Genomics England
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Genes and Entities
SS18L1
SS18L1, nBAF chromatin remodeling complex subunit
OMIM:
606472
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Panel
Mode of inheritance
Details
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Adult onset neurodegenerative disorder
R-numbers:
R58
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Amyotrophic lateral sclerosis, MONDO:0004976