about
P688
Identification of a novel contactin-associated transmembrane receptor with multiple domains implicated in protein-protein interactions.Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region.CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis.Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Contactin associated protein 1
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
Contactin associated protein 1
@en
type
label
Contactin associated protein 1
@en
altLabel
CNTNAP1
@en
caspr1
@en
contactin-associated protein 1
@en
neurexin IV
@en
neurexin-4
@en
p190
@en
prefLabel
Contactin associated protein 1
@en
P361
P527
P637
P680
P681
P682
P352
P31
P352
P361
P527
P637
XP_005257805
XP_016880727
XP_024306779
P681
P682
P702
P703
P705
ENSP00000264638
ENSP00000466571