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Gene: PAIP2B (poly(A) binding protein interacting protein 2B) Homo sapiens

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Symbol:

PAIP2B

Name:

poly(A) binding protein interacting protein 2B

RGD ID:

1605487

HGNC Page

HGNC:29200

Description:

Enables mRNA regulatory element binding translation repressor activity. Involved in negative regulation of translational initiation. Predicted to be active in cytoplasm.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

KIAA1155; PABP-interacting protein 2B; PAIP-2B; poly(A)-binding protein-interacting protein 2B; polyadenylate-binding protein-interacting protein 2B

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	71,182,738 - 71,227,103 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	71,182,738 - 71,227,103 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	71,409,868 - 71,454,233 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	71,263,376 - 71,307,741 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	2	71,260,574 - 71,304,932 (-)	NCBI		Celera
Cytogenetic Map	2	p13.3	NCBI
HuRef	2	71,146,532 - 71,191,204 (-)	NCBI		HuRef
CHM1_1	2	71,339,205 - 71,383,545 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	2	71,193,792 - 71,238,156 (-)	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

dystonia (IAGP)

Methylmalonyl-CoA Epimerase Deficiency (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

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

2-hydroxypropanoic acid (EXP)

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

6-propyl-2-thiouracil (ISO)

aflatoxin B1 (EXP,ISO)

benzo[a]pyrene (EXP,ISO)

bis(2-ethylhexyl) phthalate (EXP)

bisphenol A (EXP)

bisphenol F (EXP,ISO)

cadmium dichloride (EXP)

carbon nanotube (ISO)

cisplatin (EXP)

dexamethasone (EXP)

dorsomorphin (EXP)

doxorubicin (EXP)

endosulfan (ISO)

ethanol (ISO)

folic acid (ISO)

herbicide (EXP)

hydroquinone (EXP)

indometacin (EXP)

lead(0) (EXP)

leflunomide (EXP)

lipopolysaccharide (EXP)

methimazole (ISO)

methylmercury chloride (EXP)

nickel atom (EXP)

niclosamide (EXP)

paracetamol (ISO)

perfluorononanoic acid (EXP)

rac-lactic acid (EXP)

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

SB 431542 (EXP)

silicon dioxide (EXP)

sodium arsenite (EXP)

sunitinib (EXP)

tetrachloromethane (ISO)

thimerosal (EXP)

titanium dioxide (ISO)

trichostatin A (EXP)

triclosan (EXP)

triphenyl phosphate (EXP)

triptonide (ISO)

tris(2-butoxyethyl) phosphate (EXP)

uranium atom (EXP)

valproic acid (EXP,ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

negative regulation of translation (IBA)

negative regulation of translational initiation (IDA,IEA)

regulation of translation (IEA)

Cellular Component

cytoplasm (IBA,IC)

Molecular Function

mRNA regulatory element binding translation repressor activity (IDA,IEA)

protein binding (IPI)

translation repressor activity (IBA)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Dystonia (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:10574461	PMID:16344560	PMID:16804161	PMID:17381337	PMID:21873635	PMID:26186194	PMID:28470677	PMID:28514442	PMID:29395067	PMID:33961781	PMID:35271311

Genomics

Comparative Map Data

PAIP2B
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	71,182,738 - 71,227,103 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	71,182,738 - 71,227,103 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	71,409,868 - 71,454,233 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	71,263,376 - 71,307,741 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	2	71,260,574 - 71,304,932 (-)	NCBI		Celera
Cytogenetic Map	2	p13.3	NCBI
HuRef	2	71,146,532 - 71,191,204 (-)	NCBI		HuRef
CHM1_1	2	71,339,205 - 71,383,545 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	2	71,193,792 - 71,238,156 (-)	NCBI		T2T-CHM13v2.0

Paip2b
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	6	83,783,040 - 83,808,723 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	6	83,782,383 - 83,808,723 (-)	Ensembl		GRCm39 Ensembl
GRCm38	6	83,806,058 - 83,831,741 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	6	83,805,401 - 83,831,741 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	6	83,756,052 - 83,781,735 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	6	83,771,721 - 83,797,322 (-)	NCBI		MGSCv36	mm8
Celera	6	85,789,017 - 85,814,725 (-)	NCBI		Celera
Cytogenetic Map	6	C3	NCBI
cM Map	6	35.97	NCBI

Paip2b
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	4	117,849,625 - 117,881,021 (-)	NCBI		GRCr8
mRatBN7.2	4	116,292,001 - 116,323,387 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	4	116,292,020 - 116,323,379 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	4	121,770,507 - 121,801,540 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	4	117,545,698 - 117,576,726 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	4	116,159,474 - 116,190,518 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	4	115,484,676 - 115,516,307 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	4	115,487,313 - 115,516,296 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	4	180,073,880 - 180,105,043 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	4	118,003,247 - 118,032,312 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	4	118,247,727 - 118,276,790 (-)	NCBI
Celera	4	105,284,575 - 105,315,731 (-)	NCBI		Celera
Cytogenetic Map	4	q34	NCBI

Paip2b
(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_004955424	14,156,768 - 14,190,865 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955424	14,157,358 - 14,190,865 (+)	NCBI	ChiLan1.0	ChiLan1.0

PAIP2B
(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	12	55,161,941 - 55,206,055 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	2A	55,164,684 - 55,208,798 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	2A	71,227,562 - 71,271,642 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	2A	72,728,012 - 72,772,036 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	2A	72,733,750 - 72,772,036 (-)	Ensembl	panpan1.1		panPan2

PAIP2B
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	17	51,381,891 - 51,388,964 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	17	51,385,194 - 51,413,360 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	17	51,093,113 - 51,101,812 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	17	52,291,532 - 52,324,245 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	17	52,291,546 - 52,324,229 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	17	51,318,027 - 51,326,716 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	17	51,389,806 - 51,398,503 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	17	51,964,551 - 51,973,260 (+)	NCBI		UU_Cfam_GSD_1.0

Paip2b
(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_024406292	13,337,941 - 13,374,264 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936491	15,202,794 - 15,233,652 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936491	15,197,028 - 15,233,652 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

PAIP2B
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	3	71,452,538 - 71,499,500 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	3	71,452,753 - 71,500,176 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	3	74,881,371 - 74,940,494 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

PAIP2B
(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	14	35,930,797 - 35,967,398 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	14	35,930,819 - 35,972,073 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666045	76,058,135 - 76,096,127 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Paip2b
(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_004624762	2,335,544 - 2,375,376 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624762	2,335,522 - 2,379,674 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in PAIP2B
9 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 2p13.3-13.2(chr2:70709155-72346899)x3	copy number gain	See cases [RCV000133956]	Chr2:70709155..72346899 [GRCh38] Chr2:70936287..72574028 [GRCh37] Chr2:70789795..72427536 [NCBI36] Chr2:2p13.3-13.2	uncertain significance
GRCh38/hg38 2p16.1-11.2(chr2:58279519-83586962)x3	copy number gain	See cases [RCV000136053]	Chr2:58279519..83586962 [GRCh38] Chr2:58506654..83814086 [GRCh37] Chr2:58360158..83667597 [NCBI36] Chr2:2p16.1-11.2	pathogenic
GRCh38/hg38 2p16.3-11.2(chr2:47620388-86702722)x3	copy number gain	See cases [RCV000137586]	Chr2:47620388..86702722 [GRCh38] Chr2:47847527..86929845 [GRCh37] Chr2:47701031..86783356 [NCBI36] Chr2:2p16.3-11.2	uncertain significance
GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3	copy number gain	See cases [RCV000141494]	Chr2:7495123..87705899 [GRCh38] Chr2:7635254..88005418 [GRCh37] Chr2:7552705..87786533 [NCBI36] Chr2:2p25.1-11.2	benign
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 2p15-11.2(chr2:62245236-86978895)x3	copy number gain	See cases [RCV000448688]	Chr2:62245236..86978895 [GRCh37] Chr2:2p15-11.2	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 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 2p13.3-13.2(chr2:71435253-71724760)x3	copy number gain	not provided [RCV000682051]	Chr2:71435253..71724760 [GRCh37] Chr2:2p13.3-13.2	uncertain significance
Single allele	deletion	not provided [RCV000714264]	Chr2:40608411..146900718 [GRCh37] Chr2:2p22.1-q22.3	likely pathogenic
Single allele	duplication	not provided [RCV000677942]	Chr2:63671346..85698002 [GRCh37] Chr2:2p15-11.2	pathogenic
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
GRCh37/hg19 2p13.3-13.2(chr2:71164124-71535431)x3	copy number gain	not provided [RCV000846600]	Chr2:71164124..71535431 [GRCh37] Chr2:2p13.3-13.2	uncertain significance
NM_020459.1(PAIP2B):c.66T>A (p.Ser22Arg)	single nucleotide variant	not specified [RCV004300328]	Chr2:71202524 [GRCh38] Chr2:71429654 [GRCh37] Chr2:2p13.3	uncertain significance
NC_000002.11:g.(?_71004499)_(74779761_?)del	deletion	Dystonic disorder [RCV003113211]\|Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency [RCV003113210]\|not provided [RCV003107716]	Chr2:71004499..74779761 [GRCh37] Chr2:2p13.3-13.1	pathogenic\|no classifications from unflagged records
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
NC_000002.11:g.(?_69240632)_(74779761_?)dup	duplication	not provided [RCV003122858]	Chr2:69240632..74779761 [GRCh37] Chr2:2p13.3-13.1	uncertain significance
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1	copy number loss	See cases [RCV002287563]	Chr2:11504318..111365996 [GRCh37] Chr2:2p25.1-q13	pathogenic
NM_020459.1(PAIP2B):c.105G>C (p.Met35Ile)	single nucleotide variant	not specified [RCV004139204]	Chr2:71202485 [GRCh38] Chr2:71429615 [GRCh37] Chr2:2p13.3	uncertain significance
NM_020459.1(PAIP2B):c.32C>T (p.Pro11Leu)	single nucleotide variant	not specified [RCV004113802]	Chr2:71202558 [GRCh38] Chr2:71429688 [GRCh37] Chr2:2p13.3	uncertain significance
NM_020459.1(PAIP2B):c.59G>A (p.Gly20Glu)	single nucleotide variant	not specified [RCV004207227]	Chr2:71202531 [GRCh38] Chr2:71429661 [GRCh37] Chr2:2p13.3	uncertain significance
GRCh37/hg19 2p13.3-12(chr2:71076472-76368354)x1	copy number loss	not specified [RCV003986388]	Chr2:71076472..76368354 [GRCh37] Chr2:2p13.3-12	likely pathogenic
NM_020459.1(PAIP2B):c.28T>C (p.Ser10Pro)	single nucleotide variant	not specified [RCV004499942]	Chr2:71202562 [GRCh38] Chr2:71429692 [GRCh37] Chr2:2p13.3	uncertain significance
NM_020459.1(PAIP2B):c.198T>G (p.Asp66Glu)	single nucleotide variant	not specified [RCV004650719]	Chr2:71189962 [GRCh38] Chr2:71417092 [GRCh37] Chr2:2p13.3	uncertain significance
NM_020459.1(PAIP2B):c.230G>A (p.Arg77Gln)	single nucleotide variant	not specified [RCV004839082]	Chr2:71189930 [GRCh38] Chr2:71417060 [GRCh37] Chr2:2p13.3	uncertain significance
NM_020459.1(PAIP2B):c.109A>T (p.Met37Leu)	single nucleotide variant	not specified [RCV004839083]	Chr2:71202481 [GRCh38] Chr2:71429611 [GRCh37] Chr2:2p13.3	uncertain significance

miRNA Target Status (No longer updated)

Predicted Target Of

	Summary Value
Count of predictions:	2295
Count of miRNA genes:	1071
Interacting mature miRNAs:	1307
Transcripts:	ENST00000244221
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597316985	GWAS1413059_H	age at onset, major depressive disorder QTL GWAS1413059 (human)		0.000002	age at onset, major depressive disorder		2	71215643	71215644	Human
597065493	GWAS1161567_H	overall survival, pancreatic carcinoma QTL GWAS1161567 (human)		0.000003	overall survival, pancreatic carcinoma		2	71220545	71220546	Human
596973069	GWAS1092588_H	age at onset, major depressive disorder QTL GWAS1092588 (human)		0.000002	age at onset, major depressive disorder		2	71215643	71215644	Human
407183742	GWAS832718_H	unipolar depression, age at onset QTL GWAS832718 (human)		0.000002	unipolar depression, age at onset		2	71215643	71215644	Human

Markers in Region

RH16647

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	71,411,347 - 71,411,490	UniSTS	GRCh37
GRCh37	2	71,312,463 - 71,312,606	UniSTS	GRCh37
Build 36	2	71,165,971 - 71,166,114	RGD	NCBI36
Celera	2	71,262,060 - 71,262,203	UniSTS
Celera	2	71,163,143 - 71,163,286	RGD
Cytogenetic Map	2	p13.3	UniSTS
HuRef	2	71,049,137 - 71,049,280	UniSTS
HuRef	2	71,148,018 - 71,148,161	UniSTS
GeneMap99-GB4 RH Map	2	220.18	UniSTS

RH36348

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	71,412,082 - 71,412,183	UniSTS	GRCh37
GRCh37	2	71,313,196 - 71,313,297	UniSTS	GRCh37
Build 36	2	71,166,704 - 71,166,805	RGD	NCBI36
Celera	2	71,262,795 - 71,262,896	UniSTS
Celera	2	71,163,876 - 71,163,977	RGD
Cytogenetic Map	2	p13.3	UniSTS
HuRef	2	71,049,871 - 71,049,972	UniSTS
HuRef	2	71,148,753 - 71,148,854	UniSTS
GeneMap99-GB4 RH Map	2	220.18	UniSTS

WI-14958

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	71,412,892 - 71,413,040	UniSTS	GRCh37
Build 36	2	71,266,400 - 71,266,548	RGD	NCBI36
Celera	2	71,263,605 - 71,263,753	RGD
Cytogenetic Map	2	p13.3	UniSTS
HuRef	2	71,149,563 - 71,149,711	UniSTS
GeneMap99-GB4 RH Map	2	223.62	UniSTS
Whitehead-RH Map	2	294.9	UniSTS

RH68850

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	71,414,467 - 71,414,593	UniSTS	GRCh37
Build 36	2	71,267,975 - 71,268,101	RGD	NCBI36
Celera	2	71,265,180 - 71,265,306	RGD
Cytogenetic Map	2	p13.3	UniSTS
HuRef	2	71,151,138 - 71,151,264	UniSTS
GeneMap99-GB4 RH Map	2	220.18	UniSTS

D11S2921

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	1	p36.1	UniSTS
Cytogenetic Map	3	p24.2	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	1	p36.31	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	7	p14.1	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	9	q22.33	UniSTS
Cytogenetic Map	15	q13.2	UniSTS
Cytogenetic Map	16	q24.3	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	19	q13.11	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	14	q13.2	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	10	q24.33	UniSTS
Cytogenetic Map	5	q23.3-q31.1	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	1	p32.3	UniSTS
Cytogenetic Map	17	q11	UniSTS
Cytogenetic Map	1	q24	UniSTS
Cytogenetic Map	11	q14	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	X	q13.1	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	2	q32.3	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	4	q32.1	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	13	q12	UniSTS
Cytogenetic Map	12	p13.31	UniSTS
Cytogenetic Map	3	p21.1	UniSTS
Cytogenetic Map	3	q12.3	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	6	q22	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	20	q11	UniSTS
Cytogenetic Map	8	q22.1	UniSTS
Cytogenetic Map	5	q23.3	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	11	q25	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	1	q32.3	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	12	q21.33	UniSTS
Cytogenetic Map	7	p22.3	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	X	p11.4-p11.3	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	1	q24.1	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	10	p15.1	UniSTS
Cytogenetic Map	18	p11.31	UniSTS
Cytogenetic Map	12	p13.32	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	11	q13.5	UniSTS
Cytogenetic Map	1	p22	UniSTS
Cytogenetic Map	2	q14	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	7	p22	UniSTS
Cytogenetic Map	14	q32.33	UniSTS
Cytogenetic Map	8	p11.21	UniSTS
Cytogenetic Map	8	q24.11	UniSTS
Cytogenetic Map	4	q12	UniSTS
Cytogenetic Map	9	q22.31	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	2	q33-q34	UniSTS
Cytogenetic Map	17	q22.2	UniSTS
Cytogenetic Map	8	q24.13	UniSTS
Cytogenetic Map	22	q11.2	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	Y	p11.2	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	2	q37	UniSTS
Cytogenetic Map	18	pter-p11.3	UniSTS
Cytogenetic Map	8	q22.3	UniSTS
Cytogenetic Map	6	p21.33	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	2	q21.3	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	X	q22.1	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	14	q32.12	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	4	q34.1	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	3	q13.31	UniSTS
Cytogenetic Map	7	q21.12	UniSTS
Cytogenetic Map	15	q22.2	UniSTS
Cytogenetic Map	8	p23.1	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	12	q23.2	UniSTS
Cytogenetic Map	6	p22	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	11	p13	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	16	p13.13	UniSTS
Cytogenetic Map	1	p34	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	12	q13	UniSTS
Cytogenetic Map	19	q13.31	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	4	p14	UniSTS
Cytogenetic Map	1	q44	UniSTS
Cytogenetic Map	19	p13.1-p12	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	8	q24	UniSTS
Cytogenetic Map	18	p11.31-p11.21	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	7	p21.2	UniSTS
Cytogenetic Map	12	q23-q24.1	UniSTS
Cytogenetic Map	15	q15.1	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	5	q14.1	UniSTS
Cytogenetic Map	5	p15.33	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	1	q42.1	UniSTS
Cytogenetic Map	12	p13	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	2	q12.3	UniSTS
Cytogenetic Map	19	q13.3-q13.4	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	5	q35	UniSTS
Cytogenetic Map	8	p23-p22	UniSTS
Cytogenetic Map	12	p11	UniSTS
Cytogenetic Map	17	q21-q22	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	11	p13-p12	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	2	q12.1	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	3	q26.32	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	10	q11.22	UniSTS
Cytogenetic Map	17	p12	UniSTS
Cytogenetic Map	3	p25.1	UniSTS
Cytogenetic Map	14	q32	UniSTS
Cytogenetic Map	5	q12-q13	UniSTS
Cytogenetic Map	6	p23	UniSTS
Cytogenetic Map	20	p12.3-p11.21	UniSTS
Cytogenetic Map	17	q11.2-q12	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	12	q13.3	UniSTS
Cytogenetic Map	10	q23-q24	UniSTS
Cytogenetic Map	14	q21.3	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	12	q13-q14	UniSTS
Cytogenetic Map	6	q14.1	UniSTS
Cytogenetic Map	3	q26.33	UniSTS
Cytogenetic Map	X	p22.2	UniSTS
Cytogenetic Map	1	p31	UniSTS
Cytogenetic Map	15	q15-q21.1	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	7	q21-q22	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	2	q33.3	UniSTS
Cytogenetic Map	11	q22.1	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	12	q22	UniSTS
Cytogenetic Map	21	p11.1	UniSTS
Cytogenetic Map	14	q23.2	UniSTS
Cytogenetic Map	6	p22.3-p22.1	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	6	q15	UniSTS
Cytogenetic Map	X	q25-q26.3	UniSTS
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	12	q24.31-q24.32	UniSTS
Cytogenetic Map	16	p12.3	UniSTS
Cytogenetic Map	9	q33.2	UniSTS
Cytogenetic Map	15	q23	UniSTS
Cytogenetic Map	12	p12.2-p11.2	UniSTS
Cytogenetic Map	2	q14.3	UniSTS
Cytogenetic Map	X	p11	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	20	q13.2	UniSTS
Cytogenetic Map	10	q26	UniSTS
Cytogenetic Map	6	q22.31	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	22	q13	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	18	p11.32	UniSTS
Cytogenetic Map	12	q15	UniSTS
Cytogenetic Map	X	q22.3	UniSTS
Cytogenetic Map	2	p25.3	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	3	q13.13	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	3	q27.3	UniSTS
Cytogenetic Map	4	p13	UniSTS
Cytogenetic Map	16	p12.1	UniSTS
Cytogenetic Map	14	q32.11	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	16	q12.1	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	9	q21.13	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	20	q13.1	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	10	q23.33	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	9	p24.1-p23	UniSTS
Cytogenetic Map	15	q22	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	X	q12-q13	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	14	q23	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	1	q42.1-q43	UniSTS
Cytogenetic Map	7	q31.1-q31.3	UniSTS
Cytogenetic Map	20	q11.21	UniSTS
Cytogenetic Map	20	q12-q13.12	UniSTS
Cytogenetic Map	1	q24-q25.3	UniSTS
Cytogenetic Map	20	p12.1	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	2	p13.3	UniSTS
Cytogenetic Map	6	q25.1-q26	UniSTS
Cytogenetic Map	12	q13.11-q14.3	UniSTS
Cytogenetic Map	7	p11	UniSTS
Cytogenetic Map	12	p11.22	UniSTS
Cytogenetic Map	17	q23.1	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	9	p11	UniSTS
Cytogenetic Map	6	p24.3	UniSTS
Cytogenetic Map	9	p24.1	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	6	p22.2	UniSTS
Cytogenetic Map	12	q24.2-q24.31	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	11	p11.11	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	11	q14.1	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	15	q22-q23	UniSTS
Cytogenetic Map	9	p21	UniSTS
Cytogenetic Map	15	q13.1	UniSTS
Cytogenetic Map	15	q22-qter	UniSTS
Cytogenetic Map	10	q25	UniSTS
Cytogenetic Map	6	p22.3	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	5	p15.1	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	22	q13.31	UniSTS
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	14	q24.1	UniSTS
Cytogenetic Map	13	q34	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	20	q11.23	UniSTS
Cytogenetic Map	1	q21.1	UniSTS
Cytogenetic Map	17	q24.3	UniSTS
Cytogenetic Map	16	q11.2	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	2	q23.3	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	18	q23	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	7	p21.1	UniSTS
Cytogenetic Map	2	q37.1	UniSTS
Cytogenetic Map	8	p11.2	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	2	q21.2	UniSTS
Cytogenetic Map	15	q13.3	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	3	p22.2	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	19	p13.2-cen	UniSTS
Cytogenetic Map	19	p13.3-p13.2	UniSTS
Cytogenetic Map	13	q32.3	UniSTS
Cytogenetic Map	9	q33	UniSTS
Cytogenetic Map	1	p36-p35	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	12	q23	UniSTS
Cytogenetic Map	21	q22.13	UniSTS
Cytogenetic Map	2	q24.2	UniSTS
Cytogenetic Map	7	q31.1-q31.2	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	X	q24	UniSTS
Cytogenetic Map	4	q25-q27	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	X	q26.2	UniSTS
Cytogenetic Map	8	q13.2	UniSTS
Cytogenetic Map	8	q13.1	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	5	q23.1	UniSTS
Cytogenetic Map	4	q13.3	UniSTS
Cytogenetic Map	3	p26.1	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	3	p22-p21.3	UniSTS
Cytogenetic Map	12	q	UniSTS
Cytogenetic Map	X	q21.3	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	20	p11	UniSTS
Cytogenetic Map	6	p12.3	UniSTS
Cytogenetic Map	5	p13.1-p12	UniSTS
Cytogenetic Map	1	p36.22	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	7	q21.13	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	3	p21.1-p14.3	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	7	q36.1	UniSTS
Cytogenetic Map	10	q24.31	UniSTS
Cytogenetic Map	2	p25.1-p24.1	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	13	q12.11	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	13	q14.13	UniSTS
Cytogenetic Map	11	p15	UniSTS
Cytogenetic Map	6	q14.3-q16.1	UniSTS
Cytogenetic Map	16	p13.2	UniSTS
Cytogenetic Map	16	q22.3	UniSTS
Cytogenetic Map	1	p32-p31	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	8	p11	UniSTS
Cytogenetic Map	6	q25	UniSTS
Cytogenetic Map	8	p11.23	UniSTS
Cytogenetic Map	9	p24.3	UniSTS
Cytogenetic Map	7	q35	UniSTS
Cytogenetic Map	11	q22.3	UniSTS
Cytogenetic Map	16	p12	UniSTS
Cytogenetic Map	6	q14.3	UniSTS
Cytogenetic Map	7	q36	UniSTS
Cytogenetic Map	1	q22	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	8	p12	UniSTS
Cytogenetic Map	13	q12.2	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	6	p21.2	UniSTS
Cytogenetic Map	18	q21.1	UniSTS
Cytogenetic Map	10	p11.21	UniSTS
Cytogenetic Map	10	p14	UniSTS
Cytogenetic Map	3	p26	UniSTS
Cytogenetic Map	9	q22.3	UniSTS
Cytogenetic Map	17	q21.1-q21.3	UniSTS
Cytogenetic Map	6	q11.1	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	3	q21.1	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	22	q13.1-q13.2	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	9	q32-q33.3	UniSTS
Cytogenetic Map	8	q21.2	UniSTS
Cytogenetic Map	18	q12.1	UniSTS
Cytogenetic Map	12	p13.2-p12.3	UniSTS
Cytogenetic Map	1	p36.3-p36.2	UniSTS
Cytogenetic Map	5	q11.2	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	3	q13.2	UniSTS
Cytogenetic Map	8	p22	UniSTS
Cytogenetic Map	1	q25.1	UniSTS
Cytogenetic Map	18	q21.32	UniSTS
Cytogenetic Map	17	q21.2	UniSTS
Cytogenetic Map	15	q26.2	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	5	p15.2	UniSTS
Cytogenetic Map	12	q23.1	UniSTS
Cytogenetic Map	10	q24.2	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	1	p22.2	UniSTS
Cytogenetic Map	7	q32	UniSTS
Cytogenetic Map	5	p13	UniSTS
Cytogenetic Map	16	q23.2	UniSTS
Cytogenetic Map	10	q24-q25	UniSTS
Cytogenetic Map	7	p11.1	UniSTS
Cytogenetic Map	14	q11.2-q21	UniSTS
Cytogenetic Map	14	q12	UniSTS
Cytogenetic Map	12	q24.13	UniSTS
Cytogenetic Map	10	q21-q22	UniSTS
Cytogenetic Map	4	q22	UniSTS
Cytogenetic Map	9	q22.2	UniSTS
Cytogenetic Map	10	q23.31	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	2	p24.1	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	7	p13-p11.1	UniSTS
Cytogenetic Map	7	q21.1-q22	UniSTS
Cytogenetic Map	1	p36.3	UniSTS
Cytogenetic Map	15	q26.1	UniSTS
Cytogenetic Map	2	q32.1	UniSTS
Cytogenetic Map	5	p14.3	UniSTS
Cytogenetic Map	X	p22.13	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
Cytogenetic Map	15	q	UniSTS
Cytogenetic Map	7	q	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	10	q23	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	10	q11.21	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	13	q22.1	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	9	p13.1	UniSTS
Cytogenetic Map	9	q34.13	UniSTS

RH36004

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	2	p13.3	UniSTS
GeneMap99-GB4 RH Map	2	231.98	UniSTS

Expression

RNA-SEQ Expression

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2436	2788	2253	4973	1724	2349	6	622	1941	463	2269	7293	6462	53	3734	1	852	1741	1617	174	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_020459	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005264310	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005264311	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011532842	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011532843	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054342025	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054342026	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054342027	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB032981	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC007878	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC007881	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC093654	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL110211	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471053	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA247526	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA346299	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000244221 ⟹ ENSP00000244221

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	71,182,738 - 71,227,103 (-)	Ensembl

RefSeq Acc Id:

NM_020459 ⟹ NP_065192

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	71,182,738 - 71,227,103 (-)	NCBI
GRCh37	2	71,409,868 - 71,454,233 (-)	RGD
Build 36	2	71,263,376 - 71,307,741 (-)	NCBI Archive
Celera	2	71,260,574 - 71,304,932 (-)	RGD
HuRef	2	71,146,532 - 71,191,204 (-)	RGD
CHM1_1	2	71,339,205 - 71,383,545 (-)	NCBI
T2T-CHM13v2.0	2	71,193,792 - 71,238,156 (-)	NCBI

Sequence:

show sequence

AGTGTGCAGTAAGAGATAACCTGGCAAGTGGTAGTGGCGCTTCTCGGGTGCTGTGCTTCACGTT
TTGGTACTAAAGGCCGAGACTGTTGTGGCGACGGCGACCTCTACGGCAACGGCTTAAGCTCTCG
GAGGAGTGGCAGAGTACGATCTGAAGGAGGGGCTTCTGGTTAGCCCAGGTTCCATCATAATGAA
TGGATCCAATATGGCAAATACATCACCGAGTGTAAAATCCAAAGAGGACCAGGGGTTAAGTGGG
CACGATGAAAAGGAAAACCCATTTGCAGAGTACATGTGGATGGAGAATGAAGAGGATTTCAACA
GACAGGTGGAGGAGGAACTGCAGGAGCAAGACTTCTTGGACCGCTGCTTCCAAGAGATGCTGGA
TGAAGAAGACCAAGACTGGTTTATTCCCTCACGAGACCTGCCTCAGGCCATGGGACAGTTGCAA
CAGCAGTTAAATGGACTGTCAGTCAGTGAAGGTCATGATTCTGAAGATATTTTGAGCAAAAGTA
ACCTGAACCCAGATGCCAAGGAGTTTATTCCAGGAGAGAAGTACTGAGCCGAGAAAGCTTTGAG
GAAGACTTGTCTGTCCCCACATCTGGGGATAGTAATGCACAAAATGGTGGAGCTGAAGAGGGGG
ATGGGGCGGGCGAGGGGTGCACAGCGGGAAGGGGAGTGGTGGTCTCACAATACTGTGACTCTGA
GTAACTAATATGCTCAGTCTTATTCTAAGCCTCTGAGTATTTCTATTTTGTTCTGCTGACTTTT
GTTTGGGGAGTTTCCTGTTTTGTTTTTTTAAATAGCTCTTTCGAGTTAAGGAAATTGCATTTTC
CCCCCTTCATCAGAAGTGTTCCGCGGTGTGTATTTAAACAAAATAAGCTGACTAAGAAAAACTG
GATATTTAGGAAATGCCCCTCTCACCCTGCTGTATACTTATCAGGGACAGTGAGCACCTGGAGA
GCTTTTTGTGGAATCTATTGAGTTGGATGGGAAAAGGGACAAGCAGAAAGAGCAGGTGGTGCAA
ACTGGAATTTGAGGCTCAGCTGCCCCACCCCCGGGGTCTCCTGCAATGAACTCGGATAACCAAT
GTGCTGTCAAGCCCTTGCCTGTTTGTCCTGAACCCCATTCAAGAAAACACAGACTTAAAGTACT
TAGTTTACAGTAACTTTTGATGATTGTTGAAAGTTGTAAATCAGAAGGTAGGGCTGTGATGGTG
GTTGTCACTTGAGTCATTTAGTTACTGTTGTCCTGTTCATAAGCCTGTGTTCACCACCACCATC
AGACTCACCATTTATAAGTAGAAGAGCACTAGGGTTGATCTGCCACCTCATCTTTCATGAAGTC
TATTCCCCAGCCTCCTTTTTAAGAAAAGATACTGCTACCAAAGGCATAGGGGAGGCCTGCTGTG
CTGGCAATTAGCATGAGCCTGCAGAAGTCATCCTTGAATCTGTTGTGTCTTAATTTTATTTGGA
CAGTTTTTTTTTCCAGCCTCATCAACACTTGGTCTTCCTGGTGTCTTAATTCCCTCAGACAAGT
TTATGCACTTTTTTAAGGAAATATTTTTCAGGACACTAGTAAGAAGCTCAGTTCACAGTTTGGA
TATTTCTTCCCACATTACAGAATTATGGAAAGGAACTCAAAATCAGCCTAGGAAAGTGAGTCCT
GCTTGACCCATGTGACTGTGTACCTGACCTTCTGGGATCTTTTCAGCTATTAAAACATTTTACT
GTTCCCACATACCCAGCTTTGCAAGTTTTGTAGATTGACCTCTTAGGGTGTGTTTCTTTGTCTT
TCCTGCCTTTAACTTGCTGGGGTCTTTTGTTGCTACCCCTAAGGAACTAAACTGGGTGCCAGGA
GCTACCTTCGTGTATAGAGATGTAGATGGCAGTGTGGGGTACAGGAGAGCCATCCAGGCCATTC
TCCCAGGGATGAGGAATTGGAGAGCCCTGAAGATAATAGTGGCTTCTTTCTGATTGCTACTGTG
CTGTGTGATAGGCCTAATAGGGAAAAGATATGTAACTTGAAACAAAGTTGGTATAAATTCAGTA
TGTGGCTGTGGGACAGAGGTTGGAAGGAAAGGACTAGGGTATGGAAAGCTGAAGAAATTCTCCT
TATGAGCTCTCGTTGACTTTTTGAACAGTGATAAGCTAATGCCAGATTTAAAATACACATTTTT
TCCTATTTGAGTCTTTAGGATTATATCATTTGAAAAAATTGCCTTCCTTGTTAGGTCACATGTC
ATAGGAGAGTAGCTTAGAGAACTTGCATTACCAGACAGACACATTAATTCCCAAAGCCTCTATG
TTGAGAGAATGAAACTGTTAACTCTTTTTCAGAGAGGACTATGAATAAAGAAACTTCTTTATTC
AAGCTTCAGCTTTCAGCTGGGTTGTTTCCTCTAAAAGGGAAAGGGCATTGCAAGTGCATAGAGG
AAATCTCTCCCTTCTGGGACTGCTTTTCCTCCTTCATCCTCGTGAGCCTGTCCAAGCTCAGAAT
TCCGAAGGCTGTTAGAAATGCGTTGGGATTGCAGAGAGAAAGGAGCTTGTCTTTCCTTCTGCTG
TGCTGGTCTGTTTTGGATGTCAGTCTTCAGGACTATGAAAACTTCCTGCCAGTTTAGCATGGAC
ACTGAGGGCTGGCATTTCTAGTCTTCTTCAGACACTGAACATACTGACTCCAGGTATAGGAAGC
AGCTAGCAAATTGATTCTTTTTTAAATGCATAGGACTCTGCTTCCGGCGGTTCCTCTTGTAGTC
CAACTCTTTTTGCCATCTATTTATGTTGGGAGGTAGGGGCACAATTGTCACTCACAACACAGGC
TAGTTAGAGTTTGCTACCTTCTTAGCAGAAAATGCATGTGTGTCTTGTTGGACCTTCACTGGGG
AAAGGCTGGGAGCCTCTGGCTGTCAGTGACTTTTCTCACAGAAGAAGAACCAGCAAGCCAGACT
GGACACCTTTACCCTTTAATGGTAAGACTTGTATTTATAAGGGGTAATTTTGATGTTGAATTTA
AGCCACTACTTTGTTTAAACTTTTTTAAATTGGCAACTAGAAGTTTGAGAATTTGTATAGAAAT
GGAACATGTATTTCTAACAGTTGCCAATCTGGCTGGTCCCAATGTTAGTTTATTAGTGATTGAT
CTGTAATTATTGGGATTATTTATTCAACTCTAAAATTCCAAGATGAAAATAATTTATCTCTTTC
TTTTCAAGGGAAAAAACCCAAATGAATGCATTTTCAGTTTCTCCAGGCCTTTGAACTGCAGCAG
AAAATTCAAGGATACAGCCTAGGCCTGGGCAAATGCAGCCCTGGGTCTTTGGGCCAGTTTCTGA
CAATAATAGTTGAGTTTTGGGAATCACATAAGGGTGAAACCAGAAACGATCCTAAGGAAAGGCT
TGACCTTTGTTAACACCTTTAGTTTCCAAAGTCACAGCAGCTGGGGTCCCTCTTTTTTTTTTTT
TTTTCTTTTTTTTTGAGACATAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTATGACCA
TAGCTCACTGCAGCATCAAATTCCTAGGCTCAAGCAATCCTCCCATCTTAGCCTCCCGAGTAGC
TGGGACAACAGGTACGCACCACCACGGCCAGCTAATTATTTTTATTATTTTTATTTTTTGTAGA
GACTGGATCTTGCTCTATTTCCCAAGCTACTCTTGAATTGTTGTGCTCAAGTGATTCTCCCATC
TCAGCCTCCCAAAGTGCTGGGATTATAGGCTGGGTGTGGTGAGCCACCCCAGCCTGGGGTCTCT
TTAATTAAGGTTATAATGCTAACCATGGCTTAAAATACTAAGCAACATTTTCCAAATTGTTTAT
TACTATTGCTTTGATTTTGGAGAAGCTGGGAAGTAAGGAGGTGAGGTGAATACTCTGATAATTA
ACACGTGTTAGAGAGGAAAGTTGTGTGAAGAGGCTGCCAAAGTAAACAGCACGAATGAATCTTC
TTGTACTAGGGCTGCTGCAAACCCCAGGTAGACAAATGACAGCCCAGGCTCCTGAACCATCAGG
AACCCAGGAATCTACCCAACTGTGAGGAGGGGGCAGGCCTTCGTCAATAAGGGTCCCACCATCA
CGGGCTAATAATCTTTCTCAGTTTAGGTGATATTGAGGTATTGAAACTGTTAGAAATCTGACAG
ATTTGACCAAGATTTGGAGACGTCCACATAATTGGGAAGGACTGAGTGTCCCTAGCCACTCTCC
TCTGGGATAACGCGGACGTCATTAGTTTGCGAAGTGGGTGGGGAGAACAGGAGGATTGACTCTA
ATTTGGTGTGTAGTGGGGGCCTTGATGTCCTTCTGCCTCTGTCCACATTTCCCCATGTGACTCA
TTGCACCCTGCATTGCTCACAGGGATCATTAGTTCTCCCGGTAGACAGAGCACCTCTGCAGCCT
CTGCTCTGCTGCCTTGTGAATTTCCTACACAGACTTGGTTAGTTACAATTTGGAAACAGTTTTT
TTGGGTTTTTTTCCTTTGTTTTAATCTTCTCACAATGAAGCTGCTATTGGTGACAGGGACAGGG
GAGCAGGAAGCCAACCCAGGGAAACATGCGAGTTTCCTGCACACCACTTAGTCACCTGCCCTCA
CTGGCCAACCCCCTACTGCTGTTCCCAGTCAGTCTGGTTTTTAGAGGCATCGTGGCAATAGAAT
AGCTGGATACACTAATCTCTACAAGGTGTCAGGCAGGAGATTCACCTTCCCCAGTCCCAGGGGA
CAGGAGAGAAATCTGTAAAGGGACAGATGCACCATCTTTATTTCAAAAGAAAAAGCTCCCTCAG
ATTGTGTTACTAGGAGTCTCTTTTGTGACATTTACTGAGCTTTCTCCCCAATCTTACCTTCCTA
TTGGCTACTTTTTAAATAAAAATAAACATTTTAGGCTAATATGACAAAAATGAGATAAAATCTT
AAAAACATTGTACTAGTGTACAGTTACTAAAATGTGCTTACTACAAAACAGTAAAATATTTCAC
TCTGTAAATCATCACTAAGTAGTTATTCTGTCCTGTTGATTATGAGCCTCCAAAAATGTTTAAT
GCTTGAAGGATGGTTTGGGAGGCAGGGAATCCTTTTCTTAAAACAACTTTAATGAGGCATATGT
TACATATCATAAAACACCCATTTCAAGTGTACATTTCAGTGATTTTAGTAACTTCCCTCAGTGG
TGTAGCTGTAACTATTACTCAGTTTTAGAACATTTTTATCCCTCCCAATAAGATCCTTCATGCT
CTTTTACAGTTAATCCTGTTCTTACCCCCGGCAACCACTAATCTACTTTCTCTATAAATTTGCC
CTTTCTGGACAGTTCAAATCAATGGAATCATACAATATGTGGTCCCTTGGGTCTGGCTTTTTTA
CTTAGCTAATGTTTTTGAGGTTTGTCCATGACAGATAACGTCTTGGTAGTTTGTTCCTTTTATT
GCTGAGTAGAATTCTGTTGATGGATGTACCACATTTTGTCAGCAGAGAGCCTTTTAAACTTGGA
TTCCAACTTCCTGTTGTCTAAACGGAACCCTCCGAACGTAGGACTTATAGGGGAAGCTGCTGTG
CATGTCAAAAAAACTACTAATCAGAATGAGCTTTGTCATCCAGAGCCAGAACTGCTGCAGAAAT
TTTTATAATTTTGCAACTTCTTTTTTTACAAGGAACTTTTGTGCTACTACACATCAGGACTTTT
GAAGCATCCAATAAATCCATTTAATAAGTATGAGCATGTGTCTGAGTGGACAAGAAAGTGAAAC
CATCCATGCTACATTGGATAATTTTTCCTCCCCCAGACTGGACAGGGAATCTCAGCTTTCAAAA
CAGAGTAACCTGGCTCCACTTACAAAGCTGCACAGGCATTAAAGATCGTGCTGCCTTTGTTAGG
CAGATTTGGAGGGGAGGCCCAACAGCAAAGATGGAGAGGAAAAAGGGAGTGGAGCTTGTGGAAC
AGGAAGCCCCCCAGGGTCTGTGCAGGGCTGCTCAGCTCTTGAGGATGTTGTGGATGGTGAAGTG
GTGATGGTGTCCCGGAGCAGCCCAGCACCTCCACTGGGCCCAGAAGGTCTTGACTTCGGACACT
TACCCCTGTTTCACAAGTGTTTATAAAGCTGTTTTTGCTTTTTTTCCCCTAATCATTACTTGGT
AGTTATTAATCCTTCTTTGGGGGAGGGACAGGGCTTTAAAACTGAAGAAAATAATTTTCATAAA
AATATCAAAAATGGAAAAAAGTTACTTTGTAAAAAATTTGCTATACAAACCAAATGGCAGCTGT
TGAGAATCTCAATAAAATGTTAAATGCA

hide sequence

RefSeq Acc Id:

XM_005264310 ⟹ XP_005264367

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	71,182,738 - 71,226,416 (-)	NCBI
GRCh37	2	71,409,868 - 71,454,233 (-)	NCBI

Sequence:

show sequence

TTCATGCCTCATTTGCCTGGGAGACGTTCGCCACTTCTCTTGTGCCTTGCGGCAGCTGGAAGGT
GAACTGAGAGAGGCAGAATACGCAGAACAGGGAGTTTGGCAAGGTTCCATCATAATGAATGGAT
CCAATATGGCAAATACATCACCGAGTGTAAAATCCAAAGAGGACCAGGGGTTAAGTGGGCACGA
TGAAAAGGAAAACCCATTTGCAGAGTACATGTGGATGGAGAATGAAGAGGATTTCAACAGACAG
GTGGAGGAGGAACTGCAGGAGCAAGACTTCTTGGACCGCTGCTTCCAAGAGATGCTGGATGAAG
AAGACCAAGACTGGTTTATTCCCTCACGAGACCTGCCTCAGGCCATGGGACAGTTGCAACAGCA
GTTAAATGGACTGTCAGTCAGTGAAGGTCATGATTCTGAAGATATTTTGAGCAAAAGTAACCTG
AACCCAGATGCCAAGGAGTTTATTCCAGGAGAGAAGTACTGAGCCGAGAAAGCTTTGAGGAAGA
CTTGTCTGTCCCCACATCTGGGGATAGTAATGCACAAAATGGTGGAGCTGAAGAGGGGGATGGG
GCGGGCGAGGGGTGCACAGCGGGAAGGGGAGTGGTGGTCTCACAATACTGTGACTCTGAGTAAC
TAATATGCTCAGTCTTATTCTAAGCCTCTGAGTATTTCTATTTTGTTCTGCTGACTTTTGTTTG
GGGAGTTTCCTGTTTTGTTTTTTTAAATAGCTCTTTCGAGTTAAGGAAATTGCATTTTCCCCCC
TTCATCAGAAGTGTTCCGCGGTGTGTATTTAAACAAAATAAGCTGACTAAGAAAAACTGGATAT
TTAGGAAATGCCCCTCTCACCCTGCTGTATACTTATCAGGGACAGTGAGCACCTGGAGAGCTTT
TTGTGGAATCTATTGAGTTGGATGGGAAAAGGGACAAGCAGAAAGAGCAGGTGGTGCAAACTGG
AATTTGAGGCTCAGCTGCCCCACCCCCGGGGTCTCCTGCAATGAACTCGGATAACCAATGTGCT
GTCAAGCCCTTGCCTGTTTGTCCTGAACCCCATTCAAGAAAACACAGACTTAAAGTACTTAGTT
TACAGTAACTTTTGATGATTGTTGAAAGTTGTAAATCAGAAGGTAGGGCTGTGATGGTGGTTGT
CACTTGAGTCATTTAGTTACTGTTGTCCTGTTCATAAGCCTGTGTTCACCACCACCATCAGACT
CACCATTTATAAGTAGAAGAGCACTAGGGTTGATCTGCCACCTCATCTTTCATGAAGTCTATTC
CCCAGCCTCCTTTTTAAGAAAAGATACTGCTACCAAAGGCATAGGGGAGGCCTGCTGTGCTGGC
AATTAGCATGAGCCTGCAGAAGTCATCCTTGAATCTGTTGTGTCTTAATTTTATTTGGACAGTT
TTTTTTTCCAGCCTCATCAACACTTGGTCTTCCTGGTGTCTTAATTCCCTCAGACAAGTTTATG
CACTTTTTTAAGGAAATATTTTTCAGGACACTAGTAAGAAGCTCAGTTCACAGTTTGGATATTT
CTTCCCACATTACAGAATTATGGAAAGGAACTCAAAATCAGCCTAGGAAAGTGAGTCCTGCTTG
ACCCATGTGACTGTGTACCTGACCTTCTGGGATCTTTTCAGCTATTAAAACATTTTACTGTTCC
CACATACCCAGCTTTGCAAGTTTTGTAGATTGACCTCTTAGGGTGTGTTTCTTTGTCTTTCCTG
CCTTTAACTTGCTGGGGTCTTTTGTTGCTACCCCTAAGGAACTAAACTGGGTGCCAGGAGCTAC
CTTCGTGTATAGAGATGTAGATGGCAGTGTGGGGTACAGGAGAGCCATCCAGGCCATTCTCCCA
GGGATGAGGAATTGGAGAGCCCTGAAGATAATAGTGGCTTCTTTCTGATTGCTACTGTGCTGTG
TGATAGGCCTAATAGGGAAAAGATATGTAACTTGAAACAAAGTTGGTATAAATTCAGTATGTGG
CTGTGGGACAGAGGTTGGAAGGAAAGGACTAGGGTATGGAAAGCTGAAGAAATTCTCCTTATGA
GCTCTCGTTGACTTTTTGAACAGTGATAAGCTAATGCCAGATTTAAAATACACATTTTTTCCTA
TTTGAGTCTTTAGGATTATATCATTTGAAAAAATTGCCTTCCTTGTTAGGTCACATGTCATAGG
AGAGTAGCTTAGAGAACTTGCATTACCAGACAGACACATTAATTCCCAAAGCCTCTATGTTGAG
AGAATGAAACTGTTAACTCTTTTTCAGAGAGGACTATGAATAAAGAAACTTCTTTATTCAAGCT
TCAGCTTTCAGCTGGGTTGTTTCCTCTAAAAGGGAAAGGGCATTGCAAGTGCATAGAGGAAATC
TCTCCCTTCTGGGACTGCTTTTCCTCCTTCATCCTCGTGAGCCTGTCCAAGCTCAGAATTCCGA
AGGCTGTTAGAAATGCGTTGGGATTGCAGAGAGAAAGGAGCTTGTCTTTCCTTCTGCTGTGCTG
GTCTGTTTTGGATGTCAGTCTTCAGGACTATGAAAACTTCCTGCCAGTTTAGCATGGACACTGA
GGGCTGGCATTTCTAGTCTTCTTCAGACACTGAACATACTGACTCCAGGTATAGGAAGCAGCTA
GCAAATTGATTCTTTTTTAAATGCATAGGACTCTGCTTCCGGCGGTTCCTCTTGTAGTCCAACT
CTTTTTGCCATCTATTTATGTTGGGAGGTAGGGGCACAATTGTCACTCACAACACAGGCTAGTT
AGAGTTTGCTACCTTCTTAGCAGAAAATGCATGTGTGTCTTGTTGGACCTTCACTGGGGAAAGG
CTGGGAGCCTCTGGCTGTCAGTGACTTTTCTCACAGAAGAAGAACCAGCAAGCCAGACTGGACA
CCTTTACCCTTTAATGGTAAGACTTGTATTTATAAGGGGTAATTTTGATGTTGAATTTAAGCCA
CTACTTTGTTTAAACTTTTTTAAATTGGCAACTAGAAGTTTGAGAATTTGTATAGAAATGGAAC
ATGTATTTCTAACAGTTGCCAATCTGGCTGGTCCCAATGTTAGTTTATTAGTGATTGATCTGTA
ATTATTGGGATTATTTATTCAACTCTAAAATTCCAAGATGAAAATAATTTATCTCTTTCTTTTC
AAGGGAAAAAACCCAAATGAATGCATTTTCAGTTTCTCCAGGCCTTTGAACTGCAGCAGAAAAT
TCAAGGATACAGCCTAGGCCTGGGCAAATGCAGCCCTGGGTCTTTGGGCCAGTTTCTGACAATA
ATAGTTGAGTTTTGGGAATCACATAAGGGTGAAACCAGAAACGATCCTAAGGAAAGGCTTGACC
TTTGTTAACACCTTTAGTTTCCAAAGTCACAGCAGCTGGGGTCCCTCTTTTTTTTTTTTTTTTC
TTTTTTTTTGAGACATAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTATGACCATAGCT
CACTGCAGCATCAAATTCCTAGGCTCAAGCAATCCTCCCATCTTAGCCTCCCGAGTAGCTGGGA
CAACAGGTACGCACCACCACGGCCAGCTAATTATTTTTATTATTTTTATTTTTTGTAGAGACTG
GATCTTGCTCTATTTCCCAAGCTACTCTTGAATTGTTGTGCTCAAGTGATTCTCCCATCTCAGC
CTCCCAAAGTGCTGGGATTATAGGCTGGGTGTGGTGAGCCACCCCAGCCTGGGGTCTCTTTAAT
TAAGGTTATAATGCTAACCATGGCTTAAAATACTAAGCAACATTTTCCAAATTGTTTATTACTA
TTGCTTTGATTTTGGAGAAGCTGGGAAGTAAGGAGGTGAGGTGAATACTCTGATAATTAACACG
TGTTAGAGAGGAAAGTTGTGTGAAGAGGCTGCCAAAGTAAACAGCACGAATGAATCTTCTTGTA
CTAGGGCTGCTGCAAACCCCAGGTAGACAAATGACAGCCCAGGCTCCTGAACCATCAGGAACCC
AGGAATCTACCCAACTGTGAGGAGGGGGCAGGCCTTCGTCAATAAGGGTCCCACCATCACGGGC
TAATAATCTTTCTCAGTTTAGGTGATATTGAGGTATTGAAACTGTTAGAAATCTGACAGATTTG
ACCAAGATTTGGAGACGTCCACATAATTGGGAAGGACTGAGTGTCCCTAGCCACTCTCCTCTGG
GATAACGCGGACGTCATTAGTTTGCGAAGTGGGTGGGGAGAACAGGAGGATTGACTCTAATTTG
GTGTGTAGTGGGGGCCTTGATGTCCTTCTGCCTCTGTCCACATTTCCCCATGTGACTCATTGCA
CCCTGCATTGCTCACAGGGATCATTAGTTCTCCCGGTAGACAGAGCACCTCTGCAGCCTCTGCT
CTGCTGCCTTGTGAATTTCCTACACAGACTTGGTTAGTTACAATTTGGAAACAGTTTTTTTGGG
TTTTTTTCCTTTGTTTTAATCTTCTCACAATGAAGCTGCTATTGGTGACAGGGACAGGGGAGCA
GGAAGCCAACCCAGGGAAACATGCGAGTTTCCTGCACACCACTTAGTCACCTGCCCTCACTGGC
CAACCCCCTACTGCTGTTCCCAGTCAGTCTGGTTTTTAGAGGCATCGTGGCAATAGAATAGCTG
GATACACTAATCTCTACAAGGTGTCAGGCAGGAGATTCACCTTCCCCAGTCCCAGGGGACAGGA
GAGAAATCTGTAAAGGGACAGATGCACCATCTTTATTTCAAAAGAAAAAGCTCCCTCAGATTGT
GTTACTAGGAGTCTCTTTTGTGACATTTACTGAGCTTTCTCCCCAATCTTACCTTCCTATTGGC
TACTTTTTAAATAAAAATAAACATTTTAGGCTAATATGACAAAAATGAGATAAAATCTTAAAAA
CATTGTACTAGTGTACAGTTACTAAAATGTGCTTACTACAAAACAGTAAAATATTTCACTCTGT
AAATCATCACTAAGTAGTTATTCTGTCCTGTTGATTATGAGCCTCCAAAAATGTTTAATGCTTG
AAGGATGGTTTGGGAGGCAGGGAATCCTTTTCTTAAAACAACTTTAATGAGGCATATGTTACAT
ATCATAAAACACCCATTTCAAGTGTACATTTCAGTGATTTTAGTAACTTCCCTCAGTGGTGTAG
CTGTAACTATTACTCAGTTTTAGAACATTTTTATCCCTCCCAATAAGATCCTTCATGCTCTTTT
ACAGTTAATCCTGTTCTTACCCCCGGCAACCACTAATCTACTTTCTCTATAAATTTGCCCTTTC
TGGACAGTTCAAATCAATGGAATCATACAATATGTGGTCCCTTGGGTCTGGCTTTTTTACTTAG
CTAATGTTTTTGAGGTTTGTCCATGACAGATAACGTCTTGGTAGTTTGTTCCTTTTATTGCTGA
GTAGAATTCTGTTGATGGATGTACCACATTTTGTCAGCAGAGAGCCTTTTAAACTTGGATTCCA
ACTTCCTGTTGTCTAAACGGAACCCTCCGAACGTAGGACTTATAGGGGAAGCTGCTGTGCATGT
CAAAAAAACTACTAATCAGAATGAGCTTTGTCATCCAGAGCCAGAACTGCTGCAGAAATTTTTA
TAATTTTGCAACTTCTTTTTTTACAAGGAACTTTTGTGCTACTACACATCAGGACTTTTGAAGC
ATCCAATAAATCCATTTAATAAGTATGAGCATGTGTCTGAGTGGACAAGAAAGTGAAACCATCC
ATGCTACATTGGATAATTTTTCCTCCCCCAGACTGGACAGGGAATCTCAGCTTTCAAAACAGAG
TAACCTGGCTCCACTTACAAAGCTGCACAGGCATTAAAGATCGTGCTGCCTTTGTTAGGCAGAT
TTGGAGGGGAGGCCCAACAGCAAAGATGGAGAGGAAAAAGGGAGTGGAGCTTGTGGAACAGGAA
GCCCCCCAGGGTCTGTGCAGGGCTGCTCAGCTCTTGAGGATGTTGTGGATGGTGAAGTGGTGAT
GGTGTCCCGGAGCAGCCCAGCACCTCCACTGGGCCCAGAAGGTCTTGACTTCGGACACTTACCC
CTGTTTCACAAGTGTTTATAAAGCTGTTTTTGCTTTTTTTCCCCTAATCATTACTTGGTAGTTA
TTAATCCTTCTTTGGGGGAGGGACAGGGCTTTAAAACTGAAGAAAATAATTTTCATAAAAATAT
CAAAAATGGAAAAAAGTTACTTTGTAAAAAATTTGCTATACAAACCAAATGGCAGCTGTTGAGA
ATCTCAATAAAATGTTAAATGCA

hide sequence

RefSeq Acc Id:

XM_005264311 ⟹ XP_005264368

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	71,182,738 - 71,226,416 (-)	NCBI
GRCh37	2	71,409,868 - 71,454,233 (-)	NCBI

Sequence:

show sequence

GGGAGGGATTGCGCGTCGTGCCCTTCCCCTATTCGCGGCCCCTGCGCGTCCTCTGCCTTTTTAT
ACTTGCTCCATCTCCCCCTTGACTCCAGCCCTCATTCTTCATGCCTCATTTGCCTGGGAGACGT
TCGCCACTTCTCTTGTGCCTTGCGGTTCCATCATAATGAATGGATCCAATATGGCAAATACATC
ACCGAGTGTAAAATCCAAAGAGGACCAGGGGTTAAGTGGGCACGATGAAAAGGAAAACCCATTT
GCAGAGTACATGTGGATGGAGAATGAAGAGGATTTCAACAGACAGGTGGAGGAGGAACTGCAGG
AGCAAGACTTCTTGGACCGCTGCTTCCAAGAGATGCTGGATGAAGAAGACCAAGACTGGTTTAT
TCCCTCACGAGACCTGCCTCAGGCCATGGGACAGTTGCAACAGCAGTTAAATGGACTGTCAGTC
AGTGAAGGTCATGATTCTGAAGATATTTTGAGCAAAAGTAACCTGAACCCAGATGCCAAGGAGT
TTATTCCAGGAGAGAAGTACTGAGCCGAGAAAGCTTTGAGGAAGACTTGTCTGTCCCCACATCT
GGGGATAGTAATGCACAAAATGGTGGAGCTGAAGAGGGGGATGGGGCGGGCGAGGGGTGCACAG
CGGGAAGGGGAGTGGTGGTCTCACAATACTGTGACTCTGAGTAACTAATATGCTCAGTCTTATT
CTAAGCCTCTGAGTATTTCTATTTTGTTCTGCTGACTTTTGTTTGGGGAGTTTCCTGTTTTGTT
TTTTTAAATAGCTCTTTCGAGTTAAGGAAATTGCATTTTCCCCCCTTCATCAGAAGTGTTCCGC
GGTGTGTATTTAAACAAAATAAGCTGACTAAGAAAAACTGGATATTTAGGAAATGCCCCTCTCA
CCCTGCTGTATACTTATCAGGGACAGTGAGCACCTGGAGAGCTTTTTGTGGAATCTATTGAGTT
GGATGGGAAAAGGGACAAGCAGAAAGAGCAGGTGGTGCAAACTGGAATTTGAGGCTCAGCTGCC
CCACCCCCGGGGTCTCCTGCAATGAACTCGGATAACCAATGTGCTGTCAAGCCCTTGCCTGTTT
GTCCTGAACCCCATTCAAGAAAACACAGACTTAAAGTACTTAGTTTACAGTAACTTTTGATGAT
TGTTGAAAGTTGTAAATCAGAAGGTAGGGCTGTGATGGTGGTTGTCACTTGAGTCATTTAGTTA
CTGTTGTCCTGTTCATAAGCCTGTGTTCACCACCACCATCAGACTCACCATTTATAAGTAGAAG
AGCACTAGGGTTGATCTGCCACCTCATCTTTCATGAAGTCTATTCCCCAGCCTCCTTTTTAAGA
AAAGATACTGCTACCAAAGGCATAGGGGAGGCCTGCTGTGCTGGCAATTAGCATGAGCCTGCAG
AAGTCATCCTTGAATCTGTTGTGTCTTAATTTTATTTGGACAGTTTTTTTTTCCAGCCTCATCA
ACACTTGGTCTTCCTGGTGTCTTAATTCCCTCAGACAAGTTTATGCACTTTTTTAAGGAAATAT
TTTTCAGGACACTAGTAAGAAGCTCAGTTCACAGTTTGGATATTTCTTCCCACATTACAGAATT
ATGGAAAGGAACTCAAAATCAGCCTAGGAAAGTGAGTCCTGCTTGACCCATGTGACTGTGTACC
TGACCTTCTGGGATCTTTTCAGCTATTAAAACATTTTACTGTTCCCACATACCCAGCTTTGCAA
GTTTTGTAGATTGACCTCTTAGGGTGTGTTTCTTTGTCTTTCCTGCCTTTAACTTGCTGGGGTC
TTTTGTTGCTACCCCTAAGGAACTAAACTGGGTGCCAGGAGCTACCTTCGTGTATAGAGATGTA
GATGGCAGTGTGGGGTACAGGAGAGCCATCCAGGCCATTCTCCCAGGGATGAGGAATTGGAGAG
CCCTGAAGATAATAGTGGCTTCTTTCTGATTGCTACTGTGCTGTGTGATAGGCCTAATAGGGAA
AAGATATGTAACTTGAAACAAAGTTGGTATAAATTCAGTATGTGGCTGTGGGACAGAGGTTGGA
AGGAAAGGACTAGGGTATGGAAAGCTGAAGAAATTCTCCTTATGAGCTCTCGTTGACTTTTTGA
ACAGTGATAAGCTAATGCCAGATTTAAAATACACATTTTTTCCTATTTGAGTCTTTAGGATTAT
ATCATTTGAAAAAATTGCCTTCCTTGTTAGGTCACATGTCATAGGAGAGTAGCTTAGAGAACTT
GCATTACCAGACAGACACATTAATTCCCAAAGCCTCTATGTTGAGAGAATGAAACTGTTAACTC
TTTTTCAGAGAGGACTATGAATAAAGAAACTTCTTTATTCAAGCTTCAGCTTTCAGCTGGGTTG
TTTCCTCTAAAAGGGAAAGGGCATTGCAAGTGCATAGAGGAAATCTCTCCCTTCTGGGACTGCT
TTTCCTCCTTCATCCTCGTGAGCCTGTCCAAGCTCAGAATTCCGAAGGCTGTTAGAAATGCGTT
GGGATTGCAGAGAGAAAGGAGCTTGTCTTTCCTTCTGCTGTGCTGGTCTGTTTTGGATGTCAGT
CTTCAGGACTATGAAAACTTCCTGCCAGTTTAGCATGGACACTGAGGGCTGGCATTTCTAGTCT
TCTTCAGACACTGAACATACTGACTCCAGGTATAGGAAGCAGCTAGCAAATTGATTCTTTTTTA
AATGCATAGGACTCTGCTTCCGGCGGTTCCTCTTGTAGTCCAACTCTTTTTGCCATCTATTTAT
GTTGGGAGGTAGGGGCACAATTGTCACTCACAACACAGGCTAGTTAGAGTTTGCTACCTTCTTA
GCAGAAAATGCATGTGTGTCTTGTTGGACCTTCACTGGGGAAAGGCTGGGAGCCTCTGGCTGTC
AGTGACTTTTCTCACAGAAGAAGAACCAGCAAGCCAGACTGGACACCTTTACCCTTTAATGGTA
AGACTTGTATTTATAAGGGGTAATTTTGATGTTGAATTTAAGCCACTACTTTGTTTAAACTTTT
TTAAATTGGCAACTAGAAGTTTGAGAATTTGTATAGAAATGGAACATGTATTTCTAACAGTTGC
CAATCTGGCTGGTCCCAATGTTAGTTTATTAGTGATTGATCTGTAATTATTGGGATTATTTATT
CAACTCTAAAATTCCAAGATGAAAATAATTTATCTCTTTCTTTTCAAGGGAAAAAACCCAAATG
AATGCATTTTCAGTTTCTCCAGGCCTTTGAACTGCAGCAGAAAATTCAAGGATACAGCCTAGGC
CTGGGCAAATGCAGCCCTGGGTCTTTGGGCCAGTTTCTGACAATAATAGTTGAGTTTTGGGAAT
CACATAAGGGTGAAACCAGAAACGATCCTAAGGAAAGGCTTGACCTTTGTTAACACCTTTAGTT
TCCAAAGTCACAGCAGCTGGGGTCCCTCTTTTTTTTTTTTTTTTCTTTTTTTTTGAGACATAGT
CTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTATGACCATAGCTCACTGCAGCATCAAATTCC
TAGGCTCAAGCAATCCTCCCATCTTAGCCTCCCGAGTAGCTGGGACAACAGGTACGCACCACCA
CGGCCAGCTAATTATTTTTATTATTTTTATTTTTTGTAGAGACTGGATCTTGCTCTATTTCCCA
AGCTACTCTTGAATTGTTGTGCTCAAGTGATTCTCCCATCTCAGCCTCCCAAAGTGCTGGGATT
ATAGGCTGGGTGTGGTGAGCCACCCCAGCCTGGGGTCTCTTTAATTAAGGTTATAATGCTAACC
ATGGCTTAAAATACTAAGCAACATTTTCCAAATTGTTTATTACTATTGCTTTGATTTTGGAGAA
GCTGGGAAGTAAGGAGGTGAGGTGAATACTCTGATAATTAACACGTGTTAGAGAGGAAAGTTGT
GTGAAGAGGCTGCCAAAGTAAACAGCACGAATGAATCTTCTTGTACTAGGGCTGCTGCAAACCC
CAGGTAGACAAATGACAGCCCAGGCTCCTGAACCATCAGGAACCCAGGAATCTACCCAACTGTG
AGGAGGGGGCAGGCCTTCGTCAATAAGGGTCCCACCATCACGGGCTAATAATCTTTCTCAGTTT
AGGTGATATTGAGGTATTGAAACTGTTAGAAATCTGACAGATTTGACCAAGATTTGGAGACGTC
CACATAATTGGGAAGGACTGAGTGTCCCTAGCCACTCTCCTCTGGGATAACGCGGACGTCATTA
GTTTGCGAAGTGGGTGGGGAGAACAGGAGGATTGACTCTAATTTGGTGTGTAGTGGGGGCCTTG
ATGTCCTTCTGCCTCTGTCCACATTTCCCCATGTGACTCATTGCACCCTGCATTGCTCACAGGG
ATCATTAGTTCTCCCGGTAGACAGAGCACCTCTGCAGCCTCTGCTCTGCTGCCTTGTGAATTTC
CTACACAGACTTGGTTAGTTACAATTTGGAAACAGTTTTTTTGGGTTTTTTTCCTTTGTTTTAA
TCTTCTCACAATGAAGCTGCTATTGGTGACAGGGACAGGGGAGCAGGAAGCCAACCCAGGGAAA
CATGCGAGTTTCCTGCACACCACTTAGTCACCTGCCCTCACTGGCCAACCCCCTACTGCTGTTC
CCAGTCAGTCTGGTTTTTAGAGGCATCGTGGCAATAGAATAGCTGGATACACTAATCTCTACAA
GGTGTCAGGCAGGAGATTCACCTTCCCCAGTCCCAGGGGACAGGAGAGAAATCTGTAAAGGGAC
AGATGCACCATCTTTATTTCAAAAGAAAAAGCTCCCTCAGATTGTGTTACTAGGAGTCTCTTTT
GTGACATTTACTGAGCTTTCTCCCCAATCTTACCTTCCTATTGGCTACTTTTTAAATAAAAATA
AACATTTTAGGCTAATATGACAAAAATGAGATAAAATCTTAAAAACATTGTACTAGTGTACAGT
TACTAAAATGTGCTTACTACAAAACAGTAAAATATTTCACTCTGTAAATCATCACTAAGTAGTT
ATTCTGTCCTGTTGATTATGAGCCTCCAAAAATGTTTAATGCTTGAAGGATGGTTTGGGAGGCA
GGGAATCCTTTTCTTAAAACAACTTTAATGAGGCATATGTTACATATCATAAAACACCCATTTC
AAGTGTACATTTCAGTGATTTTAGTAACTTCCCTCAGTGGTGTAGCTGTAACTATTACTCAGTT
TTAGAACATTTTTATCCCTCCCAATAAGATCCTTCATGCTCTTTTACAGTTAATCCTGTTCTTA
CCCCCGGCAACCACTAATCTACTTTCTCTATAAATTTGCCCTTTCTGGACAGTTCAAATCAATG
GAATCATACAATATGTGGTCCCTTGGGTCTGGCTTTTTTACTTAGCTAATGTTTTTGAGGTTTG
TCCATGACAGATAACGTCTTGGTAGTTTGTTCCTTTTATTGCTGAGTAGAATTCTGTTGATGGA
TGTACCACATTTTGTCAGCAGAGAGCCTTTTAAACTTGGATTCCAACTTCCTGTTGTCTAAACG
GAACCCTCCGAACGTAGGACTTATAGGGGAAGCTGCTGTGCATGTCAAAAAAACTACTAATCAG
AATGAGCTTTGTCATCCAGAGCCAGAACTGCTGCAGAAATTTTTATAATTTTGCAACTTCTTTT
TTTACAAGGAACTTTTGTGCTACTACACATCAGGACTTTTGAAGCATCCAATAAATCCATTTAA
TAAGTATGAGCATGTGTCTGAGTGGACAAGAAAGTGAAACCATCCATGCTACATTGGATAATTT
TTCCTCCCCCAGACTGGACAGGGAATCTCAGCTTTCAAAACAGAGTAACCTGGCTCCACTTACA
AAGCTGCACAGGCATTAAAGATCGTGCTGCCTTTGTTAGGCAGATTTGGAGGGGAGGCCCAACA
GCAAAGATGGAGAGGAAAAAGGGAGTGGAGCTTGTGGAACAGGAAGCCCCCCAGGGTCTGTGCA
GGGCTGCTCAGCTCTTGAGGATGTTGTGGATGGTGAAGTGGTGATGGTGTCCCGGAGCAGCCCA
GCACCTCCACTGGGCCCAGAAGGTCTTGACTTCGGACACTTACCCCTGTTTCACAAGTGTTTAT
AAAGCTGTTTTTGCTTTTTTTCCCCTAATCATTACTTGGTAGTTATTAATCCTTCTTTGGGGGA
GGGACAGGGCTTTAAAACTGAAGAAAATAATTTTCATAAAAATATCAAAAATGGAAAAAAGTTA
CTTTGTAAAAAATTTGCTATACAAACCAAATGGCAGCTGTTGAGAATCTCAATAAAATGTTAAA
TGCA

hide sequence

RefSeq Acc Id:

XM_011532842 ⟹ XP_011531144

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	71,182,738 - 71,226,416 (-)	NCBI

Sequence:

show sequence

TGCGCGTCGTGCCCTTCCCCTATTCGCGGCCCCTGCGCGTCCTCTGCCTTTTTATACTTGCTCC
ATCTCCCCCTTGACTCCAGCCCTCATTCTTCATGCCTCATTTGCCTGGGAGACGTTCGCCACTT
CTCTTGTGCCTTGCGGTCCGTTCCATCATAATGAATGGATCCAATATGGCAAATACATCACCGA
GTGTAAAATCCAAAGAGGACCAGGGGTTAAGTGGGCACGATGAAAAGGAAAACCCATTTGCAGA
GTACATGTGGATGGAGAATGAAGAGGATTTCAACAGACAGGTGGAGGAGGAACTGCAGGAGCAA
GACTTCTTGGACCGCTGCTTCCAAGAGATGCTGGATGAAGAAGACCAAGACTGGTTTATTCCCT
CACGAGACCTGCCTCAGGCCATGGGACAGTTGCAACAGCAGTTAAATGGACTGTCAGTCAGTGA
AGGTCATGATTCTGAAGATATTTTGAGCAAAAGTAACCTGAACCCAGATGCCAAGGAGTTTATT
CCAGGAGAGAAGTACTGAGCCGAGAAAGCTTTGAGGAAGACTTGTCTGTCCCCACATCTGGGGA
TAGTAATGCACAAAATGGTGGAGCTGAAGAGGGGGATGGGGCGGGCGAGGGGTGCACAGCGGGA
AGGGGAGTGGTGGTCTCACAATACTGTGACTCTGAGTAACTAATATGCTCAGTCTTATTCTAAG
CCTCTGAGTATTTCTATTTTGTTCTGCTGACTTTTGTTTGGGGAGTTTCCTGTTTTGTTTTTTT
AAATAGCTCTTTCGAGTTAAGGAAATTGCATTTTCCCCCCTTCATCAGAAGTGTTCCGCGGTGT
GTATTTAAACAAAATAAGCTGACTAAGAAAAACTGGATATTTAGGAAATGCCCCTCTCACCCTG
CTGTATACTTATCAGGGACAGTGAGCACCTGGAGAGCTTTTTGTGGAATCTATTGAGTTGGATG
GGAAAAGGGACAAGCAGAAAGAGCAGGTGGTGCAAACTGGAATTTGAGGCTCAGCTGCCCCACC
CCCGGGGTCTCCTGCAATGAACTCGGATAACCAATGTGCTGTCAAGCCCTTGCCTGTTTGTCCT
GAACCCCATTCAAGAAAACACAGACTTAAAGTACTTAGTTTACAGTAACTTTTGATGATTGTTG
AAAGTTGTAAATCAGAAGGTAGGGCTGTGATGGTGGTTGTCACTTGAGTCATTTAGTTACTGTT
GTCCTGTTCATAAGCCTGTGTTCACCACCACCATCAGACTCACCATTTATAAGTAGAAGAGCAC
TAGGGTTGATCTGCCACCTCATCTTTCATGAAGTCTATTCCCCAGCCTCCTTTTTAAGAAAAGA
TACTGCTACCAAAGGCATAGGGGAGGCCTGCTGTGCTGGCAATTAGCATGAGCCTGCAGAAGTC
ATCCTTGAATCTGTTGTGTCTTAATTTTATTTGGACAGTTTTTTTTTCCAGCCTCATCAACACT
TGGTCTTCCTGGTGTCTTAATTCCCTCAGACAAGTTTATGCACTTTTTTAAGGAAATATTTTTC
AGGACACTAGTAAGAAGCTCAGTTCACAGTTTGGATATTTCTTCCCACATTACAGAATTATGGA
AAGGAACTCAAAATCAGCCTAGGAAAGTGAGTCCTGCTTGACCCATGTGACTGTGTACCTGACC
TTCTGGGATCTTTTCAGCTATTAAAACATTTTACTGTTCCCACATACCCAGCTTTGCAAGTTTT
GTAGATTGACCTCTTAGGGTGTGTTTCTTTGTCTTTCCTGCCTTTAACTTGCTGGGGTCTTTTG
TTGCTACCCCTAAGGAACTAAACTGGGTGCCAGGAGCTACCTTCGTGTATAGAGATGTAGATGG
CAGTGTGGGGTACAGGAGAGCCATCCAGGCCATTCTCCCAGGGATGAGGAATTGGAGAGCCCTG
AAGATAATAGTGGCTTCTTTCTGATTGCTACTGTGCTGTGTGATAGGCCTAATAGGGAAAAGAT
ATGTAACTTGAAACAAAGTTGGTATAAATTCAGTATGTGGCTGTGGGACAGAGGTTGGAAGGAA
AGGACTAGGGTATGGAAAGCTGAAGAAATTCTCCTTATGAGCTCTCGTTGACTTTTTGAACAGT
GATAAGCTAATGCCAGATTTAAAATACACATTTTTTCCTATTTGAGTCTTTAGGATTATATCAT
TTGAAAAAATTGCCTTCCTTGTTAGGTCACATGTCATAGGAGAGTAGCTTAGAGAACTTGCATT
ACCAGACAGACACATTAATTCCCAAAGCCTCTATGTTGAGAGAATGAAACTGTTAACTCTTTTT
CAGAGAGGACTATGAATAAAGAAACTTCTTTATTCAAGCTTCAGCTTTCAGCTGGGTTGTTTCC
TCTAAAAGGGAAAGGGCATTGCAAGTGCATAGAGGAAATCTCTCCCTTCTGGGACTGCTTTTCC
TCCTTCATCCTCGTGAGCCTGTCCAAGCTCAGAATTCCGAAGGCTGTTAGAAATGCGTTGGGAT
TGCAGAGAGAAAGGAGCTTGTCTTTCCTTCTGCTGTGCTGGTCTGTTTTGGATGTCAGTCTTCA
GGACTATGAAAACTTCCTGCCAGTTTAGCATGGACACTGAGGGCTGGCATTTCTAGTCTTCTTC
AGACACTGAACATACTGACTCCAGGTATAGGAAGCAGCTAGCAAATTGATTCTTTTTTAAATGC
ATAGGACTCTGCTTCCGGCGGTTCCTCTTGTAGTCCAACTCTTTTTGCCATCTATTTATGTTGG
GAGGTAGGGGCACAATTGTCACTCACAACACAGGCTAGTTAGAGTTTGCTACCTTCTTAGCAGA
AAATGCATGTGTGTCTTGTTGGACCTTCACTGGGGAAAGGCTGGGAGCCTCTGGCTGTCAGTGA
CTTTTCTCACAGAAGAAGAACCAGCAAGCCAGACTGGACACCTTTACCCTTTAATGGTAAGACT
TGTATTTATAAGGGGTAATTTTGATGTTGAATTTAAGCCACTACTTTGTTTAAACTTTTTTAAA
TTGGCAACTAGAAGTTTGAGAATTTGTATAGAAATGGAACATGTATTTCTAACAGTTGCCAATC
TGGCTGGTCCCAATGTTAGTTTATTAGTGATTGATCTGTAATTATTGGGATTATTTATTCAACT
CTAAAATTCCAAGATGAAAATAATTTATCTCTTTCTTTTCAAGGGAAAAAACCCAAATGAATGC
ATTTTCAGTTTCTCCAGGCCTTTGAACTGCAGCAGAAAATTCAAGGATACAGCCTAGGCCTGGG
CAAATGCAGCCCTGGGTCTTTGGGCCAGTTTCTGACAATAATAGTTGAGTTTTGGGAATCACAT
AAGGGTGAAACCAGAAACGATCCTAAGGAAAGGCTTGACCTTTGTTAACACCTTTAGTTTCCAA
AGTCACAGCAGCTGGGGTCCCTCTTTTTTTTTTTTTTTTCTTTTTTTTTGAGACATAGTCTCAC
TCTGTCACCCAGGCTGGAGTGCAGTGGTATGACCATAGCTCACTGCAGCATCAAATTCCTAGGC
TCAAGCAATCCTCCCATCTTAGCCTCCCGAGTAGCTGGGACAACAGGTACGCACCACCACGGCC
AGCTAATTATTTTTATTATTTTTATTTTTTGTAGAGACTGGATCTTGCTCTATTTCCCAAGCTA
CTCTTGAATTGTTGTGCTCAAGTGATTCTCCCATCTCAGCCTCCCAAAGTGCTGGGATTATAGG
CTGGGTGTGGTGAGCCACCCCAGCCTGGGGTCTCTTTAATTAAGGTTATAATGCTAACCATGGC
TTAAAATACTAAGCAACATTTTCCAAATTGTTTATTACTATTGCTTTGATTTTGGAGAAGCTGG
GAAGTAAGGAGGTGAGGTGAATACTCTGATAATTAACACGTGTTAGAGAGGAAAGTTGTGTGAA
GAGGCTGCCAAAGTAAACAGCACGAATGAATCTTCTTGTACTAGGGCTGCTGCAAACCCCAGGT
AGACAAATGACAGCCCAGGCTCCTGAACCATCAGGAACCCAGGAATCTACCCAACTGTGAGGAG
GGGGCAGGCCTTCGTCAATAAGGGTCCCACCATCACGGGCTAATAATCTTTCTCAGTTTAGGTG
ATATTGAGGTATTGAAACTGTTAGAAATCTGACAGATTTGACCAAGATTTGGAGACGTCCACAT
AATTGGGAAGGACTGAGTGTCCCTAGCCACTCTCCTCTGGGATAACGCGGACGTCATTAGTTTG
CGAAGTGGGTGGGGAGAACAGGAGGATTGACTCTAATTTGGTGTGTAGTGGGGGCCTTGATGTC
CTTCTGCCTCTGTCCACATTTCCCCATGTGACTCATTGCACCCTGCATTGCTCACAGGGATCAT
TAGTTCTCCCGGTAGACAGAGCACCTCTGCAGCCTCTGCTCTGCTGCCTTGTGAATTTCCTACA
CAGACTTGGTTAGTTACAATTTGGAAACAGTTTTTTTGGGTTTTTTTCCTTTGTTTTAATCTTC
TCACAATGAAGCTGCTATTGGTGACAGGGACAGGGGAGCAGGAAGCCAACCCAGGGAAACATGC
GAGTTTCCTGCACACCACTTAGTCACCTGCCCTCACTGGCCAACCCCCTACTGCTGTTCCCAGT
CAGTCTGGTTTTTAGAGGCATCGTGGCAATAGAATAGCTGGATACACTAATCTCTACAAGGTGT
CAGGCAGGAGATTCACCTTCCCCAGTCCCAGGGGACAGGAGAGAAATCTGTAAAGGGACAGATG
CACCATCTTTATTTCAAAAGAAAAAGCTCCCTCAGATTGTGTTACTAGGAGTCTCTTTTGTGAC
ATTTACTGAGCTTTCTCCCCAATCTTACCTTCCTATTGGCTACTTTTTAAATAAAAATAAACAT
TTTAGGCTAATATGACAAAAATGAGATAAAATCTTAAAAACATTGTACTAGTGTACAGTTACTA
AAATGTGCTTACTACAAAACAGTAAAATATTTCACTCTGTAAATCATCACTAAGTAGTTATTCT
GTCCTGTTGATTATGAGCCTCCAAAAATGTTTAATGCTTGAAGGATGGTTTGGGAGGCAGGGAA
TCCTTTTCTTAAAACAACTTTAATGAGGCATATGTTACATATCATAAAACACCCATTTCAAGTG
TACATTTCAGTGATTTTAGTAACTTCCCTCAGTGGTGTAGCTGTAACTATTACTCAGTTTTAGA
ACATTTTTATCCCTCCCAATAAGATCCTTCATGCTCTTTTACAGTTAATCCTGTTCTTACCCCC
GGCAACCACTAATCTACTTTCTCTATAAATTTGCCCTTTCTGGACAGTTCAAATCAATGGAATC
ATACAATATGTGGTCCCTTGGGTCTGGCTTTTTTACTTAGCTAATGTTTTTGAGGTTTGTCCAT
GACAGATAACGTCTTGGTAGTTTGTTCCTTTTATTGCTGAGTAGAATTCTGTTGATGGATGTAC
CACATTTTGTCAGCAGAGAGCCTTTTAAACTTGGATTCCAACTTCCTGTTGTCTAAACGGAACC
CTCCGAACGTAGGACTTATAGGGGAAGCTGCTGTGCATGTCAAAAAAACTACTAATCAGAATGA
GCTTTGTCATCCAGAGCCAGAACTGCTGCAGAAATTTTTATAATTTTGCAACTTCTTTTTTTAC
AAGGAACTTTTGTGCTACTACACATCAGGACTTTTGAAGCATCCAATAAATCCATTTAATAAGT
ATGAGCATGTGTCTGAGTGGACAAGAAAGTGAAACCATCCATGCTACATTGGATAATTTTTCCT
CCCCCAGACTGGACAGGGAATCTCAGCTTTCAAAACAGAGTAACCTGGCTCCACTTACAAAGCT
GCACAGGCATTAAAGATCGTGCTGCCTTTGTTAGGCAGATTTGGAGGGGAGGCCCAACAGCAAA
GATGGAGAGGAAAAAGGGAGTGGAGCTTGTGGAACAGGAAGCCCCCCAGGGTCTGTGCAGGGCT
GCTCAGCTCTTGAGGATGTTGTGGATGGTGAAGTGGTGATGGTGTCCCGGAGCAGCCCAGCACC
TCCACTGGGCCCAGAAGGTCTTGACTTCGGACACTTACCCCTGTTTCACAAGTGTTTATAAAGC
TGTTTTTGCTTTTTTTCCCCTAATCATTACTTGGTAGTTATTAATCCTTCTTTGGGGGAGGGAC
AGGGCTTTAAAACTGAAGAAAATAATTTTCATAAAAATATCAAAAATGGAAAAAAGTTACTTTG
TAAAAAATTTGCTATACAAACCAAATGGCAGCTGTTGAGAATCTCAATAAAATGTTAAATGCA

hide sequence

RefSeq Acc Id:

XM_054342025 ⟹ XP_054198000

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	71,193,792 - 71,237,549 (-)	NCBI

RefSeq Acc Id:

XM_054342026 ⟹ XP_054198001

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	71,193,792 - 71,237,559 (-)	NCBI

RefSeq Acc Id:

XM_054342027 ⟹ XP_054198002

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	71,193,792 - 71,237,461 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_065192	(Get FASTA)	NCBI Sequence Viewer
	XP_005264367	(Get FASTA)	NCBI Sequence Viewer
	XP_005264368	(Get FASTA)	NCBI Sequence Viewer
	XP_011531144	(Get FASTA)	NCBI Sequence Viewer
	XP_054198000	(Get FASTA)	NCBI Sequence Viewer
	XP_054198001	(Get FASTA)	NCBI Sequence Viewer
	XP_054198002	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	BAA86469	(Get FASTA)	NCBI Sequence Viewer
	EAW99774	(Get FASTA)	NCBI Sequence Viewer
	EAW99775	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000244221
	ENSP00000244221.8
GenBank Protein	Q9ULR5	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_065192 ⟸ NM_020459
- UniProtKB:	Q9ULR5 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MNGSNMANTSPSVKSKEDQGLSGHDEKENPFAEYMWMENEEDFNRQVEEELQEQDFLDRCFQEM LDEEDQDWFIPSRDLPQAMGQLQQQLNGLSVSEGHDSEDILSKSNLNPDAKEFIPGEKY hide sequence

RefSeq Acc Id:	XP_005264368 ⟸ XM_005264311
- Peptide Label:	isoform X2
- UniProtKB:	Q9ULR5 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MNGSNMANTSPSVKSKEDQGLSGHDEKENPFAEYMWMENEEDFNRQVEEELQEQDFLDRCFQEM LDEEDQDWFIPSRDLPQAMGQLQQQLNGLSVSEGHDSEDILSKSNLNPDAKEFIPGEKY hide sequence

RefSeq Acc Id:	XP_005264367 ⟸ XM_005264310
- Peptide Label:	isoform X2
- UniProtKB:	Q9ULR5 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MNGSNMANTSPSVKSKEDQGLSGHDEKENPFAEYMWMENEEDFNRQVEEELQEQDFLDRCFQEM LDEEDQDWFIPSRDLPQAMGQLQQQLNGLSVSEGHDSEDILSKSNLNPDAKEFIPGEKY hide sequence

RefSeq Acc Id:	XP_011531144 ⟸ XM_011532842
- Peptide Label:	isoform X1
- Sequence:	show sequence MPHLPGRRSPLLLCLAVRSIIMNGSNMANTSPSVKSKEDQGLSGHDEKENPFAEYMWMENEEDF NRQVEEELQEQDFLDRCFQEMLDEEDQDWFIPSRDLPQAMGQLQQQLNGLSVSEGHDSEDILSK SNLNPDAKEFIPGEKY hide sequence

Ensembl Acc Id:

ENSP00000244221 ⟸ ENST00000244221

RefSeq Acc Id:	XP_054198001 ⟸ XM_054342026
- Peptide Label:	isoform X2
- UniProtKB:	Q9ULR5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054198000 ⟸ XM_054342025
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054198002 ⟸ XM_054342027
- Peptide Label:	isoform X2
- UniProtKB:	Q9ULR5 (UniProtKB/Swiss-Prot)

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9ULR5-F1-model_v2	AlphaFold	Q9ULR5	1-123	view protein structure

Promoters

RGD ID:

6860638

Promoter ID:

EPDNEW_H3484

Type:

initiation region

Name:

PAIP2B_1

Description:

poly binding protein interacting protein 2B

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	2	71,227,103 - 71,227,163	EPDNEW

RGD ID:

6797908

Promoter ID:

HG_KWN:33186

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_020459

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	2	71,307,541 - 71,308,041 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:29200	AgrOrtholog
COSMIC	PAIP2B	COSMIC
Ensembl Genes	ENSG00000124374	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000244221	ENTREZGENE
	ENST00000244221.9	UniProtKB/Swiss-Prot
GTEx	ENSG00000124374	GTEx
HGNC ID	HGNC:29200	ENTREZGENE
Human Proteome Map	PAIP2B	Human Proteome Map
InterPro	Ataxin-2_C	UniProtKB/Swiss-Prot
	PAIP2-like	UniProtKB/Swiss-Prot
KEGG Report	hsa:400961	UniProtKB/Swiss-Prot
NCBI Gene	400961	ENTREZGENE
OMIM	611018	OMIM
PANTHER	POLYADENYLATE-BINDING PROTEIN-INTERACTING PROTEIN 2B	UniProtKB/Swiss-Prot
	PTHR13154	UniProtKB/Swiss-Prot
Pfam	PAM2	UniProtKB/Swiss-Prot
PharmGKB	KIAA1155	RGD
	PA162398595	PharmGKB
UniProt	PAI2B_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar