| 1 | FMF, MEFV, MID1, MID2, PML, TRIM10, TRIM11, TRIM13, TRIM15, TRIM17, TRIM2, TRIM21, TRIM22, TRIM23, TRIM24, TRIM25, TRIM26, TRIM27, TRIM28, TRIM3, TRIM31, TRIM32, TRIM33, TRIM34, TRIM35, TRIM36, TRIM37, TRIM38, TRIM39, TRIM4, TRIM40, TRIM41, TRIM42, TRIM43, TRIM45, TRIM46, TRIM47, TRIM48, TRIM49, TRIM5, TRIM50, TRIM52, TRIM53, TRIM54, TRIM55, TRIM56, TRIM58, TRIM59, TRIM6, TRIM60, TRIM61, TRIM62, TRIM63, TRIM64, TRIM65, TRIM67, TRIM68, TRIM69, TRIM7, TRIM71, TRIM72, TRIM73, TRIM74, TRIM75, TRIM8, TRIM9, TRIML1 |
| TRIM family proteins and their emerging roles in innate immunity. | |
| Ozato K, Shin DM, Chang TH, Morse HC 3rd. | |
| Nat Rev Immunol 8(11):849-60. Review. 2008 | |
| 2 | MID1, MID2 |
| MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders. | |
| Short KM, Hopwood B, Yi Z, Cox TC. | |
| BMC Cell Biol 3:1. Epub 2002 Jan 4. 2002 | |
| 3 | MID1, MID2 |
| MID2, a homologue of the opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development. | |
| Buchner G, et al. | |
| Hum Mol Genet 8(8):1397-407. 1999 | |
| 4 | MID1, MID2 |
| FXY2/MID2, a gene related to the X-linked opitz syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules. | |
| Perry J, Short KM, Romer JT, Swift S, Cox TC, Ashworth A. | |
| Genomics 62(3):385-94 1999 | |