CLDN10
claudin 10
Summary
This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The expression level of this gene is associated with recurrence of primary hepatocellular carcinoma. Six alternatively spliced transcript variants encoding different isoforms have been reported, but the transcript sequences of some variants are not determined.[provided by RefSeq, Jun 2010]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9584304 | 13:96,085,685 | T/C | — | benign |
| rs115306504 | 13:96,085,880 | C/A | — | benign |
| rs3751334 | 13:96,086,010 | A/G | — | benign |
| rs760145374 | 13:96,086,188 | C/T | — | uncertain significance |
| rs7333503 | 13:96,086,480 | C/T | — | benign |
| rs75607197 | 13:96,107,386 | G/A | — | — |
| rs78446689 | 13:96,109,784 | G/A | regulatory region variant | — |
| rs74475970 | 13:96,109,807 | A/G | regulatory region variant | — |
| rs76260959 | 13:96,116,805 | G/A | intron variant | — |
| rs17268442 | 13:96,127,958 | C/T | downstream gene variant | — |
| rs2095774 | 13:96,130,395 | C/A | downstream gene variant | — |
| rs9525016 | 13:96,193,271 | G/C | — | — |
| rs9516602 | 13:96,199,409 | G/A | regulatory region variant | — |
| rs2277421 | 13:96,204,808 | G/A | — | benign |
| rs930701747 | 13:96,205,009 | T/C | missense variant | pathogenic |
| rs759535516 | 13:96,205,042 | T/C | — | uncertain significance |
| rs1157773336 | 13:96,205,069 | T/C | — | uncertain significance |
| rs747253181 | 13:96,205,134 | G/T | — | uncertain significance |
| rs2501666796 | 13:96,205,145 | G/A | — | pathogenic |
| rs2501666805 | 13:96,205,149 | A/C | — | likely pathogenic |
| rs759408749 | 13:96,205,151 | C/G | missense variant | pathogenic |
| rs142907955 | 13:96,205,205 | C/A | — | uncertain significance |
| rs113108501 | 13:96,205,333 | T/C | — | benign |
| rs1886855 | 13:96,205,359 | A/C | — | benign |
| rs34449921 | 13:96,212,393 | A/C | — | benign |
| rs1188481980 | 13:96,212,407 | G/A | — | uncertain significance |
| rs371976897 | 13:96,212,421 | G/T | — | uncertain significance |
| rs375663820 | 13:96,212,436 | T/C | — | uncertain significance |
| rs374567220 | 13:96,212,483 | C/T | — | uncertain significance |
| rs771988001 | 13:96,212,523 | G/T | — | uncertain significance |
| rs760346005 | 13:96,212,536 | T/C | — | uncertain significance |
| rs1555299783 | 13:96,212,645 | C/T | — | pathogenic |
| rs79906565 | 13:96,212,655 | A/C | — | benign |
| rs387907413 | 13:96,212,673 | C/A | — | uncertain significance |
| rs374187735 | 13:96,212,684 | C/T | — | uncertain significance |
| rs201348784 | 13:96,229,525 | G/T | — | uncertain significance |
| rs2043947900 | 13:96,229,574 | A/G | — | uncertain significance |
| rs778343896 | 13:96,230,191 | C/T | — | uncertain significance |
| rs114813638 | 13:96,230,201 | A/G | — | uncertain significance |
| rs1489951611 | 13:96,230,230 | A/C | — | uncertain significance |
| rs1325774 | 13:96,230,279 | T/G | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.