Assay Details
Target Gene Details
Entrez Gene ID: | 91647 |
Gene Name: | ATP synthase mitochondrial F1 complex assembly factor 2 |
Gene Aliases: |
ATP12, ATP12p, LP3663, MC5DN1 |
Location: |
Chr.17:18015059-18039169 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 1 - Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ATPAF2 | NM_145691.3 | NP_663729.1 | ||
XM_005256848.3 | XP_005256905.1 | |||
XM_011524065.1 | XP_011522367.1 | |||
XM_017025302.1 | XP_016880791.1 | |||
XM_017025303.1 | XP_016880792.1 | |||
AF052185.1 | ||||
AF070584.1 | ||||
AK290257.1 | ||||
AK294487.1 | ||||
AK296382.1 | ||||
AY203943.1 | AAP34466.1 | |||
BC004114.2 | AAH04114.1 | |||
BC032126.2 | AAH32126.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv510701 | Chr.17:17947160 - 18052171 on Build GRCh38 | Deletion | DRC3 GID4 TOM1L2 ATPAF2 |
More Information
Additional Information:
For this assay, SNP(s) [rs80251201] 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 |