From: Formin homology 2 domains occur in multiple contexts in angiosperms
Gene | Organism | Class | Closest relatives | Gene | Organism | Class | Closest relatives |
---|---|---|---|---|---|---|---|
BvFH1 | Beta vulgaris | I | AtFH5 107/202 (52%) | NbFH6 | N. benthamiana | Ic | NbFH1 47/48 (97%); AtFH5 41/48 (85%) |
GaFH1 | Gossypium arboreum | Ic | AtFH5 131/172 (76%) | NbFH7 | N. benthamiana | Ia | NtFH2 154/181 (85%); AtFH1 60/188 (31%) |
GaFH2 | G. arboreum | Ia | MtFH1 116/171 (67%); AtFH1 105/169 (62%) | NtFH1 | Nicotiana tabacum | Ia* | StFH4 177/218 (81%); AtFH1 216/293 (73%) |
GhFH1 | Gossypium hirsutum | I | SpFH1 89/109 (81%); AtFH1 144/197 (73%) | NtFH2 | N. tabacum | Ia* | AtFH1 313/474 (66%) |
GhFH2 | G. hirsutum | Ib | LeFH1 165/227 (72%); AtFH6 158/221 (71%) | NtFH3 | N. tabacum | Ic | AtFH5 109/156 (69%) |
GmFH1 | Glycine max | II* | MtFH5 113/133 (84%); AtFH13 182/278 (65%) | NtFH4 | N. tabacum | II | GmFH1 105/165 (63%); AtFH13 97/195 (49%) |
GmFH2 | G. max | IIa | OsFH3 136/161 (84%); AtFH14 132/161 (81%) | NtFH5 | N. tabacum | Ic | StFH5 58/87 (66%); AtFH5 36/50 (72%) |
GmFH3 | G. max | II | AtFH18 125/153 (81%) | NtFH6 | N. tabacum | I | StFH5 71/150 (47%); AtFH3 56/153 (36%) |
GmFH4 | G. max | Ia | MtFH1 98/107 (91%); AtFH1 88/105 (83%) | OsFH1 | Oryza sativa | I* | SpFH1 180/205 (87%); AtFH1 299/442 (67%) |
GmFH5 | G. max | I | StFH4 77/125 (61%); AtFH1 75/112 (66%) | OsFH2 | O. sativa | Id* | AtFH11 227/409 (55%) |
GmFH6 | G. max | Ic | LeFH3 103/141 (73%); AtFH5 97/142 (68%) | OsFH3 | O. sativa | IIa* | GmFH2 136/160 (85%); AtFH14 303/461 (65%) |
HvFH1 | Hordeum vulgare | II | OsFH5 190/217 (87%); AtFH18 146/217 (67%) | OsFH4 | O. sativa | Ib* | OsFH8 373/495 (75%); AtFH6 292/486 (60%) |
HvFH2 | H. vulgare | I | OsFH13 144/168 (85%); AtFH6 114/164 (69%) | OsFH5 | O. sativa | II* | HvFH1 190/217 (87%); AtFH20 259/445 (58%) |
HvFH3 | H. vulgare | I | OsFH13 177/237 (74%); AtFH6 121/227 (53%) | OsFH6 | O. sativa | II* | AtFH18 265/382 (69%) |
HvFH4 | H. vulgare | I* | OsFH1 256/316 (81%); AtFH1 198/289 (68%) | OsFH7 | O. sativa | IIb* | HvFH5 139/163 (85%); AtFH18 264/428 (61%) |
HvFH5 | H. vulgare | IIb | OsFH7 132/153 (86%); AtFH18 103/149 (69%) | OsFH8 | O. sativa | Ib* | OsFH4 356/486 (73%); AtFH6 287/433 (66%) |
HvFH6 | H. vulgare | I | OsFH1 138/154 (89%); AtFH1 91/151 (60%) | OsFH9 | O. sativa | Id* | AtFH11 220/404 (54%) |
HvFH7 | H. vulgare | Ic* | OsFH11 156/225 (69%); AtFH5 147/226 (65%) | OsFH10 | O. sativa | Ic* | OsFH11 235/456 (51%); AtFH5 243/463 (52%) |
HvFH8 | H. vulgare | I | SpFH2 98/120 (81%); AtFH1 94/186 (50%) | OsFH11 | O. sativa | Ic* | AtFH5 265/481 (55%) |
HvFH9 | H. vulgare | I | OsFH11 70/129 (54%); AtFH5 47/110 (42%) | OsFH12 | O. sativa | II* | AtFH20 209/395 (52%) |
HvFH10 | H. vulgare | I | OsFH14 145/196 (73%); AtFH1 86/193 (44%) | OsFH13 | O. sativa | I | HvFH2 144/168 (85%); AtFH6 224/443 (50%) |
LeFH1 | Lycopersicon esculentum | Ib* | StFH1 211/235 (89%); AtFH6 318/455 (69%) | OsFH14 | O. sativa | I* | AtFH1 187/381 (49%) |
LeFH2 | L. esculentum | IIa* | StFH6 140/155 (90%); AtFH14 268/349 (76%) | OsFH15 | O. sativa | I* | OsFH1 243/425 (57%); AtFH1 228/416 (54%) |
LeFH3 | L. esculentum | Ic* | StFH5 189/196 (96%); AtFH5 292/406 (71%) | OsFH16 | O. sativa | I* | SbFH2 148/167 (88%); AtFH4 234/441 (53%) |
LeFH4 | L. esculentum | I | NtFH1 164/258 (63%); AtFH1 131/246 (53%) | PsFH1 | Pisum sativum | Ic* | AtFH5 275/439 (62%) |
LeFH5 | L. esculentum | Ia | AtFH1 155/222 (69%) | SbFH1 | Sorghum bicolor | II | HvFH1 105/126 (83%); AtFH18 93/147 (63%) |
LeFH6 | L. esculentum | II | OsFH5 95/144 (65%); AtFH20 99/178 (55%) | SbFH2 | S. bicolor | Ie | OsFH16 137/167 (82%); AtFH7 107/167 (64%) |
LeFH7 | L. esculentum | I | NbFH1 66/98 (67%); AtFH5 62/108 (57%) | SpFH1 | Sorghum propinquum | I | OsFH1 180/205 (87%); AtFH1 146/205 (71%) |
LjFH1 | Lotus japonicus | Id | AtFH11 111/140 (79%) | SpFH2 | S. propinquum | I | OsFH15 172/204 (84%); AtFH1 128/205 (62%) |
MtFH1 | Medicago truncatula | Ia | GmFH4 98/106 (92%); AtFH1 215/299 (71%) | SpFH3 | S. propinquum | I | OsFH1 93/111 (83%); AtFH1 72/91 (79%) |
MtFH2 | M. truncatula | Ia | AtFH1 143/182 (78%) | StFH1 | Solanum tuberosum | Ib* | LeFH1 211/235 (89%); AtFH6 186/248 (75%) |
MtFH3 | M. truncatula | Ic | NbFH1 135/189 (71%); AtFH5 128/188 (68%) | StFH2 | S. tuberosum | Ia | GhFH1 127/148 (85%); AtFH1 143/208 (68%) |
MtFH4 | M. truncatula | II | GmFH3 129/181 (71%); AtFH13 126/191 (65%) | StFH3 | S. tuberosum | II | OsFH6 156/216 (72%); AtFH18 150/216 (69%) |
MtFH5 | M. truncatula | II | GmFH1 102/133 (76%); AtFH18 83/166 (50%) | StFH4 | S. tuberosum | Ia | NtFH1 186/217 (85%); AtFH1 149/211 (70%) |
MtFH6 | M. truncatula | II | AtFH20 76/124 (61%) | StFH5 | S. tuberosum | Ic | LeFH3 189/196 (96%); AtFH5 152/229 (66%) |
NbFH1 | Nicotiana benthamiana | Ic | LeFH3 225/241 (93%); AtFH5 189/240 (78%) | StFH6 | S. tuberosum | IIa | LeFH2 153/155 (98%); AtFH14 123/154 (79%) |
NbFH2 | N. benthamiana | Ib | LeFH1 138/150 (92%); AtFH6 100/162 (61%) | TaFH1 | Triticum aestivum | I | HvFH4 178/196 (90%); AtFH1 145/192 (75%) |
NbFH3 | N. benthamiana | Ic | StFH5 100/124 (80%); AtFH5 91/143 (63%) | VvFH1 | Vitis vinifera | I | OsFH1 114/185 (61%); AtFH1 104/192 (54%) |
NbFH4 | N. benthamiana | I | AtFH6 115/278 (41%) | ZmFH1 | Zea mays | I | OsFH1 119/154 (77%); AtFH1 81/154 (52%) |
NbFH5 | N. benthamiana | I | NtFH2 101/146 (69%); AtFH1 77/140 (55%) |