Complex Parkinsonism (includes pallido-pyramidal syndromes)

Gene: RAB39B

Red List (low evidence)

RAB39B (RAB39B, member RAS oncogene family)
EnsemblGeneIds (GRCh38): ENSG00000155961
EnsemblGeneIds (GRCh37): ENSG00000155961
OMIM: 300774, Gene2Phenotype
RAB39B is in 10 panels

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Details

Mode of Inheritance
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert
OMIM
300774
Clinvar variants
Variants in RAB39B
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jul 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

RAB39B was added to Complex Parkinsonism (includes pallido-pyramidal syndromes)panel. Sources: Expert