rs3749507
This variant is located in the INTU gene.
▶ClinVar annotation
Benign★★★☆
5 submitters2 publicationsnot provided; Orofaciodigital syndrome 17; Short-rib thoracic dysplasia 20 with polydactyly; INTU-related disorder
View on ClinVar →About INTU
Predicted to enable phosphatidylinositol binding activity. Involved in embryonic digit morphogenesis; roof of mouth development; and tongue morphogenesis. Located in several cellular components, including ciliary basal body; cytosol; and motile cilium. Implicated in asphyxiating thoracic dystrophy and orofaciodigital syndrome XVII. [provided by Alliance of Genome Resources, Apr 2025]
View all INTU variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
Community Wiki
No community notes yet for this variant. Sign in to start one.
Comments
Sign in to join the discussion.
Loading comments…