retinoic acid induced 1

Symbol

RAI1 (may also be known as: None)

Organism

Human

Description

This gene is located within the Smith-Magenis syndrome region on chromosome 17. It is highly similar to its mouse counterpart and is expressed at high levels mainly in neuronal tissues. The protein encoded by this gene includes a polymorphic polyglutamine tract in the N-terminal domain. Expression of the mouse counterpart in neurons is induced by retinoic acid. This gene is associated with both the severity of the phenotype and the response to medication in schizophrenic patients. [provided by RefSeq, Jul 2008]

Orthologs

SymbolSpecies
CG5098 Drosophila melanogaster
Rai1 Mus musculus
Rai1 Rattus norvegicus

Links to external resources

Changes associated with this gene

GO Terms

GO IDGO TermGO Category
GO:0001501 skeletal system development biological_process
GO:0006357 regulation of transcription from RNA polymerase II promoter biological_process
GO:0040015 negative regulation of multicellular organism growth biological_process
GO:0005634 nucleus cellular_component
GO:0005737 cytoplasm cellular_component
GO:0008270 zinc ion binding molecular_function
GO:0046872 metal ion binding molecular_function