Home Details
| Official Symbol of Gene | CLEC16A |
| Species | Homo sapiens |
| Entrez Gene ID | 29013 |
| Official Full Name | C-type lectin domain containing 16A |
| Also known as | Gop-1; KIAA0350 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000038532 MIM:611303; AllianceGenome:HGNC:29013 |
| Map Location | 16p13.13 |
| Variation Type | SNP |
| refSNP ID | rs8056098 |
| Detected Sample | brain |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | 179 MS cases |
| Pubmed ID | 31228212 |
| Year | 2020 |
| Title | Post-mortem multiple sclerosis lesion pathology is influenced by single nucleotide polymorphisms |
| Risk Type | Disease risk |
| Main Result | Positive |
| Result | Three SNPs linked to MS clinical severity showed a significant association between the genotype and either the proportion of active lesions (rs2234978/FAS and rs11957313/KCNIP1) or the proportion of mixed active/inactive lesions (rs8056098/CLEC16A) |
| Mechanism/Pathway | This is in part because of the difficulty in the functional translation of genotype into disease-relevant mechanisms |

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