Assay Details
Target Gene Details
Entrez Gene ID: | 101927447 |
Gene Name: | uncharacterized LOC101927447 |
Gene Aliases: |
- |
Location: |
Chr.22:43275942-43283830 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC101927447 | NR_134582.1 | |||
DA931830.1 |
Target Gene Details
Entrez Gene ID: | 80274 |
Gene Name: | signal peptide, CUB domain and EGF like domain containing 1 |
Gene Aliases: |
- |
Location: |
Chr.22:43203223-43343388 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SCUBE1 | NM_173050.3 | NP_766638.2 | ||
XM_005261752.1 | XP_005261809.1 | |||
XM_011530389.2 | XP_011528691.1 | |||
XM_011530390.2 | XP_011528692.1 | |||
AF525689.1 | AAN77133.1 | |||
AK127719.1 | BAC87098.1 | |||
BC047916.1 | AAH47916.1 | |||
BC127263.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv955166 | Chr.22:43238095 - 43320894 on Build GRCh38 | Deletion |
![]() ![]() |
nsv834216 | Chr.22:43184904 - 43383781 on Build GRCh38 | Loss |
![]() ![]() ![]() ![]() |
nsv471202 | Chr.22:43274380 - 43344412 on Build GRCh38 | Gain |
![]() ![]() |
nsv520927 | Chr.22:43154143 - 43307985 on Build GRCh38 | Loss |
![]() ![]() ![]() ![]() ![]() |
esv33816 | Chr.22:43113758 - 43326122 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
dgv844e214 | Chr.22:43185465 - 43295588 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs74364212] 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: |
![]() ![]() ![]() ![]() |
Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)