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Gene Symbol
SLC2A4
Assay Reference Genome
Location

Chr.17:7283628 on build GRCh38
Cytoband
17p13.1
Assay ID Hs00689963_cn
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 6517

Gene Name:

 solute carrier family 2 member 4

Gene Aliases:

 GLUT4

Location:

 Chr.17:7281735-7288048 on Build GRCh38

Assay Gene Location:

 Overlaps Exon 3 - Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SLC2A4 NM_001042.2 NP_001033.1
AK300899.1
AK313372.1
AL521328.3
BC034387.1
BC069615.1 AAH69615.1
BC069621.1 AAH69621.1
BC113592.1
BC126164.1
M20747.1 AAA59189.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv2422288 Chr.17:6789933 - 7646709 on Build GRCh38 Deletion SNORD10 C17orf74 TMEM102 DLG4 TMEM256 TEKT1 SPEM1 CD68 MIR497HG SLC16A11 SNORA67 RNASEK-C17orf49 FGF11 TNFSF12-TNFSF13 LOC100996842 PLSCR3 ALOX12P2 EIF4A1 SLC35G6 CTDNEP1 ASGR2 LOC107983988 C17orf49 SLC16A13 ALOX12-AS1 GPS2 KCTD11 SHBG ELP5 MPDU1 DVL2 NEURL4 FBXO39 ACADVL TMEM256-PLSCR3 FXR2 CLEC10A SNORA48 ALOX12 ATP1B2 ZBTB4 SENP3-EIF4A1 ASGR1 TMEM95 TNK1 SAT2 BCL6B POLR2A MIR324 SENP3 SLC2A4 RNASEK ACAP1 GABARAP TNFSF13 SOX15 NLGN2 EIF5A CHRNB1 YBX2 MIR195 MIR497 PHF23 TNFSF12 CLDN7
nsv952118 Chr.17:7174582 - 7456981 on Build GRCh38 Deletion DVL2 C17orf74 NEURL4 TMEM102 DLG4 TMEM256 ACADVL TMEM256-PLSCR3 SPEM1 ASGR1 TMEM95 TNK1 FGF11 MIR324 PLSCR3 SLC2A4 ACAP1 CTDNEP1 GABARAP NLGN2 LOC107983988 EIF5A CHRNB1 YBX2 GPS2 KCTD11 PHF23 CLDN7 ELP5
esv2665200 Chr.17:7091816 - 7333062 on Build GRCh38 Deletion MIR324 DVL2 NEURL4 SLC2A4 DLG4 ACADVL CTDNEP1 GABARAP ASGR2 EIF5A YBX2 ASGR1 GPS2 PHF23 CLDN7 ELP5
nsv574322 Chr.17:7010333 - 7689462 on Build GRCh38 Loss SNORD10 C17orf74 TMEM102 DLG4 TMEM256 SPEM1 CD68 MIR497HG SLC16A11 SNORA67 RNASEK-C17orf49 FGF11 TNFSF12-TNFSF13 LOC100996842 PLSCR3 EIF4A1 SLC35G6 CTDNEP1 ASGR2 LOC107983988 C17orf49 SLC16A13 ALOX12-AS1 GPS2 KCTD11 SHBG ELP5 MPDU1 DVL2 NEURL4 ACADVL TMEM256-PLSCR3 FXR2 CLEC10A SNORA48 ALOX12 ATP1B2 TP53 ZBTB4 SENP3-EIF4A1 ASGR1 TMEM95 TNK1 SAT2 BCL6B POLR2A MIR324 SENP3 SLC2A4 RNASEK ACAP1 GABARAP TNFSF13 SOX15 NLGN2 WRAP53 EIF5A CHRNB1 YBX2 MIR195 MIR497 PHF23 TNFSF12 CLDN7
nsv1963 Chr.17:7244585 - 7333855 on Build GRCh38 Deletion EIF5A NEURL4 SLC2A4 YBX2 CTDNEP1 GPS2 CLDN7 ELP5
esv3639863 Chr.17:7280422 - 7290803 on Build GRCh38 Loss SLC2A4 YBX2

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More Information


Additional Information:

For this assay, SNP(s) [rs77409522] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Set Membership:

 Intragenic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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