IGSF5
immunoglobulin superfamily member 5
Summary
Predicted to enable PDZ domain binding activity. Predicted to be involved in cell-cell adhesion. Predicted to be located in apical plasma membrane. Predicted to be active in bicellular tight junction and cell surface. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2837148 | 21:41,118,783 | G/C | — | — |
| rs1735151 | 21:41,123,301 | T/C | intron variant | — |
| rs2837156 | 21:41,126,687 | T/C | intron variant | — |
| rs759511517 | 21:41,137,495 | C/A | — | uncertain significance |
| rs372378189 | 21:41,137,531 | G/A | — | uncertain significance |
| rs1372851339 | 21:41,137,549 | C/T | — | uncertain significance |
| rs111477785 | 21:41,137,566 | A/C | — | uncertain significance |
| rs371108598 | 21:41,137,602 | G/A | — | likely benign |
| rs199738172 | 21:41,137,635 | C/T | — | uncertain significance |
| rs112166899 | 21:41,137,689 | A/T | — | uncertain significance |
| rs1016371789 | 21:41,137,693 | A/G | — | uncertain significance |
| rs2516922504 | 21:41,137,698 | G/A | — | uncertain significance |
| rs1217761342 | 21:41,137,762 | C/T | — | uncertain significance |
| rs575362025 | 21:41,137,767 | C/G | — | uncertain significance |
| rs201139705 | 21:41,142,884 | G/A | — | likely benign |
| rs117910095 | 21:41,143,070 | G/A | — | uncertain significance |
| rs772007235 | 21:41,143,077 | C/T | — | uncertain significance |
| rs1018351 | 21:41,149,521 | T/G | — | — |
| rs774315775 | 21:41,151,044 | G/A | — | uncertain significance |
| rs756212768 | 21:41,151,062 | C/T | — | uncertain significance |
| rs371965247 | 21:41,151,131 | C/T | — | uncertain significance |
| rs569416566 | 21:41,151,132 | G/A | — | likely benign |
| rs749337072 | 21:41,151,137 | C/T | — | uncertain significance |
| rs199672249 | 21:41,151,173 | G/A | — | uncertain significance |
| rs764698988 | 21:41,151,214 | T/C | — | uncertain significance |
| rs145234708 | 21:41,160,100 | G/A | — | uncertain significance |
| rs1352961128 | 21:41,164,011 | G/C | — | uncertain significance |
| rs148668253 | 21:41,165,479 | C/T | — | uncertain significance |
| rs7278863 | 21:41,165,708 | G/A | intron variant | — |
| rs371000620 | 21:41,173,189 | C/T | — | uncertain significance |
| rs146703590 | 21:41,173,222 | C/T | — | uncertain significance |
| rs375213364 | 21:41,173,225 | C/G | — | uncertain significance |
| rs201807214 | 21:41,173,249 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.