VSIG4 V-set and immunoglobulin domain containing 4

Information
Symbol
VSIG4
Type
protein-coding
Description
V-set and immunoglobulin domain containing 4
Entrez Gene ID
11326
Genome
hg19
Position
chrX:65,241,580-65,259,922
Genome
hg38
Position
chrX:66,021,738-66,040,080
MIM
300353 OMIM
HGNC
HGNC:17032 HGNC
Ensembl
ENSG00000155659 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 24
Conflicting classifications of pathogenicity 0 2
not provided 6 0
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
72
2
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 CRIg
SYNONYM Z39IG
MIM 300353 OMIM
HGNC HGNC:17032 HGNC
Ensembl ENSG00000155659 Ensembl
AllianceGenome HGNC:17032
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000412866.2 hg38 chrX 66,021,769 66,040,060 18,292
ENST00000455586.6 hg38 chrX 66,021,740 66,040,125 18,386
ENST00000374737.9 hg38 chrX 66,021,738 66,040,080 18,343
ENST00000374737.9 hg19 chrX 65,241,580 65,259,922 18,343
ENST00000455586.6 hg19 chrX 65,241,582 65,259,967 18,386
ENST00000412866.2 hg19 chrX 65,241,611 65,259,902 18,292
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