CCDC85C
coiled-coil domain containing 85C
Summary
Predicted to be involved in cerebral cortex development. Predicted to act upstream of or within several processes, including Notch signaling pathway; establishment of cell polarity; and radial glial cell differentiation. Located in adherens junction and nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs766385345 | 14:99,981,591 | G/A | — | uncertain significance |
| rs1244982581 | 14:99,981,611 | G/A | — | uncertain significance |
| rs895199409 | 14:99,981,624 | G/A | — | uncertain significance |
| rs376773544 | 14:99,982,570 | C/A | — | uncertain significance |
| rs983184896 | 14:99,982,580 | C/A | — | uncertain significance |
| rs534603051 | 14:99,983,482 | G/T | — | likely benign |
| rs987239593 | 14:99,983,501 | G/C | — | uncertain significance |
| rs574014725 | 14:99,983,505 | C/T | — | uncertain significance |
| rs1409805803 | 14:99,983,507 | G/A | — | uncertain significance |
| rs747601740 | 14:99,983,516 | G/A | — | likely benign |
| rs377060982 | 14:99,988,552 | G/A | — | uncertain significance |
| rs2504075333 | 14:99,988,554 | G/A | — | likely benign |
| rs1013959265 | 14:100,002,357 | C/A | — | uncertain significance |
| rs80071266 | 14:100,028,474 | C/T | intron variant | — |
| rs1318325539 | 14:100,069,531 | G/A | — | uncertain significance |
| rs2055225462 | 14:100,069,567 | G/A | — | uncertain significance |
| rs2055225741 | 14:100,069,581 | T/C | — | uncertain significance |
| rs1305122749 | 14:100,069,609 | G/C | — | uncertain significance |
| rs2504202096 | 14:100,069,623 | G/A | — | uncertain significance |
| rs866814055 | 14:100,069,626 | G/A | — | uncertain significance |
| rs940604765 | 14:100,069,631 | G/T | — | uncertain significance |
| rs1426582205 | 14:100,069,731 | G/T | — | uncertain significance |
| rs568971842 | 14:100,069,786 | C/T | — | uncertain significance |
| rs2055232564 | 14:100,069,830 | G/A | — | uncertain significance |
| rs2055232731 | 14:100,069,839 | T/C | — | uncertain significance |
| rs1001188990 | 14:100,069,861 | C/T | — | uncertain significance |
| rs1707023975 | 14:100,069,977 | C/A | — | uncertain significance |
| rs2055237195 | 14:100,070,052 | T/C | — | uncertain significance |
| rs551860394 | 14:100,070,202 | G/A | — | uncertain significance |
| rs750511462 | 14:100,070,256 | T/A | — | uncertain significance |
| rs1281949461 | 14:100,070,266 | C/A | — | uncertain significance |
| rs1366750011 | 14:100,070,278 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.