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See other SLC38A10 CNV Assays ›
Gene Symbol
SLC38A10
Assay Reference Genome
Location

Chr.17:81245050 on build GRCh38
Cytoband
17q25.3
Assay ID Hs01504581_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 124565

Gene Name:

 solute carrier family 38 member 10

Gene Aliases:

 PP1744

Location:

 Chr.17:81244811-81295433 on Build GRCh38

Assay Gene Location:

 Within Exon 17
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SLC38A10 NM_001037984.2 16 4284 NP_001033073.1
XM_005257019.1 17 4402 XP_005257076.1
XM_011524288.1 17 4423 XP_011522590.1
XM_011524289.1 16 4399 XP_011522591.1
XM_011524290.1 15 3678 XP_011522592.1
AF086389.1 1 386
AI476273.1 1 63
BM129331.1 1 242
CA447446.1 1 257

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv828128 Chr.17:80659041 - 81736487 on Build GRCh38 Loss MIR4740 LOC400627 TSPAN10 MIR657 ACTG1 CCDC137 FAAP100 PDE6G BAHCC1 SLC25A10 AATK-AS1 TMEM105 LOC105371925 LOC100129503 FSCN2 MIR6786 MRPL12 RPTOR CEP131 LOC107985021 ARL16 OXLD1 BAIAP2-AS1 TEPSIN MIR1250 LOC107985022 NPLOC4 MIR3186 HGS LINC00482 LOC105371921 CHMP6 AATK LOC100130370 BAIAP2 LOC101928855 MIR338 SLC38A10 C17orf89 MIR3065
nsv2161 Chr.17:81238081 - 81282084 on Build GRCh38 Insertion SLC38A10 TEPSIN C17orf89
esv2758707 Chr.17:81152631 - 81345362 on Build GRCh38 Gain AATK-AS1 CEP131 LINC00482 TMEM105 AATK SLC38A10 TEPSIN LOC105371925 C17orf89
esv3893051 Chr.17:81244320 - 81272804 on Build GRCh38 Gain SLC38A10
dgv46n68 Chr.17:81133921 - 81288932 on Build GRCh38 Loss AATK-AS1 CEP131 AATK SLC38A10 TEPSIN LOC105371925 C17orf89
nsv576172 Chr.17:81216762 - 81282974 on Build GRCh38 Loss CEP131 SLC38A10 TEPSIN LOC105371925 C17orf89
nsv470619 Chr.17:81032233 - 81349843 on Build GRCh38 Loss CEP131 BAIAP2-AS1 MIR657 TEPSIN MIR1250 AATK-AS1 LINC00482 TMEM105 AATK BAIAP2 MIR338 SLC38A10 LOC105371925 C17orf89 MIR3065
nsv952389 Chr.17:81137501 - 81593774 on Build GRCh38 Deletion FSCN2 MIR4740 CEP131 ACTG1 TEPSIN FAAP100 BAHCC1 NPLOC4 MIR3186 AATK-AS1 LINC00482 TMEM105 AATK LOC100130370 SLC38A10 LOC105371925 C17orf89
nsv1064123 Chr.17:81168449 - 81282457 on Build GRCh38 Gain AATK-AS1 CEP131 SLC38A10 TEPSIN LOC105371925 C17orf89
nsv1160499 Chr.17:81235307 - 81320655 on Build GRCh38 Deletion LINC00482 TMEM105 SLC38A10 TEPSIN C17orf89
nsv509677 Chr.17:81227139 - 81267309 on Build GRCh38 Insertion SLC38A10 TEPSIN LOC105371925 C17orf89

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

Panther Classification:

Molecular Function -

amino acid transporter

Gene Ontology Categories:

Function(s) Process(es)


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