KEGG Orthology (KO) [BR:ko00001]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins
K19656 IFT122; intraflagellar transport protein 122
Cilium and associated proteins [BR:ko03037]
Primary cilia and associated proteins
Intraflagellar transport (IFT) complex A
K19656 IFT122; intraflagellar transport protein 122
Walczak-Sztulpa J, Eggenschwiler J, Osborn D, Brown DA, Emma F, Klingenberg C, Hennekam RC, Torre G, Garshasbi M, Tzschach A, Szczepanska M, Krawczynski M, Zachwieja J, Zwolinska D, Beales PL, Ropers HH, Latos-Bielenska A, Kuss AW
Title
Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.