rs119103234
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
Osteogenesis imperfecta, Levin type
0.810
GeneticVariation
BEFREE
Two missense mutations (C356R and C356G ) of GDD1 were identified in the two families with GDD (the original Japanese family and a new African American family), and both missense mutations occur at the cysteine residue at amino acid 356, which is evolutionarily conserved among human, mouse, zebrafish, fruit fly, and mosquito.
15124103
2004
rs119103234
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
Osteogenesis imperfecta, Levin type
0.810
GeneticVariation
UNIPROT
rs119103234
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
Osteogenesis imperfecta, Levin type
G
0.810
CausalMutation
CLINVAR
rs119103234
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
Osteogenesis imperfecta, Levin type
C
0.810
CausalMutation
CLINVAR
rs137854529
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.800
CausalMutation
CLINVAR
Decreased Aerobic Capacity in ANO5-Muscular Dystrophy.
27911336
2016
rs201725369
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.800
CausalMutation
CLINVAR
Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases.
27854218
2016
rs201725369
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.800
GeneticVariation
CLINVAR
Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases.
27854218
2016
rs137854523
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.800
GeneticVariation
CLINVAR
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs137854523
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.800
GeneticVariation
UNIPROT
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
25864073
2015
rs137854523
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.800
GeneticVariation
UNIPROT
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs137854526
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.800
GeneticVariation
UNIPROT
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs137854526
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.800
GeneticVariation
UNIPROT
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
25864073
2015
rs137854529
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.800
GeneticVariation
UNIPROT
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs137854529
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.800
GeneticVariation
UNIPROT
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
25864073
2015
rs201725369
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.800
GeneticVariation
UNIPROT
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs201725369
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.800
CausalMutation
CLINVAR
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
25891276
2015
rs201725369
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
0.800
GeneticVariation
UNIPROT
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
25864073
2015
rs11026407
ANO5;LOC102723370
Thyroid stimulating hormone measurement
C
0.800
GeneticVariation
GWASDB
A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans.
24722205
2014
rs11026407
ANO5;LOC102723370
Thyroid stimulating hormone measurement
C
0.800
GeneticVariation
GWASCAT
A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans.
24722205
2014
rs137854529
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.800
CausalMutation
CLINVAR
Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic.
25135358
2014
rs137854523
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.800
GeneticVariation
CLINVAR
Anoctamin 5 muscular dystrophy in Denmark: prevalence, genotypes, phenotypes, cardiac findings, and muscle protein expression.
23670307
2013
rs137854523
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.800
GeneticVariation
CLINVAR
ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutation.
23606453
2013
rs137854523
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.800
GeneticVariation
CLINVAR
Dilated cardiomyopathy in patients with mutations in anoctamin 5.
23041008
2013
rs137854529
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.800
CausalMutation
CLINVAR
Eosinophils in hereditary and inflammatory myopathies.
24803842
2013
rs201725369
×
Entrez Id:
203859
Gene Symbol:
ANO5
ANO5
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
T
0.800
CausalMutation
CLINVAR
Dilated cardiomyopathy in patients with mutations in anoctamin 5.
23041008
2013