Assay Details
Target Gene Details
Entrez Gene ID: | 7884 |
Gene Name: | stem-loop binding protein |
Gene Aliases: |
HBP |
Location: |
Chr.4:1692731-1712741 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLBP | NM_001306074.1 | 1 | 459 | NP_001293003.1 |
| NM_001306075.1 | 1 | 459 | NP_001293004.1 | |
| NM_006527.3 | 1 | 459 | NP_006518.1 | |
| AK091735.1 | ||||
| AK093314.1 | 1 | 66 | ||
| AK094257.1 | 1 | 273 | ||
| AK300826.1 | ||||
| AK315635.1 | ||||
| BC014908.1 | AAH14908.1 | |||
| BC015703.1 | AAH15703.1 | |||
| DB027411.1 | 1 | 66 | ||
| DB031118.1 | 1 | 66 | ||
| DC383752.1 | ||||
| U75679.1 | AAB97091.1 | |||
| Z71188.1 | CAA94918.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv428434 | Chr.4:1623665 - 1813048 on Build GRCh38 | Gain |
|
| nsv949756 | Chr.4:1710274 - 1817773 on Build GRCh38 | Deletion |
|
| dgv8901n54 | Chr.4:1644637 - 1864631 on Build GRCh38 | Loss |
|
| nsv593316 | Chr.4:1526039 - 1768630 on Build GRCh38 | Gain |
|
| nsv508989 | Chr.4:1623823 - 1846590 on Build GRCh38 | Insertion |
|
| nsv1161027 | Chr.4:1699833 - 1750693 on Build GRCh38 | Deletion |
|
| nsv470000 | Chr.4:1522203 - 1722852 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs181032842] 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