(Q21102436)

Contactin-associated protein 1

1 reference

Concanavalin A-like lectin/glucanase domain superfamily

1 reference

Galactose-binding-like domain superfamily

1 reference

Laminin G domain, protein family

1 reference

Fibrinogen, alpha/beta/gamma chain, C-terminal globular domain, protein family

1 reference

Neurexin/syndecan/glycophorin C, protein family

1 reference

EGF-like domain, protein family

1 reference

Coagulation factor 5/8 C-terminal domain, protein family

1 reference

Systematic identification of SH3 domain-mediated human protein-protein interactions by peptide array target screening

1 reference

13 November 2019

1 reference

13 November 2019

1 reference

8 April 2019

GOA

curator

IntAct protein interaction database

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

signaling receptor activity

IPI

1 reference

8 April 2019

Identification of a novel contactin-associated transmembrane receptor with multiple domains implicated in protein-protein interactions

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

integral component of membrane

TAS

cell component

4 references

8 April 2019

British Heart Foundation

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

1 reference

16 July 2018

http://www.ebi.ac.uk/QuickGO/annotations?protein=P78357&geneProductId=UniProtKB:P78357

integral component of plasma membrane

1 reference

8 April 2019

Identification of a novel contactin-associated transmembrane receptor with multiple domains implicated in protein-protein interactions

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

presynaptic active zone membrane

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

neuromuscular process controlling posture

biological process

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

neuromuscular process controlling balance

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

neuron projection development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

1 reference

8 April 2019

Identification of a novel contactin-associated transmembrane receptor with multiple domains implicated in protein-protein interactions

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

positive regulation of signal transduction

TAS

1 reference

8 April 2019

Gene Ontology Consortium

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

central nervous system myelination

1 reference

8 April 2019

CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

myelination in peripheral nervous system

IMP

3 references

8 April 2019

Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

8 April 2019

CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

8 April 2019

Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

paranodal junction assembly

IMP

4 references

8 April 2019

British Heart Foundation

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

8 April 2019

Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

neuron projection morphogenesis

4 references

8 April 2019

British Heart Foundation

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

8 April 2019

Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

8 April 2019

Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P78357

1 reference

Coagulation factor 5/8 C-terminal domain

1 reference

Fibrinogen, alpha/beta/gamma chain, C-terminal globular domain

1 reference

EGF-like domain

1 reference

Neurexin/syndecan/glycophorin C

1 reference