accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

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

Chr.17:81246027 on build GRCh38
Cytoband
17q25.3
Assay ID Hs01741275_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

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 3307 NP_001033073.1
XM_005257019.1 17 3425 XP_005257076.1
XM_011524288.1 17 3446 XP_011522590.1
XM_011524289.1 16 3422 XP_011522591.1
XM_011524290.1 15 2701 XP_011522592.1
BI194553.1 1 68
BU552914.1 1 644

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

Back To Top

More Information


Set Membership:

 Intragenic Exonic DGV Variation

Panther Classification:

Molecular Function -

amino acid transporter

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products