Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

RGD ID: 2705
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Glra2
Name: glycine receptor, alpha 2
Acc ID: DOID:9001972
Term: Syndromic X-Linked Intellectual Disability Pilorge type
Definition: Characterized by global developmental delay with variably impaired intellectual development, speech delay, and behavioral abnormalities, including autism spectrum disorder (ASD). Caused by heterozygous or hemizygous mutation in the GLRA2 gene on chromosome Xp22.
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Go Back to source page   Continue to Ontology report