CC2D2B
coiled-coil and C2 domain containing 2B
Summary
Predicted to be involved in non-motile cilium assembly and protein localization to ciliary transition zone. Predicted to be active in ciliary transition zone. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9919426 | 10:97,680,969 | G/C | — | — |
| rs201173034 | 10:97,687,018 | T/C | — | likely benign |
| rs753655014 | 10:97,697,822 | G/C | — | likely benign |
| rs41291590 | 10:97,721,616 | G/A | — | likely benign |
| rs143284507 | 10:97,736,574 | C/T | intron variant | — |
| rs146883214 | 10:97,741,780 | C/T | — | likely benign |
| rs117203733 | 10:97,758,385 | A/G | upstream gene variant | — |
| rs376825763 | 10:97,769,607 | G/T | — | uncertain significance |
| rs2496544177 | 10:97,769,675 | T/C | — | uncertain significance |
| rs373755580 | 10:97,772,362 | G/A | — | uncertain significance |
| rs2496608642 | 10:97,773,551 | A/T | — | uncertain significance |
| rs2496609528 | 10:97,773,609 | G/C | — | uncertain significance |
| rs1365787368 | 10:97,775,964 | A/G | — | uncertain significance |
| rs200962424 | 10:97,775,977 | T/C | — | uncertain significance |
| rs747173131 | 10:97,776,043 | T/C | — | uncertain significance |
| rs768630692 | 10:97,776,058 | C/T | — | uncertain significance |
| rs749151504 | 10:97,778,975 | G/A | — | uncertain significance |
| rs373032981 | 10:97,778,976 | T/C | — | uncertain significance |
| rs1293387192 | 10:97,779,015 | C/G | — | uncertain significance |
| rs774903800 | 10:97,779,026 | C/A | — | uncertain significance |
| rs764293033 | 10:97,779,472 | T/G | — | uncertain significance |
| rs116882651 | 10:97,783,706 | C/T | intron variant | — |
| rs2079625636 | 10:97,784,623 | T/C | — | uncertain significance |
| rs2496770342 | 10:97,784,646 | A/T | — | uncertain significance |
| rs753440139 | 10:97,791,716 | A/G | — | uncertain significance |
| rs372192636 | 10:97,791,737 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.