MALAT1 (metastasis associated lung adenocarcinoma transcript 1) - Rat Genome Database

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Gene: MALAT1 (metastasis associated lung adenocarcinoma transcript 1) Homo sapiens
Analyze
Symbol: MALAT1
Name: metastasis associated lung adenocarcinoma transcript 1
RGD ID: 1346754
HGNC Page HGNC:29665
Description: Enables chromatin-protein adaptor activity and miRNA inhibitor activity via base-pairing. Involved in several processes, including lncRNA-mediated post-transcriptional gene silencing; positive regulation of cardiac muscle myoblast proliferation; and positive regulation of miRNA catabolic process. Located in nucleus. Biomarker of osteoarthritis and rheumatoid arthritis.
Type: ncrna (Ensembl: lncRNA)
RefSeq Status: REVIEWED
Previously known as: HCN; LINC00047; MALAT-1; mascRNA; metastasis associated lung adenocarcinoma transcript 1 (non-protein coding); NCRNA00047; NEAT2; PRO2853
RGD Orthologs
Mouse
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381165,497,738 - 65,506,516 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1165,497,640 - 65,508,073 (+)EnsemblGRCh38hg38GRCh38
GRCh371165,265,209 - 65,273,987 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361165,022,410 - 65,030,999 (+)NCBINCBI36Build 36hg18NCBI36
Celera1162,591,512 - 62,600,220 (+)NCBICelera
Cytogenetic Map11q13.1NCBI
HuRef1161,592,326 - 61,601,033 (+)NCBIHuRef
CHM1_11165,149,225 - 65,157,932 (+)NCBICHM1_1
T2T-CHM13v2.01165,491,042 - 65,499,820 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(S)-nicotine  (EXP)
1,2-dimethylhydrazine  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-diaminotoluene  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
3-methylcholanthrene  (ISO)
4,4'-sulfonyldiphenol  (EXP)
4-hydroxyphenyl retinamide  (ISO)
4-octylphenol  (EXP)
5-fluorouracil  (EXP)
all-trans-retinoic acid  (EXP)
antimycin A  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP,ISO)
arsenous acid  (EXP)
azoxystrobin  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
bisphenol A  (ISO)
bisphenol F  (ISO)
bortezomib  (EXP)
cadmium atom  (ISO)
cadmium dichloride  (EXP,ISO)
cadmium sulfate  (EXP)
cantharidin  (EXP)
carbon nanotube  (ISO)
carmustine  (EXP)
CGP 52608  (EXP)
cisplatin  (EXP)
cobalt dichloride  (EXP)
copper atom  (EXP)
copper(0)  (EXP)
copper(II) chloride  (EXP)
copper(II) sulfate  (EXP)
coumestrol  (EXP)
cycloheximide  (EXP)
DDE  (EXP)
DDT  (EXP)
dexamethasone  (EXP)
diarsenic trioxide  (EXP)
diuron  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP)
elesclomol  (EXP)
endosulfan  (EXP)
Enterolactone  (EXP)
entinostat  (EXP)
ethanol  (ISO)
ethylbenzene  (EXP)
fipronil  (EXP)
folic acid  (EXP)
formaldehyde  (EXP)
geldanamycin  (EXP)
indometacin  (EXP)
irinotecan  (EXP)
lead diacetate  (ISO)
lead(II) chloride  (EXP)
levonorgestrel  (EXP)
lipopolysaccharide  (EXP)
lithium chloride  (EXP)
melittin  (EXP)
methylmercury chloride  (EXP)
methylphenidate  (ISO)
mono(2-ethylhexyl) phthalate  (EXP)
monobenzyl phthalate  (EXP)
N,N-diethyl-m-toluamide  (EXP)
N-acetyl-L-cysteine  (EXP)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (EXP)
N-nitrosodiethylamine  (ISO)
nicotine  (EXP)
okadaic acid  (EXP)
osthole  (EXP)
ozone  (ISO)
paracetamol  (EXP)
pentachlorophenol  (ISO)
perfluorooctane-1-sulfonic acid  (EXP)
phenethyl isothiocyanate  (EXP)
phenobarbital  (ISO)
phenylmercury acetate  (EXP)
pregnenolone 16alpha-carbonitrile  (ISO)
puromycin  (EXP)
pyrimidifen  (EXP)
quercetin  (EXP)
quinolin-8-ol  (EXP)
resveratrol  (EXP)
rotenone  (EXP)
SB 431542  (EXP)
silicon dioxide  (ISO)
silver atom  (ISO)
silver(0)  (ISO)
sodium arsenate  (ISO)
sodium arsenite  (EXP,ISO)
succimer  (ISO)
tebufenpyrad  (EXP)
temozolomide  (EXP)
testosterone undecanoate  (EXP)
tetrachloromethane  (ISO)
thimerosal  (EXP)
thiram  (EXP)
titanium dioxide  (ISO)
toluene  (EXP)
triadimefon  (EXP)
trichostatin A  (EXP)
tungsten  (ISO)
valproic acid  (EXP)
vancomycin  (ISO)
vorinostat  (EXP)
wortmannin  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Knockdown of lncRNA MALAT1 attenuates acute myocardial infarction through miR-320-Pten axis. Hu H, etal., Biomed Pharmacother. 2018 Oct;106:738-746. doi: 10.1016/j.biopha.2018.06.122. Epub 2018 Jul 11.
2. LncRNA MALAT1 mediates proliferation of LPS treated-articular chondrocytes by targeting the miR-146a-PI3K/Akt/mTOR axis. Li H, etal., Life Sci. 2020 Aug 1;254:116801. doi: 10.1016/j.lfs.2019.116801. Epub 2019 Aug 28.
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients. Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.
Additional References at PubMed
PMID:9253601   PMID:10843802   PMID:12107410   PMID:12477932   PMID:12719541   PMID:12837690   PMID:12970751   PMID:16441420   PMID:17270048   PMID:19041754   PMID:19167051   PMID:19690017  
PMID:20149803   PMID:20213048   PMID:20711585   PMID:20797886   PMID:21112873   PMID:21503572   PMID:21678027   PMID:21941126   PMID:22078878   PMID:22088988   PMID:22560368   PMID:22722759  
PMID:22751105   PMID:22858678   PMID:23073843   PMID:23129630   PMID:23153939   PMID:23243023   PMID:23555285   PMID:23726266   PMID:23847102   PMID:23898077   PMID:23973260   PMID:23985560  
PMID:24115594   PMID:24120702   PMID:24244343   PMID:24449823   PMID:24468535   PMID:24602777   PMID:24658096   PMID:24815433   PMID:24857172   PMID:24892958   PMID:24927181   PMID:24952594  
PMID:25025966   PMID:25031737   PMID:25036876   PMID:25085246   PMID:25155612   PMID:25187517   PMID:25217850   PMID:25269958   PMID:25280565   PMID:25369863   PMID:25431257   PMID:25446987  
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PMID:31350456   PMID:31361602   PMID:31372165   PMID:31388927   PMID:31397203   PMID:31408432   PMID:31436334   PMID:31479414   PMID:31485645   PMID:31494280   PMID:31500506   PMID:31552681  
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PMID:31803924   PMID:31837057   PMID:31846184   PMID:31856403   PMID:31863590   PMID:31871512   PMID:31880028   PMID:31913701   PMID:31922243   PMID:31933110   PMID:31935634   PMID:31939443  
PMID:31949884   PMID:31952940   PMID:31953613   PMID:31986419   PMID:31992741   PMID:31995604   PMID:32026279   PMID:32084582   PMID:32099751   PMID:32109146   PMID:32113834   PMID:32117213  
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PMID:32812343   PMID:32832561   PMID:32840181   PMID:32867128   PMID:32879299   PMID:32880825   PMID:32894536   PMID:32965597   PMID:32980391   PMID:32993558   PMID:33022677   PMID:33026292  
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PMID:33344634   PMID:33346423   PMID:33358903   PMID:33382018   PMID:33410422   PMID:33414433   PMID:33428963   PMID:33448307   PMID:33506040   PMID:33545365   PMID:33547935   PMID:33565328  
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PMID:33824303   PMID:33887222   PMID:33916321   PMID:33933553   PMID:33944676   PMID:33972684   PMID:34019552   PMID:34036896   PMID:34036905   PMID:34200314   PMID:34210246   PMID:34240756  
PMID:34253686   PMID:34257576   PMID:34268963   PMID:34291564   PMID:34308750   PMID:34313719   PMID:34324865   PMID:34399118   PMID:34419445   PMID:34427833   PMID:34456284   PMID:34463043  
PMID:34474594   PMID:34478876   PMID:34482739   PMID:34503385   PMID:34554676   PMID:34599867   PMID:34610246   PMID:34638541   PMID:34651657   PMID:34761722   PMID:34769245   PMID:34846099  
PMID:34858541   PMID:34883204   PMID:34893107   PMID:34896788   PMID:34918470   PMID:34943778   PMID:34962086   PMID:35006556   PMID:35007307   PMID:35013429   PMID:35075166   PMID:35084640  
PMID:35085770   PMID:35110552   PMID:35132797   PMID:35208500   PMID:35228564   PMID:35255186   PMID:35300579   PMID:35367362   PMID:35392816   PMID:35398394   PMID:35410813   PMID:35426182  
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PMID:36042115   PMID:36073002   PMID:36121635   PMID:36127791   PMID:36149748   PMID:36189916   PMID:36232884   PMID:36241224   PMID:36264775   PMID:36270460   PMID:36283602   PMID:36378551  
PMID:36410173   PMID:36420706   PMID:36452326   PMID:36529281   PMID:36552736   PMID:36685103   PMID:36710662   PMID:36734858   PMID:36812496   PMID:36813772   PMID:36852184   PMID:36861261  
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Genomics

Comparative Map Data
MALAT1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381165,497,738 - 65,506,516 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1165,497,640 - 65,508,073 (+)EnsemblGRCh38hg38GRCh38
GRCh371165,265,209 - 65,273,987 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361165,022,410 - 65,030,999 (+)NCBINCBI36Build 36hg18NCBI36
Celera1162,591,512 - 62,600,220 (+)NCBICelera
Cytogenetic Map11q13.1NCBI
HuRef1161,592,326 - 61,601,033 (+)NCBIHuRef
CHM1_11165,149,225 - 65,157,932 (+)NCBICHM1_1
T2T-CHM13v2.01165,491,042 - 65,499,820 (+)NCBIT2T-CHM13v2.0
Malat1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39195,845,718 - 5,852,700 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl195,845,717 - 5,852,706 (-)EnsemblGRCm39 Ensembl
GRCm38195,795,690 - 5,802,672 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl195,795,690 - 5,802,672 (-)EnsemblGRCm38mm10GRCm38
MGSCv37195,795,690 - 5,802,671 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36195,796,000 - 5,797,754 (-)NCBIMGSCv36mm8
Celera195,665,814 - 5,672,795 (-)NCBICelera
Cytogenetic Map19ANCBI
cM Map194.34NCBI

Variants

.
Variants in MALAT1
2 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
GRCh38/hg38 11q13.1(chr11:65327786-65626431)x3 copy number gain See cases [RCV000141334] Chr11:65327786..65626431 [GRCh38]
Chr11:65095257..65393902 [GRCh37]
Chr11:64851833..65150478 [NCBI36]
Chr11:11q13.1		 uncertain significance
GRCh37/hg19 11q13.1-13.2(chr11:64501919-67129258)x3 copy number gain See cases [RCV000511632] Chr11:64501919..67129258 [GRCh37]
Chr11:11q13.1-13.2		 likely pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11q13.1(chr11:65144318-65373538)x3 copy number gain not provided [RCV000750081] Chr11:65144318..65373538 [GRCh37]
Chr11:11q13.1		 benign
GRCh37/hg19 11q13.1-13.2(chr11:65138976-67574402) copy number gain not provided [RCV000767601] Chr11:65138976..67574402 [GRCh37]
Chr11:11q13.1-13.2		 pathogenic
dup(11)(q13.1q13.1) duplication Ependymoma [RCV000785872] Chr11:63533279..65429676 [GRCh37]
Chr11:11q13.1		 likely pathogenic
NC_000011.9:g.(?_64973914)_(70052579_?)dup duplication Aicardi-Goutieres syndrome 3 [RCV003113322]|FADD-related immunodeficiency [RCV003107753] Chr11:64973914..70052579 [GRCh37]
Chr11:11q13.1-13.3		 uncertain significance
NC_000011.9:g.(?_59596957)_(68707199_?)dup duplication Familial temporal lobe epilepsy 8 [RCV001372442] Chr11:59596957..68707199 [GRCh37]
Chr11:11q12.1-13.3		 uncertain significance
GRCh37/hg19 11q13.1-13.2(chr11:64935724-66405514) copy number loss not specified [RCV002052930] Chr11:64935724..66405514 [GRCh37]
Chr11:11q13.1-13.2		 uncertain significance
NC_000011.9:g.(?_64522783)_(66283694_?)del deletion Bardet-Biedl syndrome [RCV002014493]|Glycogen storage disease, type V [RCV002004587] Chr11:64522783..66283694 [GRCh37]
Chr11:11q13.1-13.2		 pathogenic
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25		 pathogenic
GRCh37/hg19 11q12.2-13.5(chr11:59923608-76272324)x3 copy number gain not provided [RCV003484842] Chr11:59923608..76272324 [GRCh37]
Chr11:11q12.2-13.5		 pathogenic
GRCh37/hg19 11q12.1-13.3(chr11:56895955-69295402)x3 copy number gain not specified [RCV003986944] Chr11:56895955..69295402 [GRCh37]
Chr11:11q12.1-13.3		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:298
Count of miRNA genes:178
Interacting mature miRNAs:182
Transcripts:ENST00000508832, ENST00000534336, ENST00000544868
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1357380BW64_HBody weight QTL 64 (human)2.2Body weightpercent fat after exercise training116097893786978937Human
407048663GWAS697639_Hperiodontitis QTL GWAS697639 (human)9e-09periodontitis116550436165504362Human
407223826GWAS872802_Hbody mass index QTL GWAS872802 (human)1e-08body mass indexbody mass index (BMI) (CMO:0000105)116550436165504362Human
407402577GWAS1051553_Hbone density QTL GWAS1051553 (human)1e-09bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)116550598265505983Human

Markers in Region
A005V08  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,273,335 - 65,273,533UniSTSGRCh37
Build 361165,029,911 - 65,030,109RGDNCBI36
Celera1162,599,615 - 62,599,813RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,600,428 - 61,600,626UniSTS
GeneMap99-GB4 RH Map11237.8UniSTS
G20528  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,273,335 - 65,273,533UniSTSGRCh37
Build 361165,029,911 - 65,030,109RGDNCBI36
Celera1162,599,615 - 62,599,813RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,600,428 - 61,600,626UniSTS
RH67818  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,270,848 - 65,270,978UniSTSGRCh37
Build 361165,027,424 - 65,027,554RGDNCBI36
Celera1162,597,128 - 62,597,258RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,597,941 - 61,598,071UniSTS
GeneMap99-GB4 RH Map11237.8UniSTS
STS-T94789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,270,177 - 65,270,431UniSTSGRCh37
Build 361165,026,753 - 65,027,007RGDNCBI36
Celera1162,596,457 - 62,596,711RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,597,270 - 61,597,524UniSTS
GeneMap99-GB4 RH Map11237.96UniSTS
D11S1957E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,269,275 - 65,269,366UniSTSGRCh37
Build 361165,025,851 - 65,025,942RGDNCBI36
Celera1162,595,554 - 62,595,645RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,596,368 - 61,596,459UniSTS
GeneMap99-GB4 RH Map11252.21UniSTS
WI-12191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,268,481 - 65,268,630UniSTSGRCh37
Build 361165,025,057 - 65,025,206RGDNCBI36
Celera1162,594,760 - 62,594,909RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,595,574 - 61,595,723UniSTS
GeneMap99-GB4 RH Map11247.64UniSTS
Whitehead-RH Map11327.6UniSTS
NCBI RH Map11573.2UniSTS
D11S2256E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,268,744 - 65,268,894UniSTSGRCh37
Build 361165,025,320 - 65,025,470RGDNCBI36
Celera1162,595,023 - 62,595,173RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,595,837 - 61,595,987UniSTS
D11S2289E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,268,916 - 65,269,039UniSTSGRCh37
Build 361165,025,492 - 65,025,615RGDNCBI36
Celera1162,595,195 - 62,595,318RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,596,009 - 61,596,132UniSTS
D11S4055E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,270,918 - 65,271,006UniSTSGRCh37
Build 361165,027,494 - 65,027,582RGDNCBI36
Celera1162,597,198 - 62,597,286RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,598,011 - 61,598,099UniSTS
RH17566  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,267,831 - 65,267,986UniSTSGRCh37
Build 361165,024,407 - 65,024,562RGDNCBI36
Celera1162,594,110 - 62,594,265RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,594,924 - 61,595,079UniSTS
GeneMap99-GB4 RH Map11237.8UniSTS
SHGC-35161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,270,278 - 65,270,427UniSTSGRCh37
Build 361165,026,854 - 65,027,003RGDNCBI36
Celera1162,596,558 - 62,596,707RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,597,371 - 61,597,520UniSTS
GeneMap99-GB4 RH Map11240.12UniSTS
Whitehead-RH Map11328.0UniSTS
NCBI RH Map11573.2UniSTS
SHGC-31329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,272,682 - 65,272,831UniSTSGRCh37
Build 361165,029,258 - 65,029,407RGDNCBI36
Celera1162,598,962 - 62,599,111RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,599,775 - 61,599,924UniSTS
Stanford-G3 RH Map112881.0UniSTS
GeneMap99-GB4 RH Map11247.35UniSTS
Whitehead-RH Map11327.3UniSTS
NCBI RH Map11573.2UniSTS
GeneMap99-G3 RH Map112881.0UniSTS
D11S951E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,272,468 - 65,272,604UniSTSGRCh37
Build 361165,029,044 - 65,029,180RGDNCBI36
Celera1162,598,748 - 62,598,884RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,599,561 - 61,599,697UniSTS
TNG Radiation Hybrid Map1128956.0UniSTS
Stanford-G3 RH Map112877.0UniSTS
NCBI RH Map11573.2UniSTS
GeneMap99-G3 RH Map112877.0UniSTS
D11S4570  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,267,013 - 65,267,104UniSTSGRCh37
Build 361165,023,589 - 65,023,680RGDNCBI36
Celera1162,593,292 - 62,593,383RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,594,106 - 61,594,197UniSTS
Stanford-G3 RH Map112860.0UniSTS
NCBI RH Map11573.2UniSTS
SGC35206  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,272,413 - 65,272,539UniSTSGRCh37
Build 361165,028,989 - 65,029,115RGDNCBI36
Celera1162,598,693 - 62,598,819RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,599,506 - 61,599,632UniSTS
GeneMap99-GB4 RH Map11239.91UniSTS
Whitehead-RH Map11327.1UniSTS
NCBI RH Map11573.2UniSTS
RH12529  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,266,564 - 65,266,746UniSTSGRCh37
Build 361165,023,140 - 65,023,322RGDNCBI36
Celera1162,592,843 - 62,593,025RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,593,657 - 61,593,839UniSTS
GeneMap99-GB4 RH Map11240.12UniSTS
NCBI RH Map11573.2UniSTS
1072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,271,220 - 65,271,309UniSTSGRCh37
Build 361165,027,796 - 65,027,885RGDNCBI36
Celera1162,597,500 - 62,597,589RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,598,313 - 61,598,402UniSTS
GeneMap99-GB4 RH Map11251.18UniSTS
RH42001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,273,731 - 65,273,897UniSTSGRCh37
Build 361165,030,307 - 65,030,473RGDNCBI36
Celera1162,600,011 - 62,600,177RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,600,824 - 61,600,990UniSTS
GeneMap99-GB4 RH Map11240.12UniSTS
NCBI RH Map11573.2UniSTS
SGC30658  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,271,814 - 65,271,963UniSTSGRCh37
Build 361165,028,390 - 65,028,539RGDNCBI36
Celera1162,598,094 - 62,598,243RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,598,907 - 61,599,056UniSTS
GeneMap99-GB4 RH Map11249.53UniSTS
Whitehead-RH Map11338.2UniSTS
NCBI RH Map11573.2UniSTS
A009Q43  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,268,653 - 65,268,767UniSTSGRCh37
Build 361165,025,229 - 65,025,343RGDNCBI36
Celera1162,594,932 - 62,595,046RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,595,746 - 61,595,860UniSTS
GeneMap99-GB4 RH Map11237.96UniSTS
1192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,266,890 - 65,267,026UniSTSGRCh37
Build 361165,023,466 - 65,023,602RGDNCBI36
Celera1162,593,169 - 62,593,305RGD
Cytogenetic Map11q13.1UniSTS
HuRef1161,593,983 - 61,594,119UniSTS
GeneMap99-GB4 RH Map11247.35UniSTS
NCBI RH Map11573.2UniSTS
G32792  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,268,653 - 65,268,768UniSTSGRCh37
Celera1162,594,932 - 62,595,047UniSTS
Cytogenetic Map11q13.1UniSTS


Sequence

Nucleotide Sequences
RefSeq Transcripts NR_002819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_144567 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_144568 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF132202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF203815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI805768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ535463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ535466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130345 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL050210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000769 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC025986 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC063689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC104662 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK001411 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK001418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX538238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX640764 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA394984 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF177381 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ209305 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HG975416 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000508832
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,042 - 65,505,452 (+)Ensembl
Ensembl Acc Id: ENST00000534336
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,497,640 - 65,508,073 (+)Ensembl
Ensembl Acc Id: ENST00000544868
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,042 - 65,502,995 (+)Ensembl
Ensembl Acc Id: ENST00000610481
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,500,223 - 65,500,713 (+)Ensembl
Ensembl Acc Id: ENST00000610851
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,059 - 65,506,516 (+)Ensembl
Ensembl Acc Id: ENST00000612781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,502,696 - 65,504,879 (+)Ensembl
Ensembl Acc Id: ENST00000613376
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,502,413 - 65,504,858 (+)Ensembl
Ensembl Acc Id: ENST00000616527
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,501,960 - 65,504,463 (+)Ensembl
Ensembl Acc Id: ENST00000616691
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,501,787 - 65,506,516 (+)Ensembl
Ensembl Acc Id: ENST00000617489
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,501,259 - 65,506,469 (+)Ensembl
Ensembl Acc Id: ENST00000617791
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,042 - 65,499,785 (+)Ensembl
Ensembl Acc Id: ENST00000618132
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,501,009 - 65,506,110 (+)Ensembl
Ensembl Acc Id: ENST00000618227
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,503,955 - 65,506,469 (+)Ensembl
Ensembl Acc Id: ENST00000618925
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,502,729 - 65,503,760 (+)Ensembl
Ensembl Acc Id: ENST00000619449
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,497,688 - 65,502,964 (+)Ensembl
Ensembl Acc Id: ENST00000620465
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,501,009 - 65,505,016 (+)Ensembl
Ensembl Acc Id: ENST00000620902
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,042 - 65,499,706 (+)Ensembl
Ensembl Acc Id: ENST00000685846
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,497,768 - 65,499,990 (+)Ensembl
Ensembl Acc Id: ENST00000688218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,497,762 - 65,499,990 (+)Ensembl
Ensembl Acc Id: ENST00000689729
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,497,762 - 65,499,990 (+)Ensembl
Ensembl Acc Id: ENST00000690116
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,497,768 - 65,499,990 (+)Ensembl
Ensembl Acc Id: ENST00000692086
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,497,764 - 65,499,990 (+)Ensembl
Ensembl Acc Id: ENST00000693503
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,497,764 - 65,499,990 (+)Ensembl
Ensembl Acc Id: ENST00000710847
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,500,816 (+)Ensembl
Ensembl Acc Id: ENST00000710848
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,503,624 (+)Ensembl
Ensembl Acc Id: ENST00000710849
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,500,512 - 65,506,431 (+)Ensembl
Ensembl Acc Id: ENST00000710852
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,497,708 - 65,499,782 (+)Ensembl
Ensembl Acc Id: ENST00000710855
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,498,388 - 65,499,782 (+)Ensembl
Ensembl Acc Id: ENST00000710856
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,051 - 65,503,226 (+)Ensembl
Ensembl Acc Id: ENST00000710857
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,056 - 65,503,584 (+)Ensembl
Ensembl Acc Id: ENST00000710858
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,500,570 - 65,502,995 (+)Ensembl
Ensembl Acc Id: ENST00000710859
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,506,469 (+)Ensembl
Ensembl Acc Id: ENST00000710860
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,048 - 65,504,504 (+)Ensembl
Ensembl Acc Id: ENST00000710861
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,049 - 65,503,614 (+)Ensembl
Ensembl Acc Id: ENST00000710862
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,051 - 65,506,468 (+)Ensembl
Ensembl Acc Id: ENST00000710863
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,084 - 65,504,879 (+)Ensembl
Ensembl Acc Id: ENST00000710864
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,501,542 - 65,503,614 (+)Ensembl
Ensembl Acc Id: ENST00000710865
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,504,702 - 65,505,887 (+)Ensembl
Ensembl Acc Id: ENST00000710866
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,499,982 (+)Ensembl
Ensembl Acc Id: ENST00000710867
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,501,009 - 65,504,879 (+)Ensembl
Ensembl Acc Id: ENST00000710868
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,501,732 - 65,504,463 (+)Ensembl
Ensembl Acc Id: ENST00000710869
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,502,809 - 65,506,458 (+)Ensembl
Ensembl Acc Id: ENST00000710870
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,503,349 - 65,506,469 (+)Ensembl
Ensembl Acc Id: ENST00000710871
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,502,104 - 65,506,469 (+)Ensembl
Ensembl Acc Id: ENST00000710874
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,498,210 - 65,499,752 (+)Ensembl
Ensembl Acc Id: ENST00000710875
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,502,995 (+)Ensembl
Ensembl Acc Id: ENST00000710876
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,503,630 (+)Ensembl
Ensembl Acc Id: ENST00000710877
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,504,463 (+)Ensembl
Ensembl Acc Id: ENST00000710878
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,504,463 (+)Ensembl
Ensembl Acc Id: ENST00000710879
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,504,463 (+)Ensembl
Ensembl Acc Id: ENST00000710880
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,504,872 (+)Ensembl
Ensembl Acc Id: ENST00000710925
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,497,708 - 65,506,469 (+)Ensembl
Ensembl Acc Id: ENST00000710926
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,504,463 (+)Ensembl
Ensembl Acc Id: ENST00000710927
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,497,688 - 65,499,847 (+)Ensembl
Ensembl Acc Id: ENST00000710933
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,501,202 (+)Ensembl
Ensembl Acc Id: ENST00000710934
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,502,995 (+)Ensembl
Ensembl Acc Id: ENST00000710935
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,506,469 (+)Ensembl
Ensembl Acc Id: ENST00000710936
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,506,469 (+)Ensembl
Ensembl Acc Id: ENST00000710937
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,046 - 65,506,469 (+)Ensembl
Ensembl Acc Id: ENST00000710938
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,091 - 65,506,469 (+)Ensembl
Ensembl Acc Id: ENST00000710939
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,042 - 65,505,449 (+)Ensembl
Ensembl Acc Id: ENST00000710940
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,501,516 (+)Ensembl
Ensembl Acc Id: ENST00000710941
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,502,239 (+)Ensembl
Ensembl Acc Id: ENST00000710942
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,502,582 (+)Ensembl
Ensembl Acc Id: ENST00000710943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,045 - 65,505,450 (+)Ensembl
Ensembl Acc Id: ENST00000710944
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,986 - 65,505,452 (+)Ensembl
Ensembl Acc Id: ENST00000710945
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,501,397 - 65,505,453 (+)Ensembl
Ensembl Acc Id: ENST00000710946
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,502,189 - 65,505,452 (+)Ensembl
Ensembl Acc Id: ENST00000710947
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,502,614 - 65,506,516 (+)Ensembl
Ensembl Acc Id: ENST00000710948
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,502,801 - 65,505,443 (+)Ensembl
Ensembl Acc Id: ENST00000710949
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,503,699 - 65,505,453 (+)Ensembl
Ensembl Acc Id: ENST00000710950
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,499,038 - 65,499,862 (+)Ensembl
Ensembl Acc Id: ENST00000710951
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,504,270 - 65,506,469 (+)Ensembl
RefSeq Acc Id: NR_002819
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381165,499,045 - 65,506,516 (+)NCBI
GRCh371165,265,224 - 65,273,940 (+)NCBI
Build 361165,022,410 - 65,030,999 (+)NCBI Archive
HuRef1161,592,326 - 61,601,033 (+)ENTREZGENE
T2T-CHM13v2.01165,492,349 - 65,499,820 (+)NCBI
Sequence:
RefSeq Acc Id: NR_144567
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381165,497,738 - 65,506,516 (+)NCBI
T2T-CHM13v2.01165,491,042 - 65,499,820 (+)NCBI
Sequence:
RefSeq Acc Id: NR_144568
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381165,497,738 - 65,506,516 (+)NCBI
T2T-CHM13v2.01165,491,042 - 65,499,820 (+)NCBI
Sequence:
Promoters
RGD ID:6789132
Promoter ID:HG_KWN:13329
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NR_002819,   UC001ODX.1,   UC001ODZ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361165,020,886 - 65,029,987 (+)MPROMDB
RGD ID:15096518
Promoter ID:EPDNEWNC_H1362
Type:single initiation site
Name:MALAT1_1
Description:metastasis associated lung adenocarcinoma transcript 1[Source:HGNC Symbol;Acc:HGNC:29665]
SO ACC ID:SO:0000170
Source:EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381165,499,045 - 65,499,105EPDNEWNC
RGD ID:15096521
Promoter ID:EPDNEWNC_H1363
Type:initiation region
Name:MALAT1_2
Description:metastasis associated lung adenocarcinoma transcript 1[Source:HGNC Symbol;Acc:HGNC:29665]
SO ACC ID:SO:0000170
Source:EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381165,500,240 - 65,500,300EPDNEWNC

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:29665 AgrOrtholog
COSMIC MALAT1 COSMIC
Ensembl Genes ENSG00000251562 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000534336 ENTREZGENE
GTEx ENSG00000251562 GTEx
HGNC ID HGNC:29665 ENTREZGENE
Human Proteome Map MALAT1 Human Proteome Map
NCBI Gene 378938 ENTREZGENE
OMIM 607924 OMIM
PharmGKB PA134935778 PharmGKB
RNAcentral URS0000A76CFF RNACentral
  URS0000A77400 RNACentral
  URS0000A77408 RNACentral


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-05-22 MALAT1  metastasis associated lung adenocarcinoma transcript 1    metastasis associated lung adenocarcinoma transcript 1 (non-protein coding)  Symbol and/or name change 5135510 APPROVED