Genomic Map
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Target Gene Details
Entrez Gene ID: | 864 |
Gene Name: | runt related transcription factor 3 |
Gene Aliases: |
AML2, CBFA3, PEBP2aC |
Location: |
Chr.1:24899511-24965158 on Build GRCh38 |
Assay Gene Location: | Within Exon 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RUNX3 | NM_001031680.2 | 6 | 1929 | NP_001026850.1 |
| NM_001320672.1 | 7 | 1762 | NP_001307601.1 | |
| NM_004350.2 | 5 | 1859 | NP_004341.1 | |
| XM_005246024.4 | 7 | 1637 | XP_005246081.1 | |
| XM_011542351.1 | 5 | 1770 | XP_011540653.1 | |
| AK091829.1 | 1 | 2002 | ||
| AK300056.1 | 5 | 1248 | ||
| BC013362.2 | 7 | 1736 | AAH13362.1 | |
| X79550.2 | 5 | 1454 | CAA56093.2 | |
| Z35278.1 | 5 | 1457 | CAA84541.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv508581 | Chr.1:24884488 - 24968228 on Build GRCh38 | Deletion |
 RUNX3
MIR6731
|
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Additional Information:
For this assay, SNP(s) [rs74060466] 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
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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