ZSCAN31 zinc finger and SCAN domain containing 31
Information
- Symbol
- ZSCAN31
- Type
- protein-coding
- Description
- zinc finger and SCAN domain containing 31
- Entrez Gene ID
- 64288
- Genome
- hg19
- Position
- chr6:28,292,517-28,324,048
- Genome
- hg38
- Position
- chr6:28,324,740-28,356,271
- MIM
- 610794 OMIM
- HGNC
- HGNC:14097 HGNC
- Ensembl
- ENSG00000235109 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 26 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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32 |
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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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| Category | : |
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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
|
| 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 | ZNF20-Lp |
| SYNONYM | ZNF310P |
| SYNONYM | ZNF323 |
| MIM | 610794 OMIM |
| HGNC | HGNC:14097 HGNC |
| Ensembl | ENSG00000235109 Ensembl |
| AllianceGenome | HGNC:14097 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000611469.4 | hg38 | chr6 | 28,324,740 | 28,336,375 | 11,636 |
| ENST00000446474.5 | hg38 | chr6 | 28,324,749 | 28,336,134 | 11,386 |
| ENST00000344279.11 | hg38 | chr6 | 28,324,737 | 28,336,148 | 11,412 |
| ENST00000414429.5 | hg38 | chr6 | 28,324,740 | 28,356,271 | 31,532 |
| ENST00000439158.5 | hg38 | chr6 | 28,324,737 | 28,336,134 | 11,398 |
| ENST00000396838.6 | hg38 | chr6 | 28,324,737 | 28,354,195 | 29,459 |
| ENST00000439158.5 | hg19 | chr6 | 28,292,514 | 28,303,911 | 11,398 |
| ENST00000344279.11 | hg19 | chr6 | 28,292,514 | 28,303,925 | 11,412 |
| ENST00000396838.6 | hg19 | chr6 | 28,292,514 | 28,321,972 | 29,459 |
| ENST00000414429.5 | hg19 | chr6 | 28,292,517 | 28,324,048 | 31,532 |
| ENST00000446474.5 | hg19 | chr6 | 28,292,526 | 28,303,911 | 11,386 |
| ENST00000611469.4 | hg19 | chr6 | 28,292,517 | 28,304,152 | 11,636 |
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