Assay Details
Target Gene Details
Entrez Gene ID: | 115825 |
Gene Name: | WD repeat and FYVE domain containing 2 |
Gene Aliases: |
PROF, WDF2, ZFYVE22 |
Location: |
Chr.13:51584194-51766799 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
WDFY2 | NM_052950.3 | NP_443182.1 | ||
XM_011534914.1 | XP_011533216.1 | |||
XM_011534915.2 | XP_011533217.1 | |||
XM_017020386.1 | XP_016875875.1 | |||
AF411978.1 | AAL04162.1 | |||
AK309815.1 | ||||
AK311177.1 | ||||
BC014004.2 | AAH14004.1 | |||
DA124107.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3892343 | Chr.13:51418581 - 52060832 on Build GRCh38 | Gain | LINC00282 INTS6-AS1 LOC107984562 MIR4703 UTP14C DHRS12 INTS6 CTAGE3P WDFY2 ALG11 CCDC70 ATP7B |
nsv832612 | Chr.13:51602847 - 51788389 on Build GRCh38 | Gain | DHRS12 WDFY2 |
More Information
Additional Information:
For this assay, SNP(s) [rs75306857,rs78766455] 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 |