ZNF442 zinc finger protein 442
Information
- Symbol
- ZNF442
- Type
- protein-coding
- Description
- zinc finger protein 442
- Entrez Gene ID
- 79973
- Genome
- hg19
- Position
- chr19:12,460,185-12,476,447
- Genome
- hg38
- Position
- chr19:12,345,944-12,365,683
- HGNC
- HGNC:20877 HGNC
- Ensembl
- ENSG00000198342 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 84 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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90 |
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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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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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000438182.5 | hg38 | chr19 | 12,349,583 | 12,365,641 | 16,059 |
ENST00000242804.9 | hg38 | chr19 | 12,345,944 | 12,365,683 | 19,740 |
ENST00000545749.2 | hg38 | chr19 | 12,349,701 | 12,363,631 | 13,931 |
ENST00000242804.4 | hg19 | chr19 | 12,460,185 | 12,476,447 | 16,263 |
ENST00000438182.1 | hg19 | chr19 | 12,460,397 | 12,476,455 | 16,059 |
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