Genomics England
GMS Panels
Panels
Genes and Entities
TGM6
transglutaminase 6
OMIM:
613900
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Panel
Mode of inheritance
Details
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Ataxia and cerebellar anomalies - narrow panel
Component of the following Super Panels:
- Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 2.23
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Spinocerebellar ataxia 35, 613908