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Gene Symbol
IQSEC3
Assay Reference Genome
Location

Chr.12:171332 on build GRCh38
Cytoband
12p13.33
Assay ID Hs02099650_cn
Size
Availability Made To Order
Catalog # 4400291
Price 4,505.00
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Online offer:
4505.0
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Assay Details

Target Gene Details

Entrez Gene ID:

 440073

Gene Name:

 IQ motif and Sec7 domain 3

Gene Aliases:

 -

Location:

 Chr.12:66794-178460 on Build GRCh38

Assay Gene Location:

 Overlaps Exon 15 - Intron 15
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
IQSEC3 NM_001170738.1 NP_001164209.1
NM_015232.1 NP_056047.1
XM_011520958.2 XP_011519260.1
XM_011520959.2 XP_011519261.1
XM_011520960.1 XP_011519262.1
XM_011520961.1 XP_011519263.1
XM_017019310.1 XP_016874799.1
XM_017019311.1 XP_016874800.1
AB029033.1 BAA83062.1
AK091953.1

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 IQSEC3 SLC6A12 LOC574538 LOC101929384 SLC6A13
esv3628226 Chr.12:157297 - 251505 on Build GRCh38 Gain IQSEC3 SLC6A12 LOC101929384 SLC6A13
nsv556853 Chr.12:136169 - 201168 on Build GRCh38 Gain IQSEC3 SLC6A12 LOC574538
nsv556854 Chr.12:152875 - 201168 on Build GRCh38 Loss IQSEC3 SLC6A12
dgv87n21 Chr.12:151516 - 194154 on Build GRCh38 Loss IQSEC3 SLC6A12
nsv1035539 Chr.12:119253 - 224079 on Build GRCh38 Gain IQSEC3 SLC6A12 LOC574538 LOC101929384 SLC6A13
nsv556855 Chr.12:154673 - 226756 on Build GRCh38 Loss IQSEC3 SLC6A12 LOC101929384 SLC6A13
dgv1331n100 Chr.12:148770 - 207194 on Build GRCh38 Gain IQSEC3 SLC6A12 LOC574538 LOC101929384
nsv470252 Chr.12:84652 - 194154 on Build GRCh38 Gain IQSEC3 SLC6A12 LOC574538
nsv556856 Chr.12:170292 - 218255 on Build GRCh38 Loss IQSEC3 SLC6A12 LOC101929384
esv3628221 Chr.12:114421 - 232803 on Build GRCh38 Gain IQSEC3 SLC6A12 LOC574538 LOC101929384 SLC6A13
nsv568 Chr.12:145682 - 179720 on Build GRCh38 Insertion IQSEC3 LOC574538
dgv1330n100 Chr.12:45001 - 233978 on Build GRCh38 Gain IQSEC3 SLC6A12 LOC574538 LOC101929384 SLC6A13

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More Information


Additional Information:

For this assay, SNP(s) [rs76461415] 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 Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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