CRISPLD2
cysteine rich secretory protein LCCL domain containing 2
Summary
Predicted to enable glycosaminoglycan binding activity. Involved in face morphogenesis. Located in transport vesicle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants88 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2131754 | 16:84,857,345 | A/G | regulatory region variant | — |
| rs2131755 | 16:84,857,378 | A/G | regulatory region variant | — |
| rs187750301 | 16:84,867,987 | C/T | intron variant | — |
| rs1546124 | 16:84,872,051 | G/C | 5 prime UTR variant | — |
| rs1395574123 | 16:84,872,151 | T/G | — | uncertain significance |
| rs147872508 | 16:84,872,166 | G/A | — | likely benign |
| rs139901174 | 16:84,872,182 | C/T | — | likely benign |
| rs965984074 | 16:84,872,195 | G/C | missense variant | — |
| rs1473008847 | 16:84,872,204 | C/T | — | uncertain significance |
| rs906789199 | 16:84,872,259 | G/C | — | uncertain significance |
| rs760678386 | 16:84,872,264 | G/T | — | uncertain significance |
| rs138134389 | 16:84,872,303 | G/A | — | uncertain significance |
| rs750062740 | 16:84,872,308 | G/T | — | uncertain significance |
| rs201061137 | 16:84,872,327 | A/G | — | uncertain significance |
| rs1881725990 | 16:84,879,431 | G/C | — | uncertain significance |
| rs184717285 | 16:84,879,457 | G/A | — | likely benign |
| rs2507674169 | 16:84,879,492 | T/C | — | uncertain significance |
| rs1203623828 | 16:84,879,497 | G/A | — | uncertain significance |
| rs2507674187 | 16:84,879,500 | C/T | — | uncertain significance |
| rs550003217 | 16:84,882,984 | C/T | — | likely benign |
| rs775437927 | 16:84,882,996 | G/A | — | uncertain significance |
| rs138518275 | 16:84,882,997 | C/T | — | likely benign |
| rs1293006248 | 16:84,883,001 | C/G | — | uncertain significance |
| rs140214661 | 16:84,883,003 | G/C | — | likely benign |
| rs145249439 | 16:84,883,053 | C/T | — | uncertain significance |
| rs138500867 | 16:84,883,063 | C/A | — | likely benign |
| rs780473680 | 16:84,883,077 | G/C | — | uncertain significance |
| rs2507679485 | 16:84,883,097 | G/A | — | uncertain significance |
| rs34925006 | 16:84,884,200 | C/T | — | benign |
| rs143085896 | 16:84,884,217 | C/G | — | uncertain significance |
| rs368719942 | 16:84,884,223 | G/A | — | uncertain significance |
| rs757246124 | 16:84,884,230 | G/C | — | uncertain significance |
| rs147475865 | 16:84,884,254 | G/A | — | likely benign |
| rs572744640 | 16:84,884,257 | C/T | — | likely benign |
| rs4782675 | 16:84,888,310 | C/T | downstream gene variant | — |
| rs754183179 | 16:84,888,340 | A/C | — | uncertain significance |
| rs2507687725 | 16:84,888,361 | A/G | — | uncertain significance |
| rs145328449 | 16:84,888,372 | C/T | — | uncertain significance |
| rs111454381 | 16:84,888,407 | C/T | — | benign |
| rs2646128 | 16:84,888,442 | A/G | — | benign |
| rs144759316 | 16:84,895,651 | C/T | intron variant | — |
| rs60910901 | 16:84,896,257 | A/G | regulatory region variant | — |
| rs150433030 | 16:84,900,577 | C/G | — | uncertain significance |
| rs1458330703 | 16:84,900,580 | G/A | — | uncertain significance |
| rs114234975 | 16:84,900,601 | A/G | — | benign |
| rs569725982 | 16:84,900,608 | C/G | — | uncertain significance |
| rs778905360 | 16:84,900,626 | C/A | — | uncertain significance |
| rs149615348 | 16:84,900,645 | G/A | missense variant | likely benign |
| rs148934412 | 16:84,902,472 | G/A | missense variant | — |
| rs544311455 | 16:84,906,043 | G/A | — | likely benign |
| rs533386261 | 16:84,906,092 | T/C | — | uncertain significance |
| rs1313039468 | 16:84,906,112 | A/G | — | uncertain significance |
| rs184877327 | 16:84,906,114 | C/T | — | benign |
| rs1597471122 | 16:84,906,640 | G/T | — | uncertain significance |
| rs34582606 | 16:84,906,645 | C/T | — | benign |
| rs548735529 | 16:84,906,647 | A/T | — | uncertain significance |
| rs536109763 | 16:84,906,668 | C/T | — | uncertain significance |
| rs762791289 | 16:84,906,693 | C/T | — | likely benign |
| rs201353419 | 16:84,906,694 | G/A | — | uncertain significance |
| rs143175101 | 16:84,906,696 | G/A | — | likely benign |
| rs182246977 | 16:84,907,219 | A/G | intron variant | — |
| rs7194957 | 16:84,907,521 | A/C | — | benign |
| rs370914708 | 16:84,907,552 | T/C | — | likely benign |
| rs983454189 | 16:84,907,563 | G/C | — | uncertain significance |
| rs140729826 | 16:84,911,035 | C/T | — | benign |
| rs757572271 | 16:84,911,060 | C/T | — | likely benign |
| rs35049212 | 16:84,911,093 | A/G | — | benign |
| rs183935383 | 16:84,914,002 | C/T | intron variant | — |
| rs763668278 | 16:84,914,143 | G/A | — | uncertain significance |
| rs139975503 | 16:84,914,177 | A/G | — | benign |
| rs35711987 | 16:84,914,186 | C/G | — | benign |
| rs111425745 | 16:84,914,197 | A/C | — | likely benign |
| rs200162804 | 16:84,914,211 | A/G | — | likely benign |
| rs182202972 | 16:84,914,217 | A/G | — | likely benign |
| rs772176109 | 16:84,922,847 | C/G | — | uncertain significance |
| rs759125995 | 16:84,922,867 | C/T | — | uncertain significance |
| rs140282295 | 16:84,922,868 | G/A | — | likely benign |
| rs750921409 | 16:84,922,882 | A/G | — | uncertain significance |
| rs758255060 | 16:84,922,899 | G/A | — | uncertain significance |
| rs981292423 | 16:84,922,917 | G/C | — | uncertain significance |
| rs201807614 | 16:84,922,933 | A/G | — | uncertain significance |
| rs767869124 | 16:84,922,935 | G/T | — | uncertain significance |
| rs8051626 | 16:84,934,006 | C/A | — | — |
| rs750379944 | 16:84,940,208 | G/A | — | uncertain significance |
| rs754640127 | 16:84,940,225 | C/T | — | uncertain significance |
| rs147087796 | 16:84,940,226 | G/A | — | uncertain significance |
| rs4783099 | 16:84,941,329 | C/T | regulatory region variant | — |
| rs16974880 | 16:84,942,638 | T/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.