ZXDB zinc finger X-linked duplicated B
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 20 |
Conflicting classifications of pathogenicity | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 100 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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120 |
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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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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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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 | ZNF905 |
SYNONYM | dJ83L6.1 |
MIM | 300236 OMIM |
HGNC | HGNC:13199 HGNC |
Ensembl | ENSG00000198455 Ensembl |
AllianceGenome | HGNC:13199 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000374888.3 | hg38 | chrX | 57,592,011 | 57,597,477 | 5,467 |
ENST00000374888.3 | hg19 | chrX | 57,618,444 | 57,623,910 | 5,467 |
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