Home Details
| Official Symbol of Gene | SP3 |
| Species | Homo sapiens |
| Entrez Gene ID | 6670 |
| Official Full Name | Sp3 transcription factor |
| Also known as | SPR2 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000172845 MIM:601804; AllianceGenome:HGNC:11208 |
| Map Location | 2q31.1 |
| Detected Sample | PBMC |
| Sample Detail | N/A |
| Detected Method | Southern blot, PCR |
| Disease | MS |
| Disease subtype | RRMS, SPMS |
| Population | N/A |
| Sample Size | 10 MS patients/ 8 healthycontrols |
| Pubmed ID | 10814800 |
| Year | 2000 |
| Title | Localization of the human SP3 gene to chromosome 7p14-p15.2. The lack of expression in multiple sclerosis does not reflect abnormal gene organization |
| Expression | No significance |
| Risk type | Disease risk |
| Result | Southern blot and polymerase chain reaction analysis of genomic DNA failed to demonstrate a detectable difference between MS and control PBMC. |
| Mechanism/Pathway | Sp3 belongs to a family of human transcription factors that bind GC/T box elements in order to either activate or repress transcription.MS is a putative autoimmune disease of the central nervous system (CNS) that exhibits both a genetic predisposition and evidence for an environmental infuence on susceptibility to the diseaseThe abnormal suppression of Sp3 expression in MS immune cells could well play a role in the control of the level of responsiveness of these cells. |

2023,CopyRight © HMU. College of Bioinformatics Science and Technology, Harbin, China.