CNTN5 - contactin 5 Gene

Homo sapiens

Also known as NB-2; HNB-2s

Gene ID: 53942 | Gene type: protein coding

About CNTN5

Cytogenetic location: 11q22.1 Genomic coordinates (GRCh38): 11:99,020,949-100,358,885 (from NCBI)

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

Ig_2

I-set

fn3

0
200
400
600
800
1000
1100 a.a.

Protein Preferred Names

Protein Names

contactin-5

neural adhesion molecule

Recombinant CNTN5 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P76841	CNTN5/Contactin-5 Protein, Human (HEK293, His)	O94779 (E19-Q1059)	≥95%

Related Diseases

Diseases

Alias

Coffin-Siris Syndrome 6

CSS6	Coffin-Siris Syndrome, Type 6

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

Aleutian Mink Disease

Aleutian Disease

Myopathy, Congenital, Compton-North

Compton-North Congenital Myopathy	MYPCN
Congenital Lethal Myopathy, Compton-North Type

Atrial Septal Defect 6

ASD6	Atrial Heart Septal Defect 6
Septal Defect, Atrial, Type 6

Cyclothymic Disorder

Cyclothymia	Cycloid Personality
Cyclothymic Personality	Affective Personality Disorder
Cyclothymic Personality Disorder	Cycloid Personality Disorder

Actinomycosis

Actinomycetoma	Boil
Canaliculitis	Actinomycotic Infection
Actinomycotic Madura Foot	Keratoactinomycosis
Furuncle	Actinomycotic Mycetema
Actinomycotic Mycetoma Of Foot	Madura Foot Due To Actinomadura
Actinomyces Israeli	Actinomycetes
Anaerobic Actinomyces Infection	Actinomycotic Infection Of Unspecified Site
Actinomycosis Nos	Actinomycotic Node
Actinomyces Infection	Actinomycotic Mycetoma
Mycetoma Due To Filamentous Bacteria

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-RS02930	CNTN5 Human Pre-designed siRNA Set A		/	Unkown

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

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