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| Official Symbol of Gene | ICAM1 |
| Species | Homo sapiens |
| Entrez Gene ID | 3383 |
| Official Full Name | intercellular adhesion molecule 1 |
| Also known as | BB2; CD54; P3.58 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000090339 MIM:147840; AllianceGenome:HGNC:5344 |
| Map Location | 19p13.2 |
| Variation Type | Allele |
| refSNP ID | NA |
| Detected Sample | Peripheral blood |
| Sample Detail | NA |
| Detected Method | RT-PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | NA |
| Sample Size | NA |
| Pubmed ID | 9667594 |
| Year | 1998 |
| Title | Multiple Sclerosis: The Increased Frequency of the ICAM-1 Exon 6 Gene Point Mutation Genetic Type K469 |
| Risk Type | Disease risk |
| Main Result | Positive |
| Result | The results indicate increased frequency of ICAM-1 exon 6 allele T in MS patients, which may contribute to the MS genetics background. |
| Mechanism/Pathway | Intracellular adhesion molecule-1 (ICAM-1) plays an important role in the cascade of adhesion events in the homing of inflammatory cells to the central nervous system (CNS) in experimental autoimmune encephalomyelitis (EAE) and in multiple sclerosis (MS). |

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