Annotation Detail
Information
- Associated Genes
- GRIA3
- Associated Variants
-
GRIA3 MUTATION
GRIA3 MUTATION - Associated Disease
- intellectual disability
- Source Database
- DisGeNET
- Description
- Virtually all α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor mutations, most of which occur within GRIA3, are from patients with intellectual disabilities, suggesting a link to this condition.
- Pubmed
- 25904555
- Section of the abstract supporting the evidence
- ALL_TEXT_3/3
- Number of the section of the abstract supporting the evidence
- 3
- Number of the sentence supporting the evidence
- 8
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000542883744160607
Drugs