Genomics England
GMS Panels
Panels
Genes and Entities
SLC9A1
solute carrier family 9 member A1
OMIM:
107310
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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 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Lichtenstein-Knorr syndrome OMIM:616291, Lichtenstein-Knorr syndrome MONDO:0014572