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See other LOC101928834 CNV Assays ›
Gene Symbol
LOC101928834
Assay Reference Genome
Location

Chr.10:19724495 on build GRCh38
Cytoband
10p12.31
Assay ID Hs03284352_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 101928834

Gene Name:

 uncharacterized LOC101928834

Gene Aliases:

 -

Location:

 Chr.10:19710335-19728550 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LOC101928834 NR_120646.1

Target Gene Details

Entrez Gene ID:

 340895

Gene Name:

 MAM and LDL receptor class A domain containing 1

Gene Aliases:

 C10orf112, DIET1, bA265G8.2

Location:

 Chr.10:19046931-19734478 on Build GRCh38

Assay Gene Location:

 Within Intron 44
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
MALRD1 NM_001142308.2 NP_001135780.2
XM_011519453.2 XP_011517755.1
XM_011519454.1 XP_011517756.1
XM_011519455.2 XP_011517757.1
XM_017016182.1 XP_016871671.1
XM_017016184.1 XP_016871673.1
XM_017016185.1 XP_016871674.1
XM_017016186.1 XP_016871675.1
AK297683.1
KC843478.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1039685 Chr.10:19646166 - 19750692 on Build GRCh38 Gain MALRD1 LOC101928834
nsv1049295 Chr.10:19451367 - 20220107 on Build GRCh38 Loss PLXDC2 MALRD1 LOC101928834
nsv1046998 Chr.10:19684167 - 19742539 on Build GRCh38 Loss MALRD1 LOC101928834
nsv831804 Chr.10:19570471 - 19746664 on Build GRCh38 Gain MALRD1 LOC101928834
esv3622540 Chr.10:19536634 - 19746769 on Build GRCh38 Loss MALRD1 LOC101928834
esv2759737 Chr.10:19405215 - 19736065 on Build GRCh38 Loss MALRD1 LOC101928834
nsv825266 Chr.10:19518090 - 19748253 on Build GRCh38 Loss MALRD1 LOC101928834
nsv523490 Chr.10:19686001 - 19752217 on Build GRCh38 Loss MALRD1 LOC101928834
esv34306 Chr.10:19488140 - 19829015 on Build GRCh38 Loss PLXDC2 MALRD1 LOC101928834

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More Information


Additional Information:

For this assay, SNP(s) [rs71497288] 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)


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