ZSCAN12 zinc finger and SCAN domain containing 12
Information
- Symbol
- ZSCAN12
- Type
- protein-coding
- Description
- zinc finger and SCAN domain containing 12
- Entrez Gene ID
- 9753
- Genome
- hg19
- Position
- chr6:28,352,515-28,367,524
- Genome
- hg38
- Position
- chr6:28,384,738-28,399,747
- MIM
- 603978 OMIM
- HGNC
- HGNC:13172 HGNC
- Ensembl
- ENSG00000158691 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 68 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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70 |
![]() |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | ZFP96 |
| SYNONYM | ZNF29K1 |
| SYNONYM | ZNF305 |
| SYNONYM | ZNF96 |
| SYNONYM | dJ29K1.2 |
| MIM | 603978 OMIM |
| HGNC | HGNC:13172 HGNC |
| Ensembl | ENSG00000158691 Ensembl |
| AllianceGenome | HGNC:13172 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000396827.3 | hg38 | chr6 | 28,379,219 | 28,399,731 | 20,513 |
| ENST00000361028.5 | hg38 | chr6 | 28,378,955 | 28,399,734 | 20,780 |
| ENST00000684592.1 | hg38 | chr6 | 28,384,738 | 28,399,747 | 15,010 |
| ENST00000361028.5 | hg19 | chr6 | 28,346,732 | 28,367,511 | 20,780 |
| ENST00000396827.3 | hg19 | chr6 | 28,346,996 | 28,367,508 | 20,513 |
| ENST00000684592.1 | hg19 | chr6 | 28,352,515 | 28,367,524 | 15,010 |
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