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: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NDRG2 | NM_001282211.1 | NP_001269140.1 | ||
AK293514.1 |
Target Gene Details
Entrez Gene ID: | 122664 |
Gene Name: | tubulin polymerization promoting protein family member 2 |
Gene Aliases: |
C14orf8, CT152, P18, p25beta |
Location: |
Chr.14:21024262-21036352 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TPPP2 | NM_173846.4 | 4 | 674 | NP_776245.2 |
XM_005267324.4 | 4 | 735 | XP_005267381.1 | |
XM_011536416.1 | XP_011534718.1 | |||
XM_011536417.2 | XP_011534719.1 | |||
XM_011536418.1 | XP_011534720.1 | |||
XM_011536420.2 | XP_011534722.1 | |||
XM_017020966.1 | 4 | 638 | XP_016876455.1 | |
AK093070.1 | ||||
AK098680.1 | 4 | 883 | ||
AW135537.1 | 1 | 139 | ||
AY072034.1 | 4 | 611 | AAL62338.1 | |
AY173946.1 | 4 | 611 | AAO49716.1 | |
BC038970.2 | 3 | 563 | AAH38970.1 |
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 | NDRG2 RNASE2 RNASE3 MIR6717 EDDM3A RNASE1 RNASE8 RNASE7 RNASE6 SLC39A2 RNASE13 ARHGEF40 LOC101929718 ECRP METTL17 TPPP2 EDDM3B |
nsv832740 | Chr.14:20863901 - 21076893 on Build GRCh38 | Gain | NDRG2 RNASE2 RNASE3 MIR6717 RNASE8 RNASE7 SLC39A2 RNASE13 ARHGEF40 LOC101929718 ECRP METTL17 TPPP2 |
nsv1039369 | Chr.14:21030895 - 21062142 on Build GRCh38 | Loss | RNASE8 RNASE7 RNASE13 ARHGEF40 NDRG2 TPPP2 |
More Information
Additional Information:
For this assay, SNP(s) [rs76101114] 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 Exonic Intronic Non-exonic DGV Variation |