SHISA6
shisa family member 6
Summary
Predicted to enable ionotropic glutamate receptor binding activity. Predicted to be involved in several processes, including excitatory chemical synaptic transmission; modulation of chemical synaptic transmission; and negative regulation of canonical Wnt signaling pathway. Predicted to be located in asymmetric, glutamatergic, excitatory synapse. Predicted to be part of AMPA glutamate receptor complex. Predicted to be active in dendritic spine membrane; glutamatergic synapse; and postsynaptic density membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1311805105 | 17:11,144,786 | C/T | — | uncertain significance |
| rs2543878107 | 17:11,144,833 | A/C | — | uncertain significance |
| rs2543878158 | 17:11,144,845 | A/C | — | uncertain significance |
| rs1466784964 | 17:11,144,846 | G/A | — | uncertain significance |
| rs1447301344 | 17:11,144,847 | T/G | — | uncertain significance |
| rs2543878220 | 17:11,144,864 | T/G | — | uncertain significance |
| rs973732956 | 17:11,144,882 | G/T | — | uncertain significance |
| rs1025822279 | 17:11,144,885 | G/A | — | uncertain significance |
| rs1458571854 | 17:11,144,900 | G/A | — | uncertain significance |
| rs2543878396 | 17:11,144,929 | G/T | — | uncertain significance |
| rs1197806433 | 17:11,144,947 | G/T | — | uncertain significance |
| rs775356615 | 17:11,144,948 | C/T | — | uncertain significance |
| rs768475439 | 17:11,144,960 | G/A | — | uncertain significance |
| rs2543878547 | 17:11,144,984 | C/T | — | uncertain significance |
| rs2543878590 | 17:11,144,996 | G/A | — | uncertain significance |
| rs1236709904 | 17:11,145,142 | G/A | — | uncertain significance |
| rs746771281 | 17:11,145,177 | G/T | — | uncertain significance |
| rs1907367303 | 17:11,145,218 | C/G | — | uncertain significance |
| rs2543900197 | 17:11,166,721 | C/G | — | uncertain significance |
| rs556309080 | 17:11,166,814 | C/T | — | uncertain significance |
| rs775491766 | 17:11,166,822 | C/T | — | uncertain significance |
| rs748761383 | 17:11,166,823 | G/A | — | uncertain significance |
| rs11650183 | 17:11,183,340 | G/T | — | — |
| rs8066969 | 17:11,197,243 | A/G | downstream gene variant | — |
| rs11650677 | 17:11,231,513 | G/A | intron variant | — |
| rs8076431 | 17:11,250,219 | C/T | — | — |
| rs1364757514 | 17:11,282,749 | C/T | — | uncertain significance |
| rs1015551061 | 17:11,282,771 | T/A | — | uncertain significance |
| rs1877644 | 17:11,342,608 | G/A | intron variant | — |
| rs4792143 | 17:11,385,890 | C/T | intron variant | — |
| rs2969180 | 17:11,407,901 | G/C | — | — |
| rs9911694 | 17:11,455,627 | C/T | intron variant | — |
| rs1422174780 | 17:11,459,120 | G/A | — | uncertain significance |
| rs536845860 | 17:11,461,107 | G/A | — | uncertain significance |
| rs760817325 | 17:11,461,131 | G/A | — | uncertain significance |
| rs199505983 | 17:11,461,191 | G/A | — | uncertain significance |
| rs779366882 | 17:11,461,197 | G/A | — | uncertain significance |
| rs1011806682 | 17:11,461,208 | C/T | — | uncertain significance |
| rs1221026141 | 17:11,461,214 | A/G | — | uncertain significance |
| rs1366123077 | 17:11,461,230 | T/C | — | uncertain significance |
| rs2544149898 | 17:11,461,251 | T/C | — | uncertain significance |
| rs1045705429 | 17:11,461,292 | G/A | — | uncertain significance |
| rs775370703 | 17:11,461,295 | G/A | — | uncertain significance |
| rs192374370 | 17:11,461,317 | G/A | — | uncertain significance |
| rs374985257 | 17:11,461,383 | G/A | — | uncertain significance |
| rs2072000586 | 17:11,461,392 | C/T | — | uncertain significance |
| rs1305585738 | 17:11,461,403 | G/A | — | uncertain significance |
| rs768771153 | 17:11,461,421 | G/A | — | uncertain significance |
| rs909393956 | 17:11,461,431 | G/A | — | uncertain significance |
| rs938069258 | 17:11,461,437 | G/T | — | uncertain significance |
| rs2544150287 | 17:11,461,452 | A/G | — | uncertain significance |
| rs2544150300 | 17:11,461,458 | A/G | — | uncertain significance |
| rs527767172 | 17:11,461,484 | G/A | — | uncertain significance |
| rs767092219 | 17:11,461,523 | G/A | — | uncertain significance |
| rs1017388600 | 17:11,461,582 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.