ZFX zinc finger protein X-linked
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 10 |
Benign | 0 | 4 |
Likely benign | 0 | 4 |
not provided | 6 | 0 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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10 |
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 |
Search Word
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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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 | MRXS37 |
SYNONYM | ZNF926 |
MIM | 314980 OMIM |
HGNC | HGNC:12869 HGNC |
Ensembl | ENSG00000005889 Ensembl |
AllianceGenome | HGNC:12869 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000379188.7 | hg38 | chrX | 24,149,724 | 24,216,255 | 66,532 |
ENST00000379177.5 | hg38 | chrX | 24,149,745 | 24,216,089 | 66,345 |
ENST00000338565.3 | hg38 | chrX | 24,172,715 | 24,211,986 | 39,272 |
ENST00000304543.10 | hg38 | chrX | 24,149,729 | 24,216,255 | 66,527 |
ENST00000539115.5 | hg38 | chrX | 24,149,645 | 24,216,255 | 66,611 |
ENST00000539115.5 | hg19 | chrX | 24,167,762 | 24,234,372 | 66,611 |
ENST00000379188.7 | hg19 | chrX | 24,167,841 | 24,234,372 | 66,532 |
ENST00000304543.10 | hg19 | chrX | 24,167,846 | 24,234,372 | 66,527 |
ENST00000379177.5 | hg19 | chrX | 24,167,862 | 24,234,206 | 66,345 |
ENST00000338565.3 | hg19 | chrX | 24,190,832 | 24,230,103 | 39,272 |
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