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See other NDRG2 CNV Assays ›
Gene Symbol
NDRG2
Assay Reference Genome
Location

Chr.14:21022424 on build GRCh38
Cytoband
14q11.2
Assay ID Hs01499082_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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  • Genomic Map
  • Assay Details
  • More Information

Genomic Map

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Assay Details

Target Gene Details

Entrez Gene ID:

57447

Gene Name:

NDRG family member 2

Gene Aliases:

SYLD

Location:

Chr.14:21016763-21070872 on Build GRCh38

Assay Gene Location:

Overlaps Intron 7 - Exon 7
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NDRG2 NM_001282211.1 NP_001269140.1
NM_001282212.1 NP_001269141.1
NM_001282213.1 NP_001269142.1
NM_001282214.1 NP_001269143.1
NM_001282215.1 NP_001269144.1
NM_001282216.1 NP_001269145.1
NM_001320329.1 NP_001307258.1
NM_016250.2 NP_057334.1
NM_201535.1 NP_963293.1
NM_201536.1 NP_963294.1
NM_201537.1 NP_963831.1
NM_201538.1 NP_963832.1
NM_201539.1 NP_963833.1
NM_201540.1 NP_963834.1
NM_201541.1 NP_963835.1
XM_011536996.2 XP_011535298.1
XM_011536997.1 XP_011535299.1
XM_011536998.1 XP_011535300.1
XM_011536999.1 XP_011535301.1
XM_011537001.1 XP_011535303.1
XM_011537002.1 XP_011535304.1
XM_017021480.1 XP_016876969.1
XM_017021481.1 XP_016876970.1
XM_017021482.1 XP_016876971.1
XM_017021483.1 XP_016876972.1
XM_017021484.1 XP_016876973.1
XM_017021485.1 XP_016876974.1
XM_017021486.1 XP_016876975.1
XM_017021487.1 XP_016876976.1
XM_017021488.1 XP_016876977.1
XM_017021489.1 XP_016876978.1
XM_017021490.1 XP_016876979.1
XM_017021491.1 XP_016876980.1
XM_017021492.1 XP_016876981.1
XM_017021493.1 XP_016876982.1
XM_017021494.1 XP_016876983.1
XM_017021495.1 XP_016876984.1
XM_017021496.1 XP_016876985.1
AB033074.1
AF087872.1 AAM10500.1
AF159092.3 AAD43131.2
AF304051.1 AAL08624.1
AK024521.1
AK057843.1
AK057847.1
AK090657.1
AK096999.1
AK130029.1
AK293514.1
AL136574.1 CAB66509.1
AW163815.1
BC010458.1 AAH10458.1
BC011240.1 AAH11240.1
BC093038.1 AAH93038.1
BG818977.1
BI759006.1
BM810623.1
BX247987.1 CAD62321.1
BX248031.1 CAD62350.1
BX647091.1
BX647748.1
CB153966.1
CR749252.1 CAH18108.1
DA065447.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv428293 Chr.14:20747949 - 21063624 on Build GRCh38 Gain+Loss ARHGEF40 RNASE1 RNASE3 RNASE8 EDDM3B MIR6717 NDRG2 ECRP SLC39A2 LOC101929718 RNASE13 RNASE7 TPPP2 RNASE6 METTL17 EDDM3A RNASE2
nsv832740 Chr.14:20863901 - 21076893 on Build GRCh38 Gain ARHGEF40 RNASE3 RNASE8 MIR6717 NDRG2 ECRP SLC39A2 LOC101929718 RNASE13 RNASE7 TPPP2 METTL17 RNASE2

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More Information


Set Membership:

Intragenic Non-exonic DGV Variation

Panther Classification:

Molecular Function -

serine protease

Gene Ontology Categories:

Function(s) Process(es)

negative regulation of cytokine production
signal transduction
regulation of vascular endothelial growth factor production
Wnt signaling pathway
substantia nigra development
cell differentiation
negative regulation of smooth muscle cell proliferation
negative regulation of ERK1 and ERK2 cascade
regulation of platelet-derived growth factor production
molecular_function
protein binding

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