ZNF567 zinc finger protein 567
Information
- Symbol
- ZNF567
- Type
- protein-coding
- Description
- zinc finger protein 567
- Entrez Gene ID
- 163081
- Genome
- hg19
- Position
- chr19:37,178,530-37,212,229
- Genome
- hg38
- Position
- chr19:36,687,628-36,721,327
- HGNC
- HGNC:28696 HGNC
- Ensembl
- ENSG00000189042 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
32 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
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 | : |
|
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 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000585696.5 | hg38 | chr19 | 36,711,240 | 36,721,321 | 10,082 |
ENST00000682579.1 | hg38 | chr19 | 36,687,612 | 36,721,336 | 33,725 |
ENST00000360729.8 | hg38 | chr19 | 36,689,400 | 36,721,326 | 31,927 |
ENST00000536254.6 | hg38 | chr19 | 36,687,628 | 36,721,327 | 33,700 |
ENST00000588311.5 | hg38 | chr19 | 36,703,681 | 36,723,346 | 19,666 |
ENST00000682579.1 | hg19 | chr19 | 37,178,514 | 37,212,238 | 33,725 |
ENST00000536254.6 | hg19 | chr19 | 37,178,530 | 37,212,229 | 33,700 |
ENST00000360729.8 | hg19 | chr19 | 37,180,302 | 37,212,228 | 31,927 |
ENST00000588311.5 | hg19 | chr19 | 37,194,583 | 37,214,248 | 19,666 |
ENST00000585696.5 | hg19 | chr19 | 37,202,142 | 37,212,223 | 10,082 |
Genome browser