INSIG1 insulin induced gene 1

Information
Symbol
INSIG1
Type
protein-coding
Description
insulin induced gene 1
Entrez Gene ID
3638
Genome
hg19
Position
chr7:155,089,588-155,101,945
Genome
hg38
Position
chr7:155,297,878-155,310,235
MIM
602055 OMIM
HGNC
HGNC:6083 HGNC
Ensembl
ENSG00000186480 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
not provided 1 0
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
30
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 CL6
MIM 602055 OMIM
HGNC HGNC:6083 HGNC
Ensembl ENSG00000186480 Ensembl
AllianceGenome HGNC:6083
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000340368.9 hg38 chr7 155,297,878 155,310,235 12,358
ENST00000344756.8 hg38 chr7 155,297,776 155,310,233 12,458
ENST00000342407.5 hg38 chr7 155,297,889 155,308,757 10,869
ENST00000344756.8 hg19 chr7 155,089,486 155,101,943 12,458
ENST00000340368.9 hg19 chr7 155,089,588 155,101,945 12,358
ENST00000342407.5 hg19 chr7 155,089,599 155,100,467 10,869
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