Home Details
| Official Symbol of Gene | CD44 |
| Species | Homo sapiens |
| Entrez Gene ID | 960 |
| Official Full Name | CD44 molecule (Indian blood group) |
| Also known as | IN; LHR; MC56; MDU2; MDU3; MIC4; Pgp1; CDW44; CSPG8; H-CAM; HCELL; ECM-III; HUTCH-1; HUTCH-I; ECMR-III; Hermes-1 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000026508 MIM:107269; AllianceGenome:HGNC:1681 |
| Map Location | 11p13 |
| Variation Type | N/A |
| refSNP ID | rs1467558 |
| Detected Sample | Peripheral blood |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | 364 Norwegian MS patients |
| Pubmed ID | 16764945 |
| Year | 2006 |
| Title | Coding region polymorphisms in T cell signal transduction genes.Prevalence and association to development of multiple sclerosis |
| Risk Type | Disease risk |
| Main Result | Typing the 41 SNPs with functioning DCE assay (Fischer and Lerman, 1983) in the pooled Norwegian controls (n= 4000) demonstrated that 16 of these (39%) were heterozygous in the Norwegian population , four of these displaying a minor allele frequency of less than 1% |
| Result | Heterozygosity (HZ) in 4000 controls |
| Mechanism/Pathway | Genes that control T cell activation downstream of the initial presentation of peptide antigen by HLA molecules may be regarded as prime candidate susceptibility genes in T cell mediated autoimmune diseases, such as MS |

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