ZSCAN9 zinc finger and SCAN domain containing 9
Information
- Symbol
- ZSCAN9
- Type
- protein-coding
- Description
- zinc finger and SCAN domain containing 9
- Entrez Gene ID
- 7746
- Genome
- hg19
- Position
- chr6:28,193,053-28,201,244
- Genome
- hg38
- Position
- chr6:28,225,275-28,233,466
- MIM
- 602246 OMIM
- HGNC
- HGNC:12984 HGNC
- Ensembl
- ENSG00000137185 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 46 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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48 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | PRD51 |
| SYNONYM | ZNF193 |
| MIM | 602246 OMIM |
| HGNC | HGNC:12984 HGNC |
| Ensembl | ENSG00000137185 Ensembl |
| AllianceGenome | HGNC:12984 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000425468.6 | hg38 | chr6 | 28,225,275 | 28,233,466 | 8,192 |
| ENST00000531981.5 | hg38 | chr6 | 28,225,264 | 28,227,958 | 2,695 |
| ENST00000527436.5 | hg38 | chr6 | 28,225,339 | 28,229,230 | 3,892 |
| ENST00000252207.10 | hg38 | chr6 | 28,225,275 | 28,233,487 | 8,213 |
| ENST00000531979.5 | hg38 | chr6 | 28,225,292 | 28,233,482 | 8,191 |
| ENST00000531981.5 | hg19 | chr6 | 28,193,042 | 28,195,736 | 2,695 |
| ENST00000425468.6 | hg19 | chr6 | 28,193,053 | 28,201,244 | 8,192 |
| ENST00000252207.10 | hg19 | chr6 | 28,193,053 | 28,201,265 | 8,213 |
| ENST00000531979.5 | hg19 | chr6 | 28,193,070 | 28,201,260 | 8,191 |
| ENST00000527436.5 | hg19 | chr6 | 28,193,117 | 28,197,008 | 3,892 |
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