about
P688
Neuroligins and neurexins link synaptic function to cognitive diseaseTruncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophreniaA patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1alphaCNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in DrosophilaMouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.Neurexins: synaptic cell surface proteins related to the alpha-latrotoxin receptor and laminin
P921
description
Protein in Homo sapiens
@de
human protein (annotated by UniProtKB/Swiss-Prot Q9ULB1)
@en
proteinë
@sq
proteïne
@nl
بروتين في الإنسان العاقل
@ar
name
Neurexin-1
@en
type
label
Neurexin-1
@en
altLabel
Neurexin I-alpha
@en
Neurexin-1-alpha
@en
prefLabel
Neurexin-1
@en
P361
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P31
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P361
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NP_001129131.1
NP_004792.1
NP_620072.1
XP_011531476.1
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P7260
8.A.74.1.2