Assay Details
Target Gene Details
Entrez Gene ID: | 51297 |
Gene Name: | BPI fold containing family A member 1 |
Gene Aliases: |
LUNX, NASG, PLUNC, SPLUNC1, SPURT, bA49G10.5 |
Location: |
Chr.20:33235996-33243309 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 1 - Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BPIFA1 | NM_001243193.1 | NP_001230122.1 | ||
| NM_016583.3 | NP_057667.1 | |||
| NM_130852.2 | NP_570913.1 | |||
| AB024937.1 | BAA93633.1 | |||
| AF158745.1 | AAF82622.1 | |||
| AF172993.1 | AAF70860.1 | |||
| AF417256.1 | AAO12198.1 | |||
| AF417257.1 | AAO12199.1 | |||
| AF439448.1 | AAL87636.1 | |||
| AK292778.1 | ||||
| AY359020.1 | AAQ89379.1 | |||
| BC012549.1 | AAH12549.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1056411 | Chr.20:32469234 - 33355029 on Build GRCh38 | Loss |
|
| esv2751912 | Chr.20:33179619 - 33248657 on Build GRCh38 | Loss |
|
| nsv1060241 | Chr.20:33172902 - 33244962 on Build GRCh38 | Loss |
|
More Information
Set Membership: |
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Genomic Map