ANKRD6
ankyrin repeat domain 6
Summary
Predicted to be involved in negative regulation of canonical Wnt signaling pathway; positive regulation of JNK cascade; and protein targeting to chloroplast. Predicted to act upstream of or within positive regulation of Wnt signaling pathway, planar cell polarity pathway. Located in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants69 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs369619069 | 6:90,276,717 | G/A | — | uncertain significance |
| rs1343872070 | 6:90,276,751 | A/T | — | uncertain significance |
| rs759408013 | 6:90,276,780 | C/T | — | uncertain significance |
| rs2534260729 | 6:90,276,783 | A/C | — | uncertain significance |
| rs6939321 | 6:90,299,210 | T/C | regulatory region variant | — |
| rs6454764 | 6:90,310,966 | T/C | intron variant | — |
| rs756145375 | 6:90,312,770 | G/A | — | uncertain significance |
| rs367690340 | 6:90,312,806 | C/T | — | uncertain significance |
| rs16881983 | 6:90,315,771 | C/T | stop gained | benign |
| rs61744890 | 6:90,315,776 | A/G | — | benign |
| rs3748085 | 6:90,315,789 | A/G | missense variant | benign |
| rs773293420 | 6:90,315,810 | C/G | — | uncertain significance |
| rs1286741568 | 6:90,322,027 | A/C | — | uncertain significance |
| rs1380765057 | 6:90,322,030 | C/T | — | uncertain significance |
| rs377367109 | 6:90,322,044 | G/A | — | likely benign |
| rs753650260 | 6:90,322,045 | C/T | — | uncertain significance |
| rs530838661 | 6:90,322,048 | G/A | — | uncertain significance |
| rs879053748 | 6:90,322,069 | C/T | — | uncertain significance |
| rs376144287 | 6:90,322,070 | G/A | — | uncertain significance |
| rs575602422 | 6:90,323,521 | C/A | — | uncertain significance |
| rs372154960 | 6:90,323,532 | G/A | — | uncertain significance |
| rs774393712 | 6:90,323,539 | C/T | — | uncertain significance |
| rs375469086 | 6:90,323,540 | G/A | — | likely benign |
| rs369598670 | 6:90,323,541 | C/T | — | uncertain significance |
| rs572932842 | 6:90,323,554 | T/G | — | uncertain significance |
| rs199717338 | 6:90,323,559 | A/G | — | uncertain significance |
| rs372121493 | 6:90,323,568 | C/T | — | uncertain significance |
| rs369158321 | 6:90,326,288 | C/A | — | uncertain significance |
| rs778628274 | 6:90,326,337 | C/G | — | uncertain significance |
| rs771678178 | 6:90,326,349 | C/T | — | likely benign |
| rs2273238 | 6:90,326,360 | C/T | missense variant | benign |
| rs774591302 | 6:90,327,700 | C/T | — | uncertain significance |
| rs375720646 | 6:90,327,701 | G/T | — | uncertain significance |
| rs756231723 | 6:90,327,712 | A/G | — | uncertain significance |
| rs570167442 | 6:90,327,716 | C/G | — | uncertain significance |
| rs367712968 | 6:90,327,743 | C/T | — | uncertain significance |
| rs569364324 | 6:90,331,647 | C/T | — | uncertain significance |
| rs762446880 | 6:90,333,136 | T/C | — | uncertain significance |
| rs371124170 | 6:90,333,217 | C/T | — | uncertain significance |
| rs17292811 | 6:90,333,599 | A/G | — | benign |
| rs759042899 | 6:90,333,612 | A/G | — | uncertain significance |
| rs778318877 | 6:90,333,663 | A/C | — | uncertain significance |
| rs1435788424 | 6:90,333,729 | T/C | — | uncertain significance |
| rs375712466 | 6:90,333,750 | C/T | — | uncertain significance |
| rs757199599 | 6:90,333,751 | G/A | — | uncertain significance |
| rs1234779284 | 6:90,334,277 | G/A | — | uncertain significance |
| rs1804952692 | 6:90,334,318 | G/T | — | uncertain significance |
| rs117917298 | 6:90,334,363 | A/C | — | uncertain significance |
| rs199619988 | 6:90,334,376 | A/G | — | uncertain significance |
| rs374681275 | 6:90,334,400 | C/T | — | uncertain significance |
| rs61736690 | 6:90,337,302 | A/C | missense variant | benign |
| rs200093363 | 6:90,337,366 | G/A | — | uncertain significance |
| rs186353748 | 6:90,338,839 | G/C | — | uncertain significance |
| rs201996863 | 6:90,338,844 | A/T | — | uncertain significance |
| rs9353687 | 6:90,338,863 | T/C | — | benign |
| rs9362667 | 6:90,340,187 | G/A | missense variant | benign |
| rs764493548 | 6:90,340,254 | A/C | — | uncertain significance |
| rs3210511 | 6:90,340,276 | G/A | — | benign |
| rs756061883 | 6:90,340,287 | G/A | — | uncertain significance |
| rs201701344 | 6:90,340,309 | C/A | — | uncertain significance |
| rs766315115 | 6:90,340,346 | G/A | — | uncertain significance |
| rs61739327 | 6:90,340,446 | C/T | missense variant | benign |
| rs61739328 | 6:90,340,447 | C/T | — | benign |
| rs370260550 | 6:90,340,448 | G/A | — | likely benign |
| rs61739325 | 6:90,340,454 | A/G | — | likely benign |
| rs368515909 | 6:90,340,599 | T/C | — | uncertain significance |
| rs367621106 | 6:90,340,637 | C/A | — | uncertain significance |
| rs61745976 | 6:90,340,645 | G/A | — | benign |
| rs9344950 | 6:90,340,734 | G/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.