SCLT1

sodium channel and clathrin linker 1
OMIM: 611399
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
No OMIM phenotype, Oro-facio-digital syndrome type IX, Senior-L√łken Syndrome
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Oro-facio-digital syndrome type IX (Adly (2014) Hum Mutat 35,36), No OMIM phenotype
Component of the following Super Panels:
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Oro-facio-digital syndrome type IX (Adly (2014) Hum Mutat 35,36), No OMIM phenotype