Genomic Map
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Target Gene Details
Entrez Gene ID: | 51079 |
Gene Name: | NADH:ubiquinone oxidoreductase subunit A13 |
Gene Aliases: |
B16.6, CDA016, CGI-39, GRIM-19, GRIM19 |
Location: |
Chr.19:19516210-19528204 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NDUFA13 | NM_015965.6 | NP_057049.5 | ||
| AF261134.1 | AAG44670.1 | |||
| AF286697.1 | AAG28167.1 | |||
| AK293859.1 | ||||
| BC000589.2 | AAH00589.2 | |||
| BC009189.2 | AAH09189.1 | |||
| BG705222.1 | ||||
| BM839920.1 | ||||
| BP230223.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv509723 | Chr.19:19517547 - 19595561 on Build GRCh38 | Insertion |
 NDUFA13
PBX4
CILP2
YJEFN3
|
| nsv952426 | Chr.19:19525792 - 19601091 on Build GRCh38 | Deletion |
NDUFA13
PBX4
CILP2
YJEFN3
|
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Additional Information:
For this assay, SNP(s) [rs73002997] 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
|
Panther Classification:
Gene Ontology Categories:
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