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Gene: LINC01887 (long intergenic non-protein coding RNA 1887) Homo sapiens

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Analyze

Symbol:

LINC01887

Name:

long intergenic non-protein coding RNA 1887

RGD ID:

11569695

HGNC Page

HGNC:52706

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	18	10,610,998 - 10,626,420 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	18	10,611,459 - 10,629,249 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	18	10,610,995 - 10,626,417 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Cytogenetic Map	18	p11.22	NCBI
CHM1_1	18	10,610,196 - 10,630,214 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	18	10,773,128 - 10,788,545 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 18p11.32-11.21(chr18:148963-14081888)x4	copy number gain	See cases [RCV000135515]	Chr18:148963..14081888 [GRCh38] Chr18:148963..14081887 [GRCh37] Chr18:138963..14071887 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:958974-11954935)x1	copy number loss	See cases [RCV000142225]	Chr18:958974..11954935 [GRCh38] Chr18:958975..11954934 [GRCh37] Chr18:948975..11944934 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:136227-80256240)x3	copy number gain	See cases [RCV000142244]	Chr18:136227..80256240 [GRCh38] Chr18:136227..78014123 [GRCh37] Chr18:126227..76115097 [NCBI36] Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18p11.22(chr18:9518608-10784749)x1	copy number loss	See cases [RCV000052075]	Chr18:9518608..10784749 [GRCh38] Chr18:9518606..10784747 [GRCh37] Chr18:9508606..10774747 [NCBI36] Chr18:18p11.22	uncertain significance
GRCh38/hg38 18p11.32-11.21(chr18:2425507-11904118)x3	copy number gain	See cases [RCV000136590]	Chr18:2425507..11904118 [GRCh38] Chr18:2425506..11904117 [GRCh37] Chr18:2415506..11894117 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.22-11.21(chr18:10077657-14081888)x3	copy number gain	See cases [RCV000136610]	Chr18:10077657..14081888 [GRCh38] Chr18:10077654..14081887 [GRCh37] Chr18:10067654..14071887 [NCBI36] Chr18:18p11.22-11.21	pathogenic
GRCh38/hg38 18p11.22-q11.2(chr18:8779843-24685379)x3	copy number gain	See cases [RCV000143075]	Chr18:8779843..24685379 [GRCh38] Chr18:8779841..22265343 [GRCh37] Chr18:8769841..20519341 [NCBI36] Chr18:18p11.22-q11.2	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:118760-12642431)x3	copy number gain	See cases [RCV000143194]	Chr18:118760..12642431 [GRCh38] Chr18:118760..12642430 [GRCh37] Chr18:108760..12632430 [NCBI36] Chr18:18p11.32-11.21	uncertain significance
GRCh38/hg38 18p11.32-q23(chr18:136226-80256240)x3	copy number gain	See cases [RCV000143218]	Chr18:136226..80256240 [GRCh38] Chr18:136226..78014123 [GRCh37] Chr18:126226..76115097 [NCBI36] Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:10001-15380684)x3	copy number gain	See cases [RCV000052499]	Chr18:10001..15380684 [GRCh38] Chr18:10001..15380683 [GRCh37] Chr18:1..15370683 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:53345-80209986)x3	copy number gain	See cases [RCV000052501]	Chr18:53345..80209986 [GRCh38] Chr18:53345..77967869 [GRCh37] Chr18:43345..76068860 [NCBI36] Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18p11.32-11.22(chr18:180229-10762632)x1	copy number loss	See cases [RCV000136860]	Chr18:180229..10762632 [GRCh38] Chr18:180229..10762630 [GRCh37] Chr18:170229..10752630 [NCBI36] Chr18:18p11.32-11.22	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:136226-15198991)x4	copy number gain	See cases [RCV000143434]	Chr18:136226..15198991 [GRCh38] Chr18:136226..15198990 [GRCh37] Chr18:126226..15188990 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:136226-14337134)x3	copy number gain	See cases [RCV000143477]	Chr18:136226..14337134 [GRCh38] Chr18:136226..14337133 [GRCh37] Chr18:126226..14327133 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-q11.1(chr18:53345-20948503)x3	copy number gain	See cases [RCV000052504]	Chr18:53345..20948503 [GRCh38] Chr18:53345..18528464 [GRCh37] Chr18:43345..16782462 [NCBI36] Chr18:18p11.32-q11.1	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148763-80252290)x3	copy number gain	See cases [RCV000052507]	Chr18:148763..80252290 [GRCh38] Chr18:148763..78010173 [GRCh37] Chr18:138763..76111164 [NCBI36] Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18p11.32-q11.1(chr18:148963-21040153)x3	copy number gain	See cases [RCV000052513]	Chr18:148963..21040153 [GRCh38] Chr18:148963..18620114 [GRCh37] Chr18:138963..16874112 [NCBI36] Chr18:18p11.32-q11.1	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80244381)x3	copy number gain	See cases [RCV000052514]	Chr18:148963..80244381 [GRCh38] Chr18:148963..78002264 [GRCh37] Chr18:138963..76103255 [NCBI36] Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:1919684-15325188)x3	copy number gain	See cases [RCV000052535]	Chr18:1919684..15325188 [GRCh38] Chr18:1919685..15325187 [GRCh37] Chr18:1909685..15315187 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.31-11.21(chr18:3389362-14082029)x3	copy number gain	See cases [RCV000052536]	Chr18:3389362..14082029 [GRCh38] Chr18:3389360..14082028 [GRCh37] Chr18:3379360..14072028 [NCBI36] Chr18:18p11.31-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-10900517)x1	copy number loss	See cases [RCV000137105]	Chr18:148963..10900517 [GRCh38] Chr18:148963..10900515 [GRCh37] Chr18:138963..10890515 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:118760-14089410)x4	copy number gain	See cases [RCV000137456]	Chr18:118760..14089410 [GRCh38] Chr18:118760..14089409 [GRCh37] Chr18:108760..14079409 [NCBI36] Chr18:18p11.32-11.21	pathogenic\|conflicting data from submitters
GRCh38/hg38 18p11.32-11.21(chr18:118760-14089410)x1	copy number loss	See cases [RCV000137457]	Chr18:118760..14089410 [GRCh38] Chr18:118760..14089409 [GRCh37] Chr18:108760..14079409 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.23-11.21(chr18:7290175-13049470)x1	copy number loss	See cases [RCV000137503]	Chr18:7290175..13049470 [GRCh38] Chr18:7290173..13049469 [GRCh37] Chr18:7280173..13039469 [NCBI36] Chr18:18p11.23-11.21	likely pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3	copy number gain	See cases [RCV000148072]	Chr18:148963..80252149 [GRCh38] Chr18:148963..78010032 [GRCh37] Chr18:138963..76111023 [NCBI36] Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-14081888)x1	copy number loss	See cases [RCV000148129]	Chr18:148963..14081888 [GRCh38] Chr18:148963..14081887 [GRCh37] Chr18:138963..14071887 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:133157-14089410)x1	copy number loss	See cases [RCV000138101]	Chr18:133157..14089410 [GRCh38] Chr18:133157..14089409 [GRCh37] Chr18:123157..14079409 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:118760-80254946)x3	copy number gain	See cases [RCV000138656]	Chr18:118760..80254946 [GRCh38] Chr18:118760..78012829 [GRCh37] Chr18:108760..76113817 [NCBI36] Chr18:18p11.32-q23	pathogenic\|conflicting data from submitters
GRCh38/hg38 18p11.32-11.21(chr18:112259-14122522)x1	copy number loss	See cases [RCV000053457]	Chr18:112259..14122522 [GRCh38] Chr18:112259..14122521 [GRCh37] Chr18:102259..14112521 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:131700-15121055)x1	copy number loss	See cases [RCV000053458]	Chr18:131700..15121055 [GRCh38] Chr18:131700..15121054 [GRCh37] Chr18:121700..15111054 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:149089-80254936)x3	copy number gain	See cases [RCV000139397]	Chr18:149089..80254936 [GRCh38] Chr18:149089..78012819 [GRCh37] Chr18:139089..76113807 [NCBI36] Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-13530126)x1	copy number loss	See cases [RCV000053784]	Chr18:148963..13530126 [GRCh38] Chr18:148963..13530125 [GRCh37] Chr18:138963..13520125 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-13068104)x1	copy number loss	See cases [RCV000053787]	Chr18:148963..13068104 [GRCh38] Chr18:148963..13068103 [GRCh37] Chr18:138963..13058103 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:136226-15175006)	copy number gain	See cases [RCV000140442]	Chr18:136226..15175006 [GRCh38] Chr18:136226..15175005 [GRCh37] Chr18:126226..15165005 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:118760-15024003)x1	copy number loss	See cases [RCV000141086]	Chr18:118760..15024003 [GRCh38] Chr18:118760..15024002 [GRCh37] Chr18:108760..15014002 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-13715860)x1	copy number loss	See cases [RCV000051027]	Chr18:148963..13715860 [GRCh38] Chr18:148963..13715859 [GRCh37] Chr18:138963..13705859 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3	copy number gain	See cases [RCV000051048]	Chr18:148963..80252149 [GRCh38] Chr18:148963..78010032 [GRCh37] Chr18:138963..76111023 [NCBI36] Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-14081888)x3	copy number gain	See cases [RCV000051153]	Chr18:148963..14081888 [GRCh38] Chr18:148963..14081887 [GRCh37] Chr18:138963..14071887 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-14081888)x1	copy number loss	See cases [RCV000051154]	Chr18:148963..14081888 [GRCh38] Chr18:148963..14081887 [GRCh37] Chr18:138963..14071887 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:14316-14206225)x3	copy number gain	See cases [RCV000141427]	Chr18:14316..14206225 [GRCh38] Chr18:14316..14206224 [GRCh37] Chr18:4316..14196224 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:149089-80234391)x3	copy number gain	See cases [RCV000134110]	Chr18:149089..80234391 [GRCh38] Chr18:149089..77992274 [GRCh37] Chr18:139089..76093265 [NCBI36] Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:48782-14978076)x1	copy number loss	See cases [RCV000141627]	Chr18:48782..14978076 [GRCh38] Chr18:48782..14978075 [GRCh37] Chr18:38782..14968075 [NCBI36] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:158286-14124574)x1	copy number loss	Deletion of short arm of chromosome 18 [RCV003327630]	Chr18:158286..14124574 [GRCh38] Chr18:18p11.32-11.21	pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:131700-14226905)x1	copy number loss	See cases [RCV000053461]	Chr18:131700..14226905 [GRCh38] Chr18:131700..14226904 [GRCh37] Chr18:121700..14216904 [NCBI36] Chr18:18p11.32-11.21	pathogenic

Predicted Target Of

	Summary Value
Count of predictions:	436
Count of miRNA genes:	365
Interacting mature miRNAs:	390
Transcripts:	ENST00000583691, ENST00000584734
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.

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	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system
106	248	357	154	953	241	393	154	1025	56	392	1405	1382	10	704	109	573	305	102


RefSeq Transcripts	NR_146509	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AP001180	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068260	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000579413

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,627,646 - 10,628,846 (-)	Ensembl

Ensembl Acc Id:

ENST00000583691

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,119 - 10,629,247 (-)	Ensembl

Ensembl Acc Id:

ENST00000584734

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,304 - 10,629,249 (-)	Ensembl

Ensembl Acc Id:

ENST00000743532

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,114 - 10,629,247 (-)	Ensembl

Ensembl Acc Id:

ENST00000743533

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,114 - 10,629,237 (-)	Ensembl

Ensembl Acc Id:

ENST00000743534

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,114 - 10,629,221 (-)	Ensembl

Ensembl Acc Id:

ENST00000743535

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,114 - 10,629,216 (-)	Ensembl

Ensembl Acc Id:

ENST00000743536

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,114 - 10,629,213 (-)	Ensembl

Ensembl Acc Id:

ENST00000743537

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,119 - 10,629,213 (-)	Ensembl

Ensembl Acc Id:

ENST00000743538

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,475 - 10,629,247 (-)	Ensembl

Ensembl Acc Id:

ENST00000743539

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,484 - 10,629,246 (-)	Ensembl

Ensembl Acc Id:

ENST00000743540

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,479 - 10,629,236 (-)	Ensembl

Ensembl Acc Id:

ENST00000743541

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,475 - 10,629,219 (-)	Ensembl

Ensembl Acc Id:

ENST00000743542

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,475 - 10,629,213 (-)	Ensembl

Ensembl Acc Id:

ENST00000743543

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,479 - 10,629,216 (-)	Ensembl

Ensembl Acc Id:

ENST00000743544

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,475 - 10,629,212 (-)	Ensembl

Ensembl Acc Id:

ENST00000743545

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,479 - 10,629,216 (-)	Ensembl

Ensembl Acc Id:

ENST00000743546

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,479 - 10,629,213 (-)	Ensembl

Ensembl Acc Id:

ENST00000743547

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,479 - 10,629,213 (-)	Ensembl

Ensembl Acc Id:

ENST00000743548

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,479 - 10,629,166 (-)	Ensembl

Ensembl Acc Id:

ENST00000743549

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,475 - 10,627,376 (-)	Ensembl

Ensembl Acc Id:

ENST00000743550

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,117 - 10,626,644 (-)	Ensembl

Ensembl Acc Id:

ENST00000743551

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,479 - 10,626,670 (-)	Ensembl

Ensembl Acc Id:

ENST00000743552

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,475 - 10,626,643 (-)	Ensembl

Ensembl Acc Id:

ENST00000743553

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,611,459 - 10,618,937 (-)	Ensembl

Ensembl Acc Id:

ENST00000743554

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,117 - 10,619,021 (-)	Ensembl

Ensembl Acc Id:

ENST00000743555

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,114 - 10,618,960 (-)	Ensembl

Ensembl Acc Id:

ENST00000743556

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,612,114 - 10,618,954 (-)	Ensembl

Ensembl Acc Id:

ENST00000743557

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,627,223 - 10,629,247 (-)	Ensembl

Ensembl Acc Id:

ENST00000743558

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	10,627,223 - 10,629,216 (-)	Ensembl

RefSeq Acc Id:

NR_146509

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	18	10,610,998 - 10,626,420 (-)	NCBI
T2T-CHM13v2.0	18	10,773,128 - 10,788,545 (-)	NCBI

Sequence:

show sequence

GAAAACTAAGTGGCTTCCCTTGAGGCAGCCCGAGGGCTCCACTGGACCCAGAACTCTGAGTTCTGATGCTGCCTATCATTTGCTTTTCCTCATGAGCTCCTGGACCACCTCATATCACCAGCACCCTC
TACCCAAGGTCCTGGAGCCAACACTGGAGTAAAAGAGCACAAGAGAACTCCTTAGAGGTGGAAGGATACCCTCTGAGGTCAAATCATTGGGCTTGTGGCCATGAGACCACAGACTTTGCCTGGCTTCC
AGTGACTGTCCGAGATGACCTGTGGAGTGCACCGCCTGTACTTGGACATCACTGTCTTTTCGGATCCATACCCGTCATCCTTGGAATTTCCCCTGCATCCAAACCTGTTCCTGATACAGGTGTGAGTA
ATGAATAACCCTAAGGAATATCTTGGATGTCTTCACGGGGCTTATGACTTATTCTGAGGTTTACAAAATAGAGGCCCCCAGCTGAGCAAAGAGAGGGCTGCAGCGCCGAGGGAACAGCTGCCGGACTC
ACCGGAGAGGCCTCCTGGAGCACGCCGGGACCCCCTCCACCCCCTGGCTTTGGCTGCATCAATGGCTAGTTTGCCTGAACTATATCTGAGCCACTGAGAGTATTTATTAAGCAGAGAATAATTTTGAG
TTTCACTTTTATAACTTTTGTTTCAAAAGTTGTTTTGGATAATTTAATGAAATGACTGTAAACCAGAATTCCCCTTTTCATTATTTCTTTGTGTCAATATAAAAAGAGTTGATGATTTTAAAAGCCAG
TGAGATGTCCCTGTCTGTGGATGTCAGCGGGAGGGTGGGGTCTGACGCCTTTCTCTGGTGGCTGTCCAGGAAGATTGCCCCAGCTTGCACTCCCTTTTGGCGGGTTCCAGAGCCTTCCATTTGAAAGG
AGCATCTCTCACCACTCTGCCCCACCCAGCACCAGCTCTTCTGGAACCCACTGACTTCCTAAACACTTTCTTCCTCCTTCACCTCATTGAATTCAAGACTTTAGAAAACAGCCAAAAACTCTAGAGGT
GGGGGTGGGTTCGATCTGGAAATCCCTGCTGTAATCTTTTTAAGGGAATCCACTGGAAATTATTAATTTATGTTTTAAATAAAACCATTCCTTACTTAACAGAATATTAAGCCACTCATTTTTTTAAC
AGAACTTTCGAGATATAATTAAAATGCCATAAATTTCACCCCCACACAGTGTACAATTCCAAGGTTTCCAATATAGTCACAGAAGTCTCTGCAACAATTACCACAATTTTAGACATGAAGACCATTTG
TTGGCAGCCCTACCTGCCTCTATGTGTATGTATATAATTTTAATATTGGATTGGATACTATAGTAATATTGTACTGTTACCTATTTGTGTTTTTATATTGCTGTTTTATTTTATTCAGATGAATAATA
ATTATCTCCATATAGTCATACATTTATATAGGGTTAAACACACCTTTTTACAATTCAATAAATTAAATTGGTCAGGTATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGG
ATCACCTGAGGTTGGGAGTTTGAGACCAGCGTGATCAACATGGAGAAACCCTGTCTGTACTAAAAATACAAAAAATTAGCCAGGCATGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGGCTGAG
GCAGGAGAATCACTCGAACCAAGGAGGCGGACATTGCGGTGAGCCAGGATCGCACCATTGCACTCCAGCCTGGGCAACAAGAGCAAAACTCCATCTCAAGAAGAAAAAAAAAAAAAAAGTAAATTGTT
TTTAATTACATAAGAAACACGTGTTATTGTTATAGAAATTCACATAGTGCTTCGGTCTATAGAATAAATGTATCCCCACCACCTCCCAGCCCACCCACTCGTCTGCATTCACCTACACACAGTTAAAC
ATGCACATATGTTTCCGTGACACGATCTTGCTTTGCATATTGTTCACTGACTGGCTTTTCCATATAAGATTTAATTTGGTGATTATTGCTTATCAGTACCTATAGGTCTCTCTCATTATTATTTATAA
TTACATCATTATTCCATAGGGTATTTTACCACAATTTGGTCACTTTTTCACTGAGGAATTTTTATGTCAGTTTCAGTTATTTGTTATTGTTACCAATGCTGTACTGGGCATCCCTGTATATCCACCTT
TTTGTTGCATTAGTTAAGTGGTTTTTTCCTTTTATGATTGATTTCTAAAAATAAAATACTGCAGCAAA

hide sequence

Database	Acc Id	Source(s)
COSMIC	LINC01887	COSMIC
Ensembl Genes	ENSG00000266604	Ensembl
GTEx	ENSG00000266604	GTEx
HGNC ID	HGNC:52706	ENTREZGENE
Human Proteome Map	LINC01887	Human Proteome Map
NCBI Gene	LINC01887	ENTREZGENE
RNAcentral	URS00002AF7BE	RNACentral
	URS0000587E10	RNACentral
	URS0000BC44E2	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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