CNTN5 - contactin 5 Gene
Also Known as NB-2; HNB-2s
Species: Homo sapiens
About CNTN5
This gene has 11 transcripts (splice variants), 204 orthologues and 36 paralogues. Biased expression in placenta (RPKM 1.0), thyroid (RPKM 1.0) and 5 other tissues.
Summary
The protein encoded by this gene is a member of the immunoglobulin superfamily, and contactin family, which mediate cell surface interactions during nervous system development. This protein is a glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein that functions as a cell adhesion molecule. It may play a role in the formation of axon connections in the developing nervous system. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]
CNTN5 Products (4)
| mRNA | Protein | Name |
|---|---|---|
| NM_001243270.2 | NP_001230199.1 | contactin-5 isoform 1 precursor |
| NM_001243271.2 | NP_001230200.1 | contactin-5 isoform 3 precursor |
| NM_014361.4 | NP_055176.1 | contactin-5 isoform 1 precursor |
| NM_175566.2 | NP_780775.1 | contactin-5 isoform 2 precursor |
CNTN5 Protein Structure
I-set: Immunoglobulin I-set domain (99 - 182)
Ig_2: Immunoglobulin domain (203 - 276)
I-set: Immunoglobulin I-set domain (307 - 386)
I-set: Immunoglobulin I-set domain (392 - 475)
I-set: Immunoglobulin I-set domain (486 - 568)
I-set: Immunoglobulin I-set domain (574 - 667)
fn3: Fibronectin type III domain (673 - 760)
fn3: Fibronectin type III domain (776 - 863)
fn3: Fibronectin type III domain (878 - 962)
fn3: Fibronectin type III domain (977 - 1057)
- 0
- 200
- 400
- 600
- 800
- 1000
- 1100 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
contactin-5 |
|
Recombinant CNTN5 Proteins
| Cat. No. | Product Name | Accession | Purity |
|---|---|---|---|
| HY-P76841 | CNTN5/Contactin-5 Protein, Human (HEK293, His) | O94779 (E19-Q1059) | ≥ 95%, as determined by reducing SDS-PAGE. |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Coffin-Siris Syndrome 6 |
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| Chromosome 3pter-P25 Deletion Syndrome |
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| Aleutian Mink Disease |
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| Myopathy, Congenital, Compton-North |
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| Atrial Septal Defect 6 |
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| Cyclothymic Disorder |
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| Actinomycosis |
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Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Rattus norvegicus | CNTN5 | RGD | RGD:621302 |
| Macaca mulatta | CNTN5 | VGNC | VGNC:71287 |
| Mus musculus | CNTN5 | MGD | MGI:3042287 |
| Canis familiaris | CNTN5 | VGNC | VGNC:39436 |
| Felis catus | CNTN5 | VGNC | VGNC:82001 |
| Others | CNTN5 | NCBI |