Assay Details
Target Gene Details
Entrez Gene ID: | 7392 |
Gene Name: | upstream transcription factor 2, c-fos interacting |
Gene Aliases: |
FIP, bHLHb12 |
Location: |
Chr.19:35268978-35279821 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 4 - Exon 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
USF2 | NM_001321150.1 | NP_001308079.1 | ||
NM_003367.3 | NP_003358.1 | |||
NM_207291.2 | NP_997174.1 | |||
XM_005259197.3 | XP_005259254.1 | |||
XM_011527260.2 | XP_011525562.1 | |||
XM_011527261.2 | XP_011525563.1 | |||
XM_017027199.1 | XP_016882688.1 | |||
AK297022.1 | ||||
AY147880.1 | AAN63092.1 | |||
BC049821.1 | AAH49821.1 | |||
CR536504.1 | CAG38742.1 | |||
M77476.1 | ||||
S50537.1 | AAB24368.1 | |||
X90824.1 | CAA62339.1 | |||
X90825.1 | CAA62340.1 | |||
X90826.1 | CAA62341.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv579396 | Chr.19:35268614 - 35272793 on Build GRCh38 | Gain | USF2 |
esv2758758 | Chr.19:35220175 - 35396211 on Build GRCh38 | Loss | FAM187B LSR FFAR3 FFAR1 HAMP USF2 MIR5196 CD22 MAG |
nsv953283 | Chr.19:35247998 - 35314097 on Build GRCh38 | Deletion | LSR HAMP USF2 MAG |
nsv510765 | Chr.19:35217323 - 35399766 on Build GRCh38 | Deletion | FAM187B LSR FFAR3 FFAR1 HAMP USF2 MIR5196 CD22 MAG |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |