LNX2
ligand of numb-protein X 2
Summary
Predicted to enable ubiquitin-protein transferase activity. Predicted to act upstream of or within neural precursor cell proliferation and neuron differentiation. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs551533909 | 13:28,120,962 | T/C | — | — |
| rs1421578167 | 13:28,122,543 | C/T | — | uncertain significance |
| rs1015064895 | 13:28,122,546 | G/C | — | uncertain significance |
| rs151176870 | 13:28,122,557 | C/T | — | uncertain significance |
| rs1005954431 | 13:28,122,560 | A/C | — | uncertain significance |
| rs113728980 | 13:28,122,785 | C/T | intron variant | — |
| rs770157240 | 13:28,124,480 | C/T | — | uncertain significance |
| rs2500187487 | 13:28,124,570 | A/G | — | uncertain significance |
| rs1566114523 | 13:28,127,389 | A/C | — | uncertain significance |
| rs777596691 | 13:28,130,376 | T/C | — | uncertain significance |
| rs115119970 | 13:28,130,473 | G/A | — | benign |
| rs1164768124 | 13:28,130,480 | C/T | — | uncertain significance |
| rs771032990 | 13:28,133,984 | G/A | — | uncertain significance |
| rs779509627 | 13:28,134,058 | A/G | — | uncertain significance |
| rs189923982 | 13:28,134,097 | G/A | — | uncertain significance |
| rs1192844073 | 13:28,134,098 | T/C | — | uncertain significance |
| rs2500235984 | 13:28,136,551 | T/C | — | uncertain significance |
| rs200248301 | 13:28,136,595 | G/T | — | uncertain significance |
| rs148429804 | 13:28,136,609 | C/T | — | uncertain significance |
| rs918257505 | 13:28,136,623 | T/C | — | uncertain significance |
| rs1050832471 | 13:28,136,633 | G/C | — | uncertain significance |
| rs143349167 | 13:28,136,660 | C/A | — | uncertain significance |
| rs2500237159 | 13:28,136,694 | A/C | — | uncertain significance |
| rs1470313686 | 13:28,136,815 | A/C | — | uncertain significance |
| rs1251500616 | 13:28,136,818 | C/T | — | uncertain significance |
| rs773673654 | 13:28,136,861 | G/C | — | uncertain significance |
| rs2500238781 | 13:28,136,896 | T/C | — | uncertain significance |
| rs770273316 | 13:28,141,829 | T/C | — | uncertain significance |
| rs142458399 | 13:28,141,934 | G/A | — | uncertain significance |
| rs765099031 | 13:28,141,976 | G/A | — | uncertain significance |
| rs758811088 | 13:28,143,204 | A/C | — | uncertain significance |
| rs373989400 | 13:28,143,208 | C/T | — | uncertain significance |
| rs772974167 | 13:28,143,232 | G/A | — | uncertain significance |
| rs61753155 | 13:28,143,234 | G/A | — | uncertain significance |
| rs780607318 | 13:28,143,280 | A/C | — | uncertain significance |
| rs137868420 | 13:28,143,312 | G/A | — | likely benign |
| rs781355332 | 13:28,143,346 | T/C | — | uncertain significance |
| rs370971924 | 13:28,143,413 | T/C | — | likely benign |
| rs766573794 | 13:28,155,579 | G/A | — | uncertain significance |
| rs755896884 | 13:28,155,605 | T/C | — | uncertain significance |
| rs1156429662 | 13:28,155,617 | C/T | — | uncertain significance |
| rs1253288781 | 13:28,155,653 | G/A | — | uncertain significance |
| rs116991985 | 13:28,155,831 | T/C | — | uncertain significance |
| rs9512755 | 13:28,158,229 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.