Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | acute promyelocytic leukemia | | EXP | | 11554173 | CTD Direct Evidence: therapeutic | CTD | PMID:21056550 | |
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Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | acute promyelocytic leukemia | | EXP | | 11554173 | CTD Direct Evidence: therapeutic | CTD | PMID:21056550 | |
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# | Reference Title | Reference Citation |
1. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
PMID:11679670 | PMID:11914277 | PMID:12434020 | PMID:12624257 | PMID:14573789 | PMID:15131085 | PMID:15183728 | PMID:15325244 | PMID:15766526 | PMID:16166262 | PMID:16381832 | PMID:17604727 |
PMID:17616659 | PMID:18320040 | PMID:18362358 | PMID:18449891 | PMID:18483394 | PMID:18708755 | PMID:18759964 | PMID:18766170 | PMID:18854308 | PMID:19144909 | PMID:19148136 | PMID:19250063 |
PMID:19347735 | PMID:19401561 | PMID:19498445 | PMID:19779621 | PMID:19823025 | PMID:19865490 | PMID:19883312 | PMID:20060366 | PMID:20159880 | PMID:20621999 | PMID:20626035 | PMID:20647767 |
PMID:20876285 | PMID:21037258 | PMID:21130495 | PMID:21205891 | PMID:21336967 | PMID:21354921 | PMID:21400525 | PMID:21454377 | PMID:21472816 | PMID:21532615 | PMID:21575235 | PMID:21602527 |
PMID:21778999 | PMID:21885851 | PMID:22002311 | PMID:22049078 | PMID:22049153 | PMID:22096249 | PMID:22133358 | PMID:22139073 | PMID:22249219 | PMID:22292036 | PMID:22564678 | PMID:22574716 |
PMID:22583478 | PMID:22677435 | PMID:22684875 | PMID:22781767 | PMID:22922827 | PMID:22940131 | PMID:22959509 | PMID:23083510 | PMID:23104180 | PMID:23175429 | PMID:23226427 | PMID:23233752 |
PMID:23260326 | PMID:23325924 | PMID:23380758 | PMID:23487264 | PMID:23507142 | PMID:23613938 | PMID:23649629 | PMID:23686310 | PMID:23783433 | PMID:23897768 | PMID:23907579 | PMID:23954293 |
PMID:23991964 | PMID:24026141 | PMID:24026226 | PMID:24045965 | PMID:24086143 | PMID:24089558 | PMID:24148817 | PMID:24285725 | PMID:24391925 | PMID:24392455 | PMID:24418124 | PMID:24500260 |
PMID:24600978 | PMID:24650689 | PMID:24710569 | PMID:24732594 | PMID:24852767 | PMID:24885794 | PMID:24916701 | PMID:24971479 | PMID:25033200 | PMID:25040181 | PMID:25054189 | PMID:25227104 |
PMID:25249297 | PMID:25261849 | PMID:25336585 | PMID:25367852 | PMID:25403480 | PMID:25405832 | PMID:25435430 | PMID:25584808 | PMID:25594541 | PMID:25641414 | PMID:25662703 | PMID:25672252 |
PMID:25738263 | PMID:25743273 | PMID:25815587 | PMID:25830480 | PMID:25888955 | PMID:25979194 | PMID:26031775 | PMID:26071245 | PMID:26073083 | PMID:26133725 | PMID:26223652 | PMID:26350536 |
PMID:26440600 | PMID:26474056 | PMID:26499886 | PMID:26516702 | PMID:26597031 | PMID:26640145 | PMID:26646931 | PMID:26656154 | PMID:26722459 | PMID:26821018 | PMID:26908869 | PMID:26918603 |
PMID:26968104 | PMID:27055667 | PMID:27064390 | PMID:27305142 | PMID:27343180 | PMID:27476546 | PMID:27605261 | PMID:27683052 | PMID:27713175 | PMID:27748453 | PMID:27748823 | PMID:27846323 |
PMID:27854515 | PMID:27857191 | PMID:27875659 | PMID:27930363 | PMID:28082316 | PMID:28159509 | PMID:28261881 | PMID:28299339 | PMID:28303998 | PMID:28377382 | PMID:28431233 | PMID:28628119 |
PMID:28634901 | PMID:28667493 | PMID:28798470 | PMID:28859135 | PMID:28968438 | PMID:29044221 | PMID:29094504 | PMID:29138833 | PMID:29180670 | PMID:29259008 | PMID:29299981 | PMID:29355387 |
PMID:29359963 | PMID:29383679 | PMID:29399695 | PMID:29484411 | PMID:29522280 | PMID:29559751 | PMID:29687850 | PMID:29739419 | PMID:29771408 | PMID:29880900 | PMID:29935185 | PMID:29955039 |
PMID:30025387 | PMID:30132525 | PMID:30136280 | PMID:30154547 | PMID:30178829 | PMID:30252587 | PMID:30365148 | PMID:30536619 | PMID:30548945 | PMID:30552617 | PMID:30582201 | PMID:30657555 |
PMID:30706130 | PMID:30753902 | PMID:30861602 | PMID:30911942 | PMID:30942450 | PMID:30957556 | PMID:31018244 | PMID:31102273 | PMID:31232026 | PMID:31298377 | PMID:31355416 | PMID:31379227 |
PMID:31383786 | PMID:31406207 | PMID:31427084 | PMID:31568645 | PMID:31640928 | PMID:31643078 | PMID:31648231 | PMID:31801064 | PMID:31841182 | PMID:31872565 | PMID:31876684 | PMID:32024878 |
PMID:32027086 | PMID:32054948 | PMID:32057163 | PMID:32307795 | PMID:32345959 | PMID:32369253 | PMID:32424097 | PMID:32486604 | PMID:32502422 | PMID:32513543 | PMID:32513696 | PMID:32524326 |
PMID:32705237 | PMID:32774515 | PMID:32954360 | PMID:33015786 | PMID:33051165 | PMID:33095833 | PMID:33141998 | PMID:33148068 | PMID:33155198 | PMID:33264723 | PMID:33338854 | PMID:33411678 |
PMID:33467738 | PMID:33545201 | PMID:33548740 | PMID:33751108 | PMID:33789312 | PMID:33824285 | PMID:33836616 | PMID:33970852 | PMID:33975517 | PMID:34022711 | PMID:34580516 | PMID:34592064 |
PMID:34627262 | PMID:34791478 | PMID:35064090 | PMID:35162959 | PMID:35536149 | PMID:35593364 | PMID:35666610 | PMID:36029069 | PMID:36111932 | PMID:36177782 | PMID:36202613 | PMID:36476595 |
PMID:36484570 | PMID:36555676 | PMID:37055445 | PMID:37549238 | PMID:37602450 | PMID:38514064 |
MIR16-1 (Homo sapiens - human) |
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Mir16-1 (Mus musculus - house mouse) |
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MIR16-1 (Canis lupus familiaris - dog) |
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MIR16-2 (Sus scrofa - pig) |
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Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh37/hg19 13q11-34(chr13:19053605-115108528)x3 | copy number gain | See cases [RCV001353184] | Chr13:19053605..115108528 [GRCh37] Chr13:13q11-34 |
pathogenic |
GRCh38/hg38 13q12.3-31.3(chr13:31363472-90575292)x3 | copy number gain | See cases [RCV000050293] | Chr13:31363472..90575292 [GRCh38] Chr13:31937609..91227546 [GRCh37] Chr13:30835609..90025547 [NCBI36] Chr13:13q12.3-31.3 |
pathogenic |
GRCh38/hg38 13q14.12-31.3(chr13:44967523-92738168)x1 | copy number loss | See cases [RCV000050891] | Chr13:44967523..92738168 [GRCh38] Chr13:45541658..93390421 [GRCh37] Chr13:44439658..92188422 [NCBI36] Chr13:13q14.12-31.3 |
pathogenic |
GRCh38/hg38 13q12.3-21.33(chr13:30697728-69471973)x1 | copy number loss | See cases [RCV000051373] | Chr13:30697728..69471973 [GRCh38] Chr13:31271865..70046105 [GRCh37] Chr13:30169865..68944106 [NCBI36] Chr13:13q12.3-21.33 |
pathogenic |
GRCh38/hg38 13q12.11-34(chr13:18946182-114304628)x3 | copy number gain | See cases [RCV000053726] | Chr13:18946182..114304628 [GRCh38] Chr13:19520322..115070103 [GRCh37] Chr13:18418322..114088205 [NCBI36] Chr13:13q12.11-34 |
pathogenic |
GRCh38/hg38 13q12.11-34(chr13:19837395-114327173)x3 | copy number gain | See cases [RCV000053731] | Chr13:19837395..114327173 [GRCh38] Chr13:20411535..115085141 [GRCh37] Chr13:19309535..114110750 [NCBI36] Chr13:13q12.11-34 |
pathogenic |
GRCh38/hg38 13q12.3-31.1(chr13:30318913-83610426)x3 | copy number gain | See cases [RCV000053737] | Chr13:30318913..83610426 [GRCh38] Chr13:30893050..84184561 [GRCh37] Chr13:29791050..83082562 [NCBI36] Chr13:13q12.3-31.1 |
pathogenic |
GRCh38/hg38 13q11-34(chr13:18565048-114327173)x3 | copy number gain | See cases [RCV000053719] | Chr13:18565048..114327173 [GRCh38] Chr13:19139188..115085141 [GRCh37] Chr13:18037188..114110750 [NCBI36] Chr13:13q11-34 |
pathogenic |
GRCh38/hg38 13q11-34(chr13:18850545-114327173)x3 | copy number gain | See cases [RCV000053723] | Chr13:18850545..114327173 [GRCh38] Chr13:19296527..115085141 [GRCh37] Chr13:18194527..114110750 [NCBI36] Chr13:13q11-34 |
pathogenic |
GRCh38/hg38 13q13.2-34(chr13:33528097-114327173)x3 | copy number gain | See cases [RCV000053759] | Chr13:33528097..114327173 [GRCh38] Chr13:34102234..115085141 [GRCh37] Chr13:33000234..114110750 [NCBI36] Chr13:13q13.2-34 |
pathogenic |
GRCh38/hg38 13q14.11-34(chr13:43219125-114327314)x3 | copy number gain | See cases [RCV000053762] | Chr13:43219125..114327314 [GRCh38] Chr13:43793261..115085141 [GRCh37] Chr13:42691261..114110891 [NCBI36] Chr13:13q14.11-34 |
pathogenic |
GRCh38/hg38 13q14.11-34(chr13:44164751-114327173)x3 | copy number gain | See cases [RCV000053764] | Chr13:44164751..114327173 [GRCh38] Chr13:44738887..115085141 [GRCh37] Chr13:43636887..114110750 [NCBI36] Chr13:13q14.11-34 |
pathogenic |
GRCh38/hg38 13q14.12-34(chr13:44733046-114327173)x3 | copy number gain | See cases [RCV000053767] | Chr13:44733046..114327173 [GRCh38] Chr13:45307182..115085141 [GRCh37] Chr13:44205182..114110750 [NCBI36] Chr13:13q14.12-34 |
pathogenic |
GRCh38/hg38 13q13.3-21.31(chr13:36777318-62955876)x1 | copy number loss | See cases [RCV000133696] | Chr13:36777318..62955876 [GRCh38] Chr13:37351455..63530009 [GRCh37] Chr13:36249455..62428010 [NCBI36] Chr13:13q13.3-21.31 |
pathogenic |
GRCh38/hg38 13q12.11-34(chr13:19833130-114298614)x3 | copy number gain | See cases [RCV000134104] | Chr13:19833130..114298614 [GRCh38] Chr13:20407270..115064089 [GRCh37] Chr13:19305270..114082191 [NCBI36] Chr13:13q12.11-34 |
pathogenic |
GRCh38/hg38 13q14.11-31.1(chr13:41288493-85137552)x3 | copy number gain | See cases [RCV000133944] | Chr13:41288493..85137552 [GRCh38] Chr13:41862629..85711687 [GRCh37] Chr13:40760629..84609688 [NCBI36] Chr13:13q14.11-31.1 |
pathogenic |
GRCh38/hg38 13q12.3-21.32(chr13:31553608-65470367)x3 | copy number gain | See cases [RCV000135808] | Chr13:31553608..65470367 [GRCh38] Chr13:32127745..66044499 [GRCh37] Chr13:31025745..64942500 [NCBI36] Chr13:13q12.3-21.32 |
pathogenic |
GRCh38/hg38 13q11-34(chr13:18445862-114327173)x1 | copy number loss | See cases [RCV000135610] | Chr13:18445862..114327173 [GRCh38] Chr13:19020001..115085141 [GRCh37] Chr13:10098739..114110750 [NCBI36] Chr13:13q11-34 |
pathogenic |
GRCh38/hg38 13q14.11-31.1(chr13:41143820-85137552)x1 | copy number loss | See cases [RCV000136526] | Chr13:41143820..85137552 [GRCh38] Chr13:41717956..85711687 [GRCh37] Chr13:40615956..84609688 [NCBI36] Chr13:13q14.11-31.1 |
pathogenic |
GRCh38/hg38 13q14.2-14.3(chr13:48307302-50927473)x1 | copy number loss | See cases [RCV000136624] | Chr13:48307302..50927473 [GRCh38] Chr13:48881438..51501609 [GRCh37] Chr13:47779439..50399610 [NCBI36] Chr13:13q14.2-14.3 |
pathogenic |
GRCh38/hg38 13q14.2-31.1(chr13:47117587-84300935)x1 | copy number loss | See cases [RCV000136647] | Chr13:47117587..84300935 [GRCh38] Chr13:47691722..84875070 [GRCh37] Chr13:46589723..83773071 [NCBI36] Chr13:13q14.2-31.1 |
pathogenic |
GRCh38/hg38 13q14.11-34(chr13:40942298-114340331)x1 | copy number loss | See cases [RCV000137893] | Chr13:40942298..114340331 [GRCh38] Chr13:41516434..115085141 [GRCh37] Chr13:40414434..114123908 [NCBI36] Chr13:13q14.11-34 |
pathogenic |
GRCh38/hg38 13q13.1-31.1(chr13:32531486-86757044)x3 | copy number gain | See cases [RCV000138339] | Chr13:32531486..86757044 [GRCh38] Chr13:33105623..87409299 [GRCh37] Chr13:32003623..86207300 [NCBI36] Chr13:13q13.1-31.1 |
pathogenic |
GRCh38/hg38 13q12.11-34(chr13:19833130-114327106)x3 | copy number gain | See cases [RCV000139078] | Chr13:19833130..114327106 [GRCh38] Chr13:20407270..115085141 [GRCh37] Chr13:19305270..114110683 [NCBI36] Chr13:13q12.11-34 |
pathogenic |
GRCh38/hg38 13q11-34(chr13:18456040-114340285)x3 | copy number gain | See cases [RCV000140004] | Chr13:18456040..114340285 [GRCh38] Chr13:19030180..115105760 [GRCh37] Chr13:17928180..114123862 [NCBI36] Chr13:13q11-34 |
pathogenic |
GRCh38/hg38 13q13.3-14.3(chr13:38514177-51425214)x1 | copy number loss | See cases [RCV000140788] | Chr13:38514177..51425214 [GRCh38] Chr13:39088314..51999350 [GRCh37] Chr13:37986314..50897351 [NCBI36] Chr13:13q13.3-14.3 |
pathogenic |
GRCh38/hg38 13q13.3-21.32(chr13:37864226-67963788)x1 | copy number loss | See cases [RCV000140744] | Chr13:37864226..67963788 [GRCh38] Chr13:38438363..68537920 [GRCh37] Chr13:37336363..67435921 [NCBI36] Chr13:13q13.3-21.32 |
pathogenic |
GRCh38/hg38 13q14.2-21.31(chr13:47765202-62058520)x1 | copy number loss | See cases [RCV000142223] | Chr13:47765202..62058520 [GRCh38] Chr13:48339337..62632653 [GRCh37] Chr13:47237338..61530654 [NCBI36] Chr13:13q14.2-21.31 |
pathogenic |
GRCh38/hg38 13q12.11-34(chr13:19671934-114340331)x3 | copy number gain | See cases [RCV000142924] | Chr13:19671934..114340331 [GRCh38] Chr13:20246074..115085141 [GRCh37] Chr13:19144074..114123908 [NCBI36] Chr13:13q12.11-34 |
pathogenic |
GRCh38/hg38 13q11-34(chr13:18862146-114342258)x3 | copy number gain | See cases [RCV000143462] | Chr13:18862146..114342258 [GRCh38] Chr13:19436286..115107733 [GRCh37] Chr13:18334286..114125835 [NCBI36] Chr13:13q11-34 |
pathogenic |
GRCh38/hg38 13q14.2(chr13:48591738-50064488)x3 | copy number gain | See cases [RCV000143577] | Chr13:48591738..50064488 [GRCh38] Chr13:49165874..50638624 [GRCh37] Chr13:48063875..49536625 [NCBI36] Chr13:13q14.2 |
uncertain significance |
GRCh38/hg38 13q12.3-31.3(chr13:31363472-90575292)x3 | copy number gain | See cases [RCV000148244] | Chr13:31363472..90575292 [GRCh38] Chr13:31937609..91227546 [GRCh37] Chr13:30835609..90025547 [NCBI36] Chr13:13q12.3-31.3 |
pathogenic |
GRCh38/hg38 13q12.11-34(chr13:19837395-114327173)x3 | copy number gain | See cases [RCV000148126] | Chr13:19837395..114327173 [GRCh38] Chr13:20411535..115085141 [GRCh37] Chr13:19309535..114110750 [NCBI36] Chr13:13q12.11-34 |
pathogenic |
GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3 | copy number gain | See cases [RCV000240150] | Chr13:19571503..115092569 [GRCh37] Chr13:13q12.11-34 |
pathogenic |
GRCh37/hg19 13q12.11-34(chr13:19571503-115092510) | copy number gain | See cases [RCV000449142] | Chr13:19571503..115092510 [GRCh37] Chr13:13q12.11-34 |
pathogenic |
GRCh37/hg19 13q14.11-31.3(chr13:42457841-91796698)x1 | copy number loss | See cases [RCV000446747] | Chr13:42457841..91796698 [GRCh37] Chr13:13q14.11-31.3 |
pathogenic |
GRCh37/hg19 13q13.1-21.31(chr13:32946120-62698217)x1 | copy number loss | See cases [RCV000446067] | Chr13:32946120..62698217 [GRCh37] Chr13:13q13.1-21.31 |
pathogenic |
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3 | copy number gain | See cases [RCV000445886] | Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34 |
pathogenic |
GRCh37/hg19 13q14.2-14.3(chr13:48906943-52778614)x1 | copy number loss | See cases [RCV000448535] | Chr13:48906943..52778614 [GRCh37] Chr13:13q14.2-14.3 |
pathogenic |
GRCh37/hg19 13q11-34(chr13:19436287-115107733) | copy number gain | See cases [RCV000510405] | Chr13:19436287..115107733 [GRCh37] Chr13:13q11-34 |
pathogenic |
GRCh37/hg19 13q14.2-14.3(chr13:47312129-51342279)x1 | copy number loss | See cases [RCV000511479] | Chr13:47312129..51342279 [GRCh37] Chr13:13q14.2-14.3 |
pathogenic |
GRCh37/hg19 13q11-34(chr13:19436287-115107733)x3 | copy number gain | See cases [RCV000511880] | Chr13:19436287..115107733 [GRCh37] Chr13:13q11-34 |
pathogenic |
GRCh37/hg19 13q11-22.1(chr13:19436286-74045459)x3 | copy number gain | not provided [RCV000683572] | Chr13:19436286..74045459 [GRCh37] Chr13:13q11-22.1 |
pathogenic |
NC_000013.11:g.46968080_87381985del40413906 | deletion | Chromosome 13q14 deletion syndrome [RCV000721955] | Chr13:46968080..87381985 [GRCh38] Chr13:13q14.2-31.2 |
pathogenic |
Single allele | deletion | Intellectual disability [RCV000684766] | Chr13:48225451..58070399 [GRCh37] Chr13:13q14.2-21.1 |
likely pathogenic |
GRCh37/hg19 13q11-34(chr13:19058717-115103529)x3 | copy number gain | not provided [RCV000738115] | Chr13:19058717..115103529 [GRCh37] Chr13:13q11-34 |
pathogenic |
GRCh37/hg19 13q11-34(chr13:19031237-115107157)x3 | copy number gain | not provided [RCV000750643] | Chr13:19031237..115107157 [GRCh37] Chr13:13q11-34 |
pathogenic |
GRCh37/hg19 13q14.2(chr13:50464624-50699452)x1 | copy number loss | not provided [RCV000750714] | Chr13:50464624..50699452 [GRCh37] Chr13:13q14.2 |
benign |
GRCh37/hg19 13q14.2(chr13:50578022-50728452)x3 | copy number gain | not provided [RCV000750715] | Chr13:50578022..50728452 [GRCh37] Chr13:13q14.2 |
benign |
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3 | copy number gain | not provided [RCV000849129] | Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34 |
pathogenic |
GRCh37/hg19 13q14.2-21.2(chr13:49586017-61311845)x1 | copy number loss | not provided [RCV000846575] | Chr13:49586017..61311845 [GRCh37] Chr13:13q14.2-21.2 |
uncertain significance |
GRCh37/hg19 13q14.2(chr13:50494451-50665381)x3 | copy number gain | not provided [RCV000847204] | Chr13:50494451..50665381 [GRCh37] Chr13:13q14.2 |
uncertain significance |
GRCh37/hg19 13q14.12-14.3(chr13:45487628-52639336)x3 | copy number gain | not provided [RCV001258545] | Chr13:45487628..52639336 [GRCh37] Chr13:13q14.12-14.3 |
likely pathogenic |
GRCh37/hg19 13p13-q34(chr13:1-115169878) | copy number gain | Complete trisomy 13 syndrome [RCV002280659] | Chr13:1..115169878 [GRCh37] Chr13:13p13-q34 |
pathogenic |
GRCh37/hg19 13q14.13-21.31(chr13:45819046-63910212)x1 | copy number loss | not provided [RCV001795546] | Chr13:45819046..63910212 [GRCh37] Chr13:13q14.13-21.31 |
pathogenic |
GRCh37/hg19 13p13-q34(chr13:1-115169878)x3 | copy number gain | See cases [RCV001780076] | Chr13:1..115169878 [GRCh37] Chr13:13p13-q34 |
pathogenic |
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3 | copy number gain | not provided [RCV001834436] | Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34 |
pathogenic |
GRCh37/hg19 13q14.11-33.3(chr13:42504540-108206269)x3 | copy number gain | not provided [RCV001829235] | Chr13:42504540..108206269 [GRCh37] Chr13:13q14.11-33.3 |
pathogenic |
GRCh37/hg19 13q14.11-14.3(chr13:44573371-53324137) | copy number loss | not specified [RCV002053058] | Chr13:44573371..53324137 [GRCh37] Chr13:13q14.11-14.3 |
pathogenic |
GRCh37/hg19 13q11-34(chr13:19436286-115107733) | copy number gain | not specified [RCV002053036] | Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34 |
pathogenic |
GRCh37/hg19 13q13.1-21.31(chr13:32946120-62698217) | copy number loss | not specified [RCV002053048] | Chr13:32946120..62698217 [GRCh37] Chr13:13q13.1-21.31 |
pathogenic |
GRCh37/hg19 13q11-34(chr13:19436286-114981726) | copy number gain | not specified [RCV002053035] | Chr13:19436286..114981726 [GRCh37] Chr13:13q11-34 |
pathogenic |
GRCh37/hg19 13q14.11-31.3(chr13:42457841-91796698) | copy number loss | not specified [RCV002053057] | Chr13:42457841..91796698 [GRCh37] Chr13:13q14.11-31.3 |
pathogenic |
GRCh37/hg19 13q13.3-31.1(chr13:36376204-80681753) | copy number loss | not specified [RCV002053052] | Chr13:36376204..80681753 [GRCh37] Chr13:13q13.3-31.1 |
pathogenic |
GRCh37/hg19 13q11-34(chr13:19253848-115108937)x3 | copy number gain | not provided [RCV002291540] | Chr13:19253848..115108937 [GRCh37] Chr13:13q11-34 |
pathogenic |
GRCh37/hg19 13q14.11-21.2(chr13:44076923-60520078)x1 | copy number loss | not specified [RCV003987012] | Chr13:44076923..60520078 [GRCh37] Chr13:13q14.11-21.2 |
pathogenic |
GRCh37/hg19 13q13.2-21.1(chr13:35015723-59553519)x3 | copy number gain | not specified [RCV003987040] | Chr13:35015723..59553519 [GRCh37] Chr13:13q13.2-21.1 |
pathogenic |
GRCh37/hg19 13q14.2-32.2(chr13:49547974-98214905)x1 | copy number loss | not specified [RCV003987008] | Chr13:49547974..98214905 [GRCh37] Chr13:13q14.2-32.2 |
pathogenic |
GRCh37/hg19 13q14.2-14.3(chr13:50181731-54350061)x1 | copy number loss | not provided [RCV004442840] | Chr13:50181731..54350061 [GRCh37] Chr13:13q14.2-14.3 |
uncertain significance |
GRCh37/hg19 13q13.2-21.2(chr13:34884647-61309742)x1 | copy number loss | not provided [RCV003885457] | Chr13:34884647..61309742 [GRCh37] Chr13:13q13.2-21.2 |
pathogenic |
The detailed report is available here: | Full Report | CSV | TAB | Printer | ||||
miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/). For more information about miRGate, see PMID:25858286 or access the full paper here. |
Mirn16-1 |
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alimentary part of gastrointestinal system | circulatory system | endocrine system | exocrine system | hemolymphoid system | hepatobiliary system | integumental system | musculoskeletal system | nervous system | renal system | reproductive system | respiratory system | sensory system | adipose tissue | appendage | entire extraembryonic component | |
High | ||||||||||||||||
Medium | 2 | |||||||||||||||
Low | 25 | 12 | 5 | 1 | 57 | 1 | 12 | 2 | 12 | 3 | 14 | 9 | 2 | 6 | 1 | |
Below cutoff | 16 | 9 | 8 | 2 | 32 | 1 | 19 | 12 | 22 | 8 | 13 | 14 | 1 | 1 | 6 | 1 |
RefSeq Transcripts | NR_029486 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
GenBank Nucleotide | AF480551 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AJ421734 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL137060 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068265 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
LM608159 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | ENST00000385271 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | NR_029486 | ||||||||||||||||||||||||
RefSeq Status: | PROVISIONAL | ||||||||||||||||||||||||
Type: | NON-CODING | ||||||||||||||||||||||||
Position: |
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Sequence: |
Database | Acc Id | Source(s) |
AGR Gene | HGNC:31545 | AgrOrtholog |
COSMIC | MIR16-1 | COSMIC |
Ensembl Genes | ENSG00000208006 | Ensembl, ENTREZGENE |
Ensembl Transcript | ENST00000385271 | ENTREZGENE |
GTEx | ENSG00000208006 | GTEx |
HGNC ID | HGNC:31545 | ENTREZGENE |
Human Proteome Map | MIR16-1 | Human Proteome Map |
miRBase | MI0000070 | ENTREZGENE |
NCBI Gene | 406950 | ENTREZGENE |
OMIM | 609704 | OMIM |
PharmGKB | PA164722518 | PharmGKB |
RNAcentral | URS00004BCD9C | RNACentral |
URS000056BFD0 | RNACentral | |
URS000061CB8F | RNACentral |