SLC2A4 solute carrier family 2 member 4

Information
Symbol
SLC2A4
Type
protein-coding
Description
solute carrier family 2 member 4
Entrez Gene ID
6517
Genome
hg19
Position
chr17:7,185,037-7,191,576
Genome
hg38
Position
chr17:7,281,718-7,288,257
MIM
138190 OMIM
HGNC
HGNC:11009 HGNC
Ensembl
ENSG00000181856 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 10
not provided 2 0
Uncertain significance 0 42
Ranking
ClinVar
0
0
0
54
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 GLUT4
MIM 138190 OMIM
HGNC HGNC:11009 HGNC
Ensembl ENSG00000181856 Ensembl
AllianceGenome HGNC:11009
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000424875.2 hg38 chr17 7,282,130 7,286,167 4,038
ENST00000571308.5 hg38 chr17 7,281,736 7,286,151 4,416
ENST00000317370.13 hg38 chr17 7,281,718 7,288,257 6,540
ENST00000317370.13 hg19 chr17 7,185,037 7,191,576 6,540
ENST00000571308.5 hg19 chr17 7,185,055 7,189,470 4,416
ENST00000424875.2 hg19 chr17 7,185,449 7,189,486 4,038
Genome browser