IVL involucrin

Information
Symbol
IVL
Type
protein-coding
Description
involucrin
Entrez Gene ID
3713
Genome
hg19
Position
chr1:152,881,022-152,884,362
Genome
hg38
Position
chr1:152,908,546-152,911,886
MIM
147360 OMIM
HGNC
HGNC:6187 HGNC
Ensembl
ENSG00000163207 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 18
Likely benign 0 28
Uncertain significance 0 94
Ranking
ClinVar
0
0
4
136
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
MIM 147360 OMIM
HGNC HGNC:6187 HGNC
Ensembl ENSG00000163207 Ensembl
AllianceGenome HGNC:6187
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000368764.4 hg38 chr1 152,908,546 152,911,886 3,341
ENST00000368764.4 hg19 chr1 152,881,022 152,884,362 3,341
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