INSIG2 insulin induced gene 2

Information
Symbol
INSIG2
Type
protein-coding
Description
insulin induced gene 2
Entrez Gene ID
51141
Genome
hg19
Position
chr2:118,846,047-118,868,573
Genome
hg38
Position
chr2:118,088,471-118,110,997
MIM
608660 OMIM
HGNC
HGNC:20452 HGNC
Ensembl
ENSG00000125629 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
not provided 1 0
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
18
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
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 INSIG-2
MIM 608660 OMIM
HGNC HGNC:20452 HGNC
Ensembl ENSG00000125629 Ensembl
AllianceGenome HGNC:20452
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000245787.9 hg38 chr2 118,088,471 118,110,997 22,527
ENST00000245787.9 hg19 chr2 118,846,047 118,868,573 22,527
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