A database built with INDRA combining content from numerous readers and databases. This page allows you to curate the loaded statements. For more information please see the manual.

IndraLab

Statements

databases
phosphosite cbn pc11 biopax bel_lc signor biogrid tas lincs_drug hprd trrust | geneways tees isi trips rlimsp medscan sparser reach
reading

BRAF binds PTPN11 and RAF1. 1 / 1
| 1
sparser
"LEOPARD syndrome (LS, OMIM 151100) is associated with PTPN11 , RAF1 and BRAF gene mutations, Noonan-like syndrome with loose anagen hair (NS/LAH, OMIM 607721) with SHOC2 gene mutations, cardio-facial-cutaneous syndrome (CFCS, OMIM 115150) with KRAS , BRAF , MEK1 and MEK2 gene mutations and Costello syndrome (CS, OMIM 218040) with HRAS gene mutations [ xref – xref ]."