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Gene: DISP2 (dispatched RND transporter family member 2) Homo sapiens

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Symbol:

DISP2

Name:

dispatched RND transporter family member 2

RGD ID:

1319977

HGNC Page

HGNC:19712

Description:

Predicted to be involved in smoothened signaling pathway. Predicted to be located in plasma membrane. Predicted to be active in membrane.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

C15orf36; dispatched B; dispatched homolog 2; DISPB; DKFZp547N223; HsT16908; KIAA1742; LINC00594; long intergenic non-protein coding RNA 594; protein dispatched homolog 2

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	15	40,358,219 - 40,378,621 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	15	40,358,219 - 40,378,621 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	15	40,650,420 - 40,670,822 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	15	38,437,726 - 38,450,548 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	15	38,437,725 - 38,450,548	NCBI
Celera	15	17,416,417 - 17,429,240 (+)	NCBI		Celera
Cytogenetic Map	15	q15.1	NCBI
HuRef	15	17,493,841 - 17,506,669 (+)	NCBI		HuRef
CHM1_1	15	40,770,296 - 40,783,119 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	15	38,161,218 - 38,185,816 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

Bloom syndrome (IAGP)

colorectal cancer (IAGP)

mosaic variegated aneuploidy syndrome 1 (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dichloroethane (ISO)

1-naphthyl isothiocyanate (ISO)

17beta-estradiol (EXP)

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

2,2',5,5'-tetrachlorobiphenyl (ISO)

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

4,4'-sulfonyldiphenol (ISO)

6-propyl-2-thiouracil (ISO)

aldehydo-D-glucose (ISO)

atrazine (ISO)

benzo[a]pyrene (EXP,ISO)

benzo[b]fluoranthene (ISO)

beta-lapachone (EXP)

bisphenol A (EXP,ISO)

cadmium dichloride (EXP)

carbon nanotube (ISO)

choline (ISO)

copper(II) sulfate (EXP)

D-glucose (ISO)

dibenz[a,h]anthracene (ISO)

dioxygen (ISO)

endosulfan (ISO)

ethanol (ISO)

folic acid (ISO)

FR900359 (EXP)

fucoxanthin (ISO)

glucose (ISO)

glyphosate (ISO)

L-methionine (ISO)

lipopolysaccharide (EXP)

paracetamol (ISO)

PCB138 (ISO)

resveratrol (EXP)

S-(1,2-dichlorovinyl)-L-cysteine (EXP)

silicon dioxide (EXP)

sodium arsenite (EXP)

testosterone (ISO)

titanium dioxide (ISO)

trichloroethene (ISO)

triclosan (EXP)

tunicamycin (EXP)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

smoothened signaling pathway (IBA,NAS)

Cellular Component

membrane (IBA,IEA)

plasma membrane (TAS)

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:8889548	PMID:10619433	PMID:11214970	PMID:12372301	PMID:12477932	PMID:14702039	PMID:16258256	PMID:21873635	PMID:21947380	PMID:29507755	PMID:32393512	PMID:35748872
PMID:38565786

Genomics

Comparative Map Data

DISP2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	15	40,358,219 - 40,378,621 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	15	40,358,219 - 40,378,621 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	15	40,650,420 - 40,670,822 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	15	38,437,726 - 38,450,548 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	15	38,437,725 - 38,450,548	NCBI
Celera	15	17,416,417 - 17,429,240 (+)	NCBI		Celera
Cytogenetic Map	15	q15.1	NCBI
HuRef	15	17,493,841 - 17,506,669 (+)	NCBI		HuRef
CHM1_1	15	40,770,296 - 40,783,119 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	15	38,161,218 - 38,185,816 (+)	NCBI		T2T-CHM13v2.0

Disp2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	118,610,183 - 118,625,656 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	118,610,200 - 118,641,774 (+)	Ensembl		GRCm39 Ensembl
GRCm38	2	118,779,702 - 118,795,175 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	118,779,719 - 118,811,293 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	2	118,605,455 - 118,620,911 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	2	118,471,359 - 118,486,616 (+)	NCBI		MGSCv36	mm8
Celera	2	119,934,257 - 119,949,735 (+)	NCBI		Celera
Cytogenetic Map	2	E5	NCBI
cM Map	2	59.46	NCBI

Disp2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	3	126,216,194 - 126,231,724 (+)	NCBI		GRCr8
mRatBN7.2	3	105,762,303 - 105,777,826 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	3	105,762,305 - 105,777,800 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	3	109,435,326 - 109,450,891 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	3	118,030,883 - 118,046,437 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	3	115,691,242 - 115,706,798 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	3	110,574,383 - 110,589,909 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	3	110,574,417 - 110,589,921 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	3	117,115,017 - 117,130,523 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	3	105,283,578 - 105,297,671 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	3	105,186,484 - 105,193,828 (+)	NCBI
Celera	3	104,676,684 - 104,692,189 (+)	NCBI		Celera
Cytogenetic Map	3	q35	NCBI

Disp2
(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_004955416	7,282,048 - 7,299,179 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955416	7,282,048 - 7,297,896 (+)	NCBI	ChiLan1.0	ChiLan1.0

DISP2
(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	16	29,592,195 - 29,605,034 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	15	33,743,677 - 33,764,721 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	15	19,292,340 - 19,305,143 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	15	37,547,632 - 37,560,361 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	15	37,548,049 - 37,559,623 (+)	Ensembl	panpan1.1		panPan2

DISP2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	30	7,539,080 - 7,555,937 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	30	7,539,354 - 7,551,985 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	30	7,593,249 - 7,609,832 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	30	7,658,094 - 7,681,757 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	30	7,665,153 - 7,681,743 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	30	7,582,612 - 7,606,253 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	30	7,688,562 - 7,712,227 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	30	7,817,353 - 7,840,994 (+)	NCBI		UU_Cfam_GSD_1.0

Disp2
(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_024408640	85,973,251 - 85,988,008 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936471	3,821,263 - 3,836,989 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936471	3,821,310 - 3,836,074 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

DISP2
(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	130,937,400 - 130,952,046 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	1	130,931,909 - 130,962,780 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	1	146,021,378 - 146,037,180 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

DISP2
(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	26	42,644,040 - 42,658,280 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	26	42,644,780 - 42,656,794 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666048	98,307,623 - 98,321,387 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Disp2
(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_004624804	7,656,830 - 7,674,171 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624804	7,656,871 - 7,673,933 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in DISP2
114 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 15q14-15.1(chr15:36531993-40787538)x3	copy number gain	See cases [RCV000052341]	Chr15:36531993..40787538 [GRCh38] Chr15:36824194..41079736 [GRCh37] Chr15:34611486..38867028 [NCBI36] Chr15:15q14-15.1	pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4	copy number gain	See cases [RCV000447765]	Chr15:20733395..102511616 [GRCh37] Chr15:15q11.2-26.3	pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3	copy number gain	See cases [RCV000510717]	Chr15:22770422..102429112 [GRCh37] Chr15:15q11.2-26.3	pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)	copy number gain	See cases [RCV000512019]	Chr15:22770422..102429112 [GRCh37] Chr15:15q11.2-26.3	pathogenic
NM_033510.3(DISP2):c.2952G>C (p.Trp984Cys)	single nucleotide variant	not specified [RCV004329387]	Chr15:40369064 [GRCh38] Chr15:40661265 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3511C>T (p.Arg1171Cys)	single nucleotide variant	not specified [RCV004320157]	Chr15:40369623 [GRCh38] Chr15:40661824 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1416G>T (p.Met472Ile)	single nucleotide variant	not specified [RCV004307646]	Chr15:40367528 [GRCh38] Chr15:40659729 [GRCh37] Chr15:15q15.1	uncertain significance
Single allele	duplication	not provided [RCV000677926]	Chr15:31115047..102354857 [GRCh37] Chr15:15q13.2-26.3	pathogenic
NM_033510.3(DISP2):c.2696G>A (p.Ser899Asn)	single nucleotide variant	not specified [RCV004303501]	Chr15:40368808 [GRCh38] Chr15:40661009 [GRCh37] Chr15:15q15.1	likely benign
GRCh37/hg19 15q14-15.1 chr15:34638237..42057083 complex variant	complex	Spindle cell sarcoma [RCV000714282]	Chr15:34640169..42054561 [GRCh37] Chr15:15q14-15.1	pathogenic
GRCh37/hg19 15q14-15.1(chr15:38170429-40775075)x1	copy number loss	not provided [RCV000683683]	Chr15:38170429..40775075 [GRCh37] Chr15:15q14-15.1	pathogenic
GRCh37/hg19 15q11.1-26.3(chr15:20016811-102493540)x3	copy number gain	not provided [RCV000751155]	Chr15:20016811..102493540 [GRCh37] Chr15:15q11.1-26.3	pathogenic
GRCh37/hg19 15q11.1-26.3(chr15:20071673-102461162)x3	copy number gain	not provided [RCV000751156]	Chr15:20071673..102461162 [GRCh37] Chr15:15q11.1-26.3	pathogenic
NM_033510.3(DISP2):c.582C>T (p.Pro194=)	single nucleotide variant	not provided [RCV000893250]	Chr15:40364523 [GRCh38] Chr15:40656724 [GRCh37] Chr15:15q15.1	benign
NM_033510.3(DISP2):c.1366C>A (p.Leu456Met)	single nucleotide variant	not specified [RCV004299566]	Chr15:40367478 [GRCh38] Chr15:40659679 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3851C>T (p.Ser1284Phe)	single nucleotide variant	not specified [RCV004308296]	Chr15:40369963 [GRCh38] Chr15:40662164 [GRCh37] Chr15:15q15.1	uncertain significance
GRCh37/hg19 15q15.1(chr15:40464942-41196807)x4	copy number gain	not provided [RCV001259208]	Chr15:40464942..41196807 [GRCh37] Chr15:15q15.1	uncertain significance
NC_000015.9:g.(?_32964879)_(91358519_?)dup	duplication	Bloom syndrome [RCV001343104]\|Familial colorectal cancer [RCV001325176]	Chr15:32964879..91358519 [GRCh37] Chr15:15q13.3-26.1	uncertain significance
NM_033510.3(DISP2):c.3880G>A (p.Val1294Ile)	single nucleotide variant	not specified [RCV004305859]	Chr15:40369992 [GRCh38] Chr15:40662193 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3872G>A (p.Gly1291Glu)	single nucleotide variant	not specified [RCV004218563]	Chr15:40369984 [GRCh38] Chr15:40662185 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3929C>G (p.Pro1310Arg)	single nucleotide variant	not specified [RCV004140002]	Chr15:40370041 [GRCh38] Chr15:40662242 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1871C>T (p.Thr624Met)	single nucleotide variant	not specified [RCV004238324]	Chr15:40367983 [GRCh38] Chr15:40660184 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1199C>T (p.Thr400Ile)	single nucleotide variant	not specified [RCV004135791]	Chr15:40367311 [GRCh38] Chr15:40659512 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.931A>G (p.Met311Val)	single nucleotide variant	not specified [RCV004085338]	Chr15:40365711 [GRCh38] Chr15:40657912 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2458C>G (p.Arg820Gly)	single nucleotide variant	not specified [RCV004228878]	Chr15:40368570 [GRCh38] Chr15:40660771 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.7G>A (p.Gly3Ser)	single nucleotide variant	not specified [RCV004200027]	Chr15:40358328 [GRCh38] Chr15:40650529 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3481G>A (p.Glu1161Lys)	single nucleotide variant	not specified [RCV004185303]	Chr15:40369593 [GRCh38] Chr15:40661794 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.869T>C (p.Val290Ala)	single nucleotide variant	not specified [RCV004114280]	Chr15:40365649 [GRCh38] Chr15:40657850 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3616C>T (p.Arg1206Trp)	single nucleotide variant	not specified [RCV004171596]	Chr15:40369728 [GRCh38] Chr15:40661929 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1721C>T (p.Pro574Leu)	single nucleotide variant	not specified [RCV004154441]	Chr15:40367833 [GRCh38] Chr15:40660034 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.289C>T (p.Arg97Trp)	single nucleotide variant	not specified [RCV004243024]	Chr15:40363794 [GRCh38] Chr15:40655995 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.112C>G (p.Pro38Ala)	single nucleotide variant	not specified [RCV004160072]	Chr15:40358433 [GRCh38] Chr15:40650634 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1969C>T (p.Arg657Trp)	single nucleotide variant	not specified [RCV004204008]	Chr15:40368081 [GRCh38] Chr15:40660282 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1097C>T (p.Ala366Val)	single nucleotide variant	not specified [RCV004237251]	Chr15:40367209 [GRCh38] Chr15:40659410 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2540G>C (p.Ser847Thr)	single nucleotide variant	not specified [RCV004161298]	Chr15:40368652 [GRCh38] Chr15:40660853 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.592A>G (p.Lys198Glu)	single nucleotide variant	not specified [RCV004151326]	Chr15:40364533 [GRCh38] Chr15:40656734 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2494T>A (p.Trp832Arg)	single nucleotide variant	not specified [RCV004246767]	Chr15:40368606 [GRCh38] Chr15:40660807 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2578G>A (p.Gly860Ser)	single nucleotide variant	not specified [RCV004227866]	Chr15:40368690 [GRCh38] Chr15:40660891 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.782G>A (p.Arg261Gln)	single nucleotide variant	not specified [RCV004113255]	Chr15:40365209 [GRCh38] Chr15:40657410 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3410G>C (p.Gly1137Ala)	single nucleotide variant	not specified [RCV004206490]	Chr15:40369522 [GRCh38] Chr15:40661723 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2192C>T (p.Thr731Met)	single nucleotide variant	not specified [RCV004163435]	Chr15:40368304 [GRCh38] Chr15:40660505 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2215G>A (p.Val739Ile)	single nucleotide variant	not specified [RCV004095951]	Chr15:40368327 [GRCh38] Chr15:40660528 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3859A>G (p.Ser1287Gly)	single nucleotide variant	not specified [RCV004164618]	Chr15:40369971 [GRCh38] Chr15:40662172 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2680T>G (p.Phe894Val)	single nucleotide variant	not specified [RCV004145043]	Chr15:40368792 [GRCh38] Chr15:40660993 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3629C>G (p.Ala1210Gly)	single nucleotide variant	not specified [RCV004079969]	Chr15:40369741 [GRCh38] Chr15:40661942 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3728G>T (p.Ser1243Ile)	single nucleotide variant	not specified [RCV004177962]	Chr15:40369840 [GRCh38] Chr15:40662041 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2753A>T (p.Asn918Ile)	single nucleotide variant	not specified [RCV004160280]	Chr15:40368865 [GRCh38] Chr15:40661066 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2456C>T (p.Ala819Val)	single nucleotide variant	not specified [RCV004135524]	Chr15:40368568 [GRCh38] Chr15:40660769 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.903C>A (p.Asn301Lys)	single nucleotide variant	not specified [RCV004172946]	Chr15:40365683 [GRCh38] Chr15:40657884 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3122A>G (p.His1041Arg)	single nucleotide variant	not specified [RCV004089794]	Chr15:40369234 [GRCh38] Chr15:40661435 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3923G>A (p.Arg1308His)	single nucleotide variant	not specified [RCV004089419]	Chr15:40370035 [GRCh38] Chr15:40662236 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.787C>T (p.Arg263Trp)	single nucleotide variant	not specified [RCV004221191]	Chr15:40365214 [GRCh38] Chr15:40657415 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3764A>G (p.Glu1255Gly)	single nucleotide variant	not specified [RCV004079970]	Chr15:40369876 [GRCh38] Chr15:40662077 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1631A>G (p.Asn544Ser)	single nucleotide variant	not specified [RCV004140784]	Chr15:40367743 [GRCh38] Chr15:40659944 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1334G>A (p.Gly445Asp)	single nucleotide variant	not specified [RCV004234646]	Chr15:40367446 [GRCh38] Chr15:40659647 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3508C>T (p.Arg1170Trp)	single nucleotide variant	not specified [RCV004206459]	Chr15:40369620 [GRCh38] Chr15:40661821 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2255A>C (p.Glu752Ala)	single nucleotide variant	not specified [RCV004137386]	Chr15:40368367 [GRCh38] Chr15:40660568 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3509G>A (p.Arg1170Gln)	single nucleotide variant	not specified [RCV004105322]	Chr15:40369621 [GRCh38] Chr15:40661822 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.755G>A (p.Arg252Lys)	single nucleotide variant	not specified [RCV004119081]	Chr15:40365182 [GRCh38] Chr15:40657383 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3515G>A (p.Arg1172Gln)	single nucleotide variant	not specified [RCV004193648]	Chr15:40369627 [GRCh38] Chr15:40661828 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3835C>T (p.Pro1279Ser)	single nucleotide variant	not specified [RCV004125760]	Chr15:40369947 [GRCh38] Chr15:40662148 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3611G>A (p.Cys1204Tyr)	single nucleotide variant	not specified [RCV004080210]	Chr15:40369723 [GRCh38] Chr15:40661924 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2950T>C (p.Trp984Arg)	single nucleotide variant	not specified [RCV004142235]	Chr15:40369062 [GRCh38] Chr15:40661263 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1930C>A (p.His644Asn)	single nucleotide variant	not specified [RCV004152983]	Chr15:40368042 [GRCh38] Chr15:40660243 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.113C>G (p.Pro38Arg)	single nucleotide variant	not specified [RCV004123646]	Chr15:40358434 [GRCh38] Chr15:40650635 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1114G>A (p.Ala372Thr)	single nucleotide variant	not specified [RCV004156233]	Chr15:40367226 [GRCh38] Chr15:40659427 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.988G>A (p.Ala330Thr)	single nucleotide variant	not specified [RCV004173433]	Chr15:40367100 [GRCh38] Chr15:40659301 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.4082T>C (p.Leu1361Ser)	single nucleotide variant	not specified [RCV004210553]	Chr15:40370194 [GRCh38] Chr15:40662395 [GRCh37] Chr15:15q15.1	likely benign
NM_033510.3(DISP2):c.480C>A (p.Ser160Arg)	single nucleotide variant	not specified [RCV004172516]	Chr15:40364421 [GRCh38] Chr15:40656622 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.274C>T (p.His92Tyr)	single nucleotide variant	not specified [RCV004216729]	Chr15:40363779 [GRCh38] Chr15:40655980 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3053A>G (p.Glu1018Gly)	single nucleotide variant	not specified [RCV004272938]	Chr15:40369165 [GRCh38] Chr15:40661366 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.299A>C (p.Gln100Pro)	single nucleotide variant	not specified [RCV004250643]	Chr15:40363804 [GRCh38] Chr15:40656005 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1727G>C (p.Gly576Ala)	single nucleotide variant	not specified [RCV004253468]	Chr15:40367839 [GRCh38] Chr15:40660040 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1430A>G (p.Lys477Arg)	single nucleotide variant	not specified [RCV004268492]	Chr15:40367542 [GRCh38] Chr15:40659743 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.308A>C (p.Gln103Pro)	single nucleotide variant	not specified [RCV004275719]	Chr15:40363813 [GRCh38] Chr15:40656014 [GRCh37] Chr15:15q15.1	likely benign
NM_033510.3(DISP2):c.1990G>C (p.Ala664Pro)	single nucleotide variant	not specified [RCV004273130]	Chr15:40368102 [GRCh38] Chr15:40660303 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2251G>T (p.Ala751Ser)	single nucleotide variant	not specified [RCV004327627]	Chr15:40368363 [GRCh38] Chr15:40660564 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2511C>G (p.Phe837Leu)	single nucleotide variant	not specified [RCV004349404]	Chr15:40368623 [GRCh38] Chr15:40660824 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2209G>A (p.Gly737Ser)	single nucleotide variant	not specified [RCV004337364]	Chr15:40368321 [GRCh38] Chr15:40660522 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1855G>A (p.Ala619Thr)	single nucleotide variant	not specified [RCV004340704]	Chr15:40367967 [GRCh38] Chr15:40660168 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3254A>G (p.Tyr1085Cys)	single nucleotide variant	not specified [RCV004336290]	Chr15:40369366 [GRCh38] Chr15:40661567 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.4073A>C (p.His1358Pro)	single nucleotide variant	not specified [RCV004358488]	Chr15:40370185 [GRCh38] Chr15:40662386 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.775G>A (p.Ala259Thr)	single nucleotide variant	not specified [RCV004350955]	Chr15:40365202 [GRCh38] Chr15:40657403 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.43G>A (p.Ala15Thr)	single nucleotide variant	not specified [RCV004341642]	Chr15:40358364 [GRCh38] Chr15:40650565 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.646G>A (p.Val216Ile)	single nucleotide variant	not provided [RCV003400861]	Chr15:40364880 [GRCh38] Chr15:40657081 [GRCh37] Chr15:15q15.1	likely benign
NM_033510.3(DISP2):c.627C>T (p.Asp209=)	single nucleotide variant	not provided [RCV003411149]	Chr15:40364861 [GRCh38] Chr15:40657062 [GRCh37] Chr15:15q15.1	likely benign
NM_033510.3(DISP2):c.1370C>T (p.Ala457Val)	single nucleotide variant	not provided [RCV003411150]\|not specified [RCV004614432]	Chr15:40367482 [GRCh38] Chr15:40659683 [GRCh37] Chr15:15q15.1	likely benign\|uncertain significance
GRCh37/hg19 15q11.2-21.2(chr15:22770421-50347130)x3	copy number gain	not specified [RCV003987108]	Chr15:22770421..50347130 [GRCh37] Chr15:15q11.2-21.2	pathogenic
NM_033510.3(DISP2):c.3282G>A (p.Met1094Ile)	single nucleotide variant	not specified [RCV004375928]	Chr15:40369394 [GRCh38] Chr15:40661595 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3605C>T (p.Pro1202Leu)	single nucleotide variant	not specified [RCV004375930]	Chr15:40369717 [GRCh38] Chr15:40661918 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.725G>T (p.Ser242Ile)	single nucleotide variant	not specified [RCV004375933]	Chr15:40365152 [GRCh38] Chr15:40657353 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.751C>T (p.Pro251Ser)	single nucleotide variant	not specified [RCV004375935]	Chr15:40365178 [GRCh38] Chr15:40657379 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.761G>C (p.Ser254Thr)	single nucleotide variant	not specified [RCV004375936]	Chr15:40365188 [GRCh38] Chr15:40657389 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.781C>G (p.Arg261Gly)	single nucleotide variant	not specified [RCV004375937]	Chr15:40365208 [GRCh38] Chr15:40657409 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3157G>A (p.Ala1053Thr)	single nucleotide variant	not specified [RCV004375927]	Chr15:40369269 [GRCh38] Chr15:40661470 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.616C>T (p.Arg206Trp)	single nucleotide variant	not specified [RCV004375932]	Chr15:40364850 [GRCh38] Chr15:40657051 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1049G>A (p.Arg350His)	single nucleotide variant	not specified [RCV004375909]	Chr15:40367161 [GRCh38] Chr15:40659362 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1363C>T (p.Arg455Trp)	single nucleotide variant	not specified [RCV004375910]	Chr15:40367475 [GRCh38] Chr15:40659676 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1364G>A (p.Arg455Gln)	single nucleotide variant	not specified [RCV004375911]	Chr15:40367476 [GRCh38] Chr15:40659677 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1493C>T (p.Ala498Val)	single nucleotide variant	not specified [RCV004375912]	Chr15:40367605 [GRCh38] Chr15:40659806 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1690G>C (p.Asp564His)	single nucleotide variant	not specified [RCV004375913]	Chr15:40367802 [GRCh38] Chr15:40660003 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1726G>C (p.Gly576Arg)	single nucleotide variant	not specified [RCV004375914]	Chr15:40367838 [GRCh38] Chr15:40660039 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1826T>G (p.Leu609Arg)	single nucleotide variant	not specified [RCV004375916]	Chr15:40367938 [GRCh38] Chr15:40660139 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1987A>G (p.Ser663Gly)	single nucleotide variant	not specified [RCV004375917]	Chr15:40368099 [GRCh38] Chr15:40660300 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2089T>C (p.Cys697Arg)	single nucleotide variant	not specified [RCV004375918]	Chr15:40368201 [GRCh38] Chr15:40660402 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.20G>C (p.Ser7Thr)	single nucleotide variant	not specified [RCV004375919]	Chr15:40358341 [GRCh38] Chr15:40650542 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2222G>C (p.Arg741Pro)	single nucleotide variant	not specified [RCV004375921]	Chr15:40368334 [GRCh38] Chr15:40660535 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2527C>T (p.Arg843Cys)	single nucleotide variant	not specified [RCV004375922]	Chr15:40368639 [GRCh38] Chr15:40660840 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.284A>G (p.Tyr95Cys)	single nucleotide variant	not specified [RCV004375924]	Chr15:40363789 [GRCh38] Chr15:40655990 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.301G>C (p.Glu101Gln)	single nucleotide variant	not specified [RCV004375926]	Chr15:40363806 [GRCh38] Chr15:40656007 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.743G>C (p.Arg248Thr)	single nucleotide variant	not specified [RCV004375934]	Chr15:40365170 [GRCh38] Chr15:40657371 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.788G>A (p.Arg263Gln)	single nucleotide variant	not specified [RCV004375938]	Chr15:40365215 [GRCh38] Chr15:40657416 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.25A>G (p.Ser9Gly)	single nucleotide variant	not specified [RCV004375923]	Chr15:40358346 [GRCh38] Chr15:40650547 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3458G>A (p.Gly1153Glu)	single nucleotide variant	not specified [RCV004375929]	Chr15:40369570 [GRCh38] Chr15:40661771 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1810T>G (p.Phe604Val)	single nucleotide variant	not specified [RCV004616470]	Chr15:40367922 [GRCh38] Chr15:40660123 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1594C>G (p.Gln532Glu)	single nucleotide variant	not specified [RCV004616473]	Chr15:40367706 [GRCh38] Chr15:40659907 [GRCh37] Chr15:15q15.1	uncertain significance
NC_000015.9:g.(?_38545387)_(42105565_?)dup	duplication	Mosaic variegated aneuploidy syndrome 1 [RCV004583016]	Chr15:38545387..42105565 [GRCh37] Chr15:15q14-15.1	uncertain significance
NM_033510.3(DISP2):c.2849G>A (p.Arg950His)	single nucleotide variant	not specified [RCV004616463]	Chr15:40368961 [GRCh38] Chr15:40661162 [GRCh37] Chr15:15q15.1	likely benign
NM_033510.3(DISP2):c.1951G>A (p.Gly651Ser)	single nucleotide variant	not specified [RCV004616465]	Chr15:40368063 [GRCh38] Chr15:40660264 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3469G>A (p.Gly1157Arg)	single nucleotide variant	not specified [RCV004616467]	Chr15:40369581 [GRCh38] Chr15:40661782 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1811T>C (p.Phe604Ser)	single nucleotide variant	not specified [RCV004616471]	Chr15:40367923 [GRCh38] Chr15:40660124 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1255G>C (p.Asp419His)	single nucleotide variant	not specified [RCV004616466]	Chr15:40367367 [GRCh38] Chr15:40659568 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.629T>C (p.Ile210Thr)	single nucleotide variant	not specified [RCV004616469]	Chr15:40364863 [GRCh38] Chr15:40657064 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.2778G>C (p.Glu926Asp)	single nucleotide variant	not specified [RCV004616474]	Chr15:40368890 [GRCh38] Chr15:40661091 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.3922C>T (p.Arg1308Cys)	single nucleotide variant	not specified [RCV004616468]	Chr15:40370034 [GRCh38] Chr15:40662235 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.875T>C (p.Met292Thr)	single nucleotide variant	not specified [RCV004616472]	Chr15:40365655 [GRCh38] Chr15:40657856 [GRCh37] Chr15:15q15.1	uncertain significance
NM_033510.3(DISP2):c.1606C>T (p.Arg536Cys)	single nucleotide variant	not specified [RCV004616462]	Chr15:40367718 [GRCh38] Chr15:40659919 [GRCh37] Chr15:15q15.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	948
Count of miRNA genes:	534
Interacting mature miRNAs:	595
Transcripts:	ENST00000267889, ENST00000558623, ENST00000559721
Prediction methods:	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.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
2289410	BW327_H	Body weight QTL 327 (human)	3.32	0.0001	Body fat amount		15	19980129	45980129	Human
597271034	GWAS1367108_H	aortic measurement QTL GWAS1367108 (human)		7e-09	aortic measurement	aorta measurement (CMO:0001474)	15	40363243	40363244	Human
1559411	SCL107_H	Serum cholesterol level QTL 107 (human)	3.88		Lipid level	triglyceride	15	26543552	52543552	Human
597271824	GWAS1367898_H	descending aortic diameter QTL GWAS1367898 (human)		3e-11	descending aortic diameter		15	40363243	40363244	Human
1559354	LDLPS4_H	Low density lipoprotein particle size QTL 4 (human)	2.2	0.019	LDL particle size		15	34790230	60790230	Human
2289420	BW314_H	Body weight QTL 314 (human)	2.72	0.0003	Body weight	lean mass	15	19980129	45980129	Human
1643273	BW330_H	Body Weight QTL 330 (human)	1.05	0.014	Body weight	body mass index	15	26866719	52866719	Human
597271338	GWAS1367412_H	descending aortic diameter QTL GWAS1367412 (human)		1e-12	descending aortic diameter		15	40363243	40363244	Human
2289430	BMD7_H	Bone mineral density QTL 7 (human)	3.32	0.0001	Bone mineral density		15	19980129	45980129	Human
597061282	GWAS1157356_H	vital capacity QTL GWAS1157356 (human)		2e-09	vital capacity		15	40361837	40361838	Human
2299958	PRSTS330_H	Prostate tumor susceptibility QTL 330 (human)	1.02	0.0151	Prostate tumor susceptibility		15	34790230	60790230	Human
597179279	GWAS1275353_H	protein measurement QTL GWAS1275353 (human)		9e-55	protein measurement		15	40361837	40361838	Human
597268129	GWAS1364203_H	aortic measurement QTL GWAS1364203 (human)		1e-09	aortic measurement	aorta measurement (CMO:0001474)	15	40363243	40363244	Human
1643523	BW284_H	Body Weight QTL 284 (human)	1.95	0.0013	Body weight		15	21792889	47792889	Human
597268549	GWAS1364623_H	ascending aortic diameter QTL GWAS1364623 (human)		8e-09	ascending aortic diameter		15	40370547	40370548	Human

Markers in Region

NIB1989

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	15	40,663,073 - 40,663,227	UniSTS	GRCh37
Build 36	15	38,450,365 - 38,450,519	RGD	NCBI36
Celera	15	17,429,057 - 17,429,211	RGD
Cytogenetic Map	15	q15.1	UniSTS
HuRef	15	17,506,486 - 17,506,640	UniSTS
GeneMap99-GB4 RH Map	15	127.27	UniSTS
Whitehead-RH Map	15	77.0	UniSTS
Whitehead-YAC Contig Map	15		UniSTS

A004U40

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	15	40,662,987 - 40,663,235	UniSTS	GRCh37
Build 36	15	38,450,279 - 38,450,527	RGD	NCBI36
Celera	15	17,428,971 - 17,429,219	RGD
Cytogenetic Map	15	q15.1	UniSTS
HuRef	15	17,506,400 - 17,506,648	UniSTS
GeneMap99-GB4 RH Map	15	128.95	UniSTS
Whitehead-RH Map	15	80.5	UniSTS

DISPB_1538

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	15	40,662,603 - 40,663,349	UniSTS	GRCh37
Build 36	15	38,449,895 - 38,450,641	RGD	NCBI36
Celera	15	17,428,587 - 17,429,333	RGD
HuRef	15	17,506,016 - 17,506,762	UniSTS

D15S179E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	15	40,662,991 - 40,663,088	UniSTS	GRCh37
Build 36	15	38,450,283 - 38,450,380	RGD	NCBI36
Celera	15	17,428,975 - 17,429,072	RGD
Cytogenetic Map	15	q15.1	UniSTS
HuRef	15	17,506,404 - 17,506,501	UniSTS

2178

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	15	40,663,018 - 40,663,122	UniSTS	GRCh37
Build 36	15	38,450,310 - 38,450,414	RGD	NCBI36
Celera	15	17,429,002 - 17,429,106	RGD
Cytogenetic Map	15	q15.1	UniSTS
HuRef	15	17,506,431 - 17,506,535	UniSTS
GeneMap99-GB4 RH Map	15	127.27	UniSTS
NCBI RH Map	15	90.1	UniSTS

RH77781

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	15	40,663,065 - 40,663,209	UniSTS	GRCh37
Build 36	15	38,450,357 - 38,450,501	RGD	NCBI36
Celera	15	17,429,049 - 17,429,193	RGD
Cytogenetic Map	15	q15.1	UniSTS
HuRef	15	17,506,478 - 17,506,622	UniSTS
GeneMap99-GB4 RH Map	15	127.42	UniSTS

Expression

RNA-SEQ Expression

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system	visual system
1203	2437	2780	2240	4967	1711	2333	4	607	1740	450	2265	7031	6238	53	3734	828	1736	1614	172	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_033510	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011522125	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017022687	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379033	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB051529	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC013356	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI278850	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK096153	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC037537	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC151833	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CB305650	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471125	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068263	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR627480	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY171765	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000267889 ⟹ ENSP00000267889

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	40,358,219 - 40,378,621 (+)	Ensembl

Ensembl Acc Id:

ENST00000558623

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	40,369,855 - 40,371,056 (+)	Ensembl

Ensembl Acc Id:

ENST00000559721

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	40,365,007 - 40,365,694 (+)	Ensembl

Ensembl Acc Id:

ENST00000561261

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	40,371,825 - 40,372,476 (+)	Ensembl

RefSeq Acc Id:

NM_033510 ⟹ NP_277045

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	40,358,219 - 40,378,621 (+)	NCBI
GRCh37	15	40,650,434 - 40,663,256 (+)	RGD
Build 36	15	38,437,726 - 38,450,548 (+)	NCBI Archive
Celera	15	17,416,417 - 17,429,240 (+)	RGD
HuRef	15	17,493,841 - 17,506,669 (+)	ENTREZGENE
CHM1_1	15	40,770,298 - 40,783,120 (+)	NCBI
T2T-CHM13v2.0	15	38,165,077 - 38,185,816 (+)	NCBI

Sequence:

show sequence

ATGCGCACGAGCACCCCGCCGCCGCTGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCGCGGC
TTCAGCACCAGCGCCCGGACAGCGGTGCCGCCCACGGGCATGGACGGTGACAGCAGCAGCAGCA
GCGGCGGCAGCGGTCCGGCTCCCGGCCCGGGTCCGGAAGGGGAGCAACGGCCCGAGGGGGAGCC
CTTGGCCCCAGACGGCGGCTCCCCGGACAGCACCCAGACCAAGGCTGTGCCCCCTGAGGCAAGC
CCAGAGAGAAGCTGCTCCCTCCACAGCTGCCCCCTGGAGGACCCTTCCAGCTCTTCAGGACCCC
CACCAACAACTTCCACCCTCCAGCCTGTGGGTCCATCCAGCCCCTTGGCCCCTGCCCACTTCAC
CTATCCCCGGGCACTGCAGGAATACCAGGGGGGCAGTTCCCTGCCAGGACTTGGGGATCGGGCA
GCTCTCTGCTCCCACGGCTCCAGCCTCAGCCCTTCTCCAGCCCCCTCACAGCGCGATGGGACCT
GGAAGCCACCCGCTGTGCAGCACCATGTGGTCAGCGTCAGGCAGGAACGAGCCTTCCAGATGCC
AAAGAGCTATTCCCAGCTGATTGCTGAGTGGCCAGTGGCCGTGCTGATGCTGTGTCTGGCTGTC
ATCTTCCTCTGCACCCTGGCTGGACTGTTGGGGGCCCGGCTGCCCGACTTCTCCAAGCCTTTGC
TGGGCTTTGAGCCACGGGACACAGACATTGGGAGCAAGTTAGTGGTCTGGAGAGCACTACAAGC
CCTCACAGGCCCCAGGAAGCTGCTTTTCCTTTCCCCAGACCTTGAGCTGAACAGCTCGAGCTCC
CACAACACTCTGAGGCCTGCACCCAGAGGCAGTGCCCAGGAGAGCGCTGTCCGGCCTCGGAGAA
TGGTGGAGCCCCTGGAGGACAGAAGGCAAGAGAACTTCTTCTGTGGCCCCCCTGAGAAGAGCTA
TGCAAAGCTGGTGTTCATGTCCACCTCCTCGGGCAGCCTATGGAACCTGCATGCCATCCATTCC
ATGTGTCGCATGGAACAGGACCAGATCCGCTCCCATACCAGCTTCGGGGCTCTGTGCCAGCGGA
CAGCAGCCAACCAGTGCTGCCCCAGCTGGTCCCTGGGCAACTATCTGGCTGTGCTCTCCAACCG
CTCCTCCTGCCTGGACACTACCCAAGCTGACGCAGCCCGCACACTGGCCCTGCTTCGGACCTGT
GCCCTCTACTACCACAGTGGCGCCTTGGTGCCCTCTTGTCTGGGACCTGGGCAGAACAAGTCCC
CACGCTGTGCCCAGGTTCCCACCAAGTGCTCCCAGAGTAGTGCCATCTACCAACTCCTGCACTT
TCTGCTTGACAGGGACTTTCTGAGTCCCCAGACCACTGACTACCAGGTGCCTTCCCTCAAGTAC
AGCCTGCTCTTCCTGCCCACCCCAAAGGGTGCTTCCCTCATGGACATCTACCTGGACCGGCTGG
CCACCCCCTGGGGGCTTGCTGACAACTACACCTCTGTCACTGGCATGGACCTGGGCCTCAAGCA
GGAGCTGCTGAGGCACTTCCTGGTCCAGGACACGGTGTACCCCTTGCTGGCTCTGGTTGCCATC
TTCTTCGGCATGGCCCTGTACCTGCGCTCACTCTTCCTCACGCTCATGGTGCTGCTGGGGGTGC
TGGGCTCACTGCTGGTGGCCTTCTTCCTTTACCAGGTGGCCTTCCGCATGGCCTACTTCCCCTT
CGTCAATCTGGCAGCCCTCCTCCTGCTGAGCAGCGTCTGCGCCAACCACACGCTCATCTTCTTC
GACCTGTGGCGCCTTAGCAAGAGCCAGCTGCCGTCGGGGGGGCTGGCGCAGCGCGTGGGCCGCA
CCATGCACCACTTCGGCTACCTGCTGCTGGTCTCCGGCCTCACCACGAGCGCGGCCTTCTATGC
CAGCTACCTGAGCCGCCTGCCGGCCGTTCGCTGCCTCGCCCTCTTCATGGGCACGGCTGTGCTG
GTGCACCTGGCGCTCACGCTGGTCTGGCTGCCCGCCTCCGCCGTGCTCCACGAGCGCTACCTGG
CGCGCGGCTGTGCGCGCCGGGCGCGGGGCCGGTGGGAGGGCAGCGCGCCCCGGCGGCTACTGCT
GGCGCTGCACCGGCGGCTCCGCGGCCTGCGGAGGGCGGCGGCTGGCACCTCGCGTCTGCTCTTC
CAGCGCCTGCTGCCCTGCGGCGTCATCAAGTTCCGCTACATCTGGATCTGCTGGTTCGCAGCAC
TGGCGGCAGGGGGCGCCTACATCGCCGGAGTCAGCCCCCGCCTGCGGCTGCCCACGCTGCCGCC
GCCCGGCGGCCAGGTCTTCCGGCCCAGCCACCCCTTCGAGCGCTTCGACGCGGAGTATCGCCAG
CTGTTCCTGTTCGAGCAGCTGCCGCAGGGCGAGGGCGGCCACATGCCCGTGGTTTTGGTGTGGG
GCGTCCTGCCTGTGGACACTGGCGACCCTCTGGACCCTCGTAGCAACAGCAGCCTGGTGAGGGA
CCCTGCCTTCTCGGCCAGCGGCCCTGAGGCCCAGCGCTGGCTGCTGGCACTCTGTCACCGGGCC
CGGAATCAGAGCTTCTTCGACACCCTGCAGGAAGGCTGGCCCACGCTGTGTTTCGTGGAGACCC
TCCAGCGCTGGATGGAGAGCCCCAGCTGCGCCCGCCTGGGGCCTGACCTCTGCTGCGGCCACTC
GGACTTCCCCTGGGCCCCCCAGTTTTTCCTGCACTGCCTGAAAATGATGGCTCTGGAGCAAGGC
CCCGATGGCACCCAGGACCTGGGACTCCGCTTTGATGCCCATGGCAGCCTGGCCGCCCTGGTCC
TACAATTCCAGACCAACTTCCGGAACAGTCCGGACTACAACCAGACCCAGCTCTTCTACAATGA
GGTCAGCCACTGGCTGGCAGCGGAGCTGGGCATGGCACCTCCAGGCCTCCGCCGTGGTTGGTTC
ACTAGCCGTCTAGAGCTGTATAGCCTGCAGCACAGCCTGAGCACTGAGCCTGCTGTGGTGCTGG
GCCTGGCTTTGGCGCTGGCCTTTGCCACACTGCTCCTGGGCACCTGGAATGTTCCCCTCAGCCT
ATTCTCCGTGGCAGCTGTGGCAGGCACCGTGCTGCTCACTGTAGGACTCCTGGTTCTCCTCGAG
TGGCAGCTCAACACTGCCGAGGCCCTGTTTCTCTCTGCCTCAGTGGGCCTCTCAGTAGACTTCA
CTGTCAACTACTGCATCTCCTATCACCTGTGCCCACACCCTGACCGCCTGAGCCGTGTGGCCTT
CTCTCTGCGCCAGACCAGCTGCGCCACAGCCGTGGGGGCTGCAGCCCTGTTTGCGGCAGGCGTG
CTCATGCTGCCTGCCACAGTGCTGCTCTATCGCAAGCTGGGCATCATCCTCATGATGGTCAAAT
GCGTCAGTTGTGGCTTTGCCAGCTTCTTCTTCCAATCTCTCTGCTGTTTCTTCGGGCCAGAGAA
GAACTGTGGGCAGATCCTCTGGCCCTGTGCCCACCTGCCATGGGATGCTGGTACTGGGGACCCT
GGTGGGGAGAAGGCAGGCCGCCCACGACCAGGGTCAGTGGGAGGGATGCCCGGGTCCTGCTCAG
AGCAATATGAGCTACAGCCCCTGGCACGGCGTCGGAGCCCCAGCTTTGACACCAGCACAGCCAC
CAGCAAGCTGTCCCACCGGCCCTCAGTACTCTCTGAGGATCTGCAGCTCCATGATGGTCCGTGC
TGTTCCCGGCCCCCACCAGCCCCTGCCTCCCCAAGGGAGCTGCTGCTGGACCACCAGGCAGTCT
TCAGCCAGTGCCCTGCCCTGCAGACCTCCTCCCCCTATAAGCAGGCTGGCCCCAGCCCCAAAAC
CCGGGCCAGGCAGGACTCCCAAGGGGAGGAGGCTGAGCCCCTGCCAGCCTCACCAGAAGCCCCA
GCCCACTCTCCTAAGGCCAAGGCTGCAGATCCTCCTGATGGCTTCTGTTCCTCAGCCAGCACCC
TGGAGGGGCTCAGCGTCTCTGATGAGACCTGCCTAAGCACCTCTGAGCCCAGTGCCCGTGTACC
AGATTCCGTGGGTGTGTCCCCAGATGACCTGGATGACACTGGGCAGCCAGTCCTTGAGCGAGGC
CAGCTCAATGGGAAGCGGGACACCCTGTGGCTGGCGCTGAGGGAGACAGTGTATGACCCATCAT
TGCCCGCTTCCCATCACAGCAGCTTGTCCTGGAAGGGCCGAGGGGGGCCAGGGGATGGCAGCCC
TGTGGTGCTGCCCAATAGCCAGCCAGACCTGCCAGATGTTTGGCTGCGCAGGCCCAGCACTCAC
ACGTCAGGCTATAGCAGCTGAGGGGGACCCGGGGAGGCTGGACAGGGCGCGGAACCCTGTCATG
GATGACAAGGCAAGGGCAGCAATAGGCTGGAGCCCGAAGGTATTTCTCCAGATCCACAGGGAGA
GGTCTCACCCTCCAGCTGTGGATGTTAAACCCTGCCAGATGTCCCAGCCTTGATCTGTCTGCTC
CTACTCCTCACATCTGGAGGATTCCAGCAGGAGGGGTTTTGGAGGGGACCTGCTTGCGACCTGC
TGAGGGCTTGTCTGCTCCCACAGCACCATCTAAGACCCCTCCTCTAGAAGTGGGGAAGGCCAGA
TGTGTAGCTTCGGGTATCAGAGGAGGCTGACCTGGCCCCCATCCCAAGTTACAAGAACTTCAGT
GAGACTAAGGGACCCCCATCCTAGGGATCTTGTCAGGGTTCCTTACTGACCAGAGGAGCCCGCA
GCAATCTCCACAGCCTCCTGGGTCTCACCCCTTTCATGGGCTCTTCATCAGGACACTTCCCTCT
CTTTTGGGAGCTTCTCTGGGCAGAATTGGGCTGGGACCTCTCTCCCCAACTGCCCTGCTCTCCT
CATACTCACCGGTTTGACCAGAAATTCTCCAAATCCAGCCATAGATGGCTGCTGGGTGTGCAGC
AGGAGAAGGAGGATGGTCAGCCTTGGAGCATCTCTCAATTACGGGACAGTCCCTCTTTGGAAGC
AGGCTCCTGTGCTTTCCTGTGTTAATAAACAGTAATAATCCTTTCCATCTCTGCACATTTTAGT
CTCCTTGGAATCTATCTCACTACTTCACTACAGGGTAGCCTGACATTGGTCAGGTTCTTTTGAC
ACCCAATTTATAGGTAAAGACATTGAGACTAAGTAAGATGAACTGACCTCAGGGTCACTTAGCC
ACTAAATGGCAGAGCGGTTTCATTCCACCACTACAACCTCCAGTTTCCCTTTGGCTACCTGCCT
TCTTTCACCGCTAGCACCCTCCTCCAATCTGCTTTCTCTGGTGTCTCTGACTGAATCCAGCCAC
CCTCTTTGGGCCTCCACTTCCTGAGAGAGCTGTATTCCAAAAAAACCCAGGAGTTCCTCTCCAT
CTCCCCCGTGCCTCCCTCTGGAATCTGGCTGAGATGTCTGCTGGCCCTGGGGCGTCCTAGCTGA
CCTGATTCCCAGGCTTCAGGACCGTGCCTCTTCTACAGCCACAGTGTATAAGAGGCCCCACCAG
AAGAGGTACTGAGGGGCAGAAGAGGTGAAGCCAAATCCAATCAAGGCAGGAACTCAGACCTGCC
CTTTGGGAAGTGTATGAGTCTGAAGCTGCTTCCCAGGTTAGGGTCCCCAGCTTTTTAAGGACAA
GTCTCTCTGTGGAGCGTTAAGCAGACCAAAGGCTGGTTCCTCCTTCCCAAACTTCCTGGTAGGG
AAGTTTTATCCCATGTGAGAGCTCATGACACCAGGTGGCATCAACATGTTTATTGAACACCTAC
TTTGCATATGGTATTACAAGGGGACAGAGGTGTGGAAGAAAAATTGAACACCACCCTCAAAGAG
CTCACCTTCTAGCTGGGGAGACAGCTTATGCACACATGCAGGCATCGGATGGCTCACGGACGGC
ACCATATGCCTGCCATCATCATTATTGTTGGAGCTCAAGTACCCAGGACTGGGTAACAAGAAAG
GCTTTCTGGAGGAGGAAAAACTTGAGCTGGGCTTCAGAAGACCAAGCGTCTCAGACTGGAAGGG
GCCTTGGCGATCGTTTATTCCAGCAGTTTTCAAATTTTGTAGCCTCAGGACTCTTTCTTCAAAG
AAGCTCTGTGTGGAAAAACAATATATAAAACAGGTAAAAGGCAGCTACTCTGGTGGGCGCTGGG
TGTTGGGGGTGGAGTCAGCTTAGCCTGTCTTTCCACTGCAGCCTCTCCGGGTATCTGGGGAACC
CCTCCGGCTCCTGGCAGCTTCACAGAATGTAATATGAAAGCTACTGATCCAGGCTATTTTACAG
AGGAGTATCAGGAAAGGGAAGGGATTGTTCTAGGGCCAAATAGTCTGTGGCAGAGCTGGAGGCA
AATCAGATGATGTTTTTGTTTTATTTAGTTTTTTATTATTGAGACCTACTTCCTACTCCAAGTA
GCCCATGAGAAGTGGAGCAGAAACCGAAAAGAGACATGGGAGTTGTGGAAGAGACAGAAGGCAA
TAGGCAGGTACGGCAGGATACCTTGGCTCCTTTGCAAGATAAGTAAATCAAGATGAGTAACTCC
TGACACCAGGAAGGGGAAGCTGGAACCTAATTTGAACCTGTCCCCAGGGGGTCTGCTGGGACCT
CTCTCTTCATGTCCAGGTAGCATTCGGCCTCTCTGACCTAGAGCTGCTCATCAGCCCTGGTTTC
TCTGATAATGGTGTCCCTCTGTCATCATGCAGCCAGGCTGAGAGAGCCCTGGTATCCTCAGGGA
CAATGAGCCACAGGGAGGTTAAGGGAACTCTTCCTCCCAAGCATGAGCAGAAGACACTTTGCCT
GAACATAACCACTGAAATGTTAGAATGCAGAGGGGTGGATGGGTGGGCATGAGGGATCTGAGCA
CACCCGAGGGCCCTACCTGGGGATTTCCAGGTCATATTCTTGCAGGCTGTGGCCACACAACACT
TCAGGAAGGTGAATGAGCCATAGCAGCTGATGCATTGATTAGATTTGTTCTTTATGTTGCCAGG
CCCAGAAGAACCCAGCAGTAATCTAAAACATTACCTTATACCTAGAATGGCCCAAACCAACAGC
AGGCAATCCACATCAGCAGGAAATCCAGCCTGCCTCTCTAGCCCTGACTTTGGAATGTGGAACT
TAAAGCACTTCCTATTTCCTTTGAGTTGCAGCAGATCCTTTGCTTTATTATTATTAGGGGCACT
TACAATGAGTGTATGGCCCTGGAGACATGGCTTACAAGCACGCTGTGAGGCGTACAAAAATGAG
TCAAAGCACTTATGCTTGCCCTGCAAAATTCAAGAAATGATTTCTCCCCACTCAGACACTCTAA
TAGAACTACATTAACATTTGGAACTTGAGGTCATTTCCCCTATTTGTGCCACTGATCCTTGAAC
TCACATTCTGAGTACGAGTATGTATCCTGTATGCTATTAAAATATAACTTGAGGCCGGACATGA
TGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACTAGACGTTAGGA
GTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCGCCTCTACTAAAAATACAAAAATTAGTTG
GGCGTGGTGGGGGATGCCTGTAGTCCTAGCTACCCAGGAGGCTGAGGCAGGAAAATCATTTGAA
CCCGGGATGCAGAGGTTGAAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGATGACAGAG
CAAGACACCGTCTCAAAAAATAAATAAATAAATAAGTCGGGCACGGTGGCTCACGCCTGTAATC
CCAGCACTTTGGGAGGCCAAGGCAGGTGGATCATGAGGTCAGGAGATCGAAACCATCCTGGCTA
ACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGTGTGGTGGCGGGCGCCTG
TAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGATGTGAACCCAGGAGGCAGAGCTTGCA
GTAAGCCGAGATTGCGCCACTGCACTCCAGCCTGGGCAACAGAGCGAGACTCCATCTTAAAAAA
AAAAAATATATATATATATATATGTAAACTTGATATAGTCTGTTACCATGGGAAAACCATCCTT
CCATGGCTGTGGTGATTTGGGGACTTTTAGAGTGACAGTGTTAGACAGACTGATTTTATTGGCT
GAATCTTAGATTTTACTGATATATAGCATATCCCATACCATGATATGCGGGCAATATTCCAGCT
TGAGACAATTTTTTTTTTTTTTTTTTGAGACAGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCA
GTGGCACAATTTCGGCTCACTGCACTAATTTTTTGTATTTTTAGTAGAGACAGTAGAGTATTTT
TAGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCATGATCCGCCTGCCTCGGCCTCCCAGAG
TGCTGGGATTACAGGCATGAGCCACCGCGCCTGGCCGAGACAATTTTTAAAAAGACATTTCTCA
AGAGAGTTATAAGCCAAAATTTCCCTAGCCCCCTCCAACTCATTCTGTCCTTCTCCCAGTGCAT
GTCAGGACAGGGAAGAAGGCTTTAAATCAGATTTTAAGAAAGAGGATACATTGGTTTACAACCT
TTGCCTATCGTCCAGAGAGTTTCTGATCTTTTCTTTTTTTTTGAGACGGAGTCTTGCTCTGTCG
CCCAGGCTGGAGTGTAGTGGCACGATCTTGGCTCACTGCAAGCTCTGCCTCCCAGGTTCACGCC
ATTCTCCTGCCCCAGCCTCCCGAGCAGTTGGGACTACAGGCACCTGCCACCACGCCTGGCAAAT
TTTTTGTATTTTTAGTAAAGACGGGGTTTCATTGTGTTAGCCAGGATGGTTTCGATCTCCTGAC
CTTGTGATCCGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACTACACCCG
GCCCTGATCTTTTCTTTGACGGTGGCAGTATCTCATTTTTTGATAATACACATGGGTAATGGCA
AGCTCTTGGGACCCCATGCCAAGCATCAAGATCCCATTTACCTGGTGATAGGAAAGACAGACAT
TCCTCACCCTTTCTACCCACACCCTTGTTCACAGGGATGACTGTAACTAAGGTCTGCAGGTATT
TATGCTTAGGAGAAGAAATCGTAGTTCAATTCACCAGGAATATGAGAAACAAAAGAAAGCCACT
ATGTGCTATGTAAATGTCTGGCCATCCAAAGCCACCTTATGCAGAGGAACACTGGAAGGGCCTT
GATAAATTTCTCATAATTATTATCGGGCCTCTTTGTGATTACTCACATTTTTCTCAATATAGGG
GAAAGATCAGCATTTTACCAAATCCACAACCATCAAACAAACAAGAGCTTTAATATTGCTAAAG
AAAATCACACAGCTGAGCAGATTGATGTAGATTTGAATTCATGACCACCTATCTTAACTGGACC
CTCAGCTCTGCCTAGCTAGTATTCATTCTAGCTACTAGTTTTGATTATTTGTATTGACTCTTTT
ATATTTTCTCCACCTTCCTCAAATATCTCACCTTCCCCCACCCCTCAGTGGACAAAAAAAAAAA
AAAAATTCTTCATGAAGAAAACTGAAGCCTTCAAATAGAAATTTCCTCACCTTCAAGGCACCAA
AGCCACAACTTACCTACCCCCGCTCCTGCCTGCTCCTCTCCCCATCCCTTCTGCTACAACGAAG
GAAGCAGTAATGGCTCCATCAATGGCTTCTCACACTTGGTGTCAGAGGCCTTCACACGAGGGTT
TGCACTCCCCTACAAGGACATGAAGACTTTCTAGAAGGTAGGTGGACACAGATAGTTTTAAAGT
AATCAGTTTCCAGAGCCGCCTTCTCCATATGTTCCCCTCCTTATATTGGTGGGCCTAAGAAGCC
ACAGGCCTGACAGCTGTCCTTCCCAACTTCCACTTTCCCAGTTGCCTCCCCTCCCTCATTCTGA
ATCCTACTCTGGCTCCTTGCTCTGCGCTGTAAAAAACAAATAAAAGGGCCACTTGAGAATGCTC
TGCTTGAGGAAGTCCTTGAAAGAGCAAAGCCTGGAGAGCTTCTTTGAGAAAGTTCACAGGGGCA
GCCCTGTGGCTCAGTTCTGTGCCTTCTTCATTTAAGAATTCAAATTCATTGACATGTTATATTG
TAAAATATATAAATATATATTAAAAAGGAAAAAATAATAAAAATTTTTAAAAATAATTCAACTT
CAGGTGAGACACAGTGGCTCATGCCTATAATCCCAGTGTTTTGAAAGGCTGAAGTGGGAGGATG
GCTTGAGGCCAGGAGTTTGAGACCAGCTTGGGCAACATAGCAAGATCCCGTATCTACAAAAAAT
AATTTTAAAAATTAGCTGGGCATGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTCT
GGGAGGCCGAGGCAGGTAGATCATCTGAGGTCAGGAGTTCAACACCAGCCTGGCCAACATGGCA
AAACCCTGTCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGAGCATGCCTGTAGTCCCA
GCTACTCAGGAGGCTGAGGAAGGACAATCGCTTGAACCCTGGAGGCAGAGGTTGCAGTGAGCCA
AGATCATGCCATTGCACTCCAGCCTGGGTGACAGAGCGAGACTACATCTCAAAATAAATAAATA
AATAATAAAATAAAAATAAAAATTAGCTGGGCATGGTGATATGCGCCTGTAGACCCAGCTACTC
CAGAGGCTGAAGCAAGAGGATCACTTGAACTCTGGAGTTCGAGGTTACAGTGAGCCATAATCAC
ATTATGGCACTCCAGCCTGGCAACAGAGCGAGACCTTAACTCTAAAAAAAGAAATAAAGAAGAA
TTTAAACTGAAAGTGAGATGGTTGACACAGGATACATATTAACCACATTGATTTGAATGGAAAA
ATAAAATCAGACTTTTTCTGTTAGAAGGTCAGAATTGGCTCACAGGTTTGACAGAGAGGATAGT
CTTTGCAAGTAGGATGTATGGTGGACATTTTCCCTAAAATGGAATAACTTTAATCTGCAGCTCC
ACAGTTTGAACAAAAACAGACTGAAGGCTGGGCGTGGTGGCTCATGCCTGTAATCCCAACACTT
TGGGAGGCCTAGGCGGGCAGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGA
AACCTCATCTCTACTAAAAATACAAAAAAATAGCTGGGCGTGGTGGCGGGCACCTGTAGTCCCA
GCTACTCAGGAGGCTGAGGCAGGCGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCG
AGATTGCGCCACTGCACTCCATCCTGGGCAACAGAGTCTCAAAAAAAAAAAAAAAAATTTTTGA
CTGAAAGTACAGATACAACTTCCCTTTCCAGCCAAGATGGAGGAGCAGGGGCCAAGTTTATCCT
CCTGCCTGAAACAACCAACCAAACAGTAAATACATGAAATAATGAGTTTCAAGACACTGGACAT
GAGGTAACAAAAGACAGTGATCTCTCAGAGGCAAGAAACAAACAAGGAGAACCCCTCGGTTGCC
CAGCTTACCGCTTGAGAGGATGTATTTCACGGAGGGAGAACCCAGGCAAAGCAAGTGACTCTGA
GGTGAGGGGATAGCTGGGAGTGTGGAGCAGCCAAGCTGGCTAGAGTGCTCAGGACAGGGTACTG
GAGAGGAGAAAGGTGGATATATAGAGAATTCTGGGGATCTGCAAAGGGCCCCCCTTGAGTGTTC
CACAGAGCATGATTCATCATATAAGTGTAAGGAAACCACTTGAGACAAAGGAAAGGACCACCCA
AAACAATGGGCCGGAACAGTAGCCAGAAGTCACACACAGCCTGGACCACGCCTGTCCCCATCAG
CCAGATTGGAAAACCTCAAATTTATGGAGCATTGGTCAGAGGTCTCAGAAGGGCCTTGCCTCGT
AGTGGGGATTCATTAGCCCTAGTTTAAACATTGCTGGAACCTACCTAACAAATCTCAAAAGCAA
GACCTGAATTCAGGAATCAAGCTGTTTCTAAGTAACTGAAGTGTATCCCAGAACAAAACCCAAG
AACATTAACAGAAATCCAAAATTAACGAGCACCCAAAAATGTAAAATTCACAATGGCTGGTTTT
CCAATAAAAAATTACCAGTCATGCAAACTATAACCCATCATAAGGAGAAAAATCAGTTGAAACC
ACTACAGCTGACACCTATGTGAGAATTAGACAAGGACACTAAAAGAATTATTATAACTGTATTC
CATATGTACTAAGTAGAGACTAGGAAGATATTTTTAAATACCCACTTTGAATTTTAGAGACGAA
AACTAAAATGTCTGAGATGATGGGGTGGGTGGGGTAGGCAGAAAGAGGAGGATGGGAAGAAGTA
CCAAGGGGAAGGAGGAATGATTTGGGGATGACGGCTGTGTTTATTATCTTAATTGTGGTGATGG
TTTCACAGGTATATGTAATTTCTAAACTTATCAAATTGTACACTTAAAATATGTGGTCTATGGA
ATGTTAATTATATCTCAATAAAGCTGTTAAAATTGTACTGAAACAAAACCATTGGGGGAAACTG
GGTAAAGAGTCCAAAGGACCTCCCTATACTATCATTGTAACTTCCTGTCAATTATAACGATTCC
AAAA

hide sequence

RefSeq Acc Id:

XM_054379033 ⟹ XP_054235008

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	15	38,161,218 - 38,181,428 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_277045	(Get FASTA)	NCBI Sequence Viewer
	XP_054235008	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	A7MBM2	(Get FASTA)	NCBI Sequence Viewer
	AAI51834	(Get FASTA)	NCBI Sequence Viewer
	BAB21833	(Get FASTA)	NCBI Sequence Viewer
	CAH10680	(Get FASTA)	NCBI Sequence Viewer
	EAW92407	(Get FASTA)	NCBI Sequence Viewer
	EAW92408	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000267889
	ENSP00000267889.3

RefSeq Acc Id:

NP_277045 ⟸ NM_033510

- UniProtKB:

A7MBM2 (UniProtKB/Swiss-Prot), Q6AHW3 (UniProtKB/Swiss-Prot), Q9C0C1 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MDGDSSSSSGGSGPAPGPGPEGEQRPEGEPLAPDGGSPDSTQTKAVPPEASPERSCSLHSCPLE
DPSSSSGPPPTTSTLQPVGPSSPLAPAHFTYPRALQEYQGGSSLPGLGDRAALCSHGSSLSPSP
APSQRDGTWKPPAVQHHVVSVRQERAFQMPKSYSQLIAEWPVAVLMLCLAVIFLCTLAGLLGAR
LPDFSKPLLGFEPRDTDIGSKLVVWRALQALTGPRKLLFLSPDLELNSSSSHNTLRPAPRGSAQ
ESAVRPRRMVEPLEDRRQENFFCGPPEKSYAKLVFMSTSSGSLWNLHAIHSMCRMEQDQIRSHT
SFGALCQRTAANQCCPSWSLGNYLAVLSNRSSCLDTTQADAARTLALLRTCALYYHSGALVPSC
LGPGQNKSPRCAQVPTKCSQSSAIYQLLHFLLDRDFLSPQTTDYQVPSLKYSLLFLPTPKGASL
MDIYLDRLATPWGLADNYTSVTGMDLGLKQELLRHFLVQDTVYPLLALVAIFFGMALYLRSLFL
TLMVLLGVLGSLLVAFFLYQVAFRMAYFPFVNLAALLLLSSVCANHTLIFFDLWRLSKSQLPSG
GLAQRVGRTMHHFGYLLLVSGLTTSAAFYASYLSRLPAVRCLALFMGTAVLVHLALTLVWLPAS
AVLHERYLARGCARRARGRWEGSAPRRLLLALHRRLRGLRRAAAGTSRLLFQRLLPCGVIKFRY
IWICWFAALAAGGAYIAGVSPRLRLPTLPPPGGQVFRPSHPFERFDAEYRQLFLFEQLPQGEGG
HMPVVLVWGVLPVDTGDPLDPRSNSSLVRDPAFSASGPEAQRWLLALCHRARNQSFFDTLQEGW
PTLCFVETLQRWMESPSCARLGPDLCCGHSDFPWAPQFFLHCLKMMALEQGPDGTQDLGLRFDA
HGSLAALVLQFQTNFRNSPDYNQTQLFYNEVSHWLAAELGMAPPGLRRGWFTSRLELYSLQHSL
STEPAVVLGLALALAFATLLLGTWNVPLSLFSVAAVAGTVLLTVGLLVLLEWQLNTAEALFLSA
SVGLSVDFTVNYCISYHLCPHPDRLSRVAFSLRQTSCATAVGAAALFAAGVLMLPATVLLYRKL
GIILMMVKCVSCGFASFFFQSLCCFFGPEKNCGQILWPCAHLPWDAGTGDPGGEKAGRPRPGSV
GGMPGSCSEQYELQPLARRRSPSFDTSTATSKLSHRPSVLSEDLQLHDGPCCSRPPPAPASPRE
LLLDHQAVFSQCPALQTSSPYKQAGPSPKTRARQDSQGEEAEPLPASPEAPAHSPKAKAADPPD
GFCSSASTLEGLSVSDETCLSTSEPSARVPDSVGVSPDDLDDTGQPVLERGQLNGKRDTLWLAL
RETVYDPSLPASHHSSLSWKGRGGPGDGSPVVLPNSQPDLPDVWLRRPSTHTSGYSS

hide sequence

Ensembl Acc Id:

ENSP00000267889 ⟸ ENST00000267889

RefSeq Acc Id:	XP_054235008 ⟸ XM_054379033
- Peptide Label:	isoform X1

Protein Domains

SSD

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-A7MBM2-F1-model_v2	AlphaFold	A7MBM2	1-1401	view protein structure

Promoters

RGD ID:

6792207

Promoter ID:

HG_KWN:21039

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, Jurkat, Lymphoblastoid

Transcripts:

OTTHUMT00000252249

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	15	38,437,394 - 38,437,894 (+)	MPROMDB

RGD ID:

6815115

Promoter ID:

HG_MRA:5181

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

AK096153, BC169313, BC169314

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	15	38,447,381 - 38,447,881 (+)	MPROMDB

RGD ID:

7229095

Promoter ID:

EPDNEW_H20293

Type:

multiple initiation site

Name:

DISP2_2

Description:

dispatched RND transporter family member 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H20294

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	40,351,033 - 40,351,093	EPDNEW

RGD ID:

7229097

Promoter ID:

EPDNEW_H20294

Type:

initiation region

Name:

DISP2_1

Description:

dispatched RND transporter family member 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H20293

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	40,358,231 - 40,358,291	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:19712	AgrOrtholog
COSMIC	DISP2	COSMIC
Ensembl Genes	ENSG00000140323	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000267889	ENTREZGENE
	ENST00000267889.5	UniProtKB/Swiss-Prot
Gene3D-CATH	Multidrug efflux transporter AcrB transmembrane domain	UniProtKB/Swiss-Prot
GTEx	ENSG00000140323	GTEx
HGNC ID	HGNC:19712	ENTREZGENE
Human Proteome Map	DISP2	Human Proteome Map
InterPro	Dispatched_Hh_regulator	UniProtKB/Swiss-Prot
	SSD	UniProtKB/Swiss-Prot
KEGG Report	hsa:85455	UniProtKB/Swiss-Prot
NCBI Gene	85455	ENTREZGENE
OMIM	607503	OMIM
PANTHER	PROTEIN DISPATCHED HOMOLOG 2	UniProtKB/Swiss-Prot
	PROTEIN DISPATCHED-RELATED	UniProtKB/Swiss-Prot
PharmGKB	PA134876083	PharmGKB
PROSITE	SSD	UniProtKB/Swiss-Prot
Superfamily-SCOP	Multidrug efflux transporter AcrB transmembrane domain	UniProtKB/Swiss-Prot
UniProt	A7MBM2	ENTREZGENE, UniProtKB/Swiss-Prot
	Q6AHW3	ENTREZGENE
	Q9C0C1	ENTREZGENE
UniProt Secondary	Q6AHW3	UniProtKB/Swiss-Prot
	Q9C0C1	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2017-01-25	DISP2	dispatched RND transporter family member 2	LINC00594	long intergenic non-protein coding RNA 594	Data merged from RGD:6482930	737654	PROVISIONAL
2016-01-19	DISP2	dispatched RND transporter family member 2		dispatched homolog 2 (Drosophila)	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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Imported Disease Annotations - ClinVar