Version 5.4
Mus musculus Gene: Apc
Summary
InnateDB Gene IDBG-134573.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Apc
Gene Name adenomatosis polyposis coli
Synonyms AI047805; AU020952; AW124434; CC1; mAPC; Min
Species Mus musculus
Ensembl Gene ENSMUSG00000005871
Encoded Proteins
IDBP-134575
adenomatosis polyposis coli
IDBP-134577
adenomatosis polyposis coli
IDBP-248875
adenomatosis polyposis coli
IDBP-621763
adenomatosis polyposis coli
IDBP-621770
adenomatosis polyposis coli
IDBP-621772
adenomatosis polyposis coli
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 ENSG00000134982:
This gene encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway. It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 18:34220924-34322189
Strand Forward strand
Band B1
Transcripts
ENSMUST00000079362 ENSMUSP00000078337
ENSMUST00000066133 ENSMUSP00000064214
ENSMUST00000115781 ENSMUSP00000111447
ENSMUST00000171187 ENSMUSP00000127131
ENSMUST00000170023
ENSMUST00000163295 ENSMUSP00000129095
ENSMUST00000170195
ENSMUST00000165590 ENSMUSP00000128327
ENSMUST00000167136
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 57 experimentally validated interaction(s) in this database.
They are also associated with 133 interaction(s) predicted by orthology.
Experimentally validated
Total 57 [view]
Protein-Protein 22 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 35 [view]
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 133 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005488 binding
GO:0005515 protein binding
GO:0008013 beta-catenin binding
GO:0008017 microtubule binding
GO:0019887 protein kinase regulator activity
GO:0019901 protein kinase binding
GO:0045295 gamma-catenin binding
GO:0051010 microtubule plus-end binding
Biological Process
GO:0000281 mitotic cytokinesis
GO:0001822 kidney development
GO:0001942 hair follicle development
GO:0006461 protein complex assembly
GO:0006974 cellular response to DNA damage stimulus
GO:0007026 negative regulation of microtubule depolymerization
GO:0007050 cell cycle arrest
GO:0007091 metaphase/anaphase transition of mitotic cell cycle
GO:0007094 mitotic spindle assembly checkpoint
GO:0007389 pattern specification process
GO:0007409 axonogenesis
GO:0008285 negative regulation of cell proliferation
GO:0009798 axis specification
GO:0009952 anterior/posterior pattern specification
GO:0009953 dorsal/ventral pattern formation
GO:0009954 proximal/distal pattern formation
GO:0016055 Wnt signaling pathway
GO:0016477 cell migration
GO:0019827 stem cell maintenance
GO:0030178 negative regulation of Wnt signaling pathway
GO:0030334 regulation of cell migration
GO:0030335 positive regulation of cell migration
GO:0030856 regulation of epithelial cell differentiation
GO:0030858 positive regulation of epithelial cell differentiation
GO:0031116 positive regulation of microtubule polymerization
GO:0031122 cytoplasmic microtubule organization
GO:0031274 positive regulation of pseudopodium assembly
GO:0032886 regulation of microtubule-based process
GO:0033077 T cell differentiation in thymus
GO:0035019 somatic stem cell maintenance
GO:0042483 negative regulation of odontogenesis
GO:0043065 positive regulation of apoptotic process
GO:0043066 negative regulation of apoptotic process
GO:0043409 negative regulation of MAPK cascade
GO:0043588 skin development
GO:0044336 canonical Wnt signaling pathway involved in negative regulation of apoptotic process
GO:0044337 canonical Wnt signaling pathway involved in positive regulation of apoptotic process
GO:0045595 regulation of cell differentiation
GO:0045597 positive regulation of cell differentiation
GO:0045667 regulation of osteoblast differentiation
GO:0045670 regulation of osteoclast differentiation
GO:0045732 positive regulation of protein catabolic process
GO:0045736 negative regulation of cyclin-dependent protein serine/threonine kinase activity
GO:0045785 positive regulation of cell adhesion
GO:0046716 muscle cell cellular homeostasis
GO:0048538 thymus development
GO:0050680 negative regulation of epithelial cell proliferation
GO:0051171 regulation of nitrogen compound metabolic process
GO:0051276 chromosome organization
GO:0051726 regulation of cell cycle
GO:0051781 positive regulation of cell division
GO:0051988 regulation of attachment of spindle microtubules to kinetochore
GO:0060041 retina development in camera-type eye
GO:0060070 canonical Wnt signaling pathway
GO:0060770 negative regulation of epithelial cell proliferation involved in prostate gland development
GO:0090090 negative regulation of canonical Wnt signaling pathway
Cellular Component
GO:0000776 kinetochore
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0005881 cytoplasmic microtubule
GO:0005886 plasma membrane
GO:0005913 cell-cell adherens junction
GO:0005923 tight junction
GO:0016328 lateral plasma membrane
GO:0030027 lamellipodium
GO:0030424 axon
GO:0030426 growth cone
GO:0030877 beta-catenin destruction complex
GO:0031253 cell projection membrane
GO:0032587 ruffle membrane
GO:0035371 microtubule plus-end
GO:0042995 cell projection
GO:0044295 axonal growth cone
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
ENSG00000134982
View Gene Order
ENSBTAG00000018852
Not yet available
Pathways
NETPATH
REACTOME
KEGG
mmu05213
Endometrial cancer pathway
mmu05217
Basal cell carcinoma pathway
mmu04310
Wnt signaling pathway pathway
mmu05210
Colorectal cancer pathway
mmu04810
Regulation of actin cytoskeleton pathway
mmu05200
Pathways in cancer pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
NetPath_8
Wnt pathway
REACTOME
REACT_11065
Beta-catenin phosphorylation cascade pathway
REACT_11063
Degradation of beta-catenin by the destruction complex pathway
REACT_107
Apoptotic cleavage of cellular proteins pathway
REACT_995
Apoptotic execution phase pathway
REACT_228216
truncated APC mutants destabilize the destruction complex pathway
REACT_228098
AXIN mutants destabilize the destruction complex, activating WNT signaling pathway
REACT_228143
APC truncation mutants are not K63 polyubiquitinated pathway
REACT_228243
AMER1 mutants destabilize the destruction complex pathway
REACT_228096
misspliced LRP5 mutants have enhanced beta-catenin-dependent signaling pathway
REACT_228331
Signaling by WNT in cancer pathway
REACT_228285
AXIN missense mutants destabilize the destruction complex pathway
REACT_11045
Signaling by Wnt pathway
REACT_200610
disassembly of the destruction complex and recruitment of AXIN to the membrane pathway
REACT_228196
APC truncation mutants have impaired AXIN binding pathway
REACT_200731
deactivation of the beta-catenin transactivating complex pathway
REACT_228261
T41 mutants of beta-catenin aren't phosphorylated pathway
REACT_578
Apoptosis pathway
REACT_111102
Signal Transduction pathway
REACT_228314
misspliced GSK3beta mutants stabilize beta-catenin pathway
REACT_228137
S45 mutants of beta-catenin aren't phosphorylated pathway
REACT_228048
deletions in the AMER1 gene destabilize the destruction complex pathway
REACT_228159
S33 mutants of beta-catenin aren't phosphorylated pathway
REACT_228060
truncations of AMER1 destabilize the destruction complex pathway
REACT_228229
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex pathway
REACT_200777
TCF dependent signaling in response to WNT pathway
REACT_228112
deletions in the AXIN genes in hepatocellular carcinoma result in elevated WNT signaling pathway
REACT_228188
RNF mutants show enhanced WNT signaling and proliferation pathway
REACT_228223
TCF7L2 mutants don't bind CTBP pathway
REACT_228279
XAV939 inhibits tankyrase, stabilizing AXIN pathway
REACT_228251
S37 mutants of beta-catenin aren't phosphorylated pathway
REACT_116125
Disease pathway
KEGG
hsa04810
Regulation of actin cytoskeleton pathway
hsa05210
Colorectal cancer pathway
hsa04310
Wnt signaling pathway pathway
hsa05213
Endometrial cancer pathway
hsa05217
Basal cell carcinoma pathway
hsa05200
Pathways in cancer pathway
INOH
INOH website
Wnt signaling pathway pathway
PID NCI
met_pathway
Signaling events mediated by Hepatocyte Growth Factor Receptor (c-Met)
ps1pathway
Presenilin action in Notch and Wnt signaling
p53downstreampathway
Direct p53 effectors
betacatenin_nuc_pathway
Regulation of nuclear beta catenin signaling and target gene transcription
cdc42_pathway
CDC42 signaling events
wnt_canonical_pathway
Canonical Wnt signaling pathway
cdc42_reg_pathway
Regulation of CDC42 activity
betacatenin_deg_pathway
Degradation of beta catenin
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene 11789
UniGene Mm.384171 Mm.470430
RefSeq NM_007462 XM_006525532
OMIM
CCDS CCDS29125
HPRD
IMGT
MGI ID MGI:88039
MGI Symbol Apc
EMBL
GenPept
RNA Seq Atlas 11789

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