Genomic Map
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Target Gene Details
Entrez Gene ID: | 220963 |
Gene Name: | solute carrier family 16 member 9 |
Gene Aliases: |
C10orf36, MCT9 |
Location: |
Chr.10:59650764-59710079 on Build GRCh38 |
Assay Gene Location: | Within Exon 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC16A9 | NM_001323977.1 | 6 | 3211 | NP_001310906.1 |
| NM_001323978.1 | 7 | 3639 | NP_001310907.1 | |
| NM_001323979.1 | 6 | 3326 | NP_001310908.1 | |
| NM_001323980.1 | 6 | 3556 | NP_001310909.1 | |
| NM_001323981.1 | 7 | 3769 | NP_001310910.1 | |
| NM_194298.2 | 6 | 3686 | NP_919274.1 | |
| XM_017015883.1 | 6 | 3812 | XP_016871372.1 | |
| XM_017015884.1 | 7 | 4019 | XP_016871373.1 | |
| AK021827.1 | 1 | 1440 | ||
| AK125791.1 | 6 | 3346 | BAC86293.1 | |
| AK172758.1 | 2 | 2262 | BAD18743.1 | |
| AL122071.1 | 2 | 2183 | CAB59247.1 | |
| BX092606.1 | 1 | 373 |
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Additional Information:
For this assay, SNP(s) [rs76453639,rs77437312] 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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