ZNF567-DT ZNF567 divergent transcript

Information
Symbol
ZNF567-DT
Type
ncRNA
Description
ZNF567 divergent transcript
Entrez Gene ID
101927621
Genome
hg19
Position
chr19:37,173,538-37,178,370
Genome
hg38
Position
chr19:36,682,636-36,687,468
HGNC
HGNC:51281 HGNC
Ensembl
ENSG00000225975 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
TypeID
SYNONYM LINC01534
HGNC HGNC:51281 HGNC
Ensembl ENSG00000225975 Ensembl
AllianceGenome HGNC:51281
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000665321.2 hg38 chr19 36,682,636 36,687,468 4,833
ENST00000433232.5 hg38 chr19 36,685,440 36,687,449 2,010
ENST00000590952.2 hg38 chr19 36,685,717 36,687,437 1,721
ENST00000665321.2 hg19 chr19 37,173,538 37,178,370 4,833
ENST00000433232.5 hg19 chr19 37,176,342 37,178,351 2,010
ENST00000590952.2 hg19 chr19 37,176,619 37,178,339 1,721
Genome browser