GMNC
geminin coiled-coil domain containing
Summary
Predicted to enable chromatin binding activity. Predicted to be involved in negative regulation of cell cycle and regulation of DNA-templated DNA replication initiation. Predicted to act upstream of or within several processes, including cerebrospinal fluid circulation; multi-ciliated epithelial cell differentiation; and seminiferous tubule development. Predicted to be located in extracellular region. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants22 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2474638847 | 3:190,573,116 | A/G | — | uncertain significance |
| rs2474638987 | 3:190,573,199 | G/A | — | uncertain significance |
| rs932803761 | 3:190,573,297 | G/T | — | uncertain significance |
| rs1186763421 | 3:190,573,349 | C/A | — | uncertain significance |
| rs371940723 | 3:190,573,364 | G/A | — | uncertain significance |
| rs2474639683 | 3:190,573,630 | T/G | — | uncertain significance |
| rs543732026 | 3:190,573,662 | A/G | — | uncertain significance |
| rs2108531983 | 3:190,575,600 | A/G | — | uncertain significance |
| rs1308451021 | 3:190,575,613 | G/C | — | uncertain significance |
| rs201964563 | 3:190,575,660 | T/A | — | uncertain significance |
| rs772589916 | 3:190,575,661 | C/T | — | uncertain significance |
| rs1043079134 | 3:190,575,672 | A/G | — | uncertain significance |
| rs745393906 | 3:190,576,724 | T/C | — | uncertain significance |
| rs1370738906 | 3:190,576,728 | T/C | — | uncertain significance |
| rs1231082884 | 3:190,576,781 | G/A | — | uncertain significance |
| rs2474644046 | 3:190,576,794 | C/T | — | uncertain significance |
| rs183159491 | 3:190,578,569 | C/T | — | uncertain significance |
| rs201469606 | 3:190,578,589 | G/T | — | uncertain significance |
| rs1737846719 | 3:190,578,590 | G/A | — | uncertain significance |
| rs1322225445 | 3:190,578,592 | C/T | — | uncertain significance |
| rs761367896 | 3:190,578,607 | C/T | — | uncertain significance |
| rs4577513 | 3:190,578,743 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.