RAI1 Gene Set

Dataset Pathway Commons Protein-Protein Interactions
Category physical interactions
Type interacting protein
Description retinoic acid induced 1|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] (NCBI Entrez Gene Database, 10743)
External Link http://www.ncbi.nlm.nih.gov/gene/10743
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Genes

19 interacting proteins for RAI1 from the Pathway Commons Protein-Protein Interactions dataset.

Symbol Name
CASP2 caspase 2, apoptosis-related cysteine peptidase
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1)
DDIT3 DNA-damage-inducible transcript 3
GADD45A growth arrest and DNA-damage-inducible, alpha
GATA1 GATA binding protein 1 (globin transcription factor 1)
GLI1 GLI family zinc finger 1
GSK3B glycogen synthase kinase 3 beta
HECW2 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2
LZTR1 leucine-zipper-like transcription regulator 1
MAML3 mastermind-like 3 (Drosophila)
MAPK8IP2 mitogen-activated protein kinase 8 interacting protein 2
PIN1 peptidylprolyl cis/trans isomerase, NIMA-interacting 1
RPS6KA5 ribosomal protein S6 kinase, 90kDa, polypeptide 5
SIRT7 sirtuin 7
SUMO2 small ubiquitin-like modifier 2
TESC tescalcin
TTR transthyretin
UBC ubiquitin C
ZNF496 zinc finger protein 496