Genomic Map
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Target Gene Details
Entrez Gene ID: | 54883 |
Gene Name: | CWC25 spliceosome associated protein homolog |
Gene Aliases: |
CCDC49 |
Location: |
Chr.17:38800434-38825350 on Build GRCh38 |
Assay Gene Location: | Within Intron 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CWC25 | NM_017748.4 | NP_060218.1 | ||
| NR_073428.1 | ||||
| AK000298.1 | BAA91065.1 | |||
| AK225373.1 | ||||
| AK296115.1 | ||||
| AK316077.1 | ||||
| BC008833.2 | AAH08833.1 | |||
| CR749362.1 | CAH18215.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833438 | Chr.17:38593441 - 38821266 on Build GRCh38 | Loss |
 PCGF2
PSMB3
MIR4726
SRCIN1
CISD3
CWC25
MLLT6
C17orf96
LOC105371763
PIP4K2B
MIR4734
LOC100287808
|
| nsv833439 | Chr.17:38743861 - 38923753 on Build GRCh38 | Loss |
PCGF2
PSMB3
RPL23
MIR6779
CWC25
LASP1
MIR4727
SNORA21
C17orf98
PIP4K2B
LOC100287808
|
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Additional Information:
For this assay, SNP(s) [rs143664563] 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
|
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