Assay Details
Target Gene Details
Entrez Gene ID: | 4839 |
Gene Name: | NOP2 nucleolar protein |
Gene Aliases: |
NOL1, NOP120, NSUN1, p120 |
Location: |
Chr.12:6556870-6568332 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 9 - Exon 9 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NOP2 | NM_001033714.2 | NP_001028886.1 | ||
NM_001258308.1 | NP_001245237.1 | |||
NM_001258309.1 | NP_001245238.1 | |||
NM_001258310.1 | NP_001245239.1 | |||
NM_006170.3 | NP_006161.2 | |||
XM_005253691.1 | XP_005253748.1 | |||
AK056208.1 | ||||
AK129852.1 | ||||
AK307582.1 | ||||
BC000656.2 | AAH00656.1 | |||
BC065257.1 | ||||
BC082985.1 | ||||
BC106072.1 | AAI06073.1 | |||
BC128183.1 | ||||
BC128184.1 | ||||
M32110.1 | AAA36398.1 | |||
X55504.1 | CAA39119.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv826210 | Chr.12:6561863 - 6612310 on Build GRCh38 | Gain | SCARNA11 CHD4 NOP2 |
More Information
Additional Information:
For this assay, SNP(s) [rs114838415] 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 Non-exonic DGV Variation |