Genomic Map
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Target Gene Details
Entrez Gene ID: | 28976 |
Gene Name: | acyl-CoA dehydrogenase family member 9 |
Gene Aliases: |
NPD002 |
Location: |
Chr.3:128879490-128916075 on Build GRCh38 |
Assay Gene Location: | Within Exon 19 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ACAD9 | NM_014049.4 | 18 | 2154 | NP_054768.2 |
| NR_033426.1 | 18 | 2330 | ||
| AB209427.1 | 16 | 5158 | BAD92664.1 | |
| AF078854.1 | 6 | 686 | AAD44486.1 | |
| AF327351.1 | 18 | 1984 | AAL56011.1 | |
| AK022568.1 | 17 | 2080 | BAB14104.1 | |
| AK024012.1 | 18 | 1998 | BAB14775.1 | |
| AK027186.1 | 7 | 1576 | ||
| AK130311.1 | 18 | 2025 | ||
| AK297952.1 | 18 | 2198 | ||
| BC001817.2 | 11 | 1118 | AAH01817.2 | |
| BC007970.2 | 18 | 2031 | AAH07970.1 | |
| BC013354.2 | 18 | 2008 | AAH13354.1 |
Target Gene Details
Entrez Gene ID: | 57501 |
Gene Name: | KIAA1257 |
Gene Aliases: |
- |
Location: |
Chr.3:128910186-129032431 on Build GRCh38 |
Assay Gene Location: | Within Exon 21 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| KIAA1257 | XM_011513050.2 | XP_011511352.2 | ||
| XM_017006939.1 | 16 | 6357 | XP_016862428.1 | |
| XM_017006940.1 | 16 | 6353 | XP_016862429.1 | |
| XM_017006941.1 | 16 | 5930 | XP_016862430.1 | |
| XM_017006942.1 | 16 | 6324 | XP_016862431.1 | |
| XM_017006943.1 | 16 | 6082 | XP_016862432.1 | |
| XM_017006944.1 | 15 | 5902 | XP_016862433.1 | |
| XM_017006945.1 | XP_016862434.1 | |||
| XM_017006946.1 | 14 | 5513 | XP_016862435.1 | |
| XM_017006947.1 | 13 | 5397 | XP_016862436.1 | |
| XM_017006948.1 | 15 | 5574 | XP_016862437.1 | |
| XM_017006949.1 | 14 | 5521 | XP_016862438.1 | |
| XM_017006950.1 | 14 | 11008 | XP_016862439.1 | |
| XM_017006951.1 | 14 | 11113 | XP_016862440.1 | |
| XM_017006952.1 | 13 | 5291 | XP_016862441.1 | |
| XM_017006953.1 | 13 | 5297 | XP_016862442.1 | |
| XM_017006954.1 | XP_016862443.1 |
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Additional Information:
For this assay, SNP(s) [rs116106966] 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
Exonic
non-DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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