Variant: rs587777357 

    present in Gene: TUBB
    present in Chromosome: 6
    Position on Chromosome: 30724263
    Alleles of this Variant: G/A

rs587777357 in TUBB gene and CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6 PMID 23246003 2012 Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.

rs587777357 in TUBB gene and Dysmorphic features PMID 24833723 2014 TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons.

PMID 26637975 2015 Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.

PMID 23246003 2012 Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.

rs587777357 in TUBB gene and Multiple congenital anomalies PMID 23246003 2012 Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.

PMID 24833723 2014 TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons.

PMID 26637975 2015 Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.

rs587777357 in TUBB gene and Muscle hypotonia PMID 23246003 2012 Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.

PMID 24833723 2014 TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons.

PMID 26637975 2015 Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.