NUTM2B-AS1 (NUTM2B antisense RNA 1) - Rat Genome Database

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Gene: NUTM2B-AS1 (NUTM2B antisense RNA 1) Homo sapiens
Analyze
Symbol: NUTM2B-AS1
Name: NUTM2B antisense RNA 1
RGD ID: 8699294
HGNC Page HGNC:51204
Description: ASSOCIATED WITH Adult onset; Ataxia; Autosomal dominant inheritance; INTERACTS WITH 2-hydroxypropanoic acid; aristolochic acid A; rac-lactic acid
Type: ncrna (Ensembl: lncRNA)
RefSeq Status: VALIDATED
Previously known as: OPML1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381079,691,500 - 79,826,594 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1079,661,394 - 79,826,594 (-)EnsemblGRCh38hg38GRCh38
GRCh371081,451,256 - 81,586,350 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map10q22.3NCBI
HuRef1075,446,628 - 75,455,400 (-)NCBIHuRef
CHM1_11081,805,944 - 81,867,768 (-)NCBICHM1_1
T2T-CHM13v2.01080,560,802 - 80,695,938 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References
Additional References at PubMed
PMID:8889548   PMID:14702039   PMID:15146197   PMID:16712791   PMID:37923380   PMID:38159879  


Genomics

Variants

.
Variants in NUTM2B-AS1
12 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 10q22.3-23.2(chr10:79802022-87068261)x1 copy number loss See cases [RCV000136565] Chr10:79802022..87068261 [GRCh38]
Chr10:81561459..88828018 [GRCh37]
Chr10:81263385..88817998 [NCBI36]
Chr10:10q22.3-23.2		 pathogenic
GRCh38/hg38 10q11.23-23.2(chr10:50729367-87147204)x3 copy number gain See cases [RCV000138007] Chr10:50729367..87147204 [GRCh38]
Chr10:52489127..88906961 [GRCh37]
Chr10:52159133..88896941 [NCBI36]
Chr10:10q11.23-23.2		 pathogenic
GRCh38/hg38 10q22.3-23.2(chr10:79689360-87223773)x1 copy number loss See cases [RCV000141724] Chr10:79689360..87223773 [GRCh38]
Chr10:81449116..88983530 [GRCh37]
Chr10:81119122..88973510 [NCBI36]
Chr10:10q22.3-23.2		 pathogenic
GRCh38/hg38 10q22.3-23.2(chr10:79719429-87358394)x1 copy number loss See cases [RCV000052534] Chr10:79719429..87358394 [GRCh38]
Chr10:81479185..89118151 [GRCh37]
Chr10:81149191..89108131 [NCBI36]
Chr10:10q22.3-23.2		 pathogenic
GRCh38/hg38 10q22.3-23.2(chr10:79802022-87358394)x1 copy number loss See cases [RCV000052537] Chr10:79802022..87358394 [GRCh38]
Chr10:81561459..89118151 [GRCh37]
Chr10:81541288..89108131 [NCBI36]
Chr10:10q22.3-23.2		 pathogenic
GRCh38/hg38 10q22.3(chr10:79491821-79798351)x3 copy number gain See cases [RCV000185583] Chr10:79491821..79798351 [GRCh38]
Chr10:81251577..81557993 [GRCh37]
Chr10:80943513..81550334 [NCBI36]
Chr10:10q22.3		 pathogenic|benign|uncertain significance
NM_001278495.2(NUTM2B):c.1614C>T (p.Pro538=) single nucleotide variant not provided [RCV000951288] Chr10:79710644 [GRCh38]
Chr10:81470400 [GRCh37]
Chr10:10q22.3		 likely benign
NR_120611.1:n.192CCG[(35_?)] microsatellite Oculopharyngeal myopathy with leukoencephalopathy 1 [RCV000853558] Chr10:10q22.3 pathogenic
NM_001278495.2(NUTM2B):c.2027T>C (p.Met676Thr) single nucleotide variant not provided [RCV001573518]|not specified [RCV001727888] Chr10:79711875 [GRCh38]
Chr10:81471631 [GRCh37]
Chr10:10q22.3		 benign|likely benign
NM_001278495.2(NUTM2B):c.2502_2503del (p.Tyr835fs) deletion Oculopharyngeal myopathy with leukoencephalopathy 1 [RCV001732876] Chr10:79712350..79712351 [GRCh38]
Chr10:81472106..81472107 [GRCh37]
Chr10:10q22.3		 benign
NM_001278495.2(NUTM2B):c.2490_2499del (p.Glu831fs) deletion Oculopharyngeal myopathy with leukoencephalopathy 1 [RCV001733563] Chr10:79712338..79712347 [GRCh38]
Chr10:81472094..81472103 [GRCh37]
Chr10:10q22.3		 benign
Single allele deletion not provided [RCV002227597] Chr10:79614895..80224601 [GRCh38]
Chr10:10q22.3		 uncertain significance
NM_001278495.2(NUTM2B):c.2051G>A (p.Arg684Gln) single nucleotide variant not provided [RCV003456710] Chr10:79711899 [GRCh38]
Chr10:81471655 [GRCh37]
Chr10:10q22.3		 likely benign
NM_001278495.2(NUTM2B):c.925A>G (p.Ser309Gly) single nucleotide variant not provided [RCV003417556] Chr10:79706584 [GRCh38]
Chr10:81466340 [GRCh37]
Chr10:10q22.3		 likely benign
NM_001278495.2(NUTM2B):c.1686C>T (p.Leu562=) single nucleotide variant not provided [RCV003417557] Chr10:79710716 [GRCh38]
Chr10:81470472 [GRCh37]
Chr10:10q22.3		 likely benign
NM_001278495.2(NUTM2B):c.2036G>A (p.Arg679Gln) single nucleotide variant not provided [RCV003417558] Chr10:79711884 [GRCh38]
Chr10:81471640 [GRCh37]
Chr10:10q22.3		 likely benign
NR_029407.1(LOC642361):n.91G>A single nucleotide variant not provided [RCV003417560] Chr10:79825992 [GRCh38]
Chr10:81585748 [GRCh37]
Chr10:10q22.3		 likely benign
NC_000010.11:g.79812006A>G single nucleotide variant not provided [RCV003417559] Chr10:79812006 [GRCh38]
Chr10:81571762 [GRCh37]
Chr10:10q22.3		 likely benign
NC_000010.11:g.79723614G>A single nucleotide variant not provided [RCV003886745] Chr10:79723614 [GRCh38]
Chr10:81483370 [GRCh37]
Chr10:10q22.3		 benign
NC_000010.11:g.79812193T>C single nucleotide variant not provided [RCV003886847] Chr10:79812193 [GRCh38]
Chr10:81571949 [GRCh37]
Chr10:10q22.3		 uncertain significance
NM_001278495.2(NUTM2B):c.918T>C (p.His306=) single nucleotide variant not provided [RCV003885078] Chr10:79706577 [GRCh38]
Chr10:81466333 [GRCh37]
Chr10:10q22.3		 likely benign
NC_000010.11:g.79804284T>A single nucleotide variant not provided [RCV004598869] Chr10:79804284 [GRCh38]
Chr10:81564040 [GRCh37]
Chr10:10q22.3		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:410
Count of miRNA genes:78
Interacting mature miRNAs:79
Transcripts:ENST00000419697, ENST00000430963, ENST00000470445, ENST00000477192, ENST00000483080, ENST00000484794, ENST00000488805, ENST00000495430, ENST00000496359
Prediction methods:Microtar, Miranda, Rnahybrid
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
407309188GWAS958164_Hhemoglobin measurement QTL GWAS958164 (human)8e-09hemoglobin measurementhemoglobin measurement (CMO:0000508)107974580279745803Human
2314551GLUCO52_HGlucose level QTL 52 (human)1.4Glucose level1077605006103605006Human


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
1204 2432 2788 2245 4942 1723 2345 4 622 1948 464 2268 7281 6454 52 3708 847 1731 1612 171

Sequence


Ensembl Acc Id: ENST00000419697
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,804,057 - 79,814,654 (-)Ensembl
Ensembl Acc Id: ENST00000430963
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,803,863 - 79,806,182 (-)Ensembl
Ensembl Acc Id: ENST00000477192
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,745,944 - 79,825,790 (-)Ensembl
Ensembl Acc Id: ENST00000483080
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,765,789 - 79,826,356 (-)Ensembl
Ensembl Acc Id: ENST00000484794
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,389 - 79,826,389 (-)Ensembl
Ensembl Acc Id: ENST00000488805
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,496 - 79,826,404 (-)Ensembl
Ensembl Acc Id: ENST00000495430
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,705 - 79,826,594 (-)Ensembl
Ensembl Acc Id: ENST00000496359
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,389 - 79,826,389 (-)Ensembl
Ensembl Acc Id: ENST00000596088
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,663,074 - 79,826,392 (-)Ensembl
Ensembl Acc Id: ENST00000600376
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,667,997 - 79,766,324 (-)Ensembl
Ensembl Acc Id: ENST00000601369
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,475 - 79,826,516 (-)Ensembl
Ensembl Acc Id: ENST00000610681
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,762,710 - 79,786,443 (-)Ensembl
Ensembl Acc Id: ENST00000619625
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,716,445 - 79,826,299 (-)Ensembl
Ensembl Acc Id: ENST00000653620
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,804,191 - 79,812,427 (-)Ensembl
Ensembl Acc Id: ENST00000658528
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,722,933 - 79,826,250 (-)Ensembl
Ensembl Acc Id: ENST00000659471
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,795,691 - 79,826,373 (-)Ensembl
Ensembl Acc Id: ENST00000661316
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,765,789 - 79,825,782 (-)Ensembl
Ensembl Acc Id: ENST00000662025
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,502 - 79,825,697 (-)Ensembl
Ensembl Acc Id: ENST00000665716
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,762,821 - 79,826,489 (-)Ensembl
Ensembl Acc Id: ENST00000669121
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,803,859 - 79,826,395 (-)Ensembl
Ensembl Acc Id: ENST00000670682
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,475 - 79,826,395 (-)Ensembl
Ensembl Acc Id: ENST00000671459
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,661,394 - 79,826,389 (-)Ensembl
Ensembl Acc Id: ENST00000807165
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,663,074 - 79,826,392 (-)Ensembl
Ensembl Acc Id: ENST00000807166
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,663,075 - 79,826,386 (-)Ensembl
Ensembl Acc Id: ENST00000807167
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,663,074 - 79,826,349 (-)Ensembl
Ensembl Acc Id: ENST00000807168
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,663,074 - 79,826,349 (-)Ensembl
Ensembl Acc Id: ENST00000807169
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,663,076 - 79,826,344 (-)Ensembl
Ensembl Acc Id: ENST00000807170
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,663,078 - 79,826,218 (-)Ensembl
Ensembl Acc Id: ENST00000807171
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,663,076 - 79,825,757 (-)Ensembl
Ensembl Acc Id: ENST00000807172
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,500 - 79,826,392 (-)Ensembl
Ensembl Acc Id: ENST00000807173
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,500 - 79,826,389 (-)Ensembl
Ensembl Acc Id: ENST00000807174
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,502 - 79,826,376 (-)Ensembl
Ensembl Acc Id: ENST00000807175
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,501 - 79,826,373 (-)Ensembl
Ensembl Acc Id: ENST00000807176
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,500 - 79,826,301 (-)Ensembl
Ensembl Acc Id: ENST00000807177
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,501 - 79,826,286 (-)Ensembl
Ensembl Acc Id: ENST00000807178
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,501 - 79,826,259 (-)Ensembl
Ensembl Acc Id: ENST00000807179
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,500 - 79,825,808 (-)Ensembl
Ensembl Acc Id: ENST00000807180
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,500 - 79,825,803 (-)Ensembl
Ensembl Acc Id: ENST00000807181
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,702,160 - 79,826,301 (-)Ensembl
Ensembl Acc Id: ENST00000807182
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,500 - 79,802,923 (-)Ensembl
Ensembl Acc Id: ENST00000807183
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,716,197 - 79,826,305 (-)Ensembl
Ensembl Acc Id: ENST00000807184
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,716,448 - 79,826,362 (-)Ensembl
Ensembl Acc Id: ENST00000807185
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,716,445 - 79,826,349 (-)Ensembl
Ensembl Acc Id: ENST00000807186
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,716,445 - 79,826,349 (-)Ensembl
Ensembl Acc Id: ENST00000807187
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,716,441 - 79,826,333 (-)Ensembl
Ensembl Acc Id: ENST00000807188
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,716,448 - 79,826,326 (-)Ensembl
Ensembl Acc Id: ENST00000807189
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,716,445 - 79,826,317 (-)Ensembl
Ensembl Acc Id: ENST00000807190
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,716,445 - 79,825,783 (-)Ensembl
Ensembl Acc Id: ENST00000807191
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,663,075 - 79,766,324 (-)Ensembl
Ensembl Acc Id: ENST00000807192
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,723,357 - 79,826,384 (-)Ensembl
Ensembl Acc Id: ENST00000807193
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,723,358 - 79,826,370 (-)Ensembl
Ensembl Acc Id: ENST00000807194
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,500 - 79,779,507 (-)Ensembl
Ensembl Acc Id: ENST00000807195
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,745,943 - 79,826,392 (-)Ensembl
Ensembl Acc Id: ENST00000807196
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,760,462 - 79,825,786 (-)Ensembl
Ensembl Acc Id: ENST00000807197
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,765,789 - 79,826,381 (-)Ensembl
Ensembl Acc Id: ENST00000807198
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,765,789 - 79,826,371 (-)Ensembl
Ensembl Acc Id: ENST00000807199
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,765,795 - 79,826,370 (-)Ensembl
Ensembl Acc Id: ENST00000807200
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,765,789 - 79,826,333 (-)Ensembl
Ensembl Acc Id: ENST00000807201
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,765,793 - 79,825,747 (-)Ensembl
Ensembl Acc Id: ENST00000807202
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,500 - 79,739,567 (-)Ensembl
Ensembl Acc Id: ENST00000807203
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,691,475 - 79,724,012 (-)Ensembl
Ensembl Acc Id: ENST00000807204
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,378 - 79,826,389 (-)Ensembl
Ensembl Acc Id: ENST00000807205
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,834 - 79,826,575 (-)Ensembl
Ensembl Acc Id: ENST00000807206
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,706 - 79,826,356 (-)Ensembl
Ensembl Acc Id: ENST00000807207
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,837 - 79,826,373 (-)Ensembl
Ensembl Acc Id: ENST00000807208
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,834 - 79,826,370 (-)Ensembl
Ensembl Acc Id: ENST00000807209
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,837 - 79,826,347 (-)Ensembl
Ensembl Acc Id: ENST00000807210
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,834 - 79,826,335 (-)Ensembl
Ensembl Acc Id: ENST00000807211
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,862 - 79,826,362 (-)Ensembl
Ensembl Acc Id: ENST00000807212
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,836 - 79,826,317 (-)Ensembl
Ensembl Acc Id: ENST00000807213
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,881 - 79,826,360 (-)Ensembl
Ensembl Acc Id: ENST00000807214
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,884 - 79,826,362 (-)Ensembl
Ensembl Acc Id: ENST00000807215
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,837 - 79,826,307 (-)Ensembl
Ensembl Acc Id: ENST00000807216
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,873 - 79,826,290 (-)Ensembl
Ensembl Acc Id: ENST00000807217
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,881 - 79,826,276 (-)Ensembl
Ensembl Acc Id: ENST00000807218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,834 - 79,826,222 (-)Ensembl
Ensembl Acc Id: ENST00000807219
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,704 - 79,825,728 (-)Ensembl
Ensembl Acc Id: ENST00000807220
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,837 - 79,825,789 (-)Ensembl
Ensembl Acc Id: ENST00000807221
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,834 - 79,825,782 (-)Ensembl
Ensembl Acc Id: ENST00000807222
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,834 - 79,825,781 (-)Ensembl
Ensembl Acc Id: ENST00000807223
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,836 - 79,825,755 (-)Ensembl
Ensembl Acc Id: ENST00000807224
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,883 - 79,825,783 (-)Ensembl
Ensembl Acc Id: ENST00000807225
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,802,592 - 79,826,349 (-)Ensembl
Ensembl Acc Id: ENST00000807226
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,803,736 - 79,826,370 (-)Ensembl
Ensembl Acc Id: ENST00000807227
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,803,859 - 79,826,362 (-)Ensembl
Ensembl Acc Id: ENST00000807228
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,804,059 - 79,826,376 (-)Ensembl
Ensembl Acc Id: ENST00000807229
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,884 - 79,814,716 (-)Ensembl
Ensembl Acc Id: ENST00000807230
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1079,797,834 - 79,802,923 (-)Ensembl
RefSeq Acc Id: NR_120611
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381079,762,572 - 79,826,594 (-)NCBI
CHM1_11081,804,035 - 81,868,662 (-)NCBI
T2T-CHM13v2.01080,631,874 - 80,695,938 (-)NCBI
Sequence:
RefSeq Acc Id: NR_120612
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381079,797,834 - 79,826,594 (-)NCBI
CHM1_11081,839,849 - 81,868,662 (-)NCBI
T2T-CHM13v2.01080,667,135 - 80,695,938 (-)NCBI
Sequence:
RefSeq Acc Id: NR_120613
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381079,691,500 - 79,826,594 (-)NCBI
CHM1_11081,733,537 - 81,868,662 (-)NCBI
T2T-CHM13v2.01080,560,802 - 80,695,938 (-)NCBI
Sequence:
Promoters
RGD ID:15096429
Promoter ID:EPDNEWNC_H1271
Type:initiation region
Name:NUTM2B-AS1_2
Description:NUTM2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51204]
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
GRCh381079,814,686 - 79,814,746EPDNEWNC
RGD ID:15096454
Promoter ID:EPDNEWNC_H1272
Type:initiation region
Name:NUTM2B-AS1_3
Description:NUTM2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51204]
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
GRCh381079,825,793 - 79,825,853EPDNEWNC
RGD ID:15096444
Promoter ID:EPDNEWNC_H1273
Type:initiation region
Name:NUTM2B-AS1_1
Description:NUTM2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51204]
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
GRCh381079,826,497 - 79,826,557EPDNEWNC

Additional Information

Database Acc Id Source(s)
COSMIC NUTM2B-AS1 COSMIC
Ensembl Genes ENSG00000225484 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000601369 ENTREZGENE
  ENST00000665716 ENTREZGENE
  ENST00000807205 ENTREZGENE
GTEx ENSG00000225484 GTEx
HGNC ID HGNC:51204 ENTREZGENE
Human Proteome Map NUTM2B-AS1 Human Proteome Map
NCBI Gene NUTM2B-AS1 ENTREZGENE
OMIM 618639 OMIM
RNAcentral URS0000759C3A RNACentral
  URS000075BB1D RNACentral
  URS000075CFC7 RNACentral