Genomic Map
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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 | 5321 | NP_001231737.1 |
| NM_001244810.1 | 21 | 5269 | NP_001231739.1 | |
| NM_001244812.1 | 16 | 4621 | NP_001231741.1 | |
| NM_001244813.1 | 15 | 4513 | NP_001231742.1 | |
| NM_001244814.1 | 17 | 5018 | NP_001231743.1 | |
| NM_001244815.1 | 16 | 4959 | NP_001231744.1 | |
| NM_001244816.1 | 20 | 5126 | NP_001231745.1 | |
| NM_032682.5 | 21 | 5221 | NP_116071.2 | |
| XM_006713102.2 | 20 | 5182 | XP_006713165.1 | |
| XM_011533584.2 | 21 | 5292 | XP_011531886.1 | |
| XM_011533585.2 | 20 | 5144 | XP_011531887.1 | |
| XM_017006165.1 | 20 | 5063 | XP_016861654.1 |
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
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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