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See other PEX11G CNV Assays ›
Gene Symbol
PEX11G
Assay Reference Genome
Location

Chr.19:7480325 on build GRCh38
Cytoband
Assay ID Hs04008514_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 92960

Gene Name:

 peroxisomal biogenesis factor 11 gamma

Gene Aliases:

 PEX11gamma

Location:

 Chr.19:7476875-7494977 on Build GRCh38

Assay Gene Location:

 Within Intron 8
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PEX11G NM_001270539.2 NP_001257468.1
NM_001300881.2 NP_001287810.1
NM_080662.4 NP_542393.1
XM_005272506.3 XP_005272563.1
XM_011528426.3 XP_011526728.1
XM_011528427.3 XP_011526729.1
XM_011528428.1 XP_011526730.1
XM_011528429.3 XP_011526731.1
XM_011528431.3 XP_011526733.1
XM_011528432.2 XP_011526734.1
AB095921.1 BAD01558.1
AL833945.1 CAD38800.1
BC008780.2 AAH08780.1
BI833221.1
HY002496.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2025-12-01, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1060887 Chr.19:7089546 - 7861087 on Build GRCh38 Gain CLEC4G FCER2 CAMSAP3 MCEMP1 TRAPPC5 CLEC4GP1 ZNF358 SAXO5 PEX11G XAB2 ARHGEF18-AS1 ARHGEF18 PCP2 INSR MIR6792 MCOLN1 STXBP2 CD209 EVI5L PET100 CLEC4M PNPLA6 RETN
nsv509719 Chr.19:7390693 - 7484911 on Build GRCh38 Insertion PEX11G ARHGEF18-AS1 ARHGEF18
esv2751809 Chr.19:6896369 - 7816144 on Build GRCh38 Gain MARK2P21 MBD3L3 SAXO5 PEX11G ARHGEF18-AS1 PCP2 ADGRE1 INSR MIR6792 MCOLN1 STXBP2 CD209 PET100 RETN MBD3L2B CLEC4G MBD3L5 ZNF557 FCER2 CAMSAP3 MCEMP1 TRAPPC5 ADGRE4P CLEC4GP1 ZNF358 XAB2 ARHGEF18 MBD3L4 MBD3L2 CLEC4M PNPLA6
nsv4261533 Chr.19:7476696 - 7481020 on Build GRCh38 Deletion PEX11G ARHGEF18

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More Information


Additional Information:

For this assay, SNP(s) [rs111618462,rs73488445] 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

Gene Ontology Categories:

Function(s) Process(es)


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