ZNF302 zinc finger protein 302
Information
- Symbol
- ZNF302
- Type
- protein-coding
- Description
- zinc finger protein 302
- Entrez Gene ID
- 55900
- Genome
- hg19
- Position
- chr19:35,168,622-35,177,237
- Genome
- hg38
- Position
- chr19:34,677,717-34,686,332
- HGNC
- HGNC:13848 HGNC
- Ensembl
- ENSG00000089335 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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64 |
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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 |
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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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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | HSD16 |
SYNONYM | MST154 |
SYNONYM | MSTP154 |
SYNONYM | ZNF135L |
SYNONYM | ZNF140L |
SYNONYM | ZNF327 |
HGNC | HGNC:13848 HGNC |
Ensembl | ENSG00000089335 Ensembl |
AllianceGenome | HGNC:13848 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000505242.6 | hg38 | chr19 | 34,677,678 | 34,686,396 | 8,719 |
ENST00000457781.6 | hg38 | chr19 | 34,677,662 | 34,686,397 | 8,736 |
ENST00000446502.6 | hg38 | chr19 | 34,677,717 | 34,686,332 | 8,616 |
ENST00000423823.6 | hg38 | chr19 | 34,677,689 | 34,686,391 | 8,703 |
ENST00000613363.4 | hg38 | chr19 | 34,677,639 | 34,686,394 | 8,756 |
ENST00000507959.5 | hg38 | chr19 | 34,677,702 | 34,684,405 | 6,704 |
ENST00000509528.5 | hg38 | chr19 | 34,677,647 | 34,684,541 | 6,895 |
ENST00000505365.2 | hg38 | chr19 | 34,677,836 | 34,686,396 | 8,561 |
ENST00000613363.4 | hg19 | chr19 | 35,168,544 | 35,177,299 | 8,756 |
ENST00000509528.5 | hg19 | chr19 | 35,168,552 | 35,175,446 | 6,895 |
ENST00000457781.6 | hg19 | chr19 | 35,168,567 | 35,177,302 | 8,736 |
ENST00000505242.6 | hg19 | chr19 | 35,168,583 | 35,177,301 | 8,719 |
ENST00000423823.6 | hg19 | chr19 | 35,168,594 | 35,177,296 | 8,703 |
ENST00000507959.5 | hg19 | chr19 | 35,168,607 | 35,175,310 | 6,704 |
ENST00000446502.6 | hg19 | chr19 | 35,168,622 | 35,177,237 | 8,616 |
ENST00000505365.2 | hg19 | chr19 | 35,168,741 | 35,177,301 | 8,561 |
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