TUBB4A, tubulin beta 4A class IVa, 10382

N. diseases: 107; N. variants: 29
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C2676244
Disease:
Leukodystrophy, Hypomyelinating, 6 		T 0.700 CausalMutation CLINVAR Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients. 29451896 2018
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Screening study of TUBB4A in isolated dystonia. 28655586 2017
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR [A report of atypical hypomyelinating leukodystrophy with atrophy of the basal ganglia and cerebellum caused by a de novo mutation in tubulin beta 4A (TUBB4A) gene and literature review]. 28592043 2017
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR TUBB4A-related hypomyelinating leukodystrophy: New insights from a series of 12 patients. 26643067 2016
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Dystonia-Causing Mutations as a Contribution to the Etiology of Spasmodic Dysphonia. 27188707 2016
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Large-scale TUBB4A mutational screening in isolated dystonia and controls. 26318963 2015
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C2676244
Disease:
Leukodystrophy, Hypomyelinating, 6 		T 0.700 CausalMutation CLINVAR Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions. 25356970 2015
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR TUBB4A novel mutation reinforces the genotype-phenotype correlation of hypomyelination with atrophy of the basal ganglia and cerebellum. 25168210 2015
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C2676244
Disease:
Leukodystrophy, Hypomyelinating, 6 		T 0.700 CausalMutation CLINVAR TUBB4A novel mutation reinforces the genotype-phenotype correlation of hypomyelination with atrophy of the basal ganglia and cerebellum. 25168210 2015
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR A de novo TUBB4A mutation in a patient with hypomyelination mimicking Pelizaeus-Merzbacher disease. 24974158 2015
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations? 25545912 2015
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C2676244
Disease:
Leukodystrophy, Hypomyelinating, 6 		T 0.700 CausalMutation CLINVAR A de novo TUBB4A mutation in a patient with hypomyelination mimicking Pelizaeus-Merzbacher disease. 24974158 2015
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C2676244
Disease:
Leukodystrophy, Hypomyelinating, 6 		T 0.700 CausalMutation CLINVAR Expanding the phenotypic spectrum of TUBB4A-associated hypomyelinating leukoencephalopathies. 24850488 2014
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Expanding the phenotypic spectrum of TUBB4A-associated hypomyelinating leukoencephalopathies. 24850488 2014
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation. 24785942 2014
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR TUBB4A de novo mutations cause isolated hypomyelination. 25085639 2014
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C2676244
Disease:
Leukodystrophy, Hypomyelinating, 6 		T 0.700 CausalMutation CLINVAR Novel TUBB4A mutations and expansion of the neuroimaging phenotype of hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC). 24706558 2014
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene. 24526230 2014
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Novel TUBB4A mutations and expansion of the neuroimaging phenotype of hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC). 24706558 2014
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Clinical exome sequencing identifies a novel TUBB4A mutation in a child with static hypomyelinating leukodystrophy. 24742798 2014
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia. 23424103 2013
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene. 23595291 2013
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum. 23582646 2013
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Whispering dysphonia in an Australian family (DYT4): a clinical and genetic reappraisal. 21956287 2011
dbSNP: rs886039470
rs886039470
Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR Tumoral and tissue-specific expression of the major human beta-tubulin isotypes. 20191564 2010