Genomic Map
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Target Gene Details
Entrez Gene ID: | 4904 |
Gene Name: | Y-box binding protein 1 |
Gene Aliases: |
BP-8, CBF-A, CSDA2, CSDB, DBPB, EFI-A, MDR-NF1, NSEP-1, NSEP1, YB-1, YB1 |
Location: |
Chr.1:42682235-42703803 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| YBX1 | NM_004559.4 | 8 | 2901 | NP_004550.2 |
| NR_132737.1 | 7 | 2719 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3577249 | Chr.1:42576524 - 42885152 on Build GRCh38 | Gain |
 SVBP
C1orf50
PPIH
LOC339539
LOC100129924
CLDN19
LOC105378683
ERMAP
YBX1
CCDC30
P3H1
ZNF691
|
| nsv829682 | Chr.1:42589429 - 42773568 on Build GRCh38 | Loss |
C1orf50
PPIH
CLDN19
YBX1
CCDC30
P3H1
|
| nsv945908 | Chr.1:42700845 - 42717445 on Build GRCh38 | Duplication |
YBX1
|
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Additional Information:
For this assay, SNP(s) [rs74345535] 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
|
Gene Ontology Categories:
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