Genomic Map
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Target Gene Details
Entrez Gene ID: | 57728 |
Gene Name: | WD repeat domain 19 |
Gene Aliases: |
ATD5, CED4, DYF-2, IFT144, NPHP13, ORF26, Oseg6, PWDMP, SRTD5 |
Location: |
Chr.4:39182404-39285810 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 12 - Intron 12 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| WDR19 | NM_001317924.1 | NP_001304853.1 | ||
| NM_025132.3 | NP_079408.3 | |||
| XM_011513724.1 | XP_011512026.1 | |||
| XM_011513725.2 | XP_011512027.1 | |||
| XM_011513726.2 | XP_011512028.1 | |||
| XM_011513727.1 | XP_011512029.1 | |||
| XM_017008501.1 | XP_016863990.1 | |||
| AB046858.1 | BAB13464.1 | |||
| AK026780.1 | BAB15550.1 | |||
| AK225588.1 | ||||
| AK294730.1 | ||||
| AK304161.1 | ||||
| AY029257.1 | AAK38745.1 | |||
| BC032578.1 | AAH32578.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2424590 | Chr.4:39215949 - 39217441 on Build GRCh38 | Deletion |
 WDR19
|
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Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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