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See other NAV2 CNV Assays ›
Gene Symbol
NAV2
Assay Reference Genome
Location

Chr.11:20048745 on build GRCh38
Cytoband
11p15.1
Assay ID Hs00315404_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 89797

Gene Name:

 neuron navigator 2

Gene Aliases:

 HELAD1, POMFIL2, RAINB1, STEERIN2, UNC53H2

Location:

 Chr.11:19345200-20121601 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 25 - Exon 26
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NAV2 NM_001111018.1 NP_001104488.1
NM_001111019.2 NP_001104489.1
NM_001244963.1 NP_001231892.1
NM_145117.4 NP_660093.2
NM_182964.5 NP_892009.3
XM_005253214.4 XP_005253271.1
XM_006718364.3 XP_006718427.1
XM_006718365.3 XP_006718428.1
XM_006718366.3 XP_006718429.1
XM_006718367.3 XP_006718430.1
XM_006718368.3 XP_006718431.1
XM_006718369.2 XP_006718432.1
XM_011520444.2 XP_011518746.1
XM_011520445.2 XP_011518747.1
XM_011520446.2 XP_011518748.1
XM_011520447.2 XP_011518749.1
XM_011520448.2 XP_011518750.1
XM_011520449.2 XP_011518751.1
XM_011520450.2 XP_011518752.1
XM_011520451.2 XP_011518753.1
XM_011520452.2 XP_011518754.1
XM_011520453.2 XP_011518755.1
XM_011520454.2 XP_011518756.1
XM_017018520.1 XP_016874009.1
XM_017018521.1 XP_016874010.1
XM_017018522.1 XP_016874011.1
XM_017018523.1 XP_016874012.1
XM_017018524.1 XP_016874013.1
XM_017018525.1 XP_016874014.1
XM_017018526.1 XP_016874015.1
AB037840.3
AB063115.1 BAC00853.1
AB063116.1 BAC00854.1
AF466143.1 AAL96479.1
AF466144.1 AAL96480.1
AJ488102.1 CAD32471.1
AK074287.1 BAB85038.1
AK298346.1
AK307574.1
BC150290.1

Target Gene Details

Entrez Gene ID:

 100874014

Gene Name:

 NAV2 antisense RNA 2

Gene Aliases:

 -

Location:

 Chr.11:20043775-20049303 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NAV2-AS2 NR_046672.1
BX112419.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv516382 Chr.11:20047418 - 20056950 on Build GRCh38 Gain NAV2-AS2 NAV2

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More Information


Additional Information:

For this assay, SNP(s) [rs78806867] 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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