PAX6, paired box 6, 5080

N. diseases: 340; N. variants: 118
Disease: ANTERIOR SEGMENT DYSGENESIS 5 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121907922
rs121907922
Entrez Id: 5080;26610
Gene Symbol: PAX6;ELP4
PAX6;ELP4
CUI: C4310809
Disease:
ANTERIOR SEGMENT DYSGENESIS 5 		A 0.700 CausalMutation CLINVAR PAX6 molecular analysis and genotype-phenotype correlations in families with aniridia from Australasia and Southeast Asia. 29618921 2018
dbSNP: rs121907922
rs121907922
Entrez Id: 5080;26610
Gene Symbol: PAX6;ELP4
PAX6;ELP4
CUI: C4310809
Disease:
ANTERIOR SEGMENT DYSGENESIS 5 		A 0.700 CausalMutation CLINVAR Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations. 28321846 2017
dbSNP: rs121907922
rs121907922
Entrez Id: 5080;26610
Gene Symbol: PAX6;ELP4
PAX6;ELP4
CUI: C4310809
Disease:
ANTERIOR SEGMENT DYSGENESIS 5 		A 0.700 CausalMutation CLINVAR Identification of a novel frameshift heterozygous deletion in exon 8 of the PAX6 gene in a pedigree with aniridia. 27431685 2016
dbSNP: rs121907922
rs121907922
Entrez Id: 5080;26610
Gene Symbol: PAX6;ELP4
PAX6;ELP4
CUI: C4310809
Disease:
ANTERIOR SEGMENT DYSGENESIS 5 		A 0.700 CausalMutation CLINVAR Missense mutations in the DNA-binding region and termination codon in PAX6. 12552561 2003
dbSNP: rs121907922
rs121907922
Entrez Id: 5080;26610
Gene Symbol: PAX6;ELP4
PAX6;ELP4
CUI: C4310809
Disease:
ANTERIOR SEGMENT DYSGENESIS 5 		A 0.700 CausalMutation CLINVAR Missense mutation at the C-terminus of PAX6 negatively modulates homeodomain function. 11309364 2001