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Gene: LINC01599 (long intergenic non-protein coding RNA 1599) Homo sapiens

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Analyze

Symbol:

LINC01599 (Ensembl: LINC01588)

Name:

long intergenic non-protein coding RNA 1599 (Ensembl:long intergenic non-protein coding RNA 1588)

RGD ID:

1602424

HGNC Page

HGNC:27285

Description:

ASSOCIATED WITH Brain-Lung-Thyroid Syndrome; L-2-hydroxyglutaric aciduria; L-2-hydroxyglutaric aciduria; INTERACTS WITH aflatoxin B1; Aflatoxin B2 alpha; benzo[a]pyrene

Type:

ncrna (Ensembl: lncRNA)

RefSeq Status:

VALIDATED

Previously known as:

C14orf183; putative uncharacterized protein C14orf183

RGD Orthologs

Bonobo

Green Monkey

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	14	50,007,313 - 50,105,043 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	49,927,213 - 50,105,121 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	50,474,031 - 50,571,761 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	49,620,119 - 49,629,111 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	14	30,417,514 - 30,426,499 (-)	NCBI		Celera
Cytogenetic Map	14	q21.3	NCBI
HuRef	14	30,675,796 - 30,684,781 (-)	NCBI		HuRef
CHM1_1	14	50,489,049 - 50,498,037 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	14	44,212,500 - 44,311,279 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
LINC01599	Human	Brain-Lung-Thyroid Syndrome		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Brain-lung-thyroid syndrome	ClinVar	PMID:25741868
LINC01599	Human	L-2-hydroxyglutaric aciduria		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: L-2-hydroxyglutaric aciduria	ClinVar	PMID:15385440

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
LINC01599	Human	aflatoxin B1	decreases methylation	EXP		6480464	Aflatoxin B1 results in decreased methylation of LINC01599 intron	CTD	PMID:30157460
LINC01599	Human	Aflatoxin B2 alpha	increases methylation	EXP		6480464	aflatoxin B2 results in increased methylation of LINC01599 intron	CTD	PMID:30157460
LINC01599	Human	benzo[a]pyrene	affects methylation	EXP		6480464	Benzo(a)pyrene affects the methylation of LINC01599 intron	CTD	PMID:30157460
LINC01599	Human	benzo[a]pyrene	increases methylation	EXP		6480464	Benzo(a)pyrene results in increased methylation of LINC01599 exon	CTD	PMID:27901495

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
LINC01599	Human	L-2-hydroxyglutaric aciduria		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: L-2-hydroxyglutaric aciduria	ClinVar	PMID:15385440

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations

PMID:12477932	PMID:16344560	PMID:19490893	PMID:31343991	PMID:34535262

LINC01599
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	14	50,007,313 - 50,105,043 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	49,927,213 - 50,105,121 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	50,474,031 - 50,571,761 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	49,620,119 - 49,629,111 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	14	30,417,514 - 30,426,499 (-)	NCBI		Celera
Cytogenetic Map	14	q21.3	NCBI
HuRef	14	30,675,796 - 30,684,781 (-)	NCBI		HuRef
CHM1_1	14	50,489,049 - 50,498,037 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	14	44,212,500 - 44,311,279 (-)	NCBI		T2T-CHM13v2.0

LOC100980742
(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	15	51,217,726 - 51,235,381 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	14	50,434,230 - 50,449,397 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	14	30,671,031 - 30,680,109 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	14	48,976,894 - 48,986,232 (-)	NCBI	panpan1.1	PanPan1.1	panPan2

LOC103229896
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	24	27,145,235 - 27,156,062 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666053	15,477,939 - 15,488,343 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Variants in LINC01599
5 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 14q21.3-22.1(chr14:50091150-51777325)x3	copy number gain	See cases [RCV000052059]	Chr14:50091150..51777325 [GRCh38] Chr14:50557868..52244043 [GRCh37] Chr14:49627618..51313793 [NCBI36] Chr14:14q21.3-22.1	uncertain significance
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3	copy number gain	See cases [RCV000135543]	Chr14:20151149..106855263 [GRCh38] Chr14:20619308..107263478 [GRCh37] Chr14:19689148..106334523 [NCBI36] Chr14:14q11.2-32.33	pathogenic
GRCh38/hg38 14q21.1-22.3(chr14:39196172-56714461)x3	copy number gain	See cases [RCV000140717]	Chr14:39196172..56714461 [GRCh38] Chr14:39665376..57181179 [GRCh37] Chr14:38735127..56250932 [NCBI36] Chr14:14q21.1-22.3	likely pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3	copy number gain	See cases [RCV000143373]	Chr14:20043514..106877229 [GRCh38] Chr14:20511673..107285437 [GRCh37] Chr14:19581513..106356482 [NCBI36] Chr14:14q11.2-32.33	pathogenic
L2HGDH, EX1-9DEL	deletion	L-2-hydroxyglutaric aciduria [RCV000001678]	Chr14:50000000..50247254 [GRCh38] Chr14:14q21.3	pathogenic
GRCh37/hg19 14q11.2-22.2(chr14:23164384-54733411)x3	copy number gain	See cases [RCV000447658]	Chr14:23164384..54733411 [GRCh37] Chr14:14q11.2-22.2	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3	copy number gain	See cases [RCV000446256]	Chr14:19794561..107234280 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437)	copy number gain	See cases [RCV000512041]	Chr14:20511673..107285437 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3	copy number gain	not provided [RCV000738412]	Chr14:19000422..107289053 [GRCh37] Chr14:14q11.1-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3	copy number gain	not provided [RCV000738413]	Chr14:19280733..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3	copy number gain	not provided [RCV000738414]	Chr14:19327823..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
NC_000014.8:g.(?_50092240)_(50698021_?)dup	duplication	Noonan syndrome 9 [RCV000799423]	Chr14:49625522..50231303 [GRCh38] Chr14:50092240..50698021 [GRCh37] Chr14:14q21.3	uncertain significance
GRCh37/hg19 14q21.3-22.1(chr14:50317272-51627752)x3	copy number gain	not provided [RCV001006632]	Chr14:50317272..51627752 [GRCh37] Chr14:14q21.3-22.1	uncertain significance
NC_000014.8:g.(21162263_36986276)_(36987308_50713602)del	deletion	Brain-lung-thyroid syndrome [RCV002221171]	Chr14:36986276..36987308 [GRCh37] Chr14:14q11.2-21.3	pathogenic
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2	copy number gain	See cases [RCV002286356]	Chr14:37671058..106985955 [GRCh37] Chr14:14q13.3-32.33	pathogenic
GRCh37/hg19 14q11.2-23.1(chr14:20511673-61826023)x3	copy number gain	not provided [RCV003485022]	Chr14:20511673..61826023 [GRCh37] Chr14:14q11.2-23.1	pathogenic
GRCh37/hg19 14q21.3-22.1(chr14:50503550-53302064)x1	copy number loss	not provided [RCV004819865]	Chr14:50503550..53302064 [GRCh37] Chr14:14q21.3-22.1	uncertain significance

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597450121	GWAS1546195_H	aspartate aminotransferase measurement QTL GWAS1546195 (human)		3e-25	aspartate aminotransferase measurement	blood aspartate aminotransferase activity level (CMO:0000580)	14	50045629	50045630	Human
597452842	GWAS1548916_H	serum alanine aminotransferase measurement QTL GWAS1548916 (human)		1e-08	serum alanine aminotransferase measurement	serum alanine aminotransferase activity level (CMO:0000575)	14	50045393	50045394	Human
597475914	GWAS1571988_H	DNA methylation QTL GWAS1571988 (human)		9e-09	DNA methylation		14	50056489	50056490	Human
597426196	GWAS1522270_H	urate measurement QTL GWAS1522270 (human)		7e-11	urate measurement	blood uric acid level (CMO:0000501)	14	50047194	50047195	Human
597402705	GWAS1498779_H	Erythema nodosum QTL GWAS1498779 (human)		0.000007	Erythema nodosum		14	50018609	50018610	Human
597447639	GWAS1543713_H	sex hormone-binding globulin measurement QTL GWAS1543713 (human)		7e-11	sex hormone-binding globulin measurement		14	50045629	50045630	Human
597422935	GWAS1519009_H	serum alanine aminotransferase measurement QTL GWAS1519009 (human)		1e-15	serum alanine aminotransferase measurement	serum alanine aminotransferase activity level (CMO:0000575)	14	50045629	50045630	Human
597403846	GWAS1499920_H	dementia, Alzheimer's disease neuropathologic change QTL GWAS1499920 (human)		0.000003	dementia, Alzheimer's disease neuropathologic change		14	50020073	50020074	Human
597454466	GWAS1550540_H	aspartate aminotransferase measurement QTL GWAS1550540 (human)		4e-16	aspartate aminotransferase measurement	blood aspartate aminotransferase activity level (CMO:0000580)	14	50045393	50045394	Human

SHGC-144589

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	50,558,271 - 50,558,617	UniSTS	GRCh37
Build 36	14	49,628,021 - 49,628,367	RGD	NCBI36
Celera	14	30,425,409 - 30,425,755	RGD
Cytogenetic Map	14	q21.3	UniSTS
HuRef	14	30,683,691 - 30,684,037	UniSTS

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


RefSeq Transcripts	NR_131171	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AF390030	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL109758	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL117692	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC067360	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC084561	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BF055388	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BF691660	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ027525	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU927649	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471078	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA856251	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA935043	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	LC791606	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MW804067	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MW804068	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986391	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	T90102	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000399206

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,981,712 - 50,007,520 (-)	Ensembl

Ensembl Acc Id:

ENST00000528300

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,380 - 50,007,520 (-)	Ensembl

Ensembl Acc Id:

ENST00000529902

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,555 - 50,006,519 (-)	Ensembl

Ensembl Acc Id:

ENST00000530176

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,982,184 - 50,007,520 (-)	Ensembl

Ensembl Acc Id:

ENST00000533506

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,990,990 - 49,993,134 (-)	Ensembl

Ensembl Acc Id:

ENST00000553463

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,300 - 50,011,442 (-)	Ensembl

Ensembl Acc Id:

ENST00000553914

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,300 - 50,040,209 (-)	Ensembl

Ensembl Acc Id:

ENST00000554129

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,037,595 - 50,041,229 (-)	Ensembl

Ensembl Acc Id:

ENST00000556019

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,041,643 - 50,089,175 (-)	Ensembl

Ensembl Acc Id:

ENST00000556130

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,946,154 - 49,960,662 (-)	Ensembl

Ensembl Acc Id:

ENST00000556434

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,927,571 - 49,961,960 (-)	Ensembl

Ensembl Acc Id:

ENST00000556913

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,941,936 - 49,961,960 (-)	Ensembl

Ensembl Acc Id:

ENST00000557142

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,313 - 50,091,555 (-)	Ensembl

Ensembl Acc Id:

ENST00000603228

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,313 - 50,105,102 (-)	Ensembl

Ensembl Acc Id:

ENST00000603474

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,297 - 50,040,606 (-)	Ensembl

Ensembl Acc Id:

ENST00000623502

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,083,651 - 50,092,643 (-)	Ensembl

Ensembl Acc Id:

ENST00000635379

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,927,556 - 50,089,203 (-)	Ensembl

Ensembl Acc Id:

ENST00000655269

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 50,001,297 (-)	Ensembl

Ensembl Acc Id:

ENST00000658223

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,990,944 - 49,993,121 (-)	Ensembl

Ensembl Acc Id:

ENST00000685750

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,060,123 - 50,105,102 (-)	Ensembl

Ensembl Acc Id:

ENST00000686177

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 50,001,348 (-)	Ensembl

Ensembl Acc Id:

ENST00000690038

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,313 - 50,040,570 (-)	Ensembl

Ensembl Acc Id:

ENST00000700829

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,981,668 - 50,001,288 (-)	Ensembl

Ensembl Acc Id:

ENST00000701026

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,000,068 - 50,003,441 (-)	Ensembl

Ensembl Acc Id:

ENST00000701065

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,558 - 50,001,288 (-)	Ensembl

Ensembl Acc Id:

ENST00000701392

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,308 - 50,039,893 (-)	Ensembl

Ensembl Acc Id:

ENST00000701890

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 50,001,288 (-)	Ensembl

Ensembl Acc Id:

ENST00000701948

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 50,001,311 (-)	Ensembl

Ensembl Acc Id:

ENST00000769199

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,006,623 - 50,105,108 (-)	Ensembl

Ensembl Acc Id:

ENST00000769200

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,313 - 50,105,102 (-)	Ensembl

Ensembl Acc Id:

ENST00000769201

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,314 - 50,105,102 (-)	Ensembl

Ensembl Acc Id:

ENST00000769202

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,326 - 50,105,056 (-)	Ensembl

Ensembl Acc Id:

ENST00000769203

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,020,908 - 50,105,034 (-)	Ensembl

Ensembl Acc Id:

ENST00000769204

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,021,145 - 50,105,105 (-)	Ensembl

Ensembl Acc Id:

ENST00000769205

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,037,577 - 50,105,106 (-)	Ensembl

Ensembl Acc Id:

ENST00000769206

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,556 - 50,040,605 (-)	Ensembl

Ensembl Acc Id:

ENST00000769207

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,060,122 - 50,105,077 (-)	Ensembl

Ensembl Acc Id:

ENST00000769208

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,060,119 - 50,105,064 (-)	Ensembl

Ensembl Acc Id:

ENST00000769209

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,927,213 - 49,970,319 (-)	Ensembl

Ensembl Acc Id:

ENST00000769210

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,927,554 - 49,970,324 (-)	Ensembl

Ensembl Acc Id:

ENST00000769211

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,927,554 - 49,970,291 (-)	Ensembl

Ensembl Acc Id:

ENST00000769212

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,927,554 - 49,970,240 (-)	Ensembl

Ensembl Acc Id:

ENST00000769213

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,308 - 50,047,613 (-)	Ensembl

Ensembl Acc Id:

ENST00000769214

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,314 - 50,047,550 (-)	Ensembl

Ensembl Acc Id:

ENST00000769215

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,308 - 50,047,513 (-)	Ensembl

Ensembl Acc Id:

ENST00000769216

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,308 - 50,047,512 (-)	Ensembl

Ensembl Acc Id:

ENST00000769217

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,311 - 50,046,531 (-)	Ensembl

Ensembl Acc Id:

ENST00000769218

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,005,123 - 50,039,854 (-)	Ensembl

Ensembl Acc Id:

ENST00000769219

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,006,622 - 50,040,209 (-)	Ensembl

Ensembl Acc Id:

ENST00000769220

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,006,622 - 50,040,203 (-)	Ensembl

Ensembl Acc Id:

ENST00000769221

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,314 - 50,040,725 (-)	Ensembl

Ensembl Acc Id:

ENST00000769222

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,308 - 50,040,605 (-)	Ensembl

Ensembl Acc Id:

ENST00000769223

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,313 - 50,040,570 (-)	Ensembl

Ensembl Acc Id:

ENST00000769224

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,313 - 50,040,570 (-)	Ensembl

Ensembl Acc Id:

ENST00000769225

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,315 - 50,040,568 (-)	Ensembl

Ensembl Acc Id:

ENST00000769226

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,927,554 - 49,960,729 (-)	Ensembl

Ensembl Acc Id:

ENST00000769227

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,927,554 - 49,960,677 (-)	Ensembl

Ensembl Acc Id:

ENST00000769228

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,300 - 50,040,209 (-)	Ensembl

Ensembl Acc Id:

ENST00000769229

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,311 - 50,040,209 (-)	Ensembl

Ensembl Acc Id:

ENST00000769230

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,308 - 50,039,867 (-)	Ensembl

Ensembl Acc Id:

ENST00000769231

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,300 - 50,039,857 (-)	Ensembl

Ensembl Acc Id:

ENST00000769232

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,313 - 50,039,855 (-)	Ensembl

Ensembl Acc Id:

ENST00000769233

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,313 - 50,039,854 (-)	Ensembl

Ensembl Acc Id:

ENST00000769234

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,314 - 50,039,854 (-)	Ensembl

Ensembl Acc Id:

ENST00000769235

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,313 - 50,039,481 (-)	Ensembl

Ensembl Acc Id:

ENST00000769236

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,010,355 - 50,039,854 (-)	Ensembl

Ensembl Acc Id:

ENST00000769237

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,313 - 50,030,234 (-)	Ensembl

Ensembl Acc Id:

ENST00000769238

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,313 - 50,029,725 (-)	Ensembl

Ensembl Acc Id:

ENST00000769239

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,962,010 - 49,982,278 (-)	Ensembl

Ensembl Acc Id:

ENST00000769240

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,981,149 - 50,001,288 (-)	Ensembl

Ensembl Acc Id:

ENST00000769241

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,021,144 - 50,040,568 (-)	Ensembl

Ensembl Acc Id:

ENST00000769242

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,981,668 - 50,000,948 (-)	Ensembl

Ensembl Acc Id:

ENST00000769243

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,553 - 50,007,144 (-)	Ensembl

Ensembl Acc Id:

ENST00000769244

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,553 - 50,005,460 (-)	Ensembl

Ensembl Acc Id:

ENST00000769245

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,561 - 50,003,814 (-)	Ensembl

Ensembl Acc Id:

ENST00000769246

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,553 - 50,003,783 (-)	Ensembl

Ensembl Acc Id:

ENST00000769247

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 50,003,427 (-)	Ensembl

Ensembl Acc Id:

ENST00000769248

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,553 - 50,003,447 (-)	Ensembl

Ensembl Acc Id:

ENST00000769249

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,553 - 50,003,445 (-)	Ensembl

Ensembl Acc Id:

ENST00000769250

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,558 - 50,003,437 (-)	Ensembl

Ensembl Acc Id:

ENST00000769251

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,556 - 50,003,403 (-)	Ensembl

Ensembl Acc Id:

ENST00000769252

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,981,149 - 49,992,911 (-)	Ensembl

Ensembl Acc Id:

ENST00000769253

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,449 - 50,003,160 (-)	Ensembl

Ensembl Acc Id:

ENST00000769254

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,553 - 50,003,190 (-)	Ensembl

Ensembl Acc Id:

ENST00000769255

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,556 - 50,003,177 (-)	Ensembl

Ensembl Acc Id:

ENST00000769256

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,981,681 - 49,993,095 (-)	Ensembl

Ensembl Acc Id:

ENST00000769257

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,981,686 - 49,993,098 (-)	Ensembl

Ensembl Acc Id:

ENST00000769258

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,595 - 50,002,844 (-)	Ensembl

Ensembl Acc Id:

ENST00000769259

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,960,416 - 49,970,298 (-)	Ensembl

Ensembl Acc Id:

ENST00000769260

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 50,001,318 (-)	Ensembl

Ensembl Acc Id:

ENST00000769261

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 50,001,312 (-)	Ensembl

Ensembl Acc Id:

ENST00000769262

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 50,001,290 (-)	Ensembl

Ensembl Acc Id:

ENST00000769263

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 50,001,289 (-)	Ensembl

Ensembl Acc Id:

ENST00000769264

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,553 - 50,001,298 (-)	Ensembl

Ensembl Acc Id:

ENST00000769265

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,553 - 50,001,288 (-)	Ensembl

Ensembl Acc Id:

ENST00000769266

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 50,001,152 (-)	Ensembl

Ensembl Acc Id:

ENST00000769267

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,030,920 - 50,040,605 (-)	Ensembl

Ensembl Acc Id:

ENST00000769268

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,973,173 - 49,982,796 (-)	Ensembl

Ensembl Acc Id:

ENST00000769269

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,556 - 50,001,162 (-)	Ensembl

Ensembl Acc Id:

ENST00000769270

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,553 - 50,000,948 (-)	Ensembl

Ensembl Acc Id:

ENST00000769271

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,561 - 50,000,916 (-)	Ensembl

Ensembl Acc Id:

ENST00000769272

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,973,173 - 49,982,495 (-)	Ensembl

Ensembl Acc Id:

ENST00000769273

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,308 - 50,011,343 (-)	Ensembl

Ensembl Acc Id:

ENST00000769274

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,311 - 50,011,343 (-)	Ensembl

Ensembl Acc Id:

ENST00000769275

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,007,316 - 50,011,335 (-)	Ensembl

Ensembl Acc Id:

ENST00000769276

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,999,684 - 50,003,408 (-)	Ensembl

Ensembl Acc Id:

ENST00000769277

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,000,068 - 50,003,441 (-)	Ensembl

Ensembl Acc Id:

ENST00000769278

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,000,068 - 50,003,200 (-)	Ensembl

Ensembl Acc Id:

ENST00000769279

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,037,575 - 50,040,617 (-)	Ensembl

Ensembl Acc Id:

ENST00000769280

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,037,580 - 50,040,570 (-)	Ensembl

Ensembl Acc Id:

ENST00000769281

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,037,574 - 50,040,237 (-)	Ensembl

Ensembl Acc Id:

ENST00000769282

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,060,123 - 50,062,775 (-)	Ensembl

Ensembl Acc Id:

ENST00000769283

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,037,578 - 50,040,209 (-)	Ensembl

Ensembl Acc Id:

ENST00000769284

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,038,111 - 50,040,525 (-)	Ensembl

Ensembl Acc Id:

ENST00000769285

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,037,579 - 50,039,880 (-)	Ensembl

Ensembl Acc Id:

ENST00000769286

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,038,370 - 50,040,604 (-)	Ensembl

Ensembl Acc Id:

ENST00000769287

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,103,347 - 50,105,121 (-)	Ensembl

Ensembl Acc Id:

ENST00000769288

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,103,438 - 50,105,103 (-)	Ensembl

Ensembl Acc Id:

ENST00000769289

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 49,993,101 (-)	Ensembl

Ensembl Acc Id:

ENST00000769290

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 49,993,047 (-)	Ensembl

Ensembl Acc Id:

ENST00000769291

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,002,285 - 50,003,821 (-)	Ensembl

Ensembl Acc Id:

ENST00000769292

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,442 - 49,992,916 (-)	Ensembl

Ensembl Acc Id:

ENST00000769293

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,991,553 - 49,992,914 (-)	Ensembl

Ensembl Acc Id:

ENST00000769294

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,001,872 - 50,003,179 (-)	Ensembl

Ensembl Acc Id:

ENST00000769295

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,001,872 - 50,003,166 (-)	Ensembl

Ensembl Acc Id:

ENST00000769296

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,000,068 - 50,001,288 (-)	Ensembl

Ensembl Acc Id:

ENST00000769297

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,002,448 - 50,003,460 (-)	Ensembl

Ensembl Acc Id:

ENST00000769298

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,060,123 - 50,061,128 (-)	Ensembl

Ensembl Acc Id:

ENST00000769299

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,002,448 - 50,003,438 (-)	Ensembl

Ensembl Acc Id:

ENST00000769300

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,962,010 - 49,962,964 (-)	Ensembl

Ensembl Acc Id:

ENST00000769301

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,002,565 - 50,003,429 (-)	Ensembl

Ensembl Acc Id:

ENST00000769302

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,981,668 - 49,982,515 (-)	Ensembl

Ensembl Acc Id:

ENST00000769303

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	49,981,681 - 49,982,509 (-)	Ensembl

Ensembl Acc Id:

ENST00000769304

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	50,002,565 - 50,003,302 (-)	Ensembl

RefSeq Acc Id:

NR_131171

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	50,007,313 - 50,105,043 (-)	NCBI
CHM1_1	14	50,412,171 - 50,510,446 (-)	NCBI
T2T-CHM13v2.0	14	44,212,500 - 44,311,279 (-)	NCBI

Sequence:

show sequence

AAAAAAAAAAGCCTACCTTTTGAGTTACTTTCAGAAGATAACACAGGTTCTCGAGGCTGGACAGTCCAAGATCAAGGTGCCTGCATCTGGCGTCTAGTGTGGACCCTATTCCTGGTTTGCAGCATTGT
TGGTGCTCTGAGGGTGTCAGCCAGGCCACTCATGCAGACCATTGCGGCAGCACTGAAAATGGAAGAAAGATGGGATTCTGCTGTCTTTTGTTTTGGCTGATGAACAGCACCGAGATGGAGTGGCTCCA
GCAGCCAGAACAAGCCACCATCTCCCCTGGGCTTTCACAGTAGCCTCCTGACTGGTCTTGTTGCTTCCACACTTACACTTCCTGTTCTCTGCAAGGCAGCCAGAGTGACCTTTCACTAATCCTTGTAT
GACCTCTGAAAATATGACCTGAAGCAGATGGATGCACTCACATAAGAAACATCACCTGTGGCCTTCATCGAAAATGGGCCTGCTGCTTGAAGAAGTTGGGCTCTTGGAGTTCTCTAGCACAGGGGCCA
TGAAAATCAATGACTTCCTTGTTTGCTGACGGAGCAGAGGTAGAATCTCTTGGTGTTTCCACGGAGAAAACACTGACCATGAAGAGCCAAGAAAGATGACATGATGAAGCCATCAGGGGAAGCACCAA
ACATCCTCAACTCTGCTCACCCATGGTTTTCTCCCGCCCTCCCAGAGCTCCTCCTGCTGATGGGCCCCCGACATGAAACTGGCACTCAGAATGAAGAATGCCTTTTCCAGCCTCCCTCGCTGGTGGAG
TCTCCGTGTTCCAGCCAATGAAGTAGGGCATGCAGTTGCCTGCCCCACTGAAGTCAACTTCAGCCTGAAGATTGGGAGACTTCCGAAAGTGGAAAACTTGGAAGGAGGAAGCCTGGACAGCCTGCAGT
TGAGGGGACCTGCACAAGCTCACAGGACTCTTCATCACCATGACACCACGCTCACCGCAAAATAAAAATGATCAAACCTGTAAAAAAAAAAAAAAAAAA

hide sequence


GenBank Protein	AAL58840	(Get FASTA)	NCBI Sequence Viewer
	EAW65733	(Get FASTA)	NCBI Sequence Viewer
	EAW65734	(Get FASTA)	NCBI Sequence Viewer
	Q8WXQ3	(Get FASTA)	NCBI Sequence Viewer

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q8WXQ3-F1-model_v2	AlphaFold	Q8WXQ3	1-324	view protein structure

Database	Acc Id	Source(s)
COSMIC	LINC01599	COSMIC
Ensembl Genes	ENSG00000214900	Ensembl, ENTREZGENE
Ensembl Transcript	ENST00000603228	ENTREZGENE
GTEx	ENSG00000214900	GTEx
HGNC ID	HGNC:27285	ENTREZGENE
Human Proteome Map	LINC01599	Human Proteome Map
NCBI Gene	196913	ENTREZGENE
RNAcentral	URS00008120FF	RNACentral
UniProt	CN183_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-03-25	LINC01599	long intergenic non-protein coding RNA 1599	C14orf183	chromosome 14 open reading frame 183	Symbol and/or name change	5135510	APPROVED
2011-07-27	C14orf183	chromosome 14 open reading frame 183	LOC196913	hypothetical protein LOC196913	Symbol and/or name change	5135510	APPROVED

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


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


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
		Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar