NRP2, neuropilin 2, 8828

N. diseases: 144; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 Biomarker disease BEFREE Further studies of mouse KO models of ASD genes such as Sema 3F or NRP2 may be informative to clinical phenotypes contributing to the pathogenesis in autism and epilepsy patients. 30635860 2019
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 GeneticVariation disease BEFREE The NRP2 G allele conferred a 2.29-fold increased risk to autism relative to the T allele (OR = 2.29, 95%CI = 1.23-4.29, P = 0.009). 28484884 2017
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 GeneticVariation disease LHGDN We found significant genetic association between autism and two of the SNPs of the NRP2 gene (rs849578: P = 0.017, rs849563: P = 0.027), as well as specific haplotypes, especially those formed by rs849563. 17427189 2007
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 GeneticVariation disease BEFREE We found significant genetic association between autism and two of the SNPs of the NRP2 gene (rs849578: P = 0.017, rs849563: P = 0.027), as well as specific haplotypes, especially those formed by rs849563. 17427189 2007
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 Biomarker disease CTD_human We found significant genetic association between autism and two of the SNPs of the NRP2 gene (rs849578: P = 0.017, rs849563: P = 0.027), as well as specific haplotypes, especially those formed by rs849563. 17427189 2007