FLNA, filamin A, 2316

N. diseases: 571; N. variants: 85
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853312
rs137853312
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C4281559
Disease:
FRONTOMETAPHYSEAL DYSPLASIA 1 		0.810 GeneticVariation UNIPROT Otopalatodigital spectrum disorders: refinement of the phenotypic and mutational spectrum. 27193221 2016
dbSNP: rs137853314
rs137853314
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C0265251
Disease:
Oto-Palato-digital syndrome type 1 		0.810 GeneticVariation UNIPROT Otopalatodigital spectrum disorders: refinement of the phenotypic and mutational spectrum. 27193221 2016
dbSNP: rs28935470
rs28935470
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C1844696
Disease:
OTOPALATODIGITAL SYNDROME, TYPE II 		0.810 GeneticVariation UNIPROT Otopalatodigital spectrum disorders: refinement of the phenotypic and mutational spectrum. 27193221 2016
dbSNP: rs28935470
rs28935470
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C1844696
Disease:
OTOPALATODIGITAL SYNDROME, TYPE II 		0.810 GeneticVariation BEFREE Ex vivo characterization of E254K OPD patient fibroblasts revealed they have similar motility and adhesion as control cells, implying that many core functions mediated by FLNA are unaffected, consistent with OPD only affecting specific tissues despite FLNA being widely expressed. 19773341 2009
dbSNP: rs28935470
rs28935470
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C1844696
Disease:
OTOPALATODIGITAL SYNDROME, TYPE II 		0.810 GeneticVariation UNIPROT Otopalatodigital syndrome type 2 in two siblings with a novel filamin A 629G>T mutation: clinical, pathological, and molecular findings. 17431908 2007
dbSNP: rs137853312
rs137853312
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C4281559
Disease:
FRONTOMETAPHYSEAL DYSPLASIA 1 		0.810 GeneticVariation UNIPROT In a second family with FMD, we identified a known mutation (S1186L) in a mother and her son. 16596676 2006
dbSNP: rs137853312
rs137853312
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C4281559
Disease:
FRONTOMETAPHYSEAL DYSPLASIA 1 		0.810 GeneticVariation BEFREE In a second family with FMD, we identified a known mutation (S1186L) in a mother and her son. 16596676 2006
dbSNP: rs137853314
rs137853314
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C0265251
Disease:
Oto-Palato-digital syndrome type 1 		0.810 GeneticVariation UNIPROT We present the phenotypic and molecular data of a sporadic female patient clinically diagnosed with an OPD1 syndrome who carried a novel FLNA point mutation resulting in an Asp203Tyr substitution in the actin-binding domain of the protein. 15940695 2005
dbSNP: rs137853314
rs137853314
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C0265251
Disease:
Oto-Palato-digital syndrome type 1 		0.810 GeneticVariation BEFREE We present the phenotypic and molecular data of a sporadic female patient clinically diagnosed with an OPD1 syndrome who carried a novel FLNA point mutation resulting in an Asp203Tyr substitution in the actin-binding domain of the protein. 15940695 2005
dbSNP: rs137853312
rs137853312
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C4281559
Disease:
FRONTOMETAPHYSEAL DYSPLASIA 1 		0.810 GeneticVariation UNIPROT Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans. 12612583 2003
dbSNP: rs137853314
rs137853314
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C0265251
Disease:
Oto-Palato-digital syndrome type 1 		0.810 GeneticVariation UNIPROT Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans. 12612583 2003
dbSNP: rs28935470
rs28935470
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C1844696
Disease:
OTOPALATODIGITAL SYNDROME, TYPE II 		0.810 GeneticVariation UNIPROT Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans. 12612583 2003
dbSNP: rs137853312
rs137853312
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C4281559
Disease:
FRONTOMETAPHYSEAL DYSPLASIA 1 		A 0.810 CausalMutation CLINVAR
dbSNP: rs137853314
rs137853314
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C0265251
Disease:
Oto-Palato-digital syndrome type 1 		A 0.810 CausalMutation CLINVAR
dbSNP: rs28935470
rs28935470
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C1844696
Disease:
OTOPALATODIGITAL SYNDROME, TYPE II 		T 0.810 CausalMutation CLINVAR
dbSNP: rs137853317
rs137853317
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C0265251
Disease:
Oto-Palato-digital syndrome type 1 		0.800 GeneticVariation UNIPROT Otopalatodigital spectrum disorders: refinement of the phenotypic and mutational spectrum. 27193221 2016
dbSNP: rs137853318
rs137853318
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C1844696
Disease:
OTOPALATODIGITAL SYNDROME, TYPE II 		0.800 GeneticVariation UNIPROT Otopalatodigital spectrum disorders: refinement of the phenotypic and mutational spectrum. 27193221 2016
dbSNP: rs28935469
rs28935469
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C0265251
Disease:
Oto-Palato-digital syndrome type 1 		0.800 GeneticVariation UNIPROT Otopalatodigital spectrum disorders: refinement of the phenotypic and mutational spectrum. 27193221 2016
dbSNP: rs28935471
rs28935471
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C4281559
Disease:
FRONTOMETAPHYSEAL DYSPLASIA 1 		0.800 GeneticVariation UNIPROT Otopalatodigital spectrum disorders: refinement of the phenotypic and mutational spectrum. 27193221 2016
dbSNP: rs28935472
rs28935472
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C0025237
Disease:
Melnick-Needles Syndrome 		0.800 GeneticVariation UNIPROT Otopalatodigital spectrum disorders: refinement of the phenotypic and mutational spectrum. 27193221 2016
dbSNP: rs137853318
rs137853318
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C1844696
Disease:
OTOPALATODIGITAL SYNDROME, TYPE II 		0.800 GeneticVariation UNIPROT Otopalatodigital syndrome type 2 in two siblings with a novel filamin A 629G>T mutation: clinical, pathological, and molecular findings. 17431908 2007
dbSNP: rs137853311
rs137853311
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C1848213
Disease:
Periventricular Heterotopia, X-Linked 		0.800 GeneticVariation UNIPROT A filamin A splice mutation resulting in a syndrome of facial dysmorphism, periventricular nodular heterotopia, and severe constipation reminiscent of cerebro-fronto-facial syndrome. 16299064 2006
dbSNP: rs137853311
rs137853311
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C1848213
Disease:
Periventricular Heterotopia, X-Linked 		0.800 GeneticVariation UNIPROT Ehlers-Danlos syndrome and periventricular nodular heterotopia in a Spanish family with a single FLNA mutation. 15994863 2006
dbSNP: rs137853313
rs137853313
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C1848213
Disease:
Periventricular Heterotopia, X-Linked 		0.800 GeneticVariation UNIPROT A filamin A splice mutation resulting in a syndrome of facial dysmorphism, periventricular nodular heterotopia, and severe constipation reminiscent of cerebro-fronto-facial syndrome. 16299064 2006
dbSNP: rs137853313
rs137853313
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C1848213
Disease:
Periventricular Heterotopia, X-Linked 		0.800 GeneticVariation UNIPROT Ehlers-Danlos syndrome and periventricular nodular heterotopia in a Spanish family with a single FLNA mutation. 15994863 2006