Genomics England
GMS Panels
Panels
Genes and Entities
THG1L
tRNA-histidine guanylyltransferase 1 like
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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 6.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spinocerebellar ataxia, autosomal recessive 28, OMIM:618800, MONDO:0032923