LINC02542 (long intergenic non-protein coding RNA 2542)

Gene: LINC02542 (long intergenic non-protein coding RNA 2542) Homo sapiens

Analyze

Symbol:

LINC02542

Name:

long intergenic non-protein coding RNA 2542

RGD ID:

12910210

HGNC Page

HGNC:53576

Description:

INTERACTS WITH benzo[a]pyrene

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	81,843,781 - 82,101,765 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	6	81,844,602 - 82,169,391 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	6	82,553,498 - 82,811,482 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Cytogenetic Map	6	q14.1	NCBI
HuRef	6	79,771,252 - 79,865,813 (-)	NCBI		HuRef
CHM1_1	6	82,651,123 - 82,893,216 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	6	83,053,185 - 83,311,151 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

benzo[a]pyrene (EXP)

References

Additional References at PubMed

PMID:16344560

Genomics

Variants

Variants in LINC02542
15 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3	copy number gain	See cases [RCV000139729]	Chr6:74382807..142040500 [GRCh38] Chr6:75092523..142361637 [GRCh37] Chr6:75149243..142403330 [NCBI36] Chr6:6q13-24.1	pathogenic
GRCh38/hg38 6q12-14.2(chr6:64549655-83426791)x1	copy number loss	See cases [RCV000142527]	Chr6:64549655..83426791 [GRCh38] Chr6:65259548..84136510 [GRCh37] Chr6:65316269..84193229 [NCBI36] Chr6:6q12-14.2	pathogenic
GRCh38/hg38 6q14.1-16.1(chr6:75926199-92710793)x1	copy number loss	See cases [RCV000143505]	Chr6:75926199..92710793 [GRCh38] Chr6:76635916..93420511 [GRCh37] Chr6:76692636..93477232 [NCBI36] Chr6:6q14.1-16.1	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	65
Count of miRNA genes:	64
Interacting mature miRNAs:	64
Transcripts:	ENST00000418567
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.

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

Low

493

1474

482

496

344

366

1750

310

283

140

829

434

142

350

986

Below cutoff

1498

855

893

556

1816

1088

1838

194

444

822

754

1109

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NR_149134	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_149135	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_149136	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AL355294	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL356492	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL360157	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068272	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA443454	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB182239	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988648	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000418567

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,844,604 - 81,933,578 (-)	Ensembl

RefSeq Acc Id:

ENST00000658218

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,844,604 - 81,860,397 (-)	Ensembl

RefSeq Acc Id:

ENST00000660534

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,844,606 - 81,938,437 (-)	Ensembl

RefSeq Acc Id:

ENST00000660637

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,844,604 - 82,101,800 (-)	Ensembl

RefSeq Acc Id:

ENST00000663543

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,844,604 - 82,169,391 (-)	Ensembl

RefSeq Acc Id:

ENST00000665153

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,844,604 - 81,895,717 (-)	Ensembl

RefSeq Acc Id:

ENST00000666226

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,844,604 - 82,101,765 (-)	Ensembl

RefSeq Acc Id:

ENST00000667666

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,844,602 - 82,169,338 (-)	Ensembl

RefSeq Acc Id:

ENST00000668266

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,844,604 - 82,101,792 (-)	Ensembl

RefSeq Acc Id:

ENST00000668303

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,844,604 - 82,160,755 (-)	Ensembl

RefSeq Acc Id:

ENST00000684960

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,845,540 - 81,938,452 (-)	Ensembl

RefSeq Acc Id:

ENST00000702318

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	81,845,547 - 81,938,468 (-)	Ensembl

RefSeq Acc Id:

NR_149134

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	81,843,781 - 81,938,421 (-)	NCBI
T2T-CHM13v2.0	6	83,053,185 - 83,147,737 (-)	NCBI

Sequence:

show sequence

ATTAAAGAAGCATATGGACAAGGAACTATCTCTGAAATGTTTTCAGAGCTTCTCTGGTGTTACA
TGCATAGTAAATATTTTCTTTAAATTAGATGAAAAATATGGATCCCCATCCATGTACCTTTGCT
CAACTGTCCTCAGACCAGATCCAGAATTCACCCTGCTGTTTCTCCATGAGTCTGACCTGCATCA
ACTGCCTCCCTTATTCTGGGATTCCAGTTGTGGAGCTCAAGGACAAGTCCATTCTGGGCTGGCT
GTATCCAACTTCTTTAGTCCAACTATATCCCCACTGGAAGCCAGGCTCTTTCCAACAGCTGTCA
CCCATGCCTCTTTCTATGTTTGTTATCTGTCTCTAGGTTCTGGTAACTACTTCCTTCCCTTGCC
CCTTCTGGCCTAGGGTGCTACCAATCCCTCCTCCAAATCCAACTGTCACTAGCCTCAAAGTACT
TGTAGCTTCCTCACCTTACTTTCACCTTAATAAATGGTCCCCCTACTATCTCTCTTCAAAGCAC
CCAATTTGAGTGTGCCATCTGTTTCTTGCCAGGATCCTGGTTGGTACATCAACCAAGCTGCACT
GATGGAGGAGCACTGTGCTGAACTTTAGGAATGAAGCCACAGGGCCCTCACTGCCCCCATAGTC
ACCTTGGTCATCTTCTGCCTCCCTGAAAGACTAAATTCAGTCAGTTCAGATACATACACATCCA
GACATGTCAGGGAAAACTCCATTTTGTAAGGATCTCTGCTTAAAATGCCAAAAGTTTGAAAGTT
GGCAAACACTTGAGAAAAGCACAGTTCTCTGTCTTACTCTTACTCTAAACTTGGAGATAAATGC
ATTTTTAAAATTGTGCATGTTAGAGTGCTAACGTGTACAAGATCATTTCTGGTGAGACACCACA
AACAATATTTTATGAGGCCAAAATAAGAAAGAAGGAAATGAAATAGCTCAGGAATCTCAGGAAG
AGCTCATCGAACACTTTGCCTTTATCTCAGACCATTTTATCCACAGCCCTGTTAATCAGGATTG
GATATACCTCCATGAGGGAGTCTTAAACGGAGGGAAAGAGATGCCACAACTAAAAAAAAGAATG
CAATAGAAGTTTGTCTTAATGCCTGTTCTGTGATGCACAACTTTCGTAAGCCAAAATTTTAACC
TTATGAACAATCAGTTCTGTGCTGCCCTTAGCAGAGAACCATAAATTAAAGATAAGCAATGGTT
CAGACTTTCCAGGGCCTTGACTCAGGAGTAACTCTGAAATCCCAACCAAATATGTATTTGGTTA
AGCAATTTGGCACATTTTTCTATTTTGAGGCATTAAACTATAATTACAAGTCACTTTTATTTCA
TTCCAAATAAATGTCCCTAAAGTAGATAGAACTAGAGGTTTCCTTTTTTTAAAAAAAGGAAACA
GGAAAACAACAAACAAAACCAAAAAGAACAAAAGCAAAACAAAACTTAGTCAAGCTAACAAATT
GCATGTATGGTGTGTTTTATAATTTAATCAATATAAAAAATTGAGTGTGCTAGTGCCTCAGGAG
GACTCAGAGGACTCAAATACTCAATAGGTTATCTGGAGGAATTTCTCATTGGAGAAAAAAATTA
AAGTTCTTTTGAACAACCCACATAATCAAGATAGTAATAATTTAACCTCAAGTTTTTCCTTGAT
TAAAAAATCCCTTTGCTATTCTGCTCCAGTGTTTGTAATAGATGGTTCAACAAGACTGGTGTTT
TGTTAGTTGGAAAAGTAAGCTGATATGAGGGGTGGGGAGAGGAAGGGCAGAAATTTATTAACAA
TCAGCAAGTAAAGAAAAACAGCCTGCAAATTGTAATGAAAGGAAGAAAGGACAGGAAAGGAAAG
GTAGGGCTGGTGGAGAGTGACTGTTCTGCCTGCTTACTGCACAGGCCAAGAACAAACTCACGAT
AAATACTCCAGGTCCTCAAGAAAAAGGTTTCTGTGCTGAATTATGGTAGTCTACCTGAAATTGG
GATGATGAATTAGAAAACCTCTCTCATCGCTTCAAGTCTTGTGATTTATTCATTCAGTGCCATT
TATTGTATAACTATATAATTTCTAAAGGGGGATAACTACAAGAAAAAGATGTGATTTCTTCTTT
CAGAGATCCCCAAATATAGAAAGCTATTCATATACTGCTTAGATAAACAAAGATTATCTTCTTT
TTCTACATTCTATATAATGTTCCTTAAACTCAAGCTCTCTTCTCCCCATCTCTACCTTACCCCT
CTGGGTAGCAAGGAAAAATAAAAATAATGTCATTC

hide sequence

RefSeq Acc Id:

NR_149135

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	81,843,781 - 82,101,765 (-)	NCBI
T2T-CHM13v2.0	6	83,053,185 - 83,311,151 (-)	NCBI

Sequence:

show sequence

AAGCAAGCCTGGGCAATGGCGGGCGCCCCTCCCCCAGCCTCGCTGCCGCCTTGCAGTTTGATCT
CAGACTGCTGTGCTAGCAATCAGCGAGACTCCGTGGACGTAGGACCCTCTGAGCCAGGTGCGGG
ATATTATCTCATGGTGTGCCGTTTTTTAAGCCAGTCGGAAAAGCACAGTATTCGGGTAGGAGTG
ACCCGATTTTCCAGGAGATATCTCCAGGTGCAAGATGGCTCAGTGAGACCATGTCCTACTCTTG
GCTCTGACTCAATTAGAAGGATCCAGTCCAAGAATAAGTAAATGGCATCCTTCCAGTGGAGAGC
TGACAGCTGGGATTGAAACAAGATCCAGAATTCACCCTGCTGTTTCTCCATGAGTCTGACCTGC
ATCAACTGCCTCCCTTATTCTGGGATTCCAGTTGTGGAGCTCAAGGACAAGTCCATTCTGGGCT
GGCTGTATCCAACTTCTTTAGTCCAACTATATCCCCACTGGAAGCCAGGCTCTTTCCAACAGCT
GTCACCCATGCCTCTTTCTATGTTTGTTATCTGTCTCTAGGTTCTGGTAACTACTTCCTTCCCT
TGCCCCTTCTGGCCTAGGGTGCTACCAATCCCTCCTCCAAATCCAACTGTCACTAGCCTCAAAG
TACTTGTAGCTTCCTCACCTTACTTTCACCTTAATAAATGGTCCCCCTACTATCTCTCTTCAAA
GCACCCAATTTGAGTGTGCCATCTGTTTCTTGCCAGGATCCTGGTTGGTACATCAACCAAGCTG
CACTGATGGAGGAGCACTGTGCTGAACTTTAGGAATGAAGCCACAGGGCCCTCACTGCCCCCAT
AGTCACCTTGGTCATCTTCTGCCTCCCTGAAAGACTAAATTCAGTCAGTTCAGATACATACACA
TCCAGACATGTCAGGGAAAACTCCATTTTGTAAGGATCTCTGCTTAAAATGCCAAAAGTTTGAA
AGTTGGCAAACACTTGAGAAAAGCACAGTTCTCTGTCTTACTCTTACTCTAAACTTGGAGATAA
ATGCATTTTTAAAATTGTGCATGTTAGAGTGCTAACGTGTACAAGATCATTTCTGGTGAGACAC
CACAAACAATATTTTATGAGGCCAAAATAAGAAAGAAGGAAATGAAATAGCTCAGGAATCTCAG
GAAGAGCTCATCGAACACTTTGCCTTTATCTCAGACCATTTTATCCACAGCCCTGTTAATCAGG
ATTGGATATACCTCCATGAGGGAGTCTTAAACGGAGGGAAAGAGATGCCACAACTAAAAAAAAG
AATGCAATAGAAGTTTGTCTTAATGCCTGTTCTGTGATGCACAACTTTCGTAAGCCAAAATTTT
AACCTTATGAACAATCAGTTCTGTGCTGCCCTTAGCAGAGAACCATAAATTAAAGATAAGCAAT
GGTTCAGACTTTCCAGGGCCTTGACTCAGGAGTAACTCTGAAATCCCAACCAAATATGTATTTG
GTTAAGCAATTTGGCACATTTTTCTATTTTGAGGCATTAAACTATAATTACAAGTCACTTTTAT
TTCATTCCAAATAAATGTCCCTAAAGTAGATAGAACTAGAGGTTTCCTTTTTTTAAAAAAAGGA
AACAGGAAAACAACAAACAAAACCAAAAAGAACAAAAGCAAAACAAAACTTAGTCAAGCTAACA
AATTGCATGTATGGTGTGTTTTATAATTTAATCAATATAAAAAATTGAGTGTGCTAGTGCCTCA
GGAGGACTCAGAGGACTCAAATACTCAATAGGTTATCTGGAGGAATTTCTCATTGGAGAAAAAA
ATTAAAGTTCTTTTGAACAACCCACATAATCAAGATAGTAATAATTTAACCTCAAGTTTTTCCT
TGATTAAAAAATCCCTTTGCTATTCTGCTCCAGTGTTTGTAATAGATGGTTCAACAAGACTGGT
GTTTTGTTAGTTGGAAAAGTAAGCTGATATGAGGGGTGGGGAGAGGAAGGGCAGAAATTTATTA
ACAATCAGCAAGTAAAGAAAAACAGCCTGCAAATTGTAATGAAAGGAAGAAAGGACAGGAAAGG
AAAGGTAGGGCTGGTGGAGAGTGACTGTTCTGCCTGCTTACTGCACAGGCCAAGAACAAACTCA
CGATAAATACTCCAGGTCCTCAAGAAAAAGGTTTCTGTGCTGAATTATGGTAGTCTACCTGAAA
TTGGGATGATGAATTAGAAAACCTCTCTCATCGCTTCAAGTCTTGTGATTTATTCATTCAGTGC
CATTTATTGTATAACTATATAATTTCTAAAGGGGGATAACTACAAGAAAAAGATGTGATTTCTT
CTTTCAGAGATCCCCAAATATAGAAAGCTATTCATATACTGCTTAGATAAACAAAGATTATCTT
CTTTTTCTACATTCTATATAATGTTCCTTAAACTCAAGCTCTCTTCTCCCCATCTCTACCTTAC
CCCTCTGGGTAGCAAGGAAAAATAAAAATAATGTCATTC

hide sequence

RefSeq Acc Id:

NR_149136

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	81,843,781 - 81,933,480 (-)	NCBI
T2T-CHM13v2.0	6	83,053,185 - 83,142,795 (-)	NCBI

Sequence:

show sequence

TTTCATCCATGTCAACCATGAAAGACAGAGTTGATCTCAGCCTGAGCTAGAGATGGATCCCCAT
CCATGTACCTTTGCTCAACTGTCCTCAGACCAGATCCAGAATTCACCCTGCTGTTTCTCCATGA
GTCTGACCTGCATCAACTGCCTCCCTTATTCTGGGATTCCAGTTGTGGAGCTCAAGGACAAGTC
CATTCTGGGCTGGCTGTATCCAACTTCTTTAGTCCAACTATATCCCCACTGGAAGCCAGGCTCT
TTCCAACAGCTGTCACCCATGCCTCTTTCTATGTTTGTTATCTGTCTCTAGGTTCTGGTAACTA
CTTCCTTCCCTTGCCCCTTCTGGCCTAGGGTGCTACCAATCCCTCCTCCAAATCCAACTGTCAC
TAGCCTCAAAGTACTTGTAGCTTCCTCACCTTACTTTCACCTTAATAAATGGTCCCCCTACTAT
CTCTCTTCAAAGCACCCAATTTGAGTGTGCCATCTGTTTCTTGCCAGGATCCTGGTTGGTACAT
CAACCAAGCTGCACTGATGGAGGAGCACTGTGCTGAACTTTAGGAATGAAGCCACAGGGCCCTC
ACTGCCCCCATAGTCACCTTGGTCATCTTCTGCCTCCCTGAAAGACTAAATTCAGTCAGTTCAG
ATACATACACATCCAGACATGTCAGGGAAAACTCCATTTTGTAAGGATCTCTGCTTAAAATGCC
AAAAGTTTGAAAGTTGGCAAACACTTGAGAAAAGCACAGTTCTCTGTCTTACTCTTACTCTAAA
CTTGGAGATAAATGCATTTTTAAAATTGTGCATGTTAGAGTGCTAACGTGTACAAGATCATTTC
TGGTGAGACACCACAAACAATATTTTATGAGGCCAAAATAAGAAAGAAGGAAATGAAATAGCTC
AGGAATCTCAGGAAGAGCTCATCGAACACTTTGCCTTTATCTCAGACCATTTTATCCACAGCCC
TGTTAATCAGGATTGGATATACCTCCATGAGGGAGTCTTAAACGGAGGGAAAGAGATGCCACAA
CTAAAAAAAAGAATGCAATAGAAGTTTGTCTTAATGCCTGTTCTGTGATGCACAACTTTCGTAA
GCCAAAATTTTAACCTTATGAACAATCAGTTCTGTGCTGCCCTTAGCAGAGAACCATAAATTAA
AGATAAGCAATGGTTCAGACTTTCCAGGGCCTTGACTCAGGAGTAACTCTGAAATCCCAACCAA
ATATGTATTTGGTTAAGCAATTTGGCACATTTTTCTATTTTGAGGCATTAAACTATAATTACAA
GTCACTTTTATTTCATTCCAAATAAATGTCCCTAAAGTAGATAGAACTAGAGGTTTCCTTTTTT
TAAAAAAAGGAAACAGGAAAACAACAAACAAAACCAAAAAGAACAAAAGCAAAACAAAACTTAG
TCAAGCTAACAAATTGCATGTATGGTGTGTTTTATAATTTAATCAATATAAAAAATTGAGTGTG
CTAGTGCCTCAGGAGGACTCAGAGGACTCAAATACTCAATAGGTTATCTGGAGGAATTTCTCAT
TGGAGAAAAAAATTAAAGTTCTTTTGAACAACCCACATAATCAAGATAGTAATAATTTAACCTC
AAGTTTTTCCTTGATTAAAAAATCCCTTTGCTATTCTGCTCCAGTGTTTGTAATAGATGGTTCA
ACAAGACTGGTGTTTTGTTAGTTGGAAAAGTAAGCTGATATGAGGGGTGGGGAGAGGAAGGGCA
GAAATTTATTAACAATCAGCAAGTAAAGAAAAACAGCCTGCAAATTGTAATGAAAGGAAGAAAG
GACAGGAAAGGAAAGGTAGGGCTGGTGGAGAGTGACTGTTCTGCCTGCTTACTGCACAGGCCAA
GAACAAACTCACGATAAATACTCCAGGTCCTCAAGAAAAAGGTTTCTGTGCTGAATTATGGTAG
TCTACCTGAAATTGGGATGATGAATTAGAAAACCTCTCTCATCGCTTCAAGTCTTGTGATTTAT
TCATTCAGTGCCATTTATTGTATAACTATATAATTTCTAAAGGGGGATAACTACAAGAAAAAGA
TGTGATTTCTTCTTTCAGAGATCCCCAAATATAGAAAGCTATTCATATACTGCTTAGATAAACA
AAGATTATCTTCTTTTTCTACATTCTATATAATGTTCCTTAAACTCAAGCTCTCTTCTCCCCAT
CTCTACCTTACCCCTCTGGGTAGCAAGGAAAAATAAAAATAATGTCATTC

hide sequence

Additional Information

External Database Links

Database	Acc Id	Source(s)
COSMIC	LINC02542	COSMIC
Ensembl Genes	ENSG00000226453	Ensembl
GTEx	ENSG00000226453	GTEx
HGNC ID	HGNC:53576	ENTREZGENE
Human Proteome Map	LINC02542	Human Proteome Map
NCBI Gene	LINC02542	ENTREZGENE
RNAcentral	URS0000BC4515	RNACentral
	URS0000BC4554	RNACentral
	URS0000BC45C5	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)

Send us a Message