ISG15 ISG15 ubiquitin like modifier

Information
Symbol
ISG15
Type
protein-coding
Description
ISG15 ubiquitin like modifier
Entrez Gene ID
9636
Genome
hg19
Position
chr1:948,877-949,920
Genome
hg38
Position
chr1:1,013,497-1,014,540
MIM
147571 OMIM
HGNC
HGNC:4053 HGNC
Ensembl
ENSG00000187608 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 4
Benign 0 26
Likely benign 0 98
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 124
Ranking
ClinVar
0
0
52
198
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 G1P2
SYNONYM IFI15
SYNONYM IMD38
SYNONYM IP17
SYNONYM UCRP
SYNONYM hUCRP
MIM 147571 OMIM
HGNC HGNC:4053 HGNC
Ensembl ENSG00000187608 Ensembl
AllianceGenome HGNC:4053
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000624697.4 hg38 chr1 1,001,138 1,014,540 13,403
ENST00000649529.1 hg38 chr1 1,013,497 1,014,540 1,044
ENST00000624697.4 hg19 chr1 936,518 949,920 13,403
ENST00000649529.1 hg19 chr1 948,877 949,920 1,044
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