Mus musculus Gene: Ctbp2
Summary
InnateDB Gene IDBG-211193.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Ctbp2
Gene Name C-terminal binding protein 2
Synonyms AA407280; D7Ertd45e; Gtrgeo6; Ribeye
Species Mus musculus
Ensembl Gene ENSMUSG00000030970
Encoded Proteins
C-terminal binding protein 2
C-terminal binding protein 2
C-terminal binding protein 2
C-terminal binding protein 2
C-terminal binding protein 2
C-terminal binding protein 2
C-terminal binding protein 2
C-terminal binding protein 2
C-terminal binding protein 2
C-terminal binding protein 2
C-terminal binding protein 2
C-terminal binding protein 2
C-terminal binding protein 2
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 ENSG00000175029:
This gene produces alternative transcripts encoding two distinct proteins. One protein is a transcriptional repressor, while the other isoform is a major component of specialized synapses known as synaptic ribbons. Both proteins contain a NAD+ binding domain similar to NAD+-dependent 2-hydroxyacid dehydrogenases. A portion of the 3' untranslated region was used to map this gene to chromosome 21q21.3; however, it was noted that similar loci elsewhere in the genome are likely. Blast analysis shows that this gene is present on chromosome 10. [provided by RefSeq, Jul 2008]
This gene produces alternative transcripts encoding two distinct proteins. One protein is a transcriptional repressor, while the other isoform is a major component of specialized synapses known as synaptic ribbons. Both proteins contain a NAD+ binding domain similar to NAD+-dependent 2-hydroxyacid dehydrogenases. A portion of the 3\' untranslated region was used to map this gene to chromosome 21q21.3; however, it was noted that similar loci elsewhere in the genome are likely. Blast analysis shows that this gene is present on chromosome 10. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Feb 2014]
Gene Information
Type Protein coding
Genomic Location Chromosome 7:132987563-133124354
Strand Reverse strand
Band F3
Transcripts
ENSMUST00000033269 ENSMUSP00000033269
ENSMUST00000155996 ENSMUSP00000132558
ENSMUST00000165457 ENSMUSP00000126126
ENSMUST00000169570 ENSMUSP00000130294
ENSMUST00000166439 ENSMUSP00000127448
ENSMUST00000168958 ENSMUSP00000132892
ENSMUST00000172341 ENSMUSP00000127701
ENSMUST00000165534
ENSMUST00000166400
ENSMUST00000163601 ENSMUSP00000128944
ENSMUST00000171727
ENSMUST00000164739
ENSMUST00000164896
ENSMUST00000167218 ENSMUSP00000133269
ENSMUST00000170459 ENSMUSP00000129590
ENSMUST00000171882 ENSMUSP00000129312
ENSMUST00000171022 ENSMUSP00000132399
ENSMUST00000171968 ENSMUSP00000130727
ENSMUST00000168762
ENSMUST00000168238
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 22 experimentally validated interaction(s) in this database.
They are also associated with 56 interaction(s) predicted by orthology.
Experimentally validated
Total 22 [view]
Protein-Protein 22 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 56 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003714 transcription corepressor activity
GO:0005515 protein binding
GO:0016616 oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0051287 NAD binding
Biological Process
GO:0006351 transcription, DNA-templated
GO:0008152 metabolic process
GO:0045892 negative regulation of transcription, DNA-templated
GO:0050872 white fat cell differentiation
GO:0055114 oxidation-reduction process
Cellular Component
GO:0005634 nucleus
GO:0017053 transcriptional repressor complex
GO:0030054 cell junction
GO:0045202 synapse
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
KEGG
Notch signaling pathway pathway
Wnt signaling pathway pathway
Chronic myeloid leukemia pathway
Pathways in cancer pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
Wnt 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
Wnt signaling pathway pathway
Notch signaling pathway pathway
Chronic myeloid leukemia pathway
Pathways in cancer pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene 13017
UniGene Mm.246240
RefSeq NM_001170744 NM_009980 XM_006507308 XM_006507309 XM_006507310 XM_006507311 XM_006507312 XM_006507313 XM_006507315
OMIM
CCDS CCDS21930 CCDS52417
HPRD
IMGT
MGI ID MGI:1201686
MGI Symbol Ctbp2
EMBL
GenPept
RNA Seq Atlas 13017