Assay Details
Target Gene Details
Entrez Gene ID: | 148823 |
Gene Name: | germinal center associated signaling and motility like |
Gene Aliases: |
C1orf150 |
Location: |
Chr.1:247507058-247577690 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| GCSAML | NM_001281834.1 | NP_001268763.1 | ||
| NM_001281835.1 | NP_001268764.1 | |||
| NM_001281836.1 | NP_001268765.1 | |||
| NM_001281837.1 | NP_001268766.1 | |||
| NM_001281838.1 | NP_001268767.1 | |||
| NM_001281853.1 | NP_001268782.1 | |||
| AK124520.1 | BAC85873.1 | |||
| AK126682.1 | ||||
| AK307081.1 | ||||
| AK307082.1 | ||||
| DA118297.1 | ||||
| DB095029.1 | ||||
| DC310064.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv33129 | Chr.1:246911128 - 248165533 on Build GRCh38 | Gain+Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs78398999] 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: |
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Genomic Map