Homo sapiens Protein: CNTN1 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-587188.3 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | CNTN1 | ||||||||||||||||||||||
Protein Name | contactin 1 | ||||||||||||||||||||||
Synonyms | F3; GP135; MYPCN; | ||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000448653 | ||||||||||||||||||||||
InnateDB Gene | IDBG-27462 (CNTN1) | ||||||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||||||
Function | Contactins mediate cell surface interactions during nervous system development. Involved in the formation of paranodal axo-glial junctions in myelinated peripheral nerves and in the signaling between axons and myelinating glial cells via its association with CNTNAP1. Participates in oligodendrocytes generation by acting as a ligand of NOTCH1. Its association with NOTCH1 promotes NOTCH1 activation through the released notch intracellular domain (NICD) and subsequent translocation to the nucleus. Interaction with TNR induces a repulsion of neurons and an inhibition of neurite outgrowth (By similarity). {ECO:0000250}. | ||||||||||||||||||||||
Subcellular Localization | Isoform 1: Cell membrane; Lipid-anchor, GPI- anchor; Extracellular side.Isoform 2: Cell membrane; Lipid-anchor, GPI- anchor; Extracellular side. | ||||||||||||||||||||||
Disease Associations | Compton-North congenital myopathy (CNCM) [MIM:612540]: Familial lethal form of congenital onset muscle weakness, inherited in an autosomal-recessive fashion and characterized by a secondary loss of beta2-syntrophin and alpha-dystrobrevin from the muscle sarcolemma, central nervous system involvement, and fetal akinesia. {ECO:0000269PubMed:19026398}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||||||
Tissue Specificity | Strongly expressed in brain and in neuroblastoma and retinoblastoma cell lines. Lower levels of expression in lung, pancreas, kidney and skeletal muscle. {ECO:0000269PubMed:2026173, ECO:0000269PubMed:8164510}. | ||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 15 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||
InterPro |
IPR003598
Immunoglobulin subtype 2 IPR003599 Immunoglobulin subtype IPR007110 Immunoglobulin-like domain IPR013098 Immunoglobulin I-set IPR013106 Immunoglobulin V-set domain IPR013151 Immunoglobulin |
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PFAM |
PF07679
PF07686 PF00047 |
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PRINTS | |||||||||||||||||||||||
PIRSF | |||||||||||||||||||||||
SMART |
SM00408
SM00409 |
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TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | Q12860 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-Q12860 | ||||||||||||||||||||||
TrEMBL | F8VX96 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 1272 | ||||||||||||||||||||||
UniGene | Hs.741112 | ||||||||||||||||||||||
RefSeq | NP_001242993 | ||||||||||||||||||||||
HUGO | HGNC:2171 | ||||||||||||||||||||||
OMIM | 600016 | ||||||||||||||||||||||
CCDS | CCDS58225 | ||||||||||||||||||||||
HPRD | 07189 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AC015540 AC016144 AC024900 AC074030 AC129108 AK289544 AK289698 BC036569 U07819 U07820 Z21488 | ||||||||||||||||||||||
GenPept | AAA67920 AAA67921 AAH36569 BAF82233 BAF82387 CAA79696 | ||||||||||||||||||||||