Version 5.4
Homo sapiens Gene: RAI2
Summary
InnateDB Gene IDBG-48428.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RAI2
Gene Name retinoic acid induced 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000131831
Encoded Proteins
IDBP-48430
retinoic acid induced 2
IDBP-48432
retinoic acid induced 2
IDBP-363397
retinoic acid induced 2
IDBP-363408
retinoic acid induced 2
IDBP-599245
retinoic acid induced 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this retinoic acid-induced gene has not yet been determined but it may play a role in development. The chromosomal location of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked mental retardation, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome X:17800049-17861337
Strand Reverse strand
Band p22.13
Transcripts
ENST00000331511 ENSP00000333456
ENST00000360011 ENSP00000353106
ENST00000451717 ENSP00000401323
ENST00000415486 ENSP00000392578
ENST00000545871 ENSP00000444210
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
Experimentally validated
Total 8 [view]
Protein-Protein 7 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
GO:0005515 protein binding
Biological Process
GO:0009790 embryo development
Cellular Component
GO:0005575 cellular_component
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
ENSMUSG00000043518
View Gene Order
ENSBTAG00000039049
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.446680
RefSeq NM_001172732 NM_001172739 NM_001172743 NM_021785
HUGO
OMIM
CCDS CCDS14183 CCDS55374
HPRD 02199
IMGT
EMBL
GenPept
RNA Seq Atlas

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca