Product Details

Assay Reference Genome
Location

Chr.17:28404635 on build GRCh38
Cytoband
17q11.2
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

Target Gene Details

Entrez Gene ID
113235
Gene Symbol
SLC46A1
Gene Name
solute carrier family 46 member 1
Gene Aliases
G21, HCP1, PCFT
Location
Chr.17:28394642-28406630 on build GRCh38
Assay Gene Location
Overlaps Intron 3 - Exon 3
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
SLC46A1 NM_001242366.2 NP_001229295.1
NM_080669.5 NP_542400.2
XM_005277786.3 XP_005277843.1
XM_017024110.1 XP_016879599.1
AK054669.1 BAB70789.1
AK074161.1 BAB84987.1
AK097194.1 1 301
AK295883.1 2 1116
AL832613.2 CAD89945.1
BC010691.1 AAH10691.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1062056 Chr17:28376191 - 28452023 on Build GRCh38 Gain SARM1 SLC46A1
nsv1056839 Chr17:28348199 - 28428188 on Build GRCh38 Gain MIR4723 TMEM199 SARM1 SLC46A1 SEBOX POLDIP2 VTN
nsv574653 Chr17:28227749 - 28501479 on Build GRCh38 Gain MIR4723 TMEM199 LOC105371712 SLC46A1 TMEM97 LOC101926984 SEBOX IFT20 PYY2 LOC105371930 RPS7P1 SARM1 SLC13A2 POLDIP2 VTN KRT18P55 PPY2P TNFAIP1

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