ALCAM
activated leukocyte cell adhesion molecule
Summary
This gene encodes activated leukocyte cell adhesion molecule (ALCAM), also known as CD166 (cluster of differentiation 166), which is a member of a subfamily of immunoglobulin receptors with five immunoglobulin-like domains (VVC2C2C2) in the extracellular domain. This protein binds to T-cell differentiation antigene CD6, and is implicated in the processes of cell adhesion and migration. Multiple alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, Aug 2011]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6437585 | 3:105,086,085 | C/T | regulatory region variant | — |
| rs10511244 | 3:105,182,533 | T/C | intron variant | — |
| rs77876308 | 3:105,192,464 | A/T | regulatory region variant | — |
| rs2472620019 | 3:105,238,930 | A/C | — | likely benign |
| rs371732188 | 3:105,238,977 | T/C | — | uncertain significance |
| rs147777853 | 3:105,243,201 | C/T | — | benign |
| rs759732563 | 3:105,243,203 | A/T | — | uncertain significance |
| rs141090189 | 3:105,243,209 | C/T | — | benign |
| rs191774794 | 3:105,243,227 | T/C | — | uncertain significance |
| rs537535274 | 3:105,243,256 | A/G | — | uncertain significance |
| rs2472626434 | 3:105,243,343 | A/C | — | uncertain significance |
| rs530196302 | 3:105,250,884 | T/G | — | uncertain significance |
| rs775373645 | 3:105,252,455 | C/G | — | uncertain significance |
| rs76635565 | 3:105,252,481 | A/T | — | uncertain significance |
| rs1402660874 | 3:105,252,492 | A/G | — | uncertain significance |
| rs144172449 | 3:105,253,507 | C/T | — | likely benign |
| rs770238326 | 3:105,253,521 | T/C | — | uncertain significance |
| rs200414406 | 3:105,253,528 | A/G | — | uncertain significance |
| rs761194368 | 3:105,253,539 | C/T | — | uncertain significance |
| rs1271704282 | 3:105,253,615 | C/G | — | uncertain significance |
| rs2472641838 | 3:105,253,620 | T/A | — | uncertain significance |
| rs79951414 | 3:105,253,631 | T/C | — | benign |
| rs991922265 | 3:105,258,832 | G/C | — | uncertain significance |
| rs35248527 | 3:105,258,850 | G/A | — | benign |
| rs765730707 | 3:105,258,866 | A/G | — | uncertain significance |
| rs2472650986 | 3:105,260,493 | T/G | — | uncertain significance |
| rs774291073 | 3:105,260,499 | G/T | — | uncertain significance |
| rs1044243 | 3:105,260,520 | C/T | missense variant | benign |
| rs199921428 | 3:105,260,522 | G/C | — | uncertain significance |
| rs201124902 | 3:105,260,580 | T/C | — | uncertain significance |
| rs766963393 | 3:105,264,099 | G/A | — | uncertain significance |
| rs139344282 | 3:105,264,155 | G/T | — | benign |
| rs34926152 | 3:105,264,176 | G/A | missense variant | — |
| rs145462175 | 3:105,266,355 | C/T | — | likely benign |
| rs2472663809 | 3:105,269,076 | A/G | — | uncertain significance |
| rs3772543 | 3:105,269,442 | A/G | intron variant | — |
| rs75636202 | 3:105,271,004 | C/T | — | likely benign |
| rs1372071296 | 3:105,271,005 | G/A | — | uncertain significance |
| rs759678619 | 3:105,271,351 | T/C | — | uncertain significance |
| rs142584625 | 3:105,271,401 | G/A | — | uncertain significance |
| rs9830049 | 3:105,284,045 | T/C | intron variant | — |
| rs1384891758 | 3:105,290,734 | T/C | — | uncertain significance |
| rs11559013 | 3:105,294,502 | G/T | — | — |
| rs1157 | 3:105,295,461 | G/A | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.