Genomics England
GMS Panels
Panels
Genes and Entities
SLC9A1
solute carrier family 9 member A1
OMIM:
107310
See this entity in PanelApp
Panel
Mode of inheritance
Details
Filter panels
1 panel
Green
in
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
Lichtenstein-Knorr syndrome OMIM:616291, Lichtenstein-Knorr syndrome MONDO:0014572