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

Chr.2:110732723 on build GRCh38
Cytoband
2q13
Assay ID Hs04706093_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 55289

Gene Name:

 acyl-CoA oxidase-like

Gene Aliases:

 -

Location:

 Chr.2:110732539-111118571 on Build GRCh38

Assay Gene Location:

 Overlaps Exon 1 - Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ACOXL NM_001142807.1 NP_001136279.1
XM_011511404.2 XP_011509706.1
XM_011511409.1 XP_011509711.1
XM_011511411.2 XP_011509713.1
XM_011511413.1 XP_011509715.1
XM_011511414.2 XP_011509716.1
XM_011511415.2 XP_011509717.1
XM_011511416.2 XP_011509718.1
XM_011511419.2 XP_011509721.1
XM_011511420.2 XP_011509722.1
XM_011511421.2 XP_011509723.1
XM_011511422.1 XP_011509724.1
XM_011511423.1 XP_011509725.1
XM_011511427.2 XP_011509729.1
XM_011511428.2 XP_011509730.1
XM_011511429.2 XP_011509731.1
XM_011511432.2 XP_011509734.1
XM_017004431.1 XP_016859920.1
XM_017004432.1 XP_016859921.1
AK300513.1
BC022268.1 AAH22268.1
CX788840.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv730e214 Chr.2:110395308 - 110848620 on Build GRCh38 Gain LIMS4 LOC100288570 RGPD6 LOC105373553 BUB1 ACOXL SNORD132
nsv521956 Chr.2:110634682 - 112341235 on Build GRCh38 Loss FBLN7 MIR4435-2 ZC3H8 LOC400997 BCL2L11 BUB1 ACOXL SNORD132 ZC3H6 PAFAH1B1P2 TMEM87B MIR4771-2 ANAPC1 MIR4435-2HG MERTK
esv3591965 Chr.2:110642083 - 110829253 on Build GRCh38 Gain BUB1 ACOXL SNORD132
dgv4047n100 Chr.2:110308696 - 112358403 on Build GRCh38 Loss FBLN7 LOC105375809 MIR4435-2 LOC100288570 ZC3H8 LOC105373553 LOC400997 BCL2L11 BUB1 ACOXL SNORD132 ZC3H6 LIMS4 RGPD6 PAFAH1B1P2 TMEM87B MIR4771-2 ANAPC1 MIR4435-2HG LINC01106 MERTK

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More Information


Additional Information:

For this assay, SNP(s) [rs79918262] 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:

Molecular Function -

oxidoreductase

Gene Ontology Categories:

Function(s) Process(es)


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