LMAN1L
lectin, mannose binding 1 like
Summary
This gene encodes a mannose-binding type 1 transmembrane protein that contains an N-terminal lectin-like carbohydrate recognition domain. The encoded protein is similar in structure to lectins found in leguminous plants. This lectin is thought to transport newly synthesized glycoproteins from the endoplasmic reticulum (ER) to the ER-Golgi intermediate compartment. [provided by RefSeq, Jan 2017]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs373850264 | 15:75,105,203 | C/T | — | likely benign |
| rs562811750 | 15:75,105,227 | T/C | — | uncertain significance |
| rs2505672918 | 15:75,105,242 | T/G | — | uncertain significance |
| rs771170114 | 15:75,105,250 | G/A | — | uncertain significance |
| rs777887951 | 15:75,105,343 | G/A | — | uncertain significance |
| rs112987086 | 15:75,106,719 | G/C | — | — |
| rs752475983 | 15:75,108,501 | C/T | — | uncertain significance |
| rs762943182 | 15:75,108,507 | T/A | — | uncertain significance |
| rs775944695 | 15:75,108,606 | T/C | — | uncertain significance |
| rs1471656721 | 15:75,108,621 | C/T | — | uncertain significance |
| rs374569087 | 15:75,108,627 | T/G | — | uncertain significance |
| rs768191587 | 15:75,108,808 | T/C | — | uncertain significance |
| rs1386161428 | 15:75,108,841 | G/T | — | uncertain significance |
| rs2505678907 | 15:75,111,075 | G/A | — | uncertain significance |
| rs147581891 | 15:75,111,156 | C/T | — | uncertain significance |
| rs202021967 | 15:75,111,574 | G/A | — | uncertain significance |
| rs1344279841 | 15:75,111,587 | T/A | — | uncertain significance |
| rs2505679579 | 15:75,111,592 | G/A | — | uncertain significance |
| rs115735578 | 15:75,112,459 | T/A | upstream gene variant | — |
| rs780746803 | 15:75,113,013 | G/A | — | uncertain significance |
| rs748905874 | 15:75,113,032 | A/C | — | uncertain significance |
| rs530877348 | 15:75,113,443 | C/T | — | uncertain significance |
| rs1165704643 | 15:75,113,457 | C/T | — | uncertain significance |
| rs138585415 | 15:75,113,460 | C/G | — | uncertain significance |
| rs369514887 | 15:75,113,478 | C/T | — | uncertain significance |
| rs781165467 | 15:75,113,479 | G/A | — | likely benign |
| rs372870036 | 15:75,113,505 | G/A | — | uncertain significance |
| rs1035160545 | 15:75,113,559 | G/A | — | uncertain significance |
| rs2141116836 | 15:75,114,237 | A/G | — | likely benign |
| rs199936512 | 15:75,115,043 | G/A | — | uncertain significance |
| rs764242763 | 15:75,115,913 | C/T | — | uncertain significance |
| rs543907196 | 15:75,115,914 | G/A | — | likely benign |
| rs373380418 | 15:75,115,934 | G/A | — | uncertain significance |
| rs746735462 | 15:75,116,013 | G/A | — | likely benign |
| rs193921107 | 15:75,116,706 | G/T | — | uncertain significance |
| rs756762410 | 15:75,116,728 | C/A | — | uncertain significance |
| rs2505686067 | 15:75,116,753 | A/G | — | likely benign |
| rs909490238 | 15:75,117,835 | C/A | — | likely benign |
| rs532637190 | 15:75,117,852 | C/T | — | uncertain significance |
| rs758083986 | 15:75,117,897 | C/G | — | uncertain significance |
| rs201085437 | 15:75,117,920 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.