NLGN4X gene homepage

General information
Gene symbol NLGN4X
Gene name neuroligin 4, X-linked
Chromosome X
Chromosomal band p22.33
Imprinted Unknown
Genomic reference NG_008881.1
Transcript reference NM_020742.2
Associated with diseases ID, MRXS, Asperger syndrome X-linked 2
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 59
Unique public DNA variants reported 41
Individuals with public variants 135
Hidden variants 5
Notes The establishment of this gene variant database (LSDB) was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement nÂș 200754 - the GEN2PHEN project.
Date created March 06, 2009
Date last updated December 04, 2019
Version NLGN4X:191204

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 14287
Entrez Gene 57502
PubMed articles NLGN4X
OMIM - Gene 300427
OMIM - Diseases MRXS (mental retardation, X-linked (MRXS))
Asperger syndrome X-linked 2
GeneCards NLGN4X
GeneTests NLGN4X

Active transcripts




NCBI ID     

NCBI Protein ID     

00000134 X neuroligin 4, X-linked, transcript variant 2 NM_020742.2 NP_851849.1 59

Copyright & disclaimer
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