MNX1, motor neuron and pancreas homeobox 1, 3110

N. diseases: 113; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912548
rs121912548
Entrez Id: 3110;105375606
Gene Symbol: MNX1;MNX1-AS2
MNX1;MNX1-AS2
CUI: C1531773
Disease:
Currarino triad
0.800 GeneticVariation UNIPROT Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotype. 22820079 2012
dbSNP: rs121912548
rs121912548
Entrez Id: 3110;105375606
Gene Symbol: MNX1;MNX1-AS2
MNX1;MNX1-AS2
CUI: C1531773
Disease:
Currarino triad
0.800 GeneticVariation UNIPROT MNX1 (HLXB9) mutations in Currarino patients. 19853743 2009
dbSNP: rs121912548
rs121912548
Entrez Id: 3110;105375606
Gene Symbol: MNX1;MNX1-AS2
MNX1;MNX1-AS2
CUI: C1531773
Disease:
Currarino triad
0.800 GeneticVariation UNIPROT Involvement of the HLXB9 homeobox gene in Currarino syndrome. 10631160 2000
dbSNP: rs121912548
rs121912548
Entrez Id: 3110;105375606
Gene Symbol: MNX1;MNX1-AS2
MNX1;MNX1-AS2
CUI: C1531773
Disease:
Currarino triad
0.800 GeneticVariation UNIPROT Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene. 10749657 2000
dbSNP: rs121912548
rs121912548
Entrez Id: 3110;105375606
Gene Symbol: MNX1;MNX1-AS2
MNX1;MNX1-AS2
CUI: C1531773
Disease:
Currarino triad
A 0.800 CausalMutation CLINVAR
dbSNP: rs140751051
rs140751051
Entrez Id: 3110
Gene Symbol: MNX1
MNX1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
G 0.700 GeneticVariation GWASCAT Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. 30718926 2019
dbSNP: rs13221118
rs13221118
Entrez Id: 3110
Gene Symbol: MNX1
MNX1
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs13221118
rs13221118
Entrez Id: 3110
Gene Symbol: MNX1
MNX1
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs121912546
rs121912546
Entrez Id: 3110;105375606
Gene Symbol: MNX1;MNX1-AS2
MNX1;MNX1-AS2
CUI: C1531773
Disease:
Currarino triad
A 0.700 CausalMutation CLINVAR
dbSNP: rs121912547
rs121912547
Entrez Id: 3110;645249
Gene Symbol: MNX1;MNX1-AS1
MNX1;MNX1-AS1
CUI: C1531773
Disease:
Currarino triad
T 0.700 CausalMutation CLINVAR
dbSNP: rs121912549
rs121912549
Entrez Id: 3110;105375606
Gene Symbol: MNX1;MNX1-AS2
MNX1;MNX1-AS2
CUI: C1531773
Disease:
Currarino triad
A 0.700 CausalMutation CLINVAR
dbSNP: rs1554594329
rs1554594329
Entrez Id: 3110;645249
Gene Symbol: MNX1;MNX1-AS1
MNX1;MNX1-AS1
CUI: C1531773
Disease:
Currarino triad
TG 0.700 CausalMutation CLINVAR
dbSNP: rs1563700090
rs1563700090
Entrez Id: 3110;105375606
Gene Symbol: MNX1;MNX1-AS2
MNX1;MNX1-AS2
CUI: C1531773
Disease:
Currarino triad
C 0.700 CausalMutation CLINVAR
dbSNP: rs1563700419
rs1563700419
Entrez Id: 3110;105375606
Gene Symbol: MNX1;MNX1-AS2
MNX1;MNX1-AS2
CUI: C1531773
Disease:
Currarino triad
T 0.700 CausalMutation CLINVAR