NLGN4Y neuroligin 4 Y-linked
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | HNL4Y |
MIM | 400028 OMIM |
HGNC | HGNC:15529 HGNC |
Ensembl | ENSG00000165246 Ensembl |
AllianceGenome | HGNC:15529 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000382868.5 | hg38 | chrY | 14,523,746 | 14,843,726 | 319,981 |
ENST00000684976.1 | hg38 | chrY | 14,524,529 | 14,845,654 | 321,126 |
ENST00000339174.9 | hg38 | chrY | 14,524,574 | 14,843,647 | 319,074 |
ENST00000382872.5 | hg38 | chrY | 14,522,752 | 14,845,650 | 322,899 |
ENST00000382872.5 | hg19 | chrY | 16,634,632 | 16,957,530 | 322,899 |
ENST00000382868.5 | hg19 | chrY | 16,635,626 | 16,955,606 | 319,981 |
ENST00000684976.1 | hg19 | chrY | 16,636,409 | 16,957,534 | 321,126 |
ENST00000339174.9 | hg19 | chrY | 16,636,454 | 16,955,527 | 319,074 |
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