DCC - DCC netrin 1 receptor Gene

Also Known as CRC18; CRCR1; MRMV1; HGPPS2; IGDCC1; NTN1R1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 1630

About DCC

Cytogenetic location: 18q21.2 Genomic coordinates (GRCh38): 18:52,340,197-53,535,899 (from NCBI)

This gene has 18 transcripts (splice variants), 193 orthologues, 36 paralogues and is associated with 109 phenotypes. Biased expression in testis (RPKM 2.4), brain (RPKM 1.4) and 2 other tissues.

Summary

This gene encodes a netrin 1 receptor. The transmembrane protein is a member of the immunoglobulin superfamily of cell adhesion molecules, and mediates axon guidance of neuronal growth cones towards sources of netrin 1 ligand. The cytoplasmic tail interacts with the tyrosine kinases Src and focal adhesion kinase (FAK, also known as PTK2) to mediate axon attraction. The protein partially localizes to lipid rafts, and induces Apoptosis in the absence of ligand. The protein functions as a tumor suppressor, and is frequently mutated or downregulated in colorectal Cancer and esophageal carcinoma. [provided by RefSeq, Oct 2009]

DCC Products (1)

mRNA Protein Name
NM_005215.4 NP_005206.2 netrin receptor DCC
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
11527412 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

DCC Protein Structure

Ig_2

Ig_2: Immunoglobulin domain (44 - 136)

I-set

I-set: Immunoglobulin I-set domain (141 - 222)

I-set

I-set: Immunoglobulin I-set domain (241 - 327)

I-set

I-set: Immunoglobulin I-set domain (333 - 417)

fn3

fn3: Fibronectin type III domain (430 - 514)

fn3

fn3: Fibronectin type III domain (530 - 607)

fn3

fn3: Fibronectin type III domain (625 - 708)

fn3

fn3: Fibronectin type III domain (727 - 806)

fn3

fn3: Fibronectin type III domain (846 - 931)

fn3

fn3: Fibronectin type III domain (946 - 1034)

Neogenin_C

Neogenin_C: Neogenin C-terminus (1146 - 1445)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1447 a.a.
Protein Preferred Names Protein Names

netrin receptor DCC

  • colorectal cancer suppressor

DCC Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
DCC P43146 MAZ Homo sapiens P56270
Y2H
11527412
Intra
DCC P43146 MAZ Homo sapiens P56270 11527412
Intra
DCC P43146 NTN1 Homo sapiens O95631 26190107
Intra
DCC P43146 NTN1 Homo sapiens O95631 19721007
Intra
DCC P43146 NTN1 Homo sapiens O95631 20434207
Intra
DCC P43146 MYO10 Homo sapiens Q9HD67 21642953
Intra
DCC P43146 MYO10 Homo sapiens Q9HD67 21642953
Intra
DCC P43146 MYO10 Homo sapiens Q9HD67
ITC
21642953
Intra
DCC P43146 RPS23 Homo sapiens P62266 20434207
Intra
DCC P43146 RPL5 Homo sapiens P46777 20434207
Intra
DCC P43146 RPL5 Homo sapiens P46777 20434207
Intra
DCC P43146 RPL28 Homo sapiens P46779 20434207
Intra
DCC P43146 CASP9 Homo sapiens P55211 16537496
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant DCC Proteins

Cat. No. Product Name Accession Purity
HY-P78745 Netrin receptor DCC/DCC Protein, Human (HEK293, His) P43146 (F32-N1097) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P78754 Netrin receptor DCC/DCC Protein, Human (HEK293, Fc) P43146 (F32-N1097) ≥ 90%, as determined by reducing SDS-PAGE.

DCC Antibodies

Cat. No. Product Name Application Reactivity
HY-P86845 DCC Antibody (YA6538) WB, IHC-F Human, Mouse, Rat

Related Diseases

Diseases Alias
Mirror Movements 1
  • Congenital Mirror Movement Disorder

  • Bimanual Synergia

  • Congenital Mirror Movements

  • Familial Congenital Controlateral Synkinesia

  • Familial Congenital Mirror Movements

  • Hereditary Congenital Controlateral Synkinesia

  • Hereditary Congenital Mirror Movements

  • Isolated Congenital Controlateral Synkinesia

  • Isolated Congenital Mirror Movements

  • Mirror Movements

  • MRMV1

  • Mirror Movements 1 And/Or Agenesis Of The Corpus Callosum

  • Mirror Movements, Congenital

  • Bimanual Synkinesis

  • Cmm

  • Mirror Movements, Type 1

Gaze Palsy, Familial Horizontal, With Progressive Scoliosis 2, With Impaired Intellectual Development
  • Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2

  • HGPPS2

  • Developmental Split-Brain Syndrome

  • Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2, With Impaired Intellectual Development

Esophageal Cancer
  • Esophageal Carcinoma

  • Carcinoma Of Esophagus

  • Esophageal Squamous Cell Carcinoma, Somatic

  • Esophageal Carcinoma, Somatic

  • Esophagus Cancer

  • Gastric Cardia Adenocarcinoma

  • Esophageal Neoplasms

  • Esophageal Cancer, Somatic

  • Cancer Of Esophagus

  • Cancer Of Oesophagus

  • Carcinoma Of Oesophagus

  • Ca Lower Third Oesophagus

  • Ca Middle Third Oesophagus

  • Malignant Neoplasm Of Distal Third Of Esophagus

  • Malignant Neoplasm Of Lower Third Of Oesophagus

  • Malignant Neoplasm Of Middle Third Of Oesophagus

  • Malignant Neoplasm Of Proximal Third Of Esophagus

  • Malignant Neoplasm Of Upper Third Esophagus

  • Malignant Tumor Of Abdominal Esophagus

  • Malignant Tumor Of Distal Third Of Esophagus

  • Malignant Tumor Of Proximal Third Of Esophagus

  • Malignant Tumor Of The Middle Third Of The Esophagus

  • ESCR

  • Aerodigestive Tract Cancer

  • Escc

  • Esophageal Squamous Cell Carcinoma

  • Cancer, Esophageal

  • Malignant Neoplasm Of Esophagus

  • Squamous Cell Carcinoma Of Esophagus

  • Malignant Neoplasm Of Middle Third Of Esophagus

Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Gaze Palsy, Familial Horizontal, With Progressive Scoliosis 1
  • Hgpps

  • Horizontal Gaze Palsy With Progressive Scoliosis

  • Gaze Palsy, Familial Horizontal, With Progressive Scoliosis

  • HGPPS1

  • Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 1

  • Gaze Palsy, Horizontal, With Progressive Scoliosis

  • Progressive External Ophthalmoplegia And Scoliosis

  • Familial Horizontal Gaze Palsy With Progressive Scoliosis

  • Familial Idiopathic Scoliosis Associated With Congenital Encephalopathy

  • Familial Infantile Scoliosis Associated With Bilateral Paralysis Of Conjugate Gaze

  • Ophthalmoplegia, Progressive External, And Scoliosis

  • Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, Type 1

Corpus Callosum, Agenesis Of
  • Corpus Callosum Agenesis

  • Agenesis Of The Corpus Callosum

  • Isolated Corpus Callosum Agenesis

  • Acc

  • Non Rare In Europe: Isolated Corpus Callosum Agenesis

  • Congenital Malformation Of Corpus Callosum

  • Deformity Of Corpus Callosum

  • Absence Of Corpus Callosum

  • Absent Corpus Callosum

  • Acc - [Agenesis Of Corpus Callosum]

  • Aplasia Of Corpus Callosum

  • Congenital Absence Of Corpus Callosum

  • Hypoplastic Corpus Callosum

  • Hypoplasia Of Corpus Callosum

Intellectual Disability - Hypoplastic Corpus Callosum - Preauricular Tag
  • Da Silva Syndrome

  • Intellectual Disability-Hypoplastic Corpus Callosum-Preauricular Tag Syndrome

Kallmann Syndrome
  • Hypogonadism With Anosmia

  • Kallman'S Syndrome

  • Anosmic Hypogonadism

  • Anosmic Idiopathic Hypogonadotropic Hypogonadism

  • Hypogonadotropic Hypogonadism And Anosmia

  • Hypogonadotropic Hypogonadism-Anosmia Syndrome

  • Olfacto-Genital Pathological Sequence

  • Familial Hypogonadism With Anosmia

  • Kallman Syndrome

  • Dysplasia Olfactogenitalis Of De Morsier

  • Kallmann'S Syndrome

  • Congenital Hypogonadotropic Hypogonadism With Anosmia

Corpus Callosum, Partial Agenesis Of, X-Linked
  • X-Linked Complicated Corpus Callosum Dysgenesis

  • Corpus Callosum, Partial Agenesis Of

  • Partial Agenesis Of The Corpus Callosum

  • Partial Agenesis Of Corpus Callosum

  • Agenesis Of The Corpus Callosum, X-Linked, Partial

  • ACCPX

  • Agenesis, Corpus Callosum, Partial

Non-Syndromic X-Linked Intellectual Disability Arx-Related
  • Arx-Related Intellectual Disability

  • Mrxarx

  • X-Linked Mental Retardation 29

  • X-Linked Mental Retardation 29 And Others

  • X-Linked Mental Retardation 32

  • X-Linked Mental Retardation 33

  • X-Linked Mental Retardation 38

  • X-Linked Mental Retardation 43

  • X-Linked Mental Retardation 76

  • X-Linked Mental Retardation 87

  • X-Linked Mental Retardation With Or Without Seizures Arx-Related

  • Mental Retardation, X-Linked, Type 29 And Others

Scoliosis
Gastric Squamous Cell Carcinoma
  • Squamous Cell Carcinoma Of Stomach

  • Squamous Cell Carcinoma Of The Stomach

Autism Spectrum Disorder
  • Asd

  • Autism Spectrum Disorders

  • Autistic Continuum

  • Pervasive Developmental Disorder

  • Pervasive Development Disorder

  • Autistic Behavior

  • Autistic Disorder

  • Autistic

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Childhood Autism

  • Kanner Syndrome

  • Pervasive Developmental Delay Nos

  • Pervasive Developmental Disorder, Not Otherwise Specified

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus DCC VGNC VGNC:61363
Mus musculus DCC MGD MGI:94869
Canis familiaris DCC VGNC VGNC:39799
Macaca mulatta DCC VGNC VGNC:71746
Bos taurus DCC VGNC VGNC:109406
Rattus norvegicus DCC RGD RGD:2492
Others DCC NCBI