Assay Details
Target Gene Details
Entrez Gene ID: | 146713 |
Gene Name: | RNA binding protein, fox-1 homolog 3 |
Gene Aliases: |
FOX-3, FOX3, HRNBP3, NEUN |
Location: |
Chr.17:79089345-79611101 on Build GRCh38 |
Assay Gene Location: | Within Intron 16 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RBFOX3 | NM_001082575.2 | NP_001076044.1 | ||
| XM_011524359.1 | XP_011522661.1 | |||
| XM_011524360.1 | XP_011522662.1 | |||
| XM_011524362.2 | XP_011522664.1 | |||
| XM_011524363.2 | XP_011522665.1 | |||
| XM_011524365.2 | XP_011522667.1 | |||
| XM_011524366.2 | XP_011522668.1 | |||
| XM_011524367.2 | XP_011522669.1 | |||
| XM_017024208.1 | XP_016879697.1 | |||
| XM_017024209.1 | XP_016879698.1 | |||
| XM_017024210.1 | XP_016879699.1 | |||
| XM_017024211.1 | XP_016879700.1 | |||
| AK124644.1 | ||||
| AK128131.1 | ||||
| AK293617.1 | ||||
| BM714144.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833556 | Chr.17:79037891 - 79221474 on Build GRCh38 | Loss |
|
| nsv952379 | Chr.17:79054919 - 79342518 on Build GRCh38 | Deletion |
|
| nsv523650 | Chr.17:78933797 - 79165563 on Build GRCh38 | Loss |
|
| nsv1057193 | Chr.17:78921031 - 79481744 on Build GRCh38 | Gain |
|
| nsv527899 | Chr.17:79085706 - 79165563 on Build GRCh38 | Loss |
|
| nsv2157 | Chr.17:79074896 - 79105704 on Build GRCh38 | Insertion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs114378137] 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: |
|

Genomic Map