Genomic Map
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Target Gene Details
Entrez Gene ID: | 26127 |
Gene Name: | FGFR1 oncogene partner 2 |
Gene Aliases: |
HSPC123-like, WIT3.0 |
Location: |
Chr.12:26938372-26966648 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FGFR1OP2 | NM_001171887.1 | 1 | 155 | NP_001165358.1 |
| NM_001171888.1 | 1 | 155 | NP_001165359.1 | |
| NM_015633.2 | 1 | 155 | NP_056448.1 | |
| AF161472.1 | AAF29087.1 | |||
| AK001534.1 | 1 | 144 | BAA91745.1 | |
| BC032143.2 | 1 | 30 | AAH32143.1 | |
| BI829470.1 | ||||
| DA388639.1 | 1 | 155 |
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Additional Information:
For this assay, SNP(s) [rs115084512,rs189020728] 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
|
Gene Ontology Categories:
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