Genomic Map
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Target Gene Details
Entrez Gene ID: | 11326 |
Gene Name: | V-set and immunoglobulin domain containing 4 |
Gene Aliases: |
CRIg, Z39IG |
Location: |
Chr.X:66021738-66040125 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| VSIG4 | NM_001100431.1 | 7 | 1135 | NP_001093901.1 |
| NM_001184830.1 | 7 | 1757 | NP_001171759.1 | |
| NM_001184831.1 | 6 | 1475 | NP_001171760.1 | |
| NM_001257403.1 | NP_001244332.1 | |||
| NM_007268.2 | 8 | 1417 | NP_009199.1 | |
| XM_017029251.1 | XP_016884740.1 | |||
| AJ132502.1 | 8 | 1335 | CAB51536.1 | |
| AK075153.1 | 8 | 1372 | ||
| AK075171.1 | 8 | 1399 | ||
| AK293215.1 | 8 | 1311 | ||
| AK301417.1 | 7 | 1090 | ||
| AL542949.3 | ||||
| AY358341.1 | 7 | 1748 | AAQ88707.1 | |
| BC010525.1 | 8 | 1293 | AAH10525.1 | |
| CA310184.1 | 1 | 452 | ||
| CA405669.1 | 1 | 273 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv6933 | Chr.X:66003429 - 66036427 on Build GRCh38 | Insertion |
 MIR223
VSIG4
|
| esv3576919 | Chr.X:65837678 - 66804698 on Build GRCh38 | Gain |
EDA2R
MIR223
HEPH
VSIG4
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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