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| Official Symbol of Gene | TAGAP |
| Species | Homo sapiens |
| Entrez Gene ID | 117289 |
| Official Full Name | T cell activation RhoGTPase activating protein |
| Also known as | FKSG15; IDDM21; TAGAP1; ARHGAP47 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000164691 MIM:609667; AllianceGenome:HGNC:15669 |
| Map Location | 6q25.3 |
| Detected Sample | peripheral blood |
| Sample Detail | NA |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | RRMS/PPMS/SPMS/CIS |
| Population | Germany, North Rhine-Westphalia |
| Sample Size | 141 MS |
| Pubmed ID | 25620546 |
| Year | 2014 |
| Title | Multiple sclerosis risk loci correlate with cervical cord atrophy and may explain the course of disability |
| Expression | up-regulation |
| Risk type | Phenotypic risk |
| Result | For nine loci—BATF, CYP27B1, IL12B, NFKB1,IL7, PLEK, EVI5, TAGAP and nrs669607—patients revealed significantly higher degree of atrophy; TYK2, RGS1 and CLEC16A revealed inverse effects. The weighted genetic risk score over the twelve loci showed significant correlation with MUCCA. |
| Mechanism/Pathway | We genotyped 141 MS patients for 58 variations re-ported to reach significance in GW AS. Expanded disability status scale (EDSS) and disease duration (DD) are available from regular clinical examinations. |

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