ClinGen Knowledge Base | Clinical Genome Resource

FOXP1

Name: FOXP1
HGNC ID: HGNC:3823
Cytogenetic Location: 3p13
Haploinsufficiency: Sufficient Evidence
Triplosensitivity: No Evidence

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

FOXP1 - intellectual disability-severe speech delay-mild dysmorphism syndrome | MONDO:0013352

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Sufficient Evidence for Haploinsufficiency	09/11/2017	View report

FOXP1

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Sufficient Evidence for Haploinsufficiency	09/11/2017	View report
Gene Dosage Sensitivity	No Evidence for Triplosensitivity	09/11/2017	View report

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