IHO1
interactor of HORMAD1 1
Summary
Predicted to be involved in several processes, including meiosis I cell cycle process; regulation of homologous chromosome segregation; and spermatogenesis. Predicted to be located in chromosome. Predicted to be active in condensed nuclear chromosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6794924 | 3:49,232,014 | G/C | — | — |
| rs13091206 | 3:49,238,718 | A/T | — | — |
| rs2082923 | 3:49,255,172 | T/A | — | — |
| rs747526288 | 3:49,274,093 | G/T | — | uncertain significance |
| rs13064780 | 3:49,274,826 | T/G | intron variant | — |
| rs768220494 | 3:49,278,821 | A/G | — | uncertain significance |
| rs112015135 | 3:49,281,172 | C/G | — | — |
| rs2470804811 | 3:49,281,873 | A/C | — | uncertain significance |
| rs9861805 | 3:49,283,103 | A/G | intron variant | — |
| rs563209905 | 3:49,284,309 | C/T | — | — |
| rs2470832057 | 3:49,292,916 | G/C | — | uncertain significance |
| rs1339104598 | 3:49,293,629 | G/T | — | uncertain significance |
| rs377765889 | 3:49,293,682 | C/T | — | uncertain significance |
| rs2470834889 | 3:49,293,691 | T/G | — | uncertain significance |
| rs2046820621 | 3:49,293,715 | C/T | — | uncertain significance |
| rs757884204 | 3:49,293,748 | C/T | — | uncertain significance |
| rs765987559 | 3:49,293,751 | C/T | — | uncertain significance |
| rs972211862 | 3:49,293,850 | A/T | — | uncertain significance |
| rs537002321 | 3:49,293,931 | C/T | — | uncertain significance |
| rs200632800 | 3:49,293,942 | G/A | — | uncertain significance |
| rs148252195 | 3:49,293,954 | C/T | — | uncertain significance |
| rs565921507 | 3:49,294,024 | C/T | — | uncertain significance |
| rs147141108 | 3:49,294,039 | A/G | — | uncertain significance |
| rs2107747285 | 3:49,294,053 | C/G | — | uncertain significance |
| rs2470837403 | 3:49,294,110 | A/G | — | uncertain significance |
| rs2470837436 | 3:49,294,117 | T/C | — | uncertain significance |
| rs777816251 | 3:49,294,230 | G/A | — | uncertain significance |
| rs372304968 | 3:49,294,239 | C/T | — | uncertain significance |
| rs951835846 | 3:49,294,326 | A/G | — | uncertain significance |
| rs142093447 | 3:49,294,503 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.