KRBOX4 KRAB box domain containing 4
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| not provided | 6 | 2 |
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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16 |
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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 | ZNF673 |
| MIM | 300585 OMIM |
| HGNC | HGNC:26007 HGNC |
| Ensembl | ENSG00000147121 Ensembl |
| AllianceGenome | HGNC:26007 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000298190.10 | hg38 | chrX | 46,447,292 | 46,473,669 | 26,378 |
| ENST00000377919.6 | hg38 | chrX | 46,447,294 | 46,472,526 | 25,233 |
| ENST00000487081.1 | hg38 | chrX | 46,448,233 | 46,473,594 | 25,362 |
| ENST00000344302.9 | hg38 | chrX | 46,447,297 | 46,474,639 | 27,343 |
| ENST00000478600.5 | hg38 | chrX | 46,447,297 | 46,497,422 | 50,126 |
| ENST00000298190.10 | hg19 | chrX | 46,306,727 | 46,333,104 | 26,378 |
| ENST00000377919.6 | hg19 | chrX | 46,306,729 | 46,331,961 | 25,233 |
| ENST00000344302.9 | hg19 | chrX | 46,306,732 | 46,334,074 | 27,343 |
| ENST00000478600.5 | hg19 | chrX | 46,306,732 | 46,356,857 | 50,126 |
| ENST00000487081.1 | hg19 | chrX | 46,307,668 | 46,333,029 | 25,362 |
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