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Aliases for CNTN5 Gene

Aliases for CNTN5 Gene

  • Contactin 5 2 3 5
  • Neural Recognition Molecule NB-2 3 4
  • Neural Adhesion Molecule 3
  • Contactin-5 3
  • HNB-2s 3
  • HNB-2 4
  • NB-2 3

External Ids for CNTN5 Gene

Previous GeneCards Identifiers for CNTN5 Gene

  • GC11P101085
  • GC11P100784
  • GC11P098429
  • GC11P098397
  • GC11P094826

Summaries for CNTN5 Gene

Entrez Gene Summary for CNTN5 Gene

  • 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]

GeneCards Summary for CNTN5 Gene

CNTN5 (Contactin 5) is a Protein Coding gene. Diseases associated with CNTN5 include Actinomycosis and Hirschsprung Disease 1. Among its related pathways are Metabolism of proteins and Post-translational modification- synthesis of GPI-anchored proteins. An important paralog of this gene is CNTN3.

UniProtKB/Swiss-Prot for CNTN5 Gene

  • Contactins mediate cell surface interactions during nervous system development. Has some neurite outgrowth-promoting activity in the cerebral cortical neurons but not in hippocampal neurons. Probably involved in neuronal activity in the auditory system (By similarity).

Additional gene information for CNTN5 Gene

No data available for CIViC summary , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for CNTN5 Gene

Genomics for CNTN5 Gene

GeneHancer (GH) Regulatory Elements for CNTN5 Gene

Promoters and enhancers for CNTN5 Gene
GeneHancer (GH) Identifier GH Type GH
GH Sources Gene Association Score Total Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor
Binding Sites
Gene Targets
GH11J099020 Promoter/Enhancer 1.5 EPDnew Ensembl ENCODE 650.7 -0.1 -90 1 CTCF VEZF1 RAD21 ZBTB20 CNTN5 PIR40279
GH11J099281 Promoter 0.5 EPDnew 650.1 +260.5 260521 0.1 CNTN5 RN7SKP53 GC11M099822
GH11J099066 Enhancer 0.2 ENCODE 10.6 +45.9 45934 0.5 CNTN5 GC11P099037 RN7SKP53
GH11J099339 Enhancer 0.2 FANTOM5 2.3 +319.0 319041 0.3 CNTN5 RN7SKP53 GC11M099822
GH11J099069 Enhancer 0.6 Ensembl ENCODE 0.2 +49.3 49253 0.9 CTCF POLR2A GC11P099037 CNTN5 RN7SKP53
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data from 2017 publication | Request up-to-date GeneHancer data (full dataset)

GeneHancers around CNTN5 on UCSC Golden Path with GeneCards custom track

Top Transcription factor binding sites by QIAGEN in the CNTN5 gene promoter:
  • Chx10
  • POU2F1
  • POU2F1a
  • POU3F2
  • POU3F2 (N-Oct-5a)
  • POU3F2 (N-Oct-5b)
  • Pbx1a
  • Gfi-1
  • LCR-F1
  • HNF-3beta

Genomic Locations for CNTN5 Gene

Genomic Locations for CNTN5 Gene
1,337,933 bases
Plus strand
1,337,934 bases
Plus strand

Genomic View for CNTN5 Gene

Genes around CNTN5 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
CNTN5 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for CNTN5 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for CNTN5 Gene

Proteins for CNTN5 Gene

  • Protein details for CNTN5 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Recommended name:
    Protein Accession:
    Secondary Accessions:
    • A1L4P0
    • B7ZM07
    • E9PKE8
    • O94780
    • Q49AF3

    Protein attributes for CNTN5 Gene

    1100 amino acids
    Molecular mass:
    120686 Da
    Quaternary structure:
    • Interacts with PTPRG.
    • Sequence=AAH39255.1; Type=Erroneous termination; Positions=223; Note=Translated as Ser.; Evidence={ECO:0000305};

    Three dimensional structures from OCA and Proteopedia for CNTN5 Gene

    Alternative splice isoforms for CNTN5 Gene


neXtProt entry for CNTN5 Gene

Post-translational modifications for CNTN5 Gene

  • Modification sites at PhosphoSitePlus
  • Modification sites at neXtProt

No data available for DME Specific Peptides for CNTN5 Gene

Domains & Families for CNTN5 Gene

Protein Domains for CNTN5 Gene

Suggested Antigen Peptide Sequences for CNTN5 Gene

Graphical View of Domain Structure for InterPro Entry



  • Belongs to the immunoglobulin superfamily. Contactin family.
  • Belongs to the immunoglobulin superfamily. Contactin family.
genes like me logo Genes that share domains with CNTN5: view

Function for CNTN5 Gene

Molecular function for CNTN5 Gene

UniProtKB/Swiss-Prot Function:
Contactins mediate cell surface interactions during nervous system development. Has some neurite outgrowth-promoting activity in the cerebral cortical neurons but not in hippocampal neurons. Probably involved in neuronal activity in the auditory system (By similarity).

Phenotypes From GWAS Catalog for CNTN5 Gene

genes like me logo Genes that share phenotypes with CNTN5: view

Animal Models for CNTN5 Gene

MGI Knock Outs for CNTN5:

Animal Model Products

  • Taconic Biosciences Mouse Models for CNTN5

Clone Products

No data available for Enzyme Numbers (IUBMB) , Gene Ontology (GO) - Molecular Function , Human Phenotype Ontology , miRNA , Transcription Factor Targets and HOMER Transcription for CNTN5 Gene

Localization for CNTN5 Gene

Subcellular locations from UniProtKB/Swiss-Prot for CNTN5 Gene

Cell membrane; Lipid-anchor, GPI-anchor.

Subcellular locations from

Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for CNTN5 gene
Compartment Confidence
plasma membrane 5
extracellular 5
cytosol 5
mitochondrion 3
peroxisome 2
nucleus 2
golgi apparatus 1

Subcellular locations from the

Human Protein Atlas (HPA)

Gene Ontology (GO) - Cellular Components for CNTN5 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005576 extracellular region TAS --
GO:0005829 cytosol IDA --
GO:0005886 plasma membrane TAS --
GO:0016020 membrane IEA --
GO:0031225 anchored component of membrane IEA --
genes like me logo Genes that share ontologies with CNTN5: view

Pathways & Interactions for CNTN5 Gene

genes like me logo Genes that share pathways with CNTN5: view

Gene Ontology (GO) - Biological Process for CNTN5 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0006501 C-terminal protein lipidation TAS --
GO:0007155 cell adhesion IEA --
GO:0007605 sensory perception of sound IEA --
genes like me logo Genes that share ontologies with CNTN5: view

No data available for SIGNOR curated interactions for CNTN5 Gene

Drugs & Compounds for CNTN5 Gene

No Compound Related Data Available

Transcripts for CNTN5 Gene

mRNA/cDNA for CNTN5 Gene

Unigene Clusters for CNTN5 Gene

Contactin 5:
Representative Sequences:

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for CNTN5 Gene

No ASD Table

Relevant External Links for CNTN5 Gene

GeneLoc Exon Structure for
ECgene alternative splicing isoforms for

Expression for CNTN5 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for CNTN5 Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

mRNA differential expression in normal tissues according to GTEx for CNTN5 Gene

This gene is overexpressed in Brain - Anterior cingulate cortex (BA24) (x8.1), Brain - Amygdala (x8.0), Brain - Frontal Cortex (BA9) (x7.4), Brain - Hippocampus (x6.0), and Brain - Cortex (x5.5).

Protein differential expression in normal tissues from HIPED for CNTN5 Gene

This gene is overexpressed in Plasma (42.1), Heart (13.0), and Fetal Brain (11.3).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB and MOPED for CNTN5 Gene

Protein tissue co-expression partners for CNTN5 Gene

- Elite partner

NURSA nuclear receptor signaling pathways regulating expression of CNTN5 Gene:


SOURCE GeneReport for Unigene cluster for CNTN5 Gene:


mRNA Expression by UniProt/SwissProt for CNTN5 Gene:

Tissue specificity: Expressed in brain and kidney and at very low level in placenta. Not expressed in other tissues. In brain, it is highly expressed in the occipital lobe, amygdala, cerebral cortex, frontal lobe, thalamus and temporal lobe. Expressed at moderate level in the cerebellum, substantia nigra, putamen, medulla and hippocampus. Weakly expressed in the spinal cord and caudate nucleus. Weakly or not expressed in the corpus callosum.

Evidence on tissue expression from TISSUES for CNTN5 Gene

  • Nervous system(4.5)
  • Blood(2.2)
genes like me logo Genes that share expression patterns with CNTN5: view

No data available for Phenotype-based relationships between genes and organs from Gene ORGANizer for CNTN5 Gene

Orthologs for CNTN5 Gene

This gene was present in the common ancestor of animals.

Orthologs for CNTN5 Gene

Organism Taxonomy Gene Similarity Type Details
(Pan troglodytes)
Mammalia CNTN5 34 33
  • 99.55 (n)
(Canis familiaris)
Mammalia CNTN5 34 33
  • 92.3 (n)
(Monodelphis domestica)
Mammalia CNTN5 34
  • 92 (a)
(Ornithorhynchus anatinus)
Mammalia CNTN5 34
  • 88 (a)
(Mus musculus)
Mammalia Cntn5 16 34 33
  • 85.91 (n)
(Rattus norvegicus)
Mammalia Cntn5 33
  • 85.56 (n)
(Bos Taurus)
Mammalia -- 34
  • 23 (a)
(Gallus gallus)
Aves FAR-2 34
  • 85 (a)
CNTN5 33
  • 80.19 (n)
(Anolis carolinensis)
Reptilia CNTN5 34
  • 81 (a)
tropical clawed frog
(Silurana tropicalis)
Amphibia cntn5 33
  • 74.32 (n)
(Danio rerio)
Actinopterygii cntn5 34 33
  • 64.81 (n)
wufi09g01 33
fruit fly
(Drosophila melanogaster)
Insecta Cont 35
  • 31 (a)
(Caenorhabditis elegans)
Secernentea Y54G2A.25 35
  • 28 (a)
C33F10.5a 35
  • 23 (a)
C33F10.5b 35
  • 23 (a)
Species where no ortholog for CNTN5 was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African clawed frog (Xenopus laevis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • baker's yeast (Saccharomyces cerevisiae)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rainbow trout (Oncorhynchus mykiss)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea squirt (Ciona intestinalis)
  • sea squirt (Ciona savignyi)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • wheat (Triticum aestivum)

Evolution for CNTN5 Gene

Gene Tree for CNTN5 (if available)
Gene Tree for CNTN5 (if available)
Evolutionary constrained regions (ECRs) for CNTN5: view image

Paralogs for CNTN5 Gene

Paralogs for CNTN5 Gene

(11) SIMAP similar genes for CNTN5 Gene using alignment to 3 proteins:

  • B7ZM08_HUMAN
genes like me logo Genes that share paralogs with CNTN5: view

Variants for CNTN5 Gene

Sequence variations from dbSNP and Humsavar for CNTN5 Gene

SNP ID Clin Chr 11 pos Variation AA Info Type
rs200028794 uncertain-significance, Hirschsprung disease 1 100,341,191(+) G/A coding_sequence_variant, genic_downstream_transcript_variant, missense_variant, non_coding_transcript_variant
rs186615197 likely-benign, not provided 100,061,278(+) A/T coding_sequence_variant, missense_variant, non_coding_transcript_variant
rs1000000810 -- 99,263,648(+) G/T genic_upstream_transcript_variant, intron_variant
rs1000003610 -- 99,637,562(+) AAATAA/AA intron_variant
rs1000005043 -- 99,621,960(+) G/T intron_variant

Structural Variations from Database of Genomic Variants (DGV) for CNTN5 Gene

Variant ID Type Subtype PubMed ID
dgv1263n100 CNV loss 25217958
dgv1264n100 CNV loss 25217958
dgv1265n100 CNV gain 25217958
dgv168n27 CNV loss 19166990
dgv2114n54 CNV loss 21841781
dgv2115n54 CNV loss 21841781
dgv2116n54 CNV loss 21841781
dgv2117n54 CNV loss 21841781
dgv2118n54 CNV loss 21841781
dgv2119n54 CNV loss 21841781
dgv2120n54 CNV loss 21841781
dgv2121n54 CNV loss 21841781
dgv2122n54 CNV loss 21841781
dgv2123n54 CNV loss 21841781
dgv2124n54 CNV loss 21841781
dgv2125n54 CNV loss 21841781
dgv2126n54 CNV loss 21841781
dgv2127n54 CNV loss 21841781
dgv2128n54 CNV loss 21841781
dgv2129n54 CNV loss 21841781
dgv2130n54 CNV loss 21841781
dgv2131n54 CNV loss 21841781
dgv226e214 CNV loss 21293372
dgv236e199 CNV deletion 23128226
dgv702n106 CNV deletion 24896259
dgv703n106 CNV deletion 24896259
dgv704n106 CNV deletion 24896259
dgv705n106 OTHER inversion 24896259
esv1001289 CNV deletion 20482838
esv1003185 CNV gain 20482838
esv1004847 CNV insertion 20482838
esv1010482 CNV gain 20482838
esv1010651 CNV deletion 20482838
esv1223158 CNV insertion 17803354
esv1232702 CNV deletion 17803354
esv1322572 CNV deletion 17803354
esv1754839 CNV insertion 17803354
esv2209043 CNV deletion 18987734
esv2299250 CNV deletion 18987734
esv23115 CNV loss 19812545
esv2421944 CNV deletion 20811451
esv2438747 CNV insertion 19546169
esv24648 CNV gain 19812545
esv2466796 CNV deletion 19546169
esv2656838 CNV deletion 23128226
esv2659055 CNV deletion 23128226
esv2661553 CNV deletion 23128226
esv2661704 CNV deletion 23128226
esv2662479 CNV deletion 23128226
esv2678709 CNV deletion 23128226
esv2744966 CNV deletion 23290073
esv2744967 CNV deletion 23290073
esv2744968 CNV deletion 23290073
esv2744969 CNV deletion 23290073
esv2744970 CNV deletion 23290073
esv2744971 CNV deletion 23290073
esv2744972 CNV deletion 23290073
esv2759859 CNV loss 17122850
esv2759860 CNV gain+loss 17122850
esv2760544 CNV loss 21179565
esv2761701 CNV loss 21179565
esv32699 CNV loss 17666407
esv3303151 CNV mobile element insertion 20981092
esv3305783 CNV mobile element insertion 20981092
esv3307536 CNV mobile element insertion 20981092
esv3307831 CNV mobile element insertion 20981092
esv3308952 CNV mobile element insertion 20981092
esv3309914 CNV mobile element insertion 20981092
esv3344223 CNV insertion 20981092
esv3354540 CNV insertion 20981092
esv33558 CNV gain 17666407
esv3357578 CNV insertion 20981092
esv3373814 CNV insertion 20981092
esv3376946 CNV insertion 20981092
esv3376958 OTHER inversion 20981092
esv3377401 OTHER inversion 20981092
esv3398286 CNV duplication 20981092
esv3408018 CNV insertion 20981092
esv3449728 CNV insertion 20981092
esv3548230 CNV deletion 23714750
esv3579870 CNV loss 25503493
esv3579872 CNV loss 25503493
esv3579873 CNV loss 25503493
esv3579874 CNV loss 25503493
esv3580039 CNV gain 25503493
esv3627452 CNV loss 21293372
esv3627453 CNV loss 21293372
esv3627456 CNV loss 21293372
esv3627457 CNV loss 21293372
esv3627460 CNV loss 21293372
esv3627465 CNV loss 21293372
esv3627466 CNV loss 21293372
esv3627469 CNV loss 21293372
esv3627471 CNV gain 21293372
esv3627472 CNV gain 21293372
esv3627473 CNV loss 21293372
esv3627474 CNV loss 21293372
esv3627475 CNV loss 21293372
esv3627476 CNV gain 21293372
esv3892088 CNV loss 25118596
esv3892089 CNV loss 25118596
esv4356 CNV loss 18987735
esv5885 CNV gain 19470904
esv7509 CNV loss 19470904
esv998217 CNV gain 20482838
nsv1036978 CNV loss 25217958
nsv1038289 CNV gain 25217958
nsv1038449 CNV loss 25217958
nsv1048704 CNV gain 25217958
nsv1048799 CNV loss 25217958
nsv1050495 CNV loss 25217958
nsv1052546 CNV loss 25217958
nsv1052565 CNV gain 25217958
nsv1069616 CNV deletion 25765185
nsv1069617 CNV deletion 25765185
nsv1078300 OTHER inversion 25765185
nsv1115417 CNV duplication 24896259
nsv1119906 CNV deletion 24896259
nsv1122658 CNV deletion 24896259
nsv1122659 CNV deletion 24896259
nsv1127227 CNV deletion 24896259
nsv1134167 CNV deletion 24896259
nsv1147684 CNV deletion 26484159
nsv1148549 OTHER inversion 26484159
nsv428265 CNV loss 18775914
nsv454 CNV insertion 18451855
nsv456 CNV insertion 18451855
nsv457 CNV insertion 18451855
nsv468823 CNV loss 19166990
nsv468824 CNV loss 19166990
nsv468828 CNV loss 19166990
nsv468829 CNV loss 19166990
nsv468830 CNV loss 19166990
nsv468831 CNV loss 19166990
nsv468832 CNV gain 19166990
nsv468833 CNV loss 19166990
nsv468834 CNV loss 19166990
nsv468842 CNV loss 19166990
nsv468843 CNV loss 19166990
nsv468844 CNV loss 19166990
nsv468845 CNV loss 19166990
nsv468846 CNV loss 19166990
nsv468847 CNV loss 19166990
nsv468848 CNV loss 19166990
nsv469984 CNV loss 18288195
nsv469985 CNV loss 18288195
nsv469986 CNV loss 18288195
nsv472133 CNV novel sequence insertion 20440878
nsv507610 OTHER sequence alteration 20534489
nsv513331 CNV insertion 21212237
nsv516785 CNV loss 19592680
nsv517422 CNV loss 19592680
nsv517898 CNV loss 19592680
nsv519340 CNV loss 19592680
nsv519381 CNV loss 19592680
nsv520862 CNV loss 19592680
nsv520993 CNV loss 19592680
nsv520995 CNV gain 19592680
nsv521600 CNV gain 19592680
nsv522053 CNV loss 19592680
nsv522201 CNV loss 19592680
nsv522847 CNV gain 19592680
nsv524013 CNV loss 19592680
nsv525174 CNV loss 19592680
nsv525366 CNV loss 19592680
nsv526736 CNV loss 19592680
nsv526809 CNV gain 19592680
nsv526847 CNV gain 19592680
nsv526965 CNV gain 19592680
nsv528690 CNV loss 19592680
nsv556046 CNV loss 21841781
nsv556047 CNV loss 21841781
nsv556048 CNV loss 21841781
nsv556051 CNV loss 21841781
nsv556052 CNV loss 21841781
nsv556055 CNV loss 21841781
nsv556058 CNV loss 21841781
nsv556059 CNV loss 21841781
nsv556062 CNV loss 21841781
nsv556075 CNV gain 21841781
nsv556076 CNV loss 21841781
nsv556077 CNV loss 21841781
nsv556083 CNV loss 21841781
nsv556084 CNV loss 21841781
nsv556085 CNV gain 21841781
nsv556086 CNV gain 21841781
nsv556089 CNV loss 21841781
nsv556092 CNV loss 21841781
nsv556093 CNV loss 21841781
nsv556104 CNV loss 21841781
nsv556106 CNV loss 21841781
nsv556108 CNV loss 21841781
nsv556114 CNV loss 21841781
nsv556115 CNV loss 21841781
nsv556117 CNV loss 21841781
nsv556119 CNV loss 21841781
nsv556120 CNV loss 21841781
nsv556121 CNV loss 21841781
nsv556122 CNV gain 21841781
nsv556123 CNV loss 21841781
nsv556124 CNV loss 21841781
nsv556125 CNV loss 21841781
nsv556126 CNV gain 21841781
nsv556127 CNV loss 21841781
nsv818860 CNV loss 17921354
nsv819915 CNV loss 19587683
nsv821270 CNV deletion 20802225
nsv826051 CNV loss 20364138
nsv826052 CNV loss 20364138
nsv826054 CNV loss 20364138
nsv826055 CNV loss 20364138
nsv832242 CNV loss 17160897
nsv832243 CNV gain 17160897
nsv832244 CNV loss 17160897
nsv832245 CNV gain 17160897
nsv8866 CNV loss 18304495
nsv958617 CNV deletion 24416366

Variation tolerance for CNTN5 Gene

Residual Variation Intolerance Score: 71.8% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 5.70; 73.06% of all genes are more intolerant (likely to be disease-causing)

Additional Variant Information for CNTN5 Gene

Human Gene Mutation Database (HGMD)
SNPedia medical, phenotypic, and genealogical associations of SNPs for

SNP Genotyping and Copy Number Assay Products

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for CNTN5 Gene

Disorders for CNTN5 Gene

MalaCards: The human disease database

(2) MalaCards diseases for CNTN5 Gene - From: HGMD, DISEASES, and GeneCards

Disorder Aliases PubMed IDs
  • actinomycetoma
hirschsprung disease 1
  • hirschsprung disease, susceptibility to, 1
- elite association - COSMIC cancer census association via MalaCards
Search CNTN5 in MalaCards View complete list of genes associated with diseases

Additional Disease Information for CNTN5

Genetic Association Database
Human Genome Epidemiology Navigator
ATLAS of Genetics and Cytogenetics in Oncology and Haematology
genes like me logo Genes that share disorders with CNTN5: view

No data available for UniProtKB/Swiss-Prot and Genatlas for CNTN5 Gene

Publications for CNTN5 Gene

  1. Human NB-2 of the contactin subgroup molecules: chromosomal localization of the gene (CNTN5) and distinct expression pattern from other subgroup members. (PMID: 11013081) Kamei Y … Watanabe K (Genomics 2000) 3 4 22 58
  2. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PMID: 20379614) Rose JE … Uhl GR (Molecular medicine (Cambridge, Mass.) 2010) 3 44 58
  3. Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients. (PMID: 20398908) Saus E … Estivill X (Journal of psychiatric research 2010) 3 44 58
  4. Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. (PMID: 20628086) Bailey SD … DREAM investigators (Diabetes care 2010) 3 44 58
  5. Investigation of genetic susceptibility factors for human longevity - a targeted nonsynonymous SNP study. (PMID: 20800603) Flachsbart F … Nebel A (Mutation research 2010) 3 44 58

Products for CNTN5 Gene

Sources for CNTN5 Gene

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