PLPPR2 (phospholipid phosphatase related 2)

Gene: PLPPR2 (phospholipid phosphatase related 2) Homo sapiens

Analyze

Symbol:

PLPPR2

Name:

phospholipid phosphatase related 2

RGD ID:

1604322

HGNC Page

HGNC:29566

Description:

Predicted to enable phosphatidate phosphatase activity. Predicted to be involved in phospholipid dephosphorylation; phospholipid metabolic process; and signal transduction. Predicted to be located in membrane. Predicted to be active in plasma membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

DKFZp761E1121; FLJ13055; inactive phospholipid phosphatase PLPPR2; lipid phosphate phosphatase-related protein type 2; LPPR2; phospholipid phosphatase-related protein type 2; plasticity related gene 4; plasticity-related gene 4 protein; PRG-4; PRG4

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	11,355,432 - 11,365,698 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	11,355,386 - 11,365,698 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	11,466,108 - 11,476,374 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	11,327,109 - 11,337,372 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	19	11,360,936 - 11,371,242 (+)	NCBI		Celera
Cytogenetic Map	19	p13.2	NCBI
HuRef	19	11,042,113 - 11,052,420 (+)	NCBI		HuRef
CHM1_1	19	11,467,084 - 11,477,386 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	11,482,410 - 11,492,670 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(-)-epigallocatechin 3-gallate (ISO)

1,1,1-Trichloro-2-(o-chlorophenyl)-2-(p-chlorophenyl)ethane (EXP)

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

2-hydroxypropanoic acid (EXP)

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

4,4'-sulfonyldiphenol (ISO)

acetamide (ISO)

aflatoxin B1 (EXP,ISO)

Aflatoxin B2 alpha (EXP)

alpha-Zearalanol (ISO)

aristolochic acid A (EXP)

atrazine (EXP)

benzo[a]pyrene (ISO)

benzo[e]pyrene (EXP)

bisphenol A (EXP,ISO)

bisphenol F (EXP)

chlorpyrifos (ISO)

cocaine (ISO)

dexamethasone (EXP)

diazinon (EXP)

doxorubicin (EXP)

epoxiconazole (ISO)

ethanol (ISO)

fulvestrant (EXP)

genistein (EXP)

indometacin (EXP)

methamphetamine (ISO)

methapyrilene (EXP)

ozone (EXP)

paracetamol (EXP,ISO)

perfluorooctanoic acid (ISO)

rac-lactic acid (EXP)

resveratrol (EXP)

sunitinib (EXP)

trichloroethene (ISO)

urethane (EXP)

valproic acid (EXP)

zearalenone (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

phospholipid dephosphorylation (IBA)

phospholipid metabolic process (IBA,IEA)

signal transduction (IBA)

Cellular Component

membrane (IEA)

plasma membrane (IBA)

Molecular Function

phosphatidate phosphatase activity (IBA,IEA)

protein binding (IPI)

References

References - curated

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

Additional References at PubMed

PMID:8125298	PMID:12477932	PMID:14702039	PMID:14750979	PMID:16344560	PMID:21873635	PMID:26186194	PMID:28514442	PMID:32296183	PMID:33961781

Genomics

Comparative Map Data

PLPPR2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	11,355,432 - 11,365,698 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	11,355,386 - 11,365,698 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	11,466,108 - 11,476,374 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	11,327,109 - 11,337,372 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	19	11,360,936 - 11,371,242 (+)	NCBI		Celera
Cytogenetic Map	19	p13.2	NCBI
HuRef	19	11,042,113 - 11,052,420 (+)	NCBI		HuRef
CHM1_1	19	11,467,084 - 11,477,386 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	11,482,410 - 11,492,670 (+)	NCBI		T2T-CHM13v2.0

Plppr2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	9	21,848,306 - 21,860,203 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	9	21,848,329 - 21,860,203 (+)	Ensembl		GRCm39 Ensembl
GRCm38	9	21,935,684 - 21,948,907 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	9	21,937,033 - 21,948,907 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	9	21,742,718 - 21,753,351 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	9	21,688,676 - 21,699,309 (+)	NCBI		MGSCv36	mm8
Celera	9	19,207,511 - 19,218,335 (+)	NCBI		Celera
Cytogenetic Map	9	A3	NCBI
cM Map	9	7.92	NCBI

Plppr2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	8	28,742,787 - 28,755,555 (+)	NCBI		GRCr8
mRatBN7.2	8	20,467,071 - 20,479,474 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	8	20,467,071 - 20,479,474 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	8	24,497,880 - 24,510,469 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	8	22,793,436 - 22,806,016 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	8	20,696,681 - 20,709,077 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	8	22,946,787 - 22,959,554 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	8	22,947,152 - 22,959,554 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	8	23,001,604 - 23,014,338 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	8	21,040,658 - 21,050,517 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	8	21,858,304 - 21,870,682 (+)	NCBI		Celera
Cytogenetic Map	8	q13	NCBI

Plppr2
(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_004955495	2,269,769 - 2,279,910 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955495	2,270,323 - 2,279,688 (+)	NCBI	ChiLan1.0	ChiLan1.0

PLPPR2
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	20	16,268,971 - 16,279,745 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	19	15,269,566 - 15,278,743 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	19	10,902,739 - 10,913,270 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	19	11,614,293 - 11,624,017 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	19	11,614,294 - 11,624,017 (+)	Ensembl	panpan1.1		panPan2

PLPPR2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	20	49,955,538 - 49,964,207 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	20	49,955,566 - 49,964,416 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	20	49,829,066 - 49,837,707 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	20	50,476,257 - 50,484,918 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	20	50,476,259 - 50,491,106 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	20	49,686,478 - 49,695,212 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	20	50,112,923 - 50,121,586 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	20	50,355,872 - 50,364,535 (-)	NCBI		UU_Cfam_GSD_1.0

Plppr2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024405118	208,895,903 - 208,904,817 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936659	1,450,338 - 1,459,106 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936659	1,450,314 - 1,458,800 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

PLPPR2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	2	70,047,788 - 70,055,778 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	2	70,047,637 - 70,061,904 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	70,410,308 - 70,418,868 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

PLPPR2
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	6	10,289,234 - 10,300,511 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	6	10,289,695 - 10,300,920 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666074	9,593,413 - 9,604,350 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Plppr2
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624828	3,158,726 - 3,168,030 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624828	3,159,313 - 3,168,030 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in PLPPR2
16 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	copy number gain	See cases [RCV000133888]	Chr19:11227942..44626354 [GRCh38] Chr19:11338618..45129651 [GRCh37] Chr19:11199618..49821491 [NCBI36] Chr19:19p13.2-q13.31	pathogenic
GRCh38/hg38 19p13.2-13.13(chr19:10319474-13777860)x1	copy number loss	See cases [RCV000141568]	Chr19:10319474..13777860 [GRCh38] Chr19:10430150..13888674 [GRCh37] Chr19:10291150..13749674 [NCBI36] Chr19:19p13.2-13.13	pathogenic
GRCh38/hg38 19p13.2-13.13(chr19:8831147-13331227)x3	copy number gain	See cases [RCV000052908]	Chr19:8831147..13331227 [GRCh38] Chr19:8941823..13442041 [GRCh37] Chr19:8802823..13303041 [NCBI36] Chr19:19p13.2-13.13	likely pathogenic
GRCh38/hg38 19p13.2-13.12(chr19:10315258-14048994)x3	copy number gain	See cases [RCV000052909]	Chr19:10315258..14048994 [GRCh38] Chr19:10425934..14159806 [GRCh37] Chr19:10286934..14020806 [NCBI36] Chr19:19p13.2-13.12	pathogenic
GRCh38/hg38 19p13.2-13.12(chr19:11227942-14532135)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053944]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053944]\|See cases [RCV000053944]	Chr19:11227942..14532135 [GRCh38] Chr19:11338618..14642947 [GRCh37] Chr19:11199618..14503947 [NCBI36] Chr19:19p13.2-13.12	pathogenic
GRCh38/hg38 19p13.2(chr19:11138895-11549951)x3	copy number gain	See cases [RCV000054109]	Chr19:11138895..11549951 [GRCh38] Chr19:11249571..11660766 [GRCh37] Chr19:11110571..11521766 [NCBI36] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.1105C>T (p.Arg369Cys)	single nucleotide variant	not specified [RCV004295966]	Chr19:11364436 [GRCh38] Chr19:11475112 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.1301C>G (p.Pro434Arg)	single nucleotide variant	not specified [RCV004141958]	Chr19:11364632 [GRCh38] Chr19:11475308 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.1091C>T (p.Ser364Leu)	single nucleotide variant	not specified [RCV004237472]	Chr19:11364422 [GRCh38] Chr19:11475098 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.1243C>G (p.Leu415Val)	single nucleotide variant	not specified [RCV004115864]	Chr19:11364574 [GRCh38] Chr19:11475250 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.706G>A (p.Val236Ile)	single nucleotide variant	not specified [RCV004228612]	Chr19:11362555 [GRCh38] Chr19:11473231 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.1166C>T (p.Thr389Ile)	single nucleotide variant	not specified [RCV004186613]	Chr19:11364497 [GRCh38] Chr19:11475173 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.527C>T (p.Pro176Leu)	single nucleotide variant	not specified [RCV004229888]	Chr19:11361352 [GRCh38] Chr19:11472028 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.887G>A (p.Arg296Gln)	single nucleotide variant	not specified [RCV004087164]	Chr19:11363759 [GRCh38] Chr19:11474435 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.1186C>A (p.Pro396Thr)	single nucleotide variant	not specified [RCV004158917]	Chr19:11364517 [GRCh38] Chr19:11475193 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.959C>A (p.Ala320Glu)	single nucleotide variant	not specified [RCV004213409]	Chr19:11363831 [GRCh38] Chr19:11474507 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.430G>A (p.Ala144Thr)	single nucleotide variant	not specified [RCV004100056]	Chr19:11361255 [GRCh38] Chr19:11471931 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.278G>A (p.Arg93His)	single nucleotide variant	not specified [RCV004260717]	Chr19:11359843 [GRCh38] Chr19:11470519 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.1099G>A (p.Val367Met)	single nucleotide variant	not specified [RCV004271482]	Chr19:11364430 [GRCh38] Chr19:11475106 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.167A>T (p.Tyr56Phe)	single nucleotide variant	not specified [RCV004263862]	Chr19:11359632 [GRCh38] Chr19:11470308 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.313G>A (p.Val105Ile)	single nucleotide variant	not specified [RCV004256613]	Chr19:11359878 [GRCh38] Chr19:11470554 [GRCh37] Chr19:19p13.2	likely benign
NM_001393892.1(PLPPR2):c.703C>T (p.Leu235=)	single nucleotide variant	not provided [RCV003421837]	Chr19:11362552 [GRCh38] Chr19:11473228 [GRCh37] Chr19:19p13.2	likely benign
NM_001393892.1(PLPPR2):c.1033C>T (p.Arg345Cys)	single nucleotide variant	not specified [RCV004506743]	Chr19:11364364 [GRCh38] Chr19:11475040 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.994C>T (p.Pro332Ser)	single nucleotide variant	not specified [RCV004506742]	Chr19:11364191 [GRCh38] Chr19:11474867 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.299C>T (p.Pro100Leu)	single nucleotide variant	not specified [RCV004506741]	Chr19:11359864 [GRCh38] Chr19:11470540 [GRCh37] Chr19:19p13.2	uncertain significance
NM_001393892.1(PLPPR2):c.1088C>T (p.Ser363Leu)	single nucleotide variant	not specified [RCV004506740]	Chr19:11364419 [GRCh38] Chr19:11475095 [GRCh37] Chr19:19p13.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	3640
Count of miRNA genes:	905
Interacting mature miRNAs:	1143
Transcripts:	ENST00000251473, ENST00000586380, ENST00000586431, ENST00000587801, ENST00000588196, ENST00000588360, ENST00000591329, ENST00000591608
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.

Markers in Region

RH103379

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	11,476,006 - 11,476,149	UniSTS	GRCh37
Build 36	19	11,337,006 - 11,337,149	RGD	NCBI36
Celera	19	11,370,874 - 11,371,017	RGD
Cytogenetic Map	19	p13.2	UniSTS
HuRef	19	11,052,052 - 11,052,195	UniSTS
GeneMap99-GB4 RH Map	19	71.07	UniSTS

STS-N51328

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	11,476,154 - 11,476,318	UniSTS	GRCh37
Build 36	19	11,337,154 - 11,337,318	RGD	NCBI36
Celera	19	11,371,022 - 11,371,186	RGD
Cytogenetic Map	19	p13.2	UniSTS
HuRef	19	11,052,200 - 11,052,364	UniSTS
GeneMap99-GB4 RH Map	19	68.33	UniSTS
NCBI RH Map	19	87.9	UniSTS

LPPR2__6417

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	11,475,482 - 11,476,376	UniSTS	GRCh37
Build 36	19	11,336,482 - 11,337,376	RGD	NCBI36
Celera	19	11,370,350 - 11,371,244	RGD
HuRef	19	11,051,528 - 11,052,422	UniSTS

RH98197

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	19	p13.2	UniSTS
HuRef	19	11,040,352 - 11,040,515	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

High

Medium

2235

2732

1584

489

1290

329

4263

1936

3687

307

1422

1572

170

1203

2755

Low

196

248

139

133

630

135

257

110

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001170635	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001393892	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001393893	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001393894	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001393895	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001393896	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_022737	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005260017	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027147	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027148	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451654	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451655	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321778	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321779	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC024575	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK023117	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK094869	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK225482	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL353953	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY304516	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY339628	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC009378	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471106	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR936652	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CS300733	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB169285	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HF548053	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000251473 ⟹ ENSP00000251473

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	11,355,386 - 11,365,698 (+)	Ensembl

RefSeq Acc Id:

ENST00000586380 ⟹ ENSP00000466698

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	11,355,466 - 11,359,838 (+)	Ensembl

RefSeq Acc Id:

ENST00000586431

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	11,355,431 - 11,359,708 (+)	Ensembl

RefSeq Acc Id:

ENST00000587801

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	11,359,723 - 11,363,768 (+)	Ensembl

RefSeq Acc Id:

ENST00000588196

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	11,357,696 - 11,359,894 (+)	Ensembl

RefSeq Acc Id:

ENST00000588360

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	11,361,266 - 11,364,215 (+)	Ensembl

RefSeq Acc Id:

ENST00000591329 ⟹ ENSP00000467807

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	11,355,424 - 11,359,719 (+)	Ensembl

RefSeq Acc Id:

ENST00000591608 ⟹ ENSP00000466898

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	11,355,498 - 11,365,698 (+)	Ensembl

RefSeq Acc Id:

ENST00000688289 ⟹ ENSP00000510269

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	11,355,432 - 11,365,698 (+)	Ensembl

RefSeq Acc Id:

NM_001170635 ⟹ NP_001164106

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	11,355,432 - 11,365,698 (+)	NCBI
GRCh37	19	11,466,062 - 11,476,374 (+)	RGD
GRCh37	19	11,466,062 - 11,476,374 (+)	NCBI
Celera	19	11,360,936 - 11,371,242 (+)	RGD
HuRef	19	11,042,113 - 11,052,420 (+)	ENTREZGENE
CHM1_1	19	11,467,084 - 11,477,386 (+)	NCBI
T2T-CHM13v2.0	19	11,482,410 - 11,492,670 (+)	NCBI

Sequence:

show sequence

GTCTGCGCGGCGCGGCCAGGCCCGGCCGACCGCGTCTCGGTCTTCGCGTCTGCCAGCCTGGCTG
GCAGTCCGTCTGTCCATCCCGCCGCGCCGGGGCAGTCTAGGCGGAGCGGGGGCTCAGGCGGCGG
CGGCCTCGACGCGAGTGAGTGTCGTGGTTGGGGTGCTGGACCCAGAGTGCCTACCCTCGCCTGC
CTGGGCCTCAGTTTCCACATCTGCACAATGGGGGTGACCATCCCTGCCCTGCTGGCTGCCAGGA
GCGGCTGTGAGTCTTCAGGCGTGGATGCAGCCTGGGGGAAGCCATAGGGCGCTTTCACAGGCCT
GGCCTTCACCATGGCGGGAGGGAGACCGCATCTGAAGAGGAGTTTCTCCATCATCCCCTGCTTT
GTCTTCGTGGAGGGATTCTTCTGCTATGACAGTACCTACGCCAAGCCCTACCCAGGGCCTGAGG
CTGCCAGCCGAGTGCCTCCTGCTCTTGTCTACGCACTGGTCACTGCCGGGCCCACCCTCACGAT
CCTGCTGGGAGAGCTGGCGCGTGCCTTTTTCCCTGCACCACCTTCAGCCGTCCCAGTCATCGGG
GAGAGCACCATCGTGTCTGGGGCCTGCTGCCGCTTCAGCCCCCCAGTGCGGAGGCTGGTCCGCT
TCCTGGGGGTCTACTCCTTCGGCCTCTTCACCACGACCATCTTCGCCAACGCGGGGCAGGTGGT
GACCGGCAATCCCACGCCACACTTCCTGTCCGTGTGCCGCCCCAACTACACGGCCCTGGGCTGC
CTGCCACCTTCTCCGGATCGGCCAGGTCCCGACCGCTTTGTCACTGACCAGGGTGCCTGCGCTG
GCAGTCCCAGCCTCGTGGCCGCCGCGCGCCGCGCCTTCCCCTGCAAGGATGCGGCCCTCTGCGC
CTACGCGGTCACCTACACAGCGATGTACGTGACTCTCGTGTTCCGCGTGAAGGGCTCCCGCCTG
GTCAAACCCTCGCTCTGCCTGGCCTTGCTGTGCCCGGCCTTCCTGGTGGGCGTGGTCCGCGTGG
CCGAGTACCGAAACCACTGGTCGGACGTGCTGGCTGGCTTCCTGACAGGGGCGGCCATCGCCAC
CTTTTTGGTCACCTGCGTTGTGCATAACTTTCAGAGCCGGCCACCCTCTGGCCGAAGGCTCTCT
CCCTGGGAGGACCTGGGCCAAGCCCCCACCATGGATAGCCCCCTCGAAAAGTTAAGTGTGGCGC
AGGAACCCGAGGTCTGCAGGCCGCATTCGACACCGGCACGGCTCACCCCATCCAAGTCGCAGAA
CTGCGCCCGCCGTGGCCACCTGATCCCCAGCTGTGTCTCCTCCAGGGCCCCAGCCATGTGTTCG
TCGCCCCGTGTGCCCCGTCCTCGATTGAGGTCTGAGCCGACGCCCTTGCCCCTGCCCCTACCCC
TGCCAGCGCCCACCCCCAGCCAGGGCCCCTCGCCTTCCTCCCCTGGACCTGGGGGGCCAGGCGG
GGGTGGTGGACGTGGCCGGAAGCTGCTGCTGCCCACGCCCCTGCTGCGGGACCTGTACACCCTG
AGTGGACTCTATCCCTCCCCCTTCCACCGGGACAACTTCAGCCCTTACCTGTTTGCCAGCCGTG
ACCACCTGCTGTGAGGCCCGACCACCCACCCAGAATCTGCCCAGTCCCCACTTCTTCCCTGCCA
CGCGTGTGTGTGCGTGTGCCACGTGAGTGCCAAAGTCCCCTGCCCCCCAAGCCAGCCAGACCCA
GACATTAGAAGATGGCTAGAAGGACATTTAGGAGACATCTGCCTCTCTGGCCCTCTGAGATATC
CCGATGGGCACAAATGGAAGGTGCGCACTTGCCCCTACTATTGCCCTTTTAAGGGCCAAAGCTT
GACCCCATTGGCCATTGCCTGGCTAATGAGAACCCCTGGTTCTCAGAATTTTAACCAAAAGGAG
TTGGCTCCAACCAATGGGAGCCTTCCCCTCACTTCTTAGAATCCTCCTGCAAGAGGGCAACTCC
AGCCAGTGTTCAGCGACTGAACAGCCAATAGGAGCCCTTGGTTTCCAGAATTTCTAGAGTGGGT
GGGCATGATTCCAGTCAATGGGGGACCGCCCGTGTCTAAGCATGTGCAAAGGAGAGGAGGGAGA
TGAGGTCATTGTTTGTCATTGAGTCTTCTCTCAGAATCAGCGAGCCCAGCTGTAGGGTGGGGGG
CAGGCTCCCCCATGGCAGGGTCCTTGGGGTACCCCTTTTCCTCTCAGCCCCTCCCTGTGTGCGG
CCTCTCCACCTCTCACCCACTCTCTCCTAATCCCCTACTTAAGTAGGGCTTGCCCCACTTCAGA
GGTTTTGGGGTTCAGGGTGCTGTGTCTCCCCTTGCCTGTGCCCAGGTCATCCCAAACCCTTCTG
TTATTTATTAGGGCTGTGGGAAGGGTTTTTCTTCTTTTTCTTGGAACCTGCCCCTGTTCTTCAC
ACTGCCCCCCATGCCTCAGCCTCATACAGATGTGCCATCATGGGGGGCATGGGTGGAGCAGAGG
GGCTCCCTCACCCCGGGCAGGCAAAGGCAGTGGGTAGAGGAGGCACTGCCCCCCTTTCCTGCCC
CCTCCTCATCTTTAATAAAGACCTGGCTTCTCATCTTTAATAAAGACCTGTTTGTAACAGAA

hide sequence

RefSeq Acc Id:

NM_001393892 ⟹ NP_001380821

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	11,355,432 - 11,365,698 (+)	NCBI
T2T-CHM13v2.0	19	11,482,410 - 11,492,670 (+)	NCBI

Sequence:

show sequence

GTCTGCGCGGCGCGGCCAGGCCCGGCCGACCGCGTCTCGGTCTTCGCGTCTGCCAGCCTGGCTG
GCAGTCCGTCTGTCCATCCCGCCGCGCCGGGGCAGTCTAGGCGGAGCGGGGGCTCAGGCGGCGG
CGGCCTCGACGCGAGTGAGTGTCGTGGTTGGGGTGCTGGACCCAGAGTGCCTACCCTCGCCTGC
CTGGGCCTCAGTTTCCACATCTGCACAATGGGGGTGACCATCCCTGCCCTGCTGGCTGCCAGGA
GCGGCTGTGAGTCTTCAGGCGTGGATGCAGCCTGGGGGAAGCCATAGGGCGCTTTCACAGGCCT
GGCCTTCACCATGGCGGGAGGGAGACCGCATCTGAAGAGGAGTTTCTCCATCATCCCCTGCTTT
GTCTTCGTGGAGTCGGTGCTGCTGGGCATTGTGATCCTGCTTGCTTACCGCCTGGAGTTCACGG
ACACCTTCCCTGTGCACACCCAGGGATTCTTCTGCTATGACAGTACCTACGCCAAGCCCTACCC
AGGGCCTGAGGCTGCCAGCCGAGTGCCTCCTGCTCTTGTCTACGCACTGGTCACTGCCGGGCCC
ACCCTCACGATCCTGCTGGGAGAGCTGGCGCGTGCCTTTTTCCCTGCACCACCTTCAGCCGTCC
CAGTCATCGGGGAGAGCACCATCGTGTCTGGGGCCTGCTGCCGCTTCAGCCCCCCAGTGCGGAG
GCTGGTCCGCTTCCTGGGGGTCTACTCCTTCGGCCTCTTCACCACGACCATCTTCGCCAACGCG
GGGCAGGTGGTGACCGGCAATCCCACGCCACACTTCCTGTCCGTGTGCCGCCCCAACTACACGG
CCCTGGGCTGCCTGCCACCTTCTCCGGATCGGCCAGGTCCCGACCGCTTTGTCACTGACCAGGG
TGCCTGCGCTGGCAGTCCCAGCCTCGTGGCCGCCGCGCGCCGCGCCTTCCCCTGCAAGGATGCG
GCCCTCTGCGCCTACGCGGTCACCTACACAGCGATGTACGTGACTCTCGTGTTCCGCGTGAAGG
GCTCCCGCCTGGTCAAACCCTCGCTCTGCCTGGCCTTGCTGTGCCCGGCCTTCCTGGTGGGCGT
GGTCCGCGTGGCCGAGTACCGAAACCACTGGTCGGACGTGCTGGCTGGCTTCCTGACAGGGGCG
GCCATCGCCACCTTTTTGGTCACCTGCGTTGTGCATAACTTTCAGAGCCGGCCACCCTCTGGCC
GAAGGCTCTCTCCCTGGGAGGACCTGGGCCAAGCCCCCACCATGGATAGCCCCCTCGAAAAGTT
AAGTGTGGCGCAGGAACCCGAGGTCTGCAGGCCGCATTCGACACCGGCACGGCTCACCCCATCC
AAGTCGCAGAACTGCGCCCGCCGTGGCCACCTGATCCCCAGCTGTGTCTCCTCCAGGGCCCCAG
CCATGTGTTCGTCGCCCCGTGTGCCCCGTCCTCGATTGAGGTCTGAGCCGACGCCCTTGCCCCT
GCCCCTACCCCTGCCAGCGCCCACCCCCAGCCAGGGCCCCTCGCCTTCCTCCCCTGGACCTGGG
GGGCCAGGCGGGGGTGGTGGACGTGGCCGGAAGCTGCTGCTGCCCACGCCCCTGCTGCGGGACC
TGTACACCCTGAGTGGACTCTATCCCTCCCCCTTCCACCGGGACAACTTCAGCCCTTACCTGTT
TGCCAGCCGTGACCACCTGCTGTGAGGCCCGACCACCCACCCAGAATCTGCCCAGTCCCCACTT
CTTCCCTGCCACGCGTGTGTGTGCGTGTGCCACGTGAGTGCCAAAGTCCCCTGCCCCCCAAGCC
AGCCAGACCCAGACATTAGAAGATGGCTAGAAGGACATTTAGGAGACATCTGCCTCTCTGGCCC
TCTGAGATATCCCGATGGGCACAAATGGAAGGTGCGCACTTGCCCCTACTATTGCCCTTTTAAG
GGCCAAAGCTTGACCCCATTGGCCATTGCCTGGCTAATGAGAACCCCTGGTTCTCAGAATTTTA
ACCAAAAGGAGTTGGCTCCAACCAATGGGAGCCTTCCCCTCACTTCTTAGAATCCTCCTGCAAG
AGGGCAACTCCAGCCAGTGTTCAGCGACTGAACAGCCAATAGGAGCCCTTGGTTTCCAGAATTT
CTAGAGTGGGTGGGCATGATTCCAGTCAATGGGGGACCGCCCGTGTCTAAGCATGTGCAAAGGA
GAGGAGGGAGATGAGGTCATTGTTTGTCATTGAGTCTTCTCTCAGAATCAGCGAGCCCAGCTGT
AGGGTGGGGGGCAGGCTCCCCCATGGCAGGGTCCTTGGGGTACCCCTTTTCCTCTCAGCCCCTC
CCTGTGTGCGGCCTCTCCACCTCTCACCCACTCTCTCCTAATCCCCTACTTAAGTAGGGCTTGC
CCCACTTCAGAGGTTTTGGGGTTCAGGGTGCTGTGTCTCCCCTTGCCTGTGCCCAGGTCATCCC
AAACCCTTCTGTTATTTATTAGGGCTGTGGGAAGGGTTTTTCTTCTTTTTCTTGGAACCTGCCC
CTGTTCTTCACACTGCCCCCCATGCCTCAGCCTCATACAGATGTGCCATCATGGGGGGCATGGG
TGGAGCAGAGGGGCTCCCTCACCCCGGGCAGGCAAAGGCAGTGGGTAGAGGAGGCACTGCCCCC
CTTTCCTGCCCCCTCCTCATCTTTAATAAAGACCTGGCTTCTCATCTTTAATAAAGACCTGTTT
GTAACAGAA

hide sequence

RefSeq Acc Id:

NM_001393893 ⟹ NP_001380822

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	11,355,432 - 11,365,698 (+)	NCBI
T2T-CHM13v2.0	19	11,482,410 - 11,492,670 (+)	NCBI

Sequence:

show sequence

GTCTGCGCGGCGCGGCCAGGCCCGGCCGACCGCGTCTCGGTCTTCGCGTCTGCCAGCCTGGCTG
GCAGTCCGTCTGTCCATCCCGCCGCGCCGGGGCAGTCTAGGCGGAGCGGGGGCTCAGGCGGCGG
CGGCCTCGACGCGAGTGAGTGTCGTGGTTGGGGTGCTGGACCCAGAGTGCCTACCCTCGCCTGC
CTGGGCCTCAGTTTCCACATCTGCACAATGGGGGTGACCATCCCTGCCCTGCTGGCTGCCAGGA
GCGGCTGTGAGTCTTCAGGCGTGGATGCAGCCTGGGGGAAGCCATAGGGCGCTTTCACAGGCAC
ACCCCCTGGGACTCCCACTCCCTCCCCACCTCTGCAGGCCTGGCCTTCACCATGGCGGGAGGGA
GACCGCATCTGAAGAGGAGTTTCTCCATCATCCCCTGCTTTGTCTTCGTGGAGTCGGTGCTGCT
GGGCATTGTGATCCTGCTTGCTTACCGCCTGGAGTTCACGGACACCTTCCCTGTGCACACCCAG
GGATTCTTCTGCTATGACAGTACCTACGCCAAGCCCTACCCAGGGCCTGAGGCTGCCAGCCGAG
TGCCTCCTGCTCTTGTCTACGCACTGGTCACTGCCGGGCCCACCCTCACGATCCTGCTGGGAGA
GCTGGCGCGTGCCTTTTTCCCTGCACCACCTTCAGCCGTCCCAGTCATCGGGGAGAGCACCATC
GTGTCTGGGGCCTGCTGCCGCTTCAGCCCCCCAGTGCGGAGGCTGGTCCGCTTCCTGGGGGTCT
ACTCCTTCGGCCTCTTCACCACGACCATCTTCGCCAACGCGGGGCAGGTGGTGACCGGCAATCC
CACGCCACACTTCCTGTCCGTGTGCCGCCCCAACTACACGGCCCTGGGCTGCCTGCCACCTTCT
CCGGATCGGCCAGGTCCCGACCGCTTTGTCACTGACCAGGGTGCCTGCGCTGGCAGTCCCAGCC
TCGTGGCCGCCGCGCGCCGCGCCTTCCCCTGCAAGGATGCGGCCCTCTGCGCCTACGCGGTCAC
CTACACAGCGATGTACGTGACTCTCGTGTTCCGCGTGAAGGGCTCCCGCCTGGTCAAACCCTCG
CTCTGCCTGGCCTTGCTGTGCCCGGCCTTCCTGGTGGGCGTGGTCCGCGTGGCCGAGTACCGAA
ACCACTGGTCGGACGTGCTGGCTGGCTTCCTGACAGGGGCGGCCATCGCCACCTTTTTGGTCAC
CTGCGTTGTGCATAACTTTCAGAGCCGGCCACCCTCTGGCCGAAGGCTCTCTCCCTGGGAGGAC
CTGGGCCAAGCCCCCACCATGGATAGCCCCCTCGAAAAGTTAAGTGTGGCGCAGGAACCCGAGG
TCTGCAGGCCGCATTCGACACCGGCACGGCTCACCCCATCCAAGTCGCAGAACTGCGCCCGCCG
TGGCCACCTGATCCCCAGCTGTGTCTCCTCCAGGGCCCCAGCCATGTGTTCGTCGCCCCGTGTG
CCCCGTCCTCGATTGAGGTCTGAGCCGACGCCCTTGCCCCTGCCCCTACCCCTGCCAGCGCCCA
CCCCCAGCCAGGGCCCCTCGCCTTCCTCCCCTGGACCTGGGGGGCCAGGCGGGGGTGGTGGACG
TGGCCGGAAGCTGCTGCTGCCCACGCCCCTGCTGCGGGACCTGTACACCCTGAGTGGACTCTAT
CCCTCCCCCTTCCACCGGGACAACTTCAGCCCTTACCTGTTTGCCAGCCGTGACCACCTGCTGT
GAGGCCCGACCACCCACCCAGAATCTGCCCAGTCCCCACTTCTTCCCTGCCACGCGTGTGTGTG
CGTGTGCCACGTGAGTGCCAAAGTCCCCTGCCCCCCAAGCCAGCCAGACCCAGACATTAGAAGA
TGGCTAGAAGGACATTTAGGAGACATCTGCCTCTCTGGCCCTCTGAGATATCCCGATGGGCACA
AATGGAAGGTGCGCACTTGCCCCTACTATTGCCCTTTTAAGGGCCAAAGCTTGACCCCATTGGC
CATTGCCTGGCTAATGAGAACCCCTGGTTCTCAGAATTTTAACCAAAAGGAGTTGGCTCCAACC
AATGGGAGCCTTCCCCTCACTTCTTAGAATCCTCCTGCAAGAGGGCAACTCCAGCCAGTGTTCA
GCGACTGAACAGCCAATAGGAGCCCTTGGTTTCCAGAATTTCTAGAGTGGGTGGGCATGATTCC
AGTCAATGGGGGACCGCCCGTGTCTAAGCATGTGCAAAGGAGAGGAGGGAGATGAGGTCATTGT
TTGTCATTGAGTCTTCTCTCAGAATCAGCGAGCCCAGCTGTAGGGTGGGGGGCAGGCTCCCCCA
TGGCAGGGTCCTTGGGGTACCCCTTTTCCTCTCAGCCCCTCCCTGTGTGCGGCCTCTCCACCTC
TCACCCACTCTCTCCTAATCCCCTACTTAAGTAGGGCTTGCCCCACTTCAGAGGTTTTGGGGTT
CAGGGTGCTGTGTCTCCCCTTGCCTGTGCCCAGGTCATCCCAAACCCTTCTGTTATTTATTAGG
GCTGTGGGAAGGGTTTTTCTTCTTTTTCTTGGAACCTGCCCCTGTTCTTCACACTGCCCCCCAT
GCCTCAGCCTCATACAGATGTGCCATCATGGGGGGCATGGGTGGAGCAGAGGGGCTCCCTCACC
CCGGGCAGGCAAAGGCAGTGGGTAGAGGAGGCACTGCCCCCCTTTCCTGCCCCCTCCTCATCTT
TAATAAAGACCTGGCTTCTCATCTTTAATAAAGACCTGTTTGTAACAGAA

hide sequence

RefSeq Acc Id:

NM_001393894 ⟹ NP_001380823

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	11,355,432 - 11,365,698 (+)	NCBI
T2T-CHM13v2.0	19	11,482,410 - 11,492,670 (+)	NCBI

Sequence:

show sequence

GTCTGCGCGGCGCGGCCAGGCCCGGCCGACCGCGTCTCGGTCTTCGCGTCTGCCAGCCTGGCTG
GCAGTCCGTCTGTCCATCCCGCCGCGCCGGGGCAGTCTAGGCGGAGCGGGGGCTCAGGCGGCGG
CGGCCTCGACGCGAGTGAGTGTCGTGGTTGGGGTGCTGGACCCAGAGTGCCTACCCTCGCCTGC
CTGGGCCTCAGTTTCCACATCTGCACAATGGGGGTGACCATCCCTGCCCTGCTGGCTGCCAGGA
GCGGCTGTGAGTCTTCAGGCGTGGATGCAGCCTGGGGGAAGCCATAGGGCGCTTTCACAGGCAC
ACCCCCTGGGACTCCCACTCCCTCCCCACCTCTGCAGGCCTGGCCTTCACCATGGCGGGAGGGA
GACCGCATCTGAAGAGGAGTTTCTCCATCATCCCCTGCTTTGTCTTCGTGGAGTCGGTGCTGCT
GGGCATTGTGATCCTGCTTGCTTACCGCCTGGAGTTCACGGACACCTTCCCTGTGCACACCCAG
GGATTCTTCTGCTATGACAGTACCTACGCCAAGCCCTACCCAGGGCCTGAGGCTGCCAGCCGAG
TGCCTCCTGCTCTTGTCTACGCACTGGTCACTGCCGGGCCCACCCTCACGATCCTGCTGGGAGA
GCTGGCGCGTGCCTTTTTCCCTGCACCACCTTCAGCCGTCCCAGTCATCGGGGAGAGCACCATC
GTGTCTGGGGCCTGCTGCCGCTTCAGCCCCCCAGTGCGGAGGCTGGTCCGCTTCCTGGGGGTCT
ACTCCTTCGGCCTCTTCACCACGACCATCTTCGCCAACGCGGGGCAGGTGGTGACCGGCAATCC
CACGCCACACTTCCTGTCCGTGTGCCGCCCCAACTACACGGCCCTGGGCTGCCTGCCACCTTCT
CCGGATCGGCCAGGTCCCGACCGCTTTGTCACTGACCAGGGTGCCTGCGCTGGCAGTCCCAGCC
TCGTGGCCGCCGCGCGCCGCGCCTTCCCCTGCAAGGATGCGGCCCTCTGCGCCTACGCGGTCAC
CTACACAGCGATGTACGTGACTCTCGTGTTCCGCGTGAAGGGCTCCCGCCTGGTCAAACCCTCG
CTCTGCCTGGCCTTGCTGTGCCCGGCCTTCCTGGTGGGCGTGGTCCGCGTGGCCGAGTACCGAA
ACCACTGGTCGGACGTGCTGGCTGGCTTCCTGACAGGGGCGGCCATCGCCACCTTTTTGGTCAC
CTGCGTTGTGCATAACTTTCAGAGCCGGCCACCCTCTGGCCGAAGGCTCTCTCCCTGGGAGGAC
CTGGGCCAAGCCCCCACCATGGATAGCCCCCTCGAAAAGAACCCGAGGTCTGCAGGCCGCATTC
GACACCGGCACGGCTCACCCCATCCAAGTCGCAGAACTGCGCCCGCCGTGGCCACCTGATCCCC
AGCTGTGTCTCCTCCAGGGCCCCAGCCATGTGTTCGTCGCCCCGTGTGCCCCGTCCTCGATTGA
GGTCTGAGCCGACGCCCTTGCCCCTGCCCCTACCCCTGCCAGCGCCCACCCCCAGCCAGGGCCC
CTCGCCTTCCTCCCCTGGACCTGGGGGGCCAGGCGGGGGTGGTGGACGTGGCCGGAAGCTGCTG
CTGCCCACGCCCCTGCTGCGGGACCTGTACACCCTGAGTGGACTCTATCCCTCCCCCTTCCACC
GGGACAACTTCAGCCCTTACCTGTTTGCCAGCCGTGACCACCTGCTGTGAGGCCCGACCACCCA
CCCAGAATCTGCCCAGTCCCCACTTCTTCCCTGCCACGCGTGTGTGTGCGTGTGCCACGTGAGT
GCCAAAGTCCCCTGCCCCCCAAGCCAGCCAGACCCAGACATTAGAAGATGGCTAGAAGGACATT
TAGGAGACATCTGCCTCTCTGGCCCTCTGAGATATCCCGATGGGCACAAATGGAAGGTGCGCAC
TTGCCCCTACTATTGCCCTTTTAAGGGCCAAAGCTTGACCCCATTGGCCATTGCCTGGCTAATG
AGAACCCCTGGTTCTCAGAATTTTAACCAAAAGGAGTTGGCTCCAACCAATGGGAGCCTTCCCC
TCACTTCTTAGAATCCTCCTGCAAGAGGGCAACTCCAGCCAGTGTTCAGCGACTGAACAGCCAA
TAGGAGCCCTTGGTTTCCAGAATTTCTAGAGTGGGTGGGCATGATTCCAGTCAATGGGGGACCG
CCCGTGTCTAAGCATGTGCAAAGGAGAGGAGGGAGATGAGGTCATTGTTTGTCATTGAGTCTTC
TCTCAGAATCAGCGAGCCCAGCTGTAGGGTGGGGGGCAGGCTCCCCCATGGCAGGGTCCTTGGG
GTACCCCTTTTCCTCTCAGCCCCTCCCTGTGTGCGGCCTCTCCACCTCTCACCCACTCTCTCCT
AATCCCCTACTTAAGTAGGGCTTGCCCCACTTCAGAGGTTTTGGGGTTCAGGGTGCTGTGTCTC
CCCTTGCCTGTGCCCAGGTCATCCCAAACCCTTCTGTTATTTATTAGGGCTGTGGGAAGGGTTT
TTCTTCTTTTTCTTGGAACCTGCCCCTGTTCTTCACACTGCCCCCCATGCCTCAGCCTCATACA
GATGTGCCATCATGGGGGGCATGGGTGGAGCAGAGGGGCTCCCTCACCCCGGGCAGGCAAAGGC
AGTGGGTAGAGGAGGCACTGCCCCCCTTTCCTGCCCCCTCCTCATCTTTAATAAAGACCTGGCT
TCTCATCTTTAATAAAGACCTGTTTGTAACAGAA

hide sequence

RefSeq Acc Id:

NM_001393895 ⟹ NP_001380824

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	11,355,432 - 11,365,698 (+)	NCBI
T2T-CHM13v2.0	19	11,482,410 - 11,492,670 (+)	NCBI

Sequence:

show sequence

GTCTGCGCGGCGCGGCCAGGCCCGGCCGACCGCGTCTCGGTCTTCGCGTCTGCCAGCCTGGCTG
GCAGTCCGTCTGTCCATCCCGCCGCGCCGGGGCAGTCTAGGCGGAGCGGGGGCTCAGGCGGCGG
CGGCCTCGACGCGAGTGAGTGTCGTGGTTGGGGTGCTGGACCCAGAGTGCCTACCCTCGCCTGC
CTGGGCCTCAGTTTCCACATCTGCACAATGGGGGTGACCATCCCTGCCCTGCTGGCTGCCAGGA
GCGGCTGTGAGTCTTCAGGCGTGGATGCAGCCTGGGGGAAGCCATAGGGCGCTTTCACAGGCCT
GGCCTTCACCATGGCGGGAGGGAGACCGCATCTGAAGAGGAGTTTCTCCATCATCCCCTGCTTT
GTCTTCGTGGAGGGATTCTTCTGCTATGACAGTACCTACGCCAAGCCCTACCCAGGGCCTGAGG
CTGCCAGCCGAGTGCCTCCTGCTCTTGTCTACGCACTGGTCACTGCCGGGCCCACCCTCACGAT
CCTGCTGGGAGAGCTGGCGCGTGCCTTTTTCCCTGCACCACCTTCAGCCGTCCCAGTCATCGGG
GAGAGCACCATCGTGTCTGGGGCCTGCTGCCGCTTCAGCCCCCCAGTGCGGAGGCTGGTCCGCT
TCCTGGGGGTCTACTCCTTCGGCCTCTTCACCACGACCATCTTCGCCAACGCGGGGCAGGTGGT
GACCGGCAATCCCACGCCACACTTCCTGTCCGTGTGCCGCCCCAACTACACGGCCCTGGGCTGC
CTGCCACCTTCTCCGGATCGGCCAGGTCCCGACCGCTTTGTCACTGACCAGGGTGCCTGCGCTG
GCAGTCCCAGCCTCGTGGCCGCCGCGCGCCGCGCCTTCCCCTGCAAGGATGCGGCCCTCTGCGC
CTACGCGGTCACCTACACAGCGATGTACGTGACTCTCGTGTTCCGCGTGAAGGGCTCCCGCCTG
GTCAAACCCTCGCTCTGCCTGGCCTTGCTGTGCCCGGCCTTCCTGGTGGGCGTGGTCCGCGTGG
CCGAGTACCGAAACCACTGGTCGGACGTGCTGGCTGGCTTCCTGACAGGGGCGGCCATCGCCAC
CTTTTTGGTCACCTGCGTTGTGCATAACTTTCAGAGCCGGCCACCCTCTGGCCGAAGGCTCTCT
CCCTGGGAGGACCTGGGCCAAGCCCCCACCATGGATAGCCCCCTCGAAAAGAACCCGAGGTCTG
CAGGCCGCATTCGACACCGGCACGGCTCACCCCATCCAAGTCGCAGAACTGCGCCCGCCGTGGC
CACCTGATCCCCAGCTGTGTCTCCTCCAGGGCCCCAGCCATGTGTTCGTCGCCCCGTGTGCCCC
GTCCTCGATTGAGGTCTGAGCCGACGCCCTTGCCCCTGCCCCTACCCCTGCCAGCGCCCACCCC
CAGCCAGGGCCCCTCGCCTTCCTCCCCTGGACCTGGGGGGCCAGGCGGGGGTGGTGGACGTGGC
CGGAAGCTGCTGCTGCCCACGCCCCTGCTGCGGGACCTGTACACCCTGAGTGGACTCTATCCCT
CCCCCTTCCACCGGGACAACTTCAGCCCTTACCTGTTTGCCAGCCGTGACCACCTGCTGTGAGG
CCCGACCACCCACCCAGAATCTGCCCAGTCCCCACTTCTTCCCTGCCACGCGTGTGTGTGCGTG
TGCCACGTGAGTGCCAAAGTCCCCTGCCCCCCAAGCCAGCCAGACCCAGACATTAGAAGATGGC
TAGAAGGACATTTAGGAGACATCTGCCTCTCTGGCCCTCTGAGATATCCCGATGGGCACAAATG
GAAGGTGCGCACTTGCCCCTACTATTGCCCTTTTAAGGGCCAAAGCTTGACCCCATTGGCCATT
GCCTGGCTAATGAGAACCCCTGGTTCTCAGAATTTTAACCAAAAGGAGTTGGCTCCAACCAATG
GGAGCCTTCCCCTCACTTCTTAGAATCCTCCTGCAAGAGGGCAACTCCAGCCAGTGTTCAGCGA
CTGAACAGCCAATAGGAGCCCTTGGTTTCCAGAATTTCTAGAGTGGGTGGGCATGATTCCAGTC
AATGGGGGACCGCCCGTGTCTAAGCATGTGCAAAGGAGAGGAGGGAGATGAGGTCATTGTTTGT
CATTGAGTCTTCTCTCAGAATCAGCGAGCCCAGCTGTAGGGTGGGGGGCAGGCTCCCCCATGGC
AGGGTCCTTGGGGTACCCCTTTTCCTCTCAGCCCCTCCCTGTGTGCGGCCTCTCCACCTCTCAC
CCACTCTCTCCTAATCCCCTACTTAAGTAGGGCTTGCCCCACTTCAGAGGTTTTGGGGTTCAGG
GTGCTGTGTCTCCCCTTGCCTGTGCCCAGGTCATCCCAAACCCTTCTGTTATTTATTAGGGCTG
TGGGAAGGGTTTTTCTTCTTTTTCTTGGAACCTGCCCCTGTTCTTCACACTGCCCCCCATGCCT
CAGCCTCATACAGATGTGCCATCATGGGGGGCATGGGTGGAGCAGAGGGGCTCCCTCACCCCGG
GCAGGCAAAGGCAGTGGGTAGAGGAGGCACTGCCCCCCTTTCCTGCCCCCTCCTCATCTTTAAT
AAAGACCTGGCTTCTCATCTTTAATAAAGACCTGTTTGTAACAGAA

hide sequence

RefSeq Acc Id:

NM_001393896 ⟹ NP_001380825

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	11,355,432 - 11,365,698 (+)	NCBI
T2T-CHM13v2.0	19	11,482,410 - 11,492,670 (+)	NCBI

Sequence:

show sequence

GTCTGCGCGGCGCGGCCAGGCCCGGCCGACCGCGTCTCGGTCTTCGCGTCTGCCAGCCTGGCTG
GCAGTCCGTCTGTCCATCCCGCCGCGCCGGGGCAGTCTAGGCGGAGCGGGGGCTCAGGCGGCGG
CGGCCTCGACGCGAGTGAGTGTCGTGGTTGGGGTGCTGGACCCAGAGTGCCTACCCTCGCCTGC
CTGGGCCTCAGTTTCCACATCTGCACAATGGGGGTGACCATCCCTGCCCTGCTGGCTGCCAGGA
GCGGCTGTGAGTCTTCAGGCGTGGATGCAGCCTGGGGGAAGCCATAGGGCGCTTTCACAGGCAC
ACCCCCTGGGACTCCCACTCCCTCCCCACCTCTGCAGGCCTGGCCTTCACCATGGCGGGAGGGA
GACCGCATCTGAAGAGGAGTTTCTCCATCATCCCCTGCTTTGTCTTCGTGGAGGGATTCTTCTG
CTATGACAGTACCTACGCCAAGCCCTACCCAGGGCCTGAGGCTGCCAGCCGAGTGCCTCCTGCT
CTTGTCTACGCACTGGTCACTGCCGGGCCCACCCTCACGATCCTGCTGGGAGAGCTGGCGCGTG
CCTTTTTCCCTGCACCACCTTCAGCCGTCCCAGTCATCGGGGAGAGCACCATCGTGTCTGGGGC
CTGCTGCCGCTTCAGCCCCCCAGTGCGGAGGCTGGTCCGCTTCCTGGGGGTCTACTCCTTCGGC
CTCTTCACCACGACCATCTTCGCCAACGCGGGGCAGGTGGTGACCGGCAATCCCACGCCACACT
TCCTGTCCGTGTGCCGCCCCAACTACACGGCCCTGGGCTGCCTGCCACCTTCTCCGGATCGGCC
AGGTCCCGACCGCTTTGTCACTGACCAGGGTGCCTGCGCTGGCAGTCCCAGCCTCGTGGCCGCC
GCGCGCCGCGCCTTCCCCTGCAAGGATGCGGCCCTCTGCGCCTACGCGGTCACCTACACAGCGA
TGTACGTGACTCTCGTGTTCCGCGTGAAGGGCTCCCGCCTGGTCAAACCCTCGCTCTGCCTGGC
CTTGCTGTGCCCGGCCTTCCTGGTGGGCGTGGTCCGCGTGGCCGAGTACCGAAACCACTGGTCG
GACGTGCTGGCTGGCTTCCTGACAGGGGCGGCCATCGCCACCTTTTTGGTCACCTGCGTTGTGC
ATAACTTTCAGAGCCGGCCACCCTCTGGCCGAAGGCTCTCTCCCTGGGAGGACCTGGGCCAAGC
CCCCACCATGGATAGCCCCCTCGAAAAGAACCCGAGGTCTGCAGGCCGCATTCGACACCGGCAC
GGCTCACCCCATCCAAGTCGCAGAACTGCGCCCGCCGTGGCCACCTGATCCCCAGCTGTGTCTC
CTCCAGGGCCCCAGCCATGTGTTCGTCGCCCCGTGTGCCCCGTCCTCGATTGAGGTCTGAGCCG
ACGCCCTTGCCCCTGCCCCTACCCCTGCCAGCGCCCACCCCCAGCCAGGGCCCCTCGCCTTCCT
CCCCTGGACCTGGGGGGCCAGGCGGGGGTGGTGGACGTGGCCGGAAGCTGCTGCTGCCCACGCC
CCTGCTGCGGGACCTGTACACCCTGAGTGGACTCTATCCCTCCCCCTTCCACCGGGACAACTTC
AGCCCTTACCTGTTTGCCAGCCGTGACCACCTGCTGTGAGGCCCGACCACCCACCCAGAATCTG
CCCAGTCCCCACTTCTTCCCTGCCACGCGTGTGTGTGCGTGTGCCACGTGAGTGCCAAAGTCCC
CTGCCCCCCAAGCCAGCCAGACCCAGACATTAGAAGATGGCTAGAAGGACATTTAGGAGACATC
TGCCTCTCTGGCCCTCTGAGATATCCCGATGGGCACAAATGGAAGGTGCGCACTTGCCCCTACT
ATTGCCCTTTTAAGGGCCAAAGCTTGACCCCATTGGCCATTGCCTGGCTAATGAGAACCCCTGG
TTCTCAGAATTTTAACCAAAAGGAGTTGGCTCCAACCAATGGGAGCCTTCCCCTCACTTCTTAG
AATCCTCCTGCAAGAGGGCAACTCCAGCCAGTGTTCAGCGACTGAACAGCCAATAGGAGCCCTT
GGTTTCCAGAATTTCTAGAGTGGGTGGGCATGATTCCAGTCAATGGGGGACCGCCCGTGTCTAA
GCATGTGCAAAGGAGAGGAGGGAGATGAGGTCATTGTTTGTCATTGAGTCTTCTCTCAGAATCA
GCGAGCCCAGCTGTAGGGTGGGGGGCAGGCTCCCCCATGGCAGGGTCCTTGGGGTACCCCTTTT
CCTCTCAGCCCCTCCCTGTGTGCGGCCTCTCCACCTCTCACCCACTCTCTCCTAATCCCCTACT
TAAGTAGGGCTTGCCCCACTTCAGAGGTTTTGGGGTTCAGGGTGCTGTGTCTCCCCTTGCCTGT
GCCCAGGTCATCCCAAACCCTTCTGTTATTTATTAGGGCTGTGGGAAGGGTTTTTCTTCTTTTT
CTTGGAACCTGCCCCTGTTCTTCACACTGCCCCCCATGCCTCAGCCTCATACAGATGTGCCATC
ATGGGGGGCATGGGTGGAGCAGAGGGGCTCCCTCACCCCGGGCAGGCAAAGGCAGTGGGTAGAG
GAGGCACTGCCCCCCTTTCCTGCCCCCTCCTCATCTTTAATAAAGACCTGGCTTCTCATCTTTA
ATAAAGACCTGTTTGTAACAGAA

hide sequence

RefSeq Acc Id:

NM_022737 ⟹ NP_073574

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	11,355,432 - 11,365,698 (+)	NCBI
GRCh37	19	11,466,062 - 11,476,374 (+)	NCBI
Build 36	19	11,327,109 - 11,337,372 (+)	NCBI Archive
Celera	19	11,360,936 - 11,371,242 (+)	RGD
HuRef	19	11,042,113 - 11,052,420 (+)	ENTREZGENE
CHM1_1	19	11,467,084 - 11,477,386 (+)	NCBI
T2T-CHM13v2.0	19	11,482,410 - 11,492,670 (+)	NCBI

Sequence:

show sequence

GTCTGCGCGGCGCGGCCAGGCCCGGCCGACCGCGTCTCGGTCTTCGCGTCTGCCAGCCTGGCTG
GCAGTCCGTCTGTCCATCCCGCCGCGCCGGGGCAGTCTAGGCGGAGCGGGGGCTCAGGCGGCGG
CGGCCTCGACGCGAGTGAGTGTCGTGGTTGGGGTGCTGGACCCAGAGTGCCTACCCTCGCCTGC
CTGGGCCTCAGTTTCCACATCTGCACAATGGGGGTGACCATCCCTGCCCTGCTGGCTGCCAGGA
GCGGCTGTGAGTCTTCAGGCGTGGATGCAGCCTGGGGGAAGCCATAGGGCGCTTTCACAGGCCT
GGCCTTCACCATGGCGGGAGGGAGACCGCATCTGAAGAGGAGTTTCTCCATCATCCCCTGCTTT
GTCTTCGTGGAGTCGGTGCTGCTGGGCATTGTGATCCTGCTTGCTTACCGCCTGGAGTTCACGG
ACACCTTCCCTGTGCACACCCAGGGATTCTTCTGCTATGACAGTACCTACGCCAAGCCCTACCC
AGGGCCTGAGGCTGCCAGCCGAGTGCCTCCTGCTCTTGTCTACGCACTGGTCACTGCCGGGCCC
ACCCTCACGATCCTGCTGGGAGAGCTGGCGCGTGCCTTTTTCCCTGCACCACCTTCAGCCGTCC
CAGTCATCGGGGAGAGCACCATCGTGTCTGGGGCCTGCTGCCGCTTCAGCCCCCCAGTGCGGAG
GCTGGTCCGCTTCCTGGGGGTCTACTCCTTCGGCCTCTTCACCACGACCATCTTCGCCAACGCG
GGGCAGGTGGTGACCGGCAATCCCACGCCACACTTCCTGTCCGTGTGCCGCCCCAACTACACGG
CCCTGGGCTGCCTGCCACCTTCTCCGGATCGGCCAGGTCCCGACCGCTTTGTCACTGACCAGGG
TGCCTGCGCTGGCAGTCCCAGCCTCGTGGCCGCCGCGCGCCGCGCCTTCCCCTGCAAGGATGCG
GCCCTCTGCGCCTACGCGGTCACCTACACAGCGATGTACGTGACTCTCGTGTTCCGCGTGAAGG
GCTCCCGCCTGGTCAAACCCTCGCTCTGCCTGGCCTTGCTGTGCCCGGCCTTCCTGGTGGGCGT
GGTCCGCGTGGCCGAGTACCGAAACCACTGGTCGGACGTGCTGGCTGGCTTCCTGACAGGGGCG
GCCATCGCCACCTTTTTGGTCACCTGCGTTGTGCATAACTTTCAGAGCCGGCCACCCTCTGGCC
GAAGGCTCTCTCCCTGGGAGGACCTGGGCCAAGCCCCCACCATGGATAGCCCCCTCGAAAAGAA
CCCGAGGTCTGCAGGCCGCATTCGACACCGGCACGGCTCACCCCATCCAAGTCGCAGAACTGCG
CCCGCCGTGGCCACCTGATCCCCAGCTGTGTCTCCTCCAGGGCCCCAGCCATGTGTTCGTCGCC
CCGTGTGCCCCGTCCTCGATTGAGGTCTGAGCCGACGCCCTTGCCCCTGCCCCTACCCCTGCCA
GCGCCCACCCCCAGCCAGGGCCCCTCGCCTTCCTCCCCTGGACCTGGGGGGCCAGGCGGGGGTG
GTGGACGTGGCCGGAAGCTGCTGCTGCCCACGCCCCTGCTGCGGGACCTGTACACCCTGAGTGG
ACTCTATCCCTCCCCCTTCCACCGGGACAACTTCAGCCCTTACCTGTTTGCCAGCCGTGACCAC
CTGCTGTGAGGCCCGACCACCCACCCAGAATCTGCCCAGTCCCCACTTCTTCCCTGCCACGCGT
GTGTGTGCGTGTGCCACGTGAGTGCCAAAGTCCCCTGCCCCCCAAGCCAGCCAGACCCAGACAT
TAGAAGATGGCTAGAAGGACATTTAGGAGACATCTGCCTCTCTGGCCCTCTGAGATATCCCGAT
GGGCACAAATGGAAGGTGCGCACTTGCCCCTACTATTGCCCTTTTAAGGGCCAAAGCTTGACCC
CATTGGCCATTGCCTGGCTAATGAGAACCCCTGGTTCTCAGAATTTTAACCAAAAGGAGTTGGC
TCCAACCAATGGGAGCCTTCCCCTCACTTCTTAGAATCCTCCTGCAAGAGGGCAACTCCAGCCA
GTGTTCAGCGACTGAACAGCCAATAGGAGCCCTTGGTTTCCAGAATTTCTAGAGTGGGTGGGCA
TGATTCCAGTCAATGGGGGACCGCCCGTGTCTAAGCATGTGCAAAGGAGAGGAGGGAGATGAGG
TCATTGTTTGTCATTGAGTCTTCTCTCAGAATCAGCGAGCCCAGCTGTAGGGTGGGGGGCAGGC
TCCCCCATGGCAGGGTCCTTGGGGTACCCCTTTTCCTCTCAGCCCCTCCCTGTGTGCGGCCTCT
CCACCTCTCACCCACTCTCTCCTAATCCCCTACTTAAGTAGGGCTTGCCCCACTTCAGAGGTTT
TGGGGTTCAGGGTGCTGTGTCTCCCCTTGCCTGTGCCCAGGTCATCCCAAACCCTTCTGTTATT
TATTAGGGCTGTGGGAAGGGTTTTTCTTCTTTTTCTTGGAACCTGCCCCTGTTCTTCACACTGC
CCCCCATGCCTCAGCCTCATACAGATGTGCCATCATGGGGGGCATGGGTGGAGCAGAGGGGCTC
CCTCACCCCGGGCAGGCAAAGGCAGTGGGTAGAGGAGGCACTGCCCCCCTTTCCTGCCCCCTCC
TCATCTTTAATAAAGACCTGGCTTCTCATCTTTAATAAAGACCTGTTTGTAACAGAA

hide sequence

RefSeq Acc Id:

XM_017027148 ⟹ XP_016882637

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	11,355,432 - 11,365,698 (+)	NCBI

Sequence:

show sequence

AGTCTGCGCGGCGCGGCCAGGCCCGGCCGACCGCGTCTCGGTCTTCGCGTCTGCCAGCCTGGCT
GGCAGTCCGTCTGTCCATCCCGCCGCGCCGGGGCAGTCTAGGCGGAGCGGGGGCTCAGGCGGCG
GCGGCCTCGACGCGAGTGAGTGTCGTGGTTGGGGTGCTGGACCCAGAGTGCCTACCCTCGCCTG
CCTGGGCCTCAGTTTCCACATCTGCACAATGGGGGTGACCATCCCTGCCCTGCTGGCTGCCAGG
AGCGGCTGTGAGTCTTCAGGCGTGGATGCAGCCTGGGGGAAGCCATAGGGCGCTTTCACAGGCA
CACCCCCTGGGACTCCCACTCCCTCCCCACCTCTGCAGGCCTGGCCTTCACCATGGCGGGAGGG
AGACCGCATCTGAAGAGGAGTTTCTCCATCATCCCCTGCTTTGTCTTCGTGGAGGGATTCTTCT
GCTATGACAGTACCTACGCCAAGCCCTACCCAGGGCCTGAGGCTGCCAGCCGAGTGCCTCCTGC
TCTTGTCTACGCACTGGTCACTGCCGGGCCCACCCTCACGATCCTGCTGGGAGAGCTGGCGCGT
GCCTTTTTCCCTGCACCACCTTCAGCCGTCCCAGTCATCGGGGAGAGCACCATCGTGTCTGGGG
CCTGCTGCCGCTTCAGCCCCCCAGTGCGGAGGCTGGTCCGCTTCCTGGGGGTCTACTCCTTCGG
CCTCTTCACCACGACCATCTTCGCCAACGCGGGGCAGGTGGTGACCGGCAATCCCACGCCACAC
TTCCTGTCCGTGTGCCGCCCCAACTACACGGCCCTGGGCTGCCTGCCACCTTCTCCGGATCGGC
CAGGTCCCGACCGCTTTGTCACTGACCAGGGTGCCTGCGCTGGCAGTCCCAGCCTCGTGGCCGC
CGCGCGCCGCGCCTTCCCCTGCAAGGATGCGGCCCTCTGCGCCTACGCGGTCACCTACACAGCG
ATGTACGTGACTCTCGTGTTCCGCGTGAAGGGCTCCCGCCTGGTCAAACCCTCGCTCTGCCTGG
CCTTGCTGTGCCCGGCCTTCCTGGTGGGCGTGGTCCGCGTGGCCGAGTACCGAAACCACTGGTC
GGACGTGCTGGCTGGCTTCCTGACAGGGGCGGCCATCGCCACCTTTTTGGTCACCTGCGTTGTG
CATAACTTTCAGAGCCGGCCACCCTCTGGCCGAAGGCTCTCTCCCTGGGAGGACCTGGGCCAAG
CCCCCACCATGGATAGCCCCCTCGAAAAGTTAAGTGTGGCGCAGGAACCCGAGGTCTGCAGGCC
GCATTCGACACCGGCACGGCTCACCCCATCCAAGTCGCAGAACTGCGCCCGCCGTGGCCACCTG
ATCCCCAGCTGTGTCTCCTCCAGGGCCCCAGCCATGTGTTCGTCGCCCCGTGTGCCCCGTCCTC
GATTGAGGTCTGAGCCGACGCCCTTGCCCCTGCCCCTACCCCTGCCAGCGCCCACCCCCAGCCA
GGGCCCCTCGCCTTCCTCCCCTGGACCTGGGGGGCCAGGCGGGGGTGGTGGACGTGGCCGGAAG
CTGCTGCTGCCCACGCCCCTGCTGCGGGACCTGTACACCCTGAGTGGACTCTATCCCTCCCCCT
TCCACCGGGACAACTTCAGCCCTTACCTGTTTGCCAGCCGTGACCACCTGCTGTGAGGCCCGAC
CACCCACCCAGAATCTGCCCAGTCCCCACTTCTTCCCTGCCACGCGTGTGTGTGCGTGTGCCAC
GTGAGTGCCAAAGTCCCCTGCCCCCCAAGCCAGCCAGACCCAGACATTAGAAGATGGCTAGAAG
GACATTTAGGAGACATCTGCCTCTCTGGCCCTCTGAGATATCCCGATGGGCACAAATGGAAGGT
GCGCACTTGCCCCTACTATTGCCCTTTTAAGGGCCAAAGCTTGACCCCATTGGCCATTGCCTGG
CTAATGAGAACCCCTGGTTCTCAGAATTTTAACCAAAAGGAGTTGGCTCCAACCAATGGGAGCC
TTCCCCTCACTTCTTAGAATCCTCCTGCAAGAGGGCAACTCCAGCCAGTGTTCAGCGACTGAAC
AGCCAATAGGAGCCCTTGGTTTCCAGAATTTCTAGAGTGGGTGGGCATGATTCCAGTCAATGGG
GGACCGCCCGTGTCTAAGCATGTGCAAAGGAGAGGAGGGAGATGAGGTCATTGTTTGTCATTGA
GTCTTCTCTCAGAATCAGCGAGCCCAGCTGTAGGGTGGGGGGCAGGCTCCCCCATGGCAGGGTC
CTTGGGGTACCCCTTTTCCTCTCAGCCCCTCCCTGTGTGCGGCCTCTCCACCTCTCACCCACTC
TCTCCTAATCCCCTACTTAAGTAGGGCTTGCCCCACTTCAGAGGTTTTGGGGTTCAGGGTGCTG
TGTCTCCCCTTGCCTGTGCCCAGGTCATCCCAAACCCTTCTGTTATTTATTAGGGCTGTGGGAA
GGGTTTTTCTTCTTTTTCTTGGAACCTGCCCCTGTTCTTCACACTGCCCCCCATGCCTCAGCCT
CATACAGATGTGCCATCATGGGGGGCATGGGTGGAGCAGAGGGGCTCCCTCACCCCGGGCAGGC
AAAGGCAGTGGGTAGAGGAGGCACTGCCCCCCTTTCCTGCCCCCTCCTCATCTTTAATAAAGAC
CTGGCTTCTCATCTTTAATAAAGACCTGTTTGTAACAGAA

hide sequence

RefSeq Acc Id:

XM_054321778 ⟹ XP_054177753

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	11,482,410 - 11,492,670 (+)	NCBI

RefSeq Acc Id:

XM_054321779 ⟹ XP_054177754

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	11,484,654 - 11,492,670 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001164106	(Get FASTA)	NCBI Sequence Viewer
	NP_001380821	(Get FASTA)	NCBI Sequence Viewer
	NP_001380822	(Get FASTA)	NCBI Sequence Viewer
	NP_001380823	(Get FASTA)	NCBI Sequence Viewer
	NP_001380824	(Get FASTA)	NCBI Sequence Viewer
	NP_001380825	(Get FASTA)	NCBI Sequence Viewer
	NP_073574	(Get FASTA)	NCBI Sequence Viewer
	XP_016882637	(Get FASTA)	NCBI Sequence Viewer
	XP_054177753	(Get FASTA)	NCBI Sequence Viewer
	XP_054177754	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH09378	(Get FASTA)	NCBI Sequence Viewer
	AAP72153	(Get FASTA)	NCBI Sequence Viewer
	AAQ73540	(Get FASTA)	NCBI Sequence Viewer
	BAB14414	(Get FASTA)	NCBI Sequence Viewer
	BAC04443	(Get FASTA)	NCBI Sequence Viewer
	CAH10684	(Get FASTA)	NCBI Sequence Viewer
	CAI56790	(Get FASTA)	NCBI Sequence Viewer
	CAK32397	(Get FASTA)	NCBI Sequence Viewer
	CCO13764	(Get FASTA)	NCBI Sequence Viewer
	EAW84200	(Get FASTA)	NCBI Sequence Viewer
	EAW84201	(Get FASTA)	NCBI Sequence Viewer
	EAW84202	(Get FASTA)	NCBI Sequence Viewer
	EAW84203	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000251473
	ENSP00000251473.4
	ENSP00000466698.1
	ENSP00000466898
	ENSP00000466898.1
	ENSP00000467807.1
	ENSP00000510269
	ENSP00000510269.1
GenBank Protein	Q96GM1	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_073574 ⟸ NM_022737
- Peptide Label:	isoform 1
- UniProtKB:	Q8N1U4 (UniProtKB/Swiss-Prot), Q5CZ76 (UniProtKB/Swiss-Prot), Q9H929 (UniProtKB/Swiss-Prot), Q96GM1 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAGGRPHLKRSFSIIPCFVFVESVLLGIVILLAYRLEFTDTFPVHTQGFFCYDSTYAKPYPGPE AASRVPPALVYALVTAGPTLTILLGELARAFFPAPPSAVPVIGESTIVSGACCRFSPPVRRLVR FLGVYSFGLFTTTIFANAGQVVTGNPTPHFLSVCRPNYTALGCLPPSPDRPGPDRFVTDQGACA GSPSLVAAARRAFPCKDAALCAYAVTYTAMYVTLVFRVKGSRLVKPSLCLALLCPAFLVGVVRV AEYRNHWSDVLAGFLTGAAIATFLVTCVVHNFQSRPPSGRRLSPWEDLGQAPTMDSPLEKNPRS AGRIRHRHGSPHPSRRTAPAVAT hide sequence

RefSeq Acc Id:	NP_001164106 ⟸ NM_001170635
- Peptide Label:	isoform 2
- UniProtKB:	Q96GM1 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAGGRPHLKRSFSIIPCFVFVEGFFCYDSTYAKPYPGPEAASRVPPALVYALVTAGPTLTILLG ELARAFFPAPPSAVPVIGESTIVSGACCRFSPPVRRLVRFLGVYSFGLFTTTIFANAGQVVTGN PTPHFLSVCRPNYTALGCLPPSPDRPGPDRFVTDQGACAGSPSLVAAARRAFPCKDAALCAYAV TYTAMYVTLVFRVKGSRLVKPSLCLALLCPAFLVGVVRVAEYRNHWSDVLAGFLTGAAIATFLV TCVVHNFQSRPPSGRRLSPWEDLGQAPTMDSPLEKLSVAQEPEVCRPHSTPARLTPSKSQNCAR RGHLIPSCVSSRAPAMCSSPRVPRPRLRSEPTPLPLPLPLPAPTPSQGPSPSSPGPGGPGGGGG RGRKLLLPTPLLRDLYTLSGLYPSPFHRDNFSPYLFASRDHLL hide sequence

RefSeq Acc Id:	XP_016882637 ⟸ XM_017027148
- Peptide Label:	isoform X1
- UniProtKB:	Q96GM1 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAGGRPHLKRSFSIIPCFVFVEGFFCYDSTYAKPYPGPEAASRVPPALVYALVTAGPTLTILLG ELARAFFPAPPSAVPVIGESTIVSGACCRFSPPVRRLVRFLGVYSFGLFTTTIFANAGQVVTGN PTPHFLSVCRPNYTALGCLPPSPDRPGPDRFVTDQGACAGSPSLVAAARRAFPCKDAALCAYAV TYTAMYVTLVFRVKGSRLVKPSLCLALLCPAFLVGVVRVAEYRNHWSDVLAGFLTGAAIATFLV TCVVHNFQSRPPSGRRLSPWEDLGQAPTMDSPLEKLSVAQEPEVCRPHSTPARLTPSKSQNCAR RGHLIPSCVSSRAPAMCSSPRVPRPRLRSEPTPLPLPLPLPAPTPSQGPSPSSPGPGGPGGGGG RGRKLLLPTPLLRDLYTLSGLYPSPFHRDNFSPYLFASRDHLL hide sequence

RefSeq Acc Id:

ENSP00000466698 ⟸ ENST00000586380

RefSeq Acc Id:

ENSP00000466898 ⟸ ENST00000591608

RefSeq Acc Id:

ENSP00000467807 ⟸ ENST00000591329

RefSeq Acc Id:

ENSP00000251473 ⟸ ENST00000251473

RefSeq Acc Id:	NP_001380822 ⟸ NM_001393893
- Peptide Label:	isoform 3
- UniProtKB:	A0A8I5KWF3 (UniProtKB/TrEMBL)

RefSeq Acc Id:	NP_001380823 ⟸ NM_001393894
- Peptide Label:	isoform 1
- UniProtKB:	Q96GM1 (UniProtKB/Swiss-Prot), Q8N1U4 (UniProtKB/Swiss-Prot), Q5CZ76 (UniProtKB/Swiss-Prot), Q9H929 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001380825 ⟸ NM_001393896
- Peptide Label:	isoform 4

RefSeq Acc Id:	NP_001380821 ⟸ NM_001393892
- Peptide Label:	isoform 3
- UniProtKB:	A0A8I5KWF3 (UniProtKB/TrEMBL)

RefSeq Acc Id:	NP_001380824 ⟸ NM_001393895
- Peptide Label:	isoform 4

RefSeq Acc Id:

ENSP00000510269 ⟸ ENST00000688289

RefSeq Acc Id:	XP_054177753 ⟸ XM_054321778
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054177754 ⟸ XM_054321779
- Peptide Label:	isoform X2

Protein Domains

Phosphatidic acid phosphatase type 2/haloperoxidase

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96GM1-F1-model_v2	AlphaFold	Q96GM1	1-343	view protein structure

Promoters

RGD ID:

6795765

Promoter ID:

HG_KWN:28910

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

NM_001170635, NM_022737

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	11,326,886 - 11,327,386 (+)	MPROMDB

RGD ID:

7238587

Promoter ID:

EPDNEW_H25040

Type:

initiation region

Name:

PLPPR2_1

Description:

phospholipid phosphatase related 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	19	11,355,432 - 11,355,492	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:29566	AgrOrtholog
COSMIC	PLPPR2	COSMIC
Ensembl Genes	ENSG00000105520	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000251473	ENTREZGENE
	ENST00000251473.9	UniProtKB/Swiss-Prot
	ENST00000586380.5	UniProtKB/TrEMBL
	ENST00000591329.5	UniProtKB/TrEMBL
	ENST00000591608	ENTREZGENE
	ENST00000591608.2	UniProtKB/Swiss-Prot
	ENST00000688289	ENTREZGENE
	ENST00000688289.1	UniProtKB/TrEMBL
Gene3D-CATH	Phosphatidic acid phosphatase type 2/haloperoxidase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000105520	GTEx
HGNC ID	HGNC:29566	ENTREZGENE
Human Proteome Map	PLPPR2	Human Proteome Map
InterPro	P_Acid_Pase_2/haloperoxi_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	P_Acid_Pase_2/haloperoxidase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PLPP	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:64748	UniProtKB/Swiss-Prot
NCBI Gene	64748	ENTREZGENE
OMIM	619591	OMIM
PANTHER	PTHR10165	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR10165:SF15	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	PAP2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA166181596	PharmGKB
SMART	acidPPc	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF48317	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A8I5KWF3	ENTREZGENE, UniProtKB/TrEMBL
	K7EMX8_HUMAN	UniProtKB/TrEMBL
	K7EQF7_HUMAN	UniProtKB/TrEMBL
	PLPR2_HUMAN	UniProtKB/Swiss-Prot
	Q5CZ76	ENTREZGENE
	Q8N1U4	ENTREZGENE
	Q96GM1	ENTREZGENE
	Q9H929	ENTREZGENE
UniProt Secondary	Q5CZ76	UniProtKB/Swiss-Prot
	Q8N1U4	UniProtKB/Swiss-Prot
	Q9H929	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-10-20	PLPPR2	phospholipid phosphatase related 2	LPPR2	lipid phosphate phosphatase-related protein type 2	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)

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