LYPD6B (LY6/PLAUR domain containing 6B)

Gene: LYPD6B (LY6/PLAUR domain containing 6B) Homo sapiens

Analyze

Symbol:

LYPD6B

Name:

LY6/PLAUR domain containing 6B

RGD ID:

1602653

HGNC Page

HGNC:27018

Description:

Enables acetylcholine receptor regulator activity. Predicted to be located in extracellular region and plasma membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

cancer/testis antigen 116; CT116; ly6/PLAUR domain-containing protein 6B; LYPD7

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Lypd6b (LY6/PLAUR domain containing 6B)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Lypd6b (Ly6/Plaur domain containing 6B)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Lypd6b (LY6/PLAUR domain containing 6B)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	LYPD6B (LY6/PLAUR domain containing 6B)	NCBI	Ortholog
Canis lupus familiaris (dog):	LYPD6B (LY6/PLAUR domain containing 6B)	HGNC	NCBI
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Lypd6b (LY6/PLAUR domain containing 6B)	NCBI	Ortholog
Sus scrofa (pig):	LYPD6B (LY6/PLAUR domain containing 6B)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	LYPD6B (LY6/PLAUR domain containing 6B)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Lypd6b (LY6/PLAUR domain containing 6B)	NCBI	Ortholog
Alliance orthologs ³
Mus musculus (house mouse):	Lypd6b (LY6/PLAUR domain containing 6B)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Rattus norvegicus (Norway rat):	Lypd6b (Ly6/Plaur domain containing 6B)	Alliance	DIOPT (HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	lypd6b (LY6/PLAUR domain containing 6B)	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Xenopus laevis (African clawed frog):	lypd6b.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	lypd6b	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	lypd6b.S	Alliance	DIOPT (Xenbase)

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	2	149,038,699 - 149,215,262 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	149,038,107 - 149,215,262 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	149,895,213 - 150,071,776 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	149,603,227 - 149,780,018 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	2	143,508,885 - 143,685,705 (+)	NCBI		Celera
Cytogenetic Map	2	q23.2	NCBI
HuRef	2	141,793,209 - 141,970,636 (+)	NCBI		HuRef
CHM1_1	2	149,900,822 - 150,077,602 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	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

17beta-estradiol (EXP)

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

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

4,4'-sulfonyldiphenol (ISO)

6-propyl-2-thiouracil (ISO)

all-trans-retinoic acid (EXP)

alpha-Zearalanol (ISO)

arsane (EXP)

arsenic atom (EXP)

avobenzone (EXP)

benzo[a]pyrene (EXP)

bisphenol A (EXP,ISO)

bisphenol F (ISO)

chloroprene (ISO)

copper atom (ISO)

copper(0) (ISO)

Cuprizon (ISO)

decabromodiphenyl ether (ISO)

diallyl trisulfide (EXP)

dorsomorphin (EXP)

fulvestrant (EXP)

furan (ISO)

genistein (ISO)

gentamycin (ISO)

manganese(II) chloride (ISO)

nickel sulfate (EXP)

ozone (ISO)

paracetamol (ISO)

perfluorooctanoic acid (ISO)

phenylmercury acetate (EXP)

potassium chromate (EXP)

SB 431542 (EXP)

sodium arsenate (EXP)

sodium arsenite (EXP,ISO)

titanium dioxide (ISO)

trichloroethene (ISO)

trichostatin A (EXP)

triptonide (ISO)

valproic acid (EXP)

zoledronic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Cellular Component

extracellular region (TAS)

plasma membrane (IEA,TAS)

side of membrane (IEA)

Molecular Function

acetylcholine receptor regulator activity (IBA,IDA,IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:12477932	PMID:15146197	PMID:16344560	PMID:18360792	PMID:20164180	PMID:20379614	PMID:21873635	PMID:23453885	PMID:26586467	PMID:29987050	PMID:32296183	PMID:33019770
PMID:33961781

Genomics

Comparative Map Data

LYPD6B
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	149,038,107 - 149,215,262 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	149,895,213 - 150,071,776 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	149,603,227 - 149,780,018 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	2	143,508,885 - 143,685,705 (+)	NCBI		Celera
Cytogenetic Map	2	q23.2	NCBI
HuRef	2	141,793,209 - 141,970,636 (+)	NCBI		HuRef
CHM1_1	2	149,900,822 - 150,077,602 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI		T2T-CHM13v2.0

Lypd6b
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	49,677,380 - 49,838,861 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	49,677,700 - 49,838,861 (+)	Ensembl		GRCm39 Ensembl
GRCm38	2	49,787,340 - 49,948,849 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	49,787,688 - 49,948,849 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	2	49,643,206 - 49,804,366 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	2	49,609,695 - 49,770,855 (+)	NCBI		MGSCv36	mm8
Celera	2	51,460,729 - 51,622,118 (+)	NCBI		Celera
Cytogenetic Map	2	C1.1	NCBI
cM Map	2	28.74	NCBI

Lypd6b
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	3	54,608,320 - 54,769,974 (+)	NCBI		GRCr8
mRatBN7.2	3	34,199,101 - 34,360,770 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	3	34,199,599 - 34,360,770 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	3	37,569,714 - 37,745,286 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	3	46,154,432 - 46,329,986 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	3	43,966,693 - 44,131,818 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	3	35,271,785 - 35,437,296 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	3	35,271,786 - 35,437,296 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	3	40,397,603 - 40,555,551 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	3	30,849,359 - 30,869,056 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	3	32,384,248 - 32,545,513 (+)	NCBI		Celera
Cytogenetic Map	3	q12	NCBI

Lypd6b
(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_004955440	15,014,264 - 15,027,648 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955440	14,865,736 - 15,028,655 (+)	NCBI	ChiLan1.0	ChiLan1.0

LYPD6B
(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	13	25,713,273 - 25,890,555 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	2B	25,728,237 - 25,905,525 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	2B	10,647,871 - 10,825,062 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	2B	153,478,374 - 153,575,462 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	2B	153,479,334 - 153,576,190 (+)	Ensembl	panpan1.1		panPan2

LYPD6B
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	19	50,692,220 - 50,855,061 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
Dog10K_Boxer_Tasha	19	50,813,689 - 50,978,961 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	19	52,164,791 - 52,330,414 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	19	52,246,558 - 52,329,581 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	19	50,807,650 - 50,973,190 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	19	50,942,420 - 51,108,413 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	19	52,341,463 - 52,507,252 (+)	NCBI		UU_Cfam_GSD_1.0

Lypd6b
(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_024405303	113,372,508 - 113,518,367 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936469	28,100,477 - 28,119,342 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936469	28,098,841 - 28,245,200 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

LYPD6B
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	15	2,952,546 - 2,972,920 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	15	2,957,051 - 3,179,409 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	15	2,443,118 - 2,477,085 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

LYPD6B
(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	10	34,511,293 - 34,644,953 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	10	34,634,763 - 34,644,939 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666040	164,885,952 - 165,010,527 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Lypd6b
(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_004624866	1,940,123 - 1,959,344 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624866	1,708,769 - 1,960,396 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in LYPD6B
18 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 2q22.3-24.1(chr2:147251948-157856378)x1	copy number loss	See cases [RCV000054090]	Chr2:147251948..157856378 [GRCh38] Chr2:148009516..158712890 [GRCh37] Chr2:147725986..158421136 [NCBI36] Chr2:2q22.3-24.1	pathogenic
GRCh38/hg38 2q22.3-23.3(chr2:147590324-153496674)x1	copy number loss	See cases [RCV000054091]	Chr2:147590324..153496674 [GRCh38] Chr2:148347892..154353187 [GRCh37] Chr2:148064362..154061433 [NCBI36] Chr2:2q22.3-23.3	pathogenic
GRCh38/hg38 2q23.1-23.3(chr2:148303135-153274626)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054092]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054092]\|See cases [RCV000054092]	Chr2:148303135..153274626 [GRCh38] Chr2:149060704..154131140 [GRCh37] Chr2:148777174..153839386 [NCBI36] Chr2:2q23.1-23.3	pathogenic
GRCh38/hg38 2q23.1-24.3(chr2:148917286-163204623)x1	copy number loss	See cases [RCV000054093]	Chr2:148917286..163204623 [GRCh38] Chr2:149674855..164061133 [GRCh37] Chr2:149391325..163769379 [NCBI36] Chr2:2q23.1-24.3	pathogenic
NM_177964.3(LYPD6B):c.78-7653C>T	single nucleotide variant	Lung cancer [RCV000091546]	Chr2:149197600 [GRCh38] Chr2:150054114 [GRCh37] Chr2:2q23.2	uncertain significance
GRCh38/hg38 2q22.3-24.1(chr2:143900149-158321624)x3	copy number gain	See cases [RCV000135402]	Chr2:143900149..158321624 [GRCh38] Chr2:144657717..159178136 [GRCh37] Chr2:144374187..158886382 [NCBI36] Chr2:2q22.3-24.1	pathogenic
GRCh38/hg38 2q22.3-23.2(chr2:147473194-149279840)x3	copy number gain	See cases [RCV000135391]	Chr2:147473194..149279840 [GRCh38] Chr2:148230762..150136354 [GRCh37] Chr2:147947232..149844600 [NCBI36] Chr2:2q22.3-23.2	uncertain significance
GRCh38/hg38 2q23.1-23.2(chr2:148440874-149091788)x1	copy number loss	See cases [RCV000139619]	Chr2:148440874..149091788 [GRCh38] Chr2:149198443..149948302 [GRCh37] Chr2:148914913..149656548 [NCBI36] Chr2:2q23.1-23.2	pathogenic
GRCh38/hg38 2q22.3-23.2(chr2:145471053-149582570)x1	copy number loss	See cases [RCV000141056]	Chr2:145471053..149582570 [GRCh38] Chr2:146228621..150439084 [GRCh37] Chr2:145945091..150147330 [NCBI36] Chr2:2q22.3-23.2	pathogenic
GRCh38/hg38 2q22.3-24.1(chr2:146324191-156219125)x3	copy number gain	See cases [RCV000142582]	Chr2:146324191..156219125 [GRCh38] Chr2:147081759..157075637 [GRCh37] Chr2:146798229..156783883 [NCBI36] Chr2:2q22.3-24.1	pathogenic
GRCh37/hg19 2q23.1-23.3(chr2:149811293-151128706)x3	copy number gain	See cases [RCV000240510]	Chr2:149811293..151128706 [GRCh37] Chr2:2q23.1-23.3	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3	copy number gain	not provided [RCV000752802]	Chr2:14238..243048760 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q23.1-23.2(chr2:149218583-149933863)x3	copy number gain	See cases [RCV000445916]	Chr2:149218583..149933863 [GRCh37] Chr2:2q23.1-23.2	uncertain significance
GRCh37/hg19 2q22.3-23.3(chr2:147063452-154796058)x1	copy number loss	See cases [RCV000448667]	Chr2:147063452..154796058 [GRCh37] Chr2:2q22.3-23.3	pathogenic
GRCh37/hg19 2q23.1-23.3(chr2:148842506-152370040)x1	copy number loss	See cases [RCV000448089]	Chr2:148842506..152370040 [GRCh37] Chr2:2q23.1-23.3	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	copy number gain	See cases [RCV000512056]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q22.3-23.3(chr2:146913477-151531586)x1	copy number loss	See cases [RCV000511626]	Chr2:146913477..151531586 [GRCh37] Chr2:2q22.3-23.3	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	copy number gain	See cases [RCV000511212]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q12.1-24.3(chr2:104172062-168223828)x1	copy number loss	Poly (ADP-Ribose) polymerase inhibitor response [RCV000626436]	Chr2:104172062..168223828 [GRCh37] Chr2:2q12.1-24.3	drug response
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3	copy number gain	not provided [RCV000752804]	Chr2:15672..243101834 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
NM_177964.5(LYPD6B):c.113G>A (p.Ser38Asn)	single nucleotide variant	not specified [RCV004285690]	Chr2:149205288 [GRCh38] Chr2:150061802 [GRCh37] Chr2:2q23.2	uncertain significance
GRCh37/hg19 2q22.3-24.1(chr2:147173792-158346266)x1	copy number loss	not provided [RCV001005326]	Chr2:147173792..158346266 [GRCh37] Chr2:2q22.3-24.1	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	copy number gain	Mosaic trisomy 2 [RCV002280628]	Chr2:1..243199373 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q21.3-23.3(chr2:136473383-152727396)	copy number gain	Global developmental delay [RCV001352659]	Chr2:136473383..152727396 [GRCh37] Chr2:2q21.3-23.3	pathogenic
GRCh37/hg19 2q23.1-23.3(chr2:148954840-150800195)	copy number gain	not specified [RCV002053249]	Chr2:148954840..150800195 [GRCh37] Chr2:2q23.1-23.3	uncertain significance
GRCh37/hg19 2q22.2-23.3(chr2:143258712-152867819)	copy number loss	not specified [RCV002053238]	Chr2:143258712..152867819 [GRCh37] Chr2:2q22.2-23.3	pathogenic
GRCh37/hg19 2q23.1-23.2(chr2:149218583-149933863)	copy number gain	not specified [RCV002053252]	Chr2:149218583..149933863 [GRCh37] Chr2:2q23.1-23.2	uncertain significance
GRCh37/hg19 2q22.2-23.3(chr2:142409401-152680804)x3	copy number gain	not provided [RCV001834428]	Chr2:142409401..152680804 [GRCh37] Chr2:2q22.2-23.3	pathogenic
NM_177964.5(LYPD6B):c.535G>A (p.Val179Ile)	single nucleotide variant	not specified [RCV004239146]	Chr2:149214621 [GRCh38] Chr2:150071135 [GRCh37] Chr2:2q23.2	likely benign
NM_177964.5(LYPD6B):c.103C>T (p.His35Tyr)	single nucleotide variant	not specified [RCV004145795]	Chr2:149205278 [GRCh38] Chr2:150061792 [GRCh37] Chr2:2q23.2	uncertain significance
NM_177964.5(LYPD6B):c.25A>G (p.Asn9Asp)	single nucleotide variant	not specified [RCV004145853]	Chr2:149160783 [GRCh38] Chr2:150017297 [GRCh37] Chr2:2q23.2	likely benign
NM_177964.5(LYPD6B):c.133G>T (p.Ala45Ser)	single nucleotide variant	not specified [RCV004126974]	Chr2:149205308 [GRCh38] Chr2:150061822 [GRCh37] Chr2:2q23.2	uncertain significance
NM_177964.5(LYPD6B):c.476G>A (p.Cys159Tyr)	single nucleotide variant	not specified [RCV004102208]	Chr2:149214562 [GRCh38] Chr2:150071076 [GRCh37] Chr2:2q23.2	uncertain significance
NM_177964.5(LYPD6B):c.296A>G (p.Asn99Ser)	single nucleotide variant	not specified [RCV004221033]	Chr2:149208380 [GRCh38] Chr2:150064894 [GRCh37] Chr2:2q23.2	uncertain significance
NM_177964.5(LYPD6B):c.371G>T (p.Gly124Val)	single nucleotide variant	not specified [RCV004252441]	Chr2:149213034 [GRCh38] Chr2:150069548 [GRCh37] Chr2:2q23.2	uncertain significance
NM_177964.5(LYPD6B):c.376A>C (p.Ser126Arg)	single nucleotide variant	not specified [RCV004359774]	Chr2:149213039 [GRCh38] Chr2:150069553 [GRCh37] Chr2:2q23.2	uncertain significance
NM_177964.5(LYPD6B):c.133G>A (p.Ala45Thr)	single nucleotide variant	not specified [RCV004354074]	Chr2:149205308 [GRCh38] Chr2:150061822 [GRCh37] Chr2:2q23.2	likely benign
GRCh37/hg19 2q22.3-23.3(chr2:148406827-152954124)x1	copy number loss	not provided [RCV003485050]	Chr2:148406827..152954124 [GRCh37] Chr2:2q22.3-23.3	pathogenic
GRCh37/hg19 2q21.2-23.2(chr2:134589311-149951291)x3	copy number gain	not specified [RCV003986337]	Chr2:134589311..149951291 [GRCh37] Chr2:2q21.2-23.2	likely pathogenic
NM_177964.5(LYPD6B):c.586C>T (p.Pro196Ser)	single nucleotide variant	not specified [RCV004411037]	Chr2:149214672 [GRCh38] Chr2:150071186 [GRCh37] Chr2:2q23.2	uncertain significance
NM_177964.5(LYPD6B):c.254A>G (p.Lys85Arg)	single nucleotide variant	not specified [RCV004411036]	Chr2:149208338 [GRCh38] Chr2:150064852 [GRCh37] Chr2:2q23.2	uncertain significance
NM_177964.5(LYPD6B):c.139G>A (p.Ala47Thr)	single nucleotide variant	not specified [RCV004411035]	Chr2:149205314 [GRCh38] Chr2:150061828 [GRCh37] Chr2:2q23.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2026
Count of miRNA genes:	821
Interacting mature miRNAs:	966
Transcripts:	ENST00000280115, ENST00000409029, ENST00000409642, ENST00000409876, ENST00000437627, ENST00000442722, ENST00000450639, ENST00000473800, ENST00000473975, ENST00000480545, ENST00000498249
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.

Markers in Region

RH94091

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	150,071,446 - 150,071,566	UniSTS	GRCh37
Build 36	2	149,779,692 - 149,779,812	RGD	NCBI36
Celera	2	143,685,379 - 143,685,499	RGD
Cytogenetic Map	2	q23.2	UniSTS
HuRef	2	141,970,310 - 141,970,430	UniSTS
GeneMap99-GB4 RH Map	2	502.6	UniSTS

RH70008

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	77,879,896 - 77,880,141	UniSTS	GRCh37
GRCh37	2	149,924,993 - 149,925,240	UniSTS	GRCh37
Build 36	2	149,633,239 - 149,633,486	RGD	NCBI36
Celera	4	75,181,270 - 75,181,515	UniSTS
Celera	2	143,538,892 - 143,539,139	RGD
Cytogenetic Map	2	q23.2	UniSTS
Cytogenetic Map	4	q21.1	UniSTS
Cytogenetic Map	9	q31	UniSTS
HuRef	4	73,631,724 - 73,631,969	UniSTS
HuRef	2	141,823,208 - 141,823,455	UniSTS

RH118755

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	150,069,728 - 150,070,002	UniSTS	GRCh37
Build 36	2	149,777,974 - 149,778,248	RGD	NCBI36
Celera	2	143,683,661 - 143,683,935	RGD
Cytogenetic Map	2	q23.2	UniSTS
HuRef	2	141,968,592 - 141,968,866	UniSTS
TNG Radiation Hybrid Map	2	85592.0	UniSTS

SHGC-144830

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	149,956,203 - 149,956,494	UniSTS	GRCh37
Build 36	2	149,664,449 - 149,664,740	RGD	NCBI36
Celera	2	143,570,134 - 143,570,425	RGD
Cytogenetic Map	2	q23.2	UniSTS
HuRef	2	141,854,468 - 141,854,759	UniSTS
TNG Radiation Hybrid Map	2	85628.0	UniSTS

D2S1812

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	149,956,201 - 149,956,431	UniSTS	GRCh37
Build 36	2	149,664,447 - 149,664,677	RGD	NCBI36
Celera	2	143,570,132 - 143,570,362	RGD
Cytogenetic Map	2	q23.2	UniSTS
HuRef	2	141,854,466 - 141,854,696	UniSTS
Whitehead-YAC Contig Map	2		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

visual system

adipose tissue

appendage

entire extraembryonic component

High

Medium

246

115

1301

569

688

Low

476

149

214

673

302

1297

194

528

594

150

Below cutoff

1375

2236

1266

327

860

310

2022

1331

2195

324

722

980

1470

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001317002	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001317003	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001317004	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001317005	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001317006	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_177964	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005246306	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006712279	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006712280	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006712281	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011510620	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011510623	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011510625	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017003364	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017003365	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017003366	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443401	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443402	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443403	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443404	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443405	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443406	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443407	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443408	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443409	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443410	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443411	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443412	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443413	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443414	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443416	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443417	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047443418	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340550	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340551	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340552	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340553	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340554	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340555	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340556	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340557	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340558	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340559	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340560	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340561	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340562	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340563	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340564	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340565	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340566	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340567	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340568	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340569	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340570	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054340571	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC009230	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC073271	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF435957	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC018203	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC040176	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ056975	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471058	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CN359800	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB042901	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB461489	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000280115 ⟹ ENSP00000280115

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	149,204,525 - 149,215,258 (+)	Ensembl

RefSeq Acc Id:

ENST00000409029 ⟹ ENSP00000386650

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	149,077,522 - 149,215,262 (+)	Ensembl

RefSeq Acc Id:

ENST00000409642 ⟹ ENSP00000387077

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	149,038,699 - 149,215,262 (+)	Ensembl

RefSeq Acc Id:

ENST00000409876 ⟹ ENSP00000386479

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	149,038,718 - 149,215,256 (+)	Ensembl

RefSeq Acc Id:

ENST00000437627 ⟹ ENSP00000388361

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	149,118,181 - 149,200,708 (+)	Ensembl

RefSeq Acc Id:

ENST00000442722 ⟹ ENSP00000410840

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	149,119,103 - 149,208,367 (+)	Ensembl

RefSeq Acc Id:

ENST00000450639 ⟹ ENSP00000412070

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	149,118,196 - 149,187,635 (+)	Ensembl

RefSeq Acc Id:

ENST00000473800

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	149,038,107 - 149,101,583 (+)	Ensembl

RefSeq Acc Id:

ENST00000473975

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	149,118,174 - 149,205,322 (+)	Ensembl

RefSeq Acc Id:

ENST00000480545

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	149,118,174 - 149,131,588 (+)	Ensembl

RefSeq Acc Id:

ENST00000498249

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	149,142,036 - 149,215,262 (+)	Ensembl

RefSeq Acc Id:

NM_001317002 ⟹ NP_001303931

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,118,174 - 149,215,262 (+)	NCBI
CHM1_1	2	149,980,523 - 150,077,602 (+)	NCBI
T2T-CHM13v2.0	2	149,568,559 - 149,665,643 (+)	NCBI

Sequence:

show sequence

AGTGTGTGTGCTGGGGCTGGGGCGGCTACATAGCTGTGACTACCAGGGGGTGCAGTCTCTGGGG
ACCACCACTACCGAGGCTGGGTACCATGATTATCGCGGAACACCTGCCCATTAATCTTGACCCT
GTTAAAACAATAACTGCCTATCCAGATATGCCACACTTCTGCCTGCTGTTGGCAACCCTCCTGG
ACTAGGCTGCTCTTGTTAATCACATGGATGTTGCTGATTACTCTGAGTGCAAACCTTTTCACTG
TTCCAGAGAGGAGCCTGACAACCACATTCTCCTTCTCAAGATATAAGAGTTCGGACCGCCCAGC
ACACAAGGTCAGCATGCTGCTCCTCTGTCACGCTCTCGCTATAGCTGTTGTCCAGATCGTTATC
TTCTCAGAAAGCTGGGCATTTGCCAAGAACATCAACTTCTATAATGTGAGGCCTCCTCTCGACC
CTACACCATTTCCAAATAGCTTCAAGTGCTTTACTTGTGAAAACGCAGGGGATAATTATAACTG
CAATCGATGGGCAGAAGACAAATGGTGTCCACAAAATACACAGTACTGTTTGACAGTTCATCAC
TTCACCAGCCACGGAAGAAGCACATCCATCACCAAAAAGTGTGCCTCCAGAAGTGAATGTCATT
TTGTCGGTTGCCACCACAGCCGAGATTCTGAACATACGGAGTGTAGGTCTTGCTGTGAAGGAAT
GATCTGCAATGTAGAATTACCCACCAATCACACTAATGCAGTGTTTGCCGTAATGCACGCTCAG
AGAACATCTGGCAGCAGTGCCCCCACACTCTACCTACCAGTGCTTGCCTGGGTCTTTGTGCTTC
CATTGCTGTGATGCCACCATTCCTAGGAGAGGCAGAGACCAGCCTCTAAAGCACAAGCCAAAAA
CTGTGTGAACGGTGAACTTTGGAGTGAAGATCAATCTTGCACTTGGTGAAGAGTGCACATTGGA
CCTCAAGGCGAAAGCCAGTGGTTTGCTTGGATAAAATGTTCCCGCATGAGGCCACAGGACTGAG
GATGGGAATTTGGCAGGGCCTGAGAAGATGGTCTGACTTCCAGGCTTCCTGGTCAAAGAGAGCT
ACGTTTGGGCAGTTCTGCAGAGAGGATCCTGGCAACTAGTCCCACCTGACTAGGCCTTTAGCTG
AAAGGATTTCTTGACCTCCTTGACTGCCTCAGAGGCTGCCAGGTCAAACCCTCTTGTTTATGTG
ATTAGCTCAGAGCATCTCTATGAAATCTAACCCTTCCCCTCATGAGAAAGCAGTTTTCCCCACC
AACAGCATAGTCAATGAGAAAGGCAACTGTACGAAGAAAACTTCCAGTGGAACTAATATGAAAT
CTATTTGCAAATTATGGGGGGAAATAAAGCTTTTAAATTATACAATGTAAA

hide sequence

RefSeq Acc Id:

NM_001317003 ⟹ NP_001303932

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI
CHM1_1	2	149,900,822 - 150,077,602 (+)	NCBI
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

Sequence:

show sequence

CCCGCGCGGTAGCAGCCAACGCCGGCCCCAGGCGGGTGCGCTGGGAGCCTGGGCCGGGAGCCGG
GTGAGGGCGCCGAGAGGCTCGGTGGGCGCGGGCGGCGAGATATGCCACACTTCTGCCTGCTGTT
GGCAACCCTCCTGGACTAGGCTGCTCTTGTTAATCACATGGATGTTATATAAGAGTTCGGACCG
CCCAGCACACAAGGTCAGCATGCTGCTCCTCTGTCACGCTCTCGCTATAGCTGTTGTCCAGATC
GTTATCTTCTCAGAAAGCTGGGCATTTGCCAAGAACATCAACTTCTATAATGTGAGGCCTCCTC
TCGACCCTACACCATTTCCAAATAGCTTCAAGTGCTTTACTTGTGAAAACGCAGGGGATAATTA
TAACTGCAATCGATGGGCAGAAGACAAATGGTGTCCACAAAATACACAGTACTGTTTGACAGTT
CATCACTTCACCAGCCACGGAAGAAGCACATCCATCACCAAAAAGTGTGCCTCCAGAAGTGAAT
GTCATTTTGTCGGTTGCCACCACAGCCGAGATTCTGAACATACGGAGTGTAGGTCTTGCTGTGA
AGGAATGATCTGCAATGTAGAATTACCCACCAATCACACTAATGCAGTGTTTGCCGTAATGCAC
GCTCAGAGAACATCTGGCAGCAGTGCCCCCACACTCTACCTACCAGTGCTTGCCTGGGTCTTTG
TGCTTCCATTGCTGTGATGCCACCATTCCTAGGAGAGGCAGAGACCAGCCTCTAAAGCACAAGC
CAAAAACTGTGTGAACGGTGAACTTTGGAGTGAAGATCAATCTTGCACTTGGTGAAGAGTGCAC
ATTGGACCTCAAGGCGAAAGCCAGTGGTTTGCTTGGATAAAATGTTCCCGCATGAGGCCACAGG
ACTGAGGATGGGAATTTGGCAGGGCCTGAGAAGATGGTCTGACTTCCAGGCTTCCTGGTCAAAG
AGAGCTACGTTTGGGCAGTTCTGCAGAGAGGATCCTGGCAACTAGTCCCACCTGACTAGGCCTT
TAGCTGAAAGGATTTCTTGACCTCCTTGACTGCCTCAGAGGCTGCCAGGTCAAACCCTCTTGTT
TATGTGATTAGCTCAGAGCATCTCTATGAAATCTAACCCTTCCCCTCATGAGAAAGCAGTTTTC
CCCACCAACAGCATAGTCAATGAGAAAGGCAACTGTACGAAGAAAACTTCCAGTGGAACTAATA
TGAAATCTATTTGCAAATTATGGGGGGAAATAAAGCTTTTAAATTATACAATGTAAA

hide sequence

RefSeq Acc Id:

NM_001317004 ⟹ NP_001303933

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,077,522 - 149,215,258 (+)	NCBI
CHM1_1	2	149,939,867 - 150,077,602 (+)	NCBI
T2T-CHM13v2.0	2	149,527,874 - 149,665,639 (+)	NCBI

Sequence:

show sequence

CTCTGCTGGAGCAGGACTTCAGAGTGTTTGTTTTCAGCCTGCTTTTAAAGTGATTTGAAGAGAG
TGGCTTTGAAGATTATCGCGGAACACCTGCCCATTAATCTTGACCCTGTTAAAACAATAACTGC
CTATCCAGATATGCCACACTTCTGCCTGCTGTTGGCAACCCTCCTGGACTAGGCTGCTCTTGTT
AATCACATGGATGTTATATAAGAGTTCGGACCGCCCAGCACACAAGGTCAGCATGCTGCTCCTC
TGTCACGCTCTCGCTATAGCTGTTGTCCAGATCGTTATCTTCTCAGAAAGCTGGGCATTTGCCA
AGAACATCAACTTCTATAATGTGAGGCCTCCTCTCGACCCTACACCATTTCCAAATAGCTTCAA
GTGCTTTACTTGTGAAAACGCAGGGGATAATTATAACTGCAATCGATGGGCAGAAGACAAATGG
TGTCCACAAAATACACAGTACTGTTTGACAGTTCATCACTTCACCAGCCACGGAAGAAGCACAT
CCATCACCAAAAAGTGTGCCTCCAGAAGTGAATGTCATTTTGTCGGTTGCCACCACAGCCGAGA
TTCTGAACATACGGAGTGTAGGTCTTGCTGTGAAGGAATGATCTGCAATGTAGAATTACCCACC
AATCACACTAATGCAGTGTTTGCCGTAATGCACGCTCAGAGAACATCTGGCAGCAGTGCCCCCA
CACTCTACCTACCAGTGCTTGCCTGGGTCTTTGTGCTTCCATTGCTGTGATGCCACCATTCCTA
GGAGAGGCAGAGACCAGCCTCTAAAGCACAAGCCAAAAACTGTGTGAACGGTGAACTTTGGAGT
GAAGATCAATCTTGCACTTGGTGAAGAGTGCACATTGGACCTCAAGGCGAAAGCCAGTGGTTTG
CTTGGATAAAATGTTCCCGCATGAGGCCACAGGACTGAGGATGGGAATTTGGCAGGGCCTGAGA
AGATGGTCTGACTTCCAGGCTTCCTGGTCAAAGAGAGCTACGTTTGGGCAGTTCTGCAGAGAGG
ATCCTGGCAACTAGTCCCACCTGACTAGGCCTTTAGCTGAAAGGATTTCTTGACCTCCTTGACT
GCCTCAGAGGCTGCCAGGTCAAACCCTCTTGTTTATGTGATTAGCTCAGAGCATCTCTATGAAA
TCTAACCCTTCCCCTCATGAGAAAGCAGTTTTCCCCACCAACAGCATAGTCAATGAGAAAGGCA
ACTGTACGAAGAAAACTTCCAGTGGAACTAATATGAAATCTATTTGCAAATTATGGGGGGAAAT
AAAGCTTTTAAATTATACAATGAAAAAAAAAAAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_001317005 ⟹ NP_001303934

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI
CHM1_1	2	149,900,822 - 150,077,602 (+)	NCBI
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

Sequence:

show sequence

CCCGCGCGGTAGCAGCCAACGCCGGCCCCAGGCGGGTGCGCTGGGAGCCTGGGCCGGGAGCCGG
GTGAGGGCGCCGAGAGGCTCGGTGGGCGCGGGCGGCGAGATTATCGCGGAACACCTGCCCATTA
ATCTTGACCCTGTTAAAACAATAACTGCCTATCCAGATATGCCACACTTCTGCCTGCTGTTGGC
AACCCTCCTGGACTAGGCTGCTCTTGTTAATCACATGGATGTTATATAAGAGTTCGGACCGCCC
AGCACACAAGGTCAGCATGCTGCTCCTCTGTCACGCTCTCGCTATAGCTGTTGTCCAGATCGTT
ATCTTCTCAGAAAGCTGGGCATTTGCCAAGAACATCAACTTCTATAATGTGAGGCCTCCTCTCG
ACCCTACACCATTTCCAAATAGCTTCAAGTGCTTTACTTGTGAAAACGCAGGGGATAATTATAA
CTGCAATCGATGGGCAGAAGACAAATGGTGTCCACAAAATACACAGTACTGTTTGACAGTTCAT
CACTTCACCAGCCACGGAAGAAGCACATCCATCACCAAAAAGTGTGCCTCCAGAAGTGAATGTC
ATTTTGTCGGTTGCCACCACAGCCGAGATTCTGAACATACGGAGTGTAGGTCTTGCTGTGAAGG
AATGATCTGCAATGTAGAATTACCCACCAATCACACTAATGCAGTGTTTGCCGTAATGCACGCT
CAGAGAACATCTGGCAGCAGTGCCCCCACACTCTACCTACCAGTGCTTGCCTGGGTCTTTGTGC
TTCCATTGCTGTGATGCCACCATTCCTAGGAGAGGCAGAGACCAGCCTCTAAAGCACAAGCCAA
AAACTGTGTGAACGGTGAACTTTGGAGTGAAGATCAATCTTGCACTTGGTGAAGAGTGCACATT
GGACCTCAAGGCGAAAGCCAGTGGTTTGCTTGGATAAAATGTTCCCGCATGAGGCCACAGGACT
GAGGATGGGAATTTGGCAGGGCCTGAGAAGATGGTCTGACTTCCAGGCTTCCTGGTCAAAGAGA
GCTACGTTTGGGCAGTTCTGCAGAGAGGATCCTGGCAACTAGTCCCACCTGACTAGGCCTTTAG
CTGAAAGGATTTCTTGACCTCCTTGACTGCCTCAGAGGCTGCCAGGTCAAACCCTCTTGTTTAT
GTGATTAGCTCAGAGCATCTCTATGAAATCTAACCCTTCCCCTCATGAGAAAGCAGTTTTCCCC
ACCAACAGCATAGTCAATGAGAAAGGCAACTGTACGAAGAAAACTTCCAGTGGAACTAATATGA
AATCTATTTGCAAATTATGGGGGGAAATAAAGCTTTTAAATTATACAATGTAAA

hide sequence

RefSeq Acc Id:

NM_001317006 ⟹ NP_001303935

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI
CHM1_1	2	149,900,822 - 150,077,602 (+)	NCBI
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

Sequence:

show sequence

CCCGCGCGGTAGCAGCCAACGCCGGCCCCAGGCGGGTGCGCTGGGAGCCTGGGCCGGGAGCCGG
GTGAGGGCGCCGAGAGGCTCGGTGGGCGCGGGCGGCGAGATATAAGAGTTCGGACCGCCCAGCA
CACAAGGTCAGCATGCTGCTCCTCTGTCACGCTCTCGCTATAGCTGTTGTCCAGATCGTTATCT
TCTCAGAAAGCTGGGCATTTGCCAAGAACATCAACTTCTATAATGTGAGGCCTCCTCTCGACCC
TACACCATTTCCAAATAGCTTCAAGTGCTTTACTTGTGAAAACGCAGGGGATAATTATAACTGC
AATCGATGGGCAGAAGACAAATGGTGTCCACAAAATACACAGTACTGTTTGACAGTTCATCACT
TCACCAGCCACGGAAGAAGCACATCCATCACCAAAAAGTGTGCCTCCAGAAGTGAATGTCATTT
TGTCGGTTGCCACCACAGCCGAGATTCTGAACATACGGAGTGTAGGTCTTGCTGTGAAGGAATG
ATCTGCAATGTAGAATTACCCACCAATCACACTAATGCAGTGTTTGCCGTAATGCACGCTCAGA
GAACATCTGGCAGCAGTGCCCCCACACTCTACCTACCAGTGCTTGCCTGGGTCTTTGTGCTTCC
ATTGCTGTGATGCCACCATTCCTAGGAGAGGCAGAGACCAGCCTCTAAAGCACAAGCCAAAAAC
TGTGTGAACGGTGAACTTTGGAGTGAAGATCAATCTTGCACTTGGTGAAGAGTGCACATTGGAC
CTCAAGGCGAAAGCCAGTGGTTTGCTTGGATAAAATGTTCCCGCATGAGGCCACAGGACTGAGG
ATGGGAATTTGGCAGGGCCTGAGAAGATGGTCTGACTTCCAGGCTTCCTGGTCAAAGAGAGCTA
CGTTTGGGCAGTTCTGCAGAGAGGATCCTGGCAACTAGTCCCACCTGACTAGGCCTTTAGCTGA
AAGGATTTCTTGACCTCCTTGACTGCCTCAGAGGCTGCCAGGTCAAACCCTCTTGTTTATGTGA
TTAGCTCAGAGCATCTCTATGAAATCTAACCCTTCCCCTCATGAGAAAGCAGTTTTCCCCACCA
ACAGCATAGTCAATGAGAAAGGCAACTGTACGAAGAAAACTTCCAGTGGAACTAATATGAAATC
TATTTGCAAATTATGGGGGGAAATAAAGCTTTTAAATTATACAATGTAAA

hide sequence

RefSeq Acc Id:

NM_177964 ⟹ NP_808879

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI
GRCh37	2	149,894,981 - 150,071,776 (+)	NCBI
Build 36	2	149,603,227 - 149,780,018 (+)	NCBI Archive
Celera	2	143,508,885 - 143,685,705 (+)	RGD
HuRef	2	141,793,209 - 141,970,636 (+)	RGD
CHM1_1	2	149,900,822 - 150,077,602 (+)	NCBI
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

Sequence:

show sequence

CCCGCGCGGTAGCAGCCAACGCCGGCCCCAGGCGGGTGCGCTGGGAGCCTGGGCCGGGAGCCGG
GTGAGGGCGCCGAGAGGCTCGGTGGGCGCGGGCGGCGAGATATGCCACACTTCTGCCTGCTGTT
GGCAACCCTCCTGGACTAGGCTGCTCTTGTTAATCACATGGATGTTGCTGATTACTCTGAGTGC
AAACCTTTTCACTGTTCCAGAGAGGAGCCTGACAACCACATTCTCCTTCTCAAGATATAAGAGT
TCGGACCGCCCAGCACACAAGGTCAGCATGCTGCTCCTCTGTCACGCTCTCGCTATAGCTGTTG
TCCAGATCGTTATCTTCTCAGAAAGCTGGGCATTTGCCAAGAACATCAACTTCTATAATGTGAG
GCCTCCTCTCGACCCTACACCATTTCCAAATAGCTTCAAGTGCTTTACTTGTGAAAACGCAGGG
GATAATTATAACTGCAATCGATGGGCAGAAGACAAATGGTGTCCACAAAATACACAGTACTGTT
TGACAGTTCATCACTTCACCAGCCACGGAAGAAGCACATCCATCACCAAAAAGTGTGCCTCCAG
AAGTGAATGTCATTTTGTCGGTTGCCACCACAGCCGAGATTCTGAACATACGGAGTGTAGGTCT
TGCTGTGAAGGAATGATCTGCAATGTAGAATTACCCACCAATCACACTAATGCAGTGTTTGCCG
TAATGCACGCTCAGAGAACATCTGGCAGCAGTGCCCCCACACTCTACCTACCAGTGCTTGCCTG
GGTCTTTGTGCTTCCATTGCTGTGATGCCACCATTCCTAGGAGAGGCAGAGACCAGCCTCTAAA
GCACAAGCCAAAAACTGTGTGAACGGTGAACTTTGGAGTGAAGATCAATCTTGCACTTGGTGAA
GAGTGCACATTGGACCTCAAGGCGAAAGCCAGTGGTTTGCTTGGATAAAATGTTCCCGCATGAG
GCCACAGGACTGAGGATGGGAATTTGGCAGGGCCTGAGAAGATGGTCTGACTTCCAGGCTTCCT
GGTCAAAGAGAGCTACGTTTGGGCAGTTCTGCAGAGAGGATCCTGGCAACTAGTCCCACCTGAC
TAGGCCTTTAGCTGAAAGGATTTCTTGACCTCCTTGACTGCCTCAGAGGCTGCCAGGTCAAACC
CTCTTGTTTATGTGATTAGCTCAGAGCATCTCTATGAAATCTAACCCTTCCCCTCATGAGAAAG
CAGTTTTCCCCACCAACAGCATAGTCAATGAGAAAGGCAACTGTACGAAGAAAACTTCCAGTGG
AACTAATATGAAATCTATTTGCAAATTATGGGGGGAAATAAAGCTTTTAAATTATACAATGTAA
A

hide sequence

RefSeq Acc Id:

XM_005246306 ⟹ XP_005246363

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,118,174 - 149,215,262 (+)	NCBI
GRCh37	2	149,894,981 - 150,071,776 (+)	NCBI

Sequence:

show sequence

TGTGTGCTGGGGCTGGGGCGGCTACATAGCTGTGACTACCAGGGGGTGCAGTCTCTGGGGACCA
CCACTACCGAGGCTGGGTACCATGATTATCGCGGAACACCTGCCCATTAATCTTGACCCTGTTA
AAACAATAACTGCCTATCCAGATATGCCACACTTCTGCCTGCTGTTGGCAACCCTCCTGGACTA
GGCTGCTCTTGTTAATCACATGGATGTTATGTGAAAGGCATTGTACAGAAGAAGATGAGAATCA
CAGTAAACCAAACAAAGGAAATGCAGAAGAGATATTTTCAGCTGAATATTGGAAAGTAAGATTC
CCTGCGAGCAGGATCTCAGGCAACGTCAATGAACAACATGAAGCCTGACACATTCTAATTAGTC
TAAGGAAAATGGTGACAGAGGATATATTCCGTAACGTCTCAGGAGGTCGCCTGGCTCCAGAGAG
ATATAAGAGTTCGGACCGCCCAGCACACAAGGTCAGCATGCTGCTCCTCTGTCACGCTCTCGCT
ATAGCTGTTGTCCAGATCGTTATCTTCTCAGAAAGCTGGGCATTTGCCAAGAACATCAACTTCT
ATAATGTGAGGCCTCCTCTCGACCCTACACCATTTCCAAATAGCTTCAAGTGCTTTACTTGTGA
AAACGCAGGGGATAATTATAACTGCAATCGATGGGCAGAAGACAAATGGTGTCCACAAAATACA
CAGTACTGTTTGACAGTTCATCACTTCACCAGCCACGGAAGAAGCACATCCATCACCAAAAAGT
GTGCCTCCAGAAGTGAATGTCATTTTGTCGGTTGCCACCACAGCCGAGATTCTGAACATACGGA
GTGTAGGTCTTGCTGTGAAGGAATGATCTGCAATGTAGAATTACCCACCAATCACACTAATGCA
GTGTTTGCCGTAATGCACGCTCAGAGAACATCTGGCAGCAGTGCCCCCACACTCTACCTACCAG
TGCTTGCCTGGGTCTTTGTGCTTCCATTGCTGTGATGCCACCATTCCTAGGAGAGGCAGAGACC
AGCCTCTAAAGCACAAGCCAAAAACTGTGTGAACGGTGAACTTTGGAGTGAAGATCAATCTTGC
ACTTGGTGAAGAGTGCACATTGGACCTCAAGGCGAAAGCCAGTGGTTTGCTTGGATAAAATGTT
CCCGCATGAGGCCACAGGACTGAGGATGGGAATTTGGCAGGGCCTGAGAAGATGGTCTGACTTC
CAGGCTTCCTGGTCAAAGAGAGCTACGTTTGGGCAGTTCTGCAGAGAGGATCCTGGCAACTAGT
CCCACCTGACTAGGCCTTTAGCTGAAAGGATTTCTTGACCTCCTTGACTGCCTCAGAGGCTGCC
AGGTCAAACCCTCTTGTTTATGTGATTAGCTCAGAGCATCTCTATGAAATCTAACCCTTCCCCT
CATGAGAAAGCAGTTTTCCCCACCAACAGCATAGTCAATGAGAAAGGCAACTGTACGAAGAAAA
CTTCCAGTGGAACTAATATGAAATCTATTTGCAAATTATGGGGGGAAATAAAGCTTTTAAATTA
TACAATGTAAA

hide sequence

RefSeq Acc Id:

XM_006712281 ⟹ XP_006712344

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,118,174 - 149,215,262 (+)	NCBI

Sequence:

show sequence

GCATAAGAGACTAGCCAGGCTTCAGTGTGTGTGCTGGGGCTGGGGCGGCTACATAGCTGTGACT
ACCAGGGGGTGCAGTCTCTGGGGACCACCACTACCGAGGCTGGGTACCATGATTATCGCGGAAC
ACCTGCCCATTAATCTTGACCCTGTTAAAACAATAACTGCCTATCCAGATATGCCACACTTCTG
CCTGCTGTTGGCAACCCTCCTGGACTAGGCTGCTCTTGTTAATCACATGGATGTTATATAAGAG
TTCGGACCGCCCAGCACACAAGGTCAGCATGCTGCTCCTCTGTCACGCTCTCGCTATAGCTGTT
GTCCAGATCGTTATCTTCTCAGAAAGCTGGGCATTTGCCAAGAACATCAACTTCTATAATGTGA
GGCCTCCTCTCGACCCTACACCATTTCCAAATAGCTTCAAGTGCTTTACTTGTGAAAACGCAGG
GGATAATTATAACTGCAATCGATGGGCAGAAGACAAATGGTGTCCACAAAATACACAGTACTGT
TTGACAGTTCATCACTTCACCAGCCACGGAAGAAGCACATCCATCACCAAAAAGTGTGCCTCCA
GAAGTGAATGTCATTTTGTCGGTTGCCACCACAGCCGAGATTCTGAACATACGGAGTGTAGGTC
TTGCTGTGAAGGAATGATCTGCAATGTAGAATTACCCACCAATCACACTAATGCAGTGTTTGCC
GTAATGCACGCTCAGAGAACATCTGGCAGCAGTGCCCCCACACTCTACCTACCAGTGCTTGCCT
GGGTCTTTGTGCTTCCATTGCTGTGATGCCACCATTCCTAGGAGAGGCAGAGACCAGCCTCTAA
AGCACAAGCCAAAAACTGTGTGAACGGTGAACTTTGGAGTGAAGATCAATCTTGCACTTGGTGA
AGAGTGCACATTGGACCTCAAGGCGAAAGCCAGTGGTTTGCTTGGATAAAATGTTCCCGCATGA
GGCCACAGGACTGAGGATGGGAATTTGGCAGGGCCTGAGAAGATGGTCTGACTTCCAGGCTTCC
TGGTCAAAGAGAGCTACGTTTGGGCAGTTCTGCAGAGAGGATCCTGGCAACTAGTCCCACCTGA
CTAGGCCTTTAGCTGAAAGGATTTCTTGACCTCCTTGACTGCCTCAGAGGCTGCCAGGTCAAAC
CCTCTTGTTTATGTGATTAGCTCAGAGCATCTCTATGAAATCTAACCCTTCCCCTCATGAGAAA
GCAGTTTTCCCCACCAACAGCATAGTCAATGAGAAAGGCAACTGTACGAAGAAAACTTCCAGTG
GAACTAATATGAAATCTATTTGCAAATTATGGGGGGAAATAAAGCTTTTAAATTATACAATGTA
AA

hide sequence

RefSeq Acc Id:

XM_011510620 ⟹ XP_011508922

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,118,174 - 149,215,262 (+)	NCBI

Sequence:

show sequence

TGTGTGCTGGGGCTGGGGCGGCTACATAGCTGTGACTACCAGGGGGTGCAGTCTCTGGGGACCA
CCACTACCGAGGCTGGGTACCATGATTATCGCGGAACACCTGCCCATTAATCTTGACCCTGTTA
AAACAATAACTGCCTATCCAGATATGCCACACTTCTGCCTGCTGTTGGCAACCCTCCTGGACTA
GGCTGCTCTTGTTAATCACATGGATGTTGCTGATTACTCTGAGTGCAAACCTTTTCACTGTTCC
AGAGAGGAGCCTGACAACCACATTCTCCTTCTCAAGGTGTGGTGCTTACTGCGCAGGCTGACCA
GATATAAGAGTTCGGACCGCCCAGCACACAAGGTCAGCATGCTGCTCCTCTGTCACGCTCTCGC
TATAGCTGTTGTCCAGATCGTTATCTTCTCAGAAAGCTGGGCATTTGCCAAGAACATCAACTTC
TATAATGTGAGGCCTCCTCTCGACCCTACACCATTTCCAAATAGCTTCAAGTGCTTTACTTGTG
AAAACGCAGGGGATAATTATAACTGCAATCGATGGGCAGAAGACAAATGGTGTCCACAAAATAC
ACAGTACTGTTTGACAGTTCATCACTTCACCAGCCACGGAAGAAGCACATCCATCACCAAAAAG
TGTGCCTCCAGAAGTGAATGTCATTTTGTCGGTTGCCACCACAGCCGAGATTCTGAACATACGG
AGTGTAGGTCTTGCTGTGAAGGAATGATCTGCAATGTAGAATTACCCACCAATCACACTAATGC
AGTGTTTGCCGTAATGCACGCTCAGAGAACATCTGGCAGCAGTGCCCCCACACTCTACCTACCA
GTGCTTGCCTGGGTCTTTGTGCTTCCATTGCTGTGATGCCACCATTCCTAGGAGAGGCAGAGAC
CAGCCTCTAAAGCACAAGCCAAAAACTGTGTGAACGGTGAACTTTGGAGTGAAGATCAATCTTG
CACTTGGTGAAGAGTGCACATTGGACCTCAAGGCGAAAGCCAGTGGTTTGCTTGGATAAAATGT
TCCCGCATGAGGCCACAGGACTGAGGATGGGAATTTGGCAGGGCCTGAGAAGATGGTCTGACTT
CCAGGCTTCCTGGTCAAAGAGAGCTACGTTTGGGCAGTTCTGCAGAGAGGATCCTGGCAACTAG
TCCCACCTGACTAGGCCTTTAGCTGAAAGGATTTCTTGACCTCCTTGACTGCCTCAGAGGCTGC
CAGGTCAAACCCTCTTGTTTATGTGATTAGCTCAGAGCATCTCTATGAAATCTAACCCTTCCCC
TCATGAGAAAGCAGTTTTCCCCACCAACAGCATAGTCAATGAGAAAGGCAACTGTACGAAGAAA
ACTTCCAGTGGAACTAATATGAAATCTATTTGCAAATTATGGGGGGAAATAAAGCTTTTAAATT
ATACAATGTAAA

hide sequence

RefSeq Acc Id:

XM_011510623 ⟹ XP_011508925

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

Sequence:

show sequence

ACGCCGGCCCCAGGCGGGTGCGCTGGGAGCCTGGGCCGGGAGCCGGGTGAGGGCGCCGAGAGGC
TCGGTGGGCGCGGGCGGCGAGGACTCTGCTGGAGCAGGACTTCAGAGTGTTTGTTTTCAGCCTG
CTTTTAAAGTGATTTGAAGAGAGTGGCTTTGAAGATTATCGCGGAACACCTGCCCATTAATCTT
GACCCTGTTAAAACAATAACTGCCTATCCAGATATGCCACACTTCTGCCTGCTGTTGGCAACCC
TCCTGGACTAGGCTGCTCTTGTTAATCACATGGATGTTATATAAGAGTTCGGACCGCCCAGCAC
ACAAGGTCAGCATGCTGCTCCTCTGTCACGCTCTCGCTATAGCTGTTGTCCAGATCGTTATCTT
CTCAGAAAGCTGGGCATTTGCCAAGAACATCAACTTCTATAATGTGAGGCCTCCTCTCGACCCT
ACACCATTTCCAAATAGCTTCAAGTGCTTTACTTGTGAAAACGCAGGGGATAATTATAACTGCA
ATCGATGGGCAGAAGACAAATGGTGTCCACAAAATACACAGTACTGTTTGACAGTTCATCACTT
CACCAGCCACGGAAGAAGCACATCCATCACCAAAAAGTGTGCCTCCAGAAGTGAATGTCATTTT
GTCGGTTGCCACCACAGCCGAGATTCTGAACATACGGAGTGTAGGTCTTGCTGTGAAGGAATGA
TCTGCAATGTAGAATTACCCACCAATCACACTAATGCAGTGTTTGCCGTAATGCACGCTCAGAG
AACATCTGGCAGCAGTGCCCCCACACTCTACCTACCAGTGCTTGCCTGGGTCTTTGTGCTTCCA
TTGCTGTGATGCCACCATTCCTAGGAGAGGCAGAGACCAGCCTCTAAAGCACAAGCCAAAAACT
GTGTGAACGGTGAACTTTGGAGTGAAGATCAATCTTGCACTTGGTGAAGAGTGCACATTGGACC
TCAAGGCGAAAGCCAGTGGTTTGCTTGGATAAAATGTTCCCGCATGAGGCCACAGGACTGAGGA
TGGGAATTTGGCAGGGCCTGAGAAGATGGTCTGACTTCCAGGCTTCCTGGTCAAAGAGAGCTAC
GTTTGGGCAGTTCTGCAGAGAGGATCCTGGCAACTAGTCCCACCTGACTAGGCCTTTAGCTGAA
AGGATTTCTTGACCTCCTTGACTGCCTCAGAGGCTGCCAGGTCAAACCCTCTTGTTTATGTGAT
TAGCTCAGAGCATCTCTATGAAATCTAACCCTTCCCCTCATGAGAAAGCAGTTTTCCCCACCAA
CAGCATAGTCAATGAGAAAGGCAACTGTACGAAGAAAACTTCCAGTGGAACTAATATGAAATCT
ATTTGCAAATTATGGGGGGAAATAAAGCTTTTAAATTATACAATGTAAA

hide sequence

RefSeq Acc Id:

XM_017003364 ⟹ XP_016858853

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

Sequence:

show sequence

AACGCCGGCCCCAGGCGGGTGCGCTGGGAGCCTGGGCCGGGAGCCGGGTGAGGGCGCCGAGAGG
CTCGGTGGGCGCGGGCGGCGAGGACTCTGCTGGAGCAGGACTTCAGAGTGTTTGTTTTCAGCCT
GCTTTTAAAGTGATTTGAAGAGAGTGGCTTTGAAGATATGCCACACTTCTGCCTGCTGTTGGCA
ACCCTCCTGGACTAGGCTGCTCTTGTTAATCACATGGATGTTGCTGATTACTCTGAGTGCAAAC
CTTTTCACTGTTCCAGAGAGGAGCCTGACAACCACATTCTCCTTCTCAAGATATAAGAGTTCGG
ACCGCCCAGCACACAAGGTCAGCATGCTGCTCCTCTGTCACGCTCTCGCTATAGCTGTTGTCCA
GATCGTTATCTTCTCAGAAAGCTGGGCATTTGCCAAGAACATCAACTTCTATAATGTGAGGCCT
CCTCTCGACCCTACACCATTTCCAAATAGCTTCAAGTGCTTTACTTGTGAAAACGCAGGGGATA
ATTATAACTGCAATCGATGGGCAGAAGACAAATGGTGTCCACAAAATACACAGTACTGTTTGAC
AGTTCATCACTTCACCAGCCACGGAAGAAGCACATCCATCACCAAAAAGTGTGCCTCCAGAAGT
GAATGTCATTTTGTCGGTTGCCACCACAGCCGAGATTCTGAACATACGGAGTGTAGGTCTTGCT
GTGAAGGAATGATCTGCAATGTAGAATTACCCACCAATCACACTAATGCAGTGTTTGCCGTAAT
GCACGCTCAGAGAACATCTGGCAGCAGTGCCCCCACACTCTACCTACCAGTGCTTGCCTGGGTC
TTTGTGCTTCCATTGCTGTGATGCCACCATTCCTAGGAGAGGCAGAGACCAGCCTCTAAAGCAC
AAGCCAAAAACTGTGTGAACGGTGAACTTTGGAGTGAAGATCAATCTTGCACTTGGTGAAGAGT
GCACATTGGACCTCAAGGCGAAAGCCAGTGGTTTGCTTGGATAAAATGTTCCCGCATGAGGCCA
CAGGACTGAGGATGGGAATTTGGCAGGGCCTGAGAAGATGGTCTGACTTCCAGGCTTCCTGGTC
AAAGAGAGCTACGTTTGGGCAGTTCTGCAGAGAGGATCCTGGCAACTAGTCCCACCTGACTAGG
CCTTTAGCTGAAAGGATTTCTTGACCTCCTTGACTGCCTCAGAGGCTGCCAGGTCAAACCCTCT
TGTTTATGTGATTAGCTCAGAGCATCTCTATGAAATCTAACCCTTCCCCTCATGAGAAAGCAGT
TTTCCCCACCAACAGCATAGTCAATGAGAAAGGCAACTGTACGAAGAAAACTTCCAGTGGAACT
AATATGAAATCTATTTGCAAATTATGGGGGGAAATAAAGCTTTTAAATTATACAATGTAAA

hide sequence

RefSeq Acc Id:

XM_017003365 ⟹ XP_016858854

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

Sequence:

show sequence

ACGCCGGCCCCAGGCGGGTGCGCTGGGAGCCTGGGCCGGGAGCCGGGTGAGGGCGCCGAGAGGC
TCGGTGGGCGCGGGCGGCGAGGACTCTGCTGGAGCAGGACTTCAGAGTGTTTGTTTTCAGCCTG
CTTTTAAAGTGATTTGAAGAGAGTGGCTTTGAAGATATGCCACACTTCTGCCTGCTGTTGGCAA
CCCTCCTGGACTAGGCTGCTCTTGTTAATCACATGGATGTTATATAAGAGTTCGGACCGCCCAG
CACACAAGGTCAGCATGCTGCTCCTCTGTCACGCTCTCGCTATAGCTGTTGTCCAGATCGTTAT
CTTCTCAGAAAGCTGGGCATTTGCCAAGAACATCAACTTCTATAATGTGAGGCCTCCTCTCGAC
CCTACACCATTTCCAAATAGCTTCAAGTGCTTTACTTGTGAAAACGCAGGGGATAATTATAACT
GCAATCGATGGGCAGAAGACAAATGGTGTCCACAAAATACACAGTACTGTTTGACAGTTCATCA
CTTCACCAGCCACGGAAGAAGCACATCCATCACCAAAAAGTGTGCCTCCAGAAGTGAATGTCAT
TTTGTCGGTTGCCACCACAGCCGAGATTCTGAACATACGGAGTGTAGGTCTTGCTGTGAAGGAA
TGATCTGCAATGTAGAATTACCCACCAATCACACTAATGCAGTGTTTGCCGTAATGCACGCTCA
GAGAACATCTGGCAGCAGTGCCCCCACACTCTACCTACCAGTGCTTGCCTGGGTCTTTGTGCTT
CCATTGCTGTGATGCCACCATTCCTAGGAGAGGCAGAGACCAGCCTCTAAAGCACAAGCCAAAA
ACTGTGTGAACGGTGAACTTTGGAGTGAAGATCAATCTTGCACTTGGTGAAGAGTGCACATTGG
ACCTCAAGGCGAAAGCCAGTGGTTTGCTTGGATAAAATGTTCCCGCATGAGGCCACAGGACTGA
GGATGGGAATTTGGCAGGGCCTGAGAAGATGGTCTGACTTCCAGGCTTCCTGGTCAAAGAGAGC
TACGTTTGGGCAGTTCTGCAGAGAGGATCCTGGCAACTAGTCCCACCTGACTAGGCCTTTAGCT
GAAAGGATTTCTTGACCTCCTTGACTGCCTCAGAGGCTGCCAGGTCAAACCCTCTTGTTTATGT
GATTAGCTCAGAGCATCTCTATGAAATCTAACCCTTCCCCTCATGAGAAAGCAGTTTTCCCCAC
CAACAGCATAGTCAATGAGAAAGGCAACTGTACGAAGAAAACTTCCAGTGGAACTAATATGAAA
TCTATTTGCAAATTATGGGGGGAAATAAAGCTTTTAAATTATACAATGTAAA

hide sequence

RefSeq Acc Id:

XM_017003366 ⟹ XP_016858855

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

Sequence:

show sequence

CCGCCCCGCGCGGTAGCAGCCAACGCCGGCCCCAGGCGGGTGCGCTGGGAGCCTGGGCCGGGAG
CCGGGTGAGGGCGCCGAGAGGCTCGGTGGGCGCGGGCGGCGAGGACTCTGCTGGAGCAGGACTT
CAGAGTGTTTGTTTTCAGCCTGCTTTTAAAGTGATTTGAAGAGAGTGGCTTTGAAGGTTTCCAT
CCTTACTTTTTCATATATGCCACACTTCTGCCTGCTGTTGGCAACCCTCCTGGACTAGGCTGCT
CTTGTTAATCACATGGATGTTATATAAGAGTTCGGACCGCCCAGCACACAAGGTCAGCATGCTG
CTCCTCTGTCACGCTCTCGCTATAGCTGTTGTCCAGATCGTTATCTTCTCAGAAAGCTGGGCAT
TTGCCAAGAACATCAACTTCTATAATGTGAGGCCTCCTCTCGACCCTACACCATTTCCAAATAG
CTTCAAGTGCTTTACTTGTGAAAACGCAGGGGATAATTATAACTGCAATCGATGGGCAGAAGAC
AAATGGTGTCCACAAAATACACAGTACTGTTTGACAGTTCATCACTTCACCAGCCACGGAAGAA
GCACATCCATCACCAAAAAGTGTGCCTCCAGAAGTGAATGTCATTTTGTCGGTTGCCACCACAG
CCGAGATTCTGAACATACGGAGTGTAGGTCTTGCTGTGAAGGAATGATCTGCAATGTAGAATTA
CCCACCAATCACACTAATGCAGTGTTTGCCGTAATGCACGCTCAGAGAACATCTGGCAGCAGTG
CCCCCACACTCTACCTACCAGTGCTTGCCTGGGTCTTTGTGCTTCCATTGCTGTGATGCCACCA
TTCCTAGGAGAGGCAGAGACCAGCCTCTAAAGCACAAGCCAAAAACTGTGTGAACGGTGAACTT
TGGAGTGAAGATCAATCTTGCACTTGGTGAAGAGTGCACATTGGACCTCAAGGCGAAAGCCAGT
GGTTTGCTTGGATAAAATGTTCCCGCATGAGGCCACAGGACTGAGGATGGGAATTTGGCAGGGC
CTGAGAAGATGGTCTGACTTCCAGGCTTCCTGGTCAAAGAGAGCTACGTTTGGGCAGTTCTGCA
GAGAGGATCCTGGCAACTAGTCCCACCTGACTAGGCCTTTAGCTGAAAGGATTTCTTGACCTCC
TTGACTGCCTCAGAGGCTGCCAGGTCAAACCCTCTTGTTTATGTGATTAGCTCAGAGCATCTCT
ATGAAATCTAACCCTTCCCCTCATGAGAAAGCAGTTTTCCCCACCAACAGCATAGTCAATGAGA
AAGGCAACTGTACGAAGAAAACTTCCAGTGGAACTAATATGAAATCTATTTGCAAATTATGGGG
GGAAATAAAGCTTTTAAATTATACAATGTAAA

hide sequence

RefSeq Acc Id:

XM_047443401 ⟹ XP_047299357

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,118,174 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443402 ⟹ XP_047299358

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443403 ⟹ XP_047299359

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443404 ⟹ XP_047299360

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443405 ⟹ XP_047299361

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443406 ⟹ XP_047299362

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,118,174 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443407 ⟹ XP_047299363

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443408 ⟹ XP_047299364

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,118,174 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443409 ⟹ XP_047299365

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,118,174 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443410 ⟹ XP_047299366

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443411 ⟹ XP_047299367

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443412 ⟹ XP_047299368

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,699 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443413 ⟹ XP_047299369

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,129,698 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443414 ⟹ XP_047299370

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,118,174 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443416 ⟹ XP_047299372

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,118,174 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443417 ⟹ XP_047299373

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,118,174 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_047443418 ⟹ XP_047299374

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,198,326 - 149,215,262 (+)	NCBI

RefSeq Acc Id:

XM_054340550 ⟹ XP_054196525

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,568,559 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340551 ⟹ XP_054196526

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340552 ⟹ XP_054196527

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340553 ⟹ XP_054196528

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340554 ⟹ XP_054196529

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340555 ⟹ XP_054196530

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340556 ⟹ XP_054196531

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,568,559 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340557 ⟹ XP_054196532

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,568,559 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340558 ⟹ XP_054196533

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340559 ⟹ XP_054196534

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340560 ⟹ XP_054196535

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340561 ⟹ XP_054196536

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340562 ⟹ XP_054196537

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,580,086 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340563 ⟹ XP_054196538

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,568,559 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340564 ⟹ XP_054196539

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,568,559 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340565 ⟹ XP_054196540

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,568,559 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340566 ⟹ XP_054196541

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,568,559 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340567 ⟹ XP_054196542

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,568,559 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340568 ⟹ XP_054196543

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340569 ⟹ XP_054196544

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340570 ⟹ XP_054196545

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,489,053 - 149,665,643 (+)	NCBI

RefSeq Acc Id:

XM_054340571 ⟹ XP_054196546

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	149,648,704 - 149,665,643 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001303931	(Get FASTA)	NCBI Sequence Viewer
	NP_001303932	(Get FASTA)	NCBI Sequence Viewer
	NP_001303933	(Get FASTA)	NCBI Sequence Viewer
	NP_001303934	(Get FASTA)	NCBI Sequence Viewer
	NP_001303935	(Get FASTA)	NCBI Sequence Viewer
	NP_808879	(Get FASTA)	NCBI Sequence Viewer
	XP_005246363	(Get FASTA)	NCBI Sequence Viewer
	XP_006712344	(Get FASTA)	NCBI Sequence Viewer
	XP_011508922	(Get FASTA)	NCBI Sequence Viewer
	XP_011508925	(Get FASTA)	NCBI Sequence Viewer
	XP_016858853	(Get FASTA)	NCBI Sequence Viewer
	XP_016858854	(Get FASTA)	NCBI Sequence Viewer
	XP_016858855	(Get FASTA)	NCBI Sequence Viewer
	XP_047299357	(Get FASTA)	NCBI Sequence Viewer
	XP_047299358	(Get FASTA)	NCBI Sequence Viewer
	XP_047299359	(Get FASTA)	NCBI Sequence Viewer
	XP_047299360	(Get FASTA)	NCBI Sequence Viewer
	XP_047299361	(Get FASTA)	NCBI Sequence Viewer
	XP_047299362	(Get FASTA)	NCBI Sequence Viewer
	XP_047299363	(Get FASTA)	NCBI Sequence Viewer
	XP_047299364	(Get FASTA)	NCBI Sequence Viewer
	XP_047299365	(Get FASTA)	NCBI Sequence Viewer
	XP_047299366	(Get FASTA)	NCBI Sequence Viewer
	XP_047299367	(Get FASTA)	NCBI Sequence Viewer
	XP_047299368	(Get FASTA)	NCBI Sequence Viewer
	XP_047299369	(Get FASTA)	NCBI Sequence Viewer
	XP_047299370	(Get FASTA)	NCBI Sequence Viewer
	XP_047299372	(Get FASTA)	NCBI Sequence Viewer
	XP_047299373	(Get FASTA)	NCBI Sequence Viewer
	XP_047299374	(Get FASTA)	NCBI Sequence Viewer
	XP_054196525	(Get FASTA)	NCBI Sequence Viewer
	XP_054196526	(Get FASTA)	NCBI Sequence Viewer
	XP_054196527	(Get FASTA)	NCBI Sequence Viewer
	XP_054196528	(Get FASTA)	NCBI Sequence Viewer
	XP_054196529	(Get FASTA)	NCBI Sequence Viewer
	XP_054196530	(Get FASTA)	NCBI Sequence Viewer
	XP_054196531	(Get FASTA)	NCBI Sequence Viewer
	XP_054196532	(Get FASTA)	NCBI Sequence Viewer
	XP_054196533	(Get FASTA)	NCBI Sequence Viewer
	XP_054196534	(Get FASTA)	NCBI Sequence Viewer
	XP_054196535	(Get FASTA)	NCBI Sequence Viewer
	XP_054196536	(Get FASTA)	NCBI Sequence Viewer
	XP_054196537	(Get FASTA)	NCBI Sequence Viewer
	XP_054196538	(Get FASTA)	NCBI Sequence Viewer
	XP_054196539	(Get FASTA)	NCBI Sequence Viewer
	XP_054196540	(Get FASTA)	NCBI Sequence Viewer
	XP_054196541	(Get FASTA)	NCBI Sequence Viewer
	XP_054196542	(Get FASTA)	NCBI Sequence Viewer
	XP_054196543	(Get FASTA)	NCBI Sequence Viewer
	XP_054196544	(Get FASTA)	NCBI Sequence Viewer
	XP_054196545	(Get FASTA)	NCBI Sequence Viewer
	XP_054196546	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH18203	(Get FASTA)	NCBI Sequence Viewer
	AAH40176	(Get FASTA)	NCBI Sequence Viewer
	AAM20908	(Get FASTA)	NCBI Sequence Viewer
	AAY14974	(Get FASTA)	NCBI Sequence Viewer
	AAY24304	(Get FASTA)	NCBI Sequence Viewer
	EAX11541	(Get FASTA)	NCBI Sequence Viewer
	EAX11542	(Get FASTA)	NCBI Sequence Viewer
	EAX11543	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000280115
	ENSP00000280115.8
	ENSP00000386479
	ENSP00000386479.1
	ENSP00000386650
	ENSP00000386650.1
	ENSP00000387077
	ENSP00000387077.3
	ENSP00000388361.1
	ENSP00000410840.1
	ENSP00000412070.1
GenBank Protein	Q8NI32	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_808879 ⟸ NM_177964
- Peptide Label:	isoform a
- UniProtKB:	H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLLITLSANLFTVPERSLTTTFSFSRYKSSDRPAHKVSMLLLCHALAIAVVQIVIFSESWAFAK NINFYNVRPPLDPTPFPNSFKCFTCENAGDNYNCNRWAEDKWCPQNTQYCLTVHHFTSHGRSTS ITKKCASRSECHFVGCHHSRDSEHTECRSCCEGMICNVELPTNHTNAVFAVMHAQRTSGSSAPT LYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:	XP_005246363 ⟸ XM_005246306
- Peptide Label:	isoform X7
- UniProtKB:	H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MVTEDIFRNVSGGRLAPERYKSSDRPAHKVSMLLLCHALAIAVVQIVIFSESWAFAKNINFYNV RPPLDPTPFPNSFKCFTCENAGDNYNCNRWAEDKWCPQNTQYCLTVHHFTSHGRSTSITKKCAS RSECHFVGCHHSRDSEHTECRSCCEGMICNVELPTNHTNAVFAVMHAQRTSGSSAPTLYLPVLA WVFVLPLL hide sequence

RefSeq Acc Id:	XP_006712344 ⟸ XM_006712281
- Peptide Label:	isoform X9
- UniProtKB:	Q7Z747 (UniProtKB/Swiss-Prot), Q53TK0 (UniProtKB/Swiss-Prot), D3DP90 (UniProtKB/Swiss-Prot), Q8IXK7 (UniProtKB/Swiss-Prot), Q8NI32 (UniProtKB/Swiss-Prot), H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLYKSSDRPAHKVSMLLLCHALAIAVVQIVIFSESWAFAKNINFYNVRPPLDPTPFPNSFKCFT CENAGDNYNCNRWAEDKWCPQNTQYCLTVHHFTSHGRSTSITKKCASRSECHFVGCHHSRDSEH TECRSCCEGMICNVELPTNHTNAVFAVMHAQRTSGSSAPTLYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:	XP_011508925 ⟸ XM_011510623
- Peptide Label:	isoform X9
- UniProtKB:	Q7Z747 (UniProtKB/Swiss-Prot), Q53TK0 (UniProtKB/Swiss-Prot), D3DP90 (UniProtKB/Swiss-Prot), Q8IXK7 (UniProtKB/Swiss-Prot), Q8NI32 (UniProtKB/Swiss-Prot), H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLYKSSDRPAHKVSMLLLCHALAIAVVQIVIFSESWAFAKNINFYNVRPPLDPTPFPNSFKCFT CENAGDNYNCNRWAEDKWCPQNTQYCLTVHHFTSHGRSTSITKKCASRSECHFVGCHHSRDSEH TECRSCCEGMICNVELPTNHTNAVFAVMHAQRTSGSSAPTLYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:	XP_011508922 ⟸ XM_011510620
- Peptide Label:	isoform X3
- UniProtKB:	H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MDVADYSECKPFHCSREEPDNHILLLKVWCLLRRLTRYKSSDRPAHKVSMLLLCHALAIAVVQI VIFSESWAFAKNINFYNVRPPLDPTPFPNSFKCFTCENAGDNYNCNRWAEDKWCPQNTQYCLTV HHFTSHGRSTSITKKCASRSECHFVGCHHSRDSEHTECRSCCEGMICNVELPTNHTNAVFAVMH AQRTSGSSAPTLYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:	NP_001303934 ⟸ NM_001317005
- Peptide Label:	isoform b precursor
- UniProtKB:	Q7Z747 (UniProtKB/Swiss-Prot), Q53TK0 (UniProtKB/Swiss-Prot), D3DP90 (UniProtKB/Swiss-Prot), Q8IXK7 (UniProtKB/Swiss-Prot), Q8NI32 (UniProtKB/Swiss-Prot), H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLYKSSDRPAHKVSMLLLCHALAIAVVQIVIFSESWAFAKNINFYNVRPPLDPTPFPNSFKCFT CENAGDNYNCNRWAEDKWCPQNTQYCLTVHHFTSHGRSTSITKKCASRSECHFVGCHHSRDSEH TECRSCCEGMICNVELPTNHTNAVFAVMHAQRTSGSSAPTLYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:	NP_001303932 ⟸ NM_001317003
- Peptide Label:	isoform b precursor
- UniProtKB:	Q7Z747 (UniProtKB/Swiss-Prot), Q53TK0 (UniProtKB/Swiss-Prot), D3DP90 (UniProtKB/Swiss-Prot), Q8IXK7 (UniProtKB/Swiss-Prot), Q8NI32 (UniProtKB/Swiss-Prot), H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLYKSSDRPAHKVSMLLLCHALAIAVVQIVIFSESWAFAKNINFYNVRPPLDPTPFPNSFKCFT CENAGDNYNCNRWAEDKWCPQNTQYCLTVHHFTSHGRSTSITKKCASRSECHFVGCHHSRDSEH TECRSCCEGMICNVELPTNHTNAVFAVMHAQRTSGSSAPTLYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:	NP_001303935 ⟸ NM_001317006
- Peptide Label:	isoform c precursor
- UniProtKB:	H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLLLCHALAIAVVQIVIFSESWAFAKNINFYNVRPPLDPTPFPNSFKCFTCENAGDNYNCNRWA EDKWCPQNTQYCLTVHHFTSHGRSTSITKKCASRSECHFVGCHHSRDSEHTECRSCCEGMICNV ELPTNHTNAVFAVMHAQRTSGSSAPTLYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:	NP_001303933 ⟸ NM_001317004
- Peptide Label:	isoform b precursor
- UniProtKB:	Q7Z747 (UniProtKB/Swiss-Prot), Q53TK0 (UniProtKB/Swiss-Prot), D3DP90 (UniProtKB/Swiss-Prot), Q8IXK7 (UniProtKB/Swiss-Prot), Q8NI32 (UniProtKB/Swiss-Prot), H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLYKSSDRPAHKVSMLLLCHALAIAVVQIVIFSESWAFAKNINFYNVRPPLDPTPFPNSFKCFT CENAGDNYNCNRWAEDKWCPQNTQYCLTVHHFTSHGRSTSITKKCASRSECHFVGCHHSRDSEH TECRSCCEGMICNVELPTNHTNAVFAVMHAQRTSGSSAPTLYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:	NP_001303931 ⟸ NM_001317002
- Peptide Label:	isoform a
- UniProtKB:	H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLLITLSANLFTVPERSLTTTFSFSRYKSSDRPAHKVSMLLLCHALAIAVVQIVIFSESWAFAK NINFYNVRPPLDPTPFPNSFKCFTCENAGDNYNCNRWAEDKWCPQNTQYCLTVHHFTSHGRSTS ITKKCASRSECHFVGCHHSRDSEHTECRSCCEGMICNVELPTNHTNAVFAVMHAQRTSGSSAPT LYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:	XP_016858855 ⟸ XM_017003366
- Peptide Label:	isoform X9
- UniProtKB:	Q7Z747 (UniProtKB/Swiss-Prot), Q53TK0 (UniProtKB/Swiss-Prot), D3DP90 (UniProtKB/Swiss-Prot), Q8IXK7 (UniProtKB/Swiss-Prot), Q8NI32 (UniProtKB/Swiss-Prot), H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLYKSSDRPAHKVSMLLLCHALAIAVVQIVIFSESWAFAKNINFYNVRPPLDPTPFPNSFKCFT CENAGDNYNCNRWAEDKWCPQNTQYCLTVHHFTSHGRSTSITKKCASRSECHFVGCHHSRDSEH TECRSCCEGMICNVELPTNHTNAVFAVMHAQRTSGSSAPTLYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:	XP_016858853 ⟸ XM_017003364
- Peptide Label:	isoform X6
- UniProtKB:	H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLLITLSANLFTVPERSLTTTFSFSRYKSSDRPAHKVSMLLLCHALAIAVVQIVIFSESWAFAK NINFYNVRPPLDPTPFPNSFKCFTCENAGDNYNCNRWAEDKWCPQNTQYCLTVHHFTSHGRSTS ITKKCASRSECHFVGCHHSRDSEHTECRSCCEGMICNVELPTNHTNAVFAVMHAQRTSGSSAPT LYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:	XP_016858854 ⟸ XM_017003365
- Peptide Label:	isoform X9
- UniProtKB:	Q7Z747 (UniProtKB/Swiss-Prot), Q53TK0 (UniProtKB/Swiss-Prot), D3DP90 (UniProtKB/Swiss-Prot), Q8IXK7 (UniProtKB/Swiss-Prot), Q8NI32 (UniProtKB/Swiss-Prot), H7BXI7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLYKSSDRPAHKVSMLLLCHALAIAVVQIVIFSESWAFAKNINFYNVRPPLDPTPFPNSFKCFT CENAGDNYNCNRWAEDKWCPQNTQYCLTVHHFTSHGRSTSITKKCASRSECHFVGCHHSRDSEH TECRSCCEGMICNVELPTNHTNAVFAVMHAQRTSGSSAPTLYLPVLAWVFVLPLL hide sequence

RefSeq Acc Id:

ENSP00000388361 ⟸ ENST00000437627

RefSeq Acc Id:

ENSP00000412070 ⟸ ENST00000450639

RefSeq Acc Id:

ENSP00000280115 ⟸ ENST00000280115

RefSeq Acc Id:

ENSP00000410840 ⟸ ENST00000442722

RefSeq Acc Id:

ENSP00000386479 ⟸ ENST00000409876

RefSeq Acc Id:

ENSP00000387077 ⟸ ENST00000409642

RefSeq Acc Id:

ENSP00000386650 ⟸ ENST00000409029

RefSeq Acc Id:	XP_047299368 ⟸ XM_047443412
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047299360 ⟸ XM_047443404
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047299367 ⟸ XM_047443411
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047299361 ⟸ XM_047443405
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047299363 ⟸ XM_047443407
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047299358 ⟸ XM_047443402
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047299366 ⟸ XM_047443410
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047299359 ⟸ XM_047443403
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047299357 ⟸ XM_047443401
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047299364 ⟸ XM_047443408
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047299362 ⟸ XM_047443406
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047299372 ⟸ XM_047443416
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_047299370 ⟸ XM_047443414
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_047299365 ⟸ XM_047443409
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047299373 ⟸ XM_047443417
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_047299369 ⟸ XM_047443413
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047299374 ⟸ XM_047443418
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_054196529 ⟸ XM_054340554
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054196536 ⟸ XM_054340561
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054196545 ⟸ XM_054340570
- Peptide Label:	isoform X9
- UniProtKB:	Q8NI32 (UniProtKB/Swiss-Prot), Q7Z747 (UniProtKB/Swiss-Prot), Q53TK0 (UniProtKB/Swiss-Prot), D3DP90 (UniProtKB/Swiss-Prot), Q8IXK7 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054196528 ⟸ XM_054340553
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054196534 ⟸ XM_054340559
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054196543 ⟸ XM_054340568
- Peptide Label:	isoform X9
- UniProtKB:	Q8NI32 (UniProtKB/Swiss-Prot), Q7Z747 (UniProtKB/Swiss-Prot), Q53TK0 (UniProtKB/Swiss-Prot), D3DP90 (UniProtKB/Swiss-Prot), Q8IXK7 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054196530 ⟸ XM_054340555
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054196535 ⟸ XM_054340560
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054196544 ⟸ XM_054340569
- Peptide Label:	isoform X9
- UniProtKB:	Q8NI32 (UniProtKB/Swiss-Prot), Q7Z747 (UniProtKB/Swiss-Prot), Q53TK0 (UniProtKB/Swiss-Prot), D3DP90 (UniProtKB/Swiss-Prot), Q8IXK7 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054196526 ⟸ XM_054340551
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054196533 ⟸ XM_054340558
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054196527 ⟸ XM_054340552
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054196525 ⟸ XM_054340550
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054196531 ⟸ XM_054340556
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054196539 ⟸ XM_054340564
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054196540 ⟸ XM_054340565
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054196532 ⟸ XM_054340557
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054196538 ⟸ XM_054340563
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054196541 ⟸ XM_054340566
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_054196542 ⟸ XM_054340567
- Peptide Label:	isoform X9
- UniProtKB:	Q8NI32 (UniProtKB/Swiss-Prot), Q7Z747 (UniProtKB/Swiss-Prot), Q53TK0 (UniProtKB/Swiss-Prot), D3DP90 (UniProtKB/Swiss-Prot), Q8IXK7 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054196537 ⟸ XM_054340562
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054196546 ⟸ XM_054340571
- Peptide Label:	isoform X10

Protein Domains

UPAR/Ly6

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q8NI32-F1-model_v2	AlphaFold	Q8NI32	1-183	view protein structure

Promoters

RGD ID:

6861704

Promoter ID:

EPDNEW_H4017

Type:

initiation region

Name:

LYPD6B_2

Description:

LY6/PLAUR domain containing 6B

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H4018 EPDNEW_H4019

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,467 - 149,038,527	EPDNEW

RGD ID:

6861706

Promoter ID:

EPDNEW_H4018

Type:

initiation region

Name:

LYPD6B_1

Description:

LY6/PLAUR domain containing 6B

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H4017 EPDNEW_H4019

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,038,738 - 149,038,798	EPDNEW

RGD ID:

6861708

Promoter ID:

EPDNEW_H4019

Type:

multiple initiation site

Name:

LYPD6B_3

Description:

LY6/PLAUR domain containing 6B

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H4017 EPDNEW_H4018

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	149,126,918 - 149,126,978	EPDNEW

RGD ID:

6796492

Promoter ID:

HG_KWN:35356

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

ENST00000409642, OTTHUMT00000332353, UC002TWW.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	2	149,603,179 - 149,603,679 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:27018	AgrOrtholog
COSMIC	LYPD6B	COSMIC
Ensembl Genes	ENSG00000150556	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000280115	ENTREZGENE
	ENST00000280115.8	UniProtKB/TrEMBL
	ENST00000409029	ENTREZGENE
	ENST00000409029.5	UniProtKB/Swiss-Prot
	ENST00000409642	ENTREZGENE
	ENST00000409642.8	UniProtKB/Swiss-Prot
	ENST00000409876	ENTREZGENE
	ENST00000409876.5	UniProtKB/Swiss-Prot
	ENST00000437627.5	UniProtKB/TrEMBL
	ENST00000442722.5	UniProtKB/TrEMBL
	ENST00000450639.5	UniProtKB/TrEMBL
Gene3D-CATH	2.10.60.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000150556	GTEx
HGNC ID	HGNC:27018	ENTREZGENE
Human Proteome Map	LYPD6B	Human Proteome Map
InterPro	LYPD6-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Snake_toxin-like_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:130576	UniProtKB/Swiss-Prot
NCBI Gene	130576	ENTREZGENE
PANTHER	LY6/PLAUR DOMAIN-CONTAINING PROTEIN 6B	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR31171	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	UPAR_LY6_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA162394734	PharmGKB
Superfamily-SCOP	SSF57302	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	D3DP90	ENTREZGENE
	F8WB42_HUMAN	UniProtKB/TrEMBL
	F8WCH4_HUMAN	UniProtKB/TrEMBL
	F8WEI1_HUMAN	UniProtKB/TrEMBL
	H7BXI7	ENTREZGENE, UniProtKB/TrEMBL
	LPD6B_HUMAN	UniProtKB/Swiss-Prot
	Q53TK0	ENTREZGENE
	Q7Z747	ENTREZGENE
	Q8IXK7	ENTREZGENE
	Q8NI32	ENTREZGENE
UniProt Secondary	D3DP90	UniProtKB/Swiss-Prot
	Q53TK0	UniProtKB/Swiss-Prot
	Q7Z747	UniProtKB/Swiss-Prot
	Q8IXK7	UniProtKB/Swiss-Prot

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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