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 :
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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
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
TypeID
HGNC HGNC:28696 HGNC
Ensembl ENSG00000189042 Ensembl
AllianceGenome HGNC:28696
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
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
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