ANKFN1
ankyrin repeat and fibronectin type III domain containing 1
Summary
Predicted to be involved in establishment of mitotic spindle orientation and regulation of establishment of bipolar cell polarity. Predicted to act upstream of or within behavioral fear response; equilibrioception; and locomotor rhythm. Predicted to be active in spindle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2060070 | 17:54,123,973 | G/A | intergenic variant | — |
| rs72829706 | 17:54,173,733 | A/G | intergenic variant | — |
| rs1431318 | 17:54,192,523 | A/C | — | — |
| rs7209324 | 17:54,194,519 | A/T | — | — |
| rs17819973 | 17:54,198,297 | T/A | intron variant | — |
| rs8065311 | 17:54,203,360 | G/T | intron variant | — |
| rs56335503 | 17:54,203,655 | G/C | — | — |
| rs143623822 | 17:54,230,874 | G/C | — | uncertain significance |
| rs4281786 | 17:54,260,251 | A/T | — | — |
| rs60891864 | 17:54,273,598 | C/G | intron variant | — |
| rs1019238 | 17:54,278,715 | G/A | intron variant | — |
| rs12602509 | 17:54,287,565 | T/C | intron variant | — |
| rs12453947 | 17:54,299,101 | C/T | intron variant | — |
| rs9900375 | 17:54,392,114 | T/A | — | — |
| rs763266295 | 17:54,403,586 | G/A | — | uncertain significance |
| rs781099215 | 17:54,403,594 | A/T | — | uncertain significance |
| rs758080488 | 17:54,403,620 | G/A | — | uncertain significance |
| rs866640368 | 17:54,403,670 | C/A | — | uncertain significance |
| rs1283573053 | 17:54,428,177 | A/G | — | uncertain significance |
| rs200776343 | 17:54,428,188 | C/T | — | uncertain significance |
| rs747095155 | 17:54,428,193 | T/G | — | uncertain significance |
| rs768663674 | 17:54,428,195 | C/T | — | uncertain significance |
| rs538479637 | 17:54,428,216 | C/T | — | uncertain significance |
| rs368152107 | 17:54,428,221 | C/T | — | uncertain significance |
| rs745655072 | 17:54,428,267 | C/A | — | uncertain significance |
| rs773925251 | 17:54,428,296 | A/G | — | uncertain significance |
| rs775181306 | 17:54,428,311 | C/T | — | uncertain significance |
| rs12449568 | 17:54,430,155 | C/T | intron variant | — |
| rs746200763 | 17:54,431,295 | C/G | — | uncertain significance |
| rs2544688573 | 17:54,431,332 | G/A | — | uncertain significance |
| rs2544735778 | 17:54,450,042 | A/G | — | uncertain significance |
| rs2544735922 | 17:54,450,064 | A/G | — | uncertain significance |
| rs755305438 | 17:54,450,068 | G/T | — | uncertain significance |
| rs2046844505 | 17:54,450,100 | A/C | — | uncertain significance |
| rs533848014 | 17:54,451,965 | C/T | — | uncertain significance |
| rs552321362 | 17:54,451,988 | T/A | — | uncertain significance |
| rs915504830 | 17:54,474,009 | C/A | — | — |
| rs192906563 | 17:54,490,736 | A/T | intron variant | — |
| rs570241750 | 17:54,500,622 | G/A | — | — |
| rs7211753 | 17:54,514,805 | G/A | intron variant | — |
| rs1367696385 | 17:54,517,754 | C/T | — | uncertain significance |
| rs2049156003 | 17:54,520,231 | G/T | — | uncertain significance |
| rs145617071 | 17:54,520,268 | C/T | — | uncertain significance |
| rs773243312 | 17:54,520,274 | C/T | — | uncertain significance |
| rs963379506 | 17:54,526,471 | A/T | — | uncertain significance |
| rs149587422 | 17:54,526,533 | A/G | — | uncertain significance |
| rs368025457 | 17:54,526,536 | A/G | — | uncertain significance |
| rs370040478 | 17:54,534,248 | C/A | — | uncertain significance |
| rs957728897 | 17:54,534,249 | G/A | — | uncertain significance |
| rs1176192803 | 17:54,534,715 | A/T | — | uncertain significance |
| rs1183991258 | 17:54,535,311 | A/C | — | uncertain significance |
| rs776346849 | 17:54,543,730 | C/T | — | uncertain significance |
| rs749177645 | 17:54,554,883 | G/A | — | uncertain significance |
| rs1420345473 | 17:54,558,078 | A/G | — | uncertain significance |
| rs751537629 | 17:54,558,133 | T/C | — | uncertain significance |
| rs752860469 | 17:54,558,165 | A/G | — | uncertain significance |
| rs1330943563 | 17:54,559,758 | G/C | — | uncertain significance |
| rs944125767 | 17:54,559,873 | A/G | — | uncertain significance |
| rs546366691 | 17:54,569,629 | C/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.