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 SLC6A12 CNV Assays ›
Gene Symbol
SLC6A12
Assay Reference Genome
Location

Chr.12:191047 on build GRCh38
Cytoband
12p13.33
Assay ID Hs00996375_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 6539

Gene Name:

 solute carrier family 6 member 12

Gene Aliases:

 BGT-1, BGT1, GAT2

Location:

 Chr.12:190077-214523 on Build GRCh38

Assay Gene Location:

 Within Exon 18
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SLC6A12 NM_001122847.2 16 2195 NP_001116319.1
NM_001122848.2 16 2292 NP_001116320.1
NM_001206931.1 15 2207 NP_001193860.1
NM_003044.4 17 2530 NP_003035.3
XM_005253748.4 16 2918 XP_005253805.1
XM_011521010.1 16 2436 XP_011519312.1
XM_017019841.1 16 2626 XP_016875330.1
AK096046.1 7 1032
AK125026.1 16 2610
AK131564.1 16 1808 BAD18697.1
AK313690.1
BC126215.1 15 2176
BC126217.1 15 2176
L42300.1 AAA66574.1
U27699.1 17 2452 AAA87029.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv832302 Chr.12:57392 - 234835 on Build GRCh38 Gain SLC6A13 IQSEC3 LOC101929384 LOC574538 SLC6A12
esv3628226 Chr.12:157297 - 251505 on Build GRCh38 Gain SLC6A13 IQSEC3 LOC101929384 SLC6A12
nsv556853 Chr.12:136169 - 201168 on Build GRCh38 Gain IQSEC3 LOC574538 SLC6A12
nsv556854 Chr.12:152875 - 201168 on Build GRCh38 Loss IQSEC3 SLC6A12
dgv87n21 Chr.12:151516 - 194154 on Build GRCh38 Loss IQSEC3 SLC6A12
nsv523142 Chr.12:189877 - 223694 on Build GRCh38 Gain SLC6A13 LOC101929384 SLC6A12
nsv569 Chr.12:179808 - 196558 on Build GRCh38 Deletion SLC6A12
nsv1035539 Chr.12:119253 - 224079 on Build GRCh38 Gain SLC6A13 IQSEC3 LOC101929384 LOC574538 SLC6A12
nsv556855 Chr.12:154673 - 226756 on Build GRCh38 Loss SLC6A13 IQSEC3 LOC101929384 SLC6A12
dgv1331n100 Chr.12:148770 - 207194 on Build GRCh38 Gain IQSEC3 LOC101929384 LOC574538 SLC6A12
nsv470252 Chr.12:84652 - 194154 on Build GRCh38 Gain IQSEC3 LOC574538 SLC6A12
nsv556861 Chr.12:184347 - 251448 on Build GRCh38 Loss SLC6A13 LOC101929384 SLC6A12
nsv556857 Chr.12:170292 - 268738 on Build GRCh38 Gain SLC6A13 LOC102723544 IQSEC3 LOC101929384 SLC6A12
esv3628221 Chr.12:114421 - 232803 on Build GRCh38 Gain SLC6A13 IQSEC3 LOC101929384 LOC574538 SLC6A12
dgv1330n100 Chr.12:45001 - 233978 on Build GRCh38 Gain SLC6A13 IQSEC3 LOC101929384 LOC574538 SLC6A12

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs80064579] 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 Exonic DGV Variation

Panther Classification:

Molecular Function -

primary active transporter

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products