Assay Details
Target Gene Details
Entrez Gene ID: | 2296 |
Gene Name: | forkhead box C1 |
Gene Aliases: |
ARA, FKHL7, FREAC-3, FREAC3, IGDA, IHG1, IRID1, RIEG3 |
Location: |
Chr.6:1610446-1613897 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FOXC1 | NM_001453.2 | 1 | 1555 | NP_001444.2 |
| BC134421.1 | 2 | 643 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv992n67 | Chr.6:1589856 - 1629286 on Build GRCh38 | Gain |
|
| nsv1016859 | Chr.6:1459785 - 1645585 on Build GRCh38 | Gain |
|
| nsv823397 | Chr.6:1603632 - 1622029 on Build GRCh38 | Gain |
|
| nsv1119068 | Chr.6:1610865 - 1612165 on Build GRCh38 | Deletion |
|
| nsv600807 | Chr.6:1610649 - 1623755 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs73406891] 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: |
|

Genomic Map