 [Pubmed: 22293200]

Throughput

  • Low Throughput

Curated By

  • BioGRID