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Gene: LINC02533 (long intergenic non-protein coding RNA 2533) Homo sapiens

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Symbol:

LINC02533

Name:

long intergenic non-protein coding RNA 2533

RGD ID:

12910410

HGNC Page

HGNC:53566

Description:

INTERACTS WITH aflatoxin B1; cadmium atom; sodium arsenite

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	6	4,488,798 - 4,495,771 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	6	4,488,720 - 4,509,528 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	6	4,489,032 - 4,496,005 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Cytogenetic Map	6	p25.1	NCBI
CHM1_1	6	4,490,590 - 4,498,642 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	6	4,357,719 - 4,364,687 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
LINC02533	Human	aflatoxin B1	decreases methylation	EXP		6480464	Aflatoxin B1 results in decreased methylation of LINC02533 polyA tail	CTD	PMID:30157460
LINC02533	Human	cadmium atom	increases expression	EXP		6480464	Cadmium results in increased expression of LINC02533 mRNA	CTD	PMID:33559965
LINC02533	Human	sodium arsenite	increases expression	EXP		6480464	sodium arsenite results in increased expression of LINC02533 mRNA	CTD	PMID:38568856

PMID:10737800	PMID:14702039	PMID:16344560

Variants in LINC02533
1 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 6p25.3-25.1(chr6:163083-6062800)x1	copy number loss	See cases [RCV000050686]	Chr6:163083..6062800 [GRCh38] Chr6:163083..6063033 [GRCh37] Chr6:108083..6008032 [NCBI36] Chr6:6p25.3-25.1	pathogenic
GRCh38/hg38 6p25.3-22.3(chr6:106431-18360595)x3	copy number gain	See cases [RCV000051869]	Chr6:106431..18360595 [GRCh38] Chr6:106431..18360826 [GRCh37] Chr6:51431..18468805 [NCBI36] Chr6:6p25.3-22.3	pathogenic
GRCh38/hg38 6p25.3-23(chr6:389423-13474956)x3	copy number gain	See cases [RCV000051896]	Chr6:389423..13474956 [GRCh38] Chr6:389423..13475188 [GRCh37] Chr6:334423..13583167 [NCBI36] Chr6:6p25.3-23	pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:107682-4978781)x1	copy number loss	See cases [RCV000052159]	Chr6:107682..4978781 [GRCh38] Chr6:107682..4979015 [GRCh37] Chr6:52682..4924014 [NCBI36] Chr6:6p25.3-25.1	pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:162883-5979198)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052160]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052160]\|See cases [RCV000052160]	Chr6:162883..5979198 [GRCh38] Chr6:162883..5979431 [GRCh37] Chr6:107883..5924430 [NCBI36] Chr6:6p25.3-25.1	pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:163083-5875402)x1	copy number loss	See cases [RCV000052161]	Chr6:163083..5875402 [GRCh38] Chr6:163083..5875635 [GRCh37] Chr6:108083..5820634 [NCBI36] Chr6:6p25.3-25.1	pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:164633-6284237)x1	copy number loss	See cases [RCV000052163]	Chr6:164633..6284237 [GRCh38] Chr6:164633..6284470 [GRCh37] Chr6:109633..6229469 [NCBI36] Chr6:6p25.3-25.1	pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:164633-5823601)x1	copy number loss	See cases [RCV000052164]	Chr6:164633..5823601 [GRCh38] Chr6:164633..5823834 [GRCh37] Chr6:109633..5768833 [NCBI36] Chr6:6p25.3-25.1	pathogenic
GRCh38/hg38 6p25.3-24.3(chr6:165675-9036034)x1	copy number loss	See cases [RCV000052165]	Chr6:165675..9036034 [GRCh38] Chr6:165675..9036267 [GRCh37] Chr6:110675..8981266 [NCBI36] Chr6:6p25.3-24.3	pathogenic
GRCh38/hg38 6p25.3-24.1(chr6:164360-13339881)x3	copy number gain	See cases [RCV000134022]	Chr6:164360..13339881 [GRCh38] Chr6:164360..13340113 [GRCh37] Chr6:109360..13448092 [NCBI36] Chr6:6p25.3-24.1	pathogenic
GRCh38/hg38 6p25.2-24.1(chr6:4068792-13267799)x1	copy number loss	See cases [RCV000136132]	Chr6:4068792..13267799 [GRCh38] Chr6:4069026..13268031 [GRCh37] Chr6:4014025..13376010 [NCBI36] Chr6:6p25.2-24.1	pathogenic
GRCh38/hg38 6p25.3-24.3(chr6:163083-9525496)x3	copy number gain	See cases [RCV000136567]	Chr6:163083..9525496 [GRCh38] Chr6:163083..9525729 [GRCh37] Chr6:108083..9633715 [NCBI36] Chr6:6p25.3-24.3	pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:152634-5315679)x1	copy number loss	See cases [RCV000137496]	Chr6:152634..5315679 [GRCh38] Chr6:152634..5315912 [GRCh37] Chr6:97634..5260911 [NCBI36] Chr6:6p25.3-25.1	pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:152634-6027547)x3	copy number gain	See cases [RCV000138716]	Chr6:152634..6027547 [GRCh38] Chr6:152634..6027780 [GRCh37] Chr6:97634..5972779 [NCBI36] Chr6:6p25.3-25.1	likely pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:152634-6027547)x1	copy number loss	See cases [RCV000138717]	Chr6:152634..6027547 [GRCh38] Chr6:152634..6027780 [GRCh37] Chr6:97634..5972779 [NCBI36] Chr6:6p25.3-25.1	pathogenic
GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3	copy number gain	See cases [RCV000138956]	Chr6:3224310..30657190 [GRCh38] Chr6:3224544..30624967 [GRCh37] Chr6:3169543..30732946 [NCBI36] Chr6:6p25.2-21.33	pathogenic
GRCh38/hg38 6p25.3-22.3(chr6:155807-17058414)x3	copy number gain	See cases [RCV000140307]	Chr6:155807..17058414 [GRCh38] Chr6:155807..17058645 [GRCh37] Chr6:100807..17166624 [NCBI36] Chr6:6p25.3-22.3	pathogenic
GRCh38/hg38 6p25.3-24.2(chr6:156974-11550817)x3	copy number gain	See cases [RCV000142295]	Chr6:156974..11550817 [GRCh38] Chr6:156974..11551050 [GRCh37] Chr6:101974..11659036 [NCBI36] Chr6:6p25.3-24.2	likely pathogenic
GRCh38/hg38 6p25.3-24.3(chr6:156974-7122759)x1	copy number loss	See cases [RCV000142299]	Chr6:156974..7122759 [GRCh38] Chr6:156974..7122992 [GRCh37] Chr6:101974..7067991 [NCBI36] Chr6:6p25.3-24.3	pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:156974-4907692)x1	copy number loss	See cases [RCV000142304]	Chr6:156974..4907692 [GRCh38] Chr6:156974..4907926 [GRCh37] Chr6:101974..4852925 [NCBI36] Chr6:6p25.3-25.1	pathogenic
GRCh38/hg38 6p25.2-22.3(chr6:2862640-16697788)x1	copy number loss	See cases [RCV000142435]	Chr6:2862640..16697788 [GRCh38] Chr6:2862874..16698019 [GRCh37] Chr6:2807873..16805998 [NCBI36] Chr6:6p25.2-22.3	pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:152634-6289804)x1	copy number loss	See cases [RCV000142916]	Chr6:152634..6289804 [GRCh38] Chr6:152634..6290037 [GRCh37] Chr6:97634..6235036 [NCBI36] Chr6:6p25.3-25.1	pathogenic
GRCh38/hg38 6p25.3-23(chr6:152634-14417003)x3	copy number gain	See cases [RCV000143334]	Chr6:152634..14417003 [GRCh38] Chr6:152634..14417234 [GRCh37] Chr6:97634..14525213 [NCBI36] Chr6:6p25.3-23	pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:156974-4946857)x3	copy number gain	See cases [RCV000143375]	Chr6:156974..4946857 [GRCh38] Chr6:156974..4947091 [GRCh37] Chr6:101974..4892090 [NCBI36] Chr6:6p25.3-25.1	uncertain significance
GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3	copy number gain	See cases [RCV000143497]	Chr6:156974..46789291 [GRCh38] Chr6:156974..46757028 [GRCh37] Chr6:101974..46864987 [NCBI36] Chr6:6p25.3-12.3	pathogenic
GRCh38/hg38 6p25.3-24.1(chr6:156974-13081201)x3	copy number gain	See cases [RCV000143698]	Chr6:156974..13081201 [GRCh38] Chr6:156974..13081433 [GRCh37] Chr6:101974..13189419 [NCBI36] Chr6:6p25.3-24.1	likely pathogenic
GRCh38/hg38 6p25.3-23(chr6:156974-13855925)x1	copy number loss	See cases [RCV000143782]	Chr6:156974..13855925 [GRCh38] Chr6:156974..13856156 [GRCh37] Chr6:101974..13964135 [NCBI36] Chr6:6p25.3-23	pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:144957-5239181)x3	copy number gain	See cases [RCV000051870]	Chr6:144957..5239181 [GRCh38] Chr6:144957..5239414 [GRCh37] Chr6:89957..5184413 [NCBI36] Chr6:6p25.3-25.1	pathogenic
GRCh38/hg38 6p25.1-24.3(chr6:4427090-8391140)x1	copy number loss	See cases [RCV000052177]	Chr6:4427090..8391140 [GRCh38] Chr6:4427324..8391373 [GRCh37] Chr6:4372323..8336372 [NCBI36] Chr6:6p25.1-24.3	pathogenic
Single allele	inversion	Anophthalmia-microphthalmia syndrome [RCV004009748]	Chr6:1713354..4870965 [GRCh38] Chr6:6p25.3-25.1	likely pathogenic

Predicted Target Of

	Summary Value
Count of predictions:	163
Count of miRNA genes:	153
Interacting mature miRNAs:	162
Transcripts:	ENST00000563079
Prediction methods:	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.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
2289408	BW324_H	Body weight QTL 324 (human)	3.15	0.0001	Body fat amount		6	1	20803913	Human
1643418	BW282_H	Body Weight QTL 282 (human)	2.07	0.001	Body weight		6	1	19321359	Human
2289435	BMD4_H	Bone mineral density QTL 4 (human)	3.15	0.0001	Bone mineral density		6	1	20803913	Human
2292824	PRSTS5_H	Prostate tumor susceptibility QTL 5 (human)			Prostate tumor susceptibility		6	1	19232373	Human
2289320	BW390_H	Body weight QTL 390 (human)	2.13		Body weight	BMI	6	1	19321359	Human
1643495	BW291_H	Body Weight QTL 291 (human)	2.13		Body weight	BMI	6	1	19321359	Human

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

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
614	1060	1456	1159	2565	797	1240	4	228	586	138	1281	3100	2848	47	1806	391	1068	945	100


RefSeq Transcripts	NR_149117	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AK092525	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL162718	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BF376889	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068272	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA839427	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988525	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988526	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988527	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988528	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988529	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988530	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988531	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988532	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988533	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000563079

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,491,803 - 4,495,769 (+)	Ensembl

Ensembl Acc Id:

ENST00000673975

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,491,807 - 4,495,769 (+)	Ensembl

Ensembl Acc Id:

ENST00000674020

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,744 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827245

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,489,832 - 4,509,528 (+)	Ensembl

Ensembl Acc Id:

ENST00000827246

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,489,834 - 4,509,521 (+)	Ensembl

Ensembl Acc Id:

ENST00000827247

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,745 - 4,494,793 (+)	Ensembl

Ensembl Acc Id:

ENST00000827248

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,793 - 4,494,793 (+)	Ensembl

Ensembl Acc Id:

ENST00000827249

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,720 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827250

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,763 - 4,494,614 (+)	Ensembl

Ensembl Acc Id:

ENST00000827251

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,762 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827252

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,762 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827253

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,774 - 4,494,616 (+)	Ensembl

Ensembl Acc Id:

ENST00000827254

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,778 - 4,494,614 (+)	Ensembl

Ensembl Acc Id:

ENST00000827255

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,778 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827256

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,778 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827257

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,795 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827258

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,795 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827259

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,795 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827260

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,795 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827261

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,798 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827262

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,489,802 - 4,495,245 (+)	Ensembl

Ensembl Acc Id:

ENST00000827263

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,489,823 - 4,495,245 (+)	Ensembl

Ensembl Acc Id:

ENST00000827264

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,489,788 - 4,494,614 (+)	Ensembl

Ensembl Acc Id:

ENST00000827265

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,489,806 - 4,494,614 (+)	Ensembl

Ensembl Acc Id:

ENST00000827266

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,489,806 - 4,494,614 (+)	Ensembl

Ensembl Acc Id:

ENST00000827267

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,489,808 - 4,494,614 (+)	Ensembl

Ensembl Acc Id:

ENST00000827268

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,489,808 - 4,494,614 (+)	Ensembl

Ensembl Acc Id:

ENST00000827269

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,489,820 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827270

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,490,291 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827271

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,490,291 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827272

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,490,291 - 4,494,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000827273

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,489,806 - 4,490,863 (+)	Ensembl

Ensembl Acc Id:

ENST00000827274

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	4,488,829 - 4,489,609 (+)	Ensembl

RefSeq Acc Id:

NR_149117

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	4,488,798 - 4,495,771 (+)	NCBI
T2T-CHM13v2.0	6	4,357,719 - 4,364,687 (+)	NCBI

Sequence:

show sequence

ACAATTTTAGGGTGCAGTAAAGGCAGAAAGGATAGTTGCAGAGTAGGGAATAGATGTGAGTTATAGATTAGGACTGATGGGAAGATTGTTTACCATAATTAGAGGCAAGGGGGCATAAAGAACGAGGA
AGTTACTCTTTGAAAATAGAGAACAAAGAACAAGGAAGCTGAACAAGCTGACTCTTCTTTGAAGAGGAACCCACCGTACCCAACACCAGAAAGACTATAACCTTGCTTTGAAGGCTGGGAGTCCAAGA
TCCAGGTGTCAGCAGTGTTGGTATCTCCTGTGGCCACTCTCCTGGGCTTGCAGACGGCGTCTTCTCCCTGTGTCCCCACATGACCACCCTTCTCCACCTTAGCATCCCCGGTGTCTCTGTGTGTCCGG
ATGTCCTTTTCTCATGAGGGAAGTGAACTTGACATGGTTTAGCAACCAAATAAAGCCATACGTCACTGCTGCTCTTTGAAGATAATGAAATCTGGCATCGAGATCTTTATCTTTGCAGGAACCAAAGG
CCAGAGACTTCTCAGCAAACACAAGACCAGAGAGAGAAGCATCCCTGCTGATGAGAAAGAACAGACACTCCCAGAGGACAAGGTCCACCTGTCAGGCAGCCACAGCCCAGCATACTCTGGAGTCTGAG
GTGGGGGTCAGTTGTGAAGAAAGGGAAGAAGGAAGAAAAAGGATACGTTGTGCTCCGACCACAGGCCAAGGTCAGAAGACGGTATTTACCAAGTCTCTTCCCAAAATACTTGCAAATGCACATAATCT
CAAAGTGTTTTTGAGGGCTCTTCCGATCTAAAATTGGTCCTAGTGACAAGGGGTGTTTGGGGAAATCAAAGGGCTGGCTTAACTATGTAGACCTAGGTCTGGTCTTATTTCTGGCCCATACGATCATC
ATGACCTTGGACAAATGAAACTTCCTGGGCCTCAAGTTCCTTGTATCAGAAAGGATGGCATTCAGCTGCGTACAACAGAAAACCAAATCACAGTGGCTTATCCAAGAAAAGTTCAATTTTTCTCAAAA
CTACAGCGTCCTGGGCTGATGCGGCAGCCCCAGGACGACCTCAGCATCTCACTCCTCCTTTCTTTACTCGGCCCCATCCTCAGGCTGTGACTTTCATCCTCAGGTTTGTCATCTTTTGGTGGTAAGAT
GGTTGCTCTACCTCAAGCTCACAAAAAGAAATGGGGGAAAGCAGGAAAGAAGAAAATCTGCTTCCCCAGAGACTCTGAGGCTGCACTTGCACATCTTATGGATCCAAACTGTGTCCCATGGCTGCCCC
TAGATGCAAGGGGCCTGGGGAAATGAGCGGATTCATCAGGTACACTGCAACCGTACATGAAAGGAAAGTTCTGTCAATAAAGAAGAGCGAAATCTACATTTGGTCAGGAAACAGCATTGCCTGCAATA
TGCCTCATATGAAATAAAGCCTTTCTTGCCCCCATTCTGCTACTCGGTCATTCTTGCACTCAACAAATAGATGTTGAGTGCCCACTCTCTCCAGGCCATGTTCTAGGTGCTGCGGATGCAATCCTGAA
TCTATGAACACGATTGGCAGAACAATAAATATTGATTGTCTTGGCCACTCACCAAATAAAGTGCTCCTGGGAAGGCTGAGATCTAATGCAAAGCAGCAGCTTGACTTTCTCACTCCCTGGCAACAATG
CCAAGCAAGAGAAAGCGATGGGTAAGGCCTGGCTCAAGAGTCTCACTGCAACCTGCACTGTAGATTCTACCTGCTAATTTCCTCAGCCTTCTCTGGTTTTGGGCTTCAGAATGCCCTAACTCTGGGCC
CGGCGCGGTGGCTCACGCCTGTAAACCCATCACTTTGGGAGGCCAAGGCGGGTGGATCACAAGATCAAGACCATCCTGGCCAACATGGTGAAACCCTGTCTCTACTGAAAATACAAAAATTAGCTGGG
CATGGTGGCTTGTGCTTGTAATCCAGCTACTTGGAAGGCTGAGGCTGGAGGATCGCTTGAACCCAGAAGGCAGAGGTTGCAGTGAGCTGAGATCACACCACTGCACTCCAGCCTGGCAACAGAGTGAG
ACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAGAATGCCCTAAGTCTACTCTGGACCATGAGCAAGGATAATCTGTCTTAGAGGAGAGAAGGTGAGGTTATGATTCCAGAGCATTTGGTGACCCAGG
AAGTAGACCTGCCTCCTCCTATCTGTCCACAGAGCAGTCCTAGGGGCAATAGGCCATGAGAAGATCATGCCAGGCAGTCCATTTCTATATTACCATGTAAACAAAAACTCAGCTGTGAACCCTGGAAC
GTTCGTATTCTGCAGCTGCCAGTGTAAACTGGTACAGGCCTCTTGAAGAACAGTGGGGAAAGGCACTCTGAAAGCATCCACGCCTCCATACCTGCTGATCCAGGGCTCTGATTTTCCTTCTGGGAACC
AAGCCTAGGAGAATGATTCAAGCTGCAGAAAACCTTTCTCCACTAAGATGTTTGCTGTGGCATTCAGTATAATAGCACACCAGAGAAACAATCTAAAGATTCATCAGTAGGAGAATATCTAAGTAAAT
TATGGTACATACACTCAATAAAATGTTATATGACTACTAA

hide sequence

Database	Acc Id	Source(s)
COSMIC	LINC02533	COSMIC
Ensembl Genes	ENSG00000260239	Ensembl
GTEx	ENSG00000260239	GTEx
HGNC ID	HGNC:53566	ENTREZGENE
Human Proteome Map	LINC02533	Human Proteome Map
NCBI Gene	LINC02533	ENTREZGENE
RNAcentral	URS00002BB5A0	RNACentral
	URS0000BC4576	RNACentral
	URS000199F702	RNACentral

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


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


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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