242:
219:
116:
141:
1545:
248:
147:
1423:
1132:, a component of the MICOS complex, along with other components of this complex and components of an ER membrane protein complex involved in transferring lipids to mitochondria. Additionally, this protein interacts with
1886:
Wan J, Steffen J, Yourshaw M, Mamsa H, Andersen E, Rudnik-Schöneborn S, Pope K, Howell KB, McLean CA, Kornberg AJ, Joseph J, Lockhart PJ, Zerres K, Ryan MM, Nelson SF, Koehler CM, Jen JC (November 2016).
255:
154:
1843:
Janer A, Prudent J, Paupe V, Fahiminiya S, Majewski J, Sgarioto N, Des
Rosiers C, Forest A, Lin ZY, Gingras AC, Mitchell G, McBride HM, Shoubridge EA (September 2016).
1358:
Janer A, Prudent J, Paupe V, Fahiminiya S, Majewski J, Sgarioto N, Des
Rosiers C, Forest A, Lin ZY, Gingras AC, Mitchell G, McBride HM, Shoubridge EA (September 2016).
1681:
Hendrickson SL, Lautenberger JA, Chinn LW, Malasky M, Sezgin E, Kingsley LA, Goedert JJ, Kirk GD, Gomperts ED, Buchbinder SP, Troyer JL, O'Brien SJ (September 2010).
1020:
1976:
657:
638:
77:
1064:
1277:
1259:
1996:
241:
1506:
881:
888:
218:
1031:
The encoded protein is an orphan transporter involved in lipid transfer from the endoplasmic reticulum to mitochondria. It promotes
1092:
and hyperfilamentous mitochondria due to decreased mitochondrial fission. Loss of this gene also has many other effects: premature
1932:"Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2-mediated hyperfusion of mitochondria"
1246:
1225:
2001:
1765:"Genetic variants predicting left ventricular hypertrophy in a diabetic population: a Go-DARTS study including meta-analysis"
1242:
140:
115:
1221:
1100:, destabilization of the MICOS (mitochondrial contact site and cristae organizing system) complex, loss of and shortened
1845:"SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome"
1360:"SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome"
1125:
254:
153:
57:
1616:
Palmieri F (April 2013). "The mitochondrial transporter family SLC25: identification, properties and physiopathology".
1075:
1651:
247:
146:
1763:
Parry HM, Donnelly LA, Van Zuydam N, Doney AS, Elder DH, Morris AD, Struthers AD, Palmer CN, Lang CC (July 2013).
1810:"Association analysis of allergic sensitization susceptibility loci with atopic dermatitis in Chinese population"
1734:
Palmieri F (2013). "The mitochondrial transporter family SLC25: identification, properties and physiopathology".
1017:
1014:
702:
65:
1808:
Gao J, Ma Y, Sheng Y, Zuo X, Wang W, Zheng X, Tang H, Tang X, Zhou F, Yang S, Zhang X, Sun L (December 2015).
683:
1068:
1032:
974:
962:
955:
1694:
1105:
1097:
1089:
129:
44:
1528:"SLC25A46 - Solute carrier family 25 member 46 - Homo sapiens (Human) - SLC25A46 gene & protein"
1093:
1005:
in position 22.1 and spans 27,039 base pairs. The gene produces a 46.2 kDa protein composed of 418
864:
835:
831:
805:
776:
772:
89:
860:
839:
801:
780:
1302:"Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder"
1153:
1961:
1930:
Steffen J, Vashisht AA, Wan J, Jen JC, Claypool SM, Wohlschlegel JA, Koehler CM (March 2017).
1918:
1874:
1831:
1796:
1751:
1722:
1633:
1598:
1471:
1389:
1331:
1157:
85:
37:
1141:
1951:
1943:
1908:
1900:
1864:
1856:
1821:
1786:
1776:
1743:
1712:
1702:
1625:
1588:
1580:
1461:
1453:
1379:
1371:
1321:
1313:
1300:
Abrams AJ, Hufnagel RB, Rebelo A, Zanna C, Patel N, Gonzalez MA, et al. (August 2015).
1060:
986:
334:
265:
209:
164:
1185:
1173:
1165:
1549:
1544:
1161:
1081:
1036:
309:
1698:
1956:
1931:
1913:
1888:
1869:
1844:
1791:
1764:
1717:
1682:
1593:
1568:
1466:
1441:
1384:
1359:
1326:
1301:
1109:
1085:
958:
572:
556:
551:
546:
541:
525:
1990:
1980:
1489:
1442:"Integration of cardiac proteome biology and medicine by a specialized knowledgebase"
1427:
978:
966:
512:
1683:"Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression"
69:
1826:
1809:
1113:
1002:
327:
106:
1889:"Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia"
1457:
1035:
and prevents the formation of hyperfilamentous mitochondria. This protein forms a
1707:
93:
1282:
National Center for
Biotechnology Information, U.S. National Library of Medicine
1264:
National Center for
Biotechnology Information, U.S. National Library of Medicine
1006:
410:
1747:
1629:
226:
123:
73:
1781:
1440:
Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, et al. (October 2013).
1947:
1860:
1375:
602:
470:
348:
293:
280:
192:
179:
81:
1965:
1922:
1904:
1878:
1835:
1800:
1755:
1726:
1637:
1602:
1475:
1393:
1335:
1067:. Symptoms include early-onset optic atrophy, progressive visual loss, and
1584:
1410:
928:
923:
1527:
1177:
982:
912:
747:
728:
1169:
1137:
944:
714:
669:
1189:
1149:
1133:
1101:
896:
624:
1317:
1181:
970:
1426:
This article incorporates text from this source, which is in the
587:
583:
1510:
1197:
1193:
1145:
1129:
1072:
1044:
1040:
1010:
951:
61:
1652:"SLC25A46 binary interactions found for search term SLC25A46"
1548: This article incorporates text available under the
1084:
of this protein causes mitochondrial fragmentation while
317:
1494:
Cardiac
Organellar Protein Atlas Knowledgebase (COPaKB)
1511:
solute carrier family 25, member 46; SLC25A46 - 610826
1043:) on the inner mitochondrial membrane, independent of
482:
853:
824:
794:
765:
48:, HMSN6B, solute carrier family 25 member 46, PCH1E
1238:
1236:
1234:
1217:
1215:
1213:
1411:"Entrez Gene: Solute carrier family 25 member 46"
264:
163:
1490:"SLC25A46 - Solute carrier family 25 member 46"
16:Protein-coding gene in the species Homo sapiens
1569:"UniProt: the universal protein knowledgebase"
1243:GRCm38: Ensembl release 89: ENSMUSG00000024259
8:
1222:GRCh38: Ensembl release 89: ENSG00000164209
1078:, with variable age at onset and severity.
1977:United States National Library of Medicine
598:
508:
305:
204:
101:
1955:
1912:
1868:
1825:
1790:
1780:
1716:
1706:
1592:
1465:
1383:
1325:
1975:This article incorporates text from the
1405:
1403:
1209:
1192:. This protein possibly interacts with
1065:hereditary motor and sensory neuropathy
18:
1656:IntAct Molecular Interaction Database
1563:
1561:
1559:
1522:
1520:
1518:
1023:to the mitochondrial outer membrane.
269:
230:
225:
168:
127:
122:
7:
1353:
1351:
1349:
1347:
1345:
1295:
1293:
1291:
1507:Online Mendelian Inheritance in Man
1069:peripheral sensorimotor neuropathy
956:SLC25 mitochondrial solute carrier
954:. This protein is a member of the
941:Solute carrier family 25 member 46
850:
821:
791:
762:
738:
719:
693:
674:
648:
629:
487:
405:
343:
322:
14:
1814:Journal of Dermatological Science
947:that in humans is encoded by the
367:lateral nuclear group of thalamus
1543:
1421:
1001:gene is located on the q arm of
253:
246:
240:
217:
152:
145:
139:
114:
1579:(D1): D158–D169. January 2017.
1112:, and changes in mitochondrial
1827:10.1016/j.jdermsci.2015.09.009
573:mitochondrial membrane fission
542:integral component of membrane
471:More reference expression data
429:Region I of hippocampus proper
1:
1936:Molecular Biology of the Cell
1736:Molecular Aspects of Medicine
1618:Molecular Aspects of Medicine
1458:10.1161/CIRCRESAHA.113.301151
238:
137:
1708:10.1371/journal.pone.0012862
987:neuropathy and optic atrophy
967:mitochondrial outer membrane
552:mitochondrial outer membrane
425:Epithelium of choroid plexus
1997:Genes on human chromosome 5
1076:Charcot-Marie-Tooth disease
2018:
1769:Cardiovascular Diabetology
441:superior cervical ganglion
1748:10.1016/j.mam.2012.05.005
1630:10.1016/j.mam.2012.05.005
1278:"Mouse PubMed Reference:"
1260:"Human PubMed Reference:"
1090:mitochondrial hyperfusion
1018:integral membrane protein
927:
922:
918:
911:
895:
882:Chr 5: 110.74 – 110.77 Mb
876:
857:
828:
817:
798:
769:
758:
745:
741:
726:
722:
713:
700:
696:
681:
677:
668:
655:
651:
636:
632:
623:
608:
601:
597:
581:
511:
507:
495:
490:
481:
468:
417:
408:
355:
346:
316:
308:
304:
287:
274:
237:
216:
207:
203:
186:
173:
136:
113:
104:
100:
55:
52:
42:
35:
30:
26:
21:
1782:10.1186/1475-2840-12-109
889:Chr 18: 31.69 – 31.74 Mb
1948:10.1091/mbc.E16-07-0545
1861:10.15252/emmm.201506159
1849:EMBO Molecular Medicine
1376:10.15252/emmm.201506159
1364:EMBO Molecular Medicine
1088:of this protein causes
985:in this gene result in
445:interventricular septum
1573:Nucleic Acids Research
1063:manner, cause type 6B
1059:gene, inherited in an
2002:Solute carrier family
1051:Clinical Significance
1033:mitochondrial fission
975:endoplasmic reticulum
963:transmembrane protein
449:medial dorsal nucleus
232:Chromosome 18 (mouse)
1905:10.1093/brain/aww212
1446:Circulation Research
1098:cellular respiration
130:Chromosome 5 (human)
94:SLC25A46 - orthologs
1699:2010PLoSO...512862H
1585:10.1093/nar/gkw1099
1094:cellular senescence
1061:autosomal recessive
433:trigeminal ganglion
1979:, which is in the
1009:. This gene has 8
973:transfer from the
703:ENSMUSG00000024259
566:Biological process
535:Cellular component
519:Molecular function
457:extraocular muscle
421:supraoptic nucleus
1899:(11): 2877–2890.
1055:Mutations in the
938:
937:
934:
933:
907:
906:
872:
871:
847:
846:
813:
812:
788:
787:
754:
753:
735:
734:
709:
708:
690:
689:
664:
663:
645:
644:
593:
592:
503:
502:
499:
498:
477:
476:
464:
463:
402:
401:
300:
299:
199:
198:
2009:
1969:
1959:
1926:
1916:
1882:
1872:
1839:
1829:
1804:
1794:
1784:
1759:
1730:
1720:
1710:
1667:
1666:
1664:
1663:
1648:
1642:
1641:
1613:
1607:
1606:
1596:
1565:
1554:
1547:
1541:
1539:
1538:
1524:
1513:
1504:
1498:
1497:
1486:
1480:
1479:
1469:
1437:
1431:
1425:
1424:
1420:
1418:
1417:
1407:
1398:
1397:
1387:
1355:
1340:
1339:
1329:
1297:
1286:
1285:
1274:
1268:
1267:
1256:
1250:
1240:
1229:
1219:
1039:with mitofilin (
920:
919:
891:
884:
867:
851:
842:
822:
818:RefSeq (protein)
808:
792:
783:
763:
739:
720:
694:
675:
649:
630:
599:
509:
488:
473:
453:substantia nigra
413:
411:Top expressed in
406:
359:secondary oocyte
351:
349:Top expressed in
344:
323:
306:
296:
283:
272:
257:
250:
244:
233:
221:
205:
195:
182:
171:
156:
149:
143:
132:
118:
102:
96:
47:
40:
19:
2017:
2016:
2012:
2011:
2010:
2008:
2007:
2006:
1987:
1986:
1972:
1929:
1885:
1842:
1807:
1762:
1742:(2–3): 465–84.
1733:
1680:
1676:
1674:Further reading
1671:
1670:
1661:
1659:
1650:
1649:
1645:
1624:(2–3): 465–84.
1615:
1614:
1610:
1567:
1566:
1557:
1536:
1534:
1532:www.uniprot.org
1526:
1525:
1516:
1505:
1501:
1488:
1487:
1483:
1439:
1438:
1434:
1422:
1415:
1413:
1409:
1408:
1401:
1357:
1356:
1343:
1318:10.1038/ng.3354
1306:Nature Genetics
1299:
1298:
1289:
1276:
1275:
1271:
1258:
1257:
1253:
1241:
1232:
1220:
1211:
1206:
1122:
1071:manifesting as
1053:
1029:
995:
965:located in the
929:View/Edit Mouse
924:View/Edit Human
887:
880:
877:Location (UCSC)
863:
859:
838:
834:
830:
804:
800:
779:
775:
771:
684:ENSG00000164209
577:
561:
530:
526:protein binding
469:
460:
455:
451:
447:
443:
439:
435:
431:
427:
423:
409:
398:
395:pars reticulata
393:
389:
385:
381:
377:
375:Achilles tendon
373:
371:right ventricle
369:
365:
361:
347:
291:
278:
270:
260:
259:
258:
251:
231:
208:Gene location (
190:
177:
169:
159:
158:
157:
150:
128:
105:Gene location (
56:
43:
36:
17:
12:
11:
5:
2015:
2013:
2005:
2004:
1999:
1989:
1988:
1971:
1970:
1942:(5): 600–612.
1927:
1883:
1855:(9): 1019–38.
1840:
1805:
1760:
1731:
1677:
1675:
1672:
1669:
1668:
1643:
1608:
1555:
1514:
1499:
1481:
1452:(9): 1043–53.
1432:
1399:
1370:(9): 1019–38.
1341:
1287:
1269:
1251:
1230:
1208:
1207:
1205:
1202:
1121:
1118:
1110:cell migration
1082:Overexpression
1052:
1049:
1028:
1025:
1013:and encodes a
994:
991:
936:
935:
932:
931:
926:
916:
915:
909:
908:
905:
904:
902:
900:
893:
892:
885:
878:
874:
873:
870:
869:
855:
854:
848:
845:
844:
826:
825:
819:
815:
814:
811:
810:
796:
795:
789:
786:
785:
767:
766:
760:
756:
755:
752:
751:
743:
742:
736:
733:
732:
724:
723:
717:
711:
710:
707:
706:
698:
697:
691:
688:
687:
679:
678:
672:
666:
665:
662:
661:
653:
652:
646:
643:
642:
634:
633:
627:
621:
620:
615:
610:
606:
605:
595:
594:
591:
590:
579:
578:
576:
575:
569:
567:
563:
562:
560:
559:
554:
549:
544:
538:
536:
532:
531:
529:
528:
522:
520:
516:
515:
505:
504:
501:
500:
497:
496:
493:
492:
485:
479:
478:
475:
474:
466:
465:
462:
461:
459:
458:
454:
450:
446:
442:
438:
434:
430:
426:
422:
418:
415:
414:
403:
400:
399:
397:
396:
392:
388:
387:jejunal mucosa
384:
383:biceps brachii
380:
376:
372:
368:
364:
360:
356:
353:
352:
340:
339:
331:
320:
314:
313:
310:RNA expression
302:
301:
298:
297:
289:
285:
284:
276:
273:
268:
262:
261:
252:
245:
239:
235:
234:
229:
223:
222:
214:
213:
201:
200:
197:
196:
188:
184:
183:
175:
172:
167:
161:
160:
151:
144:
138:
134:
133:
126:
120:
119:
111:
110:
98:
97:
54:
50:
49:
41:
33:
32:
28:
27:
24:
23:
15:
13:
10:
9:
6:
4:
3:
2:
2014:
2003:
2000:
1998:
1995:
1994:
1992:
1985:
1984:
1982:
1981:public domain
1978:
1967:
1963:
1958:
1953:
1949:
1945:
1941:
1937:
1933:
1928:
1924:
1920:
1915:
1910:
1906:
1902:
1898:
1894:
1890:
1884:
1880:
1876:
1871:
1866:
1862:
1858:
1854:
1850:
1846:
1841:
1837:
1833:
1828:
1823:
1820:(3): 217–20.
1819:
1815:
1811:
1806:
1802:
1798:
1793:
1788:
1783:
1778:
1774:
1770:
1766:
1761:
1757:
1753:
1749:
1745:
1741:
1737:
1732:
1728:
1724:
1719:
1714:
1709:
1704:
1700:
1696:
1693:(9): e12862.
1692:
1688:
1684:
1679:
1678:
1673:
1657:
1653:
1647:
1644:
1639:
1635:
1631:
1627:
1623:
1619:
1612:
1609:
1604:
1600:
1595:
1590:
1586:
1582:
1578:
1574:
1570:
1564:
1562:
1560:
1556:
1553:
1551:
1546:
1533:
1529:
1523:
1521:
1519:
1515:
1512:
1508:
1503:
1500:
1495:
1491:
1485:
1482:
1477:
1473:
1468:
1463:
1459:
1455:
1451:
1447:
1443:
1436:
1433:
1429:
1428:public domain
1412:
1406:
1404:
1400:
1395:
1391:
1386:
1381:
1377:
1373:
1369:
1365:
1361:
1354:
1352:
1350:
1348:
1346:
1342:
1337:
1333:
1328:
1323:
1319:
1315:
1312:(8): 926–32.
1311:
1307:
1303:
1296:
1294:
1292:
1288:
1283:
1279:
1273:
1270:
1265:
1261:
1255:
1252:
1248:
1244:
1239:
1237:
1235:
1231:
1227:
1223:
1218:
1216:
1214:
1210:
1203:
1201:
1199:
1195:
1191:
1187:
1183:
1179:
1175:
1171:
1167:
1163:
1159:
1155:
1151:
1147:
1143:
1139:
1135:
1131:
1127:
1124:This protein
1119:
1117:
1116:composition.
1115:
1111:
1107:
1104:, altered ER
1103:
1099:
1095:
1091:
1087:
1083:
1079:
1077:
1074:
1070:
1066:
1062:
1058:
1050:
1048:
1046:
1042:
1038:
1034:
1026:
1024:
1022:
1019:
1016:
1012:
1008:
1004:
1000:
992:
990:
988:
984:
980:
976:
972:
968:
964:
960:
957:
953:
950:
946:
942:
930:
925:
921:
917:
914:
910:
903:
901:
898:
894:
890:
886:
883:
879:
875:
868:
866:
862:
856:
852:
849:
843:
841:
837:
833:
827:
823:
820:
816:
809:
807:
803:
797:
793:
790:
784:
782:
778:
774:
768:
764:
761:
759:RefSeq (mRNA)
757:
750:
749:
744:
740:
737:
731:
730:
725:
721:
718:
716:
712:
705:
704:
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631:
628:
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619:
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604:
600:
596:
589:
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574:
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568:
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558:
557:mitochondrion
555:
553:
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548:
545:
543:
540:
539:
537:
534:
533:
527:
524:
523:
521:
518:
517:
514:
513:Gene ontology
510:
506:
494:
489:
486:
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480:
472:
467:
456:
452:
448:
444:
440:
436:
432:
428:
424:
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404:
394:
390:
386:
382:
379:Pars compacta
378:
374:
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366:
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357:
354:
350:
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342:
341:
338:
336:
332:
330:
329:
325:
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321:
319:
315:
311:
307:
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295:
290:
286:
282:
277:
271:18|18 B1
267:
263:
256:
249:
243:
236:
228:
224:
220:
215:
211:
206:
202:
194:
189:
185:
181:
176:
166:
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148:
142:
135:
131:
125:
121:
117:
112:
108:
103:
99:
95:
91:
87:
83:
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75:
71:
67:
63:
59:
51:
46:
39:
34:
29:
25:
20:
1974:
1973:
1939:
1935:
1896:
1892:
1852:
1848:
1817:
1813:
1772:
1768:
1739:
1735:
1690:
1686:
1660:. Retrieved
1655:
1646:
1621:
1617:
1611:
1576:
1572:
1542:
1535:. Retrieved
1531:
1502:
1493:
1484:
1449:
1445:
1435:
1414:. Retrieved
1367:
1363:
1309:
1305:
1281:
1272:
1263:
1254:
1123:
1120:Interactions
1114:phospholipid
1080:
1056:
1054:
1030:
1003:chromosome 5
998:
996:
979:mitochondria
969:involved in
948:
940:
939:
865:NP_001344390
858:
836:NP_001290179
832:NP_001290178
829:
806:NM_001357461
799:
777:NM_001303250
773:NM_001303249
770:
746:
727:
701:
682:
656:
637:
617:
612:
437:pineal gland
333:
326:
191:110,765,161
178:110,738,136
53:External IDs
1108:, impaired
1096:, impaired
1007:amino acids
292:31,742,964
279:31,689,164
31:Identifiers
1991:Categories
1662:2018-08-18
1658:. EMBL-EBI
1537:2018-08-16
1416:2018-08-17
1249:, May 2017
1228:, May 2017
1204:References
1106:morphology
1015:multi-pass
961:. It is a
337:(ortholog)
74:HomoloGene
1550:CC BY 4.0
1154:linc01142
1126:interacts
1086:knockdown
1021:localized
993:Structure
983:Mutations
861:NP_080441
840:NP_620128
802:NM_026165
781:NM_138773
603:Orthologs
82:GeneCards
1966:28057766
1923:27543974
1879:27390132
1836:26464032
1801:23879873
1756:23266187
1727:20877624
1687:PLOS ONE
1638:23266187
1603:27899622
1552:license.
1509:(OMIM):
1476:23965338
1394:27390132
1336:26168012
1245:–
1224:–
1178:HSD17B11
1158:LEPROTL1
1057:SLC25A46
1027:Function
999:SLC25A46
977:(ER) to
949:SLC25A46
913:Wikidata
582:Sources:
547:membrane
86:SLC25A46
45:SLC25A46
22:SLC25A46
1957:5328619
1914:5840878
1870:5009808
1792:3729417
1775:: 109.
1718:2943476
1695:Bibcode
1594:5210571
1467:4076475
1385:5009808
1327:4520737
1247:Ensembl
1226:Ensembl
1170:MFSD14B
1142:SLC10A6
1138:SLC10A1
1102:cristae
1037:complex
945:protein
715:UniProt
670:Ensembl
609:Species
588:QuickGO
312:pattern
70:1914703
38:Aliases
1964:
1954:
1921:
1911:
1877:
1867:
1834:
1799:
1789:
1754:
1725:
1715:
1636:
1601:
1591:
1474:
1464:
1392:
1382:
1334:
1324:
1190:TOMM22
1188:, and
1150:FUNDC1
1134:SLC7A8
1073:axonal
959:family
899:search
897:PubMed
748:Q9CQS4
729:Q96AG3
625:Entrez
483:BioGPS
170:5q22.1
62:610826
1893:Brain
1186:REEP4
1182:REEP2
1174:PQLC1
1166:VMA21
1128:with
1011:exons
971:lipid
943:is a
658:67453
639:91137
618:Mouse
613:Human
584:Amigo
363:sperm
335:Mouse
328:Human
275:Start
210:Mouse
174:Start
107:Human
78:14518
1962:PMID
1919:PMID
1875:PMID
1832:PMID
1797:PMID
1752:PMID
1723:PMID
1634:PMID
1599:PMID
1472:PMID
1390:PMID
1332:PMID
1198:MFN2
1196:and
1194:OPA1
1162:ODF4
1146:FHL3
1130:IMMT
1045:MFN2
1041:IMMT
997:The
952:gene
391:pons
318:Bgee
266:Band
227:Chr.
165:Band
124:Chr.
58:OMIM
1952:PMC
1944:doi
1909:PMC
1901:doi
1897:139
1865:PMC
1857:doi
1822:doi
1787:PMC
1777:doi
1744:doi
1713:PMC
1703:doi
1626:doi
1589:PMC
1581:doi
1462:PMC
1454:doi
1450:113
1380:PMC
1372:doi
1322:PMC
1314:doi
491:n/a
288:End
187:End
90:OMA
66:MGI
1993::
1960:.
1950:.
1940:28
1938:.
1934:.
1917:.
1907:.
1895:.
1891:.
1873:.
1863:.
1851:.
1847:.
1830:.
1818:80
1816:.
1812:.
1795:.
1785:.
1773:12
1771:.
1767:.
1750:.
1740:34
1738:.
1721:.
1711:.
1701:.
1689:.
1685:.
1654:.
1632:.
1622:34
1620:.
1597:.
1587:.
1577:45
1575:.
1571:.
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1530:.
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1492:.
1470:.
1460:.
1448:.
1444:.
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1388:.
1378:.
1366:.
1362:.
1344:^
1330:.
1320:.
1310:47
1308:.
1304:.
1290:^
1280:.
1262:.
1233:^
1212:^
1200:.
1184:,
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1172:,
1168:,
1164:,
1160:,
1156:,
1152:,
1148:,
1144:,
1140:,
1136:,
1047:.
989:.
981:.
586:/
294:bp
281:bp
193:bp
180:bp
88:;
84::
80:;
76::
72:;
68::
64:;
60::
1983:.
1968:.
1946::
1925:.
1903::
1881:.
1859::
1853:8
1838:.
1824::
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1374::
1368:8
1338:.
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1284:.
1266:.
212:)
109:)
92::
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