CIAO3
cytosolic iron-sulfur assembly component 3
Summary
Predicted to enable 4 iron, 4 sulfur cluster binding activity and metal ion binding activity. Involved in several processes, including intracellular oxygen homeostasis; iron-sulfur cluster assembly; and response to hypoxia. Part of cytosolic [4Fe-4S] assembly targeting complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201356656 | 16:780,425 | G/A | — | uncertain significance |
| rs376469524 | 16:780,439 | G/C | — | likely benign |
| rs771352387 | 16:780,446 | C/T | — | uncertain significance |
| rs765277097 | 16:780,469 | G/A | — | uncertain significance |
| rs1309269281 | 16:780,493 | T/C | — | uncertain significance |
| rs34851515 | 16:780,510 | C/T | — | benign |
| rs144802616 | 16:780,545 | C/T | — | likely benign |
| rs137994770 | 16:780,575 | C/T | — | likely benign |
| rs114620274 | 16:780,664 | G/A | — | benign |
| rs777141563 | 16:780,885 | G/A | — | uncertain significance |
| rs143356480 | 16:780,890 | C/T | — | uncertain significance |
| rs750419777 | 16:780,923 | C/T | — | uncertain significance |
| rs530672481 | 16:781,620 | C/T | — | uncertain significance |
| rs372706521 | 16:781,626 | G/A | — | uncertain significance |
| rs1169214942 | 16:781,652 | G/A | — | uncertain significance |
| rs956732494 | 16:781,665 | G/A | — | uncertain significance |
| rs1280254749 | 16:781,695 | C/T | — | likely benign |
| rs1297572992 | 16:783,310 | C/T | — | uncertain significance |
| rs780933349 | 16:783,342 | T/C | — | likely benign |
| rs144124774 | 16:783,400 | C/T | — | uncertain significance |
| rs12051245 | 16:783,865 | T/C | regulatory region variant | — |
| rs182716013 | 16:784,220 | C/T | — | likely benign |
| rs140800910 | 16:784,255 | C/G | — | uncertain significance |
| rs780075131 | 16:784,284 | C/T | — | uncertain significance |
| rs138258252 | 16:784,800 | G/A | — | uncertain significance |
| rs748256317 | 16:784,811 | C/T | — | uncertain significance |
| rs149877092 | 16:786,326 | G/A | — | uncertain significance |
| rs201910077 | 16:787,218 | C/T | — | likely benign |
| rs755304741 | 16:787,257 | T/A | — | uncertain significance |
| rs760871340 | 16:787,266 | C/T | — | uncertain significance |
| rs376966046 | 16:787,284 | C/T | — | uncertain significance |
| rs1199540910 | 16:789,665 | C/G | — | uncertain significance |
| rs766170341 | 16:789,680 | C/T | — | likely benign |
| rs8045850 | 16:789,693 | C/T | — | benign |
| rs2544197304 | 16:790,928 | G/C | — | uncertain significance |
| rs771893582 | 16:790,934 | T/A | — | uncertain significance |
| rs969700716 | 16:790,964 | C/T | — | uncertain significance |
| rs747240410 | 16:790,983 | C/A | — | uncertain significance |
| rs11648796 | 16:792,190 | A/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.