Assay Details
Target Gene Details
Entrez Gene ID: | 4299 |
Gene Name: | AF4/FMR2 family member 1 |
Gene Aliases: |
AF4, MLLT2, PBM1 |
Location: |
Chr.4:86935002-87141054 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| AFF1 | NM_001166693.2 | NP_001160165.1 | ||
| XM_005263007.3 | XP_005263064.1 | |||
| XM_005263009.3 | XP_005263066.1 | |||
| XM_005263013.3 | XP_005263070.1 | |||
| XM_011531973.2 | XP_011530275.1 | |||
| XM_017008215.1 | XP_016863704.1 | |||
| AK296149.1 | ||||
| AK300364.1 | ||||
| BC017432.1 | ||||
| DC340279.1 | ||||
| L13743.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv508297 | Chr.4:86857630 - 86947356 on Build GRCh38 | Deletion |
|
| nsv594787 | Chr.4:86300674 - 86967515 on Build GRCh38 | Gain |
|
| nsv1013308 | Chr.4:86848541 - 86949016 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs78219683] 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