Genomic Map
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Target Gene Details
Entrez Gene ID: | 51296 |
Gene Name: | solute carrier family 15 member 3 |
Gene Aliases: |
OCTP, PHT2, PTR3 |
Location: |
Chr.11:60937083-60952081 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC15A3 | NM_016582.2 | 1 | 423 | NP_057666.1 |
| NR_027391.1 | 1 | 423 | ||
| XM_011545095.2 | 1 | 718 | XP_011543397.1 | |
| AB020598.1 | 1 | 423 | BAA93432.1 | |
| AF135600.1 | 1 | 316 | AAQ13565.1 | |
| BC025710.1 | 1 | 284 | ||
| BC037974.1 | 1 | 283 | AAH37974.1 |
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Additional Information:
For this assay, SNP(s) [rs150370599] 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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