ClinGen Knowledge Base | Clinical Genome Resource

RAB39B

Name: RAB39B
HGNC ID: HGNC:16499
Cytogenetic Location: Xq28
Haploinsufficiency: Sufficient Evidence
Triplosensitivity: No Evidence

External Resources: View external resources
ClinVar Variants: View ClinVar Variants
GeneReviews®: View GeneReviews

RAB39B - early-onset parkinsonism-intellectual disability syndrome | MONDO:0010709

Curated by	Classification	Date	Report
Gene-Disease Validity	Definitive	06/04/2018	View report

RAB39B

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Sufficient Evidence for Haploinsufficiency	06/13/2017	View report
Gene Dosage Sensitivity	No Evidence for Triplosensitivity	06/13/2017	View report

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