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

Chr.17:81245363 on build GRCh38
Cytoband
17q25.3
Assay ID Hs01941947_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 3971 NP_001033073.1
XM_005257019.1 17 4089 XP_005257076.1
XM_011524288.1 17 4110 XP_011522590.1
XM_011524289.1 16 4086 XP_011522591.1
XM_011524290.1 15 3365 XP_011522592.1
AF086389.1 1 73
AI476273.1
BI194553.1 1 732
BM129331.1
CA447446.1

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 SLC25A10 CCDC137 MIR657 ACTG1 HGS AATK-AS1 AATK MIR6786 TEPSIN LOC100129503 C17orf89 MIR4740 PDE6G MIR1250 CEP131 TSPAN10 MIR338 CHMP6 LOC101928855 LOC105371925 LINC00482 BAIAP2 RPTOR MIR3186 LOC107985022 NPLOC4 OXLD1 FAAP100 BAIAP2-AS1 LOC100130370 TMEM105 LOC107985021 MIR3065 BAHCC1 LOC400627 LOC105371921 SLC38A10 MRPL12 ARL16 FSCN2
nsv2161 Chr.17:81238081 - 81282084 on Build GRCh38 Insertion SLC38A10 TEPSIN C17orf89
esv2758707 Chr.17:81152631 - 81345362 on Build GRCh38 Gain AATK-AS1 AATK CEP131 SLC38A10 TEPSIN TMEM105 LOC105371925 C17orf89 LINC00482
esv3893051 Chr.17:81244320 - 81272804 on Build GRCh38 Gain SLC38A10
dgv46n68 Chr.17:81133921 - 81288932 on Build GRCh38 Loss AATK-AS1 AATK CEP131 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 BAIAP2 MIR657 AATK-AS1 AATK BAIAP2-AS1 TEPSIN TMEM105 C17orf89 MIR1250 MIR3065 CEP131 MIR338 SLC38A10 LOC105371925 LINC00482
nsv952389 Chr.17:81137501 - 81593774 on Build GRCh38 Deletion ACTG1 AATK-AS1 MIR3186 NPLOC4 AATK FAAP100 LOC100130370 TEPSIN TMEM105 C17orf89 MIR4740 BAHCC1 CEP131 SLC38A10 FSCN2 LOC105371925 LINC00482
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 SLC38A10 TEPSIN TMEM105 C17orf89 LINC00482
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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