SEZ6L
seizure related 6 homolog like
Summary
Predicted to be involved in synapse maturation. Predicted to act upstream of or within activation of protein kinase C activity; adult locomotory behavior; and cerebellar Purkinje cell layer development. Predicted to be located in endoplasmic reticulum membrane. Predicted to be active in several cellular components, including glutamatergic synapse; neuronal cell body; and postsynaptic membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants84 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs972076408 | 22:26,565,643 | C/T | — | uncertain significance |
| rs2517433089 | 22:26,565,651 | C/A | — | uncertain significance |
| rs527371769 | 22:26,565,679 | C/G | — | uncertain significance |
| rs4822691 | 22:26,627,142 | C/T | intron variant | — |
| rs1207393 | 22:26,653,362 | C/T | — | — |
| rs373985470 | 22:26,688,383 | G/A | — | uncertain significance |
| rs2081161542 | 22:26,688,483 | C/T | — | uncertain significance |
| rs145637105 | 22:26,688,484 | G/A | — | likely benign |
| rs752005755 | 22:26,688,539 | A/G | — | uncertain significance |
| rs867362972 | 22:26,688,546 | C/T | — | uncertain significance |
| rs372902970 | 22:26,688,559 | C/G | — | uncertain significance |
| rs748983148 | 22:26,688,560 | G/A | — | uncertain significance |
| rs760566198 | 22:26,688,582 | T/C | — | uncertain significance |
| rs144766472 | 22:26,688,621 | C/G | — | uncertain significance |
| rs545994093 | 22:26,688,650 | G/A | — | uncertain significance |
| rs370632181 | 22:26,688,806 | G/A | — | uncertain significance |
| rs374087121 | 22:26,688,811 | G/T | — | uncertain significance |
| rs2081181671 | 22:26,688,858 | C/G | — | uncertain significance |
| rs141695407 | 22:26,688,864 | C/G | — | uncertain significance |
| rs756013990 | 22:26,688,869 | G/A | — | uncertain significance |
| rs2517634834 | 22:26,688,950 | G/T | — | uncertain significance |
| rs992371326 | 22:26,688,971 | G/T | — | uncertain significance |
| rs772690714 | 22:26,689,004 | A/T | — | uncertain significance |
| rs753670484 | 22:26,689,031 | G/A | — | uncertain significance |
| rs201779919 | 22:26,689,053 | A/G | — | uncertain significance |
| rs193920876 | 22:26,689,055 | G/T | — | uncertain significance |
| rs760398959 | 22:26,689,100 | G/A | — | uncertain significance |
| rs688034 | 22:26,689,635 | C/T | intron variant | — |
| rs766360176 | 22:26,690,299 | G/T | — | uncertain significance |
| rs200380172 | 22:26,690,308 | G/A | — | uncertain significance |
| rs372813703 | 22:26,690,309 | A/T | — | uncertain significance |
| rs112422707 | 22:26,692,922 | C/T | — | benign |
| rs759752155 | 22:26,692,966 | G/A | — | uncertain significance |
| rs1197271533 | 22:26,692,980 | A/G | — | uncertain significance |
| rs148526431 | 22:26,692,999 | G/A | — | uncertain significance |
| rs146559583 | 22:26,693,026 | C/A | — | uncertain significance |
| rs150343251 | 22:26,695,072 | A/G | — | uncertain significance |
| rs663048 | 22:26,695,077 | G/A | missense variant | — |
| rs591044 | 22:26,697,195 | T/C | intron variant | — |
| rs761270884 | 22:26,701,984 | G/A | — | uncertain significance |
| rs1189230337 | 22:26,702,001 | T/C | — | likely benign |
| rs193920909 | 22:26,706,631 | G/A | — | uncertain significance |
| rs770508545 | 22:26,706,652 | G/A | — | uncertain significance |
| rs199770989 | 22:26,706,681 | C/T | — | likely benign |
| rs117917851 | 22:26,706,697 | G/A | — | benign |
| rs142214073 | 22:26,706,743 | G/A | — | likely benign |
| rs201153704 | 22:26,706,745 | A/G | — | benign |
| rs190114018 | 22:26,706,755 | C/T | — | uncertain significance |
| rs774078967 | 22:26,706,769 | C/T | — | uncertain significance |
| rs201841723 | 22:26,706,773 | C/T | — | uncertain significance |
| rs140029399 | 22:26,706,780 | C/T | — | benign |
| rs142677073 | 22:26,707,818 | T/A | — | uncertain significance |
| rs773884340 | 22:26,707,863 | C/T | — | uncertain significance |
| rs1388368175 | 22:26,709,757 | T/C | — | uncertain significance |
| rs752901613 | 22:26,709,789 | G/A | — | uncertain significance |
| rs1178392073 | 22:26,709,808 | A/C | — | uncertain significance |
| rs1371320486 | 22:26,709,816 | A/G | — | likely benign |
| rs150114413 | 22:26,709,847 | G/A | — | uncertain significance |
| rs767495936 | 22:26,736,418 | A/G | — | uncertain significance |
| rs780374550 | 22:26,736,439 | G/A | — | uncertain significance |
| rs773150235 | 22:26,736,442 | G/A | — | uncertain significance |
| rs200138174 | 22:26,736,486 | C/G | — | uncertain significance |
| rs149869184 | 22:26,743,689 | A/G | — | benign |
| rs200745477 | 22:26,743,751 | A/T | — | uncertain significance |
| rs768459906 | 22:26,743,804 | G/A | — | uncertain significance |
| rs144838560 | 22:26,743,829 | C/T | — | uncertain significance |
| rs116806899 | 22:26,743,866 | A/T | — | benign |
| rs760443816 | 22:26,747,096 | C/T | — | uncertain significance |
| rs2083266010 | 22:26,747,155 | T/C | — | uncertain significance |
| rs2517745200 | 22:26,747,166 | A/C | — | uncertain significance |
| rs747914181 | 22:26,747,206 | G/A | — | uncertain significance |
| rs1476101944 | 22:26,747,219 | G/A | — | likely benign |
| rs2517769182 | 22:26,761,401 | A/C | — | uncertain significance |
| rs146313552 | 22:26,761,444 | C/T | — | likely benign |
| rs752023482 | 22:26,761,479 | G/A | — | uncertain significance |
| rs575877260 | 22:26,761,515 | C/A | — | uncertain significance |
| rs202010195 | 22:26,769,441 | C/T | — | uncertain significance |
| rs731276 | 22:26,770,390 | A/T | — | — |
| rs376385912 | 22:26,771,550 | C/A | — | uncertain significance |
| rs200000489 | 22:26,771,574 | G/T | — | uncertain significance |
| rs2517791424 | 22:26,773,712 | G/A | — | uncertain significance |
| rs761582151 | 22:26,773,740 | G/A | — | uncertain significance |
| rs115519582 | 22:26,776,228 | G/A | — | benign |
| rs542926685 | 22:26,778,086 | G/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.