Assay Details
Target Gene Details
Entrez Gene ID: | 9167 |
Gene Name: | cytochrome c oxidase subunit 7A2 like |
Gene Aliases: |
COX7AR, COX7RP, EB1, SIG81 |
Location: |
Chr.2:42335561-42368957 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
COX7A2L | NM_001319036.1 | NP_001305965.1 | ||
NM_001319037.1 | NP_001305966.1 | |||
NM_001319038.1 | NP_001305967.1 | |||
NM_001319040.1 | NP_001305969.1 | |||
NM_004718.3 | NP_004709.2 | |||
NR_134947.1 | ||||
NR_134948.1 | ||||
AB007618.1 | BAA22571.1 | |||
AF127788.1 | AAF72746.1 | |||
AK092911.1 | ||||
AK130281.1 | ||||
BC005251.1 | AAH05251.1 | |||
BC007095.1 | AAH07095.1 | |||
BF130603.1 | ||||
BI598394.1 | ||||
BT007371.1 | AAP36035.1 | |||
CA336587.1 | ||||
CD700827.1 | ||||
CF593726.1 | ||||
CR542208.1 | CAG47004.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3583758 | Chr.2:42347476 - 42362702 on Build GRCh38 | Loss |
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nsv524679 | Chr.2:42350030 - 42576225 on Build GRCh38 | Loss |
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More Information
Additional Information:
For this assay, SNP(s) [rs113951781,rs116531013] 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:
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