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See other DMBT1 CNV Assays ›
Gene Symbol
DMBT1
Assay Reference Genome
Location

Chr.10:122641444 on build GRCh38
Cytoband
10q26.13
Assay ID Hs03757892_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 1755

Gene Name:

 deleted in malignant brain tumors 1

Gene Aliases:

 GP340, SAG, muclin

Location:

 Chr.10:122560665-122643736 on Build GRCh38

Assay Gene Location:

 Within Intron 56
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
DMBT1 NM_001320644.1 NP_001307573.1
NM_004406.2 NP_004397.2
NM_007329.2 NP_015568.2
NM_017579.2 NP_060049.2
XM_006717660.3 XP_006717723.1
XM_006717665.3 XP_006717728.1
XM_011539388.2 XP_011537690.1
XM_011539389.2 XP_011537691.1
XM_011539390.2 XP_011537692.1
XM_011539391.2 XP_011537693.1
XM_011539392.2 XP_011537694.1
XM_011539393.2 XP_011537695.1
XM_011539394.2 XP_011537696.1
XM_011539395.2 XP_011537697.1
XM_011539396.2 XP_011537698.1
XM_011539398.2 XP_011537700.1
XM_011539399.2 XP_011537701.1
XM_011539400.2 XP_011537702.1
XM_011539401.2 XP_011537703.1
XM_011539402.2 XP_011537704.1
XM_011539403.2 XP_011537705.1
XM_011539405.2 XP_011537707.1
XM_011539407.2 XP_011537709.1
XM_011539408.2 XP_011537710.1
XM_011539409.2 XP_011537711.1
XM_011539410.2 XP_011537712.1
XM_011539411.2 XP_011537713.1
XM_011539413.2 XP_011537715.1
XM_011539414.2 XP_011537716.1
XM_011539415.2 XP_011537717.1
XM_017015798.1 XP_016871287.1
AF159456.1 AAD49696.1
AJ000342.1 CAA04019.1
AJ243212.1 CAB56155.1
AJ243224.1 CAB63942.1
AJ297935.1 CAC44122.1
AK304149.1
BC153299.1
BX640988.1 CAE45995.1
FJ234410.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv428240 Chr.10:122503559 - 122695299 on Build GRCh38 Gain+Loss HTRA1 DMBT1

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More Information


Additional Information:

For this assay, SNP(s) [rs75964629] 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:

Gene Ontology Categories:

Function(s) Process(es)


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