Assay Details
Target Gene Details
Entrez Gene ID: | 8725 |
Gene Name: | URI1, prefoldin like chaperone |
Gene Aliases: |
C19orf2, NNX3, PPP1R19, RMP, URI |
Location: |
Chr.19:29923644-30016612 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| URI1 | NM_001252641.1 | NP_001239570.1 | ||
| NM_003796.3 | NP_003787.2 | |||
| NR_045557.1 | ||||
| XM_005259362.2 | XP_005259419.1 | |||
| XM_005259363.4 | XP_005259420.1 | |||
| XM_011527435.1 | XP_011525737.1 | |||
| AF091095.1 | AAD08679.1 | |||
| AK001437.1 | ||||
| AK226173.1 | ||||
| AK292170.1 | ||||
| AK314313.1 | ||||
| BC026184.2 | AAH26184.2 | |||
| BC067259.1 | AAH67259.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1063678 | Chr.19:29937920 - 29987524 on Build GRCh38 | Loss |
|
| dgv3512n100 | Chr.19:29974636 - 30013166 on Build GRCh38 | Loss |
|
| nsv579283 | Chr.19:29974289 - 30048552 on Build GRCh38 | Loss |
|
| dgv3510n100 | Chr.19:29961142 - 30020645 on Build GRCh38 | Loss |
|
| nsv579282 | Chr.19:29960594 - 30000137 on Build GRCh38 | Loss |
|
| dgv3511n100 | Chr.19:29964373 - 29988391 on Build GRCh38 | Loss |
|
| dgv3509n100 | Chr.19:29954152 - 30028098 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs77841415] 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: |
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Genomic Map