Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Gastrointestinal neuromuscular disease v0.20 | SEMA3D | Bryony Thompson Marked gene: SEMA3D as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Gastrointestinal neuromuscular disease v0.20 | SEMA3D | Bryony Thompson Gene: sema3d has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Gastrointestinal neuromuscular disease v0.20 | SEMA3D |
Bryony Thompson gene: SEMA3D was added gene: SEMA3D was added to Gastrointestinal neuromuscular disease. Sources: Expert list Mode of inheritance for gene: SEMA3D was set to Unknown Publications for gene: SEMA3D were set to 28334784; 25839327 Phenotypes for gene: SEMA3D were set to Hirschsprung disease Review for gene: SEMA3D was set to RED Added comment: Reported as a common susceptibility loci. No reported evidence for an association with Mendelian disease. Sema3d null heterozygote and homozygote mouse model had normal intestinal innervation. Sources: Expert list |