Contactin-2

Summary
UniProt ID
Q02246
Gene Symbol
  • CNTN2
  • AXT
  • TAG1
  • TAX1
Organism
Homo sapiens (human)
External Links
GlyGen
Q02246
PubChem
Q02246
RaftProt
Q02246
Annotation
Keyword
  • 3D-structure
  • Cell adhesion
  • Cell membrane
  • Direct protein sequencing
  • Disulfide bond
  • Epilepsy
  • GPI-anchor
  • Immunoglobulin domain
  • Reference proteome
  • Repeat
  • Signal
Gene Ontology (GO)
Sequence
MGTATRRKPHLLLVAAVALVSSSAWSSALGSQTTFGPVFEDQPLSVLFPEESTEEQVLLACRARASPPATYRWKMNGTEMKLEPGSRHQLVGGNLVIMNPTKAQDAGVYQCLASNPVGTVVSREAILRFGFLQEFSKEERDPVKAHEGWGVMLPCNPPAHYPGLSYRWLLNEFPNFIPTDGRHFVSQTTGNLYIARTNASDLGNYSCLATSHMDFSTKSVFSKFAQLNLAAEDTRLFAPSIKARFPAETYALVGQQVTLECFAFGNPVPRIKWRKVDGSLSPQWTTAEPTLQIPSVSFEDEGTYECEAENSKGRDTVQGRIIVQAQPEWLKVISDTEADIGSNLRWGCAAAGKPRPTVRWLRNGEPLASQNRVEVLAGDLRFSKLSLEDSGMYQCVAENKHGTIYASAELAVQALAPDFRLNPVRRLIPAARGGEILIPCQPRAAPKAVVLWSKGTEILVNSSRVTVTPDGTLIIRNISRSDEGKYTCFAENFMGKANSTGILSVRDATKITLAPSSADINLGDNLTLQCHASHDPTMDLTFTWTLDDFPIDFDKPGGHYRRTNVKETIGDLTILNAQLRHGGKYTCMAQTVVDSASKEATVLVRGPPGPPGGVVVRDIGDTTIQLSWSRGFDNHSPIAKYTLQARTPPAGKWKQVRTNPANIEGNAETAQVLGLTPWMDYEFRVIASNILGTGEPSGPSSKIRTREAAPSVAPSGLSGGGGAPGELIVNWTPMSREYQNGDGFGYLLSFRRQGSTHWQTARVPGADAQYFVYSNESVRPYTPFEVKIRSYNRRGDGPESLTALVYSAEEEPRVAPTKVWAKGVSSSEMNVTWEPVQQDMNGILLGYEIRYWKAGDKEAAADRVRTAGLDTSARVSGLHPNTKYHVTVRAYNRAGTGPASPSANATTMKPPPRRPPGNISWTFSSSSLSIKWDPVVPFRNESAVTGYKMLYQNDLHLTPTLHLTGKNWIEIPVPEDIGHALVQIRTTGPGGDGIPAEVHIVRNGGTSMMVENMAVRPAPHPGTVISHSVAMLILIGSLEL
Glycosylation Sites
Displaying entries 1 - 10 of 13 in total
Position Description PubMed ID GlyTouCan ID Source
76 N-linked (GlcNAc...) asparagine
198 N-linked (GlcNAc...) asparagine
204 N-linked (GlcNAc...) asparagine
461 N-linked (GlcNAc...) asparagine
477 N-linked (GlcNAc...) asparagine
498 N-linked (GlcNAc...) asparagine
525 N-linked (GlcNAc...) asparagine
730
775
830 N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 3 entries
Pathway Name Organism
L1CAM interactions Homo sapiens
NCAM1 interactions Homo sapiens
NrCAM interactions Homo sapiens
Disease
Displaying entries 1 - 10 of 116 in total
DO ID Disease Name Source
DOID:0050523 adult T-cell leukemia/lymphoma
DOID:0050526 Gamstorp-Wohlfart syndrome
DOID:0050759 myotonic dystrophy type 2
DOID:0050841 focal hand dystonia
DOID:0050989 episodic ataxia type 1
DOID:0060041 autism spectrum disorder
DOID:0060058 lymphoma
DOID:0060061 primary cutaneous T-cell non-Hodgkin lymphoma
DOID:0060224 atrial fibrillation
DOID:0060239 Van der Woude syndrome

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024