SLC2A2 solute carrier family 2 member 2

Information
Symbol
SLC2A2
Type
protein-coding
Description
solute carrier family 2 member 2
Entrez Gene ID
6514
Genome
hg19
Position
chr3:170,714,136-170,744,509
Genome
hg38
Position
chr3:170,996,347-171,026,720
MIM
138160 OMIM
HGNC
HGNC:11006 HGNC
Ensembl
ENSG00000163581 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 64
Likely pathogenic 1 26
Benign 0 84
Likely benign 0 144
Affects 0 2
Conflicting classifications of pathogenicity 0 22
Uncertain significance 2 226
Ranking
ClinVar
0
0
104
408
14
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 GLUT2
MIM 138160 OMIM
HGNC HGNC:11006 HGNC
Ensembl ENSG00000163581 Ensembl
AllianceGenome HGNC:11006
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000314251.8 hg38 chr3 170,996,347 171,026,720 30,374
ENST00000314251.8 hg19 chr3 170,714,136 170,744,509 30,374
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