Home Details
| Official Symbol of Gene | DBP |
| Species | Homo sapiens |
| Entrez Gene ID | 1628 |
| Official Full Name | D-box binding PAR bZIP transcription factor |
| Also known as | DABP; taxREB302 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000105516 MIM:124097; AllianceGenome:HGNC:2697 |
| Map Location | 19q13.33 |
| Variation Type | polymorphisms |
| refSNP ID | N/A |
| Detected Sample | peripheral blood |
| Sample Detail | N/A |
| Detected Method | microsatellite markers |
| Disease | MS |
| Disease subtype | N/A |
| Population | Canadian |
| Sample Size | 236 sibling pairs from 187 families |
| Pubmed ID | 10680811 |
| Year | 2000 |
| Title | Genetic analysis of vitamin D related genes in Canadian multiple sclerosis patients. Canadian Collaborative Study Group |
| Risk Type | Disease risk |
| Main Result | Negative |
| Result | Within the DBP gene, TDT analysis of the HaeIII and StyI genotypes showed no preferential transmission of any allele to affected offspring. |
| Mechanism/Pathway | A high prevalence of vitamin D deficiency has been demonstrated in MS patients.DBP is involved in the metabolism and function of vitamin D. |

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