UNG uracil DNA glycosylase

Information
Symbol
UNG
Type
protein-coding
Description
uracil DNA glycosylase
Entrez Gene ID
7374
Genome
hg19
Position
chr12:109,535,402-109,548,797
Genome
hg38
Position
chr12:109,097,597-109,110,992
MIM
191525 OMIM
HGNC
HGNC:12572 HGNC
Ensembl
ENSG00000076248 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 22
Likely pathogenic 0 8
Benign 0 44
Likely benign 0 190
Conflicting classifications of pathogenicity 0 20
Uncertain significance 0 250
Ranking
ClinVar
0
0
58
450
4
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 DGU
SYNONYM HIGM4
SYNONYM HIGM5
SYNONYM UDG
SYNONYM UNG1
SYNONYM UNG15
SYNONYM UNG2
MIM 191525 OMIM
HGNC HGNC:12572 HGNC
Ensembl ENSG00000076248 Ensembl
AllianceGenome HGNC:12572
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000699561.1 hg38 chr12 109,098,172 109,105,501 7,330
ENST00000699562.1 hg38 chr12 109,098,172 109,110,961 12,790
ENST00000699563.1 hg38 chr12 109,098,172 109,126,725 28,554
ENST00000699560.1 hg38 chr12 109,098,161 109,110,956 12,796
ENST00000242576.7 hg38 chr12 109,097,597 109,110,992 13,396
ENST00000336865.6 hg38 chr12 109,098,118 109,110,975 12,858
ENST00000242576.7 hg19 chr12 109,535,402 109,548,797 13,396
ENST00000336865.6 hg19 chr12 109,535,923 109,548,780 12,858
ENST00000699560.1 hg19 chr12 109,535,966 109,548,761 12,796
ENST00000699561.1 hg19 chr12 109,535,977 109,543,306 7,330
ENST00000699562.1 hg19 chr12 109,535,977 109,548,766 12,790
ENST00000699563.1 hg19 chr12 109,535,977 109,564,530 28,554
Genome browser