APCDD1L
APC down-regulated 1 like
Summary
Predicted to enable Wnt-protein binding activity. Predicted to be involved in negative regulation of Wnt signaling pathway. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs199504715 | 20:57,035,860 | G/A | — | uncertain significance |
| rs201769185 | 20:57,035,971 | C/T | — | uncertain significance |
| rs780551687 | 20:57,036,001 | G/T | — | uncertain significance |
| rs771169748 | 20:57,036,033 | G/A | — | uncertain significance |
| rs371147444 | 20:57,036,067 | C/T | — | uncertain significance |
| rs149312027 | 20:57,036,069 | A/G | — | uncertain significance |
| rs757702271 | 20:57,036,090 | A/G | — | uncertain significance |
| rs78418340 | 20:57,036,118 | C/T | — | uncertain significance |
| rs2516092943 | 20:57,036,148 | G/C | — | uncertain significance |
| rs760246702 | 20:57,036,150 | G/A | — | uncertain significance |
| rs1241764943 | 20:57,036,205 | C/T | — | uncertain significance |
| rs750909228 | 20:57,036,211 | C/G | — | uncertain significance |
| rs200688452 | 20:57,036,313 | C/T | — | uncertain significance |
| rs763585294 | 20:57,036,333 | G/A | — | uncertain significance |
| rs1213711254 | 20:57,036,465 | A/G | — | uncertain significance |
| rs1371452278 | 20:57,036,480 | A/G | — | uncertain significance |
| rs752591174 | 20:57,036,547 | C/T | — | uncertain significance |
| rs894992227 | 20:57,036,565 | C/A | — | uncertain significance |
| rs41307189 | 20:57,036,570 | C/T | — | uncertain significance |
| rs746369561 | 20:57,036,604 | C/T | — | uncertain significance |
| rs1438540639 | 20:57,036,607 | G/A | — | uncertain significance |
| rs1459187259 | 20:57,042,167 | C/A | — | uncertain significance |
| rs374426833 | 20:57,042,181 | C/T | — | likely benign |
| rs1465609057 | 20:57,042,412 | G/A | — | uncertain significance |
| rs1448255918 | 20:57,042,427 | G/T | — | uncertain significance |
| rs1414739296 | 20:57,042,469 | A/C | — | uncertain significance |
| rs748068500 | 20:57,042,481 | G/A | — | uncertain significance |
| rs1274389051 | 20:57,042,487 | C/T | — | uncertain significance |
| rs2516101774 | 20:57,042,580 | C/A | — | uncertain significance |
| rs2516101820 | 20:57,042,596 | A/G | — | uncertain significance |
| rs201380039 | 20:57,042,647 | G/C | — | uncertain significance |
| rs1252163001 | 20:57,042,656 | G/A | — | uncertain significance |
| rs754613379 | 20:57,042,659 | T/A | — | uncertain significance |
| rs1482097793 | 20:57,042,703 | C/A | — | uncertain significance |
| rs2516105099 | 20:57,045,689 | A/G | — | uncertain significance |
| rs199788439 | 20:57,045,693 | G/A | — | uncertain significance |
| rs199697401 | 20:57,045,726 | C/A | — | uncertain significance |
| rs573179097 | 20:57,045,728 | G/T | — | uncertain significance |
| rs375466344 | 20:57,045,758 | C/T | — | likely benign |
| rs763906482 | 20:57,045,761 | A/G | — | uncertain significance |
| rs562721222 | 20:57,045,774 | C/T | — | uncertain significance |
| rs771121433 | 20:57,089,727 | C/A | — | uncertain significance |
| rs1183983452 | 20:57,089,757 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.