Genomic Map
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Target Gene Details
Entrez Gene ID: | 55208 |
Gene Name: | defective in cullin neddylation 1 domain containing 2 |
Gene Aliases: |
C13orf17 |
Location: |
Chr.13:113455819-113492047 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DCUN1D2 | NM_001014283.1 | 7 | 928 | NP_001014305.1 |
| XM_017020643.1 | 7 | 1139 | XP_016876132.1 | |
| XM_017020644.1 | 7 | 1069 | XP_016876133.1 | |
| XM_017020645.1 | 7 | 1110 | XP_016876134.1 | |
| XM_017020646.1 | 7 | 4851 | XP_016876135.1 | |
| XM_017020647.1 | 7 | 1389 | XP_016876136.1 | |
| XM_017020648.1 | 7 | 2152 | XP_016876137.1 | |
| XM_017020649.1 | 6 | 966 | XP_016876138.1 | |
| AK000099.1 | 5 | 525 | BAA90944.1 | |
| AK001566.1 | 8 | 1063 | BAA91760.1 | |
| BC056669.1 | 7 | 915 | AAH56669.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1048814 | Chr.13:113081728 - 113611496 on Build GRCh38 | Gain |
 LOC105370378
MCF2L
LOC102724474
MIR8075
F10
ADPRHL1
PROZ
TFDP1
GRTP1-AS1
LAMP1
F10-AS1
PCID2
TMCO3
GRTP1
LOC101928841
F7
CUL4A
DCUN1D2
|
| nsv1035248 | Chr.13:113454525 - 113505449 on Build GRCh38 | Loss |
TMCO3
DCUN1D2
|
| nsv456137 | Chr.13:113452383 - 113477639 on Build GRCh38 | Loss |
ADPRHL1
DCUN1D2
|
| esv2759970 | Chr.13:113384114 - 113556749 on Build GRCh38 | Loss |
TMCO3
LOC101928841
ADPRHL1
DCUN1D2
|
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Additional Information:
For this assay, SNP(s) [rs376681957] 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
Exonic
DGV Variation
|
Gene Ontology Categories:
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