49:
1555:
1575:
2456:
2457:"Search results - 22[CHR] AND "Homo sapiens"[Organism] AND ( ("genetype miscrna"[Properties] OR "genetype ncrna"[Properties] OR "genetype rrna"[Properties] OR "genetype trna"[Properties] OR "genetype scrna"[Properties] OR "genetype snrna"[Properties] OR "genetype snorna"[Properties]) NOT "genetype protein coding"[Properties] AND alive[prop]) - Gene"
1475:: Most people with 22q11.2 deletion syndrome are missing about 3 million base pairs on one copy of chromosome 22 in each cell. The deletion occurs near the middle of the chromosome at a location designated as q11.2. This region contains about 30 genes, but many of these genes have not been well characterized. A small percentage of affected individuals have shorter deletions in the same region.
2996:
McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH (1999). "The
Philadelphia story: the 22q11.2 deletion:
1505:
is a rare disorder most often caused by a chromosomal change called an inverted duplicated 22. A small extra chromosome is made up of genetic material from chromosome 22 that has been abnormally duplicated (copied). The extra genetic material causes the characteristic signs and symptoms of cat-eye
1494:
Other chromosomal conditions: Other changes in the number or structure of chromosome 22 can have a variety of effects, including intellectual disability, delayed development, physical abnormalities, and other medical problems. These changes include an extra piece of chromosome 22 in each cell
1580:
G-banding patterns of human chromosome 22 in three different resolutions (400, 550 and 850). Band length in this diagram is based on the ideograms from ISCN (2013). This type of ideogram represents actual relative band length observed under a microscope at the different moments during the
2806:
Dunham I, Shimizu N, Roe BA, Chissoe S, Hunt AR, Collins JE, Bruskiewich R, Beare DM, Clamp M, Smink LJ, Ainscough R, Almeida JP, Babbage A, Bagguley C, Bailey J, Barlow K, Bates KN, Beasley O, Bird CP, Blakey S, Bridgeman AM, Buck D, Burgess J, Burrill WD, O'Brien KP (1999).
1481:), distinctive facial features, and low calcium levels. A loss of this gene does not appear to cause learning disabilities, however. Other genes in the deleted region are also likely to contribute to the signs and symptoms of 22q11.2 deletion syndrome.
1529:, or CML. It also has been found in some cases of more rapidly progressing blood cancers (acute leukemias). The presence of the Philadelphia chromosome can help predict how the cancer will progress and provides a target for molecular therapies.
2430:
2482:
2173:
135:
31:
1535:
is a translocation of chromosomes 11 and 22. Originally known as supernumerary der (22) syndrome, it occurs when an individual has an extra chromosome composed of pieces of the 11th and 22nd chromosomes.
1499:), a missing segment of the chromosome in each cell (partial monosomy), and a circular structure called ring chromosome 22 that is caused by the breakage and reattachment of both ends of the chromosome.
2508:
Beck, Megan; Peterson, Jess F.; McConnell, Juliann; McGuire, Marianne; Asato, Miya; Losee, Joseph E.; Surti, Urvashi; Madan-Khetarpal, Suneeta; Rajkovic, Aleksandar; Yatsenko, Svetlana A. (May 2015).
1477:
The loss of one particular gene, TBX1, is thought to be responsible for many of the characteristic features of 22q11.2 deletion syndrome, such as heart defects, an opening in the roof of the mouth (a
1560:
G-banding ideogram of human chromosome 22 in resolution 850 bphs. Band length in this diagram is proportional to base-pair length. This type of ideogram is generally used in genome browsers (e.g.
1510:(a gap or split in the colored part of the eye), small skin tags or pits in front of the ear, heart defects, kidney problems, and, in some cases, delayed development.
3921:
2745:
These values (ISCN start/stop) are based on the length of bands/ideograms from the ISCN book, An
International System for Human Cytogenetic Nomenclature (2013).
306:
announced they had determined the sequence of base pairs that make up this chromosome. Chromosome 22 was the first human chromosome to be fully sequenced.
2431:"Search results - 22[CHR] AND "Homo sapiens"[Organism] AND ("genetype protein coding"[Properties] AND alive[prop]) - Gene"
3063:"Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSASP2 in the major neurological symptoms"
350:) takes an extremely conservative strategy. So CCDS's gene number prediction represents a lower bound on the total number of human protein-coding genes.
2879:
Kurzrock R, Kantarjian HM, Druker BJ, Talpaz M (2003). "Philadelphia chromosome-positive leukemias: from basic mechanisms to molecular therapeutics".
1525:, is found only in cancer cells. The Philadelphia chromosome has been identified in most cases of a slowly progressing form of blood cancer called
2916:
Maynard TM, Haskell GT, Lieberman JA, LaMantia AS (2002). "22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome".
2483:"Search results - 22[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene"
288:. Humans normally have two copies of chromosome 22 in each cell. Chromosome 22 is the second smallest human chromosome, spanning about 51 million
3018:
Rinn JL, Euskirchen G, Bertone P, Martone R, Luscombe NM, Hartman S, Harrison PM, Nelson FK, Miller P, Gerstein M, Weissman S, Snyder M (2003).
3422:
466:
207:
166:
2174:"Search results - 22[CHR] AND "Homo sapiens"[Organism] AND ("has ccds"[Properties] AND alive[prop]) - Gene"
212:
317:
being the largest and chromosome 22 having originally been identified as the smallest. However, genome sequencing has revealed that
3819:
3874:
3869:
2510:"Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the gene"
741:
2348:
499:
The following is a partial list of genes on human chromosome 22. For complete list, see the link in the infobox on the right.
3947:
3911:
3552:
3176:
2689:
2652:
2214:
494:
3916:
2555:
Liu H, Abecasis GR, Heath SC, Knowles A, Demars S, Chen YJ, Roos JL, Rapoport JL, Gogos JA, Karayiorgou M (December 2002).
334:
The following are some of the gene count estimates of human chromosome 22. Because researchers use different approaches to
1382:
3674:
3136:
1411:
3415:
3691:
1484:
1387:
403:
142:
3112:
3061:
Wilson HL, Wong AC, Shaw SR, Tse WY, Stapleton GA, Phelan MC, Hu S, Marshall J, McDermid HE, et al. (2003).
604:
424:
183:
2668:
Sethakulvichai, W.; Manitpornsut, S.; Wiboonrat, M.; Lilakiatsakun, W.; Assawamakin, A.; Tongsima, S. (2012).
30:
3537:
2561:
1357:
2628:
2615:
2235:
3942:
3408:
3358:
2378:
1421:
171:
1468:
The following conditions are caused by changes in the structure or number of copies of chromosome 22:
224:
200:
48:
3684:
3169:
1517:) of genetic material between chromosomes 9 and 22 is associated with several types of blood cancer (
1514:
1472:
1446:
1441:
2850:
Gilbert F (1998). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 22".
3738:
3522:
3389:
1526:
1431:
1396:
1372:
1055:
2640:
1522:
1489:
1392:
1339:
1316:
1293:
1270:
1326:
1303:
1280:
1257:
1237:
1217:
1197:
1173:
1153:
1133:
1113:
1088:
1068:
1045:
3644:
3617:
188:
244:
3679:
3577:
2892:
2204:
1323:
1300:
1277:
1254:
1234:
1214:
1194:
1170:
1150:
1130:
1110:
1085:
1065:
1042:
634:
382:
347:
263:
231:
130:
93:
3899:
3824:
3809:
3639:
3587:
3562:
3502:
3377:
3162:
2820:
2569:
1507:
1451:
1436:
1416:
1098:
359:
303:
8:
3567:
3384:
1574:
1565:
618:
219:
71:
2824:
2674:
2012 Ninth
International Conference on Computer Science and Software Engineering (JCSSE)
2573:
1554:
3087:
3062:
2941:
2904:
2695:
2537:
2325:
2298:
2274:
2249:
3044:
3019:
2979:
2954:
2929:
2592:
2556:
3629:
3541:
3352:
3092:
3049:
3006:
2984:
2933:
2896:
2867:
2838:
2685:
2669:
2648:
2597:
2541:
2529:
2330:
2279:
2210:
1426:
1377:
335:
2945:
2908:
2699:
2356:
147:
3718:
3597:
3082:
3074:
3039:
3031:
2974:
2966:
2925:
2888:
2859:
2828:
2730:
2677:
2587:
2577:
2521:
2509:
2320:
2310:
2269:
2261:
1532:
1502:
1401:
1367:
1187:
782:
116:
3711:
3532:
3480:
2642:
1496:
343:
339:
111:
84:
2667:
346:). Among various projects, the collaborative consensus coding sequence project (
3602:
3526:
2746:
2681:
2265:
364:
296:
285:
3936:
3582:
3310:
3305:
3300:
3295:
3290:
3285:
3280:
3275:
3270:
3265:
3260:
3255:
2315:
1456:
1406:
1362:
1103:
318:
3400:
2644:
ISCN 2013: An
International System for Human Cytogenetic Nomenclature (2013)
2404:
1352:
The following diseases are some of those related to genes on chromosome 22:
159:
3557:
3431:
3372:
3338:
3333:
3250:
3245:
3240:
3235:
3230:
3225:
3220:
3215:
3210:
3185:
3096:
3053:
3010:
2988:
2937:
2900:
2871:
2842:
2641:
International
Standing Committee on Human Cytogenetic Nomenclature (2013).
2601:
2582:
2533:
2334:
2283:
1478:
314:
267:
248:
2863:
2557:"Genetic variation in the 22q11 locus and susceptibility to schizophrenia"
3776:
3771:
3634:
3612:
3607:
3475:
3193:
3078:
2995:
2525:
875:
823:
726:
562:
3035:
547:(22q13) encoding protein cyclic AMP-dependent transcription factor ATF-4
3796:
3786:
3781:
3766:
3706:
3696:
3572:
3546:
3497:
3487:
3435:
3120:
2781:
2774:
2766:
1178:
953:
766:
746:
550:
369:
281:
2405:"Human chromosome 22: entries, gene names and cross-references to MIM"
3748:
3492:
3470:
3451:
2762:
2299:"Between a chicken and a grape: estimating the number of human genes"
1593:
706:
310:
292:
56:
36:
3734:
3518:
3325:
3202:
2970:
2833:
2808:
1518:
943:
700:
568:
514:
104:
3904:
3758:
3669:
3664:
2670:"Estimation of band level resolutions of human chromosome images"
1582:
1561:
1308:
1017:
997:
977:
967:
957:
947:
937:
922:
911:
901:
879:
847:
817:
791:
750:
710:
688:
650:
559:(22q13) encoding caspase recruitment domain-containing protein 10
538:
528:
524:
518:
508:
445:
257:
154:
3814:
3701:
3465:
3461:
3456:
3154:
2915:
1285:
1007:
987:
933:
897:
837:
833:
827:
811:
730:
721:
667:
661:
608:
592:
556:
238:
195:
2878:
2661:
2629:
Ideogram data for Homo sapience (550 bphs, Assembly GRCh38.p3)
2616:
Ideogram data for Homo sapience (400 bphs, Assembly GRCh38.p3)
2236:
Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3)
1521:). This chromosomal abnormality, which is commonly called the
888:: encoding protein RNA 2',3'-cyclic phosphate and 5'-OH ligase
3879:
3864:
3859:
3854:
3849:
3844:
3839:
3834:
3829:
3804:
3742:
2773:: Region which is negatively stained by G banding, generally
1331:
1262:
1242:
1222:
1202:
1158:
1093:
1003:
993:
973:
963:
928:
917:
907:
869:
843:
820:: pseudogene phosphatidylinositol 4-kinase alpha pseudogene 2
807:
802:
797:
787:
771:
761:
716:
694:
684:
673:
656:
644:
639:
629:
623:
614:
598:
580:
574:
534:
309:
Human chromosomes are numbered by their apparent size in the
3017:
2507:
733:
malonyl CoA-acyl carrier protein transacylase, mitochondrial
1138:
1118:
1073:
1050:
1013:
983:
891:
885:
863:
858:
853:
777:
756:
736:
697:: encoding protein immunoglobulin lambda like polypeptide 5
679:
586:
544:
504:
3110:
1336:
parvin beta (cytoskeleton organization and cell adhesion)
289:
295:
and representing between 1.5 and 2% of the total DNA in
3922:
International System for Human
Cytogenetic Nomenclature
2805:
2554:
2202:
840:
patatin-like phospholipase domain-containing protein 3
342:
on each chromosome varies (for technical details, see
3020:"The transcriptional activity of human Chromosome 22"
2296:
1267:
Wingless-type MMTV integration site family, member 7B
904:
sorting and assembly machinery component 50 homolog
850:
melanoma antigen preferentially expressed in tumors
531:
ADP-ribosylation factor GTPase-activating protein 3
3141:Human Genome Project Information Archive 1990–2003
2729:For cytogenetic banding nomenclature, see article
2379:"Chromosome 22: Chromosome summary - Homo sapiens"
553:(22q11) encoding breakpoint cluster region protein
541:activating signal cointegrator 1 complex subunit 2
3060:
2371:
3934:
2634:
2631:. Last update 2015-08-11. Retrieved 2017-04-26.
2618:. Last update 2014-03-04. Retrieved 2017-04-26.
2238:. Last update 2014-06-03. Retrieved 2017-04-26.
2196:
521:probable DNA dC->dU-editing enzyme APOBEC-3B
2952:
2449:
2349:"Statistics & Downloads for chromosome 22"
1596:of human chromosome 22 in resolution 850 bphs
1506:syndrome, including an eye abnormality called
676:: encoding protein intraflagellar transport 27
647:: family with sequence similarity 19 member A5
595:: cysteine-rich with EGF-like domain protein 2
3430:
3416:
3170:
990:mitochondrial tRNA-specific 2-thiouridylase 1
894:: encoding protein retrotransposon Gag Like 6
2647:. Karger Medical and Scientific Publishers.
2548:
882:ribosomal RNA-processing protein 7 homolog A
577:: cat eye syndrome critical region protein 1
565:(22q13) encoding chromobox protein homolog 7
2514:American Journal of Medical Genetics Part A
2475:
2341:
2290:
703:: encoding uncharacterized protein KIAA0930
3423:
3409:
3177:
3163:
2423:
2203:Tom Strachan; Andrew Read (2 April 2010).
1547:G-banding ideograms of human chromosome 22
830:phosphatidylserine decarboxylase proenzyme
713:long intergenic non-protein coding RNA 899
626:: DiGeorge syndrome critical region gene 6
47:
29:
3086:
3043:
2978:
2849:
2832:
2809:"The DNA sequence of human chromosome 22"
2591:
2581:
2324:
2314:
2273:
2230:
2228:
2226:
1463:
1347:
1290:SH3 and multiple ankyrin repeat domains 3
872:: encoding protein RNA, U12 small nuclear
601:: cold shock domain-containing protein D2
2893:10.7326/0003-4819-138-10-200305200-00010
2761:: Region which is positively stained by
611:casein kinase I isoform epsilon or CK1ε,
321:is actually smaller than chromosome 22.
2741:
2739:
2621:
2608:
1143:neurofilament, heavy polypeptide 200kDa
866:: encoding RNA, ribosomal 45S cluster 5
753:MIRLET7B host gene (non-protein coding)
670:: encoding protein HMG-box containing 4
41:One is from mother, one is from father.
3935:
2397:
2223:
2168:
2166:
1010:probable tubulin polyglutamylase TTLL1
3912:List of organisms by chromosome count
3404:
3158:
2250:"First human chromosome is sequenced"
2247:
1207:SRY (sex determining region Y)-box 10
495:Category:Genes on human chromosome 22
2736:
1313:sulfotransferase family 4A, member 1
302:In 1999, researchers working on the
2163:
1539:
1383:Desmoplastic small round cell tumor
814:phosphatidylinositol 4-kinase alpha
13:
2799:
1412:Focal Segmental Glomerulosclerosis
1163:CHK2 checkpoint homolog (S. pombe)
1000:tetratricopeptide repeat domain 28
329:
14:
3959:
3104:
1123:catechol-O-methyltransferase gene
3184:
2627:Genome Decoration Page, NCBI.
2353:HUGO Gene Nomenclature Committee
2234:Genome Decoration Page, NCBI.
1573:
1553:
1485:22q11.2 distal deletion syndrome
1388:22q11.2 distal deletion syndrome
970:THAP domain-containing protein 7
3533:Macrochromosome/Microchromosome
3111:National Institutes of Health.
2953:McDermid HE, Morrow BE (2002).
2752:
2723:
2706:
2501:
2209:. Garland Science. p. 45.
691:immunoglobulin lambda joining 3
35:Human chromosome 22 pair after
2614:Genome Decoration Page, NCBI.
2297:Pertea M, Salzberg SL (2010).
2241:
1058:(Cayler cardiofacial syndrome)
589:: Catechol-O-methyltransferase
85:
1:
2930:10.1016/S0736-5748(02)00050-3
2562:Proc. Natl. Acad. Sci. U.S.A.
2355:. 8 July 2019. Archived from
2156:
1358:Amyotrophic lateral sclerosis
980:THO complex subunit 5 homolog
950:TBC1 domain family member 10A
3948:Genes on human chromosome 22
2955:"Genomic disorders on 22q11"
1422:Metachromatic leukodystrophy
488:
7:
960:thyrotroph embryonic factor
338:, their predictions of the
10:
3964:
3573:Dinoflagellate chromosomes
2682:10.1109/JCSSE.2012.6261965
2266:10.1136/bmj.319.7223.1453a
914:neuronal-specific septin-3
653:: encoding protein FAM227A
571:: CDC42 effector protein 1
492:
280:is one of the 23 pairs of
3917:List of sequenced genomes
3892:
3795:
3757:
3727:
3685:Chromosomal translocation
3655:
3558:A chromosome/B chromosome
3549:(or accessory chromosome)
3511:
3442:
3365:
3351:
3324:
3201:
3192:
2997:report on 250 patients".
2260:(7223). BMJ Group: 1453.
1473:22q11.2 deletion syndrome
1447:Rubinstein-Taybi syndrome
1442:Renal medullary carcinoma
256:
237:
230:
218:
206:
194:
182:
177:
165:
153:
141:
129:
124:
110:
100:
83:
69:
64:
46:
28:
23:
3739:Telomere-binding protein
3553:Supernumerary chromosome
2316:10.1186/gb-2010-11-5-206
2206:Human Molecular Genetics
1527:chronic myeloid leukemia
1432:Neurofibromatosis type 2
1397:Phelan-McDermid syndrome
1373:Chronic myeloid leukemia
1247:E1A binding protein p300
1056:Asymmetric crying facies
324:
3359:Human mitochondrial DNA
3117:Genetics Home Reference
1523:Philadelphia chromosome
1490:22q13 deletion syndrome
1393:22q13 deletion syndrome
1340:22q13 deletion syndrome
1317:22q13 deletion syndrome
1294:22q13 deletion syndrome
1271:22q13 deletion syndrome
664:: GTP-binding protein 1
3675:Structural alterations
2583:10.1073/pnas.232186099
2180:. CCDS Release 20 for
1464:Chromosomal conditions
1348:Diseases and disorders
3692:Numerical alterations
3680:Chromosomal inversion
3578:Homologous chromosome
2864:10.1089/gte.1998.2.89
2248:Mayor, Susan (1999).
3900:Extrachromosomal DNA
3588:Satellite chromosome
3563:Lampbrush chromosome
3503:Nuclear organization
3378:Human Genome Project
3353:Mitochondrial genome
3079:10.1136/jmg.40.8.575
2676:. pp. 276–282.
2526:10.1002/ajmg.a.36839
1508:ocular iris coloboma
1452:Waardenburg syndrome
1437:Opitz G/BBB syndrome
1417:Li-Fraumeni syndrome
1099:Reticulon 4 receptor
794:nucleolar protein 12
365:Non-coding RNA genes
360:Protein-coding genes
304:Human Genome Project
178:External map viewers
3943:Chromosomes (human)
3593:Centromere position
3568:Polytene chromosome
3538:Circular chromosome
3385:List of human genes
3036:10.1101/gad.1055203
2825:1999Natur.402..489D
2788:: Variable region;
2574:2002PNAS...9916859L
1597:
1566:UCSC Genome Browser
619:long non-coding RNA
125:Complete gene lists
112:Centromere position
2918:Int J Dev Neurosci
2411:. 28 February 2018
2383:Ensembl Release 88
2184:. 8 September 2016
1592:
232:Full DNA sequences
53:Chromosome 22 pair
3930:
3929:
3888:
3887:
3625:Centromere number
3542:Linear chromosome
3398:
3397:
3390:Human archaeology
3347:
3346:
2691:978-1-4673-1921-8
2654:978-3-318-02253-7
2359:on 18 August 2017
2216:978-1-136-84407-2
2154:
2153:
1513:A rearrangement (
1427:Methemoglobinemia
1378:DiGeorge syndrome
1345:
1344:
1227:Apolipoprotein L1
486:
485:
336:genome annotation
275:
274:
3955:
3755:
3754:
3719:Polyploidization
3547:Extra chromosome
3462:Genetic material
3425:
3418:
3411:
3402:
3401:
3199:
3198:
3179:
3172:
3165:
3156:
3155:
3151:
3149:
3147:
3132:
3130:
3128:
3119:. Archived from
3100:
3090:
3057:
3047:
3014:
2992:
2982:
2949:
2912:
2875:
2846:
2836:
2819:(6761): 489–95.
2793:
2756:
2750:
2743:
2734:
2727:
2721:
2710:
2704:
2703:
2665:
2659:
2658:
2638:
2632:
2625:
2619:
2612:
2606:
2605:
2595:
2585:
2568:(26): 16859–64.
2552:
2546:
2545:
2520:(5): 1047–1053.
2505:
2499:
2498:
2496:
2494:
2479:
2473:
2472:
2470:
2468:
2453:
2447:
2446:
2444:
2442:
2427:
2421:
2420:
2418:
2416:
2401:
2395:
2394:
2392:
2390:
2375:
2369:
2368:
2366:
2364:
2345:
2339:
2338:
2328:
2318:
2294:
2288:
2287:
2277:
2245:
2239:
2232:
2221:
2220:
2200:
2194:
2193:
2191:
2189:
2170:
2145:
2140:
2112:
2107:
2080:
2075:
2047:
2042:
2015:
2010:
1982:
1977:
1950:
1945:
1917:
1912:
1885:
1880:
1852:
1847:
1820:
1815:
1788:
1783:
1756:
1751:
1724:
1719:
1692:
1687:
1660:
1655:
1598:
1591:
1577:
1557:
1540:Cytogenetic band
1533:Emanuel syndrome
1503:Cat-eye syndrome
1402:Emanuel syndrome
1368:Cat eye syndrome
1188:acoustic neuroma
1025:
1024:
353:
352:
271:
252:
87:
51:
33:
21:
20:
16:Human chromosome
3963:
3962:
3958:
3957:
3956:
3954:
3953:
3952:
3933:
3932:
3931:
3926:
3884:
3791:
3753:
3723:
3712:Paleopolyploidy
3657:
3651:
3507:
3481:Heterochromatin
3444:
3438:
3429:
3399:
3394:
3361:
3343:
3320:
3188:
3183:
3145:
3143:
3137:"Chromosome 22"
3135:
3126:
3124:
3113:"Chromosome 22"
3107:
2924:(3–5): 407–19.
2802:
2800:Further reading
2797:
2796:
2777:and gene rich;
2769:and gene poor;
2757:
2753:
2744:
2737:
2728:
2724:
2716:": Short arm; "
2711:
2707:
2692:
2666:
2662:
2655:
2639:
2635:
2626:
2622:
2613:
2609:
2553:
2549:
2506:
2502:
2492:
2490:
2481:
2480:
2476:
2466:
2464:
2455:
2454:
2450:
2440:
2438:
2429:
2428:
2424:
2414:
2412:
2403:
2402:
2398:
2388:
2386:
2385:. 29 March 2017
2377:
2376:
2372:
2362:
2360:
2347:
2346:
2342:
2295:
2291:
2246:
2242:
2233:
2224:
2217:
2201:
2197:
2187:
2185:
2172:
2171:
2164:
2159:
2143:
2138:
2110:
2105:
2078:
2073:
2045:
2040:
2013:
2008:
1980:
1975:
1948:
1943:
1915:
1910:
1883:
1878:
1850:
1845:
1818:
1813:
1786:
1781:
1754:
1749:
1722:
1717:
1690:
1685:
1658:
1653:
1626:
1621:
1616:
1611:
1590:
1589:
1588:
1587:
1586:
1583:mitotic process
1578:
1570:
1569:
1558:
1549:
1548:
1542:
1497:partial trisomy
1476:
1466:
1461:
1350:
1183:neurofibromin 2
1023:
497:
491:
344:gene prediction
340:number of genes
332:
330:Number of genes
327:
262:
243:
119:
78:
60:
54:
42:
40:
17:
12:
11:
5:
3961:
3951:
3950:
3945:
3928:
3927:
3925:
3924:
3919:
3914:
3909:
3908:
3907:
3896:
3894:
3890:
3889:
3886:
3885:
3883:
3882:
3877:
3872:
3867:
3862:
3857:
3852:
3847:
3842:
3837:
3832:
3827:
3822:
3817:
3812:
3807:
3801:
3799:
3793:
3792:
3790:
3789:
3784:
3779:
3774:
3769:
3763:
3761:
3752:
3751:
3746:
3731:
3729:
3725:
3724:
3722:
3721:
3716:
3715:
3714:
3709:
3704:
3699:
3689:
3688:
3687:
3682:
3672:
3667:
3661:
3659:
3653:
3652:
3650:
3649:
3648:
3647:
3642:
3637:
3632:
3622:
3621:
3620:
3615:
3610:
3605:
3603:Submetacentric
3600:
3590:
3585:
3580:
3575:
3570:
3565:
3560:
3555:
3550:
3544:
3535:
3530:
3529:or heterosome)
3523:Sex chromosome
3515:
3513:
3509:
3508:
3506:
3505:
3500:
3495:
3490:
3485:
3484:
3483:
3478:
3468:
3459:
3454:
3448:
3446:
3440:
3439:
3428:
3427:
3420:
3413:
3405:
3396:
3395:
3393:
3392:
3387:
3382:
3381:
3380:
3369:
3367:
3366:Related topics
3363:
3362:
3357:
3355:
3349:
3348:
3345:
3344:
3342:
3341:
3336:
3330:
3328:
3326:Sex chromosome
3322:
3321:
3319:
3318:
3313:
3308:
3303:
3298:
3293:
3288:
3283:
3278:
3273:
3268:
3263:
3258:
3253:
3248:
3243:
3238:
3233:
3228:
3223:
3218:
3213:
3207:
3205:
3196:
3194:Nuclear genome
3190:
3189:
3182:
3181:
3174:
3167:
3159:
3153:
3152:
3133:
3123:on 5 June 2011
3106:
3105:External links
3103:
3102:
3101:
3073:(8): 575–584.
3058:
3015:
2993:
2971:10.1086/340363
2965:(5): 1077–88.
2959:Am J Hum Genet
2950:
2913:
2887:(10): 819–30.
2881:Ann Intern Med
2876:
2847:
2834:10.1038/990031
2801:
2798:
2795:
2794:
2751:
2747:Arbitrary unit
2735:
2722:
2705:
2690:
2660:
2653:
2633:
2620:
2607:
2547:
2500:
2474:
2448:
2422:
2396:
2370:
2340:
2289:
2240:
2222:
2215:
2195:
2161:
2160:
2158:
2155:
2152:
2151:
2149:
2146:
2141:
2136:
2133:
2130:
2127:
2124:
2120:
2119:
2116:
2113:
2108:
2103:
2100:
2097:
2094:
2091:
2087:
2086:
2084:
2081:
2076:
2071:
2068:
2065:
2062:
2059:
2055:
2054:
2051:
2048:
2043:
2038:
2035:
2032:
2029:
2026:
2022:
2021:
2019:
2016:
2011:
2006:
2003:
2000:
1997:
1994:
1990:
1989:
1986:
1983:
1978:
1973:
1970:
1967:
1964:
1961:
1957:
1956:
1954:
1951:
1946:
1941:
1938:
1935:
1932:
1929:
1925:
1924:
1921:
1918:
1913:
1908:
1905:
1902:
1899:
1896:
1892:
1891:
1889:
1886:
1881:
1876:
1873:
1870:
1867:
1864:
1860:
1859:
1856:
1853:
1848:
1843:
1840:
1837:
1834:
1831:
1827:
1826:
1824:
1821:
1816:
1811:
1808:
1805:
1802:
1799:
1795:
1794:
1792:
1789:
1784:
1779:
1776:
1773:
1770:
1767:
1763:
1762:
1760:
1757:
1752:
1747:
1744:
1741:
1738:
1735:
1731:
1730:
1728:
1725:
1720:
1715:
1712:
1709:
1706:
1703:
1699:
1698:
1696:
1693:
1688:
1683:
1680:
1677:
1674:
1671:
1667:
1666:
1664:
1661:
1656:
1651:
1648:
1645:
1642:
1639:
1635:
1634:
1631:
1628:
1623:
1618:
1613:
1608:
1605:
1602:
1579:
1572:
1571:
1559:
1552:
1551:
1550:
1546:
1545:
1544:
1543:
1541:
1538:
1537:
1536:
1530:
1511:
1500:
1492:
1487:
1482:
1465:
1462:
1460:
1459:
1454:
1449:
1444:
1439:
1434:
1429:
1424:
1419:
1414:
1409:
1404:
1399:
1390:
1385:
1380:
1375:
1370:
1365:
1360:
1354:
1349:
1346:
1343:
1342:
1337:
1334:
1329:
1320:
1319:
1314:
1311:
1306:
1297:
1296:
1291:
1288:
1283:
1274:
1273:
1268:
1265:
1260:
1251:
1250:
1248:
1245:
1240:
1231:
1230:
1228:
1225:
1220:
1211:
1210:
1208:
1205:
1200:
1191:
1190:
1184:
1181:
1176:
1167:
1166:
1164:
1161:
1156:
1147:
1146:
1144:
1141:
1136:
1127:
1126:
1124:
1121:
1116:
1107:
1106:
1101:
1096:
1091:
1082:
1081:
1079:
1076:
1071:
1062:
1061:
1059:
1053:
1048:
1039:
1038:
1035:
1032:
1029:
1022:
1021:
1011:
1001:
991:
981:
971:
961:
951:
941:
940:synaptogyrin-1
931:
926:
920:
915:
905:
895:
889:
883:
873:
867:
861:
856:
851:
841:
831:
821:
815:
805:
800:
795:
785:
780:
775:
769:
764:
759:
754:
744:
739:
734:
724:
719:
714:
704:
698:
692:
682:
677:
671:
665:
659:
654:
648:
642:
637:
632:
627:
621:
612:
602:
596:
590:
584:
578:
572:
566:
560:
554:
548:
542:
532:
522:
512:
501:
490:
487:
484:
483:
480:
478:
475:
472:
469:
463:
462:
459:
457:
454:
451:
448:
442:
441:
438:
436:
433:
430:
427:
421:
420:
417:
415:
412:
409:
406:
400:
399:
396:
394:
391:
388:
385:
379:
378:
375:
372:
367:
362:
357:
331:
328:
326:
323:
273:
272:
260:
254:
253:
241:
235:
234:
228:
227:
222:
216:
215:
210:
204:
203:
198:
192:
191:
186:
180:
179:
175:
174:
169:
163:
162:
157:
151:
150:
145:
139:
138:
133:
127:
126:
122:
121:
114:
108:
107:
102:
98:
97:
90:
81:
80:
75:
67:
66:
62:
61:
55:in human male
52:
44:
43:
34:
26:
25:
15:
9:
6:
4:
3:
2:
3960:
3949:
3946:
3944:
3941:
3940:
3938:
3923:
3920:
3918:
3915:
3913:
3910:
3906:
3903:
3902:
3901:
3898:
3897:
3895:
3891:
3881:
3878:
3876:
3873:
3871:
3868:
3866:
3863:
3861:
3858:
3856:
3853:
3851:
3848:
3846:
3843:
3841:
3838:
3836:
3833:
3831:
3828:
3826:
3823:
3821:
3818:
3816:
3813:
3811:
3808:
3806:
3803:
3802:
3800:
3798:
3794:
3788:
3785:
3783:
3780:
3778:
3775:
3773:
3770:
3768:
3765:
3764:
3762:
3760:
3756:
3750:
3747:
3744:
3740:
3736:
3733:
3732:
3730:
3726:
3720:
3717:
3713:
3710:
3708:
3705:
3703:
3700:
3698:
3695:
3694:
3693:
3690:
3686:
3683:
3681:
3678:
3677:
3676:
3673:
3671:
3668:
3666:
3663:
3662:
3660:
3658:and evolution
3654:
3646:
3643:
3641:
3638:
3636:
3633:
3631:
3628:
3627:
3626:
3623:
3619:
3616:
3614:
3611:
3609:
3606:
3604:
3601:
3599:
3596:
3595:
3594:
3591:
3589:
3586:
3584:
3583:Isochromosome
3581:
3579:
3576:
3574:
3571:
3569:
3566:
3564:
3561:
3559:
3556:
3554:
3551:
3548:
3545:
3543:
3539:
3536:
3534:
3531:
3528:
3524:
3520:
3517:
3516:
3514:
3510:
3504:
3501:
3499:
3496:
3494:
3491:
3489:
3486:
3482:
3479:
3477:
3474:
3473:
3472:
3469:
3467:
3463:
3460:
3458:
3455:
3453:
3450:
3449:
3447:
3441:
3437:
3433:
3426:
3421:
3419:
3414:
3412:
3407:
3406:
3403:
3391:
3388:
3386:
3383:
3379:
3376:
3375:
3374:
3371:
3370:
3368:
3364:
3360:
3356:
3354:
3350:
3340:
3337:
3335:
3332:
3331:
3329:
3327:
3323:
3317:
3314:
3312:
3309:
3307:
3304:
3302:
3299:
3297:
3294:
3292:
3289:
3287:
3284:
3282:
3279:
3277:
3274:
3272:
3269:
3267:
3264:
3262:
3259:
3257:
3254:
3252:
3249:
3247:
3244:
3242:
3239:
3237:
3234:
3232:
3229:
3227:
3224:
3222:
3219:
3217:
3214:
3212:
3209:
3208:
3206:
3204:
3200:
3197:
3195:
3191:
3187:
3180:
3175:
3173:
3168:
3166:
3161:
3160:
3157:
3142:
3138:
3134:
3122:
3118:
3114:
3109:
3108:
3098:
3094:
3089:
3084:
3080:
3076:
3072:
3068:
3064:
3059:
3055:
3051:
3046:
3041:
3037:
3033:
3030:(4): 529–40.
3029:
3025:
3021:
3016:
3012:
3008:
3004:
3000:
2994:
2990:
2986:
2981:
2976:
2972:
2968:
2964:
2960:
2956:
2951:
2947:
2943:
2939:
2935:
2931:
2927:
2923:
2919:
2914:
2910:
2906:
2902:
2898:
2894:
2890:
2886:
2882:
2877:
2873:
2869:
2865:
2861:
2857:
2853:
2848:
2844:
2840:
2835:
2830:
2826:
2822:
2818:
2814:
2810:
2804:
2803:
2791:
2787:
2783:
2780:
2776:
2772:
2768:
2764:
2760:
2755:
2748:
2742:
2740:
2732:
2726:
2719:
2715:
2709:
2701:
2697:
2693:
2687:
2683:
2679:
2675:
2671:
2664:
2656:
2650:
2646:
2645:
2637:
2630:
2624:
2617:
2611:
2603:
2599:
2594:
2589:
2584:
2579:
2575:
2571:
2567:
2564:
2563:
2558:
2551:
2543:
2539:
2535:
2531:
2527:
2523:
2519:
2515:
2511:
2504:
2489:. 19 May 2017
2488:
2484:
2478:
2463:. 19 May 2017
2462:
2458:
2452:
2437:. 19 May 2017
2436:
2432:
2426:
2410:
2406:
2400:
2384:
2380:
2374:
2358:
2354:
2350:
2344:
2336:
2332:
2327:
2322:
2317:
2312:
2308:
2304:
2300:
2293:
2285:
2281:
2276:
2271:
2267:
2263:
2259:
2255:
2251:
2244:
2237:
2231:
2229:
2227:
2218:
2212:
2208:
2207:
2199:
2183:
2179:
2175:
2169:
2167:
2162:
2150:
2147:
2142:
2137:
2134:
2131:
2128:
2125:
2122:
2121:
2117:
2114:
2109:
2104:
2101:
2098:
2095:
2092:
2089:
2088:
2085:
2082:
2077:
2072:
2069:
2066:
2063:
2060:
2057:
2056:
2052:
2049:
2044:
2039:
2036:
2033:
2030:
2027:
2024:
2023:
2020:
2017:
2012:
2007:
2004:
2001:
1998:
1995:
1992:
1991:
1987:
1984:
1979:
1974:
1971:
1968:
1965:
1962:
1959:
1958:
1955:
1952:
1947:
1942:
1939:
1936:
1933:
1930:
1927:
1926:
1922:
1919:
1914:
1909:
1906:
1903:
1900:
1897:
1894:
1893:
1890:
1887:
1882:
1877:
1874:
1871:
1868:
1865:
1862:
1861:
1857:
1854:
1849:
1844:
1841:
1838:
1835:
1832:
1829:
1828:
1825:
1822:
1817:
1812:
1809:
1806:
1803:
1800:
1797:
1796:
1793:
1790:
1785:
1780:
1777:
1774:
1771:
1768:
1765:
1764:
1761:
1758:
1753:
1748:
1745:
1742:
1739:
1736:
1733:
1732:
1729:
1726:
1721:
1716:
1713:
1710:
1707:
1704:
1701:
1700:
1697:
1694:
1689:
1684:
1681:
1678:
1675:
1672:
1669:
1668:
1665:
1662:
1657:
1652:
1649:
1646:
1643:
1640:
1637:
1636:
1632:
1629:
1624:
1619:
1614:
1609:
1606:
1603:
1600:
1599:
1595:
1584:
1576:
1567:
1563:
1556:
1534:
1531:
1528:
1524:
1520:
1516:
1515:translocation
1512:
1509:
1504:
1501:
1498:
1493:
1491:
1488:
1486:
1483:
1480:
1474:
1471:
1470:
1469:
1458:
1457:Schizophrenia
1455:
1453:
1450:
1448:
1445:
1443:
1440:
1438:
1435:
1433:
1430:
1428:
1425:
1423:
1420:
1418:
1415:
1413:
1410:
1408:
1407:Ewing sarcoma
1405:
1403:
1400:
1398:
1394:
1391:
1389:
1386:
1384:
1381:
1379:
1376:
1374:
1371:
1369:
1366:
1364:
1363:Breast cancer
1361:
1359:
1356:
1355:
1353:
1341:
1338:
1335:
1333:
1330:
1328:
1325:
1322:
1321:
1318:
1315:
1312:
1310:
1307:
1305:
1302:
1299:
1298:
1295:
1292:
1289:
1287:
1284:
1282:
1279:
1276:
1275:
1272:
1269:
1266:
1264:
1261:
1259:
1256:
1253:
1252:
1249:
1246:
1244:
1241:
1239:
1236:
1233:
1232:
1229:
1226:
1224:
1221:
1219:
1216:
1213:
1212:
1209:
1206:
1204:
1201:
1199:
1196:
1193:
1192:
1189:
1185:
1182:
1180:
1177:
1175:
1172:
1169:
1168:
1165:
1162:
1160:
1157:
1155:
1152:
1149:
1148:
1145:
1142:
1140:
1137:
1135:
1132:
1129:
1128:
1125:
1122:
1120:
1117:
1115:
1114:q11.21-q11.23
1112:
1109:
1108:
1105:
1104:Schizophrenia
1102:
1100:
1097:
1095:
1092:
1090:
1087:
1084:
1083:
1080:
1077:
1075:
1072:
1070:
1067:
1064:
1063:
1060:
1057:
1054:
1052:
1049:
1047:
1044:
1041:
1040:
1036:
1033:
1030:
1027:
1026:
1019:
1015:
1012:
1009:
1005:
1002:
999:
995:
992:
989:
985:
982:
979:
975:
972:
969:
965:
962:
959:
955:
952:
949:
945:
942:
939:
935:
932:
930:
927:
924:
921:
919:
916:
913:
909:
906:
903:
899:
896:
893:
890:
887:
884:
881:
877:
874:
871:
868:
865:
862:
860:
857:
855:
852:
849:
845:
842:
839:
835:
832:
829:
825:
822:
819:
816:
813:
809:
806:
804:
801:
799:
796:
793:
789:
786:
784:
781:
779:
776:
773:
770:
768:
765:
763:
760:
758:
755:
752:
748:
745:
743:
740:
738:
735:
732:
728:
725:
723:
720:
718:
715:
712:
708:
705:
702:
699:
696:
693:
690:
686:
683:
681:
678:
675:
672:
669:
666:
663:
660:
658:
655:
652:
649:
646:
643:
641:
638:
636:
633:
631:
628:
625:
622:
620:
617:: encoding a
616:
613:
610:
606:
603:
600:
597:
594:
591:
588:
585:
582:
579:
576:
573:
570:
567:
564:
561:
558:
555:
552:
549:
546:
543:
540:
536:
533:
530:
526:
523:
520:
516:
513:
510:
506:
503:
502:
500:
496:
481:
479:
476:
473:
470:
468:
465:
464:
460:
458:
455:
452:
449:
447:
444:
443:
439:
437:
434:
431:
428:
426:
423:
422:
418:
416:
413:
410:
407:
405:
402:
401:
397:
395:
392:
389:
386:
384:
381:
380:
377:Release date
376:
373:
371:
368:
366:
363:
361:
358:
356:Estimated by
355:
354:
351:
349:
345:
341:
337:
322:
320:
319:chromosome 21
316:
312:
307:
305:
300:
298:
294:
291:
287:
283:
279:
278:Chromosome 22
269:
265:
261:
259:
255:
250:
246:
242:
240:
236:
233:
229:
226:
225:Chromosome 22
223:
221:
217:
214:
213:Chromosome 22
211:
209:
205:
202:
201:Chromosome 22
199:
197:
193:
190:
189:Chromosome 22
187:
185:
181:
176:
173:
170:
168:
164:
161:
158:
156:
152:
149:
146:
144:
140:
137:
134:
132:
128:
123:
118:
115:
113:
109:
106:
103:
99:
95:
91:
89:
82:
77:51,324,926 bp
76:
73:
68:
63:
58:
50:
45:
38:
32:
27:
24:Chromosome 22
22:
19:
3624:
3592:
3432:Cytogenetics
3373:Human genome
3315:
3186:Human genome
3144:. Retrieved
3140:
3125:. Retrieved
3121:the original
3116:
3070:
3066:
3027:
3023:
3005:(1): 11–24.
3002:
2998:
2962:
2958:
2921:
2917:
2884:
2880:
2858:(1): 89–97.
2855:
2851:
2816:
2812:
2789:
2785:
2778:
2770:
2765:, generally
2758:
2754:
2725:
2720:": Long arm.
2717:
2713:
2708:
2673:
2663:
2643:
2636:
2623:
2610:
2565:
2560:
2550:
2517:
2513:
2503:
2491:. Retrieved
2486:
2477:
2465:. Retrieved
2460:
2451:
2439:. Retrieved
2434:
2425:
2413:. Retrieved
2408:
2399:
2387:. Retrieved
2382:
2373:
2361:. Retrieved
2357:the original
2352:
2343:
2306:
2302:
2292:
2257:
2253:
2243:
2205:
2198:
2186:. Retrieved
2182:Homo sapiens
2181:
2177:
1479:cleft palate
1467:
1351:
498:
333:
315:chromosome 1
308:
301:
277:
276:
18:
3645:Polycentric
3635:Monocentric
3618:Holocentric
3613:Acrocentric
3608:Telocentric
3598:Metacentric
3476:Euchromatin
3436:chromosomes
3067:J Med Genet
2999:Genet Couns
2303:Genome Biol
1134:q12.1-q13.1
1046:q11.1-q11.2
1034:Description
1016:: encoding
1006:: encoding
996:: encoding
986:: encoding
976:: encoding
966:: encoding
956:: encoding
946:: encoding
936:: encoding
910:: encoding
900:: encoding
878:: encoding
846:: encoding
836:: encoding
826:: encoding
810:: encoding
790:: encoding
749:: encoding
729:: encoding
607:: encoding
537:: encoding
527:: encoding
517:: encoding
507:: encoding
482:2017-05-19
461:2018-02-28
440:2017-03-29
419:2019-07-08
398:2016-09-08
370:Pseudogenes
282:chromosomes
117:Acrocentric
3937:Categories
3797:Centromere
3728:Structures
3707:Polyploidy
3697:Aneuploidy
3498:Nucleosome
3488:Chromosome
2852:Genet Test
2782:Centromere
2309:(5): 206.
2157:References
2144:50,818,468
2139:49,100,001
2111:49,100,000
2106:48,100,001
2079:48,100,000
2074:43,800,001
2046:43,800,000
2041:40,600,001
2014:40,600,000
2009:37,200,001
1981:37,200,000
1976:31,800,001
1949:31,800,000
1944:29,200,001
1916:29,200,000
1911:25,500,001
1884:25,500,000
1879:23,100,001
1851:23,100,000
1846:21,700,001
1819:21,700,000
1814:17,400,001
1787:17,400,000
1782:15,000,001
1755:15,000,000
1750:13,700,001
1723:13,700,000
1186:bilateral
1037:Condition
747:MIRLET7BHG
493:See also:
293:base pairs
120:(15.0 Mbp)
3749:Protamine
3656:Processes
3640:Dicentric
3493:Chromatid
3471:Chromatin
3452:Karyotype
3024:Genes Dev
2763:G banding
2542:205319722
1718:9,400,001
1691:9,400,000
1686:4,300,001
1659:4,300,000
709:encoding
707:LINC00899
687:encoding
635:EP300-AS1
489:Gene list
311:karyotype
284:in human
245:NC_000022
172:Gene list
160:Gene list
148:Gene list
136:Gene list
57:karyogram
37:G-banding
3893:See also
3735:Telomere
3702:Euploidy
3630:Acentric
3527:allosome
3519:Autosome
3445:concepts
3203:Autosome
3097:12920066
3054:12600945
3011:10191425
2989:11925570
2946:22941004
2938:12175881
2909:25865321
2901:12755554
2872:10464604
2843:10591208
2792:: Stalk.
2700:16666470
2602:12477929
2534:25810350
2415:16 March
2363:7 August
2335:20441615
2284:10582915
1633:Density
1625:Basepair
1620:Basepair
1519:leukemia
944:TBC1D10A
701:KIAA0930
569:CDC42EP1
515:APOBEC3B
264:CM000684
105:Autosome
88:of genes
70:Length (
65:Features
3905:Plasmid
3759:Histone
3670:Meiosis
3665:Mitosis
3088:1735560
2821:Bibcode
2775:CG-rich
2767:AT-rich
2570:Bibcode
2409:UniProt
2326:2898077
2275:1117192
1594:G-bands
1562:Ensembl
1309:SULT4A1
1078:T-box 1
1018:protein
998:protein
978:protein
968:protein
958:protein
948:protein
938:protein
923:SHFM3P1
912:protein
902:protein
880:protein
848:protein
818:PI4KAP2
792:protein
751:protein
711:protein
689:protein
651:FAM227A
583:(22q12)
539:protein
529:protein
525:ARFGAP3
519:protein
509:protein
446:UniProt
425:Ensembl
374:Source
313:, with
258:GenBank
184:Ensembl
155:UniProt
79:(CHM13)
3466:Genome
3457:Ploidy
3095:
3085:
3052:
3045:195998
3042:
3009:
2987:
2980:447586
2977:
2944:
2936:
2907:
2899:
2870:
2841:
2813:Nature
2698:
2688:
2651:
2600:
2593:139234
2590:
2540:
2532:
2493:20 May
2467:20 May
2441:20 May
2389:19 May
2333:
2323:
2282:
2272:
2213:
2188:28 May
1630:Stain
1622:start
1612:start
1286:SHANK3
1069:q11.21
1008:enzyme
988:enzyme
934:SYNGR1
898:SAMM50
838:enzyme
834:PNPLA3
828:enzyme
812:enzyme
731:enzyme
722:MAPK12
668:HMGXB4
662:GTPBP1
609:enzyme
605:CSNK1E
593:CRELD2
557:CARD10
239:RefSeq
196:Entrez
3743:TINF2
3512:Types
3443:Basic
3146:6 May
3127:6 May
2942:S2CID
2905:S2CID
2790:stalk
2731:locus
2696:S2CID
2538:S2CID
2129:13.33
2096:13.32
2064:13.31
1869:11.23
1836:11.22
1804:11.21
1695:stalk
1627:stop
1617:stop
1607:Band
1601:Chr.
1332:PARVB
1327:q13.3
1304:q13.3
1281:q13.3
1263:WNT7B
1258:q13.3
1243:EP300
1238:q13.2
1223:APOL1
1218:q13.1
1203:SOX10
1174:q12.2
1159:CHEK2
1154:q12.1
1094:RTN4R
1028:Locus
1014:XRCC6
1004:TTLL1
994:TTC28
974:THOC5
964:THAP7
929:SOX10
918:SEPT5
908:SEPT3
876:RRP7A
870:RNU12
844:PRAME
808:PI4KA
803:PDGFB
798:PARVB
788:NOL12
772:MTP18
762:MMP11
717:MAPK1
695:IGLL5
685:IGLJ3
674:IFT27
657:FBLN1
645:TAFA5
640:EWSR1
630:EP300
624:DGCR6
615:DGCR5
599:CSDC2
581:CHEK2
575:CECR1
535:ASCC2
325:Genes
297:cells
286:cells
268:FASTA
249:FASTA
92:417 (
3525:(or
3148:2017
3129:2017
3093:PMID
3050:PMID
3007:PMID
2985:PMID
2934:PMID
2897:PMID
2868:PMID
2839:PMID
2779:acen
2771:gneg
2759:gpos
2686:ISBN
2649:ISBN
2598:PMID
2530:PMID
2495:2017
2487:NCBI
2469:2017
2461:NCBI
2443:2017
2435:NCBI
2417:2018
2391:2017
2365:2019
2331:PMID
2280:PMID
2211:ISBN
2190:2017
2178:NCBI
2148:gneg
2135:3400
2132:3290
2115:gpos
2102:3290
2099:3181
2083:gneg
2070:3181
2067:2852
2050:gpos
2037:2852
2034:2687
2031:13.2
2018:gneg
2005:2687
2002:2413
1999:13.1
1985:gpos
1972:2413
1969:2194
1966:12.3
1953:gneg
1940:2194
1937:2029
1934:12.2
1920:gpos
1907:2029
1904:1878
1901:12.1
1888:gneg
1875:1878
1872:1700
1855:gpos
1842:1700
1839:1563
1823:gneg
1810:1563
1807:1234
1791:acen
1778:1234
1775:1015
1772:11.1
1759:acen
1746:1015
1740:11.1
1727:gvar
1708:11.2
1663:gvar
1615:ISCN
1610:ISCN
1604:Arm
1139:NEFH
1119:COMT
1074:TBX1
1051:IGL@
1031:Gene
1020:Ku70
984:TRMU
892:RTL6
886:RTCB
864:RNR5
859:RBX1
854:RAC2
824:PISD
778:MYH9
757:MKL1
737:MCM5
727:MCAT
680:IGL@
587:COMT
563:CBX7
545:ATF4
511:ADM2
505:ADM2
477:379
467:NCBI
435:325
414:295
404:HGNC
383:CCDS
348:CCDS
220:UCSC
208:NCBI
167:NCBI
143:HGNC
131:CCDS
101:Type
94:CCDS
3777:H2B
3772:H2A
3083:PMC
3075:doi
3040:PMC
3032:doi
2975:PMC
2967:doi
2926:doi
2889:doi
2885:138
2860:doi
2829:doi
2817:402
2786:var
2678:doi
2588:PMC
2578:doi
2522:doi
2518:167
2321:PMC
2311:doi
2270:PMC
2262:doi
2258:319
2254:BMJ
2118:50
2053:50
1988:50
1923:50
1858:25
1743:836
1714:836
1711:576
1682:576
1679:260
1650:260
1395:or
1198:q13
1179:NF2
1089:q11
954:TEF
783:NF2
767:MN1
742:MIF
551:BCR
474:392
471:474
450:496
432:515
429:489
411:161
408:424
387:417
290:DNA
86:No.
3939::
3820:C2
3815:C1
3787:H4
3782:H3
3767:H1
3737::
3434::
3316:22
3311:21
3306:20
3301:19
3296:18
3291:17
3286:16
3281:15
3276:14
3271:13
3266:12
3261:11
3256:10
3139:.
3115:.
3091:.
3081:.
3071:40
3069:.
3065:.
3048:.
3038:.
3028:17
3026:.
3022:.
3003:10
3001:.
2983:.
2973:.
2963:70
2961:.
2957:.
2940:.
2932:.
2922:20
2920:.
2903:.
2895:.
2883:.
2866:.
2854:.
2837:.
2827:.
2815:.
2811:.
2784:.
2738:^
2694:.
2684:.
2672:.
2596:.
2586:.
2576:.
2566:99
2559:.
2536:.
2528:.
2516:.
2512:.
2485:.
2459:.
2433:.
2407:.
2381:.
2351:.
2329:.
2319:.
2307:11
2305:.
2301:.
2278:.
2268:.
2256:.
2252:.
2225:^
2176:.
2165:^
2126:q
2123:22
2093:q
2090:22
2061:q
2058:22
2028:q
2025:22
1996:q
1993:22
1963:q
1960:22
1931:q
1928:22
1898:q
1895:22
1866:q
1863:22
1833:q
1830:22
1801:q
1798:22
1769:q
1766:22
1737:p
1734:22
1705:p
1702:22
1676:12
1673:p
1670:22
1644:13
1641:p
1638:22
1568:).
1564:,
1324:22
1301:22
1278:22
1255:22
1235:22
1215:22
1195:22
1171:22
1151:22
1131:22
1111:22
1086:22
1066:22
1043:22
456:—
393:—
299:.
270:)
251:)
72:bp
3880:T
3875:Q
3870:P
3865:O
3860:N
3855:M
3850:K
3845:J
3840:I
3835:H
3830:F
3825:E
3810:B
3805:A
3745:)
3741:(
3540:/
3521:/
3464:/
3424:e
3417:t
3410:v
3339:Y
3334:X
3251:9
3246:8
3241:7
3236:6
3231:5
3226:4
3221:3
3216:2
3211:1
3178:e
3171:t
3164:v
3150:.
3131:.
3099:.
3077::
3056:.
3034::
3013:.
2991:.
2969::
2948:.
2928::
2911:.
2891::
2874:.
2862::
2856:2
2845:.
2831::
2823::
2749:.
2733:.
2718:q
2714:p
2712:"
2702:.
2680::
2657:.
2604:.
2580::
2572::
2544:.
2524::
2497:.
2471:.
2445:.
2419:.
2393:.
2367:.
2337:.
2313::
2286:.
2264::
2219:.
2192:.
1654:1
1647:0
1585:.
1495:(
925::
774::
453:—
390:—
266:(
247:(
96:)
74:)
59:.
39:.
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
