Gene content    
DCC ( by HUGO)
Deleted In Colorectal Carcinoma
Tumor suppressor gene
Deleted In Colorectal Carcinoma
Colorectal Cancer Suppressor
Immunoglobulin Superfamily DCC Subclass Member 1
Tumor Suppressor Protein DCC
IGDCC1
MRMV1
DCC Subclass
Immunoglobulin Superfamily
Member 1
CRC18
CRCR1
Colorectal Tumor Suppressor
Deleted In Colorectal Cancer Protein
Immunoglobulin Superfamily
DCC Subclass
Member 1
Netrin Receptor DCC
NCBI: 18q21.3    Ensembl: 18q21.2
DCC_HUMANSize: 1447 amino acidsMass: 158457 Da

  • Tissue specificity: Found in axons of the central and peripheral nervous system and in differentiated cell types of the intestine. Not expressed in colorectal tumor cells that lost their capacity to differentiate into mucus producing cells [IMAGE] Pathway & Disease-focused R
  • Function:
    UniProtKB/Swiss-Prot Summary: DCC_HUMAN, P43146 Function: Receptor for netrin required for axon guidance. Mediates axon attraction of neuronal growth cones in the developing nervous system upon ligand binding. Its association with UNC5 proteins may trigger signaling for axon repulsion. It also acts as a dependence receptor required for apoptosis induction when not associated with netrin ligand. Implicated as a tumor suppressor gene
  • Similarity:
    Belongs to the immunoglobulin superfamily. DCC family
                          
    Contains 6 fibronectin type-III domains
                          
    Contains 4 Ig-like C2-type (immunoglobulin-like) domains [IMAGE]
  • Protein Domain/Family    
    Source ID Domain Name Type
    InterProIPR003598Ig_sub2Immunoglobulin C2 typeDomain
    IPR003599Ig_subImmunoglobulin subtypeDomain
    IPR003961Fibronectin_type3Fibronectin, type IIIDomain
    IPR007110Ig-like_domImmunoglobulin-likeDomain
    IPR010560Neogenin_CNeogenin, C-terminalDomain
    IPR013098Ig_I-setImmunoglobulin I-setDomain
    BlocksIPB003598Immunoglobulin C-2 typeImmunoglobulin C-2 type
    IPB003962Fibronectin type III repeat signatureFibronectin type III repeat signature
    IPB010560NeogeninNeogenin, C-terminal

    Gene Ontology    
    Type Term Evidence Source Pub
    Biological Process axonogenesis TAS GOA 8861902
    negative regulation of collateral sprouting TAS GOA 19616629
    negative regulation of dendrite development TAS GOA 19616629
    negative regulation of neuron projection development TAS GOA 19616629
    Molecular Function protein binding IPI GOA 11527412
    transmembrane signaling receptor activity TAS GOA 8861902

    Disorder & Mutation    
    Source Disease
    Genatlascolorectal carcinoma,deleted in (see TSG18A) in endometrial carcinoma with lymph node metastasis,and in pancreatic carcinomas
    SWISS-PROTMirror movements 1 (MRMV1) [MIM:157600]: A disorder characterized by contralateral involuntary movements that mirror voluntary ones. While mirror movements are occasionally found in young children, persistence beyond the age of 10 is abnormal. Mirror movements occur more commonly in the upper extremities. Note=The disease is caused by mutations affecting the gene represented in this entry

    DCC cross reference    
    PubMed OMIM Entrez Gene NCKU SNP Nucleotide UniProt Genome Data Viewer HomoloGene