ZNF799 zinc finger protein 799

Information
Symbol
ZNF799
Type
protein-coding
Description
zinc finger protein 799
Entrez Gene ID
90576
Genome
hg19
Position
chr19:12,500,830-12,512,085
Genome
hg38
Position
chr19:12,390,016-12,401,271
MIM
619916 OMIM
HGNC
HGNC:28071 HGNC
Ensembl
ENSG00000196466 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 76
Ranking
ClinVar
0
0
0
78
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 HIT-40
SYNONYM HIT40
SYNONYM ZNF842
MIM 619916 OMIM
HGNC HGNC:28071 HGNC
Ensembl ENSG00000196466 Ensembl
AllianceGenome HGNC:28071
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000419318.5 hg38 chr19 12,390,016 12,400,980 10,965
ENST00000430385.3 hg38 chr19 12,390,016 12,401,271 11,256
ENST00000595766.1 hg38 chr19 12,392,138 12,401,268 9,131
ENST00000419318.5 hg19 chr19 12,500,830 12,511,794 10,965
ENST00000430385.3 hg19 chr19 12,500,830 12,512,085 11,256
ENST00000595766.1 hg19 chr19 12,502,952 12,512,082 9,131
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