CCDC144NL-AS1 (CCDC144NL antisense RNA 1)

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Gene: CCDC144NL-AS1 (CCDC144NL antisense RNA 1) Homo sapiens

Analyze

Symbol:

CCDC144NL-AS1

Name:

CCDC144NL antisense RNA 1

RGD ID:

9589987

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	17	20,938,566 - 20,982,357 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	20,841,125 - 21,002,324 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	20,841,879 - 20,885,670 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Cytogenetic Map	17	p11.2	NCBI
HuRef	17	20,026,936 - 20,045,431 (+)	NCBI		HuRef
CHM1_1	17	20,850,581 - 20,894,422 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	20,887,381 - 20,931,176 (+)	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:12477932	PMID:16344560

Genomics

Variants

Variants in CCDC144NL-AS1
1 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 17p11.2(chr17:19744033-21598663)x3	copy number gain	See cases [RCV000142733]	Chr17:19744033..21598663 [GRCh38] Chr17:19647346..21501929 [GRCh37] Chr17:19587938..21442522 [NCBI36] Chr17:17p11.2	uncertain significance
GRCh38/hg38 17p11.2(chr17:16426633-20998588)x3	copy number gain	See cases [RCV000143715]	Chr17:16426633..20998588 [GRCh38] Chr17:16329947..20901901 [GRCh37] Chr17:16270672..20842493 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:20879426-22533437)x3	copy number gain	See cases [RCV000053124]	Chr17:20879426..22533437 [GRCh38] Chr17:20782739..22032763 [GRCh37] Chr17:20723331..21956890 [NCBI36] Chr17:17p11.2	uncertain significance
GRCh38/hg38 17p11.2(chr17:19070690-21619442)x3	copy number gain	See cases [RCV000054009]	Chr17:19070690..21619442 [GRCh38] Chr17:18974003..21522709 [GRCh37] Chr17:18914728..21463302 [NCBI36] Chr17:17p11.2	uncertain significance
GRCh38/hg38 17p11.2(chr17:19239860-21530183)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054010]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054010]\|See cases [RCV000054010]	Chr17:19239860..21530183 [GRCh38] Chr17:19143173..21433444 [GRCh37] Chr17:19083766..21374037 [NCBI36] Chr17:17p11.2	uncertain significance
GRCh38/hg38 17p11.2(chr17:20935766-21621469)x1	copy number loss	See cases [RCV000051216]	Chr17:20935766..21621469 [GRCh38] Chr17:20839079..21529632 [GRCh37] Chr17:20779671..21471956 [NCBI36] Chr17:17p11.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2857
Count of miRNA genes:	1036
Interacting mature miRNAs:	1278
Transcripts:	ENST00000417232, ENST00000423473, ENST00000433763, ENST00000437829, ENST00000439794, ENST00000443508, ENST00000577537, ENST00000577841, ENST00000577860, ENST00000577968, ENST00000579168, ENST00000580056, ENST00000580278, ENST00000581958, ENST00000582324, ENST00000583481, ENST00000583962, ENST00000584433
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.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1298406	BP16_H	Blood pressure QTL 16 (human)		0.0004	Blood pressure	hypertension susceptibility	17	14778647	40778647	Human

Expression

RNA-SEQ Expression

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

Download All Expressed Objects for this Gene

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
1192	2358	2711	2215	4837	1635	2196	5	558	1385	403	2181	6489	5846	46	3684	781	1673	1526	166

Sequence

Nucleotide Sequences


RefSeq Transcripts	NR_123730	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_160712	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_160713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_160714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_160715	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_160716	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_160717	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_160718	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_160719	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_160720	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_160721	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_160722	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC087393	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC090774	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC107926	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC043529	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB066214	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000417232

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,456 - 20,930,041 (+)	Ensembl

Ensembl Acc Id:

ENST00000423473

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,578 - 20,998,028 (+)	Ensembl

Ensembl Acc Id:

ENST00000433763

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,566 - 20,958,389 (+)	Ensembl

Ensembl Acc Id:

ENST00000437829

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,949,239 - 20,979,752 (+)	Ensembl

Ensembl Acc Id:

ENST00000439794

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,497 - 20,994,142 (+)	Ensembl

Ensembl Acc Id:

ENST00000443508

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,437 - 20,930,056 (+)	Ensembl

Ensembl Acc Id:

ENST00000577537

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,433 - 20,905,230 (+)	Ensembl

Ensembl Acc Id:

ENST00000577841

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,921,068 - 20,930,046 (+)	Ensembl

Ensembl Acc Id:

ENST00000577860

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,547 - 20,932,818 (+)	Ensembl

Ensembl Acc Id:

ENST00000577968

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,929,756 - 20,938,522 (+)	Ensembl

Ensembl Acc Id:

ENST00000579168

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,955,817 - 20,958,326 (+)	Ensembl

Ensembl Acc Id:

ENST00000580056

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,520 - 20,994,292 (+)	Ensembl

Ensembl Acc Id:

ENST00000580278

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,929,755 - 20,939,519 (+)	Ensembl

Ensembl Acc Id:

ENST00000581673

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,963,722 - 20,980,238 (+)	Ensembl

Ensembl Acc Id:

ENST00000581958

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,951,431 - 21,002,276 (+)	Ensembl

Ensembl Acc Id:

ENST00000582324

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,543 - 20,899,131 (+)	Ensembl

Ensembl Acc Id:

ENST00000582583

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,538 - 20,982,357 (+)	Ensembl

Ensembl Acc Id:

ENST00000583481

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,551 - 21,002,007 (+)	Ensembl

Ensembl Acc Id:

ENST00000583962

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,465 - 20,905,230 (+)	Ensembl

Ensembl Acc Id:

ENST00000584433

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,497 - 20,958,721 (+)	Ensembl

Ensembl Acc Id:

ENST00000662319

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,920,915 - 20,933,416 (+)	Ensembl

Ensembl Acc Id:

ENST00000692309

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,440 - 20,930,050 (+)	Ensembl

Ensembl Acc Id:

ENST00000692759

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,443 - 20,930,050 (+)	Ensembl

Ensembl Acc Id:

ENST00000717326

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,508 - 20,979,989 (+)	Ensembl

Ensembl Acc Id:

ENST00000737554

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,841,269 - 20,958,697 (+)	Ensembl

Ensembl Acc Id:

ENST00000737555

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,567 - 20,964,160 (+)	Ensembl

Ensembl Acc Id:

ENST00000737556

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,547 - 20,963,713 (+)	Ensembl

Ensembl Acc Id:

ENST00000737557

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,563 - 20,963,714 (+)	Ensembl

Ensembl Acc Id:

ENST00000737558

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,460 - 20,958,697 (+)	Ensembl

Ensembl Acc Id:

ENST00000737559

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,487 - 20,958,697 (+)	Ensembl

Ensembl Acc Id:

ENST00000737560

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,565 - 20,958,697 (+)	Ensembl

Ensembl Acc Id:

ENST00000737561

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,841,125 - 20,930,041 (+)	Ensembl

Ensembl Acc Id:

ENST00000737562

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,498 - 21,002,324 (+)	Ensembl

Ensembl Acc Id:

ENST00000737563

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,567 - 20,931,833 (+)	Ensembl

Ensembl Acc Id:

ENST00000737564

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,436 - 20,930,041 (+)	Ensembl

Ensembl Acc Id:

ENST00000737565

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,483 - 20,930,041 (+)	Ensembl

Ensembl Acc Id:

ENST00000737566

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,483 - 20,930,041 (+)	Ensembl

Ensembl Acc Id:

ENST00000737567

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,487 - 20,930,041 (+)	Ensembl

Ensembl Acc Id:

ENST00000737568

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,563 - 20,930,041 (+)	Ensembl

Ensembl Acc Id:

ENST00000737569

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,572 - 20,930,041 (+)	Ensembl

Ensembl Acc Id:

ENST00000737570

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,527 - 20,925,175 (+)	Ensembl

Ensembl Acc Id:

ENST00000737571

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,489 - 20,924,832 (+)	Ensembl

Ensembl Acc Id:

ENST00000737572

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,600 - 20,924,832 (+)	Ensembl

Ensembl Acc Id:

ENST00000737573

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,559 - 20,981,825 (+)	Ensembl

Ensembl Acc Id:

ENST00000737574

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,505 - 20,979,989 (+)	Ensembl

Ensembl Acc Id:

ENST00000737575

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,921,077 - 20,958,697 (+)	Ensembl

Ensembl Acc Id:

ENST00000737576

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,488 - 20,903,413 (+)	Ensembl

Ensembl Acc Id:

ENST00000737577

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,583 - 20,903,413 (+)	Ensembl

Ensembl Acc Id:

ENST00000737578

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,527 - 20,903,014 (+)	Ensembl

Ensembl Acc Id:

ENST00000737579

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,584 - 20,903,014 (+)	Ensembl

Ensembl Acc Id:

ENST00000737580

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,969,518 - 20,999,591 (+)	Ensembl

Ensembl Acc Id:

ENST00000737581

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,456 - 20,895,850 (+)	Ensembl

Ensembl Acc Id:

ENST00000737582

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,464 - 20,895,850 (+)	Ensembl

Ensembl Acc Id:

ENST00000737583

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,533 - 20,964,264 (+)	Ensembl

Ensembl Acc Id:

ENST00000737584

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,516 - 20,964,165 (+)	Ensembl

Ensembl Acc Id:

ENST00000737585

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,565 - 20,964,081 (+)	Ensembl

Ensembl Acc Id:

ENST00000737586

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,525 - 20,963,696 (+)	Ensembl

Ensembl Acc Id:

ENST00000737587

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,868,489 - 20,892,536 (+)	Ensembl

Ensembl Acc Id:

ENST00000737588

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,566 - 20,959,703 (+)	Ensembl

Ensembl Acc Id:

ENST00000737589

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,494 - 20,958,697 (+)	Ensembl

Ensembl Acc Id:

ENST00000737590

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,496 - 20,958,699 (+)	Ensembl

Ensembl Acc Id:

ENST00000737591

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,496 - 20,958,697 (+)	Ensembl

Ensembl Acc Id:

ENST00000737592

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,496 - 20,958,697 (+)	Ensembl

Ensembl Acc Id:

ENST00000737593

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,938,498 - 20,958,697 (+)	Ensembl

Ensembl Acc Id:

ENST00000737594

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,841,191 - 20,852,400 (+)	Ensembl

Ensembl Acc Id:

ENST00000737595

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,921,013 - 20,930,820 (+)	Ensembl

Ensembl Acc Id:

ENST00000737596

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,921,031 - 20,925,175 (+)	Ensembl

Ensembl Acc Id:

ENST00000737597

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,921,028 - 20,924,918 (+)	Ensembl

Ensembl Acc Id:

ENST00000737598

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,841,257 - 20,843,919 (+)	Ensembl

Ensembl Acc Id:

ENST00000737599

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	20,930,267 - 20,931,827 (+)	Ensembl

RefSeq Acc Id:

NR_123730

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,982,357 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,931,176 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGAAGTCAGACAAGTACCGGTGATTGCCGGTTTC
TTGTCTGATTTTTGCACTTCTCTGGCAAGCTGCCCCCTCTGAAGAGTTGACTATTTGGGAGTTA
CTCACTGATGGTTCAGCCACTTCCAGAACCTACCCCAAGAGCAAGACTTGAAACCAACTCGCAC
CCTCAAAGCTCCGGAAGCCATTCAGTGTTTCCATCTTGGCTGAGTGAGTTCTTCACTGAAACTC
AATTTGACTTTGACAGTCATCTAATGAGAACTCAAAAGTCATTCTTGGTTCAGCCACAGTCAAA
GAACTTGCAGAGCATTCTCTGACGAGGTCCTCAAGGACAACTGAGAGAAGGTCCCATTCCAGGT
CTTGCCCAAGTCTTTCTGATTGGTGGGACTTAAATCACACCCAAAATTCCAGCTGCAGGAGAGC
TCTGAGATTTCATCTTTCCAACCTCTGTGTGCTACGTGGGGGTTGGAGCACTTGCTGACAAGCC
TTGCAACCACCATTGACAGGATGTCCTCCACCTTTTCAATCTGATTTGCTCTTTGCCATGCAGA
CCTGTGGATGAAGAGCCAGAGTCCTCCAAGGTGAAGCTGGACTGAATATTTCTGTCCATAAGAC
TATTAGAATCCCCCAAAGTGGGATACCAGTGAGGACCTCACCAGCAGCTGCTGTCTCTCCAATG
CAGCTCCACAGGGCCTGTGAGCAGGGCTGGCTATGAGATCCTGCCCTGAAGAGCAGTACTGGGC
TGCTCTGCTAGGCACCTGCATGTCCTGCAAAGCCATCTGCAACCATCAGAGCCAGCGCACCTGT
GCAGCCTCCTGCGGTGAGTTCTGGGACCTGAGCCCAGGGGACAGTGTGATCACCCCCAACGCCT
GTCCCCAGAGCACCCTCTGGCCCCACAGTCAGGTGGCTGAGGAGAGGATGGCAGGAGGAGATGT
ACAGTGTGGCACCTCTTATCCCTCCACCTTCCTGCTCTGGCCACACTGCCTCCTTTCAGTGTCG
AACATGCCATGTTCTTCCCTGCCTCGGGTTCTTTGCACATGTTGTTCCCGCTGCCTGGAATGCA
TGCTCTCTATCATCTTCCCTCAGCTCCCTCCTACCCAACTTTCAGGTCTCGGCCCAAACATCGG
GGGTCTCCTCTGACCACACAGTAGTACTGGGCCCTCCTTTGTACTGCTAGTGTTACTTTCTTTT
GAAACTTTTAATTACAGAACTTACCACACATATACATAGAGAGGACTGCACAATGATGCCCTCC
TCATCCATTACCAGCTTCACAAATCATTTAAATTCTGCCTTGTACTTTCCCAACCAGTTGTTTT
GGCTTGTGTATTTTAAAGCAAAGCCAAGACCTCATATCATTTTACCTGCAGATACTGGGCCATA
AAGATCTGTAAAACATAACCCAAATATCCTATCACTGCCAGCAATAATTTATTAACATCATCTA
ATATTCAGGCCATATCCAATTTTCCCTGATTGTCTTGAAAACTATCCATTGCTTGCTGTTCTTT
TTCATAATCTGTCTTTTTCCTTGATAGAACTTACCACAATTT

hide sequence

RefSeq Acc Id:

NR_160712

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,982,357 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,931,176 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGGATGTCCTCCACCTTTTCAATCTGATTTGCTC
TTTGCCATGCAGACCTGTGGATGAAGAGCCAGAGTCCTCCAAGGTGAAGCTGGACTGAATATTT
CTGTCCATAAGACTATTAGAATCCCCCAAAGTGGGATACCAGTGAGGACCTCACCAGCAGCTGC
TGTCTCTCCAATGCAGCTCCACAGGGCCTGTGAGCAGGGCTGGCTATGAGATCCTGCCCTGAAG
AGCAGTACTGGGCTGCTCTGCTAGGCACCTGCATGTCCTGCAAAGCCATCTGCAACCATCAGAG
CCAGCGCACCTGTGCAGCCTCCTGCGGTGAGTTCTGGGACCTGAGCCCAGGGGACAGTGTGATC
ACCCCCAACGCCTGTCCCCAGAGCACCCTCTGGCCCCACAGTCAGGTGGCTGAGGAGAGGATGG
CAGGAGGAGATGTACAGTGTGGCACCTCTTATCCCTCCACCTTCCTGCTCTGGCCACACTGCCT
CCTTTCAGTGTCGAACATGCCATGTTCTTCCCTGCCTCGGGTTCTTTGCACATGTTGTTCCCGC
TGCCTGGAATGCATGCTCTCTATCATCTTCCCTCAGCTCCCTCCTACCCAACTTTCAGGTCTCG
GCCCAAACATCGGGGGTCTCCTCTGACCACACAGTAGTACTGGGCCCTCCTTTGTACTGCTAGT
GTTACTTTCTTTTGAAACTTTTAATTACAGAACTTACCACACATATACATAGAGAGGACTGCAC
AATGATGCCCTCCTCATCCATTACCAGCTTCACAAATCATTTAAATTCTGCCTTGTACTTTCCC
AACCAGTTGTTTTGGCTTGTGTATTTTAAAGCAAAGCCAAGACCTCATATCATTTTACCTGCAG
ATACTGGGCCATAAAGATCTGTAAAACATAACCCAAATATCCTATCACTGCCAGCAATAATTTA
TTAACATCATCTAATATTCAGGCCATATCCAATTTTCCCTGATTGTCTTGAAAACTATCCATTG
CTTGCTGTTCTTTTTCATAATCTGTCTTTTTCCTTGATAGAACTTACCACAATTT

hide sequence

RefSeq Acc Id:

NR_160713

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,980,349 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,929,168 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGTCCCATTCCAGGTCTTGCCCAAGTCTTTCTGA
TTGGTGGGACTTAAATCACACCCAAAATTCCAGCTGCAGGAGAGCTCTGAGATTTCATCTTTCC
AACCTCTGTGTGCTACGTGGGGGTTGGAGCACTTGCTGACAAGCCTTGCAACCACCATTGACAG
GATGTCCTCCACCTTTTCAATCTGATTTGCTCTTTGCCATGCAGACCTGTGGATGAAGAGCCAG
AGTCCTCCAAGGTGAAGCTGGACTGAATATTTCTGTCCATAAGACTATTAGAATCCCCCAAAGT
GGGATACCAGTGAGGACCTCACCAGCAGCTGCTGTCTCTCCAATGCAGAGCTTCCTGCCTCCTG
CCCAGCCCCTGCTGTCAGAGATACTTGGTGCTTCCAGTTCTGGAGACTTCCTTGAGTTCTGTGA
CTCAAAACAACTTCCTTCCCCTGTGGGCATCAACAATGAGAGATCTTCAGATGCGATCAGGCAC
TCCAGTCCTTCCATCTCCCACAATGTTGGAGACCTGTGTTCCCTGCTGTAGAAACCTCTGCCAT
TCCCTTTATCTCTGAAGACAGATGGACTTGACTGTCAGCTTAGCTTGGTTTCAGGAGGAAAGGA
AGATAAACCCCTGTGTTTAAGCTGCCGTGTTAAATGGGAGGCACCTGGTCTTTTTTCTTTTTCT
TTTTTAAAGACTGGGTCTCGCTCTGTTATCCAAGCTGCAGTGCAGTGATGTGATCATAGCTCAC
CTCAGCCTTGAACTCTCAGGCTCAAGCGATCCTCCAGCCTCAGCCTCCTGAATTGCTGGGATTA
TAGCACCTGGCCAATTTTAAAATCTTTCTGTAGCGACAGGATCTCACTATGTTGCCCAGGCTGG
TCTTGAACCCCTGGCCTCAAGGAATTCTCCCACAACCTCCCAAAGTGCTAAGATTACAGGCAAG
AGCCATGGTGCCCAGCCACCTCTGGTCTTCCCTCAGTTTGCTTTCATTAAAGGACAAACACATG
CCTTGCAAAA

hide sequence

RefSeq Acc Id:

NR_160714

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,980,349 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,929,168 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGAAGTCAGACAAGTACCGGTGATTGCCGGTTTC
TTGTCTGATTTTTGCACTTCTCTGGCAAGCTGCCCCCTCTGAAGAGTTGACTATTTGGGAGTTA
CTCACTGATGGTTCAGCCACTTCCAGAACCTACCCCAAGAGCAAGACTTGAAACCAACTCGCAC
CCTCAAAGCTCCGGAAGCCATTCAGTGTTTCCATCTTGGCTGAGTGAGTTCTTCACTGAAACTC
AATTTGACTTTGACAGTCATCTAATGAGAACTCAAAAGTCATTCTTGGTTCAGCCACAGTCAAA
GAACTTGCAGAGCATTCTCTGACGAGGTCCTCAAGGACAACTGAGAGAAGGTCCCATTCCAGGT
CTTGCCCAAGTCTTTCTGATTGGTGGGACTTAAATCACACCCAAAATTCCAGCTGCAGGAGAGC
TCTGAGATTTCATCTTTCCAACCTCTGTGTGCTACGTGGGGGTTGGAGCACTTGCTGACAAGCC
TTGCAACCACCATTGACAGGATGTCCTCCACCTTTTCAATCTGATTTGCTCTTTGCCATGCAGA
CCTGTGGATGAAGAGCCAGAGTCCTCCAAGGTGAAGCTGGACTGAATATTTCTGTCCATAAGAC
TATTAGAATCCCCCAAAGTGGGATACCAGTGAGGACCTCACCAGCAGCTGCTGTCTCTCCAATG
CAGAGCTTCCTGCCTCCTGCCCAGCCCCTGCTGTCAGAGATACTTGGTGCTTCCAGTTCTGGAG
ACTTCCTTGAGTTCTGTGACTCAAAACAACTTCCTTCCCCTGTGGGCATCAACAATGAGAGATC
TTCAGATGCGATCAGGCACTCCAGTCCTTCCATCTCCCACAATGTTGGAGACCTGTGTTCCCTG
CTGTAGAAACCTCTGCCATTCCCTTTATCTCTGAAGACAGATGGACTTGACTGTCAGCTTAGCT
TGGTTTCAGGAGGAAAGGAAGATAAACCCCTGTGTTTAAGCTGCCGTGTTAAATGGGAGGCACC
TGGTCTTTTTTCTTTTTCTTTTTTAAAGACTGGGTCTCGCTCTGTTATCCAAGCTGCAGTGCAG
TGATGTGATCATAGCTCACCTCAGCCTTGAACTCTCAGGCTCAAGCGATCCTCCAGCCTCAGCC
TCCTGAATTGCTGGGATTATAGCACCTGGCCAATTTTAAAATCTTTCTGTAGCGACAGGATCTC
ACTATGTTGCCCAGGCTGGTCTTGAACCCCTGGCCTCAAGGAATTCTCCCACAACCTCCCAAAG
TGCTAAGATTACAGGCAAGAGCCATGGTGCCCAGCCACCTCTGGTCTTCCCTCAGTTTGCTTTC
ATTAAAGGACAAACACATGCCTTGCAAAA

hide sequence

RefSeq Acc Id:

NR_160715

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,958,697 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,907,512 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGTCCCATTCCAGGTCTTGCCCAAGTCTTTCTGA
TTGGTGGGACTTAAATCACACCCAAAATTCCAGCTGCAGGAGAGCTCTGAGATTTCATCTTTCC
AACCTCTGTGTGCTACGTGGGGGTTGGAGCACTTGCTGACAAGCCTTGCAACCACCATTGACAG
GATGTCCTCCACCTTTTCAATCTGATTTGCTCTTTGCCATGCAGACCTGTGGATGAAGAGCCAG
AGTCCTCCAAGGTGAAGCTGGACTGAATATTTCTGTCCATAAGACTATTAGAATCCCCCAAAGT
GGGATACCAGTGAGGACCTCACCAGCAGCTGCTGTCTCTCCAATGCAGGTAGATGAGCCTCAGA
AATAACCGCTGCTTGTGGTTTGCTGTGTATTCCTCTAGATGTTTTTCTTTACACATATTAGTGA
GTGTGGAGAGAGAGTGTGTATGTGTTCTGTAAATTTGATTACACTGCGCATTTATTCCGAAATC
CATTTCACTTTACCGTTGGAACGTAAGCTCTGTGAGGGCAGAGACTTTTGTTTATTGCACTTGC
TGTTAGAGCTCTTGTCTGTAACAGTGGCTGGCACATGGTCACATCATAGTAGAAGCTCAATAAA
TATTTGTTGAATGAATGAAAAAA

hide sequence

RefSeq Acc Id:

NR_160716

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,980,349 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,929,168 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGCAGAAAGGTGTTAAATGGTTTGCAGAATTGTT
GGGAAGGCTAAGCTTCCAGGAGCAGCTCCCAAAGTCTCCACACACAACTGGACCACCAGGGAAC
CTGCTCCCTCCACCAGGACAGGACTTGGAAACCTGCCACCGCAATTACCAGCACCAGAAGGATC
TTGTCTCTGCTAAGTCTCTGTCGACATAGTGAATACCCTGTGCCCTGCCTCTCTCTCCCTGACT
CAGGTCCCATTCCAGGTCTTGCCCAAGTCTTTCTGATTGGTGGGACTTAAATCACACCCAAAAT
TCCAGCTGCAGGAGAGCTCTGAGATTTCATCTTTCCAACCTCTGTGTGCTACGTGGGGGTTGGA
GCACTTGCTGACAAGCCTTGCAACCACCATTGACAGGATGTCCTCCACCTTTTCAATCTGATTT
GCTCTTTGCCATGCAGACCTGTGGATGAAGAGCCAGAGTCCTCCAAGGTGAAGCTGGACTGAAT
ATTTCTGTCCATAAGACTATTAGAATCCCCCAAAGTGGGATACCAGTGAGGACCTCACCAGCAG
CTGCTGTCTCTCCAATGCAGAGCTTCCTGCCTCCTGCCCAGCCCCTGCTGTCAGAGATACTTGG
TGCTTCCAGTTCTGGAGACTTCCTTGAGTTCTGTGACTCAAAACAACTTCCTTCCCCTGTGGGC
ATCAACAATGAGAGATCTTCAGATGCGATCAGGCACTCCAGTCCTTCCATCTCCCACAATGTTG
GAGACCTGTGTTCCCTGCTGTAGAAACCTCTGCCATTCCCTTTATCTCTGAAGACAGATGGACT
TGACTGTCAGCTTAGCTTGGTTTCAGGAGGAAAGGAAGATAAACCCCTGTGTTTAAGCTGCCGT
GTTAAATGGGAGGCACCTGGTCTTTTTTCTTTTTCTTTTTTAAAGACTGGGTCTCGCTCTGTTA
TCCAAGCTGCAGTGCAGTGATGTGATCATAGCTCACCTCAGCCTTGAACTCTCAGGCTCAAGCG
ATCCTCCAGCCTCAGCCTCCTGAATTGCTGGGATTATAGCACCTGGCCAATTTTAAAATCTTTC
TGTAGCGACAGGATCTCACTATGTTGCCCAGGCTGGTCTTGAACCCCTGGCCTCAAGGAATTCT
CCCACAACCTCCCAAAGTGCTAAGATTACAGGCAAGAGCCATGGTGCCCAGCCACCTCTGGTCT
TCCCTCAGTTTGCTTTCATTAAAGGACAAACACATGCCTTGCAAAA

hide sequence

RefSeq Acc Id:

NR_160717

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,982,357 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,931,176 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGAAGTCAGACAAGTACCGGTGATTGCCGGTTTC
TTGTCTGATTTTTGCACTTCTCTGGCAAGCTGCCCCCTCTGAAGAGTTGACTATTTGGGAGTTA
CTCACTGATGGTTCAGCCACTTCCAGAACCTACCCCAAGAGCAAGACTTGAAACCAACTCGCAC
CCTCAAAGCTCCGGAAGCCATTCAGTGTTTCCATCTTGGCTGAGTGAGTTCTTCACTGAAACTC
AATTTGACTTTGACAGTCATCTAATGAGAACTCAAAAGTCATTCTTGGTTCAGCCACAGTCAAA
GAACTTGCAGAGCATTCTCTGACGAGGTCCTCAAGGACAACTGAGAGAAGGGATGTCCTCCACC
TTTTCAATCTGATTTGCTCTTTGCCATGCAGACCTGTGGATGAAGAGCCAGAGTCCTCCAAGGT
GAAGCTGGACTGAATATTTCTGTCCATAAGACTATTAGAATCCCCCAAAGTGGGATACCAGTGA
GGACCTCACCAGCAGCTGCTGTCTCTCCAATGCAGCTCCACAGGGCCTGTGAGCAGGGCTGGCT
ATGAGATCCTGCCCTGAAGAGCAGTACTGGGCTGCTCTGCTAGGCACCTGCATGTCCTGCAAAG
CCATCTGCAACCATCAGAGCCAGCGCACCTGTGCAGCCTCCTGCGGTGAGTTCTGGGACCTGAG
CCCAGGGGACAGTGTGATCACCCCCAACGCCTGTCCCCAGAGCACCCTCTGGCCCCACAGTCAG
GTGGCTGAGGAGAGGATGGCAGGAGGAGATGTACAGTGTGGCACCTCTTATCCCTCCACCTTCC
TGCTCTGGCCACACTGCCTCCTTTCAGTGTCGAACATGCCATGTTCTTCCCTGCCTCGGGTTCT
TTGCACATGTTGTTCCCGCTGCCTGGAATGCATGCTCTCTATCATCTTCCCTCAGCTCCCTCCT
ACCCAACTTTCAGGTCTCGGCCCAAACATCGGGGGTCTCCTCTGACCACACAGTAGTACTGGGC
CCTCCTTTGTACTGCTAGTGTTACTTTCTTTTGAAACTTTTAATTACAGAACTTACCACACATA
TACATAGAGAGGACTGCACAATGATGCCCTCCTCATCCATTACCAGCTTCACAAATCATTTAAA
TTCTGCCTTGTACTTTCCCAACCAGTTGTTTTGGCTTGTGTATTTTAAAGCAAAGCCAAGACCT
CATATCATTTTACCTGCAGATACTGGGCCATAAAGATCTGTAAAACATAACCCAAATATCCTAT
CACTGCCAGCAATAATTTATTAACATCATCTAATATTCAGGCCATATCCAATTTTCCCTGATTG
TCTTGAAAACTATCCATTGCTTGCTGTTCTTTTTCATAATCTGTCTTTTTCCTTGATAGAACTT
ACCACAATTT

hide sequence

RefSeq Acc Id:

NR_160718

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,980,349 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,929,168 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGAAGTCAGACAAGTACCGGTGATTGCCGGTTTC
TTGTCTGATTTTTGCACTTCTCTGGCAAGCTGCCCCCTCTGAAGAGTTGACTATTTGGGAGTTA
CTCACTGATGGTTCAGCCACTTCCAGAACCTACCCCAAGAGCAAGACTTGAAACCAACTCGCAC
CCTCAAAGCTCCGGAAGCCATTCAGTGTTTCCATCTTGGCTGAGTGAGTTCTTCACTGAAACTC
AATTTGACTTTGACAGTCATCTAATGAGAACTCAAAAGTCATTCTTGGTTCAGCCACAGTCAAA
GAACTTGCAGAGCATTCTCTGACGAGGTCCTCAAGGACAACTGAGAGAAGGGATGTCCTCCACC
TTTTCAATCTGATTTGCTCTTTGCCATGCAGACCTGTGGATGAAGAGCCAGAGTCCTCCAAGGT
GAAGCTGGACTGAATATTTCTGTCCATAAGACTATTAGAATCCCCCAAAGTGGGATACCAGTGA
GGACCTCACCAGCAGCTGCTGTCTCTCCAATGCAGAGCTTCCTGCCTCCTGCCCAGCCCCTGCT
GTCAGAGATACTTGGTGCTTCCAGTTCTGGAGACTTCCTTGAGTTCTGTGACTCAAAACAACTT
CCTTCCCCTGTGGGCATCAACAATGAGAGATCTTCAGATGCGATCAGGCACTCCAGTCCTTCCA
TCTCCCACAATGTTGGAGACCTGTGTTCCCTGCTGTAGAAACCTCTGCCATTCCCTTTATCTCT
GAAGACAGATGGACTTGACTGTCAGCTTAGCTTGGTTTCAGGAGGAAAGGAAGATAAACCCCTG
TGTTTAAGCTGCCGTGTTAAATGGGAGGCACCTGGTCTTTTTTCTTTTTCTTTTTTAAAGACTG
GGTCTCGCTCTGTTATCCAAGCTGCAGTGCAGTGATGTGATCATAGCTCACCTCAGCCTTGAAC
TCTCAGGCTCAAGCGATCCTCCAGCCTCAGCCTCCTGAATTGCTGGGATTATAGCACCTGGCCA
ATTTTAAAATCTTTCTGTAGCGACAGGATCTCACTATGTTGCCCAGGCTGGTCTTGAACCCCTG
GCCTCAAGGAATTCTCCCACAACCTCCCAAAGTGCTAAGATTACAGGCAAGAGCCATGGTGCCC
AGCCACCTCTGGTCTTCCCTCAGTTTGCTTTCATTAAAGGACAAACACATGCCTTGCAAAA

hide sequence

RefSeq Acc Id:

NR_160719

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,958,697 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,907,512 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGAAGTCAGACAAGTACCGGTGATTGCCGGTTTC
TTGTCTGATTTTTGCACTTCTCTGGCAAGCTGCCCCCTCTGAAGAGTTGACTATTTGGGAGTTA
CTCACTGATGGTTCAGCCACTTCCAGAACCTACCCCAAGAGCAAGACTTGAAACCAACTCGCAC
CCTCAAAGCTCCGGAAGCCATTCAGTGTTTCCATCTTGGCTGAGTGAGTTCTTCACTGAAACTC
AATTTGACTTTGACAGTCATCTAATGAGAACTCAAAAGTCATTCTTGGTTCAGCCACAGTCAAA
GAACTTGCAGAGCATTCTCTGACGAGGTCCTCAAGGACAACTGAGAGAAGGTCCCATTCCAGGT
CTTGCCCAAGTCTTTCTGATTGGTGGGACTTAAATCACACCCAAAATTCCAGCTGCAGGAGAGC
TCTGAGATTTCATCTTTCCAACCTCTGTGTGCTACGTGGGGGTTGGAGCACTTGCTGACAAGCC
TTGCAACCACCATTGACAGGATGTCCTCCACCTTTTCAATCTGATTTGCTCTTTGCCATGCAGA
CCTGTGGATGAAGAGCCAGAGTCCTCCAAGGTGAAGCTGGACTGAATATTTCTGTCCATAAGAC
TATTAGAATCCCCCAAAGTGGGATACCAGTGAGGACCTCACCAGCAGCTGCTGTCTCTCCAATG
CAGGTAGATGAGCCTCAGAAATAACCGCTGCTTGTGGTTTGCTGTGTATTCCTCTAGATGTTTT
TCTTTACACATATTAGTGAGTGTGGAGAGAGAGTGTGTATGTGTTCTGTAAATTTGATTACACT
GCGCATTTATTCCGAAATCCATTTCACTTTACCGTTGGAACGTAAGCTCTGTGAGGGCAGAGAC
TTTTGTTTATTGCACTTGCTGTTAGAGCTCTTGTCTGTAACAGTGGCTGGCACATGGTCACATC
ATAGTAGAAGCTCAATAAATATTTGTTGAATGAATGAAAAAA

hide sequence

RefSeq Acc Id:

NR_160720

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,958,697 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,907,512 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGAAGTCAGACAAGTACCGGTGATTGCCGGTTTC
TTGTCTGATTTTTGCACTTCTCTGGCAAGCTGCCCCCTCTGAAGAGTTGACTATTTGGGAGTTA
CTCACTGATGGTTCAGCCACTTCCAGAACCTACCCCAAGAGCAAGACTTGAAACCAACTCGCAC
CCTCAAAGCTCCGGAAGCCATTCAGTGTTTCCATCTTGGCTGAGTGAGTTCTTCACTGAAACTC
AATTTGACTTTGACAGTCATCTAATGAGAACTCAAAAGTCATTCTTGGTTCAGCCACAGTCAAA
GAACTTGCAGAGCATTCTCTGACGAGGTCCTCAAGGACAACTGAGAGAAGGGATGTCCTCCACC
TTTTCAATCTGATTTGCTCTTTGCCATGCAGACCTGTGGATGAAGAGCCAGAGTCCTCCAAGGT
GAAGCTGGACTGAATATTTCTGTCCATAAGACTATTAGAATCCCCCAAAGTGGGATACCAGTGA
GGACCTCACCAGCAGCTGCTGTCTCTCCAATGCAGGTAGATGAGCCTCAGAAATAACCGCTGCT
TGTGGTTTGCTGTGTATTCCTCTAGATGTTTTTCTTTACACATATTAGTGAGTGTGGAGAGAGA
GTGTGTATGTGTTCTGTAAATTTGATTACACTGCGCATTTATTCCGAAATCCATTTCACTTTAC
CGTTGGAACGTAAGCTCTGTGAGGGCAGAGACTTTTGTTTATTGCACTTGCTGTTAGAGCTCTT
GTCTGTAACAGTGGCTGGCACATGGTCACATCATAGTAGAAGCTCAATAAATATTTGTTGAATG
AATGAAAAAA

hide sequence

RefSeq Acc Id:

NR_160721

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,982,357 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,931,176 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGTCTTGCCCAAGTCTTTCTGATTGGTGGGACTT
AAATCACACCCAAAATTCCAGCTGCAGGAGAGCTCTGAGATTTCATCTTTCCAACCTCTGTGTG
CTACGTGGGGGTTGGAGCACTTGCTGACAAGCCTTGCAACCACCATTGACAGGATGTCCTCCAC
CTTTTCAATCTGATTTGCTCTTTGCCATGCAGACCTGTGGATGAAGAGCCAGAGTCCTCCAAGG
TGAAGCTGGACTGAATATTTCTGTCCATAAGACTATTAGAATCCCCCAAAGTGGGATACCAGTG
AGGACCTCACCAGCAGCTGCTGTCTCTCCAATGCAGCTCCACAGGGCCTGTGAGCAGGGCTGGC
TATGAGATCCTGCCCTGAAGAGCAGTACTGGGCTGCTCTGCTAGGCACCTGCATGTCCTGCAAA
GCCATCTGCAACCATCAGAGCCAGCGCACCTGTGCAGCCTCCTGCGGTGAGTTCTGGGACCTGA
GCCCAGGGGACAGTGTGATCACCCCCAACGCCTGTCCCCAGAGCACCCTCTGGCCCCACAGTCA
GGTGGCTGAGGAGAGGATGGCAGGAGGAGATGTACAGTGTGGCACCTCTTATCCCTCCACCTTC
CTGCTCTGGCCACACTGCCTCCTTTCAGTGTCGAACATGCCATGTTCTTCCCTGCCTCGGGTTC
TTTGCACATGTTGTTCCCGCTGCCTGGAATGCATGCTCTCTATCATCTTCCCTCAGCTCCCTCC
TACCCAACTTTCAGGTCTCGGCCCAAACATCGGGGGTCTCCTCTGACCACACAGTAGTACTGGG
CCCTCCTTTGTACTGCTAGTGTTACTTTCTTTTGAAACTTTTAATTACAGAACTTACCACACAT
ATACATAGAGAGGACTGCACAATGATGCCCTCCTCATCCATTACCAGCTTCACAAATCATTTAA
ATTCTGCCTTGTACTTTCCCAACCAGTTGTTTTGGCTTGTGTATTTTAAAGCAAAGCCAAGACC
TCATATCATTTTACCTGCAGATACTGGGCCATAAAGATCTGTAAAACATAACCCAAATATCCTA
TCACTGCCAGCAATAATTTATTAACATCATCTAATATTCAGGCCATATCCAATTTTCCCTGATT
GTCTTGAAAACTATCCATTGCTTGCTGTTCTTTTTCATAATCTGTCTTTTTCCTTGATAGAACT
TACCACAATTT

hide sequence

RefSeq Acc Id:

NR_160722

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	20,938,566 - 20,980,349 (+)	NCBI
T2T-CHM13v2.0	17	20,887,381 - 20,929,168 (+)	NCBI

Sequence:

show sequence

AGAGAAGGGTGTCCCAGATGTAGGCAAAGCGTCCTCCATGTGTTCCTGGAGGACCGTCCCAAGT
CCTTCTCCATTCTCCCAACCTCTTGGGCCTGGGATGTCCTCCACCTTTTCAATCTGATTTGCTC
TTTGCCATGCAGACCTGTGGATGAAGAGCCAGAGTCCTCCAAGGTGAAGCTGGACTGAATATTT
CTGTCCATAAGACTATTAGAATCCCCCAAAGTGGGATACCAGTGAGGACCTCACCAGCAGCTGC
TGTCTCTCCAATGCAGAGCTTCCTGCCTCCTGCCCAGCCCCTGCTGTCAGAGATACTTGGTGCT
TCCAGTTCTGGAGACTTCCTTGAGTTCTGTGACTCAAAACAACTTCCTTCCCCTGTGGGCATCA
ACAATGAGAGATCTTCAGATGCGATCAGGCACTCCAGTCCTTCCATCTCCCACAATGTTGGAGA
CCTGTGTTCCCTGCTGTAGAAACCTCTGCCATTCCCTTTATCTCTGAAGACAGATGGACTTGAC
TGTCAGCTTAGCTTGGTTTCAGGAGGAAAGGAAGATAAACCCCTGTGTTTAAGCTGCCGTGTTA
AATGGGAGGCACCTGGTCTTTTTTCTTTTTCTTTTTTAAAGACTGGGTCTCGCTCTGTTATCCA
AGCTGCAGTGCAGTGATGTGATCATAGCTCACCTCAGCCTTGAACTCTCAGGCTCAAGCGATCC
TCCAGCCTCAGCCTCCTGAATTGCTGGGATTATAGCACCTGGCCAATTTTAAAATCTTTCTGTA
GCGACAGGATCTCACTATGTTGCCCAGGCTGGTCTTGAACCCCTGGCCTCAAGGAATTCTCCCA
CAACCTCCCAAAGTGCTAAGATTACAGGCAAGAGCCATGGTGCCCAGCCACCTCTGGTCTTCCC
TCAGTTTGCTTTCATTAAAGGACAAACACATGCCTTGCAAAA

hide sequence

Additional Information

External Database Links

Database	Acc Id	Source(s)
COSMIC	CCDC144NL-AS1	COSMIC
Ensembl Genes	ENSG00000233098	Ensembl, ENTREZGENE
Ensembl Transcript	ENST00000582583	ENTREZGENE
	ENST00000584433	ENTREZGENE
	ENST00000737590	ENTREZGENE
	ENST00000737592	ENTREZGENE
GTEx	ENSG00000233098	GTEx
Human Proteome Map	CCDC144NL-AS1	Human Proteome Map
NCBI Gene	LOC339260	ENTREZGENE
RNAcentral	URS0000E60A1A	RNACentral
	URS0000E60A2F	RNACentral
	URS0000E60A34	RNACentral
	URS0000E60A40	RNACentral
	URS0000E60A5E	RNACentral
	URS0000E60A90	RNACentral
	URS0000E60A96	RNACentral
	URS0000E60AAD	RNACentral
	URS0000E60AB8	RNACentral
	URS0000E60ACB	RNACentral
	URS0000E60B42	RNACentral
	URS0000E60B49	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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