Genomic Map
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Target Gene Details
Entrez Gene ID: | 1763 |
Gene Name: | DNA replication helicase/nuclease 2 |
Gene Aliases: |
DNA2L, hDNA2 |
Location: |
Chr.10:68414064-68472521 on Build GRCh38 |
Assay Gene Location: | Within Intron 19 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DNA2 | NM_001080449.2 | NP_001073918.2 | ||
| NR_102264.1 | ||||
| XM_006717680.3 | XP_006717743.1 | |||
| XM_011539417.1 | XP_011537719.1 | |||
| XM_017015799.1 | XP_016871288.1 | |||
| AK307939.1 | ||||
| BC028188.1 | AAH28188.1 | |||
| BC041115.2 | AAH41115.1 | |||
| BC053574.1 | AAH53574.1 | |||
| BC063664.1 | AAH63664.1 | |||
| BC111740.1 | AAI11741.1 | |||
| D42046.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv919n100 | Chr.10:68400084 - 68752800 on Build GRCh38 | Gain |
 TET1
RUFY2
DNA2
CCAR1
SLC25A16
|
| nsv551434 | Chr.10:68384017 - 68503822 on Build GRCh38 | Loss |
RUFY2
DNA2
SLC25A16
|
| nsv1047983 | Chr.10:68414663 - 68849311 on Build GRCh38 | Gain |
SNORD98
TET1
MIR1254-1
DNA2
CCAR1
SLC25A16
STOX1
|
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Additional Information:
For this assay, SNP(s) [rs149422990] 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:
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