Genes in panel

Ataxia and cerebellar anomalies - narrow panel

Gene: TUBB

Red List (low evidence)

TUBB (tubulin beta class I)
EnsemblGeneIds (GRCh38): ENSG00000196230
EnsemblGeneIds (GRCh37): ENSG00000196230
OMIM: 191130, Gene2Phenotype
TUBB is in 12 panels

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History Filter Activity

9 Jan 2019, Gel status: 1

Panel promoted to version 1.0

Louise Daugherty (Genomics England Curator)

Rebecca Foulger: Comment on list classification

19 Dec 2018, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: TUBB was added gene: TUBB was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Red Mode of inheritance for gene: TUBB was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: TUBB were set to 23246003, 27010057 Phenotypes for gene: TUBB were set to Cortical dysplasia, complex, with other brain malformations 6, 615771