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See other GLB1L2 CNV Assays ›
Gene Symbol
GLB1L2
Assay Reference Genome
Location

Chr.11:134364376 on build GRCh38
Cytoband
11q25
Assay ID Hs01911591_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 89944

Gene Name:

 galactosidase beta 1 like 2

Gene Aliases:

 MST114, MSTP114

Location:

 Chr.11:134331874-134376324 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 7 - Intron 8
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
GLB1L2 NM_138342.3 NP_612351.2
XM_006718937.1 XP_006719000.1
AF173889.1 AAQ13636.1
AK074703.1 BAC11149.1
AK074855.1 BAC11247.1
AK074947.1 BAC11309.1
AY358497.1 AAQ88861.1
BC008326.1 AAH08326.1
BC040641.1 AAH40641.1
BX640934.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv4e196 Chr.11:134304439 - 134744665 on Build GRCh38 Duplication GLB1L3 LOC283177 GLB1L2 B3GAT1
dgv1305n100 Chr.11:134363845 - 134416469 on Build GRCh38 Gain GLB1L2 B3GAT1
nsv556608 Chr.11:134348406 - 134876236 on Build GRCh38 Gain LOC283177 GLB1L2 B3GAT1
nsv521581 Chr.11:134126584 - 134772738 on Build GRCh38 Gain JAM3 ACAD8 GLB1L3 VPS26B LOC283177 THYN1 NCAPD3 GLB1L2 B3GAT1
nsv1053071 Chr.11:134355691 - 134379382 on Build GRCh38 Loss GLB1L2 B3GAT1
esv3628169 Chr.11:134353064 - 134485281 on Build GRCh38 Gain LOC283177 GLB1L2 B3GAT1
dgv1304n100 Chr.11:134322594 - 134754120 on Build GRCh38 Gain LOC283177 GLB1L2 B3GAT1
nsv561 Chr.11:134353547 - 134380498 on Build GRCh38 Insertion GLB1L2 B3GAT1
esv2760555 Chr.11:134282136 - 134860776 on Build GRCh38 Gain+Loss GLB1L3 LOC283177 GLB1L2 B3GAT1
esv3628170 Chr.11:134357170 - 134435562 on Build GRCh38 Gain GLB1L2 B3GAT1
nsv521623 Chr.11:134307381 - 134756993 on Build GRCh38 Gain GLB1L3 LOC283177 GLB1L2 B3GAT1

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More Information


Additional Information:

For this assay, SNP(s) [rs114723326] 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 Intronic Non-exonic DGV Variation

Panther Classification:

Molecular Function -

galactosidase

Gene Ontology Categories:

Function(s) Process(es)


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