Bos taurus Gene: RAI1
Summary
InnateDB Gene IDBG-638248.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RAI1
Gene Name Uncharacterized protein
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000004768
Encoded Proteins
retinoic acid induced 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000108557:
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 19:35252242-35263546
Strand Reverse strand
Band
Transcripts
ENSBTAT00000006264 ENSBTAP00000006264
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 14 interaction(s) predicted by orthology.
Predicted by orthology
Total 14 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0008270 zinc ion binding
GO:0035326 enhancer binding
Biological Process
GO:0001501 skeletal system development
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0032922 circadian regulation of gene expression
GO:0040015 negative regulation of multicellular organism growth
GO:0045893 positive regulation of transcription, DNA-templated
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL E1B9X1
UniProt Splice Variant
Entrez Gene 528972
UniGene Bt.103121
RefSeq XM_002695826 XM_005195693 XM_005195694 XM_005195695 XM_005195696 XM_005195697 XM_005195698 XM_005220467 XM_005220468 XM_005220469 XM_005220470 XM_005220471 XM_607410
HUGO HGNC:9834
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02048998
GenPept
RNA Seq Atlas 528972