2. Gene
  3. CNTN3 - contactin 3 Gene

CNTN3 - contactin 3 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as PCS; PANG; BIG-1

Gene ID: 5067 | Gene type: protein coding

About CNTN3

Cytogenetic location: 3p12.3 Genomic coordinates (GRCh38): 3:74,262,568-74,614,659 (from NCBI)

This gene has 2 transcripts (splice variants), 124 orthologues and 36 paralogues. Broad expression in brain (RPKM 2.7), prostate (RPKM 1.8) and 18 other tissues.

Summary

Predicted to be involved in cell adhesion and nervous system development. Predicted to be located in extracellular region and plasma membrane. Predicted to be active in neuron projection. [provided by Alliance of Genome Resources, Apr 2022]

CNTN3 Products(2)

mRNA Protein Name
NM_001393376.1 NP_001380305.1 contactin-3 precursor
NM_020872.3 NP_065923.1 contactin-3 precursor

CNTN3 Protein Structure

I-set

I-set: Immunoglobulin I-set domain (40 - 116)

Ig_2

Ig_2: Immunoglobulin domain (131 - 201)

I-set

I-set: Immunoglobulin I-set domain (232 - 309)

I-set

I-set: Immunoglobulin I-set domain (319 - 403)

I-set

I-set: Immunoglobulin I-set domain (409 - 496)

I-set

I-set: Immunoglobulin I-set domain (501 - 594)

fn3

fn3: Fibronectin type III domain (600 - 687)

fn3

fn3: Fibronectin type III domain (704 - 790)

fn3

fn3: Fibronectin type III domain (805 - 891)

fn3

fn3: Fibronectin type III domain (906 - 986)

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  • 1028 a.a.
Protein Preferred Names Protein Names

contactin-3

brain-derived immunoglobulin superfamily protein 1

Recombinant CNTN3 Proteins

Cat. No. Product Name Accession Purity
HY-P72947 Contactin-3/CNTN3 Protein, Human (N708D, HEK293, Fc) Q9P232 (M1-S1002) ≥95%
HY-P74229 Contactin-3/CNTN3 Protein, Human (N708D, HEK293, His) Q9P232 (E20-S1002, N708D) ≥95%

Related Diseases

Diseases Alias
Plasmacytoma

Solitary Plasmacytoma

Solitary Myeloma

Myeloma - Solitary

Myeloma, Solitary

Plasmacytoma - Category

Solitary Osseous Plasmacytoma

Solitary Plasmacytoma Without Mention Of Remission

Localised Malignant Plasma Cell Tumour Nos

Plasmacytoma Nos
Pilocytic Astrocytoma Of Cerebellum

Cerebellar Pilocytic Astrocytoma
Cerebellar Astrocytoma

Astrocytoma Of Cerebellum
Chromosome 3pter-P25 Deletion Syndrome

3p- Syndrome

3p Deletion Syndrome

Distal Monosomy 3p

Chromosome 3, Monosomy 3p

3p Partial Monosomy Syndrome

Chromosome 3, Deletion 3p

Chromosome 3p Deletion Syndrome

Del Syndrome

Deletion 3p

Monosomy 3p

Partial Monosomy 3p

Distal 3p Deletion

Monosomy 3pter

Telomeric Monosomy 3p

Chromosome Deletion Syndrome 3pter-P25
Pneumonic Tularemia

Pulmonary Tularemia

Bronchopneumonic Tularemia

Pneumonic Tularaemia
Miles-Carpenter Syndrome

X-Linked Intellectual Disability, Miles-Carpenter Type

Mcs

Mental Retardation, X-Linked, Syndromic 4

Mental Retardation, X-Linked, With Congenital Contractures And Low Fingertip Arches

Mrxs4

Miles-Carpenter X-Linked Mental Retardation Syndrome
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

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS02928 CNTN3 Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus CNTN3 MGD MGI:99534
Felis catus CNTN3 VGNC VGNC:97386
Bos taurus CNTN3 VGNC VGNC:27538
Canis familiaris CNTN3 VGNC VGNC:39434
Macaca mulatta CNTN3 VGNC VGNC:71285
Rattus norvegicus CNTN3 RGD RGD:3253
Others CNTN3 NCBI