ZBTB42 zinc finger and BTB domain containing 42
Information
- Symbol
- ZBTB42
- Type
- protein-coding
- Description
- zinc finger and BTB domain containing 42
- Entrez Gene ID
- 100128927
- Genome
- hg19
- Position
- chr14:105,267,438-105,271,049
- Genome
- hg38
- Position
- chr14:104,801,101-104,804,712
- MIM
- 613915 OMIM
- HGNC
- HGNC:32550 HGNC
- Ensembl
- ENSG00000179627 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 16 |
| Likely benign | 0 | 10 |
| Uncertain significance | 0 | 60 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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8 |
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78 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | LCCS6 |
| SYNONYM | ZNF925 |
| MIM | 613915 OMIM |
| HGNC | HGNC:32550 HGNC |
| Ensembl | ENSG00000179627 Ensembl |
| AllianceGenome | HGNC:32550 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000555360.1 | hg38 | chr14 | 104,800,596 | 104,802,486 | 1,891 |
| ENST00000342537.8 | hg38 | chr14 | 104,801,101 | 104,804,712 | 3,612 |
| ENST00000555360.1 | hg19 | chr14 | 105,266,933 | 105,268,823 | 1,891 |
| ENST00000342537.8 | hg19 | chr14 | 105,267,438 | 105,271,049 | 3,612 |
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