MYO3B-AS1 (MYO3B antisense RNA 1)

Gene: MYO3B-AS1 (MYO3B antisense RNA 1) Homo sapiens

Analyze

Symbol:

MYO3B-AS1

Name:

MYO3B antisense RNA 1

RGD ID:

13793304

HGNC Page

HGNC:40713

Description:

Type:

ncrna (Ensembl: lncRNA)

RefSeq Status:

VALIDATED

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	170,340,517 - 170,350,943 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	170,332,085 - 170,408,564 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	171,197,027 - 171,207,453 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Cytogenetic Map	2	q31.1	NCBI
HuRef	2	163,084,536 - 163,087,650 (-)	NCBI		HuRef
CHM1_1	2	171,203,393 - 171,206,513 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	2	170,817,647 - 170,828,073 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

References

Additional References at PubMed

PMID:16344560

Genomics

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 2q24.3-31.1(chr2:164066038-172097886)x1	copy number loss	See cases [RCV000054123]	Chr2:164066038..172097886 [GRCh38] Chr2:164922548..172962614 [GRCh37] Chr2:164630794..172670860 [NCBI36] Chr2:2q24.3-31.1	pathogenic
GRCh38/hg38 2q24.3-31.1(chr2:164850117-175559190)x1	copy number loss	See cases [RCV000051201]	Chr2:164850117..175559190 [GRCh38] Chr2:165706627..176423918 [GRCh37] Chr2:165414873..176132164 [NCBI36] Chr2:2q24.3-31.1	pathogenic
GRCh38/hg38 2q24.3-32.1(chr2:163965382-182195062)x1	copy number loss	See cases [RCV000054122]	Chr2:163965382..182195062 [GRCh38] Chr2:164821892..183059789 [GRCh37] Chr2:164530138..182768034 [NCBI36] Chr2:2q24.3-32.1	pathogenic
GRCh38/hg38 2q31.1(chr2:170101430-171243609)x1	copy number loss	See cases [RCV000054126]	Chr2:170101430..171243609 [GRCh38] Chr2:170957940..172100119 [GRCh37] Chr2:170666186..171808365 [NCBI36] Chr2:2q31.1	pathogenic
GRCh38/hg38 2q24.1-31.1(chr2:154294042-175989372)x3	copy number gain	See cases [RCV000142286]	Chr2:154294042..175989372 [GRCh38] Chr2:155150555..176854100 [GRCh37] Chr2:154858801..176562346 [NCBI36] Chr2:2q24.1-31.1	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	3523
Count of miRNA genes:	830
Interacting mature miRNAs:	965
Transcripts:	ENST00000413923, ENST00000424391, ENST00000438635, ENST00000457834, ENST00000593578, ENST00000593599, ENST00000593861, ENST00000594762, ENST00000595011, ENST00000595528, ENST00000596641, ENST00000597915, ENST00000598749, ENST00000599635, ENST00000600365, ENST00000600436, ENST00000600489, ENST00000607977, ENST00000608050, ENST00000608085, ENST00000608325, ENST00000608503, ENST00000608716, ENST00000609097, ENST00000609459, ENST00000609532, ENST00000609666, ENST00000609725, ENST00000609890, ENST00000609996, ENST00000610113, ENST00000610274
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.

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

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

224

Low

149

Below cutoff

499

475

719

514

1552

499

913

139

261

701

231

978

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NG_034020	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_110576	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC012594	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC068280	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX117364	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CD557506	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB057224	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000413923

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,114 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000424391

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,101 - 170,350,943 (-)	Ensembl

RefSeq Acc Id:

ENST00000438635

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,344,849 - 170,351,055 (-)	Ensembl

RefSeq Acc Id:

ENST00000457834

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,344,835 - 170,351,071 (-)	Ensembl

RefSeq Acc Id:

ENST00000593578

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,334,013 - 170,344,927 (-)	Ensembl

RefSeq Acc Id:

ENST00000593599

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,191 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000593861

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,334,765 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000594762

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,334,099 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000595011

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,263 - 170,351,108 (-)	Ensembl

RefSeq Acc Id:

ENST00000595528

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,982 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000596641

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,340,518 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000597915

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,928 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000598749

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,340,639 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000599635

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,334,372 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000600365

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,334,859 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000600436

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,334,372 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000600489

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,344,799 - 170,351,118 (-)	Ensembl

RefSeq Acc Id:

ENST00000607977

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,207 - 170,346,276 (-)	Ensembl

RefSeq Acc Id:

ENST00000608050

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,588 - 170,351,103 (-)	Ensembl

RefSeq Acc Id:

ENST00000608085

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,594 - 170,350,763 (-)	Ensembl

RefSeq Acc Id:

ENST00000608325

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,238 - 170,351,108 (-)	Ensembl

RefSeq Acc Id:

ENST00000608503

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,195 - 170,347,997 (-)	Ensembl

RefSeq Acc Id:

ENST00000608716

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,195 - 170,350,627 (-)	Ensembl

RefSeq Acc Id:

ENST00000609097

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,218 - 170,346,276 (-)	Ensembl

RefSeq Acc Id:

ENST00000609459

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,587 - 170,351,102 (-)	Ensembl

RefSeq Acc Id:

ENST00000609532

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,321 - 170,351,099 (-)	Ensembl

RefSeq Acc Id:

ENST00000609666

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,340,523 - 170,351,111 (-)	Ensembl

RefSeq Acc Id:

ENST00000609725

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,606 - 170,350,792 (-)	Ensembl

RefSeq Acc Id:

ENST00000609890

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,196 - 170,350,581 (-)	Ensembl

RefSeq Acc Id:

ENST00000609996

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,195 - 170,350,373 (-)	Ensembl

RefSeq Acc Id:

ENST00000610113

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,591 - 170,351,117 (-)	Ensembl

RefSeq Acc Id:

ENST00000610274

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,165 - 170,351,108 (-)	Ensembl

RefSeq Acc Id:

ENST00000610954

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,587 - 170,351,106 (-)	Ensembl

RefSeq Acc Id:

ENST00000613316

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,587 - 170,350,942 (-)	Ensembl

RefSeq Acc Id:

ENST00000616148

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,587 - 170,350,870 (-)	Ensembl

RefSeq Acc Id:

ENST00000620227

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,587 - 170,350,848 (-)	Ensembl

RefSeq Acc Id:

ENST00000622590

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,587 - 170,350,916 (-)	Ensembl

RefSeq Acc Id:

ENST00000625235

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,340,553 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000625384

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,933 - 170,341,410 (-)	Ensembl

RefSeq Acc Id:

ENST00000625393

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,113 - 170,344,901 (-)	Ensembl

RefSeq Acc Id:

ENST00000625406

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,937 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000625440

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,334,801 - 170,344,926 (-)	Ensembl

RefSeq Acc Id:

ENST00000625454

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,334,049 - 170,341,410 (-)	Ensembl

RefSeq Acc Id:

ENST00000625790

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,346,300 - 170,351,012 (-)	Ensembl

RefSeq Acc Id:

ENST00000625968

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,196 - 170,408,564 (-)	Ensembl

RefSeq Acc Id:

ENST00000626351

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,334,083 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000626618

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,346,309 - 170,348,654 (-)	Ensembl

RefSeq Acc Id:

ENST00000626724

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,587 - 170,350,641 (-)	Ensembl

RefSeq Acc Id:

ENST00000626776

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,925 - 170,344,883 (-)	Ensembl

RefSeq Acc Id:

ENST00000626959

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,337,849 - 170,344,883 (-)	Ensembl

RefSeq Acc Id:

ENST00000627214

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,153 - 170,350,892 (-)	Ensembl

RefSeq Acc Id:

ENST00000627332

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,928 - 170,344,883 (-)	Ensembl

RefSeq Acc Id:

ENST00000627387

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,925 - 170,344,926 (-)	Ensembl

RefSeq Acc Id:

ENST00000627454

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,931 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000627884

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,924 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000628002

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,342,104 - 170,343,656 (-)	Ensembl

RefSeq Acc Id:

ENST00000628338

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,587 - 170,351,030 (-)	Ensembl

RefSeq Acc Id:

ENST00000628535

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,153 - 170,350,973 (-)	Ensembl

RefSeq Acc Id:

ENST00000629445

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,955 - 170,344,882 (-)	Ensembl

RefSeq Acc Id:

ENST00000629469

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,154 - 170,350,343 (-)	Ensembl

RefSeq Acc Id:

ENST00000629973

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,334,043 - 170,344,883 (-)	Ensembl

RefSeq Acc Id:

ENST00000630033

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,340,594 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000630277

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,928 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000630367

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,332,085 - 170,344,880 (-)	Ensembl

RefSeq Acc Id:

ENST00000630496

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,959 - 170,343,600 (-)	Ensembl

RefSeq Acc Id:

ENST00000630498

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,341,098 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000630532

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,587 - 170,350,988 (-)	Ensembl

RefSeq Acc Id:

ENST00000630561

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,927 - 170,345,826 (-)	Ensembl

RefSeq Acc Id:

ENST00000630683

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,343,587 - 170,350,978 (-)	Ensembl

RefSeq Acc Id:

ENST00000630733

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,334,074 - 170,341,253 (-)	Ensembl

RefSeq Acc Id:

ENST00000630778

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,340,522 - 170,344,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000631125

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,999 - 170,341,410 (-)	Ensembl

RefSeq Acc Id:

ENST00000631172

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	170,333,924 - 170,344,883 (-)	Ensembl

RefSeq Acc Id:

NR_110576

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	170,340,517 - 170,350,943 (-)	NCBI
T2T-CHM13v2.0	2	170,817,647 - 170,828,073 (-)	NCBI

Sequence:

show sequence

TTTGGAAAAGTATAAACCTAAGGCATCACCTTTACAGAAAATATCTTCCACGGAAACATCTAAA
GGCCACAGATCAGCCCTGGGGTTCAGAGGGATCCTGACAGCTACTCCTCAAGATCCTCTCTGTT
GTGATTCATCCCCCCGGGGCCCTACAGTTTCTCCTTCCTGACTCTTACATTTCTTTGGATGGCA
TCATTATTTACCTGTCTCCTCCCATAGTTAGGTGCCAAGCACTGTGGATTCTGCCTCTCAGTGT
CCAGACACCCATTTTCCTTCCCACTGTTCCTTCCCCATGGAGAAGCCTGTGGCTGGCTGACAGC
AGAGAGAGATGCTCAACTTGGAGAAGGTGTTACCTGGGCCAGGTGGGGAAGGTTTGTTTGCAGA
GCAAAGAAGTGAAGGAAGTATTAACCCTTTGCATGGCCTCCTGAGAATCCGACAAGACGTAAAT
AGCCAAGAATATCTGTGAAACTTCATCACTGAGTTACAATATTTATCACTGCAAGTGTGTTGTT
CATTGACACTATAAAGCCATGTGGAATTAAGCAGCCTTGAAACACAAAATGGAGAAAGGCTAAG
AGCTGAGAATTGTTGCCTTCAGGGAAATACAATCAATGTCAAGCAAACAACCACCCCAAAATGG
TTAGCTTTATCAGCATTCAGGCCTACAGTGAACGCAAATGTTCCAGATCTGAGTTTCAATTTTT
AAAGAATAAACATATGCAAATGACCATTAGTCTTAGTAGTTTTAGGGCTCAGAATGATCTTATC
TTGTTAACATTCAGGGCAACTGCTTATACCCATTTGAATGTCATTTAGAGGGCTAGGAAAGACT
GCTTCAACATTTGATGACTAAATGGCAGGGCTCAGCCACAATGCTCACTCCGAGAAATGAGAAA
TAGACACACCAGTATGCTAGATGCTGATGCAGTTCAGGAAATGCTACCCCAAAATATGGCCCCT
CAGCATACTGAGTATTTTAAGCAGAAGGCAATTAAGAAAACCACAAAAACAGAAAGGTCCCTCT
GACCTTCTCCCACCCTCTCTCTCTTGAAGATCCTCATGTGACAGGTGACCTGCCATATAATCAG
AAGGAAGAAATGTTACACAGAGAGGCTGAGAAGAATCTGAGGACTTGCTAAGTTTTCCCCAGTT
TATTACCATTAGATCATATGCCTTTTTTGTTCAATCATACTTCTATACAACTGTCCATCATTCA
TTAAACCTAACCACAAAAGTAGTTTTCACTCGGTTTTTGAGTGAAGGCTCCTGTGTCACATAAA
ACTTACATTAAATAAATTTGTTCCACTTTTC

hide sequence

Promoters

RGD ID:

15095495

Promoter ID:

EPDNEWNC_H333

Type:

initiation region

Name:

MYO3B-AS1_1

Description:

MYO3B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40713]

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 Assembly	Chr	Position (strand)	Source
GRCh38	2	170,343,670 - 170,343,730	EPDNEWNC

RGD ID:

15095509

Promoter ID:

EPDNEWNC_H334

Type:

initiation region

Name:

MYO3B-AS1_2

Description:

MYO3B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40713]

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 Assembly	Chr	Position (strand)	Source
GRCh38	2	170,351,071 - 170,351,131	EPDNEWNC

Additional Information

External Database Links

Database	Acc Id	Source(s)
COSMIC	MYO3B-AS1	COSMIC
Ensembl Genes	ENSG00000231898	Ensembl, ENTREZGENE
Ensembl Transcript	ENST00000609666	ENTREZGENE
GTEx	ENSG00000231898	GTEx
HGNC ID	HGNC:40713	ENTREZGENE
Human Proteome Map	MYO3B-AS1	Human Proteome Map
NCBI Gene	MYO3B-AS1	ENTREZGENE
RNAcentral	URS000075A229	RNACentral

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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