Assay Details
Target Gene Details
Entrez Gene ID: | 10911 |
Gene Name: | urotensin 2 |
Gene Aliases: |
PRO1068, U-II, UCN2, UII |
Location: |
Chr.1:7846345-7913615 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
UTS2 | NM_006786.3 | NP_006777.1 | ||
NM_021995.2 | NP_068835.1 | |||
XM_011540537.2 | XP_011538839.1 | |||
XM_011540538.1 | XP_011538840.1 | |||
XM_017000116.1 | XP_016855605.1 | |||
XM_017000117.1 | XP_016855606.1 | |||
XM_017000118.1 | XP_016855607.1 | |||
XM_017000119.1 | XP_016855608.1 | |||
AF104118.1 | AAD13070.1 | |||
AF140630.1 | AAD55577.1 | |||
AY358375.1 | AAQ88741.1 | |||
BC126443.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3585131 | Chr.1:7848735 - 7849453 on Build GRCh38 | Loss | UTS2 |
esv2660700 | Chr.1:7848692 - 7849434 on Build GRCh38 | Deletion | UTS2 |
More Information
Additional Information:
For this assay, SNP(s) [rs370567193] 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 Intronic Non-exonic DGV Variation |