Assay Details
Target Gene Details
Entrez Gene ID: | 27158 |
Gene Name: | NADPH dependent diflavin oxidoreductase 1 |
Gene Aliases: |
NR1, bA350O14.9 |
Location: |
Chr.9:137205667-137219361 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 4 - Exon 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NDOR1 | NM_001144026.2 | NP_001137498.1 | ||
NM_001144027.2 | NP_001137499.1 | |||
NM_001144028.2 | NP_001137500.1 | |||
NM_014434.3 | NP_055249.1 | |||
XM_011518545.1 | XP_011516847.1 | |||
XM_011518547.1 | XP_011516849.1 | |||
XM_011518548.2 | XP_011516850.1 | |||
XM_017014626.1 | XP_016870115.1 | |||
XM_017014627.1 | XP_016870116.1 | |||
AF199509.1 | AAF25205.1 | |||
AK026089.1 | ||||
AK074403.1 | ||||
AK225995.1 | ||||
AK290026.1 | ||||
AY077845.1 | AAL77754.1 | |||
BC015735.1 | AAH15735.1 | |||
BC093782.1 | AAH93782.1 | |||
BC111943.1 | AAI11944.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv13010n54 | Chr.9:137191539 - 137233413 on Build GRCh38 | Loss |
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nsv616012 | Chr.9:137197680 - 137223834 on Build GRCh38 | Loss |
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nsv616007 | Chr.9:137079368 - 137240666 on Build GRCh38 | Loss |
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dgv13009n54 | Chr.9:137173890 - 137327859 on Build GRCh38 | Loss |
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nsv524322 | Chr.9:136795692 - 137482216 on Build GRCh38 | Loss |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
nsv951207 | Chr.9:137136949 - 137379148 on Build GRCh38 | Deletion |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
nsv1161918 | Chr.9:137118319 - 137438026 on Build GRCh38 | Duplication |
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esv2422220 | Chr.9:136584135 - 137350098 on Build GRCh38 | Deletion |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs77510769] 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: |
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Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)