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Gene: LINC03124 (long intergenic non-protein coding RNA 3124) Homo sapiens

Analyze

Symbol:

LINC03124

Name:

long intergenic non-protein coding RNA 3124

RGD ID:

1353501

HGNC Page

HGNC:25077

Description:

INTERACTS WITH aflatoxin B1; arsane; arsenic atom

Type:

ncrna (Ensembl: lncRNA)

RefSeq Status:

VALIDATED

Previously known as:

C2orf27; C2orf27A; C2orf27B; chromosome 2 open reading frame 27A; hypothetical protein LOC29798; MGC138394; uncharacterized protein C2orf27; uncharacterized protein C2orf27A

RGD Orthologs

Bonobo

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	131,682,499 - 131,767,404 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	131,647,982 - 131,774,655 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	132,440,072 - 132,524,977 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	132,196,534 - 132,241,449 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	2	132,313,795 - 132,358,709	NCBI
Celera	2	126,204,833 - 126,250,421 (+)	NCBI		Celera
Cytogenetic Map	2	q21.1-q21.2	NCBI
HuRef	2	124,473,328 - 124,518,239 (+)	NCBI		HuRef
CHM1_1	2	132,483,532 - 132,529,363 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	132,117,144 - 132,202,925 (+)	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

aflatoxin B1 (EXP)

arsane (EXP)

arsenic atom (EXP)

cyclosporin A (EXP)

entinostat (EXP)

folic acid (EXP)

hydroquinone (EXP)

mercury dibromide (EXP)

panobinostat (EXP)

paraoxon (EXP)

phenylmercury acetate (EXP)

sodium arsenite (EXP)

titanium dioxide (EXP)

valproic acid (EXP)

References

References - curated

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:8619474	PMID:9110174	PMID:12477932	PMID:15489334	PMID:15815621	PMID:29954144	PMID:33961781

Genomics

Comparative Map Data

LINC03124
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	131,682,499 - 131,767,404 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	131,647,982 - 131,774,655 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	132,440,072 - 132,524,977 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	132,196,534 - 132,241,449 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	2	132,313,795 - 132,358,709	NCBI
Celera	2	126,204,833 - 126,250,421 (+)	NCBI		Celera
Cytogenetic Map	2	q21.1-q21.2	NCBI
HuRef	2	124,473,328 - 124,518,239 (+)	NCBI		HuRef
CHM1_1	2	132,483,532 - 132,529,363 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	132,117,144 - 132,202,925 (+)	NCBI		T2T-CHM13v2.0

LOC112439094
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	23	20,326,825 - 20,336,719 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	22	23,666,359 - 23,676,273 (-)	NCBI		NHGRI_mPanPan1
PanPan1.1	2B	132,572,243 - 132,575,361 (+)	NCBI	panpan1.1	PanPan1.1	panPan2

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 2q14.1-21.3(chr2:118086324-134964738)x1	copy number loss	See cases [RCV000054058]	Chr2:118086324..134964738 [GRCh38] Chr2:118843900..135722308 [GRCh37] Chr2:118560370..135438778 [NCBI36] Chr2:2q14.1-21.3	pathogenic
GRCh38/hg38 2q14.3-22.1(chr2:123445762-140592538)x1	copy number loss	See cases [RCV000136714]	Chr2:123445762..140592538 [GRCh38] Chr2:124203338..141350107 [GRCh37] Chr2:123919808..141066577 [NCBI36] Chr2:2q14.3-22.1	pathogenic
GRCh38/hg38 2q21.1-21.2(chr2:131451345-131736366)x3	copy number gain	See cases [RCV000139297]	Chr2:131451345..131736366 [GRCh38] Chr2:132208918..132493939 [GRCh37] Chr2:131925388..132210409 [NCBI36] Chr2:2q21.1-21.2	likely benign
GRCh38/hg38 2q21.1-21.2(chr2:131451345-131736366)x1	copy number loss	See cases [RCV000139301]	Chr2:131451345..131736366 [GRCh38] Chr2:132208918..132493939 [GRCh37] Chr2:131925388..132210409 [NCBI36] Chr2:2q21.1-21.2	likely benign
GRCh38/hg38 2q21.1-21.2(chr2:131409034-131940119)x1	copy number loss	See cases [RCV000139880]	Chr2:131409034..131940119 [GRCh38] Chr2:132166607..132697692 [GRCh37] Chr2:131883077..132414162 [NCBI36] Chr2:2q21.1-21.2	uncertain significance
GRCh38/hg38 2q21.1-21.2(chr2:131100857-132436431)x3	copy number gain	See cases [RCV000141447]	Chr2:131100857..132436431 [GRCh38] Chr2:131858430..133194004 [GRCh37] Chr2:131574900..132910474 [NCBI36] Chr2:2q21.1-21.2	uncertain significance
GRCh38/hg38 2q21.1-21.2(chr2:131291207-132406186)x3	copy number gain	See cases [RCV000142215]	Chr2:131291207..132406186 [GRCh38] Chr2:132048780..133163759 [GRCh37] Chr2:131765250..132880229 [NCBI36] Chr2:2q21.1-21.2	likely benign\|uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3	copy number gain	not provided [RCV000752802]	Chr2:14238..243048760 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q21.1-21.2(chr2:132352058-132510828)x3	copy number gain	not provided [RCV000753134]	Chr2:132352058..132510828 [GRCh37] Chr2:2q21.1-21.2	benign
GRCh37/hg19 2q21.1-21.2(chr2:132352058-132649834)x3	copy number gain	not provided [RCV000753135]	Chr2:132352058..132649834 [GRCh37] Chr2:2q21.1-21.2	benign
GRCh37/hg19 2q21.1-21.2(chr2:132290940-132515623)x3	copy number gain	See cases [RCV000449149]	Chr2:132290940..132515623 [GRCh37] Chr2:2q21.1-21.2	benign
GRCh37/hg19 2q21.1-21.2(chr2:132290940-132508293)x3	copy number gain	See cases [RCV000447171]	Chr2:132290940..132508293 [GRCh37] Chr2:2q21.1-21.2	benign\|likely benign
GRCh37/hg19 2q14.3-22.1(chr2:128490257-138210164)x1	copy number loss	See cases [RCV000445892]	Chr2:128490257..138210164 [GRCh37] Chr2:2q14.3-22.1	pathogenic
GRCh37/hg19 2q21.1-21.2(chr2:132287932-132558490)x3	copy number gain	See cases [RCV000448742]	Chr2:132287932..132558490 [GRCh37] Chr2:2q21.1-21.2	benign
GRCh37/hg19 2q21.1-21.2(chr2:132287932-132508293)x3	copy number gain	See cases [RCV000447831]	Chr2:132287932..132508293 [GRCh37] Chr2:2q21.1-21.2	benign
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	copy number gain	See cases [RCV000512056]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q21.1-21.2(chr2:130920847-134220436)x3	copy number gain	See cases [RCV000511730]	Chr2:130920847..134220436 [GRCh37] Chr2:2q21.1-21.2	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	copy number gain	See cases [RCV000511212]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q12.1-24.3(chr2:104172062-168223828)x1	copy number loss	Poly (ADP-Ribose) polymerase inhibitor response [RCV000626436]	Chr2:104172062..168223828 [GRCh37] Chr2:2q12.1-24.3	drug response
GRCh37/hg19 2q14.2-22.1(chr2:120571363-141627287)x1	copy number loss	See cases [RCV000512348]	Chr2:120571363..141627287 [GRCh37] Chr2:2q14.2-22.1	pathogenic
Single allele	deletion	not provided [RCV000714264]	Chr2:40608411..146900718 [GRCh37] Chr2:2p22.1-q22.3	likely pathogenic
GRCh37/hg19 2q21.1-21.2(chr2:132352058-132755417)x3	copy number gain	not provided [RCV000753136]	Chr2:132352058..132755417 [GRCh37] Chr2:2q21.1-21.2	benign
GRCh37/hg19 2q21.1-21.2(chr2:132478453-133015071)x3	copy number gain	not provided [RCV000753137]	Chr2:132478453..133015071 [GRCh37] Chr2:2q21.1-21.2	benign
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3	copy number gain	not provided [RCV000752804]	Chr2:15672..243101834 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q21.1-21.2(chr2:132343339-132649834)x3	copy number gain	not provided [RCV000753133]	Chr2:132343339..132649834 [GRCh37] Chr2:2q21.1-21.2	benign
GRCh37/hg19 2q21.1(chr2:132483583-132497065)x3	copy number gain	not provided [RCV000753138]	Chr2:132483583..132497065 [GRCh37] Chr2:2q21.1	benign
GRCh37/hg19 2q21.1-21.2(chr2:130916858-134213436)x3	copy number gain	not provided [RCV000846479]	Chr2:130916858..134213436 [GRCh37] Chr2:2q21.1-21.2	uncertain significance
GRCh37/hg19 2q14.3-21.2(chr2:122952356-133826358)x1	copy number loss	See cases [RCV001194541]	Chr2:122952356..133826358 [GRCh37] Chr2:2q14.3-21.2	likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	copy number gain	Mosaic trisomy 2 [RCV002280628]	Chr2:1..243199373 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q14.3-22.2(chr2:122699106-143799629)x1	copy number loss	not provided [RCV001832883]	Chr2:122699106..143799629 [GRCh37] Chr2:2q14.3-22.2	pathogenic
GRCh37/hg19 2q13-22.3(chr2:111484468-146333604)x3	copy number gain	not provided [RCV001832896]	Chr2:111484468..146333604 [GRCh37] Chr2:2q13-22.3	pathogenic
GRCh37/hg19 2q13-22.3(chr2:112475655-145691999)x3	copy number gain	2q13q22.3 microduplication syndrome [RCV002226436]	Chr2:112475655..145691999 [GRCh37] Chr2:2q13-22.3	pathogenic
GRCh37/hg19 2q21.1-21.2(chr2:131853044-133195255)x3	copy number gain	See cases [RCV002292205]	Chr2:131853044..133195255 [GRCh37] Chr2:2q21.1-21.2	uncertain significance
GRCh37/hg19 2q21.1-21.2(chr2:132058665-133163759)x3	copy number gain	not provided [RCV002472400]	Chr2:132058665..133163759 [GRCh37] Chr2:2q21.1-21.2	uncertain significance
GRCh37/hg19 2q21.1-21.2(chr2:131777624-134871884)x1	copy number loss	not provided [RCV003484904]	Chr2:131777624..134871884 [GRCh37] Chr2:2q21.1-21.2	uncertain significance
GRCh37/hg19 2q12.2-21.2(chr2:106755586-134302739)x1	copy number loss	not specified [RCV003986380]	Chr2:106755586..134302739 [GRCh37] Chr2:2q12.2-21.2	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	756
Count of miRNA genes:	525
Interacting mature miRNAs:	585
Transcripts:	ENST00000355171, ENST00000463645, ENST00000466372, ENST00000481510
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.

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
597394067	GWAS1490141_H	adolescent idiopathic scoliosis QTL GWAS1490141 (human)		0.0000003	adolescent idiopathic scoliosis		2	131713032	131713033	Human

Markers in Region

RH11944

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	132,552,599 - 132,552,749	UniSTS	GRCh37
GRCh37	2	132,524,762 - 132,524,912	UniSTS	GRCh37
Build 36	2	132,241,232 - 132,241,382	RGD	NCBI36
Celera	2	126,250,206 - 126,250,356	RGD
Cytogenetic Map	2	q21	UniSTS
Cytogenetic Map	2	q21.2	UniSTS
HuRef	2	124,518,024 - 124,518,174	UniSTS
HuRef	2	124,545,824 - 124,545,974	UniSTS
GeneMap99-GB4 RH Map	2	478.96	UniSTS
NCBI RH Map	2	1021.7	UniSTS

RH99290

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	2	q21.2	UniSTS
Cytogenetic Map	2	q21	UniSTS

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
1203	2430	2788	2244	4942	1709	2317	4	609	1812	451	2268	7124	6316	51	3708	840	1730	1597	170

Sequence

Nucleotide Sequences


RefSeq Transcripts	NR_149013	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_149014	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_149015	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_149016	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_167887	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_167888	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_167889	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC093724	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC093838	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC226740	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC244624	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF038169	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI302788	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI418663	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK309649	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC071972	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC093716	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC112189	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX648270	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471058	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MG828590	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000463645

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,733,656 - 131,751,669 (+)	Ensembl

Ensembl Acc Id:

ENST00000466372

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,736,552 - 131,750,763 (+)	Ensembl

Ensembl Acc Id:

ENST00000481510

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,758,031 - 131,767,107 (+)	Ensembl

Ensembl Acc Id:

ENST00000623058

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,722,417 - 131,751,584 (+)	Ensembl

Ensembl Acc Id:

ENST00000624391

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,722,375 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000652878

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,647,990 - 131,723,045 (+)	Ensembl

Ensembl Acc Id:

ENST00000653458

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,699,779 (+)	Ensembl

Ensembl Acc Id:

ENST00000655714

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,684,897 - 131,699,861 (+)	Ensembl

Ensembl Acc Id:

ENST00000657415

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,468 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000666411

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,437 - 131,699,644 (+)	Ensembl

Ensembl Acc Id:

ENST00000779756

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,648,013 - 131,773,756 (+)	Ensembl

Ensembl Acc Id:

ENST00000779757

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,647,982 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779758

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,438 - 131,774,655 (+)	Ensembl

Ensembl Acc Id:

ENST00000779759

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,774,645 (+)	Ensembl

Ensembl Acc Id:

ENST00000779760

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,609 - 131,774,645 (+)	Ensembl

Ensembl Acc Id:

ENST00000779761

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,483 - 131,774,195 (+)	Ensembl

Ensembl Acc Id:

ENST00000779762

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,773,834 (+)	Ensembl

Ensembl Acc Id:

ENST00000779763

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,773,756 (+)	Ensembl

Ensembl Acc Id:

ENST00000779764

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,453 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779765

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,464 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779766

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,481 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779767

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,483 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779768

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,483 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779769

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,483 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779770

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,483 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779771

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,483 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779772

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,488 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779773

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779774

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779775

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779776

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779777

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779778

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779779

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779780

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779781

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,492 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779782

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,767,400 (+)	Ensembl

Ensembl Acc Id:

ENST00000779784

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,495 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779785

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,497 - 131,767,406 (+)	Ensembl

Ensembl Acc Id:

ENST00000779786

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,497 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779788

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,497 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779790

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779791

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779792

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779793

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779794

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779795

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779796

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779797

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,767,402 (+)	Ensembl

Ensembl Acc Id:

ENST00000779798

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779799

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,767,402 (+)	Ensembl

Ensembl Acc Id:

ENST00000779800

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,497 - 131,767,400 (+)	Ensembl

Ensembl Acc Id:

ENST00000779801

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779802

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,504 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779803

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,767,400 (+)	Ensembl

Ensembl Acc Id:

ENST00000779804

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,505 - 131,767,400 (+)	Ensembl

Ensembl Acc Id:

ENST00000779805

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,506 - 131,767,400 (+)	Ensembl

Ensembl Acc Id:

ENST00000779806

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,519 - 131,767,402 (+)	Ensembl

Ensembl Acc Id:

ENST00000779807

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,528 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779808

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,544 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779809

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,761 - 131,767,402 (+)	Ensembl

Ensembl Acc Id:

ENST00000779810

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,754,749 (+)	Ensembl

Ensembl Acc Id:

ENST00000779811

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,753,523 (+)	Ensembl

Ensembl Acc Id:

ENST00000779812

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,753,248 (+)	Ensembl

Ensembl Acc Id:

ENST00000779813

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,752,719 (+)	Ensembl

Ensembl Acc Id:

ENST00000779814

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,752,212 (+)	Ensembl

Ensembl Acc Id:

ENST00000779815

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,752,168 (+)	Ensembl

Ensembl Acc Id:

ENST00000779816

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,504 - 131,752,157 (+)	Ensembl

Ensembl Acc Id:

ENST00000779817

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,751,794 (+)	Ensembl

Ensembl Acc Id:

ENST00000779818

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,528 - 131,751,717 (+)	Ensembl

Ensembl Acc Id:

ENST00000779819

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,493 - 131,751,390 (+)	Ensembl

Ensembl Acc Id:

ENST00000779820

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,517 - 131,751,390 (+)	Ensembl

Ensembl Acc Id:

ENST00000779821

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,482 - 131,751,180 (+)	Ensembl

Ensembl Acc Id:

ENST00000779822

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,751,184 (+)	Ensembl

Ensembl Acc Id:

ENST00000779823

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,738,881 (+)	Ensembl

Ensembl Acc Id:

ENST00000779824

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,483 - 131,734,053 (+)	Ensembl

Ensembl Acc Id:

ENST00000779825

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,734,053 (+)	Ensembl

Ensembl Acc Id:

ENST00000779826

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,734,053 (+)	Ensembl

Ensembl Acc Id:

ENST00000779827

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,734,053 (+)	Ensembl

Ensembl Acc Id:

ENST00000779828

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,734,053 (+)	Ensembl

Ensembl Acc Id:

ENST00000779829

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,734,053 (+)	Ensembl

Ensembl Acc Id:

ENST00000779830

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,497 - 131,734,047 (+)	Ensembl

Ensembl Acc Id:

ENST00000779831

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,672,749 - 131,722,948 (+)	Ensembl

Ensembl Acc Id:

ENST00000779832

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,681,830 - 131,723,096 (+)	Ensembl

Ensembl Acc Id:

ENST00000779833

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,681,848 - 131,722,948 (+)	Ensembl

Ensembl Acc Id:

ENST00000779834

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,681,857 - 131,722,953 (+)	Ensembl

Ensembl Acc Id:

ENST00000779835

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,438 - 131,723,202 (+)	Ensembl

Ensembl Acc Id:

ENST00000779836

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,453 - 131,723,094 (+)	Ensembl

Ensembl Acc Id:

ENST00000779837

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,723,096 (+)	Ensembl

Ensembl Acc Id:

ENST00000779838

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,431 - 131,722,953 (+)	Ensembl

Ensembl Acc Id:

ENST00000779839

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,438 - 131,722,950 (+)	Ensembl

Ensembl Acc Id:

ENST00000779840

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,453 - 131,722,953 (+)	Ensembl

Ensembl Acc Id:

ENST00000779841

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,483 - 131,722,953 (+)	Ensembl

Ensembl Acc Id:

ENST00000779842

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,488 - 131,722,953 (+)	Ensembl

Ensembl Acc Id:

ENST00000779843

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,485 - 131,722,948 (+)	Ensembl

Ensembl Acc Id:

ENST00000779844

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,722,952 (+)	Ensembl

Ensembl Acc Id:

ENST00000779845

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,722,948 (+)	Ensembl

Ensembl Acc Id:

ENST00000779846

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,722,948 (+)	Ensembl

Ensembl Acc Id:

ENST00000779847

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,483 - 131,722,939 (+)	Ensembl

Ensembl Acc Id:

ENST00000779848

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,722,945 (+)	Ensembl

Ensembl Acc Id:

ENST00000779849

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,722,945 (+)	Ensembl

Ensembl Acc Id:

ENST00000779850

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,722,953 (+)	Ensembl

Ensembl Acc Id:

ENST00000779851

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,722,943 (+)	Ensembl

Ensembl Acc Id:

ENST00000779852

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,497 - 131,722,948 (+)	Ensembl

Ensembl Acc Id:

ENST00000779853

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,722,942 (+)	Ensembl

Ensembl Acc Id:

ENST00000779854

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,722,948 (+)	Ensembl

Ensembl Acc Id:

ENST00000779855

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,722,943 (+)	Ensembl

Ensembl Acc Id:

ENST00000779856

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,722,941 (+)	Ensembl

Ensembl Acc Id:

ENST00000779857

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,522 - 131,722,948 (+)	Ensembl

Ensembl Acc Id:

ENST00000779858

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,537 - 131,722,953 (+)	Ensembl

Ensembl Acc Id:

ENST00000779859

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,722,830 (+)	Ensembl

Ensembl Acc Id:

ENST00000779860

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,456 - 131,722,779 (+)	Ensembl

Ensembl Acc Id:

ENST00000779861

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,722,779 (+)	Ensembl

Ensembl Acc Id:

ENST00000779862

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,722,779 (+)	Ensembl

Ensembl Acc Id:

ENST00000779863

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,722,779 (+)	Ensembl

Ensembl Acc Id:

ENST00000779864

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,528 - 131,722,779 (+)	Ensembl

Ensembl Acc Id:

ENST00000779865

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,550 - 131,722,617 (+)	Ensembl

Ensembl Acc Id:

ENST00000779866

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,728,115 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779867

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,755,903 - 131,773,759 (+)	Ensembl

Ensembl Acc Id:

ENST00000779868

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,468 - 131,699,644 (+)	Ensembl

Ensembl Acc Id:

ENST00000779869

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,699,644 (+)	Ensembl

Ensembl Acc Id:

ENST00000779870

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,499 - 131,699,640 (+)	Ensembl

Ensembl Acc Id:

ENST00000779871

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,468 - 131,698,426 (+)	Ensembl

Ensembl Acc Id:

ENST00000779872

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,485 - 131,698,425 (+)	Ensembl

Ensembl Acc Id:

ENST00000779873

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,698,426 (+)	Ensembl

Ensembl Acc Id:

ENST00000779874

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,698,426 (+)	Ensembl

Ensembl Acc Id:

ENST00000779875

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,698,394 (+)	Ensembl

Ensembl Acc Id:

ENST00000779876

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,497 - 131,698,394 (+)	Ensembl

Ensembl Acc Id:

ENST00000779877

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,501 - 131,698,394 (+)	Ensembl

Ensembl Acc Id:

ENST00000779878

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,699 - 131,698,394 (+)	Ensembl

Ensembl Acc Id:

ENST00000779879

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,753,602 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779880

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,753,602 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779881

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,753,795 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779882

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,753,809 - 131,767,403 (+)	Ensembl

Ensembl Acc Id:

ENST00000779883

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,754,002 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779884

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,754,069 - 131,767,400 (+)	Ensembl

Ensembl Acc Id:

ENST00000779885

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,754,612 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779886

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,754,692 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779887

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,755,085 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779888

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,755,519 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779889

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,755,886 - 131,767,406 (+)	Ensembl

Ensembl Acc Id:

ENST00000779890

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,756,297 - 131,767,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000779891

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,756,527 - 131,767,406 (+)	Ensembl

Ensembl Acc Id:

ENST00000779892

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,755,909 - 131,766,721 (+)	Ensembl

Ensembl Acc Id:

ENST00000779893

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,525 - 131,688,120 (+)	Ensembl

Ensembl Acc Id:

ENST00000779894

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,755,885 - 131,759,018 (+)	Ensembl

Ensembl Acc Id:

ENST00000779895

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,755,920 - 131,758,981 (+)	Ensembl

Ensembl Acc Id:

ENST00000779896

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,755,885 - 131,758,682 (+)	Ensembl

Ensembl Acc Id:

ENST00000779897

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,672,221 - 131,674,525 (+)	Ensembl

Ensembl Acc Id:

ENST00000779898

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,672,528 - 131,674,537 (+)	Ensembl

Ensembl Acc Id:

ENST00000779899

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,722,062 - 131,723,950 (+)	Ensembl

Ensembl Acc Id:

ENST00000779900

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,672,876 - 131,674,524 (+)	Ensembl

Ensembl Acc Id:

ENST00000779901

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,673,256 - 131,674,520 (+)	Ensembl

Ensembl Acc Id:

ENST00000779902

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,673,304 - 131,674,527 (+)	Ensembl

Ensembl Acc Id:

ENST00000779903

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,682,491 - 131,683,327 (+)	Ensembl

Ensembl Acc Id:

ENST00000779904

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	131,722,055 - 131,722,779 (+)	Ensembl

RefSeq Acc Id:

NR_149013

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	131,682,499 - 131,767,404 (+)	NCBI
T2T-CHM13v2.0	2	132,117,144 - 132,202,925 (+)	NCBI

Sequence:

show sequence

AGTTCCTGCGACGCCCCTGCAGCAGCAGCAGCGTGGTCAGAGCGAGCTTCTGAGCGGTGGTTCA
TCTGCGTTGCTCTAAATGGGACTGTTTCATTATTTTGATGGCTGAAGAATATTTCCTAGTGTAT
GTATATGAGAGTTTCTTGATCTCTTTATCTGTGGATGAACAGCTACTTTGAAATATATGATACA
TTTGTGTTAAGGCTAGTCACGCTGCTGTGGAATAGAAGGCCAGAATTGATCACTATCATCTGAG
AGTAACTTTGTACCCATCACTGATTCCTTCCGAGACTGCCTCCACTTCCCCAGCAGCCTCTGAT
TTCTTCATGTGGCTGCAGATGGCAGGATTTCCCAAAGGTTTATGGCTGCAACATATTCCGTGGT
GTATCTGTACAGCAGTTTCCTCATTCCTGCAGCTGTGTTTGAACAGGTCATTTACCATGCGGTC
CTCCAGGTTCAACAGTATGGCTCCAAATGATGAAATTTCATTCTGATTTTCTGGCTGAAGACTA
TTCTGTTTGTGTATGTCCACCACAGTTACTTTATCCCTTCATCTGTGGATGGGCAGTTGGTTGG
CAGAGAATTTGAACTGGAGATGAACTTTATTATCCAGGATGCTGAGAGTATAACATGCATGACA
GAGCTTTTAGAGCACTGTGATGTAACATGTCAAGCAGAAATAGGGAGCATGTTTACAGCCATTC
TATGAAAAAGTGTTCGGAATGTACAGACTAGCACAGAAGCTGGACTAATTGAACAAGTATTGCT
GAAAATGAGTGCTGTAGATGACATGATAGCAGTGGTACATGATCAGCATTGTCCACATTTACAA
TCGATGGAGAAACAGTGAAATTCAGTGTTATGTTAATGGACAACTGGTATCTTATGGTGATATG
GCTTGGCATGTTAACACAAATGACAGCTATGACAAGTGCTTTCTTGGATCATCAGAAACTGCTG
ATGCAAATAGGGTATTCTGTGGTCAACTTGGTGCCGTGTATGTGTTCAGTGAAGCACTCAACCC
AGCACAGATATTTGCAATTCATCAGTTAGGACCTAGATATAAGAGTACCTTCAAGTTTAAATCT
GAGAGTGATATTCATTTGGCAGAACATCATAAACAGGTTTTGTATGATGGGAAACTTGCAAGTA
GCATTACCTTTACATATACTGCTAAGGCCACTGATGCTCAACTCTGCCTGGAATCATCACCAAA
AGAGAATGCATCAATTTTTGTGCATTCCCAACATGCTCTAATGCTTCAGATTCAAGTGCTTTTT
CCACTGTTTCCCCAATTGGATAATCGGCAGCTCAATGACAGTCAAGTGGAAACAACTGTCTGGG
GCCTAATGTCCACCTAAGACGTGGTGTTCACCTGGGGTCTGATGTTCAGCTGAAGACTGGATGT
CCACCTGGAGCTGAGGAATCCACCCAGGGACTGGTGTTGAACTGGGGCCTGATGACCACCGGGG
GACAAGGTATCCACACCAGGCTTGATGTCCACCTGTCACCAGATGTCTACCTCCTGCTTCAGGT
GCAGAAATACAGCGATTTCCAGTGCCAGCTGTTGAGCCAGTGCCAGCACCAGGGGCAGATTCCC
CTCCAGGGACAGCGCTGGAGCTAGAGGAAGCTCCAGAGCCCTCCTGCCGCTGCCCTGGGACTGC
CCAGGACCAGCCCAGTGAGGAGCTGCCTGACTTCATGGCACCTCCTGTAGAGCCACCGGCCTCA
GCCCTGGAGCTGAAAGTGTGGCTGGAGCTAGAGGTGGCAGAGAGGGGTGGCCAGCACAGCTCCA
GCCAGCAGCTCCCACACTGCTCCCAGTCCTGGGCACAGTGGAAGCTATGGAGGCAGAGACCAGG
GTTTGCAATCTGGGCTCCTCTGCCTCACTGGAGAGGGACTTCTCTCATTCAGCAGAGCAGCAGC
CCTGCTGCTGAAGGGCCTGCTGCTACTGCTGCTGGGGCTGTTTGCCTGCCTGCAGGAGGTGCTG
GAGAGCAAGAAAAGGAGCCTGTGAGCAGGGGTTCCAGCAGGTCCTCCTGCTCCCAGAGGCGACC
TCCTCCTCCAGGCATGGAGGTTTGCCCTCAGCTGGGCATCTGGGCCATTTGCCCCTAACGTGCT
GCCCAGGATGGCCTCCTCTTGACAGGCGGACAGGGGGTGAGGGGGCCAGGGGGCATCTCCAAAG
GAAGCTTTTAAACTCAGCAGCTGCACCCCAGAATCTGTATGCCTGCACCTGCCCAAGGATTTAT
TCATAGCTTACCTAAGAATTTCAAATTTCTACCATAACACTGAATAAAGTTTGACTTTTTGAAA
CTTC

hide sequence

RefSeq Acc Id:

NR_149014

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	131,682,499 - 131,699,850 (+)	NCBI
T2T-CHM13v2.0	2	132,117,144 - 132,134,495 (+)	NCBI

Sequence:

show sequence

AGTTCCTGCGACGCCCCTGCAGCAGCAGCAGCGTGGTCAGAGCGAGCTTCTGAGCGGTGGTTCA
TCTGCGTTGCTCTAAATGGGACTGTTTCATTATTTTGATGGCTGAAGAATATTTCCTAGTGTAT
GTATATGAGAGTTTCTTGATCTCTTTATCTGTGGATGAACAGCTACTTTGAAATATATGATACA
TTTGTGTTAAGGCTAGTCACGCTGCTGTGGAATAGAAGGCCAGAATTGATCACTATCATCTGAG
AGTAACTTTGTACCCATCACTGATTCCTTCCGAGACTGCCTCCACTTCCCCAGCAGCCTCTGAT
TTCTTCATGTGGCTGCAGATGGCAGGATTTCCCAAAGGTTTATGGCTGCAACATATTCCGTGGT
GTATCTGTACAGCAGTTTCCTCATTCCTGCAGCTGTGTTTGAACAGGTCATTTACCATGCGGTC
CTCCAGGTTCAACAGTATGGCTCCAAATGATGAAATTTCATTCTGATTTTCTGGCTGAAGACTA
TTCTGTTTGTGTATGTCCACCACAGTTACTTTATCCCTTCATCTGTGGATGGGCAGGAAACTCC
AAACTGTCCAAGGGATAGTTCTGTTGTGATTACTTCATTGAGAAATTTAACTTATGAGCAGTTG
AAAGGAATGCAAGTTGCTGGAAAATCAGAATGAAGAGTGCAAAATGACCAAGCTACAATGTATT
GTCATTATTCACTCTGATGTGAAAAAGGCAGTGAATTCAATAGAAAATAACTTTGCAGAATAAA
ATCTCAGGTGTGTTTTTTTAGTGCCACAGTCTTGGATGATGGGCTTCTAGATGTTGAGTCCTAG
AAGCTCTCAACATCTCTTCTTAATTGGAGAAAGTGTTAAGCCCCAAAGTAGCTGGAGCAGTACA
TCTTCAATTTTTGACAAGAAAGCAGGAACTTGGTTACTTTGAGTGTTATTCATTAGTTTCTGCT
TTCATTGAGAATGCAGCAAAAGCCAACGAGGCTGCTGCTAACTCCTTGCTGGACATCTTCTGCC
ACTATCACAGGAACTGTGATCTCACTGGACAATTAACTAGGGAGCCTTTCATCTTGAATGACTG
CTGCACAAATGATCTTCAAAGCATTTTAGCCACCAGAGGAATTCTCTTCAAATACCCAAAATCC
ATCAGTATCTTGAATCATGCTGGATTTTGAAGAATTCTTAACAAGCCATGTAAAGGGGGCTCTC
TGGCCTTGAAATAGTGATGTTTTTTATACAGAAAGGAGAATGCCGAATGTTCAGACTACCATGC
ACTGTTAAATTTGATTTCAAGAAATTACAGGAAAACTTTCCAAAGTTCCGTCTCACAGAATTTA
TTTTTACAAAGAATTCCAAGATAAGTTTAGTTTTATGGAAGATTTTTATGTGGTTTTTACTCAC
TCTTCATCTCAGACATCAACCGATGATTACATCACTTATTTAGCTAGTAAATTTATTAATATAA
AACTCAGAGACATTCCAATATCCACATTGCTTACATCATCAGGCATAGATTCAATGTCAGCTAT
GACAATTGAAAATAAGCTGTTTTGTGATTTAAAGGTTTAAATTTCTCTAACCAAACAGCTTGAT
CCAGATGCAGCACTGCAAATGTTAATATTTGTTCTGGAAGAGCAATCAAATAAGACTTAAGAGG
AAAAGGAATGGCCACAATCCACCTGAAATTTTTTTTAAAAAAGTATGCAGCCTACTAAATCAGA
ATGAAAATAGAAGTACAAGATTATAAACAAAATGCAATCAAACTTTTCTTAAGCTTACCTAAAG
TTATTTTATCTGAAAATTTCAAGCAACTTTGATCAACATTAAATTGACAATCTAAACTAACAAG
TCTTTTGAATTTATGTATGGTAGTAAACATTCTCTCTATTAATTTTATTACCTAAGGCTAAACC
TAAAATTTTTAAGCAAAATTAGAAAGTCTTCACTTATCAAAAAATAAAGTTTGTTACATTTAGT
ATTTTCCCAATAAAATTGGTCATTCTTGGTTTTTTATTTGGAGAATCTGTGCAAAATTTCACTG
AAAATAAATTAGAACTAGAAATTATTTCTAAATACCAAAAAAAAAATGAAGAATGGTTTCACAA
AGAAAAAAAGAAAACTTGCTTAATTAGCAGAGTATCATCTCTGTGATTTTTGTGATTATTTGAT
CAGTGTCCTGAGATGGATACAATGGCAAGTAATGACAAAATTAAAATAAGCATGCAGATTTTTT
TAAATTAAGTGCCAAAAAATAATTGGTCATGCAAAGCCCTTAAAAATATTGTGGCCTAATTCTA
AAGTTTTTTGCTACTATGCTACATCACACGCAACATCAGTTAAGTGCTCATTCTGTGACAGGTA
GTACATTACATTTTAGCAAACTACACAAGACCCCTATGTGATAATATGCTTCAGGGTTGTAAGG
TTGGGTGCATTTACTAGTCTTGAATTTTCTGGGAGTATACAAACCCAATATTAGTCTAGATGCC
CACAAATCTATTTAGACGTCACAGTAGAATGGAGAGTAATCTTGACCACAGGAAGCTGTGTTGT
GGCATTTATTTTGAAATTATTTTTTCTTGATTTTTTTGCCTTTTGTTTTGTGAGTTTTATAATG
TACAGAATATTTTTAAATTATTATATATATCAACTAATTAGTCTTCATTTAAACTTACGCCTCT
GGGGTCTTACTTGGGTTTCTCCTAACAATATTATACACATATTTGCAATAATTTCTCTCATACT
GCTTTTAACTCATTTAATTTTTCAACTTTTTAAGAATAACAAAAGTGATATTAATTGTAAAAAT
GCTGAAGTGACATATGAATTTATGAAGTGCATATGTATTTTTTAGTTTACCAATGAGATGGGAG
AAATGCTGTCTTATATTTTAACATACATTTTGGCCATTACACAGATGAAGCAACTTTTCATTTG
TTAATACATAATGCATACTTTTTCTTCTGTGCAATTCCTCTTTGTATTCTTTGCTCATTTTCCC
ACTGGGATTTGCAAGTTCTTTATTATTTGATAATCTCTATACATTCTGAATATCAATTTTTTGT
TATATATACCATGTAAATATTTTCTTCTAATTTGTTATTTGTCTTTTAATGGTATTTATCAATT
GTTTGCTAAAAATGAGTTTGTTTAGTTAGTAAAATTTGTCTATCTTTAACTTCATGATATTTGT
ATATCATGTCATGAGGAAAAGGCATGAATATTTTAAAAACTTCCTTGTAGTGTTAATTTTATTT
TTTATTTCATTCTTTAAGTTATTTGAAATTTATTGTTTATTTCTTCAAATTCCAAATAATAACC
AACTTTCTCAAAGCAATACTTCTTTCTACTGATTTCAAACGTTACATTTGTCTTCTCTGAAGTT
CTTGTTTTTTTGATACCTGACTGTCACACTACTGCTGTGGATGTGCTTCATACCATCACAGTAC
TGCAGGGTTATAAGATTATCTGATAGCCAATAGAAGCAGACGTCTACTCACTGTCATTCTTTTG
TCTTTTGGAGAATAAAGTTAGCTATTTTTA

hide sequence

RefSeq Acc Id:

NR_149015

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	131,682,499 - 131,699,850 (+)	NCBI
T2T-CHM13v2.0	2	132,117,144 - 132,134,495 (+)	NCBI

Sequence:

show sequence

AGTTCCTGCGACGCCCCTGCAGCAGCAGCAGCGTGGTCAGAGCGAGCTTCTGAGCGGTGGTTCA
TCTGCGTTGCTCTAAATGGGACTGTTTCATTATTTTGATGGCTGAAGAATATTTCCTAGTCTAC
TTTGAAATATATGATACATTTGTGTTAAGGCTAGTCACGCTGCTGTGGAATAGAAGGCCAGAAT
TGATCACTATCATCTGAGAGTAACTTTGTACCCATCACTGATTCCTTCCGAGACTGCCTCCACT
TCCCCAGCAGCCTCTGATTTCTTCATGTGGCTGCAGATGGCAGGATTTCCCAAAGGTTTATGGC
TGCAACATATTCCGTGGTGTATCTGTACAGCAGTTTCCTCATTCCTGCAGCTGTGTTTGAACAG
GTCATTTACCATGCGGTCCTCCAGGTTCAACAGTATGGCTCCAAATGATGAAATTTCATTCTGA
TTTTCTGGCTGAAGACTATTCTGTTTGTGTATGTCCACCACAGTTACTTTATCCCTTCATCTGT
GGATGGGCAGGAAACTCCAAACTGTCCAAGGGATAGTTCTGTTGTGATTACTTCATTGAGAAAT
TTAACTTATGAGCAGTTGAAAGGAATGCAAGTTGCTGGAAAATCAGAATGAAGAGTGCAAAATG
ACCAAGCTACAATGTATTGTCATTATTCACTCTGATGTGAAAAAGGCAGTGAATTCAATAGAAA
ATAACTTTGCAGAATAAAATCTCAGGTGTGTTTTTTTAGTGCCACAGTCTTGGATGATGGGCTT
CTAGATGTTGAGTCCTAGAAGCTCTCAACATCTCTTCTTAATTGGAGAAAGTGTTAAGCCCCAA
AGTAGCTGGAGCAGTACATCTTCAATTTTTGACAAGAAAGCAGGAACTTGGTTACTTTGAGTGT
TATTCATTAGTTTCTGCTTTCATTGAGAATGCAGCAAAAGCCAACGAGGCTGCTGCTAACTCCT
TGCTGGACATCTTCTGCCACTATCACAGGAACTGTGATCTCACTGGACAATTAACTAGGGAGCC
TTTCATCTTGAATGACTGCTGCACAAATGATCTTCAAAGCATTTTAGCCACCAGAGGAATTCTC
TTCAAATACCCAAAATCCATCAGTATCTTGAATCATGCTGGATTTTGAAGAATTCTTAACAAGC
CATGTAAAGGGGGCTCTCTGGCCTTGAAATAGTGATGTTTTTTATACAGAAAGGAGAATGCCGA
ATGTTCAGACTACCATGCACTGTTAAATTTGATTTCAAGAAATTACAGGAAAACTTTCCAAAGT
TCCGTCTCACAGAATTTATTTTTACAAAGAATTCCAAGATAAGTTTAGTTTTATGGAAGATTTT
TATGTGGTTTTTACTCACTCTTCATCTCAGACATCAACCGATGATTACATCACTTATTTAGCTA
GTAAATTTATTAATATAAAACTCAGAGACATTCCAATATCCACATTGCTTACATCATCAGGCAT
AGATTCAATGTCAGCTATGACAATTGAAAATAAGCTGTTTTGTGATTTAAAGGTTTAAATTTCT
CTAACCAAACAGCTTGATCCAGATGCAGCACTGCAAATGTTAATATTTGTTCTGGAAGAGCAAT
CAAATAAGACTTAAGAGGAAAAGGAATGGCCACAATCCACCTGAAATTTTTTTTAAAAAAGTAT
GCAGCCTACTAAATCAGAATGAAAATAGAAGTACAAGATTATAAACAAAATGCAATCAAACTTT
TCTTAAGCTTACCTAAAGTTATTTTATCTGAAAATTTCAAGCAACTTTGATCAACATTAAATTG
ACAATCTAAACTAACAAGTCTTTTGAATTTATGTATGGTAGTAAACATTCTCTCTATTAATTTT
ATTACCTAAGGCTAAACCTAAAATTTTTAAGCAAAATTAGAAAGTCTTCACTTATCAAAAAATA
AAGTTTGTTACATTTAGTATTTTCCCAATAAAATTGGTCATTCTTGGTTTTTTATTTGGAGAAT
CTGTGCAAAATTTCACTGAAAATAAATTAGAACTAGAAATTATTTCTAAATACCAAAAAAAAAA
TGAAGAATGGTTTCACAAAGAAAAAAAGAAAACTTGCTTAATTAGCAGAGTATCATCTCTGTGA
TTTTTGTGATTATTTGATCAGTGTCCTGAGATGGATACAATGGCAAGTAATGACAAAATTAAAA
TAAGCATGCAGATTTTTTTAAATTAAGTGCCAAAAAATAATTGGTCATGCAAAGCCCTTAAAAA
TATTGTGGCCTAATTCTAAAGTTTTTTGCTACTATGCTACATCACACGCAACATCAGTTAAGTG
CTCATTCTGTGACAGGTAGTACATTACATTTTAGCAAACTACACAAGACCCCTATGTGATAATA
TGCTTCAGGGTTGTAAGGTTGGGTGCATTTACTAGTCTTGAATTTTCTGGGAGTATACAAACCC
AATATTAGTCTAGATGCCCACAAATCTATTTAGACGTCACAGTAGAATGGAGAGTAATCTTGAC
CACAGGAAGCTGTGTTGTGGCATTTATTTTGAAATTATTTTTTCTTGATTTTTTTGCCTTTTGT
TTTGTGAGTTTTATAATGTACAGAATATTTTTAAATTATTATATATATCAACTAATTAGTCTTC
ATTTAAACTTACGCCTCTGGGGTCTTACTTGGGTTTCTCCTAACAATATTATACACATATTTGC
AATAATTTCTCTCATACTGCTTTTAACTCATTTAATTTTTCAACTTTTTAAGAATAACAAAAGT
GATATTAATTGTAAAAATGCTGAAGTGACATATGAATTTATGAAGTGCATATGTATTTTTTAGT
TTACCAATGAGATGGGAGAAATGCTGTCTTATATTTTAACATACATTTTGGCCATTACACAGAT
GAAGCAACTTTTCATTTGTTAATACATAATGCATACTTTTTCTTCTGTGCAATTCCTCTTTGTA
TTCTTTGCTCATTTTCCCACTGGGATTTGCAAGTTCTTTATTATTTGATAATCTCTATACATTC
TGAATATCAATTTTTTGTTATATATACCATGTAAATATTTTCTTCTAATTTGTTATTTGTCTTT
TAATGGTATTTATCAATTGTTTGCTAAAAATGAGTTTGTTTAGTTAGTAAAATTTGTCTATCTT
TAACTTCATGATATTTGTATATCATGTCATGAGGAAAAGGCATGAATATTTTAAAAACTTCCTT
GTAGTGTTAATTTTATTTTTTATTTCATTCTTTAAGTTATTTGAAATTTATTGTTTATTTCTTC
AAATTCCAAATAATAACCAACTTTCTCAAAGCAATACTTCTTTCTACTGATTTCAAACGTTACA
TTTGTCTTCTCTGAAGTTCTTGTTTTTTTGATACCTGACTGTCACACTACTGCTGTGGATGTGC
TTCATACCATCACAGTACTGCAGGGTTATAAGATTATCTGATAGCCAATAGAAGCAGACGTCTA
CTCACTGTCATTCTTTTGTCTTTTGGAGAATAAAGTTAGCTATTTTTA

hide sequence

RefSeq Acc Id:

NR_149016

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	131,682,499 - 131,699,850 (+)	NCBI
T2T-CHM13v2.0	2	132,117,144 - 132,134,495 (+)	NCBI

Sequence:

show sequence

AGTTCCTGCGACGCCCCTGCAGCAGCAGCAGCGTGGTCAGAGCGAGCTTCTGAGCGGTGGTGGG
TTCCATGTGATGGTGGAGTAGGAGACAGGTCTCCGCGGTCAGTGGCGGGGGCGTGGACCCCACC
GGGAACCCTCCCTGCTCCTTCCCTGCCTCTCCCTGTTTTCGTGCCCGCACTTCTTCGTGGGCAT
CTGGGCCCGAGTCCTCCGCTTGGGGGCGGTTGTGCGGTCCTGGCTACTGCAGCGTCCGCACCCC
GGCCGGGAAGGCTATGCCAATGTCCGACCCGCGTCCAGCGTATAGGAGCGCCCTGGCCCACAGC
TGGCGGTAAAACGCGGGACCTGGGTCCCTCGGAGCCCCAGGGGCCTCTGAGCTGGAGTCTAGGA
TTATTTTTGATGCCTCAGCACCTTTAAAAAGAGACCTCGCTAGAGCAGGGGGCATCTGTATTTT
CAGTTCTTTGAGGAGTCTCCAGCTATTTAGCTGTTTTCCATGGTTCATCTGCGTTGCTCTAAAT
GGGACTGTTTCATTATTTTGATGGCTGAAGAATATTTCCTAGTGTATGTATATGAGAGTTTCTT
GATCTCTTTATCTGTGGATGAACAGCTACTTTGAAATATATGATACATTTGTGTTAAGGCTAGT
CACGCTGCTGTGGAATAGAAGGCCAGAATTGATCACTATCATCTGAGAGTAACTTTGTACCCAT
CACTGATTCCTTCCGAGACTGCCTCCACTTCCCCAGCAGCCTCTGATTTCTTCATGTGGCTGCA
GATGGCAGGATTTCCCAAAGGTTTATGGCTGCAACATATTCCGTGGTGTATCTGTACAGCAGTT
TCCTCATTCCTGCAGCTGTGTTTGAACAGGTCATTTACCATGCGGTCCTCCAGGTTCAACAGTA
TGGCTCCAAATGATGAAATTTCATTCTGATTTTCTGGCTGAAGACTATTCTGTTTGTGTATGTC
CACCACAGTTACTTTATCCCTTCATCTGTGGATGGGCAGGAAACTCCAAACTGTCCAAGGGATA
GTTCTGTTGTGATTACTTCATTGAGAAATTTAACTTATGAGCAGTTGAAAGGAATGCAAGTTGC
TGGAAAATCAGAATGAAGAGTGCAAAATGACCAAGCTACAATGTATTGTCATTATTCACTCTGA
TGTGAAAAAGGCAGTGAATTCAATAGAAAATAACTTTGCAGAATAAAATCTCAGGTGTGTTTTT
TTAGTGCCACAGTCTTGGATGATGGGCTTCTAGATGTTGAGTCCTAGAAGCTCTCAACATCTCT
TCTTAATTGGAGAAAGTGTTAAGCCCCAAAGTAGCTGGAGCAGTACATCTTCAATTTTTGACAA
GAAAGCAGGAACTTGGTTACTTTGAGTGTTATTCATTAGTTTCTGCTTTCATTGAGAATGCAGC
AAAAGCCAACGAGGCTGCTGCTAACTCCTTGCTGGACATCTTCTGCCACTATCACAGGAACTGT
GATCTCACTGGACAATTAACTAGGGAGCCTTTCATCTTGAATGACTGCTGCACAAATGATCTTC
AAAGCATTTTAGCCACCAGAGGAATTCTCTTCAAATACCCAAAATCCATCAGTATCTTGAATCA
TGCTGGATTTTGAAGAATTCTTAACAAGCCATGTAAAGGGGGCTCTCTGGCCTTGAAATAGTGA
TGTTTTTTATACAGAAAGGAGAATGCCGAATGTTCAGACTACCATGCACTGTTAAATTTGATTT
CAAGAAATTACAGGAAAACTTTCCAAAGTTCCGTCTCACAGAATTTATTTTTACAAAGAATTCC
AAGATAAGTTTAGTTTTATGGAAGATTTTTATGTGGTTTTTACTCACTCTTCATCTCAGACATC
AACCGATGATTACATCACTTATTTAGCTAGTAAATTTATTAATATAAAACTCAGAGACATTCCA
ATATCCACATTGCTTACATCATCAGGCATAGATTCAATGTCAGCTATGACAATTGAAAATAAGC
TGTTTTGTGATTTAAAGGTTTAAATTTCTCTAACCAAACAGCTTGATCCAGATGCAGCACTGCA
AATGTTAATATTTGTTCTGGAAGAGCAATCAAATAAGACTTAAGAGGAAAAGGAATGGCCACAA
TCCACCTGAAATTTTTTTTAAAAAAGTATGCAGCCTACTAAATCAGAATGAAAATAGAAGTACA
AGATTATAAACAAAATGCAATCAAACTTTTCTTAAGCTTACCTAAAGTTATTTTATCTGAAAAT
TTCAAGCAACTTTGATCAACATTAAATTGACAATCTAAACTAACAAGTCTTTTGAATTTATGTA
TGGTAGTAAACATTCTCTCTATTAATTTTATTACCTAAGGCTAAACCTAAAATTTTTAAGCAAA
ATTAGAAAGTCTTCACTTATCAAAAAATAAAGTTTGTTACATTTAGTATTTTCCCAATAAAATT
GGTCATTCTTGGTTTTTTATTTGGAGAATCTGTGCAAAATTTCACTGAAAATAAATTAGAACTA
GAAATTATTTCTAAATACCAAAAAAAAAATGAAGAATGGTTTCACAAAGAAAAAAAGAAAACTT
GCTTAATTAGCAGAGTATCATCTCTGTGATTTTTGTGATTATTTGATCAGTGTCCTGAGATGGA
TACAATGGCAAGTAATGACAAAATTAAAATAAGCATGCAGATTTTTTTAAATTAAGTGCCAAAA
AATAATTGGTCATGCAAAGCCCTTAAAAATATTGTGGCCTAATTCTAAAGTTTTTTGCTACTAT
GCTACATCACACGCAACATCAGTTAAGTGCTCATTCTGTGACAGGTAGTACATTACATTTTAGC
AAACTACACAAGACCCCTATGTGATAATATGCTTCAGGGTTGTAAGGTTGGGTGCATTTACTAG
TCTTGAATTTTCTGGGAGTATACAAACCCAATATTAGTCTAGATGCCCACAAATCTATTTAGAC
GTCACAGTAGAATGGAGAGTAATCTTGACCACAGGAAGCTGTGTTGTGGCATTTATTTTGAAAT
TATTTTTTCTTGATTTTTTTGCCTTTTGTTTTGTGAGTTTTATAATGTACAGAATATTTTTAAA
TTATTATATATATCAACTAATTAGTCTTCATTTAAACTTACGCCTCTGGGGTCTTACTTGGGTT
TCTCCTAACAATATTATACACATATTTGCAATAATTTCTCTCATACTGCTTTTAACTCATTTAA
TTTTTCAACTTTTTAAGAATAACAAAAGTGATATTAATTGTAAAAATGCTGAAGTGACATATGA
ATTTATGAAGTGCATATGTATTTTTTAGTTTACCAATGAGATGGGAGAAATGCTGTCTTATATT
TTAACATACATTTTGGCCATTACACAGATGAAGCAACTTTTCATTTGTTAATACATAATGCATA
CTTTTTCTTCTGTGCAATTCCTCTTTGTATTCTTTGCTCATTTTCCCACTGGGATTTGCAAGTT
CTTTATTATTTGATAATCTCTATACATTCTGAATATCAATTTTTTGTTATATATACCATGTAAA
TATTTTCTTCTAATTTGTTATTTGTCTTTTAATGGTATTTATCAATTGTTTGCTAAAAATGAGT
TTGTTTAGTTAGTAAAATTTGTCTATCTTTAACTTCATGATATTTGTATATCATGTCATGAGGA
AAAGGCATGAATATTTTAAAAACTTCCTTGTAGTGTTAATTTTATTTTTTATTTCATTCTTTAA
GTTATTTGAAATTTATTGTTTATTTCTTCAAATTCCAAATAATAACCAACTTTCTCAAAGCAAT
ACTTCTTTCTACTGATTTCAAACGTTACATTTGTCTTCTCTGAAGTTCTTGTTTTTTTGATACC
TGACTGTCACACTACTGCTGTGGATGTGCTTCATACCATCACAGTACTGCAGGGTTATAAGATT
ATCTGATAGCCAATAGAAGCAGACGTCTACTCACTGTCATTCTTTTGTCTTTTGGAGAATAAAG
TTAGCTATTTTTA

hide sequence

RefSeq Acc Id:

NR_167887

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	131,682,499 - 131,767,404 (+)	NCBI
T2T-CHM13v2.0	2	132,117,144 - 132,202,925 (+)	NCBI

Sequence:

show sequence

AGTTCCTGCGACGCCCCTGCAGCAGCAGCAGCGTGGTCAGAGCGAGCTTCTGAGCGGTGGTGGG
TTCCATGTGATGGTGGAGTAGGAGACAGGTCTCCGCGGTCAGTGGCGGGGGCGTGGACCCCACC
GGGAACCCTCCCTGCTCCTTCCCTGCCTCTCCCTGTTTTCGTGCCCGCACTTCTTCGTGGGCAT
CTGGGCCCGAGTCCTCCGCTTGGGGGCGGTTGTGCGGTCCTGGCTACTGCAGCGTCCGCACCCC
GGCCGGGAAGGCTATGCCAATGTCCGACCCGCGTCCAGCGTATAGGAGCGCCCTGGCCCACAGC
TGGCGGTAAAACGCGGGACCTGGGTCCCTCGGAGCCCCAGGGGCCTCTGAGCTGGAGTCTAGGA
TTATTTTTGATGCCTCAGCACCTTTAAAAAGAGACCTCGCTAGAGCAGGGGGCATCTGTATTTT
CAGTTCTTTGAGGAGTCTCCAGCTATTTAGCTGTTTTCCATGGTTCATCTGCGTTGCTCTAAAT
GGGACTGTTTCATTATTTTGATGGCTGAAGAATATTTCCTAGTGTATGTATATGAGAGTTTCTT
GATCTCTTTATCTGTGGATGAACAGCTACTTTGAAATATATGATACATTTGTGTTAAGGCTAGT
CACGCTGCTGTGGAATAGAAGGCCAGAATTGATCACTATCATCTGAGAGTAACTTTGTACCCAT
CACTGATTCCTTCCGAGACTGCCTCCACTTCCCCAGCAGCCTCTGATTTCTTCATGTGGCTGCA
GATGGCAGGATTTCCCAAAGGTTTATGGCTGCAACATATTCCGTGGTGTATCTGTACAGCAGTT
TCCTCATTCCTGCAGCTGTGTTTGAACAGGTCATTTACCATGCGGTCCTCCAGGTTCAACAGTA
TGGCTCCAAATGATGAAATTTCATTCTGATTTTCTGGCTGAAGACTATTCTGTTTGTGTATGTC
CACCACAGTTACTTTATCCCTTCATCTGTGGATGGGCAGTTGGTTGGCAGAGAATTTGAACTGG
AGATGAACTTTATTATCCAGGATGCTGAGAGTATAACATGCATGACAGAGCTTTTAGAGCACTG
TGATGTAACATGTCAAGCAGAAATAGGGAGCATGTTTACAGCCATTCTATGAAAAAGTGTTCGG
AATGTACAGACTAGCACAGAAGCTGGACTAATTGAACAAGTATTGCTGAAAATGAGTGCTGTAG
ATGACATGATAGCAGAGTACCTTCAAGTTTAAATCTGAGAGTGATATTCATTTGGCAGAACATC
ATAAACAGGTTTTGTATGATGGGAAACTTGCAAGTAGCATTACCTTTACATATACTGCTAAGGC
CACTGATGCTCAACTCTGCCTGGAATCATCACCAAAAGAGAATGCATCAATTTTTGTGCATTCC
CAACATGCTCTAATGCTTCAGATTCAAGTGCTTTTTCCACTGTTTCCCCAATTGGATAATCGGC
AGCTCAATGACAGTCAAGTGGAAACAACTGTCTGCTCCTGCTTCAGGTGCAGAAATACAGCGAT
TTCCAGTGCCAGCTGTTGAGCCAGTGCCAGCACCAGGGGCAGATTCCCCTCCAGGGACAGCGCT
GGAGCTAGAGGAAGCTCCAGAGCCCTCCTGCCGCTGCCCTGGGACTGCCCAGGACCAGCCCAGT
GAGGAGCTGCCTGACTTCATGGCACCTCCTGTAGAGCCACCGGCCTCAGCCCTGGAGCTGAAAG
TGTGGCTGGAGCTAGAGGTGGCAGAGAGGGGTGGCCAGCACAGCTCCAGCCAGCAGCTCCCACA
CTGCTCCCAGTCCTGGGCACAGTGGAAGCTATGGAGGCAGAGACCAGGGTTTGCAATCTGGGCT
CCTCTGCCTCACTGGAGAGGGACTTCTCTCATTCAGCAGAGCAGCAGCCCTGCTGCTGAAGGGC
CTGCTGCTACTGCTGCTGGGGCTGTTTGCCTGCCTGCAGGAGGTGCTGGAGAGCAAGAAAAGGA
GCCTGTGAGCAGGGGTTCCAGCAGGTCCTCCTGCTCCCAGAGGCGACCTCCTCCTCCAGGCATG
GAGGTTTGCCCTCAGCTGGGCATCTGGGCCATTTGCCCCTAACGTGCTGCCCAGGATGGCCTCC
TCTTGACAGGCGGACAGGGGGTGAGGGGGCCAGGGGGCATCTCCAAAGGAAGCTTTTAAACTCA
GCAGCTGCACCCCAGAATCTGTATGCCTGCACCTGCCCAAGGATTTATTCATAGCTTACCTAAG
AATTTCAAATTTCTACCATAACACTGAATAAAGTTTGACTTTTTGAAACTTC

hide sequence

RefSeq Acc Id:

NR_167888

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	131,682,499 - 131,767,404 (+)	NCBI
T2T-CHM13v2.0	2	132,117,144 - 132,202,925 (+)	NCBI

Sequence:

show sequence

AGTTCCTGCGACGCCCCTGCAGCAGCAGCAGCGTGGTCAGAGCGAGCTTCTGAGCGGTGGTGGG
TTCCATGTGATGGTGGAGTAGGAGACAGGTCTCCGCGGTCAGTGGCGGGGGCGTGGACCCCACC
GGGAACCCTCCCTGCTCCTTCCCTGCCTCTCCCTGTTTTCGTGCCCGCACTTCTTCGTGGGCAT
CTGGGCCCGAGTCCTCCGCTTGGGGGCGGTTGTGCGGTCCTGGCTACTGCAGCGTCCGCACCCC
GGCCGGGAAGGCTATGCCAATGTCCGACCCGCGTCCAGCGTATAGGAGCGCCCTGGCCCACAGC
TGGCGGTAAAACGCGGGACCTGGGTCCCTCGGAGCCCCAGGGGCCTCTGAGCTGGAGTCTAGGA
TTATTTTTGATGCCTCAGCACCTTTAAAAAGAGACCTCGCTAGAGCAGGGGGCATCTGTATTTT
CAGTTCTTTGAGGAGTCTCCAGCTATTTAGCTGTTTTCCATGGTTCATCTGCGTTGCTCTAAAT
GGGACTGTTTCATTATTTTGATGGCTGAAGAATATTTCCTAGTGTATGTATATGAGAGTTTCTT
GATCTCTTTATCTGTGGATGAACAGCTACTTTGAAATATATGATACATTTGTGTTAAGGCTAGT
CACGCTGCTGTGGAATAGAAGGCCAGAATTGATCACTATCATCTGAGAGTAACTTTGTACCCAT
CACTGATTCCTTCCGAGACTGCCTCCACTTCCCCAGCAGCCTCTGATTTCTTCATGTGGCTGCA
GATGGCAGGATTTCCCAAAGGTTTATGGCTGCAACATATTCCGTGGTGTATCTGTACAGCAGTT
TCCTCATTCCTGCAGCTGTGTTTGAACAGGTCATTTACCATGCGGTCCTCCAGGTTCAACAGTA
TGGCTCCAAATGATGAAATTTCATTCTGATTTTCTGGCTGAAGACTATTCTGTTTGTGTATGTC
CACCACAGTTACTTTATCCCTTCATCTGTGGATGGGCAGTTGGTTGGCAGAGAATTTGAACTGG
AGATGAACTTTATTATCCAGGATGCTGAGAGTATAACATGCATGACAGAGCTTTTAGAGCACTG
TGATGTAACATGTCAAGCAGAAATAGGGAGCATGTTTACAGCCATTCTATGAAAAAGTGTTCGG
AATGTACAGACTAGCACAGAAGCTGGACTAATTGAACAAGTATTGCTGAAAATGAGTGCTGTAG
ATGACATGATAGCAGTGGTACATGATCAGCATTGTCCACATTTACAATCGATGGAGAAACAGTG
AAATTCAGTGTTATGTTAATGGACAACTGGTATCTTATGGTGATATGGCTTGGCATGTTAACAC
AAATGACAGTACCTTCAAGTTTAAATCTGAGAGTGATATTCATTTGGCAGAACATCATAAACAG
GTTTTGTATGATGGGAAACTTGCAAGTAGCATTACCTTTACATATACTGCTAAGGCCACTGATG
CTCAACTCTGCCTGGAATCATCACCAAAAGAGAATGCATCAATTTTTGTGCATTCCCAACATGC
TCTAATGCTTCAGATTCAAGTGCTTTTTCCACTGTTTCCCCAATTGGATAATCGGCAGCTCAAT
GACAGTCAAGTGGAAACAACTGTCTGCTCCTGCTTCAGGTGCAGAAATACAGCGATTTCCAGTG
CCAGCTGTTGAGCCAGTGCCAGCACCAGGGGCAGATTCCCCTCCAGGGACAGCGCTGGAGCTAG
AGGAAGCTCCAGAGCCCTCCTGCCGCTGCCCTGGGACTGCCCAGGACCAGCCCAGTGAGGAGCT
GCCTGACTTCATGGCACCTCCTGTAGAGCCACCGGCCTCAGCCCTGGAGCTGAAAGTGTGGCTG
GAGCTAGAGGTGGCAGAGAGGGGTGGCCAGCACAGCTCCAGCCAGCAGCTCCCACACTGCTCCC
AGTCCTGGGCACAGTGGAAGCTATGGAGGCAGAGACCAGGGTTTGCAATCTGGGCTCCTCTGCC
TCACTGGAGAGGGACTTCTCTCATTCAGCAGAGCAGCAGCCCTGCTGCTGAAGGGCCTGCTGCT
ACTGCTGCTGGGGCTGTTTGCCTGCCTGCAGGAGGTGCTGGAGAGCAAGAAAAGGAGCCTGTGA
GCAGGGGTTCCAGCAGGTCCTCCTGCTCCCAGAGGCGACCTCCTCCTCCAGGCATGGAGGTTTG
CCCTCAGCTGGGCATCTGGGCCATTTGCCCCTAACGTGCTGCCCAGGATGGCCTCCTCTTGACA
GGCGGACAGGGGGTGAGGGGGCCAGGGGGCATCTCCAAAGGAAGCTTTTAAACTCAGCAGCTGC
ACCCCAGAATCTGTATGCCTGCACCTGCCCAAGGATTTATTCATAGCTTACCTAAGAATTTCAA
ATTTCTACCATAACACTGAATAAAGTTTGACTTTTTGAAACTTC

hide sequence

RefSeq Acc Id:

NR_167889

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	131,682,499 - 131,767,404 (+)	NCBI
T2T-CHM13v2.0	2	132,117,144 - 132,202,925 (+)	NCBI

Sequence:

show sequence

AGTTCCTGCGACGCCCCTGCAGCAGCAGCAGCGTGGTCAGAGCGAGCTTCTGAGCGGTGGTGGG
TTCCATGTGATGGTGGAGTAGGAGACAGGTCTCCGCGGTCAGTGGCGGGGGCGTGGACCCCACC
GGGAACCCTCCCTGCTCCTTCCCTGCCTCTCCCTGTTTTCGTGCCCGCACTTCTTCGTGGGCAT
CTGGGCCCGAGTCCTCCGCTTGGGGGCGGTTGTGCGGTCCTGGCTACTGCAGCGTCCGCACCCC
GGCCGGGAAGGCTATGCCAATGTCCGACCCGCGTCCAGCGTATAGGAGCGCCCTGGCCCACAGC
TGGCGGTAAAACGCGGGACCTGGGTCCCTCGGAGCCCCAGGGGCCTCTGAGCTGGAGTCTAGGA
TTATTTTTGATGCCTCAGCACCTTTAAAAAGAGACCTCGCTAGAGCAGGGGGCATCTGTATTTT
CAGTTCTTTGAGGAGTCTCCAGCTATTTAGCTGTTTTCCATGGTTCATCTGCGTTGCTCTAAAT
GGGACTGTTTCATTATTTTGATGGCTGAAGAATATTTCCTAGTGTATGTATATGAGAGTTTCTT
GATCTCTTTATCTGTGGATGAACAGCTACTTTGAAATATATGATACATTTGTGTTAAGGCTAGT
CACGCTGCTGTGGAATAGAAGGCCAGAATTGATCACTATCATCTGAGAGTAACTTTGTACCCAT
CACTGATTCCTTCCGAGACTGCCTCCACTTCCCCAGCAGCCTCTGATTTCTTCATGTGGCTGCA
GATGGCAGGATTTCCCAAAGGTTTATGGCTGCAACATATTCCGTGGTGTATCTGTACAGCAGTT
TCCTCATTCCTGCAGCTGTGTTTGAACAGGTCATTTACCATGCGGTCCTCCAGGTTCAACAGTA
TGGCTCCAAATGATGAAATTTCATTCTGATTTTCTGGCTGAAGACTATTCTGTTTGTGTATGTC
CACCACAGTTACTTTATCCCTTCATCTGTGGATGGGCAGTTGGTTGGCAGAGAATTTGAACTGG
AGATGAACTTTATTATCCAGGATGCTGAGAGTATAACATGCATGACAGAGCTTTTAGAGCACTG
TGATGTAACATGTCAAGCAGAAATAGGGAGCATGTTTACAGCCATTCTATGAAAAAGTGTTCGG
AATGTACAGACTAGCACAGAAGCTGGACTAATTGAACAAGTATTGCTGAAAATGAGTGCTGTAG
ATGACATGATAGCAGAGTACCTTCAAGTTTAAATCTGAGAGTGATATTCATTTGGCAGAACATC
ATAAACAGGTTTTGTATGATGGGAAACTTGCAAGTAGCATTACCTTTACATATACTGCTAAGGC
CACTGATGCTCAACTCTGCCTGGAATCATCACCAAAAGAGAATGCATCAATTTTTGTGCATTCC
CAACATGCTCTAATGCTTCAGATTCAAGTGCTTTTTCCACTGTTTCCCCAATTGGATAATCGGC
AGCTCAATGACAGTCAAGTGGAAACAACTGTCTGGGGCCTAATGTCCACCTAAGACGTGGTGTT
CACCTGGGGTCTGATGTTCAGCTGAAGACTGGATGTCCACCTGGAGCTGAGGAATCCACCCAGG
GACTGGTGTTGAACTGGGGCCTGATGACCACCGGGGGACAAGGTATCCACACCAGGCTTGATGT
CCACCTGTCACCAGATGTCTACCTCCTGCTTCAGGTGCAGAAATACAGCGATTTCCAGTGCCAG
CTGTTGAGCCAGTGCCAGCACCAGGGGCAGATTCCCCTCCAGGGACAGCGCTGGAGCTAGAGGA
AGCTCCAGAGCCCTCCTGCCGCTGCCCTGGGACTGCCCAGGACCAGCCCAGTGAGGAGCTGCCT
GACTTCATGGCACCTCCTGTAGAGCCACCGGCCTCAGCCCTGGAGCTGAAAGTGTGGCTGGAGC
TAGAGGTGGCAGAGAGGGGTGGCCAGCACAGCTCCAGCCAGCAGCTCCCACACTGCTCCCAGTC
CTGGGCACAGTGGAAGCTATGGAGGCAGAGACCAGGGTTTGCAATCTGGGCTCCTCTGCCTCAC
TGGAGAGGGACTTCTCTCATTCAGCAGAGCAGCAGCCCTGCTGCTGAAGGGCCTGCTGCTACTG
CTGCTGGGGCTGTTTGCCTGCCTGCAGGAGGTGCTGGAGAGCAAGAAAAGGAGCCTGTGAGCAG
GGGTTCCAGCAGGTCCTCCTGCTCCCAGAGGCGACCTCCTCCTCCAGGCATGGAGGTTTGCCCT
CAGCTGGGCATCTGGGCCATTTGCCCCTAACGTGCTGCCCAGGATGGCCTCCTCTTGACAGGCG
GACAGGGGGTGAGGGGGCCAGGGGGCATCTCCAAAGGAAGCTTTTAAACTCAGCAGCTGCACCC
CAGAATCTGTATGCCTGCACCTGCCCAAGGATTTATTCATAGCTTACCTAAGAATTTCAAATTT
CTACCATAACACTGAATAAAGTTTGACTTTTTGAAACTTC

hide sequence

Protein Sequences


GenBank Protein	AAB97362	(Get FASTA)	NCBI Sequence Viewer
	AAH93716	(Get FASTA)	NCBI Sequence Viewer
	AAI12190	(Get FASTA)	NCBI Sequence Viewer
	AAX82001	(Get FASTA)	NCBI Sequence Viewer
	EAX11684	(Get FASTA)	NCBI Sequence Viewer
	EAX11685	(Get FASTA)	NCBI Sequence Viewer
	EAX11686	(Get FASTA)	NCBI Sequence Viewer

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P0DPF5-F1-model_v2	AlphaFold	P0DPF5	1-203	view protein structure

Additional Information

External Database Links

Database	Acc Id	Source(s)
COSMIC	LINC03124	COSMIC
Ensembl Genes	ENSG00000197927	Ensembl
	ENSG00000287151	Ensembl, ENTREZGENE
Ensembl Transcript	ENST00000666411	ENTREZGENE
	ENST00000779776	ENTREZGENE
	ENST00000779785	ENTREZGENE
	ENST00000779795	ENTREZGENE
	ENST00000779799	ENTREZGENE
	ENST00000779869	ENTREZGENE
GTEx	ENSG00000197927	GTEx
	ENSG00000287151	GTEx
HGNC ID	HGNC:25077	ENTREZGENE
Human Proteome Map	LINC03124	Human Proteome Map
NCBI Gene	29798	ENTREZGENE
PharmGKB	PA164717121	PharmGKB
RNAcentral	URS0000EEFC63	RNACentral
	URS0000EF108F	RNACentral
	URS0000EF50A1	RNACentral
	URS0000EF61C6	RNACentral
	URS0000EF6DF6	RNACentral
	URS0001BBE3B9	RNACentral
	URS0001BBE3BD	RNACentral
	URS0001BBE41A	RNACentral
	URS0001BBE460	RNACentral
	URS0001BBE518	RNACentral
	URS0001BBE531	RNACentral
	URS0001BBE5F0	RNACentral
	URS0002180AAA	RNACentral

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2023-12-25	LINC03124	long intergenic non-protein coding RNA 3124	C2orf27A	chromosome 2 open reading frame 27A	Symbol and/or name change	19259463	PROVISIONAL

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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