LARGE2 (LARGE xylosyl- and glucuronyltransferase 2)

Gene: LARGE2 (LARGE xylosyl- and glucuronyltransferase 2) Homo sapiens

Analyze

Symbol:

LARGE2

Name:

LARGE xylosyl- and glucuronyltransferase 2

RGD ID:

1605885

HGNC Page

HGNC:16522

Description:

Predicted to enable dystroglycan binding activity; glucuronosyltransferase activity; and xylosyltransferase activity. Involved in protein O-linked mannosylation. Predicted to be located in intracellular membrane-bounded organelle. Predicted to be active in Golgi apparatus.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FLJ35207; glycosyltransferase-like 1B; glycosyltransferase-like protein LARGE2; GYLTL1B; like-glycosyltransferase 2; ortholog of mouse glycosyltransferase-like 1B; PP5656; xylosyl- and glucuronyltransferase LARGE2

RGD Orthologs

Alliance Genes

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	45,921,621 - 45,929,096 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	45,921,621 - 45,929,096 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	45,943,172 - 45,950,647 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	45,899,772 - 45,907,223 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	11	46,090,798 - 46,098,250 (+)	NCBI		Celera
Cytogenetic Map	11	p11.2	NCBI
HuRef	11	45,650,018 - 45,657,284 (+)	NCBI		HuRef
CHM1_1	11	45,940,615 - 45,949,059 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	11	46,077,548 - 46,085,010 (+)	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

congenital disorder of glycosylation type IIc (IAGP)

genetic disease (IAGP)

infantile Refsum disease (IAGP)

intellectual disability (IAGP)

Zellweger syndrome (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

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

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

2,4-dinitrotoluene (ISO)

2,6-dinitrotoluene (ISO)

2-palmitoylglycerol (EXP)

4,4'-sulfonyldiphenol (ISO)

4-hydroxyphenyl retinamide (ISO)

6-propyl-2-thiouracil (ISO)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP,ISO)

bisphenol A (ISO)

bisphenol F (ISO)

chrysene (ISO)

decabromodiphenyl ether (ISO)

dorsomorphin (EXP)

endosulfan (ISO)

folic acid (ISO)

fulvestrant (EXP)

gentamycin (ISO)

inulin (ISO)

methylmercury chloride (EXP)

mono(2-ethylhexyl) phthalate (ISO)

nickel atom (EXP)

paracetamol (ISO)

perfluorooctane-1-sulfonic acid (ISO)

phenylmercury acetate (EXP)

pirinixic acid (ISO)

potassium dichromate (ISO)

progesterone (EXP)

SB 431542 (EXP)

trichloroethene (ISO)

triptonide (ISO)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

muscle cell cellular homeostasis (ISS)

protein glycosylation (IEA)

protein O-linked glycosylation (TAS)

protein O-linked mannosylation (IBA,IDA,IEA)

Cellular Component

Golgi apparatus (IBA,IEA)

Golgi membrane (IEA,TAS)

intracellular membrane-bounded organelle (ISO)

membrane (IEA)

Molecular Function

dystroglycan binding (ISO)

glucuronosyltransferase activity (IBA,IEA,ISS,TAS)

glycosyltransferase activity (IEA)

manganese ion binding (TAS)

metal ion binding (IEA)

protein binding (IPI)

transferase activity (IEA)

UDP-glycosyltransferase activity (IEA)

UDP-xylosyltransferase activity (TAS)

xylosyltransferase activity (IBA,IEA,ISS)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Intellectual disability (IAGP)

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:12477932	PMID:14702039	PMID:15489334	PMID:15498874	PMID:15661757	PMID:15752776	PMID:15958417	PMID:16341674	PMID:16344560	PMID:19587235	PMID:19724895	PMID:19851296
PMID:20198315	PMID:21873635	PMID:23223448	PMID:24144296	PMID:25138275	PMID:25455932	PMID:26186194	PMID:26220087	PMID:28514442	PMID:32586342	PMID:33961781	PMID:35271311
PMID:35696571

Genomics

Comparative Map Data

LARGE2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	45,921,621 - 45,929,096 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	45,921,621 - 45,929,096 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	45,943,172 - 45,950,647 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	45,899,772 - 45,907,223 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	11	46,090,798 - 46,098,250 (+)	NCBI		Celera
Cytogenetic Map	11	p11.2	NCBI
HuRef	11	45,650,018 - 45,657,284 (+)	NCBI		HuRef
CHM1_1	11	45,940,615 - 45,949,059 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	11	46,077,548 - 46,085,010 (+)	NCBI		T2T-CHM13v2.0

Large2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	92,195,391 - 92,201,437 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	92,195,391 - 92,205,214 (-)	Ensembl		GRCm39 Ensembl
GRCm38	2	92,365,046 - 92,371,086 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	92,365,046 - 92,374,869 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	2	92,205,203 - 92,211,193 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	2	92,165,891 - 92,171,850 (-)	NCBI		MGSCv36	mm8
Celera	2	93,758,175 - 93,764,164 (-)	NCBI		Celera
Cytogenetic Map	2	E1	NCBI
cM Map	2	50.97	NCBI

Large2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	3	98,791,543 - 98,800,251 (-)	NCBI		GRCr8
mRatBN7.2	3	78,334,627 - 78,347,167 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	3	78,336,056 - 78,342,184 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	3	81,811,835 - 81,817,967 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	3	90,410,876 - 90,417,008 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	3	88,261,971 - 88,268,105 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	3	81,276,020 - 81,285,457 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	3	81,276,028 - 81,282,157 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	3	87,979,489 - 87,990,560 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	3	76,762,507 - 76,768,638 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	3	76,658,936 - 76,665,066 (-)	NCBI
Celera	3	77,538,049 - 77,544,180 (-)	NCBI		Celera
Cytogenetic Map	3	q24	NCBI

Large2
(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_004955422	2,045,986 - 2,050,863 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955422	2,045,986 - 2,052,086 (-)	NCBI	ChiLan1.0	ChiLan1.0

LARGE2
(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	9	48,131,104 - 48,137,222 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	11	48,137,961 - 48,144,072 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	11	45,876,788 - 45,882,899 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	11	46,368,507 - 46,374,454 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	11	46,368,624 - 46,374,203 (+)	Ensembl	panpan1.1		panPan2

LARGE2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	18	43,497,134 - 43,503,177 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	18	43,497,484 - 43,502,619 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	18	42,225,385 - 42,231,185 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	18	44,153,316 - 44,159,124 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	18	44,153,447 - 44,158,590 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	18	43,637,574 - 43,643,378 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	18	43,190,737 - 43,195,957 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	18	43,922,802 - 43,928,608 (-)	NCBI		UU_Cfam_GSD_1.0

Large2
(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_024404947	20,982,067 - 20,987,714 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936562	3,093,857 - 3,099,311 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936562	3,093,719 - 3,099,311 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

LARGE2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	2	16,545,448 - 16,550,888 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	2	16,545,436 - 16,550,922 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	17,962,525 - 17,968,338 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

LARGE2
(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	1	19,411,127 - 19,424,016 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	1	19,413,123 - 19,419,104 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666038	116,690,272 - 116,697,931 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Large2
(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_004624767	2,583,978 - 2,589,107 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624767	2,583,981 - 2,589,257 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in LARGE2
10 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 11p13-11.2(chr11:35663578-46959820)x1	copy number loss	See cases [RCV000052679]	Chr11:35663578..46959820 [GRCh38] Chr11:35685126..46981371 [GRCh37] Chr11:35641702..46937947 [NCBI36] Chr11:11p13-11.2	pathogenic
GRCh38/hg38 11p12-11.2(chr11:36508280-48643003)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052680]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052680]\|See cases [RCV000052680]	Chr11:36508280..48643003 [GRCh38] Chr11:36529830..48664555 [GRCh37] Chr11:36486406..48621131 [NCBI36] Chr11:11p12-11.2	pathogenic
GRCh38/hg38 11p11.2(chr11:44136593-46121139)x1	copy number loss	See cases [RCV000052681]	Chr11:44136593..46121139 [GRCh38] Chr11:44158143..46142690 [GRCh37] Chr11:44114719..46099266 [NCBI36] Chr11:11p11.2	pathogenic
GRCh38/hg38 11p12-11.2(chr11:41118322-48643003)x1	copy number loss	See cases [RCV000135405]	Chr11:41118322..48643003 [GRCh38] Chr11:41139872..48664555 [GRCh37] Chr11:41096448..48621131 [NCBI36] Chr11:11p12-11.2	pathogenic
GRCh38/hg38 11p12-11.12(chr11:39179252-49135735)x1	copy number loss	See cases [RCV000137391]	Chr11:39179252..49135735 [GRCh38] Chr11:39200802..49157287 [GRCh37] Chr11:39157378..49113863 [NCBI36] Chr11:11p12-11.12	pathogenic
GRCh38/hg38 11p12-11.12(chr11:42727555-49135735)x3	copy number gain	See cases [RCV000139422]	Chr11:42727555..49135735 [GRCh38] Chr11:42749105..49157287 [GRCh37] Chr11:42705681..49113863 [NCBI36] Chr11:11p12-11.12	likely pathogenic
GRCh38/hg38 11p12-11.2(chr11:42553659-46114792)x1	copy number loss	See cases [RCV000142289]	Chr11:42553659..46114792 [GRCh38] Chr11:42575209..46136343 [GRCh37] Chr11:42531785..46092919 [NCBI36] Chr11:11p12-11.2	pathogenic
GRCh37/hg19 11p12-11.2(chr11:42475897-48372559)x1	copy number loss	See cases [RCV000446383]	Chr11:42475897..48372559 [GRCh37] Chr11:11p12-11.2	pathogenic
GRCh37/hg19 11p11.2(chr11:45873733-46409298)x1	copy number loss	See cases [RCV000446153]	Chr11:45873733..46409298 [GRCh37] Chr11:11p11.2	likely pathogenic
GRCh37/hg19 11p14.2-11.12(chr11:26574629-50508019)x3	copy number gain	See cases [RCV000448603]	Chr11:26574629..50508019 [GRCh37] Chr11:11p14.2-11.12	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)	copy number gain	See cases [RCV000511729]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3	copy number gain	See cases [RCV000510881]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3	copy number gain	not provided [RCV000737348]	Chr11:198510..134934063 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3	copy number gain	not provided [RCV000749874]	Chr11:70864..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p11.2(chr11:45229091-46342834)x3	copy number gain	not provided [RCV000750026]	Chr11:45229091..46342834 [GRCh37] Chr11:11p11.2	uncertain significance
GRCh37/hg19 11p11.2(chr11:44266593-46123796)x4	copy number gain	not provided [RCV001259092]	Chr11:44266593..46123796 [GRCh37] Chr11:11p11.2	uncertain significance
NC_000011.9:g.(?_45827353)_(47804770_?)dup	duplication	Leukocyte adhesion deficiency type II [RCV001296459]	Chr11:45827353..47804770 [GRCh37] Chr11:11p11.2	uncertain significance
Single allele	deletion	Intellectual disability [RCV001293382]	Chr11:118359328..118372573 [GRCh37] Chr11:11p15.3-q23.3	pathogenic
GRCh37/hg19 11p12-11.2(chr11:40117145-46920718)x1	copy number loss	not provided [RCV001836486]	Chr11:40117145..46920718 [GRCh37] Chr11:11p12-11.2	pathogenic
NC_000011.9:g.(?_45827353)_(46401497_?)del	deletion	Peroxisome biogenesis disorder [RCV001953896]	Chr11:45827353..46401497 [GRCh37] Chr11:11p11.2	pathogenic
NC_000011.9:g.(?_45827353)_(47804770_?)del	deletion	Leukocyte adhesion deficiency type II [RCV003119908]	Chr11:45827353..47804770 [GRCh37] Chr11:11p11.2	pathogenic
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3	copy number gain	MISSED ABORTION [RCV002282973]	Chr11:32799481..134938470 [GRCh37] Chr11:11p13-q25	pathogenic
GRCh37/hg19 11p11.2-q12.2(chr11:51581311-54891247)x3	copy number gain	See cases [RCV002286338]	Chr11:51581311..54891247 [GRCh37] Chr11:11p11.2-q12.2	pathogenic
NM_001300721.2(LARGE2):c.1068C>G (p.Phe356Leu)	single nucleotide variant	Inborn genetic diseases [RCV002777814]	Chr11:45926501 [GRCh38] Chr11:45948052 [GRCh37] Chr11:11p11.2	uncertain significance
NM_001300721.2(LARGE2):c.1115G>A (p.Arg372Gln)	single nucleotide variant	Inborn genetic diseases [RCV002777815]	Chr11:45926548 [GRCh38] Chr11:45948099 [GRCh37] Chr11:11p11.2	uncertain significance
NM_001300721.2(LARGE2):c.1772G>A (p.Arg591Gln)	single nucleotide variant	Inborn genetic diseases [RCV002977823]	Chr11:45928194 [GRCh38] Chr11:45949745 [GRCh37] Chr11:11p11.2	likely benign
NM_001300721.2(LARGE2):c.536A>G (p.Tyr179Cys)	single nucleotide variant	Inborn genetic diseases [RCV002712788]	Chr11:45924549 [GRCh38] Chr11:45946100 [GRCh37] Chr11:11p11.2	uncertain significance
NM_001300721.2(LARGE2):c.325A>T (p.Ser109Cys)	single nucleotide variant	Inborn genetic diseases [RCV002789868]	Chr11:45923512 [GRCh38] Chr11:45945063 [GRCh37] Chr11:11p11.2	uncertain significance
NM_001300721.2(LARGE2):c.895G>A (p.Ala299Thr)	single nucleotide variant	Inborn genetic diseases [RCV002672538]	Chr11:45926234 [GRCh38] Chr11:45947785 [GRCh37] Chr11:11p11.2	uncertain significance
NM_001300721.2(LARGE2):c.1450C>T (p.Arg484Trp)	single nucleotide variant	Inborn genetic diseases [RCV002965503]	Chr11:45927439 [GRCh38] Chr11:45948990 [GRCh37] Chr11:11p11.2	uncertain significance
NM_001300721.2(LARGE2):c.1922T>C (p.Val641Ala)	single nucleotide variant	Inborn genetic diseases [RCV002965764]	Chr11:45928344 [GRCh38] Chr11:45949895 [GRCh37] Chr11:11p11.2	uncertain significance
NM_001300721.2(LARGE2):c.1217G>A (p.Arg406Gln)	single nucleotide variant	Inborn genetic diseases [RCV002677330]	Chr11:45926763 [GRCh38] Chr11:45948314 [GRCh37] Chr11:11p11.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	3942
Count of miRNA genes:	806
Interacting mature miRNAs:	975
Transcripts:	ENST00000325468, ENST00000389968, ENST00000401752, ENST00000414027, ENST00000525609, ENST00000528236, ENST00000529052, ENST00000530437, ENST00000531526, ENST00000531847, ENST00000534410, ENST00000536139
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

SHGC-148984

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	45,949,110 - 45,949,416	UniSTS	GRCh37
Build 36	11	45,905,686 - 45,905,992	RGD	NCBI36
Celera	11	46,096,713 - 46,097,019	RGD
Cytogenetic Map	11	p11.2	UniSTS
HuRef	11	45,655,747 - 45,656,053	UniSTS
TNG Radiation Hybrid Map	11	22220.0	UniSTS

Expression

RNA-SEQ Expression

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

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

adipose tissue

appendage

entire extraembryonic component

High

Medium

403

986

191

221

1475

269

232

572

879

167

690

Low

636

695

678

383

1154

384

181

386

142

749

677

157

Below cutoff

1296

1906

435

2273

1755

2860

126

1006

1642

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001300721	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001300722	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_152312	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005252787	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006718140	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006718141	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519886	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519888	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519889	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519890	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519891	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519892	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519893	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017017173	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426344	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426345	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426346	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426347	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426348	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426349	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367622	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367623	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367624	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367625	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367626	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367627	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367628	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367629	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367630	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367631	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367632	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367633	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367634	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367635	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367636	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367637	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC068385	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF258588	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK055829	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK092526	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK096021	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC037291	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM840813	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB204404	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HF584352	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000325468 ⟹ ENSP00000324570

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	45,922,778 - 45,929,096 (+)	Ensembl

RefSeq Acc Id:

ENST00000401752 ⟹ ENSP00000385235

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	45,922,656 - 45,929,096 (+)	Ensembl

RefSeq Acc Id:

ENST00000414027

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	45,924,617 - 45,926,830 (+)	Ensembl

RefSeq Acc Id:

ENST00000525609

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	45,924,454 - 45,926,552 (+)	Ensembl

RefSeq Acc Id:

ENST00000528236

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	45,924,150 - 45,929,096 (+)	Ensembl

RefSeq Acc Id:

ENST00000529052 ⟹ ENSP00000431932

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	45,921,621 - 45,929,096 (+)	Ensembl

RefSeq Acc Id:

ENST00000530437

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	45,926,363 - 45,929,082 (+)	Ensembl

RefSeq Acc Id:

ENST00000531526 ⟹ ENSP00000432869

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	45,921,645 - 45,929,096 (+)	Ensembl

RefSeq Acc Id:

ENST00000531847 ⟹ ENSP00000434325

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	45,928,036 - 45,929,096 (+)	Ensembl

RefSeq Acc Id:

ENST00000534410 ⟹ ENSP00000433328

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	45,926,451 - 45,927,938 (+)	Ensembl

RefSeq Acc Id:

NM_001300721 ⟹ NP_001287650

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI
CHM1_1	11	45,941,652 - 45,949,059 (+)	NCBI
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

Sequence:

show sequence

GCCTCTCCCCTGGTTCCCGCACCCTGGCCGGCGGCTGCGAGCGCAGGGCCCAGCCCGGGAGCCG
CTGGAGCAGGGCCTGCGATGGAGCCTGCAGCCCCGGGTCGCGTCCCTCCCTGAGCGCCCCCGTC
GGCGGCCATGCTGCCCCGAGGGCGCCCCCGGGCGCTGGGGGCCGCCGCGCTGTTGCTGCTGCTG
CTGCTGCTCGGATTCCTCCTGTTCGGTGGGGACCTGGGGTGTGAGCGCCGCGAGCCTGGCGGGC
GAGCGGGGGCCCCGGGATGCTTCCCCGGCCCGCTCATGCCACGTGTCCCCCCAGACGGGAGGCT
GCGGAGAGCCGCCGCCCTCGACGGAGACCCGGGGGCCGGCCCCGGGGACCACAACCGCTCCGAC
TGCGGCCCGCAGCCGCCGCCGCCGCCCAAGTGCGAGCTCTTGCATGTGGCCATCGTGTGTGCGG
GGCATAACTCCAGCCGAGACGTCATCACCCTGGTGAAGTCCATGCTCTTCTACAGGAAAAATCC
ACTGCACCTCCACTTGGTGACTGACGCCGTGGCCAGAAACATCCTGGAGACGCTCTTCCACACA
TGGATGGTGCCTGCTGTCCGTGTCAGCTTTTATCATGCCGACCAGCTCAAGCCCCAGGTCTCCT
GGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAATGAAGCTGGTGCTGCCCAGTGCCTT
GCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGATGTCACCTTCGCCTCTGACATCTCG
GAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAGGCGATCGGTCTTGTGGAGAACCAGA
GTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGCCCTGGCCTGCCTTGGGCCGGGGATT
TAACACAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCGGCAGGCTGGCTGGGAGCAGATGTGG
AGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCCACCTCACTGGCTGACCAGGACATCT
TCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGCAGCGTCTGCCTTGTGTCTGGAATGTGCA
GCTGTCAGATCACACACTGGCCGAGCGCTGCTACTCTGAGGCGTCTGACCTCAAGGTGATCCAC
TGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAGCATGTGGAATTCTTCCGCAATTTCTACC
TGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGAGAGAGCTCTTTGTGTGCCCCAGCCAGCC
CCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGCACAACTGGACGAGGAAGACCCCTGCTTT
GAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTGCATGTCACTTTCCTGCCCCATGAACCGC
CACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCCAGCTGTCCATGGACCGGCTGCAGATGTT
GGAAGCCCTGTGCAGGCACTGGCCTGGCCCCATGAGCCTGGCCTTGTACCTGACAGACGCAGAA
GCTCAGCAGTTCCTGCATTTCGTCGAGGCCTCACCAGTGCTTGCTGCCCGGCAGGACGTGGCCT
ACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCGTCAACCAGCTTCGCAACGTGGCCTTGGC
CCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACATTGACTTCCTGCCTGCCTATTCTCTCTAC
GACTACCTCAGGGCCTCCATTGAGCAGCTGGGGCTGGGCAGCCGGCGCAAGGCAGCACTGGTGG
TGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCTTCCCCCATTCCAAGGTGGAGCTGTTGGC
CTTGCTGGATGCGGGCACTCTCTACACCTTCAGGTACCACGAGTGGCCCCGAGGCCACGCACCC
ACAGACTATGCCCGCTGGCGGGAGGCTCAGGCCCCGTACCGTGTGCAATGGGCGGCCAACTATG
AACCCTACGTGGTGGTGCCACGAGACTGTCCCCGCTATGATCCTCGCTTTGTGGGCTTCGGCTG
GAACAAAGTGGCCCACATTGTGGAGCTGGATGCCCAGGAATATGAGCTCCTGGTGCTGCCCGAG
GCCTTCACCATCCATCTGCCCCACGCTCCAAGCCTGGACATCTCCCGCTTCCGCTCCAGCCCCA
CCTATCGTGACTGCCTCCAGGCCCTCAAGGACGAATTCCACCAGGACTTGTCCCGCCACCATGG
GGCTGCTGCCCTCAAATACCTCCCAGCCCTGCAGCAGCCCCAGAGCCCTGCCCGAGGCTGAGGC
TGGGCCGGCGCTGCCCCTCATCTTAGCATTGGGCAGACACCAGGGCAACCTGCCCTCCGCCATC
CCTGCTATTTAAATTATTTAAGGTCTCTGGGAAGGGCTGGGGCAGAGCATCTGTGGGGTGGGGT
CTTCCCCTTGCTGCTATTGTATGGCTGGGGACTGGTCTCTCTCTGCCCCAGCCAGTTTGGGGCT
GGTTCCCCCATCTTGAATTGTTTATCCCTTTTTCATAATTAAAGTTTTAAAACATC

hide sequence

RefSeq Acc Id:

NM_001300722 ⟹ NP_001287651

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,921,621 - 45,929,096 (+)	NCBI
CHM1_1	11	45,940,591 - 45,949,059 (+)	NCBI
T2T-CHM13v2.0	11	46,077,548 - 46,085,010 (+)	NCBI

Sequence:

show sequence

AAGCAAACAACTTCAACTTTCCATGAGTGCTAGCCAGCCCTGGGAGGCTCCGCTGCCAGAAGGA
ACGTCAAGGGGCCTGCGATGGAGCCTGCAGCCCCGGGTCGCGTCCCTCCCTGAGCGCCCCCGTC
GGCGGCCATGCTGCCCCGAGGGCGCCCCCGGGCGCTGGGGGCCGCCGCGCTGTTGCTGCTGCTG
CTGCTGCTCGGATTCCTCCTGTTCGACGGGAGGCTGCGGAGAGCCGCCGCCCTCGACGGAGACC
CGGGGGCCGGCCCCGGGGACCACAACCGCTCCGACTGCGGCCCGCAGCCGCCGCCGCCGCCCAA
GTGCGAGCTCTTGCATGTGGCCATCGTGTGTGCGGGGCATAACTCCAGCCGAGACGTCATCACC
CTGGTGAAGTCCATGCTCTTCTACAGGAAAAATCCACTGCACCTCCACTTGGTGACTGACGCCG
TGGCCAGAAACATCCTGGAGACGCTCTTCCACACATGGATGGTGCCTGCTGTCCGTGTCAGCTT
TTATCATGCCGACCAGCTCAAGCCCCAGGTCTCCTGGATCCCCAACAAGCACTACTCCGGCCTC
TATGGGCTAATGAAGCTGGTGCTGCCCAGTGCCTTGCCTGCTGAGCTGGCCCGCGTCATTGTCC
TGGACACGGATGTCACCTTCGCCTCTGACATCTCGGAGCTCTGGGCCCTCTTTGCTCACTTTTC
TGACACGCAGGCGATCGGTCTTGTGGAGAACCAGAGTGACTGGTACCTGGGCAACCTCTGGAAG
AACCACAGGCCCTGGCCTGCCTTGGGCCGGGGATTTAACACAGGTGTGATCCTGCTGCGGCTGG
ACCGGCTCCGGCAGGCTGGCTGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAG
CCTGCCTGCCACCTCACTGGCTGACCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCGGGG
CTAGTGCAGCGTCTGCCTTGTGTCTGGAATGTGCAGCTGTCAGATCACACACTGGCCGAGCGCT
GCTACTCTGAGGCGTCTGACCTCAAGGTGATCCACTGGAACTCACCAAAGAAGCTTCGGGTGAA
GAACAAGCATGTGGAATTCTTCCGCAATTTCTACCTGACCTTCCTGGAGTACGATGGGAACCTG
CTGCGGAGAGAGCTCTTTGTGTGCCCCAGCCAGCCCCCACCTGGTGCTGAGCAGTTGCAGCAGG
CCCTGGCACAACTGGACGAGGAAGACCCCTGCTTTGAGTTCCGGCAGCAGCAGCTCACTGTGCA
CCGTGTGCATGTCACTTTCCTGCCCCATGAACCGCCACCCCCCCGGCCTCACGATGTCACCCTT
GTGGCCCAGCTGTCCATGGACCGGCTGCAGATGTTGGAAGCCCTGTGCAGGCACTGGCCTGGCC
CCATGAGCCTGGCCTTGTACCTGACAGACGCAGAAGCTCAGCAGTTCCTGCATTTCGTCGAGGC
CTCACCAGTGCTTGCTGCCCGGCAGGACGTGGCCTACCATGTGGTGTACCGTGAGGGGCCCCTA
TACCCCGTCAACCAGCTTCGCAACGTGGCCTTGGCCCAGGCCCTCACGCCTTACGTCTTCCTCA
GTGACATTGACTTCCTGCCTGCCTATTCTCTCTACGACTACCTCAGGGCCTCCATTGAGCAGCT
GGGGCTGGGCAGCCGGCGCAAGGCAGCACTGGTGGTGCCGGCATTCGAGACCCTGCGCTACCGC
TTCAGCTTCCCCCATTCCAAGGTGGAGCTGTTGGCCTTGCTGGATGCGGGCACTCTCTACACCT
TCAGGTACCACGAGTGGCCCCGAGGCCACGCACCCACAGACTATGCCCGCTGGCGGGAGGCTCA
GGCCCCGTACCGTGTGCAATGGGCGGCCAACTATGAACCCTACGTGGTGGTGCCACGAGACTGT
CCCCGCTATGATCCTCGCTTTGTGGGCTTCGGCTGGAACAAAGTGGCCCACATTGTGGAGCTGG
ATGCCCAGGAATATGAGCTCCTGGTGCTGCCCGAGGCCTTCACCATCCATCTGCCCCACGCTCC
AAGCCTGGACATCTCCCGCTTCCGCTCCAGCCCCACCTATCGTGACTGCCTCCAGGCCCTCAAG
GACGAATTCCACCAGGACTTGTCCCGCCACCATGGGGCTGCTGCCCTCAAATACCTCCCAGCCC
TGCAGCAGCCCCAGAGCCCTGCCCGAGGCTGAGGCTGGGCCGGCGCTGCCCCTCATCTTAGCAT
TGGGCAGACACCAGGGCAACCTGCCCTCCGCCATCCCTGCTATTTAAATTATTTAAGGTCTCTG
GGAAGGGCTGGGGCAGAGCATCTGTGGGGTGGGGTCTTCCCCTTGCTGCTATTGTATGGCTGGG
GACTGGTCTCTCTCTGCCCCAGCCAGTTTGGGGCTGGTTCCCCCATCTTGAATTGTTTATCCCT
TTTTCATAATTAAAGTTTTAAAACATC

hide sequence

RefSeq Acc Id:

NM_152312 ⟹ NP_689525

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,921,621 - 45,929,096 (+)	NCBI
GRCh37	11	45,943,172 - 45,950,647 (+)	NCBI
Build 36	11	45,899,772 - 45,907,223 (+)	NCBI Archive
Celera	11	46,090,798 - 46,098,250 (+)	RGD
HuRef	11	45,650,018 - 45,657,284 (+)	ENTREZGENE
CHM1_1	11	45,940,591 - 45,949,059 (+)	NCBI
T2T-CHM13v2.0	11	46,077,548 - 46,085,010 (+)	NCBI

Sequence:

show sequence

AAGCAAACAACTTCAACTTTCCATGAGTGCTAGCCAGCCCTGGGAGGCTCCGCTGCCAGAAGGA
ACGTCAAGGGGCCTGCGATGGAGCCTGCAGCCCCGGGTCGCGTCCCTCCCTGAGCGCCCCCGTC
GGCGGCCATGCTGCCCCGAGGGCGCCCCCGGGCGCTGGGGGCCGCCGCGCTGTTGCTGCTGCTG
CTGCTGCTCGGATTCCTCCTGTTCGGTGGGGACCTGGGGTGTGAGCGCCGCGAGCCTGGCGGGC
GAGCGGGGGCCCCGGGATGCTTCCCCGGCCCGCTCATGCCACGTGTCCCCCCAGACGGGAGGCT
GCGGAGAGCCGCCGCCCTCGACGGAGACCCGGGGGCCGGCCCCGGGGACCACAACCGCTCCGAC
TGCGGCCCGCAGCCGCCGCCGCCGCCCAAGTGCGAGCTCTTGCATGTGGCCATCGTGTGTGCGG
GGCATAACTCCAGCCGAGACGTCATCACCCTGGTGAAGTCCATGCTCTTCTACAGGAAAAATCC
ACTGCACCTCCACTTGGTGACTGACGCCGTGGCCAGAAACATCCTGGAGACGCTCTTCCACACA
TGGATGGTGCCTGCTGTCCGTGTCAGCTTTTATCATGCCGACCAGCTCAAGCCCCAGGTCTCCT
GGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAATGAAGCTGGTGCTGCCCAGTGCCTT
GCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGATGTCACCTTCGCCTCTGACATCTCG
GAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAGGCGATCGGTCTTGTGGAGAACCAGA
GTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGCCCTGGCCTGCCTTGGGCCGGGGATT
TAACACAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCGGCAGGCTGGCTGGGAGCAGATGTGG
AGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCCACCTCACTGGCTGACCAGGACATCT
TCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGCAGCGTCTGCCTTGTGTCTGGAATGTGCA
GCTGTCAGATCACACACTGGCCGAGCGCTGCTACTCTGAGGCGTCTGACCTCAAGGTGATCCAC
TGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAGCATGTGGAATTCTTCCGCAATTTCTACC
TGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGAGAGAGCTCTTTGTGTGCCCCAGCCAGCC
CCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGCACAACTGGACGAGGAAGACCCCTGCTTT
GAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTGCATGTCACTTTCCTGCCCCATGAACCGC
CACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCCAGCTGTCCATGGACCGGCTGCAGATGTT
GGAAGCCCTGTGCAGGCACTGGCCTGGCCCCATGAGCCTGGCCTTGTACCTGACAGACGCAGAA
GCTCAGCAGTTCCTGCATTTCGTCGAGGCCTCACCAGTGCTTGCTGCCCGGCAGGACGTGGCCT
ACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCGTCAACCAGCTTCGCAACGTGGCCTTGGC
CCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACATTGACTTCCTGCCTGCCTATTCTCTCTAC
GACTACCTCAGGGCCTCCATTGAGCAGCTGGGGCTGGGCAGCCGGCGCAAGGCAGCACTGGTGG
TGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCTTCCCCCATTCCAAGGTGGAGCTGTTGGC
CTTGCTGGATGCGGGCACTCTCTACACCTTCAGGTACCACGAGTGGCCCCGAGGCCACGCACCC
ACAGACTATGCCCGCTGGCGGGAGGCTCAGGCCCCGTACCGTGTGCAATGGGCGGCCAACTATG
AACCCTACGTGGTGGTGCCACGAGACTGTCCCCGCTATGATCCTCGCTTTGTGGGCTTCGGCTG
GAACAAAGTGGCCCACATTGTGGAGCTGGATGCCCAGGAATATGAGCTCCTGGTGCTGCCCGAG
GCCTTCACCATCCATCTGCCCCACGCTCCAAGCCTGGACATCTCCCGCTTCCGCTCCAGCCCCA
CCTATCGTGACTGCCTCCAGGCCCTCAAGGACGAATTCCACCAGGACTTGTCCCGCCACCATGG
GGCTGCTGCCCTCAAATACCTCCCAGCCCTGCAGCAGCCCCAGAGCCCTGCCCGAGGCTGAGGC
TGGGCCGGCGCTGCCCCTCATCTTAGCATTGGGCAGACACCAGGGCAACCTGCCCTCCGCCATC
CCTGCTATTTAAATTATTTAAGGTCTCTGGGAAGGGCTGGGGCAGAGCATCTGTGGGGTGGGGT
CTTCCCCTTGCTGCTATTGTATGGCTGGGGACTGGTCTCTCTCTGCCCCAGCCAGTTTGGGGCT
GGTTCCCCCATCTTGAATTGTTTATCCCTTTTTCATAATTAAAGTTTTAAAACATC

hide sequence

RefSeq Acc Id:

XM_005252787 ⟹ XP_005252844

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,924,506 - 45,929,096 (+)	NCBI
GRCh37	11	45,943,172 - 45,950,647 (+)	NCBI

Sequence:

show sequence

CCCCAGGTCTCCTGGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAATGAAGCTGGTGC
TGCCCAGTGCCTTGCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGATGTCACCTTCGC
CTCTGACATCTCGGAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAGGCGATCGGTCTT
GTGGAGAACCAGAGTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGCCCTGGCCTGCCT
TGGGCCGGGGATTTAACACAGGACATCTTCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGC
AGCGTCTGCCTTGTGTCTGGAATGTGCAGCTGTCAGATCACACACTGGCCGAGCGCTGCTACTC
TGAGGCGTCTGACCTCAAGGTGATCCACTGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAG
CATGTGGAATTCTTCCGCAATTTCTACCTGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGA
GAGAGCTCTTTGTGTGCCCCAGCCAGCCCCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGC
ACAACTGGACGAGGAAGACCCCTGCTTTGAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTG
CATGTCACTTTCCTGCCCCATGAACCGCCACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCC
AGCTGTCCATGGACCGGCTGCAGATGTTGGAAGCCCTGTGCAGGCACTGGCCTGGCCCCATGAG
CCTGGCCTTGTACCTGACAGACGCAGAAGCTCAGCAGTTCCTGCATTTCGTCGAGGCCTCACCA
GTGCTTGCTGCCCGGCAGGACGTGGCCTACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCG
TCAACCAGCTTCGCAACGTGGCCTTGGCCCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACAT
TGACTTCCTGCCTGCCTATTCTCTCTACGACTACCTCAGGGCCTCCATTGAGCAGCTGGGGCTG
GGCAGCCGGCGCAAGGCAGCACTGGTGGTGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCT
TCCCCCATTCCAAGGTGGAGCTGTTGGCCTTGCTGGATGCGGGCACTCTCTACACCTTCAGGTA
CCACGAGTGGCCCCGAGGCCACGCACCCACAGACTATGCCCGCTGGCGGGAGGCTCAGGCCCCG
TACCGTGTGCAATGGGCGGCCAACTATGAACCCTACGTGGTGGTGCCACGAGACTGTCCCCGCT
ATGATCCTCGCTTTGTGGGCTTCGGCTGGAACAAAGTGGCCCACATTGTGGAGCTGGATGCCCA
GGCCAGGCAAGCCAGGCAGCCACTGCTCCTCTGCCCCACCCTGCAGGAATATGAGCTCCTGGTG
CTGCCCGAGGCCTTCACCATCCATCTGCCCCACGCTCCAAGCCTGGACATCTCCCGCTTCCGCT
CCAGCCCCACCTATCGTGACTGCCTCCAGGCCCTCAAGGACGAATTCCACCAGGACTTGTCCCG
CCACCATGGGGCTGCTGCCCTCAAATACCTCCCAGCCCTGCAGCAGCCCCAGAGCCCTGCCCGA
GGCTGAGGCTGGGCCGGCGCTGCCCCTCATCTTAGCATTGGGCAGACACCAGGGCAACCTGCCC
TCCGCCATCCCTGCTATTTAAATTATTTAAGGTCTCTGGGAAGGGCTGGGGCAGAGCATCTGTG
GGGTGGGGTCTTCCCCTTGCTGCTATTGTATGGCTGGGGACTGGTCTCTCTCTGCCCCAGCCAG
TTTGGGGCTGGTTCCCCCATCTTGAATTGTTTATCCCTTTTTCATAATTAAAGTTTTAAAACAT
C

hide sequence

RefSeq Acc Id:

XM_006718140 ⟹ XP_006718203

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

Sequence:

show sequence

ACCCTGGCCGGCGGCTGCGAGCGCAGGGCCCAGCCCGGGAGCCGCTGGAGCAGGGCCTGCGATG
GAGCCTGCAGCCCCGGGTCGCGTCCCTCCCTGAGCGCCCCCGTCGGCGGCCATGCTGCCCCGAG
GGCGCCCCCGGGCGCTGGGGGCCGCCGCGCTGTTGCTGCTGCTGCTGCTGCTCGGATTCCTCCT
GTTCGACGGGAGGCTGCGGAGAGCCGCCGCCCTCGACGGAGACCCGGGGGCCGGCCCCGGGGAC
CACAACCGCTCCGACTGCGGCCCGCAGCCGCCGCCGCCGCCCAAGTGCGAGCTCTTGCATGTGG
CCATCGTGTGTGCGGGGCATAACTCCAGCCGAGACGTCATCACCCTGGTGAAGTCCATGCTCTT
CTACAGGAAAAATCCACTGCACCTCCACTTGGTGACTGACGCCGTGGCCAGAAACATCCTGGAG
ACGCTCTTCCACACATGGATGGTGCCTGCTGTCCGTGTCAGCTTTTATCATGCCGACCAGCTCA
AGCCCCAGGTCTCCTGGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAATGAAGCTGGT
GCTGCCCAGTGCCTTGCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGATGTCACCTTC
GCCTCTGACATCTCGGAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAGGCGATCGGTC
TTGTGGAGAACCAGAGTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGCCCTGGCCTGC
CTTGGGCCGGGGATTTAACACAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCGGCAGGCTGGC
TGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCCACCTCACTGG
CTGACCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGCAGCGTCTGCCTTG
TGTCTGGAATGTGCAGCTGTCAGATCACACACTGGCCGAGCGCTGCTACTCTGAGGCGTCTGAC
CTCAAGGTGATCCACTGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAGCATGTGGAATTCT
TCCGCAATTTCTACCTGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGAGAGAGCTCTTTGT
GTGCCCCAGCCAGCCCCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGCACAACTGGACGAG
GAAGACCCCTGCTTTGAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTGCATGTCACTTTCC
TGCCCCATGAACCGCCACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCCAGCTGTCCATGGA
CCGGCTGCAGATGTTGGAAGCCCTGTGCAGGCACTGGCCTGGCCCCATGAGCCTGGCCTTGTAC
CTGACAGACGCAGAAGCTCAGCAGTTCCTGCATTTCGTCGAGGCCTCACCAGTGCTTGCTGCCC
GGCAGGACGTGGCCTACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCGTCAACCAGCTTCG
CAACGTGGCCTTGGCCCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACATTGACTTCCTGCCT
GCCTATTCTCTCTACGACTACCTCAGGGCCTCCATTGAGCAGCTGGGGCTGGGCAGCCGGCGCA
AGGCAGCACTGGTGGTGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCTTCCCCCATTCCAA
GGTGGAGCTGTTGGCCTTGCTGGATGCGGGCACTCTCTACACCTTCAGGTACCACGAGTGGCCC
CGAGGCCACGCACCCACAGACTATGCCCGCTGGCGGGAGGCTCAGGCCCCGTACCGTGTGCAAT
GGGCGGCCAACTATGAACCCTACGTGGTGGTGCCACGAGACTGTCCCCGCTATGATCCTCGCTT
TGTGGGCTTCGGCTGGAACAAAGTGGCCCACATTGTGGAGCTGGATGCCCAGGAATATGAGCTC
CTGGTGCTGCCCGAGGCCTTCACCATCCATCTGCCCCACGCTCCAAGCCTGGACATCTCCCGCT
TCCGCTCCAGCCCCACCTATCGTGACTGCCTCCAGGCCCTCAAGGACGAATTCCACCAGGACTT
GTCCCGCCACCATGGGGCTGCTGCCCTCAAATACCTCCCAGCCCTGCAGCAGCCCCAGAGCCCT
GCCCGAGGCTGAGGCTGGGCCGGCGCTGCCCCTCATCTTAGCATTGGGCAGACACCAGGGCAAC
CTGCCCTCCGCCATCCCTGCTATTTAAATTATTTAAGGTCTCTGGGAAGGGCTGGGGCAGAGCA
TCTGTGGGGTGGGGTCTTCCCCTTGCTGCTATTGTATGGCTGGGGACTGGTCTCTCTCTGCCCC
AGCCAGTTTGGGGCTGGTTCCCCCATCTTGAATTGTTTATCCCTTTTTCATAATTAAAGTTTTA
AAACATC

hide sequence

RefSeq Acc Id:

XM_006718141 ⟹ XP_006718204

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,928,069 (+)	NCBI

Sequence:

show sequence

AGCGCAGGGCCCAGCCCGGGAGCCGCTGGAGCAGGGCCTGCGATGGAGCCTGCAGCCCCGGGTC
GCGTCCCTCCCTGAGCGCCCCCGTCGGCGGCCATGCTGCCCCGAGGGCGCCCCCGGGCGCTGGG
GGCCGCCGCGCTGTTGCTGCTGCTGCTGCTGCTCGGATTCCTCCTGTTCGGTGGGGACCTGGGG
TGTGAGCGCCGCGAGCCTGGCGGGCGAGCGGGGGCCCCGGGATGCTTCCCCGGCCCGCTCATGC
CACGTGTCCCCCCAGACGGGAGGCTGCGGAGAGCCGCCGCCCTCGACGGAGACCCGGGGGCCGG
CCCCGGGGACCACAACCGCTCCGACTGCGGCCCGCAGCCGCCGCCGCCGCCCAAGTGCGAGCTC
TTGCATGTGGCCATCGTGTGTGCGGGGCATAACTCCAGCCGAGACGTCATCACCCTGGTGAAGT
CCATGCTCTTCTACAGGAAAAATCCACTGCACCTCCACTTGGTGACTGACGCCGTGGCCAGAAA
CATCCTGGAGACGCTCTTCCACACATGGATGGTGCCTGCTGTCCGTGTCAGCTTTTATCATGCC
GACCAGCTCAAGCCCCAGGTCTCCTGGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAA
TGAAGCTGGTGCTGCCCAGTGCCTTGCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGA
TGTCACCTTCGCCTCTGACATCTCGGAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAG
GCGATCGGTCTTGTGGAGAACCAGAGTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGC
CCTGGCCTGCCTTGGGCCGGGGATTTAACACAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCG
GCAGGCTGGCTGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCC
ACCTCACTGGCTGACCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGCAGC
GTCTGCCTTGTGTCTGGAATGTGCAGCTGTCAGATCACACACTGGCCGAGCGCTGCTACTCTGA
GGCGTCTGACCTCAAGGTGATCCACTGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAGCAT
GTGGAATTCTTCCGCAATTTCTACCTGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGAGAG
AGCTCTTTGTGTGCCCCAGCCAGCCCCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGCACA
ACTGGACGAGGAAGACCCCTGCTTTGAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTGCAT
GTCACTTTCCTGCCCCATGAACCGCCACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCCAGC
TGTCCATGGACCGGCTGCAGATGTTGGAAGCCCTGTGCAGGCACTGGCCTGGCCCCATGAGCCT
GGCCTTGTACCTGACAGACGCAGAAGCTCAGCAGTTCCTGCATTTCGTCGAGGCCTCACCAGTG
CTTGCTGCCCGGCAGGACGTGGCCTACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCGTCA
ACCAGCTTCGCAACGTGGCCTTGGCCCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACATTGA
CTTCCTGCCTGCCTATTCTCTCTACGACTACCTCAGGGAGGCCAGGGCCGGCTTCAACAGCAGC
TCCACCTGTGGTTGTGCCCACCCGTCGCATCAGGCAAGATGGCCCATGGTGGTCTAGTCCTGTG
GCTAATGCCCTGATGAGTGTCACTGGCCCAGTCCTAGATGCCCCGCTCTTCTCCCCTGCTCATG
GGTGCTCCTCCTCAGGGCCTCCATTGAGCAGCTGGGGCTGGGCAGCCGGCGCAAGGCAGCACTG
GTGGTGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCTTCCCCCATTCCAAGGTGGAGCTGT
TGGCCTTGCTGGATGCGGGCACTCTCTACACCTTCAG

hide sequence

RefSeq Acc Id:

XM_011519886 ⟹ XP_011518188

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

Sequence:

show sequence

AGCGCAGGGCCCAGCCCGGGAGCCGCTGGAGCAGGGCCTGCGATGGAGCCTGCAGCCCCGGGTC
GCGTCCCTCCCTGAGCGCCCCCGTCGGCGGCCATGCTGCCCCGAGGGCGCCCCCGGGCGCTGGG
GGCCGCCGCGCTGTTGCTGCTGCTGCTGCTGCTCGGATTCCTCCTGTTCGGTGGGGACCTGGGG
TGTGAGCGCCGCGAGCCTGGCGGGCGAGCGGGGGCCCCGGGATGCTTCCCCGGCCCGCTCATGC
CACGTGTCCCCCCAGACGGGAGGCTGCGGAGAGCCGCCGCCCTCGACGGAGACCCGGGGGCCGG
CCCCGGGGACCACAACCGCTCCGACTGCGGCCCGCAGCCGCCGCCGCCGCCCAAGTGCGAGCTC
TTGCATGTGGCCATCGTGTGTGCGGGGCATAACTCCAGCCGAGACGTCATCACCCTGGTGAAGT
CCATGCTCTTCTACAGGAAAAATCCACTGCACCTCCACTTGGTGACTGACGCCGTGGCCAGAAA
CATCCTGGAGACGCTCTTCCACACATGGATGGTGCCTGCTGTCCGTGTCAGCTTTTATCATGCC
GACCAGCTCAAGCCCCAGGTCTCCTGGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAA
TGAAGCTGGTGCTGCCCAGTGCCTTGCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGA
TGTCACCTTCGCCTCTGACATCTCGGAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAG
GCGATCGGTCTTGTGGAGAACCAGAGTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGC
CCTGGCCTGCCTTGGGCCGGGGATTTAACACAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCG
GCAGGCTGGCTGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCC
ACCTCACTGGCTGACCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGCAGC
GTCTGCCTTGTGTCTGGAATGTGCAGCTGTCAGATCACACACTGGCCGAGCGCTGCTACTCTGA
GGCGTCTGACCTCAAGGTGATCCACTGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAGCAT
GTGGAATTCTTCCGCAATTTCTACCTGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGAGAG
AGCTCTTTGTGTGCCCCAGCCAGCCCCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGCACA
ACTGGACGAGGAAGACCCCTGCTTTGAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTGCAT
GTCACTTTCCTGCCCCATGAACCGCCACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCCAGC
TGTCCATGGACCGGCTGCAGATGTTGGAAGCCCTGTGCAGGCACTGGCCTGGCCCCATGAGCCT
GGCCTTGTACCTGACAGACGCAGAAGCTCAGCAGTTCCTGCATTTCGTCGAGGCCTCACCAGTG
CTTGCTGCCCGGCAGGACGTGGCCTACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCGTCA
ACCAGCTTCGCAACGTGGCCTTGGCCCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACATTGA
CTTCCTGCCTGCCTATTCTCTCTACGACTACCTCAGGGCCTCCATTGAGCAGCTGGGGCTGGGC
AGCCGGCGCAAGGCAGCACTGGTGGTGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCTTCC
CCCATTCCAAGGTGGAGCTGTTGGCCTTGCTGGATGCGGGCACTCTCTACACCTTCAGGTACCA
CGAGTGGCCCCGAGGCCACGCACCCACAGACTATGCCCGCTGGCGGGAGGCTCAGGCCCCGTAC
CGTGTGCAATGGGCGGCCAACTATGAACCCTACGTGGTGGTGCCACGAGACTGTCCCCGCTATG
ATCCTCGCTTTGTGGGCTTCGGCTGGAACAAAGTGGCCCACATTGTGGAGCTGGATGCCCAGGC
CAGGCAAGCCAGGCAGCCACTGCTCCTCTGCCCCACCCTGCAGGAATATGAGCTCCTGGTGCTG
CCCGAGGCCTTCACCATCCATCTGCCCCACGCTCCAAGCCTGGACATCTCCCGCTTCCGCTCCA
GCCCCACCTATCGTGACTGCCTCCAGGCCCTCAAGGACGAATTCCACCAGGACTTGTCCCGCCA
CCATGGGGCTGCTGCCCTCAAATACCTCCCAGCCCTGCAGCAGCCCCAGAGCCCTGCCCGAGGC
TGAGGCTGGGCCGGCGCTGCCCCTCATCTTAGCATTGGGCAGACACCAGGGCAACCTGCCCTCC
GCCATCCCTGCTATTTAAATTATTTAAGGTCTCTGGGAAGGGCTGGGGCAGAGCATCTGTGGGG
TGGGGTCTTCCCCTTGCTGCTATTGTATGGCTGGGGACTGGTCTCTCTCTGCCCCAGCCAGTTT
GGGGCTGGTTCCCCCATCTTGAATTGTTTATCCCTTTTTCATAATTAAAGTTTTAAAACATC

hide sequence

RefSeq Acc Id:

XM_011519888 ⟹ XP_011518190

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

Sequence:

show sequence

AGCGCAGGGCCCAGCCCGGGAGCCGCTGGAGCAGGGCCTGCGATGGAGCCTGCAGCCCCGGGTC
GCGTCCCTCCCTGAGCGCCCCCGTCGGCGGCCATGCTGCCCCGAGGGCGCCCCCGGGCGCTGGG
GGCCGCCGCGCTGTTGCTGCTGCTGCTGCTGCTCGGATTCCTCCTGTTCGGTGGGGACCTGGGG
TGTGAGCGCCGCGAGCCTGGCGGGCGAGCGGGGGCCCCGGGATGCTTCCCCGGCCCGCTCATGC
CACGTGTCCCCCCAGACGGGAGGCTGCGGAGAGCCGCCGCCCTCGACGGAGACCCGGGGGCCGG
CCCCGGGGACCACAACCGCTCCGACTGCGGCCCGCAGCCGCCGCCGCCGCCCAAGTGCGAGCTC
TTGCATGTGGCCATCGTGTGTGCGGGGCATAACTCCAGCCGAGACGTCATCACCCTGGTGAAGT
CCATGCTCTTCTACAGGAAAAATCCACTGCACCTCCACTTGGTGACTGACGCCGTGGCCAGAAA
CATCCTGGAGACGCTCTTCCACACATGGATGGTGCCTGCTGTCCGTGTCAGCTTTTATCATGCC
GACCAGCTCAAGCCCCAGGTCTCCTGGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAA
TGAAGCTGGTGCTGCCCAGTGCCTTGCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGA
TGTCACCTTCGCCTCTGACATCTCGGAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAG
GCGATCGGTCTTGTGGAGAACCAGAGTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGC
CCTGGCCTGCCTTGGGCCGGGGATTTAACACAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCG
GCAGGCTGGCTGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCC
ACCTCACTGGCTGACCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGCAGC
GTCTGCCTTGTGTCTGGAATGTGCAGCTGTCAGATCACACACTGGCCGAGCGCTGCTACTCTGA
GGCGTCTGACCTCAAGGTGATCCACTGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAGCAT
GTGGAATTCTTCCGCAATTTCTACCTGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGAGAG
AGCTCTTTGTGTGCCCCAGCCAGCCCCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGCACA
ACTGGACGAGGAAGACCCCTGCTTTGAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTGCAT
GTCACTTTCCTGCCCCATGAACCGCCACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCCAGC
TGTCCATGGACCGGACGTGGCCTACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCGTCAAC
CAGCTTCGCAACGTGGCCTTGGCCCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACATTGACT
TCCTGCCTGCCTATTCTCTCTACGACTACCTCAGGGCCTCCATTGAGCAGCTGGGGCTGGGCAG
CCGGCGCAAGGCAGCACTGGTGGTGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCTTCCCC
CATTCCAAGGTGGAGCTGTTGGCCTTGCTGGATGCGGGCACTCTCTACACCTTCAGGTACCACG
AGTGGCCCCGAGGCCACGCACCCACAGACTATGCCCGCTGGCGGGAGGCTCAGGCCCCGTACCG
TGTGCAATGGGCGGCCAACTATGAACCCTACGTGGTGGTGCCACGAGACTGTCCCCGCTATGAT
CCTCGCTTTGTGGGCTTCGGCTGGAACAAAGTGGCCCACATTGTGGAGCTGGATGCCCAGGCCA
GGCAAGCCAGGCAGCCACTGCTCCTCTGCCCCACCCTGCAGGAATATGAGCTCCTGGTGCTGCC
CGAGGCCTTCACCATCCATCTGCCCCACGCTCCAAGCCTGGACATCTCCCGCTTCCGCTCCAGC
CCCACCTATCGTGACTGCCTCCAGGCCCTCAAGGACGAATTCCACCAGGACTTGTCCCGCCACC
ATGGGGCTGCTGCCCTCAAATACCTCCCAGCCCTGCAGCAGCCCCAGAGCCCTGCCCGAGGCTG
AGGCTGGGCCGGCGCTGCCCCTCATCTTAGCATTGGGCAGACACCAGGGCAACCTGCCCTCCGC
CATCCCTGCTATTTAAATTATTTAAGGTCTCTGGGAAGGGCTGGGGCAGAGCATCTGTGGGGTG
GGGTCTTCCCCTTGCTGCTATTGTATGGCTGGGGACTGGTCTCTCTCTGCCCCAGCCAGTTTGG
GGCTGGTTCCCCCATCTTGAATTGTTTATCCCTTTTTCATAATTAAAGTTTTAAAACATC

hide sequence

RefSeq Acc Id:

XM_011519889 ⟹ XP_011518191

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

Sequence:

show sequence

ACCCTGGCCGGCGGCTGCGAGCGCAGGGCCCAGCCCGGGAGCCGCTGGAGCAGGGCCTGCGATG
GAGCCTGCAGCCCCGGGTCGCGTCCCTCCCTGAGCGCCCCCGTCGGCGGCCATGCTGCCCCGAG
GGCGCCCCCGGGCGCTGGGGGCCGCCGCGCTGTTGCTGCTGCTGCTGCTGCTCGGATTCCTCCT
GTTCGACGGGAGGCTGCGGAGAGCCGCCGCCCTCGACGGAGACCCGGGGGCCGGCCCCGGGGAC
CACAACCGCTCCGACTGCGGCCCGCAGCCGCCGCCGCCGCCCAAGTGCGAGCTCTTGCATGTGG
CCATCGTGTGTGCGGGGCATAACTCCAGCCGAGACGTCATCACCCTGGTGAAGTCCATGCTCTT
CTACAGGAAAAATCCACTGCACCTCCACTTGGTGACTGACGCCGTGGCCAGAAACATCCTGGAG
ACGCTCTTCCACACATGGATGGTGCCTGCTGTCCGTGTCAGCTTTTATCATGCCGACCAGCTCA
AGCCCCAGGTCTCCTGGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAATGAAGCTGGT
GCTGCCCAGTGCCTTGCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGATGTCACCTTC
GCCTCTGACATCTCGGAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAGGCGATCGGTC
TTGTGGAGAACCAGAGTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGCCCTGGCCTGC
CTTGGGCCGGGGATTTAACACAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCGGCAGGCTGGC
TGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCCACCTCACTGG
CTGACCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGCAGCGTCTGCCTTG
TGTCTGGAATGTGCAGCTGTCAGATCACACACTGGCCGAGCGCTGCTACTCTGAGGCGTCTGAC
CTCAAGGTGATCCACTGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAGCATGTGGAATTCT
TCCGCAATTTCTACCTGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGAGAGAGCTCTTTGT
GTGCCCCAGCCAGCCCCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGCACAACTGGACGAG
GAAGACCCCTGCTTTGAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTGCATGTCACTTTCC
TGCCCCATGAACCGCCACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCCAGCTGTCCATGGA
CCGGCTGCAGATGTTGGAAGCCCTGTGCAGGCACTGGCCTGGCCCCATGAGCCTGGCCTTGTAC
CTGACAGACGCAGAAGCTCAGCAGTTCCTGCATTTCGTCGAGGCCTCACCAGTGCTTGCTGCCC
GGCAGGACGTGGCCTACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCGTCAACCAGCTTCG
CAACGTGGCCTTGGCCCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACATTGACTTCCTGCCT
GCCTATTCTCTCTACGACTACCTCAGGGCCTCCATTGAGCAGCTGGGGCTGGGCAGCCGGCGCA
AGGCAGCACTGGTGGTGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCTTCCCCCATTCCAA
GGTGGAGCTGTTGGCCTTGCTGGATGCGGGCACTCTCTACACCTTCAGGTACCACGAGTGGCCC
CGAGGCCACGCACCCACAGACTATGCCCGCTGGCGGGAGGCTCAGGCCCCGTACCGTGTGCAAT
GGGCGGCCAACTATGAACCCTACGTGGTGGTGCCACGAGACTGTCCCCGCTATGATCCTCGCTT
TGTGGGCTTCGGCTGGAACAAAGTGGCCCACATTGTGGAGCTGGATGCCCAGGCCAGGCAAGCC
AGGCAGCCACTGCTCCTCTGCCCCACCCTGCAGGAATATGAGCTCCTGGTGCTGCCCGAGGCCT
TCACCATCCATCTGCCCCACGCTCCAAGCCTGGACATCTCCCGCTTCCGCTCCAGCCCCACCTA
TCGTGACTGCCTCCAGGCCCTCAAGGACGAATTCCACCAGGACTTGTCCCGCCACCATGGGGCT
GCTGCCCTCAAATACCTCCCAGCCCTGCAGCAGCCCCAGAGCCCTGCCCGAGGCTGAGGCTGGG
CCGGCGCTGCCCCTCATCTTAGCATTGGGCAGACACCAGGGCAACCTGCCCTCCGCCATCCCTG
CTATTTAAATTATTTAAGGTCTCTGGGAAGGGCTGGGGCAGAGCATCTGTGGGGTGGGGTCTTC
CCCTTGCTGCTATTGTATGGCTGGGGACTGGTCTCTCTCTGCCCCAGCCAGTTTGGGGCTGGTT
CCCCCATCTTGAATTGTTTATCCCTTTTTCATAATTAAAGTTTTAAAACATC

hide sequence

RefSeq Acc Id:

XM_011519890 ⟹ XP_011518192

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

Sequence:

show sequence

AGCGCAGGGCCCAGCCCGGGAGCCGCTGGAGCAGGGCCTGCGATGGAGCCTGCAGCCCCGGGTC
GCGTCCCTCCCTGAGCGCCCCCGTCGGCGGCCATGCTGCCCCGAGGGCGCCCCCGGGCGCTGGG
GGCCGCCGCGCTGTTGCTGCTGCTGCTGCTGCTCGGATTCCTCCTGTTCGGTGGGGACCTGGGG
TGTGAGCGCCGCGAGCCTGGCGGGCGAGCGGGGGCCCCGGGATGCTTCCCCGGCCCGCTCATGC
CACGTGTCCCCCCAGACGGGAGGCTGCGGAGAGCCGCCGCCCTCGACGGAGACCCGGGGGCCGG
CCCCGGGGACCACAACCGCTCCGACTGCGGCCCGCAGCCGCCGCCGCCGCCCAAGTGCGAGCTC
TTGCATGTGGCCATCGTGTGTGCGGGGCATAACTCCAGCCGAGACGTCATCACCCTGGTGAAGT
CCATGCTCTTCTACAGGAAAAATCCACTGCACCTCCACTTGGTGACTGACGCCGTGGCCAGAAA
CATCCTGGAGACGCTCTTCCACACATGGATGGTGCCTGCTGTCCGTGTCAGCTTTTATCATGCC
GACCAGCTCAAGCCCCAGGTCTCCTGGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAA
TGAAGCTGGTGCTGCCCAGTGCCTTGCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGA
TGTCACCTTCGCCTCTGACATCTCGGAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAG
GCGATCGGTCTTGTGGAGAACCAGAGTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGC
CCTGGCCTGCCTTGGGCCGGGGATTTAACACAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCG
GCAGGCTGGCTGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCC
ACCTCACTGGCTGACCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGCAGC
GTCTGCCTTGTGTCTGGAATGTGCAGCTGTCAGATCACACACTGGCCGAGCGCTGCTACTCTGA
GGCGTCTGACCTCAAGGTGATCCACTGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAGCAT
GTGGAATTCTTCCGCAATTTCTACCTGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGAGAG
AGCTCTTTGTGTGCCCCAGCCAGCCCCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGCACA
ACTGGACGAGGAAGACCCCTGCTTTGAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTGCAT
GTCACTTTCCTGCCCCATGAACCGCCACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCCAGC
TGTCCATGGACCGGACGTGGCCTACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCGTCAAC
CAGCTTCGCAACGTGGCCTTGGCCCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACATTGACT
TCCTGCCTGCCTATTCTCTCTACGACTACCTCAGGGCCTCCATTGAGCAGCTGGGGCTGGGCAG
CCGGCGCAAGGCAGCACTGGTGGTGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCTTCCCC
CATTCCAAGGTGGAGCTGTTGGCCTTGCTGGATGCGGGCACTCTCTACACCTTCAGGTACCACG
AGTGGCCCCGAGGCCACGCACCCACAGACTATGCCCGCTGGCGGGAGGCTCAGGCCCCGTACCG
TGTGCAATGGGCGGCCAACTATGAACCCTACGTGGTGGTGCCACGAGACTGTCCCCGCTATGAT
CCTCGCTTTGTGGGCTTCGGCTGGAACAAAGTGGCCCACATTGTGGAGCTGGATGCCCAGGAAT
ATGAGCTCCTGGTGCTGCCCGAGGCCTTCACCATCCATCTGCCCCACGCTCCAAGCCTGGACAT
CTCCCGCTTCCGCTCCAGCCCCACCTATCGTGACTGCCTCCAGGCCCTCAAGGACGAATTCCAC
CAGGACTTGTCCCGCCACCATGGGGCTGCTGCCCTCAAATACCTCCCAGCCCTGCAGCAGCCCC
AGAGCCCTGCCCGAGGCTGAGGCTGGGCCGGCGCTGCCCCTCATCTTAGCATTGGGCAGACACC
AGGGCAACCTGCCCTCCGCCATCCCTGCTATTTAAATTATTTAAGGTCTCTGGGAAGGGCTGGG
GCAGAGCATCTGTGGGGTGGGGTCTTCCCCTTGCTGCTATTGTATGGCTGGGGACTGGTCTCTC
TCTGCCCCAGCCAGTTTGGGGCTGGTTCCCCCATCTTGAATTGTTTATCCCTTTTTCATAATTA
AAGTTTTAAAACATC

hide sequence

RefSeq Acc Id:

XM_011519891 ⟹ XP_011518193

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

Sequence:

show sequence

AGCGCAGGGCCCAGCCCGGGAGCCGCTGGAGCAGGGCCTGCGATGGAGCCTGCAGCCCCGGGTC
GCGTCCCTCCCTGAGCGCCCCCGTCGGCGGCCATGCTGCCCCGAGGGCGCCCCCGGGCGCTGGG
GGCCGCCGCGCTGTTGCTGCTGCTGCTGCTGCTCGGATTCCTCCTGTTCGGTGGGGACCTGGGG
TGTGAGCGCCGCGAGCCTGGCGGGCGAGCGGGGGCCCCGGGATGCTTCCCCGGCCCGCTCATGC
CACGTGTCCCCCCAGACGGGAGGCTGCGGAGAGCCGCCGCCCTCGACGGAGACCCGGGGGCCGG
CCCCGGGGACCACAACCGCTCCGACTGCGGCCCGCAGCCGCCGCCGCCGCCCAAGTGCGAGCTC
TTGCATGTGGCCATCGTGTGTGCGGGGCATAACTCCAGCCGAGACGTCATCACCCTGGTGAAGT
CCATGCTCTTCTACAGGAAAAATCCACTGCACCTCCACTTGGTGACTGACGCCGTGGCCAGAAA
CATCCTGGAGACGCTCTTCCACACATGGATGGTGCCTGCTGTCCGTGTCAGCTTTTATCATGCC
GACCAGCTCAAGCCCCAGGTCTCCTGGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAA
TGAAGCTGGTGCTGCCCAGTGCCTTGCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGA
TGTCACCTTCGCCTCTGACATCTCGGAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAG
GCGATCGGTCTTGTGGAGAACCAGAGTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGC
CCTGGCCTGCCTTGGGCCGGGGATTTAACACAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCG
GCAGGCTGGCTGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCC
ACCTCACTGGCTGACCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGCAGC
GTCTGCCTTGTGTCTGGAATGTGCAGCTGTCAGATCACACACTGGCCGAGCGCTGCTACTCTGA
GGCGTCTGACCTCAAGGTGATCCACTGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAGCAT
GTGGAATTCTTCCGCAATTTCTACCTGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGAGAG
AGCTCTTTGTGTGCCCCAGCCAGCCCCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGCACA
ACTGGACGAGGAAGACCCCTGCTTTGAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTGCAT
GTCACTTTCCTGCCCCATGAACCGCCACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCCAGC
TGTCCATGGACCGGCTGCAGATGTTGGAAGCCCTGTGCAGGCACTGGCCTGGCCCCATGAGCCT
GGCCTTGTACCTGACAGACGCAGAAGCTCAGCAGTTCCTGCATTTCGTCGAGGCCTCACCAGTG
CTTGCTGCCCGGCAGGACGTGGCCTACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCGTCA
ACCAGCTTCGCAACGTGGCCTTGGCCCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACATTGA
CTTCCTGCCTGCCTATTCTCTCTACGACTACCTCAGGGCCTCCATTGAGCAGCTGGGGCTGGGC
AGCCGGCGCAAGGCAGCACTGGTGGTGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCTTCC
CCCATTCCAAGGTGGAGCTGTTGGCCTTGCTGGATGCGGGCACTCTCTACACCTTCAGGAATAT
GAGCTCCTGGTGCTGCCCGAGGCCTTCACCATCCATCTGCCCCACGCTCCAAGCCTGGACATCT
CCCGCTTCCGCTCCAGCCCCACCTATCGTGACTGCCTCCAGGCCCTCAAGGACGAATTCCACCA
GGACTTGTCCCGCCACCATGGGGCTGCTGCCCTCAAATACCTCCCAGCCCTGCAGCAGCCCCAG
AGCCCTGCCCGAGGCTGAGGCTGGGCCGGCGCTGCCCCTCATCTTAGCATTGGGCAGACACCAG
GGCAACCTGCCCTCCGCCATCCCTGCTATTTAAATTATTTAAGGTCTCTGGGAAGGGCTGGGGC
AGAGCATCTGTGGGGTGGGGTCTTCCCCTTGCTGCTATTGTATGGCTGGGGACTGGTCTCTCTC
TGCCCCAGCCAGTTTGGGGCTGGTTCCCCCATCTTGAATTGTTTATCCCTTTTTCATAATTAAA
GTTTTAAAACATC

hide sequence

RefSeq Acc Id:

XM_011519892 ⟹ XP_011518194

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

Sequence:

show sequence

AGCGCAGGGCCCAGCCCGGGAGCCGCTGGAGCAGGGCCTGCGATGGAGCCTGCAGCCCCGGGTC
GCGTCCCTCCCTGAGCGCCCCCGTCGGCGGCCATGCTGCCCCGAGGGCGCCCCCGGGCGCTGGG
GGCCGCCGCGCTGTTGCTGCTGCTGCTGCTGCTCGGATTCCTCCTGTTCGGTGGGGACCTGGGG
TGTGAGCGCCGCGAGCCTGGCGGGCGAGCGGGGGCCCCGGGATGCTTCCCCGGCCCGCTCATGC
CACGTGTCCCCCCAGACGGGAGGCTGCGGAGAGCCGCCGCCCTCGACGGAGACCCGGGGGCCGG
CCCCGGGGACCACAACCGCTCCGACTGCGGCCCGCAGCCGCCGCCGCCGCCCAAGTGCGAGCTC
TTGCATGTGGCCATCGTGTGTGCGGGGCATAACTCCAGCCGAGACGTCATCACCCTGGTGAAGT
CCATGCTCTTCTACAGGAAAAATCCACTGCACCTCCACTTGGTGACTGACGCCGTGGCCAGAAA
CATCCTGGAGACGCTCTTCCACACATGGATGGTGCCTGCTGTCCGTGTCAGCTTTTATCATGCC
GACCAGCTCAAGCCCCAGGTCTCCTGGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAA
TGAAGCTGGTGCTGCCCAGTGCCTTGCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGA
TGTCACCTTCGCCTCTGACATCTCGGAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAG
GCGATCGGTCTTGTGGAGAACCAGAGTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGC
CCTGGCCTGCCTTGGGCCGGGGATTTAACACAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCG
GCAGGCTGGCTGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCC
ACCTCACTGGCTGACCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGCAGC
GTCTGCCTTGTGTCTGGAATGTGCAGCTGTCAGATCACACACTGGCCGAGCGCTGCTACTCTGA
GGCGTCTGACCTCAAGGTGATCCACTGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAGCAT
GTGGAATTCTTCCGCAATTTCTACCTGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGAGAG
AGCTCTTTGTGTGCCCCAGCCAGCCCCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGCACA
ACTGGACGAGGAAGACCCCTGCTTTGAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTGCAT
GTCACTTTCCTGCCCCATGAACCGCCACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCCAGC
TGTCCATGGACCGGCTGCAGATGTTGGAAGCCCTGTGCAGGCACTGGCCTGGCCCCATGAGCCT
GGCCTTGTACCTGACAGACGCAGAAGCTCAGCAGTTCCTGCATTTCGTCGAGGCCTCACCAGTG
CTTGCTGCCCGGCAGGACGTGGCCTACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCGTCA
ACCAGCTTCGCAACGTGGCCTTGGCCCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACATTGA
CTTCCTGCCTGCCTATTCTCTCTACGACTACCTCAGGGCCTCCATTGAGCAGCTGGGGCTGGGC
AGCCGGCGCAAGGCAGCACTGGTGGTGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCTTCC
CCCATTCCAAGGTGGAGCTGTTGGCCTTGCTGGATGCGGGCACTCTCTACACCTTCAGGTACCA
CGAGTGGCCCCGAGGCCACGCACCCACAGACTATGCCCGCTGGCGGGAGGCTCAGGCCCCGTAC
CGTGTGCAATGGGCGGCCAACTATGAACCCTACGTGGTGGTGCCACGAGACTGTCCCCGCTATG
ATCCTCGCTTTGTGGGCTTCGGCTGGAACAAAGTGGCCCACATTGTGGAGCTGGATGCCCAGCT
CTCAGGGGCTACAGGGTAAGCCTGTTCTCTGGAGCTGCACCTTCCCCGCAGGCCAGGCAAGCCA
GGCAGCCACTGCTC

hide sequence

RefSeq Acc Id:

XM_011519893 ⟹ XP_011518195

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

Sequence:

show sequence

AGCGCAGGGCCCAGCCCGGGAGCCGCTGGAGCAGGGCCTGCGATGGAGCCTGCAGCCCCGGGTC
GCGTCCCTCCCTGAGCGCCCCCGTCGGCGGCCATGCTGCCCCGAGGGCGCCCCCGGGCGCTGGG
GGCCGCCGCGCTGTTGCTGCTGCTGCTGCTGCTCGGATTCCTCCTGTTCGGTGGGGACCTGGGG
TGTGAGCGCCGCGAGCCTGGCGGGCGAGCGGGGGCCCCGGGATGCTTCCCCGGCCCGCTCATGC
CACGTGTCCCCCCAGACGGGAGGCTGCGGAGAGCCGCCGCCCTCGACGGAGACCCGGGGGCCGG
CCCCGGGGACCACAACCGCTCCGACTGCGGCCCGCAGCCGCCGCCGCCGCCCAAGTGCGAGCTC
TTGCATGTGGCCATCGTGTGTGCGGGGCATAACTCCAGCCGAGACGTCATCACCCTGGTGAAGT
CCATGCTCTTCTACAGGAAAAATCCACTGCACCTCCACTTGGTGACTGACGCCGTGGCCAGAAA
CATCCTGGAGACGCTCTTCCACACATGGATGGTGCCTGCTGTCCGTGTCAGCTTTTATCATGCC
GACCAGCTCAAGCCCCAGGTCTCCTGGATCCCCAACAAGCACTACTCCGGCCTCTATGGGCTAA
TGAAGCTGGTGCTGCCCAGTGCCTTGCCTGCTGAGCTGGCCCGCGTCATTGTCCTGGACACGGA
TGTCACCTTCGCCTCTGACATCTCGGAGCTCTGGGCCCTCTTTGCTCACTTTTCTGACACGCAG
GCGATCGGTCTTGTGGAGAACCAGAGTGACTGGTACCTGGGCAACCTCTGGAAGAACCACAGGC
CCTGGCCTGCCTTGGGCCGGGGATTTAACACAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCG
GCAGGCTGGCTGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCC
ACCTCACTGGCTGACCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCGGGGCTAGTGCAGC
GTCTGCCTTGTGTCTGGAATGTGCAGCTGTCAGATCACACACTGGCCGAGCGCTGCTACTCTGA
GGCGTCTGACCTCAAGGTGATCCACTGGAACTCACCAAAGAAGCTTCGGGTGAAGAACAAGCAT
GTGGAATTCTTCCGCAATTTCTACCTGACCTTCCTGGAGTACGATGGGAACCTGCTGCGGAGAG
AGCTCTTTGTGTGCCCCAGCCAGCCCCCACCTGGTGCTGAGCAGTTGCAGCAGGCCCTGGCACA
ACTGGACGAGGAAGACCCCTGCTTTGAGTTCCGGCAGCAGCAGCTCACTGTGCACCGTGTGCAT
GTCACTTTCCTGCCCCATGAACCGCCACCCCCCCGGCCTCACGATGTCACCCTTGTGGCCCAGC
TGTCCATGGACCGGACGTGGCCTACCATGTGGTGTACCGTGAGGGGCCCCTATACCCCGTCAAC
CAGCTTCGCAACGTGGCCTTGGCCCAGGCCCTCACGCCTTACGTCTTCCTCAGTGACATTGACT
TCCTGCCTGCCTATTCTCTCTACGACTACCTCAGGGCCTCCATTGAGCAGCTGGGGCTGGGCAG
CCGGCGCAAGGCAGCACTGGTGGTGCCGGCATTCGAGACCCTGCGCTACCGCTTCAGCTTCCCC
CATTCCAAGGTGGAGCTGTTGGCCTTGCTGGATGCGGGCACTCTCTACACCTTCAGGAATATGA
GCTCCTGGTGCTGCCCGAGGCCTTCACCATCCATCTGCCCCACGCTCCAAGCCTGGACATCTCC
CGCTTCCGCTCCAGCCCCACCTATCGTGACTGCCTCCAGGCCCTCAAGGACGAATTCCACCAGG
ACTTGTCCCGCCACCATGGGGCTGCTGCCCTCAAATACCTCCCAGCCCTGCAGCAGCCCCAGAG
CCCTGCCCGAGGCTGAGGCTGGGCCGGCGCTGCCCCTCATCTTAGCATTGGGCAGACACCAGGG
CAACCTGCCCTCCGCCATCCCTGCTATTTAAATTATTTAAGGTCTCTGGGAAGGGCTGGGGCAG
AGCATCTGTGGGGTGGGGTCTTCCCCTTGCTGCTATTGTATGGCTGGGGACTGGTCTCTCTCTG
CCCCAGCCAGTTTGGGGCTGGTTCCCCCATCTTGAATTGTTTATCCCTTTTTCATAATTAAAGT
TTTAAAACATC

hide sequence

RefSeq Acc Id:

XM_047426344 ⟹ XP_047282300

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

RefSeq Acc Id:

XM_047426345 ⟹ XP_047282301

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

RefSeq Acc Id:

XM_047426346 ⟹ XP_047282302

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

RefSeq Acc Id:

XM_047426347 ⟹ XP_047282303

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

RefSeq Acc Id:

XM_047426348 ⟹ XP_047282304

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

RefSeq Acc Id:

XM_047426349 ⟹ XP_047282305

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,656 - 45,929,096 (+)	NCBI

RefSeq Acc Id:

XM_054367622 ⟹ XP_054223597

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367623 ⟹ XP_054223598

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367624 ⟹ XP_054223599

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367625 ⟹ XP_054223600

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367626 ⟹ XP_054223601

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367627 ⟹ XP_054223602

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367628 ⟹ XP_054223603

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367629 ⟹ XP_054223604

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367630 ⟹ XP_054223605

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367631 ⟹ XP_054223606

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367632 ⟹ XP_054223607

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367633 ⟹ XP_054223608

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367634 ⟹ XP_054223609

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367635 ⟹ XP_054223610

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,083,983 (+)	NCBI

RefSeq Acc Id:

XM_054367636 ⟹ XP_054223611

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,078,583 - 46,085,010 (+)	NCBI

RefSeq Acc Id:

XM_054367637 ⟹ XP_054223612

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	46,080,420 - 46,085,010 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001287650	(Get FASTA)	NCBI Sequence Viewer
	NP_001287651	(Get FASTA)	NCBI Sequence Viewer
	NP_689525	(Get FASTA)	NCBI Sequence Viewer
	XP_005252844	(Get FASTA)	NCBI Sequence Viewer
	XP_006718203	(Get FASTA)	NCBI Sequence Viewer
	XP_006718204	(Get FASTA)	NCBI Sequence Viewer
	XP_011518188	(Get FASTA)	NCBI Sequence Viewer
	XP_011518190	(Get FASTA)	NCBI Sequence Viewer
	XP_011518191	(Get FASTA)	NCBI Sequence Viewer
	XP_011518192	(Get FASTA)	NCBI Sequence Viewer
	XP_011518193	(Get FASTA)	NCBI Sequence Viewer
	XP_011518194	(Get FASTA)	NCBI Sequence Viewer
	XP_011518195	(Get FASTA)	NCBI Sequence Viewer
	XP_047282300	(Get FASTA)	NCBI Sequence Viewer
	XP_047282301	(Get FASTA)	NCBI Sequence Viewer
	XP_047282302	(Get FASTA)	NCBI Sequence Viewer
	XP_047282303	(Get FASTA)	NCBI Sequence Viewer
	XP_047282304	(Get FASTA)	NCBI Sequence Viewer
	XP_047282305	(Get FASTA)	NCBI Sequence Viewer
	XP_054223597	(Get FASTA)	NCBI Sequence Viewer
	XP_054223598	(Get FASTA)	NCBI Sequence Viewer
	XP_054223599	(Get FASTA)	NCBI Sequence Viewer
	XP_054223600	(Get FASTA)	NCBI Sequence Viewer
	XP_054223601	(Get FASTA)	NCBI Sequence Viewer
	XP_054223602	(Get FASTA)	NCBI Sequence Viewer
	XP_054223603	(Get FASTA)	NCBI Sequence Viewer
	XP_054223604	(Get FASTA)	NCBI Sequence Viewer
	XP_054223605	(Get FASTA)	NCBI Sequence Viewer
	XP_054223606	(Get FASTA)	NCBI Sequence Viewer
	XP_054223607	(Get FASTA)	NCBI Sequence Viewer
	XP_054223608	(Get FASTA)	NCBI Sequence Viewer
	XP_054223609	(Get FASTA)	NCBI Sequence Viewer
	XP_054223610	(Get FASTA)	NCBI Sequence Viewer
	XP_054223611	(Get FASTA)	NCBI Sequence Viewer
	XP_054223612	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAG23791	(Get FASTA)	NCBI Sequence Viewer
	AAH37291	(Get FASTA)	NCBI Sequence Viewer
	BAC03909	(Get FASTA)	NCBI Sequence Viewer
	BAC04675	(Get FASTA)	NCBI Sequence Viewer
	BAG51581	(Get FASTA)	NCBI Sequence Viewer
	CCQ43849	(Get FASTA)	NCBI Sequence Viewer
	EAW68020	(Get FASTA)	NCBI Sequence Viewer
	EAW68021	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000324570.5
	ENSP00000385235
	ENSP00000385235.1
	ENSP00000431932
	ENSP00000431932.1
	ENSP00000432869
	ENSP00000432869.1
	ENSP00000433328.1
	ENSP00000434325.1
GenBank Protein	Q8N3Y3	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_689525 ⟸ NM_152312
- Peptide Label:	isoform a precursor
- UniProtKB:	Q8NAK3 (UniProtKB/Swiss-Prot), Q8N8Y6 (UniProtKB/Swiss-Prot), A6NN75 (UniProtKB/Swiss-Prot), Q8WY62 (UniProtKB/Swiss-Prot), Q8N3Y3 (UniProtKB/Swiss-Prot), B3KP69 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLPRGRPRALGAAALLLLLLLLGFLLFGGDLGCERREPGGRAGAPGCFPGPLMPRVPPDGRLRR AAALDGDPGAGPGDHNRSDCGPQPPPPPKCELLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLH LHLVTDAVARNILETLFHTWMVPAVRVSFYHADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPA ELARVIVLDTDVTFASDISELWALFAHFSDTQAIGLVENQSDWYLGNLWKNHRPWPALGRGFNT GVILLRLDRLRQAGWEQMWRLTARRELLSLPATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLS DHTLAERCYSEASDLKVIHWNSPKKLRVKNKHVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPP GAEQLQQALAQLDEEDPCFEFRQQQLTVHRVHVTFLPHEPPPPRPHDVTLVAQLSMDRLQMLEA LCRHWPGPMSLALYLTDAEAQQFLHFVEASPVLAARQDVAYHVVYREGPLYPVNQLRNVALAQA LTPYVFLSDIDFLPAYSLYDYLRASIEQLGLGSRRKAALVVPAFETLRYRFSFPHSKVELLALL DAGTLYTFRYHEWPRGHAPTDYARWREAQAPYRVQWAANYEPYVVVPRDCPRYDPRFVGFGWNK VAHIVELDAQEYELLVLPEAFTIHLPHAPSLDISRFRSSPTYRDCLQALKDEFHQDLSRHHGAA ALKYLPALQQPQSPARG hide sequence

RefSeq Acc Id:

XP_005252844 ⟸ XM_005252787

- Peptide Label:

isoform X16

- Sequence:

show sequence

MSPSPLTSRSSGPSLLTFLTRRRSVLWRTRVTGTWATSGRTTGPGLPWAGDLTQDIFNAVIKEH
PGLVQRLPCVWNVQLSDHTLAERCYSEASDLKVIHWNSPKKLRVKNKHVEFFRNFYLTFLEYDG
NLLRRELFVCPSQPPPGAEQLQQALAQLDEEDPCFEFRQQQLTVHRVHVTFLPHEPPPPRPHDV
TLVAQLSMDRLQMLEALCRHWPGPMSLALYLTDAEAQQFLHFVEASPVLAARQDVAYHVVYREG
PLYPVNQLRNVALAQALTPYVFLSDIDFLPAYSLYDYLRASIEQLGLGSRRKAALVVPAFETLR
YRFSFPHSKVELLALLDAGTLYTFRYHEWPRGHAPTDYARWREAQAPYRVQWAANYEPYVVVPR
DCPRYDPRFVGFGWNKVAHIVELDAQARQARQPLLLCPTLQEYELLVLPEAFTIHLPHAPSLDI
SRFRSSPTYRDCLQALKDEFHQDLSRHHGAAALKYLPALQQPQSPARG

hide sequence

RefSeq Acc Id:	XP_006718203 ⟸ XM_006718140
- Peptide Label:	isoform X7
- UniProtKB:	E9PIZ2 (UniProtKB/TrEMBL), B3KP69 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLPRGRPRALGAAALLLLLLLLGFLLFDGRLRRAAALDGDPGAGPGDHNRSDCGPQPPPPPKCE LLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLHLHLVTDAVARNILETLFHTWMVPAVRVSFYH ADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPAELARVIVLDTDVTFASDISELWALFAHFSDT QAIGLVENQSDWYLGNLWKNHRPWPALGRGFNTGVILLRLDRLRQAGWEQMWRLTARRELLSLP ATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLSDHTLAERCYSEASDLKVIHWNSPKKLRVKNK HVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPPGAEQLQQALAQLDEEDPCFEFRQQQLTVHRV HVTFLPHEPPPPRPHDVTLVAQLSMDRLQMLEALCRHWPGPMSLALYLTDAEAQQFLHFVEASP VLAARQDVAYHVVYREGPLYPVNQLRNVALAQALTPYVFLSDIDFLPAYSLYDYLRASIEQLGL GSRRKAALVVPAFETLRYRFSFPHSKVELLALLDAGTLYTFRYHEWPRGHAPTDYARWREAQAP YRVQWAANYEPYVVVPRDCPRYDPRFVGFGWNKVAHIVELDAQEYELLVLPEAFTIHLPHAPSL DISRFRSSPTYRDCLQALKDEFHQDLSRHHGAAALKYLPALQQPQSPARG hide sequence

RefSeq Acc Id:

XP_006718204 ⟸ XM_006718141

- Peptide Label:

isoform X14

- Sequence:

show sequence

MLPRGRPRALGAAALLLLLLLLGFLLFGGDLGCERREPGGRAGAPGCFPGPLMPRVPPDGRLRR
AAALDGDPGAGPGDHNRSDCGPQPPPPPKCELLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLH
LHLVTDAVARNILETLFHTWMVPAVRVSFYHADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPA
ELARVIVLDTDVTFASDISELWALFAHFSDTQAIGLVENQSDWYLGNLWKNHRPWPALGRGFNT
GVILLRLDRLRQAGWEQMWRLTARRELLSLPATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLS
DHTLAERCYSEASDLKVIHWNSPKKLRVKNKHVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPP
GAEQLQQALAQLDEEDPCFEFRQQQLTVHRVHVTFLPHEPPPPRPHDVTLVAQLSMDRLQMLEA
LCRHWPGPMSLALYLTDAEAQQFLHFVEASPVLAARQDVAYHVVYREGPLYPVNQLRNVALAQA
LTPYVFLSDIDFLPAYSLYDYLREARAGFNSSSTCGCAHPSHQARWPMVV

hide sequence

RefSeq Acc Id:	NP_001287651 ⟸ NM_001300722
- Peptide Label:	isoform b
- UniProtKB:	B3KP69 (UniProtKB/TrEMBL), E9PIZ2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLPRGRPRALGAAALLLLLLLLGFLLFDGRLRRAAALDGDPGAGPGDHNRSDCGPQPPPPPKCE LLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLHLHLVTDAVARNILETLFHTWMVPAVRVSFYH ADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPAELARVIVLDTDVTFASDISELWALFAHFSDT QAIGLVENQSDWYLGNLWKNHRPWPALGRGFNTGVILLRLDRLRQAGWEQMWRLTARRELLSLP ATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLSDHTLAERCYSEASDLKVIHWNSPKKLRVKNK HVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPPGAEQLQQALAQLDEEDPCFEFRQQQLTVHRV HVTFLPHEPPPPRPHDVTLVAQLSMDRLQMLEALCRHWPGPMSLALYLTDAEAQQFLHFVEASP VLAARQDVAYHVVYREGPLYPVNQLRNVALAQALTPYVFLSDIDFLPAYSLYDYLRASIEQLGL GSRRKAALVVPAFETLRYRFSFPHSKVELLALLDAGTLYTFRYHEWPRGHAPTDYARWREAQAP YRVQWAANYEPYVVVPRDCPRYDPRFVGFGWNKVAHIVELDAQEYELLVLPEAFTIHLPHAPSL DISRFRSSPTYRDCLQALKDEFHQDLSRHHGAAALKYLPALQQPQSPARG hide sequence

RefSeq Acc Id:	NP_001287650 ⟸ NM_001300721
- Peptide Label:	isoform a precursor
- UniProtKB:	Q8NAK3 (UniProtKB/Swiss-Prot), Q8N8Y6 (UniProtKB/Swiss-Prot), A6NN75 (UniProtKB/Swiss-Prot), Q8WY62 (UniProtKB/Swiss-Prot), Q8N3Y3 (UniProtKB/Swiss-Prot), B3KP69 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLPRGRPRALGAAALLLLLLLLGFLLFGGDLGCERREPGGRAGAPGCFPGPLMPRVPPDGRLRR AAALDGDPGAGPGDHNRSDCGPQPPPPPKCELLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLH LHLVTDAVARNILETLFHTWMVPAVRVSFYHADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPA ELARVIVLDTDVTFASDISELWALFAHFSDTQAIGLVENQSDWYLGNLWKNHRPWPALGRGFNT GVILLRLDRLRQAGWEQMWRLTARRELLSLPATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLS DHTLAERCYSEASDLKVIHWNSPKKLRVKNKHVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPP GAEQLQQALAQLDEEDPCFEFRQQQLTVHRVHVTFLPHEPPPPRPHDVTLVAQLSMDRLQMLEA LCRHWPGPMSLALYLTDAEAQQFLHFVEASPVLAARQDVAYHVVYREGPLYPVNQLRNVALAQA LTPYVFLSDIDFLPAYSLYDYLRASIEQLGLGSRRKAALVVPAFETLRYRFSFPHSKVELLALL DAGTLYTFRYHEWPRGHAPTDYARWREAQAPYRVQWAANYEPYVVVPRDCPRYDPRFVGFGWNK VAHIVELDAQEYELLVLPEAFTIHLPHAPSLDISRFRSSPTYRDCLQALKDEFHQDLSRHHGAA ALKYLPALQQPQSPARG hide sequence

RefSeq Acc Id:	XP_011518191 ⟸ XM_011519889
- Peptide Label:	isoform X5
- UniProtKB:	B3KP69 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLPRGRPRALGAAALLLLLLLLGFLLFDGRLRRAAALDGDPGAGPGDHNRSDCGPQPPPPPKCE LLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLHLHLVTDAVARNILETLFHTWMVPAVRVSFYH ADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPAELARVIVLDTDVTFASDISELWALFAHFSDT QAIGLVENQSDWYLGNLWKNHRPWPALGRGFNTGVILLRLDRLRQAGWEQMWRLTARRELLSLP ATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLSDHTLAERCYSEASDLKVIHWNSPKKLRVKNK HVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPPGAEQLQQALAQLDEEDPCFEFRQQQLTVHRV HVTFLPHEPPPPRPHDVTLVAQLSMDRLQMLEALCRHWPGPMSLALYLTDAEAQQFLHFVEASP VLAARQDVAYHVVYREGPLYPVNQLRNVALAQALTPYVFLSDIDFLPAYSLYDYLRASIEQLGL GSRRKAALVVPAFETLRYRFSFPHSKVELLALLDAGTLYTFRYHEWPRGHAPTDYARWREAQAP YRVQWAANYEPYVVVPRDCPRYDPRFVGFGWNKVAHIVELDAQARQARQPLLLCPTLQEYELLV LPEAFTIHLPHAPSLDISRFRSSPTYRDCLQALKDEFHQDLSRHHGAAALKYLPALQQPQSPAR G hide sequence

RefSeq Acc Id:	XP_011518188 ⟸ XM_011519886
- Peptide Label:	isoform X2
- UniProtKB:	B3KP69 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLPRGRPRALGAAALLLLLLLLGFLLFGGDLGCERREPGGRAGAPGCFPGPLMPRVPPDGRLRR AAALDGDPGAGPGDHNRSDCGPQPPPPPKCELLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLH LHLVTDAVARNILETLFHTWMVPAVRVSFYHADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPA ELARVIVLDTDVTFASDISELWALFAHFSDTQAIGLVENQSDWYLGNLWKNHRPWPALGRGFNT GVILLRLDRLRQAGWEQMWRLTARRELLSLPATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLS DHTLAERCYSEASDLKVIHWNSPKKLRVKNKHVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPP GAEQLQQALAQLDEEDPCFEFRQQQLTVHRVHVTFLPHEPPPPRPHDVTLVAQLSMDRLQMLEA LCRHWPGPMSLALYLTDAEAQQFLHFVEASPVLAARQDVAYHVVYREGPLYPVNQLRNVALAQA LTPYVFLSDIDFLPAYSLYDYLRASIEQLGLGSRRKAALVVPAFETLRYRFSFPHSKVELLALL DAGTLYTFRYHEWPRGHAPTDYARWREAQAPYRVQWAANYEPYVVVPRDCPRYDPRFVGFGWNK VAHIVELDAQARQARQPLLLCPTLQEYELLVLPEAFTIHLPHAPSLDISRFRSSPTYRDCLQAL KDEFHQDLSRHHGAAALKYLPALQQPQSPARG hide sequence

RefSeq Acc Id:	XP_011518193 ⟸ XM_011519891
- Peptide Label:	isoform X8
- UniProtKB:	B3KP69 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLPRGRPRALGAAALLLLLLLLGFLLFGGDLGCERREPGGRAGAPGCFPGPLMPRVPPDGRLRR AAALDGDPGAGPGDHNRSDCGPQPPPPPKCELLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLH LHLVTDAVARNILETLFHTWMVPAVRVSFYHADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPA ELARVIVLDTDVTFASDISELWALFAHFSDTQAIGLVENQSDWYLGNLWKNHRPWPALGRGFNT GVILLRLDRLRQAGWEQMWRLTARRELLSLPATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLS DHTLAERCYSEASDLKVIHWNSPKKLRVKNKHVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPP GAEQLQQALAQLDEEDPCFEFRQQQLTVHRVHVTFLPHEPPPPRPHDVTLVAQLSMDRLQMLEA LCRHWPGPMSLALYLTDAEAQQFLHFVEASPVLAARQDVAYHVVYREGPLYPVNQLRNVALAQA LTPYVFLSDIDFLPAYSLYDYLRASIEQLGLGSRRKAALVVPAFETLRYRFSFPHSKVELLALL DAGTLYTFRNMSSWCCPRPSPSICPTLQAWTSPASAPAPPIVTASRPSRTNSTRTCPATMGLLP SNTSQPCSSPRALPEAEAGPALPLILALGRHQGNLPSAIPAI hide sequence

RefSeq Acc Id:

XP_011518190 ⟸ XM_011519888

- Peptide Label:

isoform X4

- Sequence:

show sequence

MLPRGRPRALGAAALLLLLLLLGFLLFGGDLGCERREPGGRAGAPGCFPGPLMPRVPPDGRLRR
AAALDGDPGAGPGDHNRSDCGPQPPPPPKCELLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLH
LHLVTDAVARNILETLFHTWMVPAVRVSFYHADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPA
ELARVIVLDTDVTFASDISELWALFAHFSDTQAIGLVENQSDWYLGNLWKNHRPWPALGRGFNT
GVILLRLDRLRQAGWEQMWRLTARRELLSLPATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLS
DHTLAERCYSEASDLKVIHWNSPKKLRVKNKHVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPP
GAEQLQQALAQLDEEDPCFEFRQQQLTVHRVHVTFLPHEPPPPRPHDVTLVAQLSMDRTWPTMW
CTVRGPYTPSTSFATWPWPRPSRLTSSSVTLTSCLPILSTTTSGPPLSSWGWAAGARQHWWCRH
SRPCATASASPIPRWSCWPCWMRALSTPSGTTSGPEATHPQTMPAGGRLRPRTVCNGRPTMNPT
WWCHETVPAMILALWASAGTKWPTLWSWMPRPGKPGSHCSSAPPCRNMSSWCCPRPSPSICPTL
QAWTSPASAPAPPIVTASRPSRTNSTRTCPATMGLLPSNTSQPCSSPRALPEAEAGPALPLILA
LGRHQGNLPSAIPAI

hide sequence

RefSeq Acc Id:

XP_011518192 ⟸ XM_011519890

- Peptide Label:

isoform X6

- Sequence:

show sequence

MLPRGRPRALGAAALLLLLLLLGFLLFGGDLGCERREPGGRAGAPGCFPGPLMPRVPPDGRLRR
AAALDGDPGAGPGDHNRSDCGPQPPPPPKCELLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLH
LHLVTDAVARNILETLFHTWMVPAVRVSFYHADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPA
ELARVIVLDTDVTFASDISELWALFAHFSDTQAIGLVENQSDWYLGNLWKNHRPWPALGRGFNT
GVILLRLDRLRQAGWEQMWRLTARRELLSLPATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLS
DHTLAERCYSEASDLKVIHWNSPKKLRVKNKHVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPP
GAEQLQQALAQLDEEDPCFEFRQQQLTVHRVHVTFLPHEPPPPRPHDVTLVAQLSMDRTWPTMW
CTVRGPYTPSTSFATWPWPRPSRLTSSSVTLTSCLPILSTTTSGPPLSSWGWAAGARQHWWCRH
SRPCATASASPIPRWSCWPCWMRALSTPSGTTSGPEATHPQTMPAGGRLRPRTVCNGRPTMNPT
WWCHETVPAMILALWASAGTKWPTLWSWMPRNMSSWCCPRPSPSICPTLQAWTSPASAPAPPIV
TASRPSRTNSTRTCPATMGLLPSNTSQPCSSPRALPEAEAGPALPLILALGRHQGNLPSAIPAI

hide sequence

RefSeq Acc Id:

XP_011518195 ⟸ XM_011519893

- Peptide Label:

isoform X15

- Sequence:

show sequence

MLPRGRPRALGAAALLLLLLLLGFLLFGGDLGCERREPGGRAGAPGCFPGPLMPRVPPDGRLRR
AAALDGDPGAGPGDHNRSDCGPQPPPPPKCELLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLH
LHLVTDAVARNILETLFHTWMVPAVRVSFYHADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPA
ELARVIVLDTDVTFASDISELWALFAHFSDTQAIGLVENQSDWYLGNLWKNHRPWPALGRGFNT
GVILLRLDRLRQAGWEQMWRLTARRELLSLPATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLS
DHTLAERCYSEASDLKVIHWNSPKKLRVKNKHVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPP
GAEQLQQALAQLDEEDPCFEFRQQQLTVHRVHVTFLPHEPPPPRPHDVTLVAQLSMDRTWPTMW
CTVRGPYTPSTSFATWPWPRPSRLTSSSVTLTSCLPILSTTTSGPPLSSWGWAAGARQHWWCRH
SRPCATASASPIPRWSCWPCWMRALSTPSGI

hide sequence

RefSeq Acc Id:	XP_011518194 ⟸ XM_011519892
- Peptide Label:	isoform X10
- UniProtKB:	B3KP69 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLPRGRPRALGAAALLLLLLLLGFLLFGGDLGCERREPGGRAGAPGCFPGPLMPRVPPDGRLRR AAALDGDPGAGPGDHNRSDCGPQPPPPPKCELLHVAIVCAGHNSSRDVITLVKSMLFYRKNPLH LHLVTDAVARNILETLFHTWMVPAVRVSFYHADQLKPQVSWIPNKHYSGLYGLMKLVLPSALPA ELARVIVLDTDVTFASDISELWALFAHFSDTQAIGLVENQSDWYLGNLWKNHRPWPALGRGFNT GVILLRLDRLRQAGWEQMWRLTARRELLSLPATSLADQDIFNAVIKEHPGLVQRLPCVWNVQLS DHTLAERCYSEASDLKVIHWNSPKKLRVKNKHVEFFRNFYLTFLEYDGNLLRRELFVCPSQPPP GAEQLQQALAQLDEEDPCFEFRQQQLTVHRVHVTFLPHEPPPPRPHDVTLVAQLSMDRLQMLEA LCRHWPGPMSLALYLTDAEAQQFLHFVEASPVLAARQDVAYHVVYREGPLYPVNQLRNVALAQA LTPYVFLSDIDFLPAYSLYDYLRASIEQLGLGSRRKAALVVPAFETLRYRFSFPHSKVELLALL DAGTLYTFRYHEWPRGHAPTDYARWREAQAPYRVQWAANYEPYVVVPRDCPRYDPRFVGFGWNK VAHIVELDAQLSGATG hide sequence

RefSeq Acc Id:

ENSP00000434325 ⟸ ENST00000531847

RefSeq Acc Id:

ENSP00000432869 ⟸ ENST00000531526

RefSeq Acc Id:

ENSP00000385235 ⟸ ENST00000401752

RefSeq Acc Id:

ENSP00000433328 ⟸ ENST00000534410

RefSeq Acc Id:

ENSP00000324570 ⟸ ENST00000325468

RefSeq Acc Id:

ENSP00000431932 ⟸ ENST00000529052

RefSeq Acc Id:	XP_047282300 ⟸ XM_047426344
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047282303 ⟸ XM_047426347
- Peptide Label:	isoform X11

RefSeq Acc Id:	XP_047282304 ⟸ XM_047426348
- Peptide Label:	isoform X12

RefSeq Acc Id:	XP_047282301 ⟸ XM_047426345
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047282305 ⟸ XM_047426349
- Peptide Label:	isoform X13

RefSeq Acc Id:	XP_047282302 ⟸ XM_047426346
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_054223606 ⟸ XM_054367631
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_054223598 ⟸ XM_054367623
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054223604 ⟸ XM_054367629
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_054223597 ⟸ XM_054367622
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054223607 ⟸ XM_054367632
- Peptide Label:	isoform X11

RefSeq Acc Id:	XP_054223600 ⟸ XM_054367625
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054223602 ⟸ XM_054367627
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054223611 ⟸ XM_054367636
- Peptide Label:	isoform X15

RefSeq Acc Id:	XP_054223608 ⟸ XM_054367633
- Peptide Label:	isoform X12

RefSeq Acc Id:	XP_054223601 ⟸ XM_054367626
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054223603 ⟸ XM_054367628
- Peptide Label:	isoform X7
- UniProtKB:	E9PIZ2 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054223599 ⟸ XM_054367624
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054223609 ⟸ XM_054367634
- Peptide Label:	isoform X13

RefSeq Acc Id:	XP_054223605 ⟸ XM_054367630
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_054223610 ⟸ XM_054367635
- Peptide Label:	isoform X14

RefSeq Acc Id:	XP_054223612 ⟸ XM_054367637
- Peptide Label:	isoform X16

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q8N3Y3-F1-model_v2	AlphaFold	Q8N3Y3	1-721	view protein structure

Promoters

RGD ID:

6788973

Promoter ID:

HG_KWN:12748

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

ENST00000389968, ENST00000401752

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	45,900,586 - 45,901,086 (+)	MPROMDB

RGD ID:

6788975

Promoter ID:

HG_KWN:12750

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562, Lymphoblastoid

Transcripts:

UC001NBZ.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	45,905,961 - 45,906,461 (+)	MPROMDB

RGD ID:

7220157

Promoter ID:

EPDNEW_H15824

Type:

initiation region

Name:

GYLTL1B_1

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	45,922,676 - 45,922,736	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:16522	AgrOrtholog
COSMIC	LARGE2	COSMIC
Ensembl Genes	ENSG00000165905	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000325468.9	UniProtKB/Swiss-Prot
	ENST00000401752	ENTREZGENE
	ENST00000401752.6	UniProtKB/Swiss-Prot
	ENST00000529052	ENTREZGENE
	ENST00000529052.5	UniProtKB/TrEMBL
	ENST00000531526	ENTREZGENE
	ENST00000531526.5	UniProtKB/Swiss-Prot
	ENST00000531847.1	UniProtKB/TrEMBL
	ENST00000534410.1	UniProtKB/TrEMBL
GTEx	ENSG00000165905	GTEx
HGNC ID	HGNC:16522	ENTREZGENE
Human Proteome Map	LARGE2	Human Proteome Map
InterPro	Glyco_trans_8	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Nucleotide-diphossugar_trans	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:120071	UniProtKB/Swiss-Prot
NCBI Gene	120071	ENTREZGENE
OMIM	609709	OMIM
PANTHER	GLYCOSYLTRANSFERASE-RELATED	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	LARGE XYLOSYL- AND GLUCURONYLTRANSFERASE 2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	Glyco_transf_49	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Glyco_transf_8	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA142671704	PharmGKB
Superfamily-SCOP	SSF53448	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A6NN75	ENTREZGENE
	B3KP69	ENTREZGENE, UniProtKB/TrEMBL
	E9PIZ2	ENTREZGENE, UniProtKB/TrEMBL
	H0YDB8_HUMAN	UniProtKB/TrEMBL
	H0YDU6_HUMAN	UniProtKB/TrEMBL
	LARG2_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
	Q8N8Y6	ENTREZGENE
	Q8NAK3	ENTREZGENE
	Q8WY62	ENTREZGENE
UniProt Secondary	A6NN75	UniProtKB/Swiss-Prot
	Q8N8Y6	UniProtKB/Swiss-Prot
	Q8NAK3	UniProtKB/Swiss-Prot
	Q8WY62	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-06-07	LARGE2	LARGE xylosyl- and glucuronyltransferase 2	GYLTL1B	glycosyltransferase-like 1B	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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