Genomic Map
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Target Gene Details
Entrez Gene ID: | 56964 |
Gene Name: | WD repeat domain 93 |
Gene Aliases: |
- |
Location: |
Chr.15:89690074-89744390 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| WDR93 | NM_001284395.1 | NP_001271324.1 | ||
| NM_020212.1 | NP_064597.1 | |||
| XM_006720614.1 | XP_006720677.1 | |||
| XM_006720615.1 | XP_006720678.1 | |||
| XM_006720618.2 | XP_006720681.1 | |||
| XM_011521794.2 | XP_011520096.1 | |||
| XM_011521795.1 | XP_011520097.1 | |||
| XM_011521796.2 | XP_011520098.1 | |||
| XM_011521798.2 | XP_011520100.1 | |||
| XM_011521800.1 | XP_011520102.1 | |||
| XM_011521802.2 | XP_011520104.1 | |||
| XM_017022415.1 | XP_016877904.1 | |||
| XM_017022416.1 | XP_016877905.1 | |||
| AK097525.1 | BAC05088.1 | |||
| BC064626.1 | AAH64626.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1046117 | Chr.15:89683716 - 89765410 on Build GRCh38 | Gain |
 PEX11A
WDR93
MESP1
|
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Additional Information:
For this assay, SNP(s) [rs114097065] 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
|
Panther Classification:
Gene Ontology Categories:
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