Assay Details
Target Gene Details
Entrez Gene ID: | 100847015 |
Gene Name: | microRNA 5691 |
Gene Aliases: |
- |
Location: |
Chr.11:9090312-9090379 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MIR5691 | NR_049874.1 |
Target Gene Details
Entrez Gene ID: | 57758 |
Gene Name: | signal peptide, CUB domain and EGF like domain containing 2 |
Gene Aliases: |
CEGB1, CEGF1, CEGP1 |
Location: |
Chr.11:9019500-9091603 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SCUBE2 | NM_001170690.1 | NP_001164161.1 | ||
NM_020974.2 | NP_066025.2 | |||
XM_005253032.4 | XP_005253089.2 | |||
XM_005253033.4 | XP_005253090.2 | |||
XM_005253034.4 | XP_005253091.2 | |||
XM_005253035.4 | XP_005253092.2 | |||
XM_005253036.4 | XP_005253093.2 | |||
XM_005253037.4 | XP_005253094.2 | |||
XM_011520246.2 | XP_011518548.1 | |||
XM_011520247.2 | XP_011518549.1 | |||
XM_011520248.2 | XP_011518550.1 | |||
XM_017018080.1 | XP_016873569.1 | |||
XM_017018081.1 | XP_016873570.1 | |||
XM_017018082.1 | XP_016873571.1 | |||
AK123039.1 | BAC85521.1 | |||
AK131552.1 | BAD18686.1 | |||
BC111690.1 | AAI11691.1 | |||
DN995815.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv467706 | Chr.11:9056105 - 9093452 on Build GRCh38 | Loss |
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nsv553454 | Chr.11:9037645 - 9103754 on Build GRCh38 | Loss |
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nsv951307 | Chr.11:9087954 - 9098353 on Build GRCh38 | Deletion |
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esv33264 | Chr.11:8986065 - 9289584 on Build GRCh38 | Loss |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs112511786,rs73412019] 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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Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)