Assay Details
Target Gene Details
Entrez Gene ID: | 2304 |
Gene Name: | forkhead box E1 |
Gene Aliases: |
FKHL15, FOXE2, HFKH4, HFKL5, NMTC4, TITF2, TTF-2, TTF2 |
Location: |
Chr.9:97853255-97856715 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FOXE1 | NM_004473.3 | 1 | 3053 | NP_004464.2 |
U89995.1 | 1 | 3081 | AAC51294.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv950914 | Chr.9:97850419 - 97857618 on Build GRCh38 | Deletion | FOXE1 PTCSC2 |
nsv6627 | Chr.9:97813976 - 97858752 on Build GRCh38 | Deletion | FOXE1 PTCSC2 |
More Information
Additional Information:
For this assay, SNP(s) [rs76305281] 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 |