Assay Details
Target Gene Details
Entrez Gene ID: | 79443 |
Gene Name: | FYVE and coiled-coil domain containing 1 |
Gene Aliases: |
CATC2, CTRCT18, RUFY3, ZFYVE7 |
Location: |
Chr.3:45917899-45995824 on Build GRCh38 |
Assay Gene Location: | Within Exon 20 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FYCO1 | NM_024513.3 | 18 | 4851 | NP_078789.2 |
XM_006713333.3 | 19 | 6016 | XP_006713396.1 | |
XM_006713334.3 | 18 | 5932 | XP_006713397.1 | |
XM_011534111.2 | 19 | 4929 | XP_011532413.1 | |
AJ292348.2 | 18 | 4835 | CAC33883.1 | |
AK023397.1 | BAB14559.1 | |||
AK074165.1 | 6 | 1003 | BAB84991.1 | |
AL833308.2 | 11 | 2837 | CAD89924.1 | |
BC007218.1 | AAH07218.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv834678 | Chr.3:45762802 - 45968764 on Build GRCh38 | Gain | LZTFL1 CCR9 FYCO1 SLC6A20 CXCR6 |
More Information
Additional Information:
For this assay, SNP(s) [rs111480321] 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 |