CD101
CD101 molecule
Summary
Predicted to enable hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides. Predicted to be involved in cell surface receptor signaling pathway. Predicted to act upstream of or within positive regulation of myeloid leukocyte differentiation. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants75 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs779243846 | 1:117,544,447 | G/A | — | uncertain significance |
| rs148682462 | 1:117,545,835 | C/T | intron variant | — |
| rs953836951 | 1:117,552,574 | A/G | — | uncertain significance |
| rs367625011 | 1:117,552,690 | C/T | — | uncertain significance |
| rs372247398 | 1:117,552,697 | G/A | — | likely benign |
| rs945577895 | 1:117,552,738 | G/A | — | uncertain significance |
| rs150988152 | 1:117,552,805 | C/A | — | uncertain significance |
| rs1480547666 | 1:117,552,808 | A/G | — | uncertain significance |
| rs1652896781 | 1:117,554,318 | G/A | — | uncertain significance |
| rs374815004 | 1:117,554,333 | A/G | — | uncertain significance |
| rs374093963 | 1:117,554,393 | C/T | — | uncertain significance |
| rs3754112 | 1:117,554,421 | G/A | — | benign |
| rs760470424 | 1:117,554,478 | A/G | — | uncertain significance |
| rs1398611926 | 1:117,554,486 | C/A | — | uncertain significance |
| rs371618655 | 1:117,554,491 | C/A | — | uncertain significance |
| rs1451142319 | 1:117,554,535 | T/A | — | uncertain significance |
| rs1401544040 | 1:117,554,581 | G/C | — | uncertain significance |
| rs183726045 | 1:117,555,057 | A/G | intron variant | — |
| rs147095176 | 1:117,556,125 | A/G | — | likely benign |
| rs757375727 | 1:117,556,261 | G/A | — | uncertain significance |
| rs34814219 | 1:117,556,271 | T/C | — | benign |
| rs1245011373 | 1:117,556,346 | C/A | — | uncertain significance |
| rs1653036944 | 1:117,556,376 | A/G | — | uncertain significance |
| rs377516933 | 1:117,559,769 | C/T | — | uncertain significance |
| rs776869170 | 1:117,559,880 | A/T | — | uncertain significance |
| rs768501974 | 1:117,560,024 | C/G | — | uncertain significance |
| rs761625520 | 1:117,560,035 | C/T | — | uncertain significance |
| rs375148372 | 1:117,560,051 | A/G | — | uncertain significance |
| rs17235773 | 1:117,560,058 | C/G | — | benign |
| rs375022404 | 1:117,560,059 | T/C | — | uncertain significance |
| rs1429854528 | 1:117,560,077 | G/C | — | uncertain significance |
| rs575575884 | 1:117,560,089 | T/C | — | uncertain significance |
| rs192424330 | 1:117,560,779 | G/A | — | likely benign |
| rs767958842 | 1:117,560,797 | T/A | — | uncertain significance |
| rs370564335 | 1:117,560,807 | C/T | — | uncertain significance |
| rs145387761 | 1:117,560,831 | A/G | — | uncertain significance |
| rs1432023868 | 1:117,561,014 | T/A | — | uncertain significance |
| rs200402907 | 1:117,561,015 | C/T | — | uncertain significance |
| rs2526803146 | 1:117,561,020 | T/A | — | uncertain significance |
| rs116063197 | 1:117,561,030 | G/A | — | benign |
| rs750267090 | 1:117,561,048 | A/G | — | uncertain significance |
| rs755902934 | 1:117,561,069 | C/T | — | uncertain significance |
| rs1653382101 | 1:117,561,103 | C/G | — | uncertain significance |
| rs34882009 | 1:117,561,116 | T/G | — | benign |
| rs776066139 | 1:117,561,125 | C/T | — | uncertain significance |
| rs763269950 | 1:117,561,126 | G/A | — | likely benign |
| rs751714684 | 1:117,561,132 | C/T | — | uncertain significance |
| rs376092353 | 1:117,561,170 | G/T | — | uncertain significance |
| rs1653587671 | 1:117,564,244 | C/G | — | uncertain significance |
| rs377288960 | 1:117,564,272 | A/T | — | uncertain significance |
| rs141474998 | 1:117,564,288 | A/G | — | likely benign |
| rs1483372589 | 1:117,564,296 | C/A | — | uncertain significance |
| rs199628070 | 1:117,564,453 | A/T | — | uncertain significance |
| rs2101138275 | 1:117,564,479 | G/A | — | uncertain significance |
| rs200228819 | 1:117,564,491 | G/A | — | uncertain significance |
| rs147808609 | 1:117,564,544 | C/T | — | likely benign |
| rs753859485 | 1:117,564,566 | A/G | — | uncertain significance |
| rs371042116 | 1:117,568,142 | C/T | — | uncertain significance |
| rs756329414 | 1:117,568,199 | C/T | — | uncertain significance |
| rs1447144956 | 1:117,568,289 | G/A | — | uncertain significance |
| rs1317713884 | 1:117,568,331 | G/T | — | uncertain significance |
| rs779120171 | 1:117,568,349 | C/A | — | uncertain significance |
| rs534163385 | 1:117,568,351 | C/T | — | likely benign |
| rs201768380 | 1:117,568,361 | T/C | — | uncertain significance |
| rs1243826285 | 1:117,568,362 | C/T | — | uncertain significance |
| rs12093834 | 1:117,568,500 | G/A | — | benign |
| rs2526832284 | 1:117,568,504 | G/C | — | uncertain significance |
| rs138020050 | 1:117,568,510 | C/A | — | benign |
| rs146527698 | 1:117,571,397 | G/A | intron variant | — |
| rs1464469515 | 1:117,576,514 | G/C | — | uncertain significance |
| rs199980381 | 1:117,576,544 | C/T | — | uncertain significance |
| rs1654632020 | 1:117,576,559 | C/T | — | uncertain significance |
| rs34512192 | 1:117,576,612 | A/G | — | benign |
| rs34248572 | 1:117,576,631 | C/T | — | benign |
| rs775079689 | 1:117,576,689 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.