ZBTB4 zinc finger and BTB domain containing 4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 18 |
Likely benign | 0 | 18 |
Uncertain significance | 0 | 162 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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194 |
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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
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 |
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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 | KAISO-L1 |
SYNONYM | ZNF903 |
MIM | 612308 OMIM |
HGNC | HGNC:23847 HGNC |
Ensembl | ENSG00000174282 Ensembl |
AllianceGenome | HGNC:23847 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000380599.9 | hg38 | chr17 | 7,459,378 | 7,479,631 | 20,254 |
ENST00000311403.4 | hg38 | chr17 | 7,459,366 | 7,484,263 | 24,898 |
ENST00000311403.4 | hg19 | chr17 | 7,362,685 | 7,387,582 | 24,898 |
ENST00000380599.9 | hg19 | chr17 | 7,362,697 | 7,382,950 | 20,254 |
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