NLGN2 neuroligin 2

Information
Symbol
NLGN2
Type
protein-coding
Description
neuroligin 2
Entrez Gene ID
57555
Genome
hg19
Position
chr17:7,311,164-7,323,179
Genome
hg38
Position
chr17:7,407,845-7,419,860
MIM
606479 OMIM
HGNC
HGNC:14290 HGNC
Ensembl
ENSG00000169992 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 34
Likely benign 0 82
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 118
Ranking
ClinVar
0
0
14
220
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
MIM 606479 OMIM
HGNC HGNC:14290 HGNC
Ensembl ENSG00000169992 Ensembl
AllianceGenome HGNC:14290
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000575301.5 hg38 chr17 7,404,874 7,418,684 13,811
ENST00000302926.7 hg38 chr17 7,407,845 7,419,860 12,016
ENST00000575301.5 hg19 chr17 7,308,193 7,322,003 13,811
ENST00000302926.7 hg19 chr17 7,311,164 7,323,179 12,016
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