PLIN2 (perilipin 2) - Rat Genome Database

Name: PLIN2
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

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Gene: PLIN2 (perilipin 2) Homo sapiens

Analyze

Symbol:

PLIN2

Name:

perilipin 2

RGD ID:

730882

HGNC Page

HGNC

Description:

Predicted to be involved in lipid storage and positive regulation of sequestering of triglyceride. Localizes to lipid droplet.

Type:

protein-coding

RefSeq Status:

REVIEWED

Also known as:

ADFP; adipophilin; adipose differentiation-related protein; ADRP; MGC10598; perilipin-2

RGD Orthologs

Mouse

Rat

Chinchilla

Bonobo

Dog

Squirrel

Pig

Green Monkey

Naked Mole-Rat

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Plin2 (perilipin 2)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Rattus norvegicus (Norway rat):	Plin2 (perilipin 2)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Plin2 (perilipin 2)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	PLIN2 (perilipin 2)	NCBI	Ortholog
Canis lupus familiaris (dog):	PLIN2 (perilipin 2)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Plin2 (perilipin 2)	NCBI	Ortholog
Sus scrofa (pig):	PLIN2 (perilipin 2)	HGNC	Ensembl, NCBI, OrthoDB
Chlorocebus sabaeus (African green monkey):	PLIN2 (perilipin 2)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Plin2 (perilipin 2)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Plin2 (perilipin 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|TreeFam)
Mus musculus (house mouse):	Plin2 (perilipin 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|Roundup\|TreeFam)
Danio rerio (zebrafish):	plin2 (perilipin 2)	Alliance	DIOPT (Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|Roundup\|TreeFam\|ZFIN)
Drosophila melanogaster (fruit fly):	Lsd-2	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|Roundup)

Related Pseudogenes:

LOC645965

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.p13 Ensembl	9	19,108,375 - 19,149,290 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh38	9	19,108,391 - 19,127,518 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh37	9	19,115,759 - 19,127,490 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
GRCh37	9	19,115,759 - 19,127,604 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	9	19,105,759 - 19,117,573 (-)	NCBI	NCBI36		hg18	NCBI36
Build 34	9	19,105,759 - 19,117,573	NCBI
Celera	9	19,041,952 - 19,053,704 (-)	NCBI
Cytogenetic Map	9	p22.1	NCBI
HuRef	9	19,077,611 - 19,089,275 (-)	NCBI		HuRef
CHM1_1	9	19,115,770 - 19,127,537 (-)	NCBI		CHM1_1

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

Experimental Liver Cirrhosis (EXP)

fatty liver disease (EXP,ISO)

Hypertriglyceridemia (ISO)

Insulin Resistance (ISO)

Stomach Neoplasms (EXP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-schisandrin B (ISO)

(-)-epigallocatechin 3-gallate (EXP)

(S)-nicotine (ISO)

1,1-dichloroethene (ISO)

1,2-dimethylhydrazine (ISO)

1,3-dinitrobenzene (ISO)

1,4-phenylenediamine (EXP)

1-chloro-2,4-dinitrobenzene (EXP)

1-naphthyl isothiocyanate (ISO)

17beta-estradiol (EXP,ISO)

2,2',4,4',5,5'-hexachlorobiphenyl (ISO)

2,2',4,4'-Tetrabromodiphenyl ether (EXP)

2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)propanoic acid (EXP)

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

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

2-hydroxypropanoic acid (EXP)

3,3',4,4',5-pentachlorobiphenyl (ISO)

3,3',5-triiodo-L-thyronine (ISO)

3-isobutyl-1-methyl-7H-xanthine (EXP,ISO)

3H-1,2-dithiole-3-thione (ISO)

4,4'-sulfonyldiphenol (EXP)

5-aza-2'-deoxycytidine (EXP)

5-fluorouracil (EXP)

6-(4-chlorophenyl)imidazo[2,1-b][1,3]thiazole-5-carbaldehyde O-(3,4-dichlorobenzyl)oxime (EXP)

6-propyl-2-thiouracil (ISO)

acetylsalicylic acid (ISO)

aflatoxin B1 (EXP)

all-trans-retinoic acid (EXP,ISO)

alpha-linolenic acid (ISO)

amphetamine (ISO)

arachidonic acid (ISO)

arsane (EXP)

arsenic atom (EXP)

arsenous acid (EXP)

atrazine (EXP)

avobenzone (EXP)

benzene-1,2,4-triol (EXP)

benzo[a]pyrene (EXP,ISO)

benzoates (EXP)

beta-naphthoflavone (ISO)

bezafibrate (EXP)

bis(2-ethylhexyl) phthalate (ISO)

bisphenol A (EXP,ISO)

boron nitride (EXP)

bromobenzene (ISO)

buspirone (ISO)

butanal (EXP)

cadmium atom (ISO)

cadmium dichloride (EXP,ISO)

cannabidiol (ISO)

capsaicin (ISO)

carbon nanotube (EXP,ISO)

celecoxib (EXP)

chloropicrin (EXP)

chloroprene (ISO)

chlorpromazine (ISO)

ciglitazone (EXP)

ciprofibrate (EXP,ISO)

cisplatin (EXP,ISO)

clofibrate (ISO)

clofibric acid (EXP)

Clofop (EXP)

copper atom (EXP)

copper(0) (EXP)

crocidolite asbestos (EXP)

cyclosporin A (EXP,ISO)

deoxynivalenol (EXP)

dexamethasone (EXP,ISO)

diarsenic trioxide (EXP)

dibenz[a,h]anthracene (ISO)

dibenzo[a,l]pyrene (ISO)

dibutyl phthalate (EXP,ISO)

dichloroacetic acid (ISO)

dioxygen (EXP,ISO)

diuron (ISO)

doxorubicin (EXP)

epoxiconazole (ISO)

ethanol (ISO)

ethyl methanesulfonate (EXP)

farnesol (EXP)

fenofibrate (EXP,ISO)

folic acid (ISO)

formaldehyde (EXP)

fumonisin B1 (ISO)

gamma-linolenic acid (EXP)

gemfibrozil (ISO)

glafenine (ISO)

glutathione (ISO)

GW 4064 (EXP)

GW 501516 (EXP)

GW 7647 (EXP)

hexadecanoic acid (EXP,ISO)

ibuprofen (EXP,ISO)

indole-3-methanol (ISO)

indometacin (EXP)

isotretinoin (EXP)

lead diacetate (ISO)

leflunomide (EXP)

Licarin A (ISO)

metformin (ISO)

methapyrilene (ISO)

methotrexate (EXP,ISO)

methyl methanesulfonate (EXP)

mono(2-ethylhexyl) phthalate (ISO)

Monobutylphthalate (ISO)

N-[2-(4-bromocinnamylamino)ethyl]isoquinoline-5-sulfonamide (ISO)

N-acetyl-L-cysteine (ISO)

N-nitrosodiethylamine (ISO)

N-nitrosodimethylamine (ISO)

naproxen (ISO)

nickel dichloride (EXP)

nickel sulfate (EXP)

nicotine (ISO)

nimesulide (EXP)

nitrofen (ISO)

ochratoxin A (EXP)

octadecanoic acid (EXP)

oleic acid (EXP,ISO)

oxaliplatin (ISO)

paracetamol (EXP,ISO)

perflubutane (EXP)

perfluorobutyric acid (EXP)

perfluorodecanoic acid (EXP)

perfluorododecanoic acid (EXP)

perfluoroheptanoic acid (EXP)

perfluorohexanesulfonic acid (EXP)

perfluorohexanoic acid (EXP)

perfluorononanoic acid (EXP)

perfluorooctane-1-sulfonic acid (EXP,ISO)

perfluorooctanoic acid (EXP,ISO)

perfluoroundecanoic acid (EXP)

phenformin (ISO)

phenobarbital (EXP,ISO)

phorbol 13-acetate 12-myristate (EXP)

pioglitazone (EXP)

pirinixic acid (EXP,ISO)

potassium chromate (EXP)

potassium dichromate (EXP)

pregnenolone 16alpha-carbonitrile (ISO)

propiconazole (ISO)

quinolin-8-ol (EXP)

rac-lactic acid (EXP)

resveratrol (ISO)

rimonabant (ISO)

rotenone (ISO)

serpentine asbestos (EXP)

silicon dioxide (EXP)

sodium arsenate (EXP)

sodium arsenite (ISO)

sodium dichromate (ISO)

sodium fluoride (ISO)

Soman (ISO)

steviol (ISO)

stevioside (ISO)

streptozocin (ISO)

sumatriptan (ISO)

sunitinib (EXP)

Tesaglitazar (EXP)

tetrachloroethene (ISO)

tetrachloromethane (ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

tolcapone (ISO)

topotecan (ISO)

tributylstannane (ISO)

Tributyltin oxide (ISO)

triphenyl phosphate (ISO)

troglitazone (EXP,ISO)

trovafloxacin (ISO)

tunicamycin (EXP,ISO)

valproic acid (EXP)

vancomycin (ISO)

vinclozolin (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

lipid storage (IBA,ISO)

long-chain fatty acid transport (IEA,ISO)

positive regulation of sequestering of triglyceride (IBA)

regulation of metabolic process (TAS)

response to drug (IEA,ISO)

response to organic cyclic compound (IEA,ISO)

Cellular Component

cytoplasm (ISO)

cytosol (IBA,ISO)

endoplasmic reticulum (TAS)

extracellular region (TAS)

lipid droplet (IBA,IDA,ISO)

nucleus (IEA,ISO)

plasma membrane (ISO,TAS)

Molecular Function

protein binding (IPI,ISO)

Molecular Pathway Annotations Click to see Annotation Detail View

hypoxia inducible factor pathway (EXP)

References

References - curated


1.	GOA_HUMAN data from the GO Consortium
2.	Imai Y, etal., Gastroenterology. 2007 May;132(5):1947-54. Epub 2007 Feb 23.
3.	Nishikimi T, etal., Regul Pept. 2009 Apr 10;154(1-3):44-53. doi: 10.1016/j.regpep.2009.02.006. Epub 2009 Feb 15.
4.	Pipeline to import Pathway Interaction Database annotations from NCI into RGD
5.	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:1518805	PMID:7829101	PMID:9003395	PMID:9799447	PMID:12114189	PMID:12387890	PMID:12477932	PMID:12591929	PMID:14671211	PMID:14707038	PMID:14741744	PMID:15136565
PMID:15146197	PMID:15336557	PMID:15489334	PMID:15545278	PMID:16230742	PMID:16391323	PMID:16489205	PMID:16808905	PMID:16884492	PMID:16936283	PMID:17200350	PMID:17322100
PMID:17446422	PMID:17620659	PMID:17927964	PMID:18188946	PMID:18393390	PMID:18606814	PMID:18624398	PMID:18827892	PMID:18832575	PMID:19054096	PMID:19169702	PMID:19351497
PMID:19460752	PMID:19602560	PMID:19638644	PMID:19717842	PMID:19843633	PMID:19851831	PMID:20032580	PMID:20118912	PMID:20143336	PMID:20661576	PMID:20887090	PMID:21566511
PMID:21828233	PMID:21873635	PMID:22238364	PMID:22496505	PMID:22667335	PMID:22949030	PMID:22952953	PMID:23129790	PMID:23603836	PMID:23688400	PMID:23931576	PMID:23977392
PMID:24405744	PMID:24577896	PMID:25172666	PMID:25279712	PMID:25559404	PMID:25595097	PMID:26166692	PMID:26181025	PMID:26443937	PMID:26598603	PMID:26636961	PMID:26728854
PMID:26731658	PMID:26742848	PMID:27157138	PMID:27308945	PMID:27467545	PMID:27567691	PMID:27591428	PMID:28005267	PMID:28404922	PMID:28713961	PMID:29422264	PMID:29529198
PMID:29733984	PMID:29749470	PMID:30178542	PMID:30288961	PMID:30351430	PMID:30400205	PMID:30425097	PMID:30467901	PMID:30559250	PMID:30591149	PMID:30626683	PMID:30639242
PMID:30649995	PMID:30782775	PMID:30879968	PMID:31273897	PMID:31504629	PMID:31520166	PMID:31701069	PMID:31857696	PMID:31941931	PMID:31981756	PMID:32296183	PMID:32814053

Genomics

Comparative Map Data

PLIN2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38.p13 Ensembl	9	19,108,375 - 19,149,290 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh38	9	19,108,391 - 19,127,518 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh37	9	19,115,759 - 19,127,490 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
GRCh37	9	19,115,759 - 19,127,604 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	9	19,105,759 - 19,117,573 (-)	NCBI	NCBI36		hg18	NCBI36
Build 34	9	19,105,759 - 19,117,573	NCBI
Celera	9	19,041,952 - 19,053,704 (-)	NCBI
Cytogenetic Map	9	p22.1	NCBI
HuRef	9	19,077,611 - 19,089,275 (-)	NCBI		HuRef
CHM1_1	9	19,115,770 - 19,127,537 (-)	NCBI		CHM1_1

Plin2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	4	86,545,147 - 86,588,518 (-)	NCBI	GRCm39		mm39
GRCm38	4	86,626,910 - 86,670,217 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	4	86,648,386 - 86,670,060 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	4	86,302,469 - 86,315,963 (-)	NCBI	GRCm37		mm9	NCBIm37
MGSCv36	4	86,127,797 - 86,141,225 (-)	NCBI			mm8
Celera	4	85,171,641 - 85,185,400 (-)	NCBI		Celera
Cytogenetic Map	4	C4	NCBI
cM Map	4	40.69	NCBI

Plin2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
mRatBN7.2	5	101,156,643 - 101,211,738 (-)	NCBI
Rnor_6.0 Ensembl	5	104,984,414 - 105,010,857 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_6.0	5	104,984,413 - 105,010,863 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_5.0	5	108,972,976 - 108,999,210 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	5	105,718,496 - 105,732,817 (-)	NCBI	RGSC3.4		rn4	RGSC3.4
RGSC_v3.1	5	105,723,721 - 105,738,043 (-)	NCBI
Celera	5	99,654,064 - 99,667,851 (-)	NCBI		Celera
Cytogenetic Map	5	q32	NCBI

Plin2
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955434	21,574,292 - 21,580,988 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955434	21,573,860 - 21,580,990 (-)	NCBI	ChiLan1.0	ChiLan1.0

PLIN2
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
PanPan1.1	9	19,421,928 - 19,537,676 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	9	19,421,928 - 19,462,222 (-)	Ensembl	panpan1.1		panPan2
Mhudiblu_PPA_v0	9	18,928,455 - 18,951,132 (-)	NCBI	Mhudiblu_PPA_v0		panPan3

PLIN2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1 Ensembl	11	38,940,065 - 38,959,070 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
CanFam3.1	11	38,940,063 - 38,959,126 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1

Plin2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
SpeTri2.0	NW_004936652	1,039,248 - 1,059,983 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

PLIN2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	1	203,683,862 - 203,709,274 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	1	203,683,867 - 203,709,277 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	1	227,334,036 - 227,357,123 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

PLIN2
(Chlorocebus sabaeus - African green monkey)

No map positions available.

Plin2
(Heterocephalus glaber - naked mole-rat)

Molerat Assembly	Chr	Position (strand)	Source	Genome Browsers
Molerat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla 1.0	NW_004624736	23,114,149 - 23,122,634 (-)	NCBI

Position Markers

ADFP_2401

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	9	19,115,622 - 19,116,406	UniSTS	GRCh37
Build 36	9	19,105,622 - 19,106,406	RGD	NCBI36
Celera	9	19,041,815 - 19,042,599	RGD
HuRef	9	19,077,474 - 19,078,258	UniSTS

STS-W55904

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	9	19,115,973 - 19,116,215	UniSTS	GRCh37
Build 36	9	19,105,973 - 19,106,215	RGD	NCBI36
Celera	9	19,042,166 - 19,042,408	RGD
Cytogenetic Map	9	p22.1	UniSTS
HuRef	9	19,077,825 - 19,078,067	UniSTS
GeneMap99-GB4 RH Map	9	64.22	UniSTS
NCBI RH Map	9	230.1	UniSTS

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1466
Count of miRNA genes:	776
Interacting mature miRNAs:	912
Transcripts:	ENST00000276914, ENST00000380464, ENST00000380465, ENST00000411567, ENST00000434144, ENST00000464326, ENST00000472715, ENST00000475923, ENST00000494753
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
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.

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	visual system	adipose tissue	appendage	entire extraembryonic component	pharyngeal arch
High	1	26	4	4	20	4	64	3	1	26	1				105	5
Medium	2182	2658	1499	604	1744	456	4197	1947	1069	340	1325	1444	152	1	1099	2718	6	2
Low	231	307	220	15	167	3	86	227	2634	49	109	131	20			65
Below cutoff	22		3	1	15	2	10	20	30	4	20	32	1

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001122	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_038064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017014259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AF443203	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK296125	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK297920	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK312983	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL591206	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC005127	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BE311586	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI494696	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471071	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CN277218	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR536541	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X97324	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Reference Sequences

RefSeq Acc Id:

ENST00000276914 ⟹ ENSP00000276914

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	9	19,115,761 - 19,127,492 (-)	Ensembl

RefSeq Acc Id:

ENST00000380464 ⟹ ENSP00000369831

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	9	19,123,313 - 19,127,490 (-)	Ensembl

RefSeq Acc Id:

ENST00000380465 ⟹ ENSP00000369832

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	9	19,123,235 - 19,127,476 (-)	Ensembl

RefSeq Acc Id:

ENST00000434144 ⟹ ENSP00000403421

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	9	19,121,100 - 19,149,278 (-)	Ensembl

RefSeq Acc Id:

ENST00000464326

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	9	19,108,375 - 19,118,446 (-)	Ensembl

RefSeq Acc Id:

ENST00000472715

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	9	19,125,633 - 19,127,490 (-)	Ensembl

RefSeq Acc Id:

ENST00000475923

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	9	19,125,506 - 19,127,475 (-)	Ensembl

RefSeq Acc Id:

ENST00000494753

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	9	19,129,737 - 19,149,290 (-)	Ensembl

RefSeq Acc Id:

NM_001122 ⟹ NP_001113

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	9	19,115,761 - 19,127,492 (-)	NCBI
GRCh37	9	19,115,759 - 19,127,604 (-)	ENTREZGENE
Build 36	9	19,105,759 - 19,117,573 (-)	NCBI Archive
HuRef	9	19,077,611 - 19,089,275 (-)	ENTREZGENE
CHM1_1	9	19,115,770 - 19,127,537 (-)	NCBI

Sequence:

show sequence

CCGAGGGTGACACTCGGGCTTGGGACAGGGCGTGCTGCCGCGGGTCACGTGCTGCGGAGGCTTG
GGGAGGGGCGGCGAGGCGGGGTTTATAGCCCGGGCGCCCGCGGGCCCCACGCTTTGACCGGGTC
GTGGCAGCCGGAGTCGTCTTCGGGACGCGCCTGCTCTTCGCCTTTCGCTGCAGTCCGTCGATTT
CTTTCTCCAGGAAGAAAAATGGCATCCGTTGCAGTTGATCCACAACCGAGTGTGGTGACTCGGG
TGGTCAACCTGCCCTTGGTGAGCTCCACGTATGACCTCATGTCCTCAGCCTATCTCAGTACAAA
GGACCAGTATCCCTACCTGAAGTCTGTGTGTGAGATGGCAGAGAACGGTGTGAAGACCATCACC
TCCGTGGCCATGACCAGTGCTCTGCCCATCATCCAGAAGCTAGAGCCGCAAATTGCAGTTGCCA
ATACCTATGCCTGTAAGGGGCTAGACAGGATTGAGGAGAGACTGCCTATTCTGAATCAGCCATC
AACTCAGATTGTTGCCAATGCCAAAGGCGCTGTGACTGGGGCAAAAGATGCTGTGACGACTACT
GTGACTGGGGCCAAGGATTCTGTGGCCAGCACGATCACAGGGGTGATGGACAAGACCAAAGGGG
CAGTGACTGGCAGTGTGGAGAAGACCAAGTCTGTGGTCAGTGGCAGCATTAACACAGTCTTGGG
GAGTCGGATGATGCAGCTCGTGAGCAGTGGCGTAGAAAATGCACTCACCAAATCAGAGCTGTTG
GTAGAACAGTACCTCCCTCTCACTGAGGAAGAACTAGAAAAAGAAGCAAAAAAAGTTGAAGGAT
TTGATCTGGTTCAGAAGCCAAGTTATTATGTTAGACTGGGATCCCTGTCTACCAAGCTTCACTC
CCGTGCCTACCAGCAGGCTCTCAGCAGGGTTAAAGAAGCTAAGCAAAAAAGCCAACAGACCATT
TCTCAGCTCCATTCTACTGTTCACCTGATTGAATTTGCCAGGAAGAATGTGTATAGTGCCAATC
AGAAAATTCAGGATGCTCAGGATAAGCTCTACCTCTCATGGGTAGAGTGGAAAAGGAGCATTGG
ATATGATGATACTGATGAGTCCCACTGTGCTGAGCACATTGAGTCACGTACTCTTGCAATTGCC
CGCAACCTGACTCAGCAGCTCCAGACCACGTGCCACACCCTCCTGTCCAACATCCAAGGTGTAC
CACAGAACATCCAAGATCAAGCCAAGCACATGGGGGTGATGGCAGGCGACATCTACTCAGTGTT
CCGCAATGCTGCCTCCTTTAAAGAAGTGTCTGACAGCCTCCTCACTTCTAGCAAGGGGCAGCTG
CAGAAAATGAAGGAATCTTTAGATGACGTGATGGATTATCTTGTTAACAACACGCCCCTCAACT
GGCTGGTAGGTCCCTTTTATCCTCAGCTGACTGAGTCTCAGAATGCTCAGGACCAAGGTGCAGA
GATGGACAAGAGCAGCCAGGAGACCCAGCGATCTGAGCATAAAACTCATTAAACCTGCCCCTAT
CACTAGTGCATGCTGTGGCCAGACAGATGACACCTTTTGTTATGTTGAAATTAACTTGCTAGGC
AACCCTAAATTGGGAAGCAAGTAGCTAGTATAAAGGCCCTCAATTGTAGTTGTTTCCAGCTGAA
TTAAGAGCTTTAAAGTTTCTGGCATTAGCAGATGATTTCTGTTCACCTGGTAAGAAAAGAATGA
TAGGCTTGTCAGAGCCTATAGCCAGAACTCAGAAAAAATTCAAATGCACTTATGTTCTCATTCT
ATGGCCATTGTGTTGCCTCTGTTACTGTTTGTATTGAATAAAAACATCTTCATGTGGGCTGGGG
TAGAAACTGGTGTCTGCTCTGGTGTGATCTGAAAAGGCGTCTTCACTGCTTTATCTCATGATGC
TTGCTTGTAAAACTTGATTTTAGTTTTTCATTTCTCAAATAGGAATACTACCTTTGAATTCAAT
AAAATTCACTGCAGGATAGACCAGTTAAAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NR_038064

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	9	19,115,761 - 19,127,492 (-)	NCBI
GRCh37	9	19,115,759 - 19,127,604 (-)	ENTREZGENE
HuRef	9	19,077,611 - 19,089,275 (-)	ENTREZGENE
CHM1_1	9	19,115,770 - 19,127,537 (-)	NCBI

Sequence:

show sequence

CCGAGGGTGACACTCGGGCTTGGGACAGGGCGTGCTGCCGCGGGTCACGTGCTGCGGAGGCTTG
GGGAGGGGCGGCGAGGCGGGGTTTATAGCCCGGGCGCCCGCGGGCCCCACGCTTTGACCGGGTC
GTGGCAGCCGGAGTCGTCTTCGGGACGCGCCTGCTCTTCGCCTTTCGCTGCAGTCCGTCGATTT
CTTTCTCCAGGAAGAAAAATGGCATCCGTTGCAGTTGATCCACAACCGGTATGAATTTTGAGTA
GCCTTTGTCTACTTTCTCTCCTTTTGTGTTTTGAGAGATTAATAAGCATACCCTCCCTACTTTG
ATTGCAGAGTGTGGTGACTCGGGTGGTCAACCTGCCCTTGGTGAGCTCCACGTATGACCTCATG
TCCTCAGCCTATCTCAGTACAAAGGACCAGTATCCCTACCTGAAGTCTGTGTGTGAGATGGCAG
AGAACGGTGTGAAGACCATCACCTCCGTGGCCATGACCAGTGCTCTGCCCATCATCCAGAAGCT
AGAGCCGCAAATTGCAGTTGCCAATACCTATGCCTGTAAGGGGCTAGACAGGATTGAGGAGAGA
CTGCCTATTCTGAATCAGCCATCAACTCAGATTGTTGCCAATGCCAAAGGCGCTGTGACTGGGG
CAAAAGATGCTGTGACGACTACTGTGACTGGGGCCAAGGATTCTGTGGCCAGCACGATCACAGG
GGTGATGGACAAGACCAAAGGGGCAGTGACTGGCAGTGTGGAGAAGACCAAGTCTGTGGTCAGT
GGCAGCATTAACACAGTCTTGGGGAGTCGGATGATGCAGCTCGTGAGCAGTGGCGTAGAAAATG
CACTCACCAAATCAGAGCTGTTGGTAGAACAGTACCTCCCTCTCACTGAGGAAGAACTAGAAAA
AGAAGCAAAAAAAGTTGAAGGATTTGATCTGGTTCAGAAGCCAAGTTATTATGTTAGACTGGGA
TCCCTGTCTACCAAGCTTCACTCCCGTGCCTACCAGCAGGCTCTCAGCAGGGTTAAAGAAGCTA
AGCAAAAAAGCCAACAGACCATTTCTCAGCTCCATTCTACTGTTCACCTGATTGAATTTGCCAG
GAAGAATGTGTATAGTGCCAATCAGAAAATTCAGGATGCTCAGGATAAGCTCTACCTCTCATGG
GTAGAGTGGAAAAGGAGCATTGGATATGATGATACTGATGAGTCCCACTGTGCTGAGCACATTG
AGTCACGTACTCTTGCAATTGCCCGCAACCTGACTCAGCAGCTCCAGACCACGTGCCACACCCT
CCTGTCCAACATCCAAGGTGTACCACAGAACATCCAAGATCAAGCCAAGCACATGGGGGTGATG
GCAGGCGACATCTACTCAGTGTTCCGCAATGCTGCCTCCTTTAAAGAAGTGTCTGACAGCCTCC
TCACTTCTAGCAAGGGGCAGCTGCAGAAAATGAAGGAATCTTTAGATGACGTGATGGATTATCT
TGTTAACAACACGCCCCTCAACTGGCTGGTAGGTCCCTTTTATCCTCAGCTGACTGAGTCTCAG
AATGCTCAGGACCAAGGTGCAGAGATGGACAAGAGCAGCCAGGAGACCCAGCGATCTGAGCATA
AAACTCATTAAACCTGCCCCTATCACTAGTGCATGCTGTGGCCAGACAGATGACACCTTTTGTT
ATGTTGAAATTAACTTGCTAGGCAACCCTAAATTGGGAAGCAAGTAGCTAGTATAAAGGCCCTC
AATTGTAGTTGTTTCCAGCTGAATTAAGAGCTTTAAAGTTTCTGGCATTAGCAGATGATTTCTG
TTCACCTGGTAAGAAAAGAATGATAGGCTTGTCAGAGCCTATAGCCAGAACTCAGAAAAAATTC
AAATGCACTTATGTTCTCATTCTATGGCCATTGTGTTGCCTCTGTTACTGTTTGTATTGAATAA
AAACATCTTCATGTGGGCTGGGGTAGAAACTGGTGTCTGCTCTGGTGTGATCTGAAAAGGCGTC
TTCACTGCTTTATCTCATGATGCTTGCTTGTAAAACTTGATTTTAGTTTTTCATTTCTCAAATA
GGAATACTACCTTTGAATTCAATAAAATTCACTGCAGGATAGACCAGTTAAAAAAAAAAAAAAA
AAAA

hide sequence

RefSeq Acc Id:

XM_017014259 ⟹ XP_016869748

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	9	19,108,391 - 19,127,518 (-)	NCBI

Sequence:

show sequence

ATAGCCCGGGCGCCCGCGGGCCCCACGCTTTGACCGGGTCGTGGCAGCCGGAGTCGTCTTCGGG
ACGCGCCTGCTCTTCGCCTTTCGCTGCAGTCCGTCGATTTCTTTCTCCAGGAAGAAAAATGGCA
TCCGTTGCAGTTGATCCACAACCGAGTGTGGTGACTCGGGTGGTCAACCTGCCCTTGGTGAGCT
CCACGTATGACCTCATGTCCTCAGCCTATCTCAGTACAAAGGACCAGTATCCCTACCTGAAGTC
TGTGTGTGAGATGGCAGAGAACGGTGTGAAGACCATCACCTCCGTGGCCATGACCAGTGCTCTG
CCCATCATCCAGAAGCTAGAGCCGCAAATTGCAGTTGCCAATACCTATGCCTGTAAGGGGCTAG
ACAGGATTGAGGAGAGACTGCCTATTCTGAATCAGCCATCAACTCAGATTGTTGCCAATGCCAA
AGGCGCTGTGACTGGGGCAAAAGATGCTGTGACGACTACTGTGACTGGGGCCAAGGATTCTGTG
GCCAGCACGATCACAGGGGTGATGGACAAGACCAAAGGGGCAGTGACTGGCAGTGTGGAGAAGA
CCAAGTCTGTGGTCAGTGGCAGCATTAACACAGTCTTGGGGAGTCGGATGATGCAGCTCGTGAG
CAGTGGCGTAGAAAATGCACTCACCAAATCAGAGCTGTTGGTAGAACAGTACCTCCCTCTCACT
GAGGAAGAACTAGAAAAAGAAGCAAAAAAAGTTGAAGGATTTGATCTGGTTCAGAAGCCAAGTT
ATTATGTTAGACTGGGATCCCTGTCTACCAAGCTTCACTCCCGTGCCTACCAGCAGGCTCTCAG
CAGGGTTAAAGAAGCTAAGCAAAAAAGCCAACAGACCATTTCTCAGCTCCATTCTACTGTTCAC
CTGATTGAATTTGCCAGGAAGAATGTGTATAGTGCCAATCAGAAAATTCAGGATGCTCAGGATA
AGCTCTACCTCTCATGGGTAGAGTGGAAAAGGAGCATTGGATATGATGATACTGATGAGTCCCA
CTGTGCTGAGCACATTGAGTCACGTACTCTTGCAATTGCCCGCAACCTGACTCAGCAGCTCCAG
ACCACGTGCCACACCCTCCTGTCCAACATCCAAGGTGTACCACAGAACATCCAAGATCAAGCCA
AGCACATGGGGGTGATGGCAGGCGACATCTACTCAGTGTTCCGCAATGCTGCCTCCTTTAAAGA
AGTGTCTGACAGCCTCCTCACTTCTAGCAAGGGGCAGCTGCAGAAAATGAAGGAATCTTTAGAT
GACGTGATGGATTATCTTGTTAACAACACGCCCCTCAACTGGCTGGTGTTTGATTTCACCACCA
TAGACTTGACATCTGAGACTGATGAAATTCCAGATATTATAGCTTTGGAAGAGGAGAACGGATC
AAATAATTCACATGCTAATGGCCCTGTCCTCTCAGGGCAAGATGTTGAATAACTAACAACAATA
AAATACCCCTTTTGGTTGAATACGCAATTTGTATTACATTAAACTTCCTGTTTTTATTCCTGTG
ACTTTGAAGAGTGTTAATCTATTTTTTGGCTACATTGGTCTTAATTGCAATGACACTCTGATCT
AAACTTTTGTAAGAGATCCTAGTTCTGTGTCATATAATCATTTAATATAATTAAAGTTTAATTG
CTGAAATACTTATAATGA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001113	(Get FASTA)	NCBI Sequence Viewer
	XP_016869748	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH05127	(Get FASTA)	NCBI Sequence Viewer
	AAL35614	(Get FASTA)	NCBI Sequence Viewer
	BAG35820	(Get FASTA)	NCBI Sequence Viewer
	BAG58871	(Get FASTA)	NCBI Sequence Viewer
	BAG60238	(Get FASTA)	NCBI Sequence Viewer
	CAA65989	(Get FASTA)	NCBI Sequence Viewer
	CAG38778	(Get FASTA)	NCBI Sequence Viewer
	EAW58648	(Get FASTA)	NCBI Sequence Viewer
	EAW58649	(Get FASTA)	NCBI Sequence Viewer
	EAW58650	(Get FASTA)	NCBI Sequence Viewer
	EAW58651	(Get FASTA)	NCBI Sequence Viewer
	Q99541	(Get FASTA)	NCBI Sequence Viewer

Reference Sequences

RefSeq Acc Id:

NP_001113 ⟸ NM_001122

- UniProtKB:

Q99541 (UniProtKB/Swiss-Prot), Q6FHZ7 (UniProtKB/TrEMBL)

- Sequence:

show sequence

MASVAVDPQPSVVTRVVNLPLVSSTYDLMSSAYLSTKDQYPYLKSVCEMAENGVKTITSVAMTS
ALPIIQKLEPQIAVANTYACKGLDRIEERLPILNQPSTQIVANAKGAVTGAKDAVTTTVTGAKD
SVASTITGVMDKTKGAVTGSVEKTKSVVSGSINTVLGSRMMQLVSSGVENALTKSELLVEQYLP
LTEEELEKEAKKVEGFDLVQKPSYYVRLGSLSTKLHSRAYQQALSRVKEAKQKSQQTISQLHST
VHLIEFARKNVYSANQKIQDAQDKLYLSWVEWKRSIGYDDTDESHCAEHIESRTLAIARNLTQQ
LQTTCHTLLSNIQGVPQNIQDQAKHMGVMAGDIYSVFRNAASFKEVSDSLLTSSKGQLQKMKES
LDDVMDYLVNNTPLNWLVGPFYPQLTESQNAQDQGAEMDKSSQETQRSEHKTH

hide sequence

RefSeq Acc Id:

XP_016869748 ⟸ XM_017014259

- Peptide Label:

isoform X1

- Sequence:

show sequence

MASVAVDPQPSVVTRVVNLPLVSSTYDLMSSAYLSTKDQYPYLKSVCEMAENGVKTITSVAMTS
ALPIIQKLEPQIAVANTYACKGLDRIEERLPILNQPSTQIVANAKGAVTGAKDAVTTTVTGAKD
SVASTITGVMDKTKGAVTGSVEKTKSVVSGSINTVLGSRMMQLVSSGVENALTKSELLVEQYLP
LTEEELEKEAKKVEGFDLVQKPSYYVRLGSLSTKLHSRAYQQALSRVKEAKQKSQQTISQLHST
VHLIEFARKNVYSANQKIQDAQDKLYLSWVEWKRSIGYDDTDESHCAEHIESRTLAIARNLTQQ
LQTTCHTLLSNIQGVPQNIQDQAKHMGVMAGDIYSVFRNAASFKEVSDSLLTSSKGQLQKMKES
LDDVMDYLVNNTPLNWLVFDFTTIDLTSETDEIPDIIALEEENGSNNSHANGPVLSGQDVE

hide sequence

RefSeq Acc Id:

ENSP00000369832 ⟸ ENST00000380465

RefSeq Acc Id:

ENSP00000369831 ⟸ ENST00000380464

RefSeq Acc Id:

ENSP00000276914 ⟸ ENST00000276914

RefSeq Acc Id:

ENSP00000403421 ⟸ ENST00000434144

Promoters

RGD ID:

6807552

Promoter ID:

HG_KWN:62746

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

ENST00000380464, OTTHUMT00000051829, OTTHUMT00000051830, OTTHUMT00000051835, OTTHUMT00000051836

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	9	19,117,431 - 19,118,312 (-)	MPROMDB

RGD ID:

6851712

Promoter ID:

EP73658

Type:

multiple initiation site

Name:

HS_ADFP

Description:

Adipose differentiation-related protein.

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

NEDO full length human cDNA sequencing project.; Oligo-capping

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	9	19,117,490 - 19,117,550	EPD

RGD ID:

7214743

Promoter ID:

EPDNEW_H13117

Type:

initiation region

Name:

PLIN2_1

Description:

perilipin 2

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	9	19,127,492 - 19,127,552	EPDNEW

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 9p24.3-13.1(chr9:204193-38815478)x3	copy number gain	See cases [RCV000050357]	Chr9:204193..38815478 [GRCh38] Chr9:204193..38815475 [GRCh37] Chr9:194193..38805475 [NCBI36] Chr9:9p24.3-13.1	pathogenic\|conflicting interpretations of pathogenicity\|conflicting data from submitters
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	copy number gain	See cases [RCV000050348]	Chr9:193412..138179445 [GRCh38] Chr9:204193..141073897 [GRCh37] Chr9:194193..140193718 [NCBI36] Chr9:9p24.3-q34.3	pathogenic
GRCh38/hg38 9p24.3-13.1(chr9:204193-38741440)x3	copy number gain	See cases [RCV000051106]	Chr9:204193..38741440 [GRCh38] Chr9:204193..38741437 [GRCh37] Chr9:194193..38731437 [NCBI36] Chr9:9p24.3-13.1	pathogenic
GRCh38/hg38 9p24.3-13.1(chr9:203993-38815619)x3	copy number gain	See cases [RCV000053703]	Chr9:203993..38815619 [GRCh38] Chr9:203993..38815616 [GRCh37] Chr9:193993..38805616 [NCBI36] Chr9:9p24.3-13.1	pathogenic
GRCh38/hg38 9p24.3-21.3(chr9:204193-22086858)x3	copy number gain	See cases [RCV000053704]	Chr9:204193..22086858 [GRCh38] Chr9:204193..22086857 [GRCh37] Chr9:194193..22076857 [NCBI36] Chr9:9p24.3-21.3	pathogenic
GRCh38/hg38 9p24.3-13.3(chr9:204193-34599437)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053706]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053706]\|See cases [RCV000053706]	Chr9:204193..34599437 [GRCh38] Chr9:204193..34599435 [GRCh37] Chr9:194193..34589435 [NCBI36] Chr9:9p24.3-13.3	pathogenic
GRCh38/hg38 9p24.3-13.3(chr9:204193-33284638)x3	copy number gain	See cases [RCV000053707]	Chr9:204193..33284638 [GRCh38] Chr9:204193..33284636 [GRCh37] Chr9:194193..33274636 [NCBI36] Chr9:9p24.3-13.3	pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124532)x3	copy number gain	See cases [RCV000053745]	Chr9:193412..138124532 [GRCh38] Chr9:204193..141018984 [GRCh37] Chr9:194193..140138805 [NCBI36] Chr9:9p24.3-q34.3	pathogenic
GRCh38/hg38 9p24.3-13.1(chr9:220253-38815419)x3	copy number gain	See cases [RCV000053747]	Chr9:220253..38815419 [GRCh38] Chr9:220253..38815416 [GRCh37] Chr9:210253..38805416 [NCBI36] Chr9:9p24.3-13.1	pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]\|See cases [RCV000053748]	Chr9:193412..138179445 [GRCh38] Chr9:266045..141073897 [GRCh37] Chr9:256045..140193718 [NCBI36] Chr9:9p24.3-q34.3	pathogenic
GRCh38/hg38 9p23-21.1(chr9:9543538-30266463)x3	copy number gain	See cases [RCV000053749]	Chr9:9543538..30266463 [GRCh38] Chr9:9543538..30266461 [GRCh37] Chr9:9533538..30256461 [NCBI36] Chr9:9p23-21.1	pathogenic
GRCh38/hg38 9p23-13.3(chr9:13526091-34261642)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053750]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053750]\|See cases [RCV000053750]	Chr9:13526091..34261642 [GRCh38] Chr9:13526090..34261640 [GRCh37] Chr9:13516090..34251640 [NCBI36] Chr9:9p23-13.3	pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	copy number gain	See cases [RCV000053746]	Chr9:193412..138114463 [GRCh38] Chr9:214367..141008915 [GRCh37] Chr9:204367..140128736 [NCBI36] Chr9:9p24.3-q34.3	pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	copy number gain	See cases [RCV000133791]	Chr9:204193..138179445 [GRCh38] Chr9:204193..141073897 [GRCh37] Chr9:194193..140193718 [NCBI36] Chr9:9p24.3-q34.3	pathogenic
GRCh38/hg38 9p24.3-21.1(chr9:220257-29424848)x3	copy number gain	See cases [RCV000134037]	Chr9:220257..29424848 [GRCh38] Chr9:220257..29424846 [GRCh37] Chr9:210257..29414846 [NCBI36] Chr9:9p24.3-21.1	pathogenic
GRCh38/hg38 9p24.3-q21.11(chr9:13997-68401065)x3	copy number gain	See cases [RCV000135344]	Chr9:13997..68401065 [GRCh38] Chr9:13997..71015981 [GRCh37] Chr9:3997..70205801 [NCBI36] Chr9:9p24.3-q21.11	pathogenic
GRCh38/hg38 9p24.3-q21.12(chr9:193412-70630731)x3	copy number gain	See cases [RCV000136152]	Chr9:193412..70630731 [GRCh38] Chr9:220253..73245647 [GRCh37] Chr9:210253..72435467 [NCBI36] Chr9:9p24.3-q21.12	pathogenic
GRCh38/hg38 9p24.3-q21.13(chr9:193412-74615913)x3	copy number gain	See cases [RCV000135954]	Chr9:193412..74615913 [GRCh38] Chr9:204193..77230829 [GRCh37] Chr9:194193..76420649 [NCBI36] Chr9:9p24.3-q21.13	pathogenic
GRCh38/hg38 9p24.1-21.2(chr9:4661872-27661572)x3	copy number gain	See cases [RCV000136680]	Chr9:4661872..27661572 [GRCh38] Chr9:4661872..27661570 [GRCh37] Chr9:4651872..27651570 [NCBI36] Chr9:9p24.1-21.2	pathogenic
GRCh38/hg38 9p24.1-13.2(chr9:7162304-37038771)x3	copy number gain	See cases [RCV000137741]	Chr9:7162304..37038771 [GRCh38] Chr9:7162304..37038768 [GRCh37] Chr9:7152304..37028768 [NCBI36] Chr9:9p24.1-13.2	pathogenic
GRCh38/hg38 9p24.3-q21.11(chr9:204104-66233120)x4	copy number gain	See cases [RCV000137888]	Chr9:204104..66233120 [GRCh38] Chr9:204104..47212321 [GRCh37] Chr9:194104..47002141 [NCBI36] Chr9:9p24.3-q21.11	pathogenic\|conflicting data from submitters
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	copy number gain	See cases [RCV000138783]	Chr9:193412..138124524 [GRCh38] Chr9:204090..141018976 [GRCh37] Chr9:194090..140138797 [NCBI36] Chr9:9p24.3-q34.3	pathogenic
GRCh38/hg38 9p24.3-21.3(chr9:459131-24207894)x3	copy number gain	See cases [RCV000138499]	Chr9:459131..24207894 [GRCh38] Chr9:459131..24207892 [GRCh37] Chr9:449131..24197892 [NCBI36] Chr9:9p24.3-21.3	pathogenic
GRCh38/hg38 9p24.3-q21.11(chr9:204104-67549861)x3	copy number gain	See cases [RCV000139208]	Chr9:204104..67549861 [GRCh38] Chr9:204104..66516698 [GRCh37] Chr9:194104..66256518 [NCBI36] Chr9:9p24.3-q21.11	pathogenic
GRCh38/hg38 9p24.3-13.3(chr9:204104-34151476)x3	copy number gain	See cases [RCV000139015]	Chr9:204104..34151476 [GRCh38] Chr9:204104..34151474 [GRCh37] Chr9:194104..34141474 [NCBI36] Chr9:9p24.3-13.3	pathogenic\|likely benign
GRCh38/hg38 9p24.3-13.1(chr9:204104-38768294)x3	copy number gain	See cases [RCV000139126]	Chr9:204104..38768294 [GRCh38] Chr9:204104..38768291 [GRCh37] Chr9:194104..38758291 [NCBI36] Chr9:9p24.3-13.1	pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	copy number gain	See cases [RCV000138962]	Chr9:193412..138159073 [GRCh38] Chr9:204104..141053525 [GRCh37] Chr9:194104..140173346 [NCBI36] Chr9:9p24.3-q34.3	pathogenic\|conflicting data from submitters
GRCh38/hg38 9p22.2-q21.11(chr9:18344605-68257015)	copy number gain	See cases [RCV000140448]	Chr9:18344605..68257015 [GRCh38] Chr9:18344603..68995221 [GRCh37] Chr9:18334603..68285041 [NCBI36] Chr9:9p22.2-q21.11	pathogenic
GRCh38/hg38 9p24.3-21.2(chr9:204104-27963369)x3	copy number gain	See cases [RCV000139621]	Chr9:204104..27963369 [GRCh38] Chr9:204104..27963367 [GRCh37] Chr9:194104..27953367 [NCBI36] Chr9:9p24.3-21.2	pathogenic
GRCh38/hg38 9p24.3-q22.1(chr9:203861-88130444)x4	copy number gain	See cases [RCV000141904]	Chr9:203861..88130444 [GRCh38] Chr9:203861..90745359 [GRCh37] Chr9:193861..89935179 [NCBI36] Chr9:9p24.3-q22.1	pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	copy number gain	See cases [RCV000141876]	Chr9:203861..138125937 [GRCh38] Chr9:203861..141020389 [GRCh37] Chr9:193861..140140210 [NCBI36] Chr9:9p24.3-q34.3	pathogenic
GRCh38/hg38 9p24.3-21.1(chr9:203861-31423873)x4	copy number gain	See cases [RCV000141662]	Chr9:203861..31423873 [GRCh38] Chr9:203861..31423871 [GRCh37] Chr9:193861..31413871 [NCBI36] Chr9:9p24.3-21.1	pathogenic
GRCh38/hg38 9p24.3-q21.31(chr9:193412-79877816)x3	copy number gain	See cases [RCV000143012]	Chr9:193412..79877816 [GRCh38] Chr9:204104..82492731 [GRCh37] Chr9:194104..81682551 [NCBI36] Chr9:9p24.3-q21.31	pathogenic
GRCh38/hg38 9p24.3-13.1(chr9:203861-38381642)	copy number gain	See cases [RCV000143411]	Chr9:203861..38381642 [GRCh38] Chr9:203861..38381639 [GRCh37] Chr9:193861..38371639 [NCBI36] Chr9:9p24.3-13.1	pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	copy number gain	See cases [RCV000143476]	Chr9:203862..138125937 [GRCh38] Chr9:203862..141020389 [GRCh37] Chr9:193862..140140210 [NCBI36] Chr9:9p24.3-q34.3	pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	copy number gain	See cases [RCV000148113]	Chr9:193412..138179445 [GRCh38] Chr9:204193..141073897 [GRCh37] Chr9:194193..140193718 [NCBI36] Chr9:9p24.3-q34.3	pathogenic
GRCh38/hg38 9p24.3-13.1(chr9:204193-38815478)x3	copy number gain	See cases [RCV000148159]	Chr9:204193..38815478 [GRCh38] Chr9:204193..38815475 [GRCh37] Chr9:194193..38805475 [NCBI36] Chr9:9p24.3-13.1	pathogenic
GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	copy number gain	See cases [RCV000139207]	Chr9:193412..138159073 [GRCh38] Chr9:68420641..141053525 [GRCh37] Chr9:67910461..140173346 [NCBI36] Chr9:9p11.2-q34.3	pathogenic
GRCh37/hg19 9p24.3-13.1(chr9:163131-38763958)x3	copy number gain	See cases [RCV000240201]	Chr9:163131..38763958 [GRCh37] Chr9:9p24.3-13.1	pathogenic
GRCh37/hg19 9p24.3-11.2(chr9:213161-47212321)x4	copy number gain	See cases [RCV000240048]	Chr9:213161..47212321 [GRCh37] Chr9:9p24.3-11.2	pathogenic
GRCh37/hg19 9p24.3-13.1(chr9:213161-39092820)x3	copy number gain	See cases [RCV000239869]	Chr9:213161..39092820 [GRCh37] Chr9:9p24.3-13.1	pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3	copy number gain	See cases [RCV000240081]	Chr9:163131..141122114 [GRCh37] Chr9:9p24.3-q34.3	pathogenic
GRCh37/hg19 9p24.3-22.1(chr9:213161-19450250)x3	copy number gain	See cases [RCV000240225]	Chr9:213161..19450250 [GRCh37] Chr9:9p24.3-22.1	pathogenic
GRCh37/hg19 9p24.3-q13(chr9:203861-68188391)x4	copy number gain	See cases [RCV000449165]	Chr9:203861..68188391 [GRCh37] Chr9:9p24.3-q13	pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407)	copy number gain	See cases [RCV000449375]	Chr9:62525..141006407 [GRCh37] Chr9:9p24.3-q34.3	pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	copy number gain	See cases [RCV000447207]	Chr9:203861..141020389 [GRCh37] Chr9:9p24.3-q34.3	pathogenic
GRCh37/hg19 9p24.3-13.1(chr9:32396-39140211)	copy number gain	See cases [RCV000447246]	Chr9:32396..39140211 [GRCh37] Chr9:9p24.3-13.1	pathogenic
GRCh37/hg19 9p24.3-q13(chr9:203861-67983174)x4	copy number gain	See cases [RCV000446521]	Chr9:203861..67983174 [GRCh37] Chr9:9p24.3-q13	pathogenic
GRCh37/hg19 9p24.3-q21.11(chr9:13997-70919878)x4	copy number gain	See cases [RCV000448242]	Chr9:13997..70919878 [GRCh37] Chr9:9p24.3-q21.11	pathogenic
GRCh37/hg19 9p24.3-q21.11(chr9:203861-69002883)x3	copy number gain	See cases [RCV000448569]	Chr9:203861..69002883 [GRCh37] Chr9:9p24.3-q21.11	pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203864-141020389)x3	copy number gain	See cases [RCV000448978]	Chr9:203864..141020389 [GRCh37] Chr9:9p24.3-q34.3	pathogenic
GRCh37/hg19 9p22.2-21.1(chr9:17684434-30889762)x3	copy number gain	See cases [RCV000510665]	Chr9:17684434..30889762 [GRCh37] Chr9:9p22.2-21.1	pathogenic
GRCh37/hg19 9p24.1-21.1(chr9:5900425-30008330)x3	copy number gain	See cases [RCV000510425]	Chr9:5900425..30008330 [GRCh37] Chr9:9p24.1-21.1	pathogenic
GRCh37/hg19 9p22.1(chr9:18580904-19377336)x4	copy number gain	See cases [RCV000511542]	Chr9:18580904..19377336 [GRCh37] Chr9:9p22.1	likely benign
GRCh37/hg19 9p24.3-13.1(chr9:203861-38787480)x3	copy number gain	See cases [RCV000510864]	Chr9:203861..38787480 [GRCh37] Chr9:9p24.3-13.1	pathogenic
GRCh37/hg19 9p22.2-13.3(chr9:17132123-35567051)x3	copy number gain	See cases [RCV000510986]	Chr9:17132123..35567051 [GRCh37] Chr9:9p22.2-13.3	pathogenic
GRCh37/hg19 9p23-21.2(chr9:10320113-26205565)x1	copy number loss	PARP Inhibitor response [RCV000626433]	Chr9:10320113..26205565 [GRCh37] Chr9:9p23-21.2	drug response
GRCh37/hg19 9p24.3-11.2(chr9:204193-44259464)x4	copy number gain	Syndromic hydrocephalus due to diffuse villous hyperplasia of choroid plexus [RCV000677299]	Chr9:204193..44259464 [GRCh37] Chr9:9p24.3-11.2	likely pathogenic
GRCh37/hg19 9p24.3-q21.33(chr9:203861-88189913)x3	copy number gain	See cases [RCV000512431]	Chr9:203861..88189913 [GRCh37] Chr9:9p24.3-q21.33	pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389)	copy number gain	See cases [RCV000512392]	Chr9:203862..141020389 [GRCh37] Chr9:9p24.3-q34.3	pathogenic
GRCh37/hg19 9p24.3-21.3(chr9:203861-20653468)x3	copy number gain	not provided [RCV000683170]	Chr9:203861..20653468 [GRCh37] Chr9:9p24.3-21.3	pathogenic
GRCh37/hg19 9p22.1(chr9:18935985-19603778)x3	copy number gain	not provided [RCV000683139]	Chr9:18935985..19603778 [GRCh37] Chr9:9p22.1	uncertain significance
GRCh37/hg19 9p22.1-21.3(chr9:18944282-19964747)x3	copy number gain	not provided [RCV000683150]	Chr9:18944282..19964747 [GRCh37] Chr9:9p22.1-21.3	uncertain significance
GRCh37/hg19 9p24.3-13.1(chr9:203861-38787480)x3	copy number gain	not provided [RCV000683172]	Chr9:203861..38787480 [GRCh37] Chr9:9p24.3-13.1	pathogenic
GRCh37/hg19 9p24.3-q13(chr9:203861-67983174)x4	copy number gain	not provided [RCV000683173]	Chr9:203861..67983174 [GRCh37] Chr9:9p24.3-q13	pathogenic
GRCh37/hg19 9p24.3-21.2(chr9:203861-26397133)x3	copy number gain	not provided [RCV000683171]	Chr9:203861..26397133 [GRCh37] Chr9:9p24.3-21.2	pathogenic
GRCh37/hg19 9p24.3-q13(chr9:203861-68262804)x3,4	copy number gain	not provided [RCV000683174]	Chr9:203861..68262804 [GRCh37] Chr9:9p24.3-q13	pathogenic
GRCh37/hg19 9p24.3-q21.12(chr9:203861-72717793)x3	copy number gain	not provided [RCV000683176]	Chr9:203861..72717793 [GRCh37] Chr9:9p24.3-q21.12	pathogenic
GRCh37/hg19 9p24.3-q21.11(chr9:203861-70985795)x4	copy number gain	not provided [RCV000683175]	Chr9:203861..70985795 [GRCh37] Chr9:9p24.3-q21.11	pathogenic
GRCh37/hg19 9p22.1(chr9:19102828-19127877)x1	copy number loss	not provided [RCV000748272]	Chr9:19102828..19127877 [GRCh37] Chr9:9p22.1	benign
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141122247)x3	copy number gain	not provided [RCV000748055]	Chr9:10590..141122247 [GRCh37] Chr9:9p24.3-q34.3	pathogenic
GRCh37/hg19 9p24.3-21.3(chr9:46587-22012051)x3	copy number gain	not provided [RCV000748062]	Chr9:46587..22012051 [GRCh37] Chr9:9p24.3-21.3	pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141107672)x3	copy number gain	not provided [RCV000748053]	Chr9:10590..141107672 [GRCh37] Chr9:9p24.3-q34.3	pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:46587-141066491)x3	copy number gain	not provided [RCV000748063]	Chr9:46587..141066491 [GRCh37] Chr9:9p24.3-q34.3	pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141114095)x2	copy number gain	not provided [RCV000748054]	Chr9:10590..141114095 [GRCh37] Chr9:9p24.3-q34.3	pathogenic
GRCh37/hg19 9p24.2-21.3(chr9:4420767-22195820)x3	copy number gain	not provided [RCV000748122]	Chr9:4420767..22195820 [GRCh37] Chr9:9p24.2-21.3	pathogenic
NM_001122.4(PLIN2):c.493G>C (p.Gly165Arg)	single nucleotide variant	not provided [RCV000897363]	Chr9:19120982 [GRCh38] Chr9:19120980 [GRCh37] Chr9:9p22.1	benign
GRCh37/hg19 9p24.3-13.1(chr9:203861-38472979)x3	copy number gain	not provided [RCV000848175]	Chr9:203861..38472979 [GRCh37] Chr9:9p24.3-13.1	pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3	copy number gain	not provided [RCV000845900]	Chr9:203861..141020388 [GRCh37] Chr9:9p24.3-q34.3	pathogenic
GRCh37/hg19 9p24.3-13.1(chr9:214309-39156958)	copy number gain	not provided [RCV000767644]	Chr9:214309..39156958 [GRCh37] Chr9:9p24.3-13.1	pathogenic
GRCh37/hg19 9p24.3-22.1(chr9:203861-19448473)x3	copy number gain	not provided [RCV000845664]	Chr9:203861..19448473 [GRCh37] Chr9:9p24.3-22.1	pathogenic
GRCh37/hg19 9p22.2-22.1(chr9:18214877-19289427)x3	copy number gain	not provided [RCV000847984]	Chr9:18214877..19289427 [GRCh37] Chr9:9p22.2-22.1	uncertain significance
GRCh37/hg19 9p22.1(chr9:19080351-19544088)x3	copy number gain	not provided [RCV001006219]	Chr9:19080351..19544088 [GRCh37] Chr9:9p22.1	uncertain significance
GRCh37/hg19 9p24.3-q13(chr9:203861-67986965)x3	copy number gain	not provided [RCV000845815]	Chr9:203861..67986965 [GRCh37] Chr9:9p24.3-q13	pathogenic
NM_001122.4(PLIN2):c.971C>T (p.Thr324Met)	single nucleotide variant	not provided [RCV000964305]	Chr9:19116591 [GRCh38] Chr9:19116589 [GRCh37] Chr9:9p22.1	benign
GRCh37/hg19 9p24.3-q21.11(chr9:203861-70984588)x3	copy number gain	not provided [RCV001006167]	Chr9:203861..70984588 [GRCh37] Chr9:9p24.3-q21.11	pathogenic
GRCh37/hg19 9p22.1(chr9:19108473-19329836)x1	copy number loss	not provided [RCV001260066]	Chr9:19108473..19329836 [GRCh37] Chr9:9p22.1	uncertain significance

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:248	AgrOrtholog
COSMIC	PLIN2	COSMIC
Ensembl Genes	ENSG00000147872	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein	ENSP00000276914	ENTREZGENE, UniProtKB/Swiss-Prot
	ENSP00000369831	UniProtKB/TrEMBL
	ENSP00000369832	UniProtKB/TrEMBL
	ENSP00000403421	UniProtKB/TrEMBL
Ensembl Transcript	ENST00000276914	ENTREZGENE, UniProtKB/Swiss-Prot
	ENST00000380464	UniProtKB/TrEMBL
	ENST00000380465	UniProtKB/TrEMBL
	ENST00000434144	UniProtKB/TrEMBL
GTEx	ENSG00000147872	GTEx
HGNC ID	HGNC:248	ENTREZGENE
Human Proteome Map	PLIN2	Human Proteome Map
InterPro	Perilipin	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:123	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	123	ENTREZGENE
OMIM	103195	OMIM
Pfam	Perilipin	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA24569	PharmGKB
PIRSF	PAT	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	PLIN2_HUMAN	UniProtKB/Swiss-Prot
	Q5SYF3_HUMAN	UniProtKB/TrEMBL
	Q5SYF4_HUMAN	UniProtKB/TrEMBL
	Q5SYF5_HUMAN	UniProtKB/TrEMBL
	Q6FHZ7	ENTREZGENE, UniProtKB/TrEMBL
	Q99541	ENTREZGENE
UniProt Secondary	Q9BSC3	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2011-08-16	PLIN2	perilipin 2	PLIN2	perilipin 2	Symbol and/or name change	5135510	APPROVED
2011-07-27	PLIN2	perilipin 2	ADFP	adipose differentiation-related protein	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 - CTD

Imported Annotations - PID (archival)