Assay Details
Target Gene Details
Entrez Gene ID: | 56163 |
Gene Name: | ring finger protein 17 |
Gene Aliases: |
Mmip-2, SPATA23, TDRD4 |
Location: |
Chr.13:24747641-24888816 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RNF17 | XM_011535152.2 | XP_011533454.1 | ||
XM_011535155.2 | XP_011533457.1 | |||
XM_011535156.2 | XP_011533458.1 | |||
XM_011535157.2 | XP_011533459.1 | |||
XM_011535158.2 | XP_011533460.1 | |||
XM_011535159.2 | XP_011533461.1 | |||
XM_011535160.2 | XP_011533462.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv561345 | Chr.13:24606013 - 24763162 on Build GRCh38 | Gain | ATP12A RNF17 |
dgv1621n100 | Chr.13:24694944 - 24762408 on Build GRCh38 | Gain | ATP12A RNF17 |
dgv3093n54 | Chr.13:24700388 - 24756889 on Build GRCh38 | Gain | ATP12A RNF17 |
More Information
Additional Information:
For this assay, SNP(s) [rs79358695] 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 |