Gene: KIDINS220 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57498
Gene Symbol: KIDINS220
KIDINS220 		0.630 GeneticVariation disease BEFREE Our work reveals a non-classical spastic paraplegia, intellectual disability, nystagmus, and obesity phenotype for a KIDINS220 mutation, which broadens both the clinical and genetic spectrum for ADHSP. 31630374 2019
Entrez Id: 57498
Gene Symbol: KIDINS220
KIDINS220 		0.630 Biomarker disease GENOMICS_ENGLAND Heterozygous KIDINS220 mutation leads to spastic paraplegia and obesity in an Asian girl. 29667355 2018
Entrez Id: 57498
Gene Symbol: KIDINS220
KIDINS220 		0.630 GeneticVariation disease BEFREE Heterozygous mutations in KIDINS220 were recently suggested a cause of spastic paraplegia, intellectual disability, nystagmus and obesity. 28934391 2017
Entrez Id: 57498
Gene Symbol: KIDINS220
KIDINS220 		0.630 Biomarker disease GENOMICS_ENGLAND Altogether, we here show that de novo protein-truncating KIDINS220 variants cause a new syndrome, SINO. 27005418 2016
Entrez Id: 57498
Gene Symbol: KIDINS220
KIDINS220 		0.630 GermlineCausalMutation disease ORPHANET Altogether, we here show that de novo protein-truncating KIDINS220 variants cause a new syndrome, SINO. 27005418 2016
Entrez Id: 57498
Gene Symbol: KIDINS220
KIDINS220 		0.630 GeneticVariation disease BEFREE Heterozygous KIDINS220/ARMS nonsense variants cause spastic paraplegia, intellectual disability, nystagmus, and obesity. 27005418 2016
Entrez Id: 57498
Gene Symbol: KIDINS220
KIDINS220 		0.630 GeneticVariation disease CLINVAR
Entrez Id: 57498
Gene Symbol: KIDINS220
KIDINS220 		0.630 CausalMutation disease CLINVAR
Entrez Id: 57498
Gene Symbol: KIDINS220
KIDINS220 		0.630 Biomarker disease GENOMICS_ENGLAND