Assay Details
Target Gene Details
Entrez Gene ID: | 101927179 |
Gene Name: | uncharacterized LOC101927179 |
Gene Aliases: |
- |
Location: |
Chr.4:47831345-47896848 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LOC101927179 | NR_125880.1 | |||
| NR_125881.1 | ||||
| AL599247.1 | ||||
| BX280044.1 |
Target Gene Details
Entrez Gene ID: | 152518 |
Gene Name: | nuclear transcription factor, X-box binding like 1 |
Gene Aliases: |
CDZFP, HOZFP, OZFP, URCC5 |
Location: |
Chr.4:47847233-47914667 on Build GRCh38 |
Assay Gene Location: | Within Intron 23 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NFXL1 | NM_001278623.1 | NP_001265552.1 | ||
| NM_001278624.1 | NP_001265553.1 | |||
| NM_152995.5 | NP_694540.3 | |||
| NR_103795.1 | ||||
| AB085695.1 | ||||
| AB181916.1 | ||||
| AK131285.1 | BAD18459.1 | |||
| AK302440.1 | ||||
| AY134856.1 | AAN08626.1 | |||
| BC018019.1 | AAH18019.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv5202n100 | Chr.4:47486414 - 47904818 on Build GRCh38 | Gain |
|
| nsv4328 | Chr.4:47814450 - 47860236 on Build GRCh38 | Deletion |
|
| nsv594118 | Chr.4:47558369 - 47915713 on Build GRCh38 | Loss |
|
| nsv829924 | Chr.4:47668888 - 47864648 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs77032921] 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