Product Details

Assay Reference Genome
Location

Chr.11:131394134 on build GRCh38
Cytoband
11q25
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs116478757] 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.

Target Gene Details

Entrez Gene ID
50863
Gene Symbol
NTM
Gene Name
neurotrimin
Gene Aliases
HNT, IGLON2, NTRI
Location
Chr.11:131370326-132336822 on build GRCh38
Assay Gene Location
Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
NTM NM_001048209.1 NP_001041674.1
XM_005271580.3 XP_005271637.1
XM_005271582.3 XP_005271639.1
XM_006718855.3 XP_006718918.1
XM_017017852.1 XP_016873341.1
XM_017017853.1 XP_016873342.1
XM_017017855.1 XP_016873344.1
XM_017017861.1 XP_016873350.1
XM_017017865.1 XP_016873354.1
AK293487.1
AK294137.1
AK315964.1
AY358331.1 AAQ88697.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv3892109 Chr11:131358314 - 131494601 on Build GRCh38 Loss NTM
nsv1035733 Chr11:130509478 - 131429821 on Build GRCh38 Gain C11orf44 LOC100507431 NTM MIR8052 LOC103611081 SNX19
nsv1039087 Chr11:131230668 - 131438530 on Build GRCh38 Gain NTM

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