Assay Details
Target Gene Details
Entrez Gene ID: | 153020 |
Gene Name: | RasGEF domain family member 1B |
Gene Aliases: |
GPIG4 |
Location: |
Chr.4:81426393-81471928 on Build GRCh38 |
Assay Gene Location: | Within Exon 15 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RASGEF1B | NM_001300735.1 | 14 | 1992 | NP_001287664.1 |
| NM_001300736.1 | 13 | 1869 | NP_001287665.1 | |
| NM_152545.2 | 14 | 1995 | NP_689758.1 | |
| XM_017007812.1 | 12 | 1713 | XP_016863301.1 | |
| XM_017007813.1 | 14 | 2083 | XP_016863302.1 | |
| AK056257.1 | 14 | 1974 | BAB71130.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv4404 | Chr.4:81419832 - 81464994 on Build GRCh38 | Deletion |
|
| nsv829985 | Chr.4:81278174 - 81432502 on Build GRCh38 | Loss |
|
| nsv829986 | Chr.4:81424009 - 81588706 on Build GRCh38 | Gain+Loss |
|
| esv3601152 | Chr.4:81315107 - 81441130 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs114716983] 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