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: | Within Exon 11 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
USF2 | NM_001321150.1 | 8 | 974 | NP_001308079.1 |
NM_003367.3 | 10 | 1367 | NP_003358.1 | |
NM_207291.2 | 9 | 1166 | NP_997174.1 | |
XM_005259197.3 | 9 | 1358 | XP_005259254.1 | |
XM_017027199.1 | 8 | 1157 | XP_016882688.1 | |
AI240594.1 | ||||
BC049821.1 | 10 | 1280 | AAH49821.1 | |
M77476.1 | 7 | 967 | ||
S50537.1 | 6 | 907 | AAB24368.1 | |
X90824.1 | 8 | 1082 | CAA62339.1 | |
X90825.1 | 9 | 1151 | CAA62340.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2758758 | Chr.19:35220175 - 35396211 on Build GRCh38 | Loss | FAM187B FFAR3 LSR MAG FFAR1 CD22 HAMP MIR5196 USF2 |
nsv953283 | Chr.19:35247998 - 35314097 on Build GRCh38 | Deletion | LSR MAG HAMP USF2 |
nsv510765 | Chr.19:35217323 - 35399766 on Build GRCh38 | Deletion | FAM187B FFAR3 LSR MAG FFAR1 CD22 HAMP MIR5196 USF2 |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |