Assay Details
Target Gene Details
Entrez Gene ID: | 27086 |
Gene Name: | forkhead box P1 |
Gene Aliases: |
12CC4, HSPC215, MFH, QRF1, hFKH1B |
Location: |
Chr.3:70954714-71583989 on Build GRCh38 |
Assay Gene Location: | Within Exon 32 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FOXP1 | NM_001244808.1 | 21 | 5037 | NP_001231737.1 |
NM_001244810.1 | 21 | 4985 | NP_001231739.1 | |
NM_001244812.1 | 16 | 4337 | NP_001231741.1 | |
NM_001244813.1 | 15 | 4229 | NP_001231742.1 | |
NM_001244814.1 | 17 | 4734 | NP_001231743.1 | |
NM_001244815.1 | 16 | 4675 | NP_001231744.1 | |
NM_001244816.1 | 20 | 4842 | NP_001231745.1 | |
NM_032682.5 | 21 | 4937 | NP_116071.2 | |
XM_006713102.2 | 20 | 4898 | XP_006713165.1 | |
XM_011533584.2 | 21 | 5008 | XP_011531886.1 | |
XM_011533585.2 | 20 | 4860 | XP_011531887.1 | |
XM_017006165.1 | 20 | 4779 | XP_016861654.1 | |
AF250920.1 | 20 | 4842 | AAL56661.1 | |
AK026898.1 | 1 | 1737 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv834727 | Chr.3:70884108 - 71058881 on Build GRCh38 | Loss | FOXP1 |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |