Mus musculus Gene: Aes
Summary
InnateDB Gene IDBG-178824.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Aes
Gene Name amino-terminal enhancer of split
Synonyms AL024115; Esp1; Grg; Grg-5; Grg5; Tle5
Species Mus musculus
Ensembl Gene ENSMUSG00000054452
Encoded Proteins
amino-terminal enhancer of split
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a protein that belongs to the Aes (amino-terminal enhancer of split) subgroup of the Groucho/transducin-like Enhancer of split (TLE) family of proteins that function as transcriptional corepressors. The encoded protein plays a role in neurological development and cell-fate determination. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jan 2013]
Gene Information
Type Protein coding
Genomic Location Chromosome 10:81559494-81566362
Strand Forward strand
Band C1
Transcripts
ENSMUST00000002518 ENSMUSP00000002518
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 15 experimentally validated interaction(s) in this database.
They are also associated with 28 interaction(s) predicted by orthology.
Experimentally validated
Total 15 [view]
Protein-Protein 15 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 28 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003714 transcription corepressor activity
GO:0005515 protein binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0001501 skeletal system development
GO:0006351 transcription, DNA-templated
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0010629 negative regulation of gene expression
GO:0016055 Wnt signaling pathway
GO:0031668 cellular response to extracellular stimulus
GO:0032091 negative regulation of protein binding
GO:0040008 regulation of growth
GO:0045892 negative regulation of transcription, DNA-templated
GO:0060761 negative regulation of response to cytokine stimulus
GO:0070555 response to interleukin-1
GO:0090090 negative regulation of canonical Wnt signaling pathway
GO:2000210 positive regulation of anoikis
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Disease pathway
deletions in the AMER1 gene destabilize the destruction complex pathway
Signaling by Wnt pathway
Signaling by WNT in cancer pathway
Degradation of beta-catenin by the destruction complex pathway
repression of WNT target genes pathway
AMER1 mutants destabilize the destruction complex pathway
AXIN mutants destabilize the destruction complex, activating WNT signaling pathway
T41 mutants of beta-catenin aren't phosphorylated pathway
APC truncation mutants have impaired AXIN binding pathway
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex pathway
deletions in the AXIN genes in hepatocellular carcinoma result in elevated WNT signaling pathway
S37 mutants of beta-catenin aren't phosphorylated pathway
AXIN missense mutants destabilize the destruction complex pathway
APC truncation mutants are not K63 polyubiquitinated pathway
S45 mutants of beta-catenin aren't phosphorylated pathway
misspliced GSK3beta mutants stabilize beta-catenin pathway
TCF7L2 mutants don't bind CTBP pathway
truncations of AMER1 destabilize the destruction complex pathway
Signal Transduction pathway
truncated APC mutants destabilize the destruction complex pathway
S33 mutants of beta-catenin aren't phosphorylated pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
AndrogenReceptor pathway
REACTOME
Degradation of beta-catenin by the destruction complex pathway
truncated APC mutants destabilize the destruction complex pathway
AXIN mutants destabilize the destruction complex, activating WNT signaling pathway
APC truncation mutants are not K63 polyubiquitinated pathway
AMER1 mutants destabilize the destruction complex pathway
Signaling by WNT in cancer pathway
AXIN missense mutants destabilize the destruction complex pathway
Signaling by Wnt pathway
APC truncation mutants have impaired AXIN binding pathway
T41 mutants of beta-catenin aren't phosphorylated pathway
Signal Transduction pathway
misspliced GSK3beta mutants stabilize beta-catenin pathway
S45 mutants of beta-catenin aren't phosphorylated pathway
deletions in the AMER1 gene destabilize the destruction complex pathway
S33 mutants of beta-catenin aren't phosphorylated pathway
truncations of AMER1 destabilize the destruction complex pathway
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex pathway
repression of WNT target genes pathway
deletions in the AXIN genes in hepatocellular carcinoma result in elevated WNT signaling pathway
TCF7L2 mutants don't bind CTBP pathway
S37 mutants of beta-catenin aren't phosphorylated pathway
Disease pathway
KEGG
INOH
PID NCI
Presenilin action in Notch and Wnt signaling
Regulation of nuclear beta catenin signaling and target gene transcription
Cross-References
SwissProt P63002
TrEMBL B7ZNK7 Q3TYD9
UniProt Splice Variant
Entrez Gene 14797
UniGene
RefSeq NM_001276288 NM_010347
OMIM
CCDS CCDS24062
HPRD
IMGT
MGI ID MGI:95806
MGI Symbol Aes
EMBL AK131845 AK158714 BC132217 BC132219 BC145299 CH466553 L12140 X73359 X73361
GenPept AAA03023 AAI32218 AAI32220 AAI45300 BAE20827 BAE34624 CAA51769 CAA51771 EDL31398 EDL31399
RNA Seq Atlas 14797