BEX3 brain expressed X-linked 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 6 | 0 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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2 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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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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Target data | : |
MGeND data only
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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 | Bex |
SYNONYM | DXS6984E |
SYNONYM | HGR74 |
SYNONYM | NADE |
SYNONYM | NGFRAP1 |
MIM | 300361 OMIM |
HGNC | HGNC:13388 HGNC |
Ensembl | ENSG00000166681 Ensembl |
AllianceGenome | HGNC:13388 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000361298.9 | hg38 | chrX | 103,376,538 | 103,378,164 | 1,627 |
ENST00000372645.3 | hg38 | chrX | 103,376,395 | 103,378,077 | 1,683 |
ENST00000372634.1 | hg38 | chrX | 103,376,916 | 103,378,071 | 1,156 |
ENST00000372635.1 | hg38 | chrX | 103,376,407 | 103,378,060 | 1,654 |
ENST00000372645.3 | hg19 | chrX | 102,631,323 | 102,633,005 | 1,683 |
ENST00000372635.1 | hg19 | chrX | 102,631,335 | 102,632,988 | 1,654 |
ENST00000361298.9 | hg19 | chrX | 102,631,466 | 102,633,092 | 1,627 |
ENST00000372634.1 | hg19 | chrX | 102,631,844 | 102,632,999 | 1,156 |
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