FZD9, frizzled class receptor 9, 8326

N. diseases: 20; N. variants: 1
Disease: Williams Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.240 Biomarker disease MGD Control of bone formation by the serpentine receptor Frizzled-9. 21402791 2011
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.240 GeneticVariation disease BEFREE Heterozygous mice (the same frizzled 9 genotype as Williams syndrome patients) were intermediate between wild type and null mice for all developmental neuronanatomic defects. 15930120 2005
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.240 Biomarker disease BEFREE Fzd9-/- mice show no obvious features of WBS, but reveal a role for Fzd9 in lymphoid development and maturation. 15572594 2005
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.240 Biomarker disease MGD Heterozygous mice (the same frizzled 9 genotype as Williams syndrome patients) were intermediate between wild type and null mice for all developmental neuronanatomic defects. 15930120 2005
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.240 GeneticVariation disease BEFREE A cognitive phenotypic map of WMS is presented, which combines previous data with five further WMS subjects and three atypical WMS subjects with deletions; two larger (deleted for D7S489L) and one smaller, deleted for genes telomeric to FZD9, through LIMK1, but not WSCR1 or telomeric. 10953236 2000
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.240 Biomarker disease BEFREE We previously identified a novel frizzled gene, FZD3, now renamed FZD9, in the Williams-Beuren syndrome (WBS) deletion region at chromosomal band 7q11.23 and showed that its product can interact with the Drosophila wingless protein. 10198163 1999