PVT1 (Pvt1 oncogene) - Rat Genome Database

Name: PVT1
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: PVT1 (Pvt1 oncogene) Homo sapiens

Analyze

Symbol:

PVT1

Name:

Pvt1 oncogene

RGD ID:

1348372

HGNC Page

HGNC:9709

Description:

Predicted to act upstream of or within response to wounding. Implicated in hepatocellular carcinoma. Biomarker of hepatocellular carcinoma.

Type:

ncrna (Ensembl: lncRNA)

RefSeq Status:

REVIEWED

Previously known as:

LINC00079; MGC21751; MIR1204HG; MYC; NCRNA00079; onco-lncRNA-100; Pvt1 oncogene (non-protein coding); TP53LC09

RGD Orthologs

Mouse

Rat

Alliance Genes

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	8	127,794,524 - 128,101,256 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	8	127,794,526 - 128,187,101 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	8	128,806,779 - 129,113,499 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	8	128,875,961 - 129,182,681 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	8	124,987,142 - 125,293,818 (+)	NCBI		Celera
Cytogenetic Map	8	q24.21	NCBI
HuRef	8	124,224,893 - 124,436,191 (+)	NCBI		HuRef
CHM1_1	8	128,943,166 - 129,153,800 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

hepatocellular carcinoma (IEP,IGI,IMP)

Hodgkin's lymphoma (EXP)

immunoglobulin alpha deficiency (EXP)

Neoplasm Invasiveness (EXP)

Sepsis (ISO)

trichorhinophalangeal syndrome type I (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,1-dichloroethene (ISO)

1,2-dichloroethane (ISO)

17beta-estradiol (EXP)

2,3,7,8-tetrachlorodibenzodioxine (ISO)

2-acetamidofluorene (ISO)

2-acetyl-1-alkyl-sn-glycero-3-phosphocholine (EXP)

2-hydroxypropanoic acid (EXP)

4,4'-sulfonyldiphenol (ISO)

4-hydroxyphenyl retinamide (ISO)

5-fluorouracil (EXP)

aflatoxin B1 (EXP,ISO)

all-trans-retinoic acid (ISO)

arsane (EXP)

arsenic atom (EXP)

arsenite(3-) (EXP)

atrazine (ISO)

benzene (ISO)

benzo[a]pyrene (EXP)

benzo[e]pyrene (EXP)

bisphenol A (EXP)

bisphenol F (ISO)

butanal (EXP)

cadmium dichloride (EXP)

cantharidin (EXP)

cyclosporin A (EXP)

dioxygen (ISO)

dorsomorphin (EXP)

doxorubicin (EXP,ISO)

fipronil (EXP)

fulvestrant (EXP)

ibuprofen (ISO)

lead(0) (EXP)

leflunomide (EXP,ISO)

lidocaine (ISO)

mercury dibromide (EXP)

methapyrilene (EXP)

methylmercury chloride (EXP)

monosodium L-glutamate (ISO)

N-acetyl-1,4-benzoquinone imine (EXP)

N-nitrosodiethylamine (ISO)

nickel atom (EXP)

Nutlin-3 (EXP)

p-chloromercuribenzoic acid (EXP)

p-toluidine (ISO)

perfluorooctane-1-sulfonic acid (ISO)

phenobarbital (ISO)

phenylmercury acetate (EXP)

rac-lactic acid (EXP)

SB 431542 (EXP)

sodium arsenate (ISO)

sodium arsenite (EXP)

sulindac sulfide (EXP)

temozolomide (EXP)

titanium dioxide (ISO)

trichostatin A (EXP)

triptonide (ISO)

trovafloxacin (ISO)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

response to wounding (ISO)

References

References - curated

#	Reference Title	Reference Citation
1.	PVT1 regulates inflammation and cardiac function via the MAPK/NF-κB pathway in a sepsis model.	Feng F, etal., Exp Ther Med. 2018 Dec;16(6):4471-4478. doi: 10.3892/etm.2018.6814. Epub 2018 Oct 1.
2.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
4.	Long Non-Coding RNA PVT1/miR-150/ HIG2 Axis Regulates the Proliferation, Invasion and the Balance of Iron Metabolism of Hepatocellular Carcinoma.	Xu Y, etal., Cell Physiol Biochem. 2018;49(4):1403-1419. doi: 10.1159/000493445. Epub 2018 Sep 11.

Additional References at PubMed

PMID:2181290	PMID:2470097	PMID:2725491	PMID:3024964	PMID:12477932	PMID:14702039	PMID:16341674	PMID:17395743	PMID:17503467	PMID:17881614	PMID:17908964	PMID:19270707
PMID:19549893	PMID:20694011	PMID:21037568	PMID:21316338	PMID:21526116	PMID:21814516	PMID:21833088	PMID:22110125	PMID:22869583	PMID:23547836	PMID:23801869	PMID:23817571
PMID:23934736	PMID:24132900	PMID:24196785	PMID:24204837	PMID:24220699	PMID:24390342	PMID:24529757	PMID:24709693	PMID:24780616	PMID:24821155	PMID:24861552	PMID:24926545
PMID:25043044	PMID:25043274	PMID:25086665	PMID:25245984	PMID:25261932	PMID:25279986	PMID:25400777	PMID:25624916	PMID:25864709	PMID:25883951	PMID:25890171	PMID:25956062
PMID:26097562	PMID:26427660	PMID:26490983	PMID:26517688	PMID:26545364	PMID:26850852	PMID:26908628	PMID:26925791	PMID:27028998	PMID:27232880	PMID:27272214	PMID:27366943
PMID:27484035	PMID:27588491	PMID:27756785	PMID:27794184	PMID:27813492	PMID:27928058	PMID:27986464	PMID:28187158	PMID:28235236	PMID:28258379	PMID:28265576	PMID:28276314
PMID:28296507	PMID:28351322	PMID:28381186	PMID:28404954	PMID:28409552	PMID:28520497	PMID:28534994	PMID:28602700	PMID:28611215	PMID:28656879	PMID:28657147	PMID:28731781
PMID:28800314	PMID:28848163	PMID:28866116	PMID:28874676	PMID:28882595	PMID:28972861	PMID:29035442	PMID:29046366	PMID:29050519	PMID:29081406	PMID:29115513	PMID:29117863
PMID:29193797	PMID:29244840	PMID:29262850	PMID:29277611	PMID:29280051	PMID:29286144	PMID:29417297	PMID:29445147	PMID:29452232	PMID:29467491	PMID:29501773	PMID:29505758
PMID:29510227	PMID:29512788	PMID:29552759	PMID:29620147	PMID:29693171	PMID:29693417	PMID:29706652	PMID:29715456	PMID:29731168	PMID:29739059	PMID:29749550	PMID:29760406
PMID:29845201	PMID:29948619	PMID:29957467	PMID:29975928	PMID:30076414	PMID:30076714	PMID:30083911	PMID:30141114	PMID:30222365	PMID:30252166	PMID:30295989	PMID:30304557
PMID:30317572	PMID:30347597	PMID:30371726	PMID:30504754	PMID:30590312	PMID:30649422	PMID:30661902	PMID:30679629	PMID:30794914	PMID:30820968	PMID:30825877	PMID:30832754
PMID:30909189	PMID:30914434	PMID:30943439	PMID:30993787	PMID:31002139	PMID:31028131	PMID:31221783	PMID:31222482	PMID:31277104	PMID:31297833	PMID:31309249	PMID:31320749
PMID:31322217	PMID:31326971	PMID:31369196	PMID:31371698	PMID:31485648	PMID:31509024	PMID:31577086	PMID:31577719	PMID:31601234	PMID:31604907	PMID:31626590	PMID:31627090
PMID:31677796	PMID:31696483	PMID:31699956	PMID:31707347	PMID:31755246	PMID:31850702	PMID:31877167	PMID:31894346	PMID:31932969	PMID:31957871	PMID:31986409	PMID:32003019
PMID:32171788	PMID:32196583	PMID:32202906	PMID:32249539	PMID:32293498	PMID:32342557	PMID:32358016	PMID:32385030	PMID:32407172	PMID:32428696	PMID:32441301	PMID:32499447
PMID:32562719	PMID:32572930	PMID:32602581	PMID:32614682	PMID:32689767	PMID:32725807	PMID:32727463	PMID:32729021	PMID:32734834	PMID:32781203	PMID:32812642	PMID:32827544
PMID:32830409	PMID:32866660	PMID:32918701	PMID:32921988	PMID:32945498	PMID:32945521	PMID:32960438	PMID:32960485	PMID:32992461	PMID:33049089	PMID:33067424	PMID:33106979
PMID:33148262	PMID:33167678	PMID:33174011	PMID:33188158	PMID:33275233	PMID:33327894	PMID:33369809	PMID:33408314	PMID:33430890	PMID:33443959	PMID:33453148	PMID:33558065
PMID:33600954	PMID:33670447	PMID:33712566	PMID:33728345	PMID:33733809	PMID:33752525	PMID:33825599	PMID:33878452	PMID:33896835	PMID:33907980	PMID:33947142	PMID:33962657
PMID:33981772	PMID:34001726	PMID:34033197	PMID:34200314	PMID:34237962	PMID:34245303	PMID:34288373	PMID:34418232	PMID:34515320	PMID:34518442	PMID:34546507	PMID:34555308
PMID:34564701	PMID:34592894	PMID:34617244	PMID:34775377	PMID:34816674	PMID:34844154	PMID:34859258	PMID:34859371	PMID:34898354	PMID:34922601	PMID:34981911	PMID:35036445
PMID:35038974	PMID:35098439	PMID:35103897	PMID:35130573	PMID:35152842	PMID:35274773	PMID:35399100	PMID:35414508	PMID:35417913	PMID:35435126	PMID:35441392	PMID:35451342
PMID:35664988	PMID:35706414	PMID:35723715	PMID:35735229	PMID:35763386	PMID:35820706	PMID:36041701	PMID:36065882	PMID:36164442	PMID:36348010	PMID:36370492	PMID:36397317
PMID:36524545	PMID:36565414	PMID:36624401	PMID:36718632	PMID:36724291	PMID:36941464	PMID:37009655	PMID:37202742	PMID:37236049	PMID:37270938	PMID:37392551	PMID:37401860
PMID:37496441	PMID:37531296	PMID:37573419	PMID:37789776	PMID:37930852	PMID:38091883	PMID:38309019

Genomics

Comparative Map Data

PVT1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	8	127,794,526 - 128,187,101 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	8	128,806,779 - 129,113,499 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	8	128,875,961 - 129,182,681 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	8	124,987,142 - 125,293,818 (+)	NCBI		Celera
Cytogenetic Map	8	q24.21	NCBI
HuRef	8	124,224,893 - 124,436,191 (+)	NCBI		HuRef
CHM1_1	8	128,943,166 - 129,153,800 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI		T2T-CHM13v2.0

Pvt1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	15	61,909,835 - 62,132,064 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	15	61,909,817 - 62,249,945 (+)	Ensembl		GRCm39 Ensembl
GRCm38	15	62,037,986 - 62,260,215 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	15	62,037,986 - 62,378,096 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	15	61,869,542 - 62,082,530 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	15	61,869,542 - 62,082,530 (+)	NCBI		MGSCv36	mm8
Celera	15	63,612,668 - 63,756,556 (+)	NCBI		Celera
Cytogenetic Map	15	D1	NCBI
cM Map	15	26.24	NCBI

Pvt1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	7	95,545,916 - 95,769,306 (+)	NCBI		GRCr8
mRatBN7.2	7	93,656,528 - 93,879,938 (+)	NCBI	mRatBN7.2	mRatBN7.2
Rnor_6.0	7	102,648,394 - 102,871,316 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_5.0	7	103,219,764 - 103,441,799 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
Celera	7	90,324,385 - 90,542,415 (+)	NCBI		Celera
Cytogenetic Map	7	q33	NCBI

Variants

Variants in PVT1
63 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 8q23.3-24.3(chr8:113580402-145054634)x3	copy number gain	See cases [RCV000050638]	Chr8:113580402..145054634 [GRCh38] Chr8:114592631..146280020 [GRCh37] Chr8:114661807..146250824 [NCBI36] Chr8:8q23.3-24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3	copy number gain	See cases [RCV000051206]	Chr8:241530..145049449 [GRCh38] Chr8:191530..146274835 [GRCh37] Chr8:181530..146245639 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:95606052-145054775)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]\|See cases [RCV000053677]	Chr8:95606052..145054775 [GRCh38] Chr8:96618280..146280161 [GRCh37] Chr8:96687456..146250965 [NCBI36] Chr8:8q22.1-24.3	pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3	copy number gain	See cases [RCV000053678]	Chr8:124514090..145054634 [GRCh38] Chr8:125526331..146280020 [GRCh37] Chr8:125595512..146250824 [NCBI36] Chr8:8q24.13-24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3	copy number gain	See cases [RCV000053602]	Chr8:241530..145054634 [GRCh38] Chr8:191530..146280020 [GRCh37] Chr8:181530..146250824 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]\|See cases [RCV000053604]	Chr8:244417..145054775 [GRCh38] Chr8:194417..146280161 [GRCh37] Chr8:184417..146250965 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q24.21-24.23(chr8:126626164-137169427)x1	copy number loss	See cases [RCV000054306]	Chr8:126626164..137169427 [GRCh38] Chr8:127638409..138181670 [GRCh37] Chr8:127707591..138250852 [NCBI36] Chr8:8q24.21-24.23	pathogenic
NR_003367.2(PVT1):n.972-2158A>G	single nucleotide variant	Lung cancer [RCV000107027]	Chr8:128068002 [GRCh38] Chr8:129080248 [GRCh37] Chr8:8q24.21	uncertain significance
NR_003367.2(PVT1):n.372-3935A>G	single nucleotide variant	Lung cancer [RCV000107024]	Chr8:127935573 [GRCh38] Chr8:128947819 [GRCh37] Chr8:8q24.21	uncertain significance
NR_003367.2(PVT1):n.971+7027A>G	single nucleotide variant	Lung cancer [RCV000107025]	Chr8:127996318 [GRCh38] Chr8:129008564 [GRCh37] Chr8:8q24.21	uncertain significance
NR_003367.2(PVT1):n.972-36600G>T	single nucleotide variant	Lung cancer [RCV000107026]	Chr8:128033560 [GRCh38] Chr8:129045806 [GRCh37] Chr8:8q24.21	uncertain significance
GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3	copy number gain	See cases [RCV000134353]	Chr8:94682154..145068656 [GRCh38] Chr8:95694382..146294042 [GRCh37] Chr8:95763558..146264846 [NCBI36] Chr8:8q22.1-24.3	pathogenic
GRCh38/hg38 8q21.3-24.23(chr8:86300584-137022587)x3	copy number gain	See cases [RCV000135621]	Chr8:86300584..137022587 [GRCh38] Chr8:87312813..138034830 [GRCh37] Chr8:87381929..138104012 [NCBI36] Chr8:8q21.3-24.23	pathogenic\|likely pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124498498-145068712)x3	copy number gain	See cases [RCV000137346]	Chr8:124498498..145068712 [GRCh38] Chr8:125510739..146294098 [GRCh37] Chr8:125579920..146264902 [NCBI36] Chr8:8q24.13-24.3	pathogenic
GRCh38/hg38 8q21.3-24.3(chr8:87931152-145068712)x3	copy number gain	See cases [RCV000138551]	Chr8:87931152..145068712 [GRCh38] Chr8:88943380..146294098 [GRCh37] Chr8:89012496..146264902 [NCBI36] Chr8:8q21.3-24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3	copy number gain	See cases [RCV000138643]	Chr8:241605..145054781 [GRCh38] Chr8:191605..146280167 [GRCh37] Chr8:181605..146250971 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3	copy number gain	See cases [RCV000139036]	Chr8:77480050..145068712 [GRCh38] Chr8:78392286..146294098 [GRCh37] Chr8:78554841..146264902 [NCBI36] Chr8:8q21.13-24.3	pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:97382873-145070385)x3	copy number gain	See cases [RCV000140447]	Chr8:97382873..145070385 [GRCh38] Chr8:98395101..146295771 [GRCh37] Chr8:98464277..146266575 [NCBI36] Chr8:8q22.1-24.3	pathogenic
GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3	copy number gain	See cases [RCV000139539]	Chr8:46031340..139285494 [GRCh38] Chr8:46942962..140297737 [GRCh37] Chr8:47062127..140366919 [NCBI36] Chr8:8q11.1-24.3	pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:100867343-145070385)x3	copy number gain	See cases [RCV000141694]	Chr8:100867343..145070385 [GRCh38] Chr8:101879571..146295771 [GRCh37] Chr8:101948747..146266575 [NCBI36] Chr8:8q22.3-24.3	pathogenic
GRCh38/hg38 8q24.13-24.21(chr8:122454392-128513076)x3	copy number gain	See cases [RCV000133620]	Chr8:122454392..128513076 [GRCh38] Chr8:123466631..129525322 [GRCh37] Chr8:123535812..129594504 [NCBI36] Chr8:8q24.13-24.21	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3	copy number gain	See cases [RCV000141808]	Chr8:208048..145070385 [GRCh38] Chr8:158048..146295771 [GRCh37] Chr8:148048..146266575 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3	copy number gain	See cases [RCV000142021]	Chr8:21291522..145070385 [GRCh38] Chr8:21149033..146295771 [GRCh37] Chr8:21193313..146266575 [NCBI36] Chr8:8p21.3-q24.3	pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:103306336-145068712)x3	copy number gain	See cases [RCV000142810]	Chr8:103306336..145068712 [GRCh38] Chr8:104318564..146294098 [GRCh37] Chr8:104387740..146264902 [NCBI36] Chr8:8q22.3-24.3	pathogenic\|likely pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3	copy number gain	See cases [RCV000142858]	Chr8:226452..145068712 [GRCh38] Chr8:176452..146294098 [GRCh37] Chr8:166452..146264902 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3	copy number gain	See cases [RCV000142597]	Chr8:78614077..145054634 [GRCh38] Chr8:79526312..146280020 [GRCh37] Chr8:79688867..146250824 [NCBI36] Chr8:8q21.13-24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3	copy number gain	See cases [RCV000148092]	Chr8:241530..145054634 [GRCh38] Chr8:191530..146280020 [GRCh37] Chr8:181530..146250824 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q21.2-24.3(chr8:85765999-145070385)x3	copy number gain	See cases [RCV000143659]	Chr8:85765999..145070385 [GRCh38] Chr8:86778228..146295771 [GRCh37] Chr8:86863079..146266575 [NCBI36] Chr8:8q21.2-24.3	pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3	copy number gain	See cases [RCV000148117]	Chr8:124514090..145054634 [GRCh38] Chr8:125526331..146280020 [GRCh37] Chr8:125595512..146250824 [NCBI36] Chr8:8q24.13-24.3	pathogenic
GRCh38/hg38 8q24.21(chr8:127118340-127858575)x3	copy number gain	See cases [RCV000050763]	Chr8:127118340..127858575 [GRCh38] Chr8:128130585..128870821 [GRCh37] Chr8:128199767..128940003 [NCBI36] Chr8:8q24.21	pathogenic
GRCh37/hg19 8q13.2-24.3(chr8:68912432-146295771)x2	copy number gain	See cases [RCV002292707]	Chr8:68912432..146295771 [GRCh37] Chr8:8q13.2-24.3	pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:84712253-146295771)x3	copy number gain	See cases [RCV002285066]	Chr8:84712253..146295771 [GRCh37] Chr8:8q21.2-24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3	copy number gain	See cases [RCV000447507]	Chr8:158991..146280828 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q22.1-24.3(chr8:98432250-146222672)x4	copy number gain	See cases [RCV000448954]	Chr8:98432250..146222672 [GRCh37] Chr8:8q22.1-24.3	pathogenic
GRCh37/hg19 8q24.21-24.22(chr8:128295596-133200773)x1	copy number loss	See cases [RCV000448960]	Chr8:128295596..133200773 [GRCh37] Chr8:8q24.21-24.22	likely pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)	copy number gain	See cases [RCV000510234]	Chr8:158049..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q21.3-24.3(chr8:93047482-141355635)x3	copy number gain	See cases [RCV000511761]	Chr8:93047482..141355635 [GRCh37] Chr8:8q21.3-24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3	copy number gain	See cases [RCV000511095]	Chr8:158049..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841154-146295771)x3	copy number gain	See cases [RCV000511002]	Chr8:86841154..146295771 [GRCh37] Chr8:8q21.2-24.3	pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841228-142689874)x3	copy number gain	See cases [RCV000510854]	Chr8:86841228..142689874 [GRCh37] Chr8:8q21.2-24.3	pathogenic
GRCh37/hg19 8q23.3-24.3(chr8:114853126-146295771)x3	copy number gain	See cases [RCV000512401]	Chr8:114853126..146295771 [GRCh37] Chr8:8q23.3-24.3	pathogenic
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3	copy number gain	See cases [RCV000512169]	Chr8:12490999..146295771 [GRCh37] Chr8:8p23.1-q24.3	pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:121694649-146295771)x3	copy number gain	not provided [RCV000683044]	Chr8:121694649..146295771 [GRCh37] Chr8:8q24.12-24.3	pathogenic
Single allele	deletion	Trichorhinophalangeal dysplasia type I [RCV000735900]	Chr8:114508086..129040004 [GRCh37] Chr8:8q23.3-24.21	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3	copy number gain	not provided [RCV000747254]	Chr8:164984..146293414 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3	copy number gain	not provided [RCV000747248]	Chr8:10213..146293414 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q24.13-24.3(chr8:126892814-143750028)x1	copy number loss	not provided [RCV001006144]	Chr8:126892814..143750028 [GRCh37] Chr8:8q24.13-24.3	pathogenic
GRCh37/hg19 8q24.13-24.3(chr8:125496223-146295771)x3	copy number gain	not provided [RCV000845705]	Chr8:125496223..146295771 [GRCh37] Chr8:8q24.13-24.3	pathogenic
GRCh37/hg19 8q24.13-24.22(chr8:124120772-135265846)x1	copy number loss	not provided [RCV000848438]	Chr8:124120772..135265846 [GRCh37] Chr8:8q24.13-24.22	pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:122193546-146295771)x3	copy number gain	not provided [RCV000849762]	Chr8:122193546..146295771 [GRCh37] Chr8:8q24.12-24.3	pathogenic
GRCh37/hg19 8q24.13-24.21(chr8:123074293-131113892)x1	copy number loss	not provided [RCV000848164]	Chr8:123074293..131113892 [GRCh37] Chr8:8q24.13-24.21	pathogenic
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3	copy number gain	not provided [RCV000848192]	Chr8:31936551..146295771 [GRCh37] Chr8:8p12-q24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	copy number gain	not provided [RCV000848478]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q24.21-24.3(chr8:128877995-146295771)x3	copy number gain	not provided [RCV001006146]	Chr8:128877995..146295771 [GRCh37] Chr8:8q24.21-24.3	pathogenic
GRCh38/hg38 8q23.3-24.23(chr8:115586904-135607135)x3	copy number gain	Neurodevelopmental disorder [RCV003327615]	Chr8:115586904..135607135 [GRCh38] Chr8:8q23.3-24.23	pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:121042467-146295771)x3	copy number gain	not provided [RCV001006140]	Chr8:121042467..146295771 [GRCh37] Chr8:8q24.12-24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)	copy number gain	Polydactyly [RCV002280629]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q24.21-24.3(chr8:128878931-141662233)x3	copy number gain	not provided [RCV001795855]	Chr8:128878931..141662233 [GRCh37] Chr8:8q24.21-24.3	uncertain significance
GRCh37/hg19 8q24.21(chr8:128717255-128918996)x3	copy number gain	not provided [RCV001834390]	Chr8:128717255..128918996 [GRCh37] Chr8:8q24.21	likely benign
GRCh37/hg19 8q13.2-24.3(chr8:70382990-146295771)	copy number gain	not specified [RCV002053772]	Chr8:70382990..146295771 [GRCh37] Chr8:8q13.2-24.3	pathogenic
GRCh37/hg19 8q22.1-24.3(chr8:96496503-146295711)	copy number gain	not provided [RCV002221452]	Chr8:96496503..146295711 [GRCh37] Chr8:8q22.1-24.3	pathogenic
GRCh37/hg19 8q24.13-24.21(chr8:124534271-129054138)x4	copy number gain	Distal trisomy 8q [RCV003458956]	Chr8:124534271..129054138 [GRCh37] Chr8:8q24.13-24.21	pathogenic
GRCh37/hg19 8q24.11-24.22(chr8:118071721-132774256)x1	copy number loss	not specified [RCV003986782]	Chr8:118071721..132774256 [GRCh37] Chr8:8q24.11-24.22	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	copy number gain	not specified [RCV003986742]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q23.3-24.3(chr8:113392581-146364022)x3	copy number gain	not provided [RCV003885521]	Chr8:113392581..146364022 [GRCh37] Chr8:8q23.3-24.3	pathogenic
GRCh37/hg19 8q23.3-24.22(chr8:112234557-133668379)x1	copy number loss	not provided [RCV002474553]	Chr8:112234557..133668379 [GRCh37] Chr8:8q23.3-24.22	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	4054
Count of miRNA genes:	1001
Interacting mature miRNAs:	1244
Transcripts:	ENST00000504719, ENST00000512617, ENST00000513868, ENST00000517525, ENST00000517790, ENST00000517838, ENST00000518528, ENST00000519481, ENST00000520913, ENST00000521122, ENST00000521600, ENST00000521951, ENST00000522414, ENST00000522875, ENST00000522963, ENST00000523068, ENST00000523190, ENST00000523328, ENST00000523427, ENST00000524165
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region

D8S1720

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	128,949,753 - 128,949,884	UniSTS	GRCh37
Build 36	8	129,018,935 - 129,019,066	RGD	NCBI36
Celera	8	125,130,542 - 125,130,675	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	8	124,272,137 - 124,272,272	UniSTS
Marshfield Genetic Map	8	140.61	RGD
Marshfield Genetic Map	8	140.61	UniSTS
Genethon Genetic Map	8	139.7	UniSTS
deCODE Assembly Map	8	137.06	UniSTS
Whitehead-YAC Contig Map	8		UniSTS

SGC34443

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	128,994,985 - 128,995,111	UniSTS	GRCh37
Build 36	8	129,064,167 - 129,064,293	RGD	NCBI36
Celera	8	125,175,783 - 125,175,909	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	8	124,317,392 - 124,317,518	UniSTS
GeneMap99-GB4 RH Map	8	496.14	UniSTS
Whitehead-RH Map	8	653.1	UniSTS

RH68431

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	128,995,025 - 128,995,191	UniSTS	GRCh37
Build 36	8	129,064,207 - 129,064,373	RGD	NCBI36
Celera	8	125,175,823 - 125,175,989	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	8	124,317,432 - 124,317,598	UniSTS
GeneMap99-GB4 RH Map	8	493.61	UniSTS

SHGC-82342

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	129,064,182 - 129,064,392	UniSTS	GRCh37
Build 36	8	129,133,364 - 129,133,574	RGD	NCBI36
Celera	8	125,244,489 - 125,244,699	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	8	124,386,676 - 124,386,886	UniSTS

SHGC-151203

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	128,949,764 - 128,950,061	UniSTS	GRCh37
Build 36	8	129,018,946 - 129,019,243	RGD	NCBI36
Celera	8	125,130,553 - 125,130,852	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	8	124,272,148 - 124,272,449	UniSTS
TNG Radiation Hybrid Map	5	709.0	UniSTS
TNG Radiation Hybrid Map	8	62621.0	UniSTS

SHGC-144185

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	128,859,640 - 128,859,910	UniSTS	GRCh37
Build 36	8	128,928,822 - 128,929,092	RGD	NCBI36
Celera	8	125,040,418 - 125,040,688	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	8	124,181,183 - 124,181,453	UniSTS
TNG Radiation Hybrid Map	8	62667.0	UniSTS

STS-T95511

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	129,113,252 - 129,113,489	UniSTS	GRCh37
Build 36	8	129,182,434 - 129,182,671	RGD	NCBI36
Celera	8	125,293,571 - 125,293,808	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	8	124,435,944 - 124,436,181	UniSTS
GeneMap99-GB4 RH Map	8	489.94	UniSTS

G17834

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	128,986,445 - 128,986,598	UniSTS	GRCh37
Build 36	8	129,055,627 - 129,055,780	RGD	NCBI36
Celera	8	125,167,244 - 125,167,397	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	8	124,308,853 - 124,309,006	UniSTS

SHGC-152351

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	128,949,805 - 128,950,106	UniSTS	GRCh37
GRCh37	8	128,949,795 - 128,950,106	UniSTS	GRCh37
Build 36	8	129,018,977 - 129,019,288	RGD	NCBI36
Celera	8	125,130,594 - 125,130,897	UniSTS
Celera	8	125,130,584 - 125,130,897	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	8	124,272,179 - 124,272,494	UniSTS
HuRef	8	124,272,189 - 124,272,494	UniSTS
TNG Radiation Hybrid Map	17	14915.0	UniSTS

G31084

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	129,008,730 - 129,008,861	UniSTS	GRCh37
Build 36	8	129,077,912 - 129,078,043	RGD	NCBI36
Celera	8	125,189,528 - 125,189,659	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	8	124,331,128 - 124,331,259	UniSTS

AFMB299YE9

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	129,055,938 - 129,056,144	UniSTS	GRCh37
Build 36	8	129,125,120 - 129,125,326	RGD	NCBI36
Celera	8	125,236,246 - 125,236,452	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	11	61,164,280 - 61,165,111	UniSTS
HuRef	8	124,378,435 - 124,378,639	UniSTS
Whitehead-YAC Contig Map	8		UniSTS

D8S1087

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	128,957,099 - 128,957,406	UniSTS	GRCh37
Build 36	8	129,026,281 - 129,026,588	RGD	NCBI36
Celera	8	125,137,891 - 125,138,198	RGD
Cytogenetic Map	8	q24	UniSTS
HuRef	8	124,279,488 - 124,279,795	UniSTS
Whitehead-YAC Contig Map	8		UniSTS

L17705

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	3	p24.2	UniSTS
Cytogenetic Map	15	q22.3	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	9	q21.13	UniSTS
Cytogenetic Map	22	q11.22	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	9	p13.3-p12	UniSTS
Cytogenetic Map	16	q11.2	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	8	p11.21	UniSTS
Cytogenetic Map	4	q21.23	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	X	q21.1	UniSTS
Cytogenetic Map	Y	p11.2	UniSTS
Cytogenetic Map	1	q23.1	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	14	q21	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	1	p36.31	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	3	q12.3	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	5	q21	UniSTS
Cytogenetic Map	1	p22.1	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	12	q21.1	UniSTS
Cytogenetic Map	X	p22.12	UniSTS
Cytogenetic Map	5	q33.3	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	1	q25	UniSTS
Cytogenetic Map	1	p35.3	UniSTS
Cytogenetic Map	17	q25.2	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	6	q14.1	UniSTS
Cytogenetic Map	7	q36.1	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	8	q24	UniSTS
Cytogenetic Map	1	p21.3	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	19	q13.13	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	17	q21.1	UniSTS
Cytogenetic Map	6	q16.1	UniSTS
Cytogenetic Map	16	p12.3	UniSTS
Cytogenetic Map	X	p22.3	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	1	q42.12	UniSTS
Cytogenetic Map	14	q32.12	UniSTS
Cytogenetic Map	6	q22.31	UniSTS
Cytogenetic Map	10	p14	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	4	p16.1	UniSTS
Cytogenetic Map	3	q13.13	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	5	q31.3	UniSTS
Cytogenetic Map	X	q24	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	15	q22	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	18	q21.31	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	12	q13.11-q14.3	UniSTS
Cytogenetic Map	20	q11.22-q11.23	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	3	q13.33	UniSTS
Cytogenetic Map	14	q12	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	15	q26.3	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	9	q21.33	UniSTS
Cytogenetic Map	2	q13	UniSTS
Cytogenetic Map	11	q12.2	UniSTS
Cytogenetic Map	2	q14.3	UniSTS
Cytogenetic Map	1	p36-p35	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	11	q12	UniSTS
Cytogenetic Map	10	q26.11	UniSTS
Cytogenetic Map	X	q21.3	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	19	q	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	6	p12.1	UniSTS
Cytogenetic Map	5	p13.2	UniSTS
Cytogenetic Map	4	p16	UniSTS
Cytogenetic Map	16	p13.11	UniSTS
Cytogenetic Map	5	p13.1	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	5	q34	UniSTS
Cytogenetic Map	18	q21.33	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	10	q24.32	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	2	p14	UniSTS
Cytogenetic Map	16	p13.2	UniSTS
Cytogenetic Map	12	q24.33	UniSTS
Cytogenetic Map	1	p36.3	UniSTS
Cytogenetic Map	1	p36.3-p36.2	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	9	p13.2	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	12	q14.2	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	19	q13.31	UniSTS
Cytogenetic Map	15	q13.3	UniSTS
Cytogenetic Map	6	p21.2	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	4	q22	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	13	q14.11	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	3	q21.3	UniSTS

D11S2977

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	4	q32	UniSTS
Cytogenetic Map	8	q24	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	X	p11.3	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

104

655

271

151

Low

2192

2046

1356

363

1224

201

3822

1406

1347

223

1182

1441

168

1173

2335

Below cutoff

139

932

327

242

243

463

743

2327

130

449

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NR_003367	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186119	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186120	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186121	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186123	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186124	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186125	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186126	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186127	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186128	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186129	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186130	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186131	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186132	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186133	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186134	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186135	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186136	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186137	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186138	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186139	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186140	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186141	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186142	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186143	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186144	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186145	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186146	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186147	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186148	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186149	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186150	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186151	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186152	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186153	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186154	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186155	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186156	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186157	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186158	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186159	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186160	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186161	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186162	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186163	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186164	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186165	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186166	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186167	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_186168	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190187	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC026248	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC084123	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC103705	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC103819	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK128687	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK129745	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY336081	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC033263	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC041065	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM821521	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX280136	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX648921	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068270	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	D79458	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M25802	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M25803	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M26714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M31519	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M34428	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M34431	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125224	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125225	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125228	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125230	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125231	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125233	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125234	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125235	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125236	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125239	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125242	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125243	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125256	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MF125263	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MG562504	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MG562505	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MG562506	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MG562507	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MG562508	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MG562509	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA989217	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA989218	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA989219	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X04620	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000504719

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,535 - 127,932,706 (+)	Ensembl

RefSeq Acc Id:

ENST00000512617

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,984,004 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000513868

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,890,628 - 128,101,253 (+)	Ensembl

RefSeq Acc Id:

ENST00000517525

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,538 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000517790

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,209 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000517838

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,890,587 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000518528

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,139 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000519481

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,854,398 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000520913

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,854,396 - 127,932,696 (+)	Ensembl

RefSeq Acc Id:

ENST00000521122

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,854,396 - 127,932,708 (+)	Ensembl

RefSeq Acc Id:

ENST00000521600

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,989,217 - 128,096,578 (+)	Ensembl

RefSeq Acc Id:

ENST00000521951

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,557 - 127,940,454 (+)	Ensembl

RefSeq Acc Id:

ENST00000522414

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,388 - 128,099,890 (+)	Ensembl

RefSeq Acc Id:

ENST00000522875

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,989,261 - 128,096,656 (+)	Ensembl

RefSeq Acc Id:

ENST00000522963

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,221 - 127,932,720 (+)	Ensembl

RefSeq Acc Id:

ENST00000523068

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,796,033 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000523190

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,975,950 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000523328

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,565 - 127,932,709 (+)	Ensembl

RefSeq Acc Id:

ENST00000523427

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,567 - 127,891,257 (+)	Ensembl

RefSeq Acc Id:

ENST00000524165

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,557 - 127,932,710 (+)	Ensembl

RefSeq Acc Id:

ENST00000612011

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,939,508 - 127,939,676 (+)	Ensembl

RefSeq Acc Id:

ENST00000613916

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,096,518 - 128,096,654 (+)	Ensembl

RefSeq Acc Id:

ENST00000615125

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,541 - 127,794,734 (+)	Ensembl

RefSeq Acc Id:

ENST00000615442

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,855,155 - 127,855,319 (+)	Ensembl

RefSeq Acc Id:

ENST00000616386

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,070,160 - 128,070,272 (+)	Ensembl

RefSeq Acc Id:

ENST00000617087

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,989,162 - 127,989,291 (+)	Ensembl

RefSeq Acc Id:

ENST00000650846

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,120,269 - 128,187,031 (+)	Ensembl

RefSeq Acc Id:

ENST00000650930

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,230 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000651568

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,854,400 - 127,932,712 (+)	Ensembl

RefSeq Acc Id:

ENST00000651587

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,541 - 128,187,101 (+)	Ensembl

RefSeq Acc Id:

ENST00000651664

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,890,226 - 127,932,712 (+)	Ensembl

RefSeq Acc Id:

ENST00000652492

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,027,509 - 128,101,099 (+)	Ensembl

RefSeq Acc Id:

ENST00000652695

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,859,787 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000652728

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,351 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000652816

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,537 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000652883

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,233 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000652993

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,046,371 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000653406

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,891,959 - 127,932,708 (+)	Ensembl

RefSeq Acc Id:

ENST00000653497

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,994,949 - 128,101,254 (+)	Ensembl

RefSeq Acc Id:

ENST00000653522

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,527 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000653608

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,367 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000653845

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,538 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000653853

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,008,879 - 128,101,252 (+)	Ensembl

RefSeq Acc Id:

ENST00000653990

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,983,878 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000654091

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,565 - 127,999,334 (+)	Ensembl

RefSeq Acc Id:

ENST00000654105

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,683 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000654324

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,550 - 128,101,252 (+)	Ensembl

RefSeq Acc Id:

ENST00000654369

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,346 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000655099

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,984,004 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000655148

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,409 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000655594

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,846,054 - 127,852,712 (+)	Ensembl

RefSeq Acc Id:

ENST00000655783

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,984,000 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000656077

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,046,604 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000656168

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,409 - 127,820,382 (+)	Ensembl

RefSeq Acc Id:

ENST00000656396

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,967 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000656402

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,590 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000656411

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,984,004 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000656491

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,609 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000656532

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,358 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000656693

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,802 - 127,990,365 (+)	Ensembl

RefSeq Acc Id:

ENST00000656880

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,537 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000656948

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,854,709 - 127,932,706 (+)	Ensembl

RefSeq Acc Id:

ENST00000656999

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,998,029 - 128,101,255 (+)	Ensembl

RefSeq Acc Id:

ENST00000657112

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,559 - 128,083,366 (+)	Ensembl

RefSeq Acc Id:

ENST00000657183

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,542 - 127,932,696 (+)	Ensembl

RefSeq Acc Id:

ENST00000657211

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,538 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000657289

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,533 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000657297

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,559 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000657356

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,567 - 128,099,887 (+)	Ensembl

RefSeq Acc Id:

ENST00000657384

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,198 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000657449

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,575 - 128,101,254 (+)	Ensembl

RefSeq Acc Id:

ENST00000657451

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,763 - 128,101,254 (+)	Ensembl

RefSeq Acc Id:

ENST00000657517

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,535 - 127,852,712 (+)	Ensembl

RefSeq Acc Id:

ENST00000657596

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,346 - 127,932,700 (+)	Ensembl

RefSeq Acc Id:

ENST00000657667

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,754 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000657682

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,406 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000657693

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,555 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000657844

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,233 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000657945

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,408 - 128,099,677 (+)	Ensembl

RefSeq Acc Id:

ENST00000658018

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,317 - 128,101,250 (+)	Ensembl

RefSeq Acc Id:

ENST00000658065

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,409 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000658158

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,152 - 128,096,763 (+)	Ensembl

RefSeq Acc Id:

ENST00000658242

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,912,004 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000658305

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,046,599 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000658350

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,997,754 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000658429

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,039,647 - 128,101,252 (+)	Ensembl

RefSeq Acc Id:

ENST00000658556

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,550 - 127,932,708 (+)	Ensembl

RefSeq Acc Id:

ENST00000658840

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,997,045 - 127,999,334 (+)	Ensembl

RefSeq Acc Id:

ENST00000659106

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,997,045 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000659326

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,196 - 127,996,681 (+)	Ensembl

RefSeq Acc Id:

ENST00000659625

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,802 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000659666

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,984,004 - 128,101,252 (+)	Ensembl

RefSeq Acc Id:

ENST00000659892

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,984,171 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000659912

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,820 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000660069

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,048,250 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000660122

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,984,004 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000660146

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,285 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000660200

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,537 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000660438

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,155 - 128,017,217 (+)	Ensembl

RefSeq Acc Id:

ENST00000660456

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,773 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000660631

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,565 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000660659

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,282 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000660781

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,193 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000660896

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,928 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000660912

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,204 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000661160

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,180 - 127,932,708 (+)	Ensembl

RefSeq Acc Id:

ENST00000661205

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,796 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000661391

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,285 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000661625

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,346 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000661830

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,533 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000661988

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,413 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000662061

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,590 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000662410

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,560 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000662413

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,565 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000662709

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,984,004 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000662766

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,537 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000663059

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,799 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000663461

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,890,601 - 128,101,252 (+)	Ensembl

RefSeq Acc Id:

ENST00000663715

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,217 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000663753

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,559 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000664139

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,531 - 127,932,708 (+)	Ensembl

RefSeq Acc Id:

ENST00000664214

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,527 - 127,932,707 (+)	Ensembl

RefSeq Acc Id:

ENST00000664265

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,563 - 128,083,335 (+)	Ensembl

RefSeq Acc Id:

ENST00000664293

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,559 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000664299

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,808 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000664610

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,998,216 - 128,070,873 (+)	Ensembl

RefSeq Acc Id:

ENST00000664742

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,984,004 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000664924

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,854,728 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000664995

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,353 - 128,101,247 (+)	Ensembl

RefSeq Acc Id:

ENST00000665166

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,854,635 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000665175

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,082,378 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000665246

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,196 - 127,932,708 (+)	Ensembl

RefSeq Acc Id:

ENST00000665372

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,565 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000665698

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,559 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000665721

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,700 - 127,995,300 (+)	Ensembl

RefSeq Acc Id:

ENST00000665737

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,559 - 128,101,254 (+)	Ensembl

RefSeq Acc Id:

ENST00000665856

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,538 - 127,943,442 (+)	Ensembl

RefSeq Acc Id:

ENST00000666039

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,046,607 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000666076

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,984,004 - 127,995,613 (+)	Ensembl

RefSeq Acc Id:

ENST00000666080

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,555 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000666105

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,409 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000666147

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,997,046 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000666223

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,409 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000666353

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,542 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000666452

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,984,004 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000666776

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,808 - 128,099,890 (+)	Ensembl

RefSeq Acc Id:

ENST00000666777

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,600 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000666842

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,200 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000666878

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,332 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000667149

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,932 - 127,942,997 (+)	Ensembl

RefSeq Acc Id:

ENST00000667204

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,600 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000667305

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,526 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000667418

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,576 - 128,071,539 (+)	Ensembl

RefSeq Acc Id:

ENST00000667539

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,555 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000667630

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,095,298 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000667714

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,675 - 128,101,255 (+)	Ensembl

RefSeq Acc Id:

ENST00000668098

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,997,045 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000668123

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,808 - 128,101,255 (+)	Ensembl

RefSeq Acc Id:

ENST00000668215

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,400 - 128,096,758 (+)	Ensembl

RefSeq Acc Id:

ENST00000668351

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,401 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000668479

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,048,135 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000668480

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,409 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000668619

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,047,339 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000669082

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,854,500 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000669132

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,537 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000669272

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,813 - 127,942,997 (+)	Ensembl

RefSeq Acc Id:

ENST00000669407

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,916,449 - 127,943,001 (+)	Ensembl

RefSeq Acc Id:

ENST00000669416

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,149 - 127,932,710 (+)	Ensembl

RefSeq Acc Id:

ENST00000669509

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,378 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000669951

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,561 - 127,996,667 (+)	Ensembl

RefSeq Acc Id:

ENST00000670009

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,400 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000670204

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,855,209 - 128,017,216 (+)	Ensembl

RefSeq Acc Id:

ENST00000670223

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,537 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000670532

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,926 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000670535

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,049,400 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000670602

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,890,196 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000670626

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,890,715 - 127,996,670 (+)	Ensembl

RefSeq Acc Id:

ENST00000670714

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,795,552 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000670795

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,561 - 127,995,232 (+)	Ensembl

RefSeq Acc Id:

ENST00000671088

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,854,724 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000671092

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,998,358 - 128,099,834 (+)	Ensembl

RefSeq Acc Id:

ENST00000671587

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	128,045,317 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000685606

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,975,942 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000685634

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,975,956 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000689722

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,975,956 - 127,996,660 (+)	Ensembl

RefSeq Acc Id:

ENST00000690350

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,526 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000690788

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,975,952 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000692433

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,975,936 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000692980

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,541 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000700930

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,916,498 - 128,101,252 (+)	Ensembl

RefSeq Acc Id:

ENST00000701558

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,916,477 - 127,932,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000701700

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,916,477 - 128,101,251 (+)	Ensembl

RefSeq Acc Id:

ENST00000701841

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,916,483 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000701958

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,975,935 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000702405

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,975,952 - 128,101,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000702532

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	127,794,541 - 128,101,254 (+)	Ensembl

RefSeq Acc Id:

NR_003367

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
GRCh37	8	128,902,874 - 129,113,499 (+)	NCBI
Build 36	8	128,875,961 - 129,182,681 (+)	NCBI Archive
HuRef	8	124,224,893 - 124,436,191 (+)	NCBI
CHM1_1	8	128,847,026 - 129,153,800 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

Sequence:

show sequence

CTCCGGGCAGAGCGCGTGTGGCGGCCGAGCACATGGGCCCGCGGGCCGGGCGGGCTCGGGGCGG
CCGGGACGAGGAGGGGCGACGACGAGCTGCGAGCAAAGATGTGCCCCGGGACCCCCGGCACCTT
CCAGTGGATTTCCTTGCGGAAAGGATGTTGGCGGTCCCTGTGACCTGTGGAGACACGGCCAGAT
CTGCCCTCCAGCCTGATCTTTTGGCCAGAAGGAGATTAAAAAGATGCCCCTCAAGATGGCTGTG
CCTGTCAGCTGCATGGAGCTTCGTTCAAGTATTTTCTGAGCCTGATGGATTTACAGTGATCTTC
AGTGGTCTGGGGAATAACGCTGGTGGAACCATGCACTGGAATGACACACGCCCGGCACATTTCA
GGATACTAAAAGTGGTTTTAAGGGAGGCTGTGGCTGAATGCCTCATGGATTCTTACAGCTTGGA
TGTCCATGGGGGACGAAGGACTGCAGCTGGCTGAGAGGGTTGAGATCTCTGTTTACTTAGATCT
CTGCCAACTTCCTTTGGGTCTCCCTATGGAATGTAAGACCCCGACTCTTCCTGGTGAAGCATCT
GATGCACGTTCCATCCGGCGCTCAGCTGGGCTTGAGCTGACCATACTCCCTGGAGCCTTCTCCC
GAGGTGCGCGGGTGACCTTGGCACATACAGCCATCATGATGGTACTTTAAGTGGAGGCTGAATC
ATCTCCCCTTTGAGCTGCTTGGCACGTGGCTCCCTTGGTGTTCCCCTTTTACTGCCAGGACACT
GAGATTTGGAGAGAGTCTCACTCTGTGGTCCAGGCTGAAGTACAGTGGCATGATCCCAGGTCAC
TGCAACCCCCACCTCCCGGGTTCAAGTGATCCTCCTGCCTCAGCCTCCCGAGTAGCTGGTATTA
CAGGCGTGTGCCACAAAGCCTGGCTAAGTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGT
TGGCCAGGTTGGTCTCGAACTCCTGACCTCAAGTGATCCACTCACTTTGGCCTTTCAACGTGCT
GGGATTACAGGCGAGAGTCACCGCACCCGGACGACTCTGACATTTTTGAAGAGTCCAGAATCCT
GTTACACCTGGGATTTAGGCACTTTCAATCTGAAAAAATACATATCCTTTCAGCACTCTGGACG
GACTTGAGAACTGTCCTTACGTGACCTAAAGCTGGAGTATTTTGAGATTGGAGAATTAAGAGCC
AGTCTTGGTGCTCTGTGTTCACCTGGTTCATCTGAGGAGCTGCATCTACCCTGCCCATGCCATA
GATCCTGCCCTGTTTGCTTCTCCTGTTGCTGCTAGTGGACATGAGAAGGACAGAATAACGGGCT
CCCAGATTCACAAGCCCCACCAAGAGGATCACCCCAGGAACGCTTGGAGGCTGAGGAGTTCACT
GAGGCTACTGCATCTTGAGACTCAGGATGAAGACCCAGCTTGGGGCTGTCAAAGAGGCCTGAAG
AGGCAGAACACCCCAGAGGAGCCTGGGGCCACCACCCAGCATCACTGTGGGAAAACGGCAGCAG
GAAATGTCCTCTCGCCTGCGTGCTCCACCTCGGTCCACGCCTTCCCTCCTTCTGGAAGCCTTGC
CTGACCACTGGCCTGCCCCTTCTATGGGAATCACTACTGACCTTGCAGCTTATTATAGACTTAT
ATGTTTTTTGCATGTCTGACACCCATGACTCCACCTGGACCTTATGGCTCCACCCAGAAGCAAT
TCAGCCCAACAGGAGGACAGCTTCAACCCATTACGATTTCATCTCTGCCCCAACCACTCAGCAG
CAAGCACCTGTTACCTGTCCACCCCCACCCCTTCCCCCAAACTGCCTTTGAAAAATCCCTAACC
TATGAGCTTTGAATAAGATGAGTACGAACTTCATCGCCCACGTGGCGTGGCCGGCCTCGTGTCT
ATTAAATTCTTTTTCTACTAAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NR_186119

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186120

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186121

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186123

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186124

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186125

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186126

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186127

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186128

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186129

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186130

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186131

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186132

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186133

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186134

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186135

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186136

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186137

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186138

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186139

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186140

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186141

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186142

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186143

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186144

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186145

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186146

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186147

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186148

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186149

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186150

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186151

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186152

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186153

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186154

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186155

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186156

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186157

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186158

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186159

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186160

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186161

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186162

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186163

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186164

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186165

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186166

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186167

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

RefSeq Acc Id:

NR_186168

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,524 - 128,101,256 (+)	NCBI
T2T-CHM13v2.0	8	128,922,013 - 129,229,130 (+)	NCBI

Promoters

RGD ID:

15096262

Promoter ID:

EPDNEWNC_H1104

Type:

multiple initiation site

Name:

PVT1_1

Description:

Pvt1 oncogene [Source:HGNC Symbol;Acc:HGNC:9709]

SO ACC ID:

SO:0000170

Source:

EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,794,541 - 127,794,601	EPDNEWNC

RGD ID:

15096261

Promoter ID:

EPDNEWNC_H1105

Type:

initiation region

Name:

PVT1_2

Description:

Pvt1 oncogene [Source:HGNC Symbol;Acc:HGNC:9709]

SO ACC ID:

SO:0000170

Source:

EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	127,795,813 - 127,795,873	EPDNEWNC

RGD ID:

6806978

Promoter ID:

HG_KWN:62085

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

ENST00000398994, NR_003367, UC003YSJ.2, UC010MDP.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	128,875,766 - 128,876,266 (+)	MPROMDB

RGD ID:

6813495

Promoter ID:

HG_ACW:78839

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, HeLa_S3, Lymphoblastoid, NB4

Transcripts:

PVT1.RAPR07, PVT1.SAPR07, PVT1.TAPR07, PVT1.VFAPR07, PVT1.VHAPR07, PVT1.VLAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	128,876,496 - 128,877,382 (+)	MPROMDB

RGD ID:

6813497

Promoter ID:

HG_ACW:78856

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

PVT1.VNAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	129,020,786 - 129,021,287 (+)	MPROMDB

RGD ID:

6813493

Promoter ID:

HG_ACW:78860

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid, NB4

Transcripts:

PVT1.AAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	129,075,074 - 129,075,574 (+)	MPROMDB

RGD ID:

6813491

Promoter ID:

HG_ACW:78867

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, K562, Lymphoblastoid, NB4

Transcripts:

PVT1.BAPR07, PVT1.KAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	129,129,911 - 129,131,047 (+)	MPROMDB

RGD ID:

6813494

Promoter ID:

HG_ACW:78871

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

PVT1.PAPR07-UNSPLICED

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	129,163,601 - 129,164,101 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:9709	AgrOrtholog
COSMIC	PVT1	COSMIC
Ensembl Genes	ENSG00000249859	Ensembl, ENTREZGENE
Ensembl Transcript	ENST00000513868	ENTREZGENE
	ENST00000652816	ENTREZGENE
	ENST00000660631	ENTREZGENE
	ENST00000662413	ENTREZGENE
	ENST00000667305	ENTREZGENE
GTEx	ENSG00000249859	GTEx
HGNC ID	HGNC:9709	ENTREZGENE
Human Proteome Map	PVT1	Human Proteome Map
NCBI Gene	5820	ENTREZGENE
OMIM	165140	OMIM
PharmGKB	PA34053	PharmGKB
RNAcentral	URS00026A19E9	RNACentral
	URS00026A1A1F	RNACentral
	URS00026A1A2D	RNACentral
	URS00026A1A5F	RNACentral
	URS00026A1AEA	RNACentral
	URS00026A1B19	RNACentral
	URS00026A1BB0	RNACentral
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	URS0002853A3B	RNACentral

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2018-05-22	PVT1	Pvt1 oncogene		Pvt1 oncogene (non-protein coding)	Symbol and/or name change	5135510	APPROVED

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)

Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD