MMP28 (matrix metallopeptidase 28)

Gene: MMP28 (matrix metallopeptidase 28) Homo sapiens

Analyze

Symbol:

MMP28

Name:

matrix metallopeptidase 28

RGD ID:

1323102

HGNC Page

HGNC:14366

Description:

Predicted to enable metalloendopeptidase activity. Predicted to be involved in collagen catabolic process and extracellular matrix organization. Predicted to act upstream of or within negative regulation of macrophage chemotaxis. Located in collagen-containing extracellular matrix.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

epilysin; matrix metalloprotease MMP25; matrix metalloproteinase 28; matrix metalloproteinase-28; MM28; MMP-25; MMP-28; MMP25; putative MMP28 gene product; uncharacterized protein LOC79148

RGD Orthologs

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Mmp28 (matrix metallopeptidase 28 (epilysin))	HGNC	Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, Panther, PhylomeDB
Rattus norvegicus (Norway rat):	Mmp28 (matrix metallopeptidase 28)	HGNC	HomoloGene, NCBI, Panther
Chinchilla lanigera (long-tailed chinchilla):	Mmp28 (matrix metallopeptidase 28)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	MMP28 (matrix metallopeptidase 28)	NCBI	Ortholog
Canis lupus familiaris (dog):	MMP28 (matrix metallopeptidase 28)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, Panther
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Mmp28 (matrix metallopeptidase 28)	NCBI	Ortholog
Sus scrofa (pig):	MMP28 (matrix metallopeptidase 28)	HGNC	Ensembl, NCBI, OrthoDB
Chlorocebus sabaeus (green monkey):	MMP28 (matrix metallopeptidase 28)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Mmp28 (matrix metallopeptidase 28)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Gemin5 (gem (nuclear organelle) associated protein 5)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Mmp28 (matrix metallopeptidase 28)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Mmp28 (matrix metallopeptidase 28 (epilysin))	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	mmp28 (matrix metallopeptidase 28)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Caenorhabditis elegans (roundworm):	zmp-3	Alliance	DIOPT (Ensembl Compara\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	mmp28.L	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	mmp28.S	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	mmp28	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)

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	17	35,756,249 - 35,795,641 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	35,756,249 - 35,795,707 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	34,083,268 - 34,122,645 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	31,116,989 - 31,146,753 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	17	31,116,988 - 31,146,741	NCBI
Celera	17	31,003,010 - 31,032,922 (-)	NCBI		Celera
Cytogenetic Map	17	q12	NCBI
HuRef	17	30,278,035 - 30,307,831 (-)	NCBI		HuRef
CHM1_1	17	34,157,411 - 34,187,192 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	17	36,704,182 - 36,743,551 (-)	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

Arterial Occlusive Diseases (IEP)

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dichloroethane (ISO)

1,2-dimethylhydrazine (ISO)

17beta-estradiol (EXP,ISO)

17beta-estradiol 3-benzoate (ISO)

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

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

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

3,4-methylenedioxymethamphetamine (ISO)

4,4'-sulfonyldiphenol (ISO)

all-trans-retinoic acid (EXP)

amphotericin B (EXP)

antirheumatic drug (EXP)

arsane (EXP)

arsenic atom (EXP)

arsenous acid (EXP)

benzo[a]pyrene (EXP)

bis(2-ethylhexyl) phthalate (EXP)

bisphenol A (ISO)

C60 fullerene (ISO)

cisplatin (EXP)

diarsenic trioxide (EXP)

ethanol (ISO)

fenvalerate (ISO)

fluoranthene (ISO)

gentamycin (ISO)

microcystin-LR (ISO)

monosodium L-glutamate (ISO)

ozone (ISO)

paracetamol (ISO)

PCB138 (ISO)

pterostilbene (ISO)

simvastatin (EXP)

sodium fluoride (ISO)

sulforaphane (EXP)

testosterone (ISO)

triclosan (EXP)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

collagen catabolic process (IBA)

extracellular matrix organization (IBA)

negative regulation of macrophage chemotaxis (IEA,ISO)

proteolysis (IEA)

Cellular Component

collagen-containing extracellular matrix (HDA)

cytoplasm (IEA)

extracellular matrix (IEA,NAS)

extracellular region (IEA)

extracellular space (IBA)

Molecular Function

metal ion binding (IEA)

metalloendopeptidase activity (IBA,IEA,TAS)

metallopeptidase activity (IEA)

protein binding (IPI)

zinc ion binding (IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	Assessment of gene expression profiles in peripheral occlusive arterial disease.	Bubenek S, etal., Can J Cardiol. 2012 Nov-Dec;28(6):712-20. doi: 10.1016/j.cjca.2012.03.013. Epub 2012 Jun 19.
2.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
3.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:8889548	PMID:11121398	PMID:11255011	PMID:11574168	PMID:12164918	PMID:12477932	PMID:12975309	PMID:14506071	PMID:14730609	PMID:15185874	PMID:15593191	PMID:15953044
PMID:16344560	PMID:18778487	PMID:19375502	PMID:19379669	PMID:19921252	PMID:20003223	PMID:20144149	PMID:21152186	PMID:21615884	PMID:21723775	PMID:21801383	PMID:21873635
PMID:22040290	PMID:23549873	PMID:23803888	PMID:23964118	PMID:24167355	PMID:24385575	PMID:24710352	PMID:25429835	PMID:26186194	PMID:27068509	PMID:28293015	PMID:28514442
PMID:29373068	PMID:29729262	PMID:30021884	PMID:30913394	PMID:32268921	PMID:32296183	PMID:33191847	PMID:33961781	PMID:35256949

Genomics

Comparative Map Data

MMP28
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	17	35,756,249 - 35,795,641 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	35,756,249 - 35,795,707 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	34,083,268 - 34,122,645 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	31,116,989 - 31,146,753 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	17	31,116,988 - 31,146,741	NCBI
Celera	17	31,003,010 - 31,032,922 (-)	NCBI		Celera
Cytogenetic Map	17	q12	NCBI
HuRef	17	30,278,035 - 30,307,831 (-)	NCBI		HuRef
CHM1_1	17	34,157,411 - 34,187,192 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	17	36,704,182 - 36,743,551 (-)	NCBI		T2T-CHM13v2.0

Mmp28
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	11	83,331,594 - 83,353,890 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	11	83,331,594 - 83,353,897 (-)	Ensembl		GRCm39 Ensembl
GRCm38	11	83,440,768 - 83,463,040 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	11	83,440,768 - 83,463,071 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	11	83,255,378 - 83,276,463 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	11	83,258,071 - 83,279,156 (-)	NCBI		MGSCv36	mm8
Celera	11	93,036,503 - 93,057,585 (-)	NCBI		Celera
Cytogenetic Map	11	C	NCBI
cM Map	11	50.39	NCBI

Mmp28
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	10	68,738,651 - 68,762,377 (-)	NCBI		GRCr8
mRatBN7.2	10	68,241,138 - 68,264,866 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	10	68,241,138 - 68,264,866 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	10	72,863,750 - 72,884,732 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	10	72,369,134 - 72,390,115 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	10	67,833,186 - 67,854,165 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	10	70,660,691 - 70,681,672 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	10	70,660,691 - 70,681,672 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	10	71,122,715 - 71,143,696 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	10	71,526,718 - 71,547,699 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	10	71,541,276 - 71,562,259 (-)	NCBI
Celera	10	67,185,212 - 67,206,220 (-)	NCBI		Celera
Cytogenetic Map	10	q26	NCBI

Mmp28
(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_004955481	10,207,704 - 10,232,816 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955481	10,207,704 - 10,242,666 (-)	NCBI	ChiLan1.0	ChiLan1.0

MMP28
(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	19	28,681,345 - 28,710,941 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	17	30,560,619 - 30,590,184 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	17	20,999,658 - 21,039,476 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	17	21,293,767 - 21,333,684 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	17	21,293,767 - 21,323,691 (+)	Ensembl	panpan1.1		panPan2

MMP28
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	9	37,873,364 - 37,907,724 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	9	37,884,430 - 37,907,719 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	9	37,097,600 - 37,131,941 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	9	38,685,116 - 38,719,456 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	9	38,696,188 - 38,718,859 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	9	37,467,864 - 37,502,250 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	9	37,753,363 - 37,787,721 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	9	37,840,856 - 37,875,211 (+)	NCBI		UU_Cfam_GSD_1.0

Mmp28
(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_024405602	36,886,239 - 36,909,510 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936490	165,376 - 188,823 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936490	165,462 - 188,788 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

MMP28
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	12	39,739,630 - 39,766,791 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	12	39,739,074 - 39,766,794 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1

MMP28
(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	16	29,241,938 - 29,272,231 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	16	29,240,569 - 29,272,077 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666075	702,510 - 732,930 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Mmp28
(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_004624875	3,243,147 - 3,266,558 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624875	3,240,386 - 3,266,811 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in MMP28
15 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_024302.4(MMP28):c.1419C>T (p.Pro473=)	single nucleotide variant	Malignant melanoma [RCV000071417]	Chr17:35766644 [GRCh38] Chr17:34093663 [GRCh37] Chr17:31117776 [NCBI36] Chr17:17q12	not provided
NM_024302.4(MMP28):c.890G>A (p.Gly297Glu)	single nucleotide variant	Malignant melanoma [RCV000071418]	Chr17:35768340 [GRCh38] Chr17:34095359 [GRCh37] Chr17:31119472 [NCBI36] Chr17:17q12	not provided
GRCh38/hg38 17q12(chr17:35129859-35767049)x3	copy number gain	See cases [RCV000136983]	Chr17:35129859..35767049 [GRCh38] Chr17:33456878..34094068 [GRCh37] Chr17:30480991..31118181 [NCBI36] Chr17:17q12	uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	copy number gain	See cases [RCV000511439]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	copy number gain	See cases [RCV000512441]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17q12(chr17:32351496-34455576)x1	copy number loss	not provided [RCV000683918]	Chr17:32351496..34455576 [GRCh37] Chr17:17q12	uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3	copy number gain	not provided [RCV000739325]	Chr17:12344..81057996 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3	copy number gain	not provided [RCV000739324]	Chr17:8547..81060040 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3	copy number gain	not provided [RCV000739320]	Chr17:7214..81058310 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p11.2-q21.2(chr17:21690653-38772647)x3	copy number gain	not provided [RCV000846852]	Chr17:21690653..38772647 [GRCh37] Chr17:17p11.2-q21.2	pathogenic
NM_024302.5(MMP28):c.194C>T (p.Ala65Val)	single nucleotide variant	Inborn genetic diseases [RCV003252540]	Chr17:35779073 [GRCh38] Chr17:34106077 [GRCh37] Chr17:17q12	uncertain significance
NM_145272.4(C17orf50):c.386C>T (p.Pro129Leu)	single nucleotide variant	Inborn genetic diseases [RCV002752285]	Chr17:35764479 [GRCh38] Chr17:34091498 [GRCh37] Chr17:17q12	uncertain significance
NM_145272.4(C17orf50):c.511G>C (p.Ala171Pro)	single nucleotide variant	Inborn genetic diseases [RCV002778997]	Chr17:35764604 [GRCh38] Chr17:34091623 [GRCh37] Chr17:17q12	uncertain significance
NM_145272.4(C17orf50):c.76G>A (p.Glu26Lys)	single nucleotide variant	Inborn genetic diseases [RCV002762609]	Chr17:35764069 [GRCh38] Chr17:34091088 [GRCh37] Chr17:17q12	uncertain significance
NM_145272.4(C17orf50):c.314T>C (p.Leu105Pro)	single nucleotide variant	Inborn genetic diseases [RCV002886770]	Chr17:35764307 [GRCh38] Chr17:34091326 [GRCh37] Chr17:17q12	uncertain significance
NM_145272.4(C17orf50):c.356C>T (p.Pro119Leu)	single nucleotide variant	Inborn genetic diseases [RCV002782234]	Chr17:35764449 [GRCh38] Chr17:34091468 [GRCh37] Chr17:17q12	uncertain significance
NM_145272.4(C17orf50):c.185G>A (p.Gly62Asp)	single nucleotide variant	Inborn genetic diseases [RCV002956756]	Chr17:35764178 [GRCh38] Chr17:34091197 [GRCh37] Chr17:17q12	uncertain significance
NM_145272.4(C17orf50):c.225G>C (p.Gln75His)	single nucleotide variant	Inborn genetic diseases [RCV002983425]	Chr17:35764218 [GRCh38] Chr17:34091237 [GRCh37] Chr17:17q12	uncertain significance
NM_024302.5(MMP28):c.193G>A (p.Ala65Thr)	single nucleotide variant	Inborn genetic diseases [RCV002965439]	Chr17:35779074 [GRCh38] Chr17:34106078 [GRCh37] Chr17:17q12	uncertain significance
NM_024302.5(MMP28):c.865G>A (p.Gly289Ser)	single nucleotide variant	Inborn genetic diseases [RCV003201785]	Chr17:35768365 [GRCh38] Chr17:34095384 [GRCh37] Chr17:17q12	uncertain significance
GRCh37/hg19 17q11.2-12(chr17:30572862-35843988)	copy number loss	Chromosome 17q12 deletion syndrome [RCV003319594]	Chr17:30572862..35843988 [GRCh37] Chr17:17q11.2-12	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	3793
Count of miRNA genes:	857
Interacting mature miRNAs:	1001
Transcripts:	ENST00000250144, ENST00000587639, ENST00000587687, ENST00000587923, ENST00000589061, ENST00000589103, ENST00000590643, ENST00000593125
Prediction methods:	Microtar, Miranda, Pita, 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

D17S1833

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	34,124,050 - 34,124,205	UniSTS	GRCh37
Build 36	17	31,148,163 - 31,148,318	RGD	NCBI36
Celera	17	31,034,332 - 31,034,487	RGD
Cytogenetic Map	17	q21.1	UniSTS
HuRef	17	30,309,241 - 30,309,396	UniSTS
Marshfield Genetic Map	17	57.71	UniSTS
Marshfield Genetic Map	17	57.71	RGD
Genethon Genetic Map	17	58.3	UniSTS
deCODE Assembly Map	17	63.12	UniSTS

MMP28_924.2

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	34,092,713 - 34,093,509	UniSTS	GRCh37
Build 36	17	31,116,826 - 31,117,622	RGD	NCBI36
Celera	17	31,002,847 - 31,003,643	RGD
HuRef	17	30,277,872 - 30,278,668	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

1771

714

408

117

2994

819

1514

617

926

1001

1803

Low

531

1608

698

166

550

1035

1184

1974

128

558

399

152

203

938

Below cutoff

652

359

246

670

244

172

170

159

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001032278	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_024302	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_032950	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_111988	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525225	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525226	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525227	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525228	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525229	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525230	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525231	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525232	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017025061	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017025062	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017025063	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017025064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450943	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436731	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317173	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317174	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317175	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317176	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317177	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317178	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317179	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317180	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317181	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317182	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317183	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA813101	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC006237	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC015849	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF219624	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF315683	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF330002	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF336346	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK122604	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY358987	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC002631	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC011774	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM702847	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471147	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA761282	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA768574	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY027589	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000605424 ⟹ ENSP00000473853

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	35,765,865 - 35,795,641 (-)	Ensembl

RefSeq Acc Id:

ENST00000612292 ⟹ ENSP00000484562

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	35,768,315 - 35,779,311 (-)	Ensembl

RefSeq Acc Id:

ENST00000612672 ⟹ ENSP00000483539

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	35,778,505 - 35,795,707 (-)	Ensembl

RefSeq Acc Id:

ENST00000615136 ⟹ ENSP00000483299

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	35,766,340 - 35,795,624 (-)	Ensembl

RefSeq Acc Id:

ENST00000615317 ⟹ ENSP00000482385

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	35,756,249 - 35,768,326 (-)	Ensembl

RefSeq Acc Id:

ENST00000616383

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	35,778,505 - 35,779,368 (-)	Ensembl

RefSeq Acc Id:

ENST00000619655 ⟹ ENSP00000481051

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	35,756,250 - 35,795,707 (-)	Ensembl

RefSeq Acc Id:

NM_001032278 ⟹ NP_001027449

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,778,505 - 35,795,641 (-)	NCBI
GRCh37	17	34,083,316 - 34,122,711 (-)	NCBI
Build 36	17	31,129,622 - 31,146,753 (-)	NCBI Archive
HuRef	17	30,278,035 - 30,307,831 (-)	ENTREZGENE
CHM1_1	17	34,170,060 - 34,187,263 (-)	NCBI
T2T-CHM13v2.0	17	36,726,415 - 36,743,551 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCTCGGTCCCCGGGGCCGGCGGACCCGCGGGCAGGCACTGCCCGGGCTGGACGACGT
CTGGCCGGCTCCCGGCGAAGGGCAGCGGAGGAGCGGCCCAGAGCGCGCAGCTAGGGCACTGGCG
AAACCCCGGGACAGTCCCTCTCCGTGCGGGGGCGGCGCAGAGCAGTCCCATCCCCGGGGTCCCG
GGCGCGGCTGACTGCCGGCTGGTTCCCTGCGCGCAGTAGCTCCCCGAGCCGGGCTGCACCGGAG
GCGGCGAGATGGTCGCGCGCGTCGGCCTCCTGCTGCGCGCCCTGCAGCTGCTACTGTGGGGCCA
CCTGGACGCCCAGCCCGCGGAGCGCGGAGGCCAGGAGCTGCGCAAGGAGGCGGAGGCATTCCTA
GAGAAGTACGGATACCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGATG
CCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACCCT
GCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTGAG
AGGATCAGTGACTTGTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAAGC
AAGGTGAGCACTGTTAAAATCCGGCTAGGCCAAGATTTCCCAATGTCTTGAAGCCAATGGCTAG
GAAAACAGCTGAGCCTGGGACTGGACTTTGTCAGTAACCTCTCTTCCCTAGGGCACGGGAGGAG
TGGGTGAATAGGACCTCTTGGCTTGAGGACCATGATTGTGAATACAGACATTTAATTCAGAATG
ACACCTACATTGATGAATTTTCATTGTACAAGTGTTTTTCCAGATCAAACACAAAACCCATGTA
ATTCCTTGATAAATTTTCAATGCAGGGCAGATAAACTGTTGCTAACATTTTTCATTTATATTTA
CTGAAGTTATTTTCATCAGAATTCATTCTTTTTCATAAGTTATTAAACAAATGTGTGATCTATT
GA

hide sequence

RefSeq Acc Id:

NM_024302 ⟹ NP_077278

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,765,865 - 35,795,641 (-)	NCBI
GRCh37	17	34,083,316 - 34,122,711 (-)	NCBI
Build 36	17	31,116,989 - 31,146,753 (-)	NCBI Archive
HuRef	17	30,278,035 - 30,307,831 (-)	ENTREZGENE
CHM1_1	17	34,157,411 - 34,187,263 (-)	NCBI
T2T-CHM13v2.0	17	36,713,803 - 36,743,551 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCTCGGTCCCCGGGGCCGGCGGACCCGCGGGCAGGCACTGCCCGGGCTGGACGACGT
CTGGCCGGCTCCCGGCGAAGGGCAGCGGAGGAGCGGCCCAGAGCGCGCAGCTAGGGCACTGGCG
AAACCCCGGGACAGTCCCTCTCCGTGCGGGGGCGGCGCAGAGCAGTCCCATCCCCGGGGTCCCG
GGCGCGGCTGACTGCCGGCTGGTTCCCTGCGCGCAGTAGCTCCCCGAGCCGGGCTGCACCGGAG
GCGGCGAGATGGTCGCGCGCGTCGGCCTCCTGCTGCGCGCCCTGCAGCTGCTACTGTGGGGCCA
CCTGGACGCCCAGCCCGCGGAGCGCGGAGGCCAGGAGCTGCGCAAGGAGGCGGAGGCATTCCTA
GAGAAGTACGGATACCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGATG
CCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACCCT
GCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTGAG
AGGATCAGTGACTTGTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAAGC
AAGGTAACAAATGGTACAAGCAGCACCTCTCCTACCGCCTGGTGAACTGGCCTGAGCATCTGCC
GGAGCCGGCAGTTCGGGGCGCCGTGCGCGCCGCCTTCCAGTTGTGGAGCAACGTCTCAGCGCTG
GAGTTCTGGGAGGCCCCAGCCACAGGCCCCGCTGACATCCGGCTCACCTTCTTCCAAGGGGACC
ACAACGATGGGCTGGGCAATGCCTTTGATGGCCCAGGGGGCGCCCTGGCGCACGCCTTCCTGCC
CCGCCGCGGCGAAGCGCACTTCGACCAAGATGAGCGCTGGTCCCTGAGCCGCCGCCGCGGGCGC
AACCTGTTCGTGGTGCTGGCGCACGAGATCGGTCACACGCTTGGCCTCACCCACTCGCCCGCGC
CGCGCGCGCTCATGGCGCCCTACTACAAGAGGCTGGGCCGCGACGCGCTGCTCAGCTGGGACGA
CGTGCTGGCCGTGCAGAGCCTGTATGGGAAGCCCCTAGGGGGCTCAGTGGCCGTCCAGCTCCCA
GGAAAGCTGTTCACTGACTTTGAGACCTGGGACTCCTACAGCCCCCAAGGAAGGCGCCCTGAAA
CGCAGGGCCCTAAATACTGCCACTCTTCCTTCGATGCCATCACTGTAGACAGGCAACAGCAACT
GTACATTTTTAAAGGGAGCCATTTCTGGGAGGTGGCAGCTGATGGCAACGTCTCAGAGCCCCGT
CCACTGCAGGAAAGATGGGTCGGGCTGCCCCCCAACATTGAGGCTGCGGCAGTGTCATTGAATG
ATGGAGATTTCTACTTCTTCAAAGGGGGTCGATGCTGGAGGTTCCGGGGCCCCAAGCCAGTGTG
GGGTCTCCCACAGCTGTGCCGGGCAGGGGGCCTGCCCCGCCATCCTGACGCCGCCCTCTTCTTC
CCTCCTCTGCGCCGCCTCATCCTCTTCAAGGGTGCCCGCTACTACGTGCTGGCCCGAGGGGGAC
TGCAAGTGGAGCCCTACTACCCCCGAAGTCTGCAGGACTGGGGAGGCATCCCTGAGGAGGTCAG
CGGCGCCCTGCCGAGGCCCGATGGCTCCATCATCTTCTTCCGAGATGACCGCTACTGGCGCCTC
GACCAGGCCAAACTGCAGGCAACCACCTCGGGCCGCTGGGCCACCGAGCTGCCCTGGATGGGCT
GCTGGCATGCCAACTCGGGGAGCGCCCTGTTCTGAAGGCACCTCCTCACCTCAGAAACTGGTGG
TGCTCTCAGGGCAAAATCATGTTCCCCACCCCCGGGGCAGAACCCCTCTTAGAAGCCTCTGAGT
CCCTCTGCAGAAGACCGGGCAGCAAAGCCTCCATCTGGAAGTCTGTCTGCCTTTGTTCCTTGAA
GAATGCAGCATTGTCTTTGTCTGTCCCCACCACATGGAGGTGGGGGTGGGATCAATCTTAGGAA
AAGCAAAAAAGGGTCCCAGATCCCTTGGCCCTTTCCTCCGAGGACTTCTATCCTCCCCAGGCCT
TTGTTTCTTCGGCTAAAGGTACAGTTCCTTTCAAGAGGTAACAGCACTGGGATCCAAGCAGGGG
GATGAAAAACTCAGCAGAGAAATTCGAGACCATTTTGCAAGACTGTGCCCTTCTCCTCAGGACC
CCCTGGCTCAGTTCTTGAAAAACGGTGTCATATTTAGTCAGAGGCCCCACCCCCAGGAAGCATG
GATGGGGATGAAGGCACAGGCGTCTCCAACCTCAGAGGCCCTTTGTGGGGTCAGGACACAGAGT
GGGAGGGAGACTGATGCAGGCCTACCAGTCCCTGGCTTTTTGTCTGGGGCTGGAATAAAGAGGT
GCCTTCAGCTGGTGGGCCGAGAGGCAGGAA

hide sequence

RefSeq Acc Id:

NM_032950 ⟹ NP_116568

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,765,865 - 35,795,641 (-)	NCBI
CHM1_1	17	34,157,411 - 34,187,263 (-)	NCBI
T2T-CHM13v2.0	17	36,713,803 - 36,743,551 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCTCGGTCCCCGGGGCCGGCGGACCCGCGGGCAGGCACTGCCCGGGCTGGACGACGT
CTGGCCGGCTCCCGGCGAAGGGCAGCGGAGGAGCGGCCCAGAGCGCGCAGCTAGGGCACTGGCG
AAACCCCGGGACAGTCCCTCTCCGTGCGGGGGCGGCGCAGAGCAGTCCCATCCCCGGGGTCCCG
GGCGCGGCTGACTGCCGGCTGGTTCCCTGCGCGCAGTAGCTCCCCGAGCCGGGCTGCACCGGAG
GCGGCGAGATGGTCGCGCGCGTCGGCCTCCTGCTGCGCGCCCTGCAGCTGCTACTGTGGGGCCA
CCTGGACGCCCAGCCCGCGGAGCGCGGAGGCCAGGAGCTGCGCAAGGAGGCGGAGGCATTCCTA
GAGAAGTACGGATACCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGATG
CCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACCCT
GCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTGAG
AGGATCAGTGACTTGTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAAGC
AAGGTAACAAATGGTACAAGCAGCACCTCTCCTACCGCCTGGTGAACTGGCCTGAGCATCTGCC
GGAGCCGGCAGTTCGGGGCGCCGTGCGCGCCGCCTTCCAGTTGTGGAGCAACGTCTCAGCGCTG
GAGTTCTGGGAGGCCCCAGCCACAGGCCCCGCTGACATCCGGCTCACCTTCTTCCAAGGGGACC
ACAACGATGGGCTGGGCAATGCCTTTGATGGCCCAGGGGGCGCCCTGGCGCACGCCTTCCTGCC
CCGCCGCGGCGAAGCGCACTTCGACCAAGATGAGCGCTGGTCCCTGAGCCGCCGCCGCGGGCGC
AACCTGTTCGTGGTGCTGGCGCACGAGATCGGTCACACGCTTGGCCTCACCCACTCGCCCGCGC
CGCGCGCGCTCATGGCGCCCTACTACAAGAGGCTGGGCCGCGACGCGCTGCTCAGCTGGGACGA
CGTGCTGGCCGTGCAGAGCCTGTATGGGAAGCCCCTAGGGGGCTCAGTGGCCGTCCAGCTCCCA
GGAAAGCTGTTCACTGACTTTGAGACCTGGGACTCCTACAGCCCCCAAGGAAGGCGCCCTGAAA
CGCAGGGCCCTAAATACTGCCACTCTTCCTTCGATGCCATCACTGTAGACAGGCAACAGCAACT
GTACATTTTTAAAGGGAGCCATTTCTGGGAGGTGGCAGCTGATGGCAACGTCTCAGAGCCCCGT
CCACTGCAGGAAAGATGGGTCGGGCTGCCCCCCAACATTGAGGCTGCGGCAGTGTCATTGAATG
ATGGAGATTTCTACTTCTTCAAAGTGCAATCCGTTTGATTGATATGAATACCAACCATCGTGGG
CTCCAGCTTAAAGGAGAGCAGAGGGGGTCGATGCTGGAGGTTCCGGGGCCCCAAGCCAGTGTGG
GGTCTCCCACAGCTGTGCCGGGCAGGGGGCCTGCCCCGCCATCCTGACGCCGCCCTCTTCTTCC
CTCCTCTGCGCCGCCTCATCCTCTTCAAGGGTGCCCGCTACTACGTGCTGGCCCGAGGGGGACT
GCAAGTGGAGCCCTACTACCCCCGAAGTCTGCAGGACTGGGGAGGCATCCCTGAGGAGGTCAGC
GGCGCCCTGCCGAGGCCCGATGGCTCCATCATCTTCTTCCGAGATGACCGCTACTGGCGCCTCG
ACCAGGCCAAACTGCAGGCAACCACCTCGGGCCGCTGGGCCACCGAGCTGCCCTGGATGGGCTG
CTGGCATGCCAACTCGGGGAGCGCCCTGTTCTGAAGGCACCTCCTCACCTCAGAAACTGGTGGT
GCTCTCAGGGCAAAATCATGTTCCCCACCCCCGGGGCAGAACCCCTCTTAGAAGCCTCTGAGTC
CCTCTGCAGAAGACCGGGCAGCAAAGCCTCCATCTGGAAGTCTGTCTGCCTTTGTTCCTTGAAG
AATGCAGCATTGTCTTTGTCTGTCCCCACCACATGGAGGTGGGGGTGGGATCAATCTTAGGAAA
AGCAAAAAAGGGTCCCAGATCCCTTGGCCCTTTCCTCCGAGGACTTCTATCCTCCCCAGGCCTT
TGTTTCTTCGGCTAAAGGTACAGTTCCTTTCAAGAGGTAACAGCACTGGGATCCAAGCAGGGGG
ATGAAAAACTCAGCAGAGAAATTCGAGACCATTTTGCAAGACTGTGCCCTTCTCCTCAGGACCC
CCTGGCTCAGTTCTTGAAAAACGGTGTCATATTTAGTCAGAGGCCCCACCCCCAGGAAGCATGG
ATGGGGATGAAGGCACAGGCGTCTCCAACCTCAGAGGCCCTTTGTGGGGTCAGGACACAGAGTG
GGAGGGAGACTGATGCAGGCCTACCAGTCCCTGGCTTTTTGTCTGGGGCTGGAATAAAGAGGTG
CCTTCAGCTGGTGGGCCGAGAGGCAGGAA

hide sequence

RefSeq Acc Id:

NR_111988

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,756,249 - 35,795,641 (-)	NCBI
CHM1_1	17	34,147,803 - 34,187,263 (-)	NCBI
T2T-CHM13v2.0	17	36,704,182 - 36,743,551 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCTCGGTCCCCGGGGCCGGCGGACCCGCGGGCAGGCACTGCCCGGGCTGGACGACGT
CTGGCCGGCTCCCGGCGAAGGGCAGCGGAGGAGCGGCCCAGAGCGCGCAGCTAGGGCACTGGCG
AAACCCCGGGACAGTCCCTCTCCGTGCGGGGGCGGCGCAGAGCAGTCCCATCCCCGGGGTCCCG
GGCGCGGCTGACTGCCGGCTGGTTCCCTGCGCGCAGTAGCTCCCCGAGCCGGGCTGCACCGGAG
GCGGCGAGATGGTCGCGCGCGTCGGCCTCCTGCTGCGCGCCCTGCAGCTGCTACTGTGGGGCCA
CCTGGACGCCCAGCCCGCGGAGCGCGGAGGCCAGGAGCTGCGCAAGGAGGCGGAGGCATTCCTA
GAGAAGTACGGATACCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGATG
CCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACCCT
GCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTGAG
AGGATCAGTGACTTGTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAAGC
AAGGTAACAAATGGTACAAGCAGCACCTCTCCTACCGCCTGGTGAACTGGCCTGAGCATCTGCC
GGAGCCGGCAGTTCGGGGCGCCGTGCGCGCCGCCTTCCAGTTGTGGAGCAACGTCTCAGCGCTG
GAGTTCTGGGAGGCCCCAGCCACAGGCCCCGCTGACATCCGGCTCACCTTCTTCCAAGGGGACC
ACAACGATGGGCTGGGCAATGCCTTTGATGGCCCAGGGGGCGCCCTGGCGCACGCCTTCCTGCC
CCGCCGCGGCGAAGCGCACTTCGACCAAGATGAGCGCTGGTCCCTGAGCCGCCGCCGCGGGCGC
AACCTGTTCGTGGTGCTGGCGCACGAGATCGGTCACACGCTTGGCCTCACCCACTCGCCCGCGC
CGCGCGCGCTCATGGCGCCCTACTACAAGAGGCTGGGCCGCGACGCGCTGCTCAGCTGGGACGA
CGTGCTGGCCGTGCAGAGCCTGTATGGGAAGCCCCTAGGGGGCTCAGTGGCCGTCCAGCTCCCA
GGAAAGCTGTTCACTGACTTTGAGACCTGGGACTCCTACAGCCCCCAAGGAAGGCGCCCTGAAA
CGCAGGGCCCTAAATACTGCCACTCTTCCTTCGATGCCATCACTGTAGGGAGCCATTTCTGGGA
GGTGGCAGCTGATGGCAACGTCTCAGAGCCCCGTCCACTGCAGGAAAGATGGGTCGGGCTGCCC
CCCAACATTGAGGCTGCGGCAGTGTCATTGAATGATGGAGATTTCTACTTCTTCAAAGGGGGTC
GATGCTGGAGGTTCCGGGGCCCCAAGCCAGTGTGGGGTCTCCCACAGCTGTGCCGGGCAGGGGG
CCTGCCCCGCCATCCTGACGCCGCCCTCTTCTTCCCTCCTCTGCGCCGCCTCATCCTCTTCAAG
GGTGCCCGCTACTACGTGCTGGCCCGAGGGGGACTGCAAGTGGAGCCCTACTACCCCCGAAGTC
TGCAGGACTGGGGAGGCATCCCTGAGGAGGTCAGCGGCGCCCTGCCGAGGCCCGATGGCTCCAT
CATCTTCTTCCGAGATGACCGCTACTGGCGCCTCGACCAGGCCAAACTGCAGGCAACCACCTCG
GGCCGCTGGGCCACCGAGCTGCCCTGGATGGGCTGCTGGCATGCCAACTCGGGGAGCGCCCTGT
TCTGAAGGCACCTCCTCACCTCAGAAACTGGTGGTGCTCTCAGGGCAAAATCATGTTCCCCACC
CCCGGGGCAGAACCCCTCTTAGAAGCCTCTGAGTCCCTCTGCAGAAGACCGGGCAGCAAAGCCT
CCATCTGGAAGTCTGTCTGCCTTTGTTCCTTGAAGAATGCAGCATTGTCTTTGTCTGTCCCCAC
CACATGGAGGTGGGGGTGGGATCAATCTTAGGAAAAGCAAAAAAGGGTCCCAGATCCCTTGGCC
CTTTCCTCCGAGGACTTCTATCCTCCCCAGGCCTTTGTTTCTTCGGCTAAAGCCTGAGGACAAA
GTTCTGGGAGATCGGCATTGACTATGTAAGTAACAACAACGGCCTAAAGAAGCAACAAGAAAGG
AACCGAGTGCCTGGAGAACTTCATGGAGCAGAGCCACTTGCCTACTTTGGATCATCTGTCTCTA
AGAGAGGGAAATAAACATTTCTTTTGTGTGA

hide sequence

RefSeq Acc Id:

XM_011525225 ⟹ XP_011523527

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,765,865 - 35,795,641 (-)	NCBI

Sequence:

show sequence

AGCAGCGGCGCGGGGTGGGTGGGGCGGGAGTGCCGGGCCTCCGCCCCCTCCGCCTGCCTTTCCT
TCCTCCCTCCCTCGGTCCCCGGGGCCGGCGGACCCGCGGGCAGGCACTGCCCGGGCTGGACGAC
GTCTGGCCGGCTCCCGGCGAAGGGCAGCGGAGGAGCGGCCCAGAGCGCGCAGCTAGGGCACTGG
CGAAACCCCGGGACAGTCCCTCTCCGTGCGGGGGCGGCGCAGAGCAGTCCCATCCCCGGGGTCC
CGGGCGCGGCTGACTGCCGGCTGGTTCCCTGCGCGCAGTAGCTCCCCGAGCCGGGCTGCACCGG
AGGCGGCGAGATGGTCGCGCGCGTCGGCCTCCTGCTGCGCGCCCTGCAGCTGCTACTGTGGGGC
CACCTGGACGCCCAGCCCGCGGAGCGCGGAGGCCAGGAGCTGCGCAAGGAGGCGGAGGCATTCC
TAGAGAAGTACGGATACCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGA
TGCCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACC
CTGCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTG
AGAGGATCAGTGACTTGTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAA
GCAAGGGGGCGCCCTGGCGCACGCCTTCCTGCCCCGCCGCGGCGAAGCGCACTTCGACCAAGAT
GAGCGCTGGTCCCTGAGCCGCCGCCGCGGGCGCAACCTGTTCGTGGTGCTGGCGCACGAGATCG
GTCACACGCTTGGCCTCACCCACTCGCCCGCGCCGCGCGCGCTCATGGCGCCCTACTACAAGAG
GCTGGGCCGCGACGCGCTGCTCAGCTGGGACGACGTGCTGGCCGTGCAGAGCCTGTATGGGAAG
CCCCTAGGGGGCTCAGTGGCCGTCCAGCTCCCAGGAAAGCTGTTCACTGACTTTGAGACCTGGG
ACTCCTACAGCCCCCAAGGAAGGCGCCCTGAAACGCAGGGCCCTAAATACTGCCACTCTTCCTT
CGATGCCATCACTGTAGACAGGCAACAGCAACTGTACATTTTTAAAGGGAGCCATTTCTGGGAG
GTGGCAGCTGATGGCAACGTCTCAGAGCCCCGTCCACTGCAGGAAAGATGGGTCGGGCTGCCCC
CCAACATTGAGGCTGCGGCAGTGTCATTGAATGATGGAGATTTCTACTTCTTCAAAGGGGGTCG
ATGCTGGAGGTTCCGGGGCCCCAAGCCAGTGTGGGGTCTCCCACAGCTGTGCCGGGCAGGGGGC
CTGCCCCGCCATCCTGACGCCGCCCTCTTCTTCCCTCCTCTGCGCCGCCTCATCCTCTTCAAGG
GTGCCCGCTACTACGTGCTGGCCCGAGGGGGACTGCAAGTGGAGCCCTACTACCCCCGAAGTCT
GCAGGACTGGGGAGGCATCCCTGAGGAGGTCAGCGGCGCCCTGCCGAGGCCCGATGGCTCCATC
ATCTTCTTCCGAGATGACCGCTACTGGCGCCTCGACCAGGCCAAACTGCAGGCAACCACCTCGG
GCCGCTGGGCCACCGAGCTGCCCTGGATGGGCTGCTGGCATGCCAACTCGGGGAGCGCCCTGTT
CTGAAGGCACCTCCTCACCTCAGAAACTGGTGGTGCTCTCAGGGCAAAATCATGTTCCCCACCC
CCGGGGCAGAACCCCTCTTAGAAGCCTCTGAGTCCCTCTGCAGAAGACCGGGCAGCAAAGCCTC
CATCTGGAAGTCTGTCTGCCTTTGTTCCTTGAAGAATGCAGCATTGTCTTTGTCTGTCCCCACC
ACATGGAGGTGGGGGTGGGATCAATCTTAGGAAAAGCAAAAAAGGGTCCCAGATCCCTTGGCCC
TTTCCTCCGAGGACTTCTATCCTCCCCAGGCCTTTGTTTCTTCGGCTAAAGGTACAGTTCCTTT
CAAGAGGTAACAGCACTGGGATCCAAGCAGGGGGATGAAAAACTCAGCAGAGAAATTCGAGACC
ATTTTGCAAGACTGTGCCCTTCTCCTCAGGACCCCCTGGCTCAGTTCTTGAAAAACGGTGTCAT
ATTTAGTCAGAGGCCCCACCCCCAGGAAGCATGGATGGGGATGAAGGCACAGGCGTCTCCAACC
TCAGAGGCCCTTTGTGGGGTCAGGACACAGAGTGGGAGGGAGACTGATGCAGGCCTACCAGTCC
CTGGCTTTTTGTCTGGGGCTGGAATAAAGAGGTGCCTTCAGCTGGTGGGCCGAGAGGCAGGAAG
CAGCCTT

hide sequence

RefSeq Acc Id:

XM_011525226 ⟹ XP_011523528

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,765,865 - 35,795,641 (-)	NCBI

Sequence:

show sequence

TGCCTTTCCTTCCTCCCTCCCTCGGTCCCCGGGGCCGGCGGACCCGCGGGCAGGCACTGCCCGG
GCTGGACGACGTCTGGCCGGCTCCCGGCGAAGGGCAGCGGAGGAGCGGCCCAGAGCGCGCAGCT
AGGGCACTGGCGAAACCCCGGGACAGTCCCTCTCCGTGCGGGGGCGGCGCAGAGCAGTCCCATC
CCCGGGGTCCCGGGCGCGGCTGACTGCCGGCTGGTTCCCTGCGCGCAGTAGCTCCCCGAGCCGG
GCTGCACCGGAGGCGGCGAGATGGTCGCGCGCGTCGGCCTCCTGCTGCGCGCCCTGCAGCTGCT
ACTGTGGGGCCACCTGGACGCCCAGCCCGCGGAGCGCGGAGGCCAGGAGCTGCGCAAGGAGGCG
GAGGAGGAAACTGAGGCATGAAAAATGCCTCACAGAAGAGGGTTAGGGACACCTCCAGGAGCAG
AGGGAGTTTCAACCCCACCACCTCCTCACCCGGGAAGTTGGATCTGCCTCCACTCCACAGAATG
TGAGAGCACCCAGCCCTGACAGCATTAAGGAGCCCCTTCCTGCATTCCTAGAGAAGTACGGATA
CCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGATGCCATCAGAGCGTTT
CAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACCCTGCGCCAGATGACTC
GTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTGAGAGGATCAGTGACTT
GTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAAGCAAGGTAACAAATGG
TACAAGCAGCACCTCTCCTACCGCCTGGTGAACTGGCCTGAGCATCTGCCGGAGCCGGCAGTTC
GGGGCGCCGTGCGCGCCGCCTTCCAGTTGTGGAGCAACGTCTCAGCGCTGGAGTTCTGGGAGGC
CCCAGCCACAGGCCCCGCTGACATCCGGCTCACCTTCTTCCAAGGGGACCACAACGATGGGCTG
GGCAATGCCTTTGATGGCCCAGGGGGCGCCCTGGCGCACGCCTTCCTGCCCCGCCGCGGCGAAG
CGCACTTCGACCAAGATGAGCGCTGGTCCCTGAGCCGCCGCCGCGGGCGCAACCTGTTCGTGGT
GCTGGCGCACGAGATCGGTCACACGCTTGGCCTCACCCACTCGCCCGCGCCGCGCGCGCTCATG
GCGCCCTACTACAAGAGGCTGGGCCGCGACGCGCTGCTCAGCTGGGACGACGTGCTGGCCGTGC
AGAGCCTGTATGGGAAGCCCCTAGGGGGCTCAGTGGCCGTCCAGCTCCCAGGAAAGCTGTTCAC
TGACTTTGAGACCTGGGACTCCTACAGCCCCCAAGGAAGGCGCCCTGAAACGCAGGGCCCTAAA
TACTGCCACTCTTCCTTCGATGCCATCACTGTAGACAGGCAACAGCAACTGTACATTTTTAAAG
GGAGCCATTTCTGGGAGGTGGCAGCTGATGGCAACGTCTCAGAGCCCCGTCCACTGCAGGAAAG
ATGGGTCGGGCTGCCCCCCAACATTGAGGCTGCGGCAGTGTCATTGAATGATGGAGATTTCTAC
TTCTTCAAAGGGGGTCGATGCTGGAGGTTCCGGGGCCCCAAGCCAGTGTGGGGTCTCCCACAGC
TGTGCCGGGCAGGGGGCCTGCCCCGCCATCCTGACGCCGCCCTCTTCTTCCCTCCTCTGCGCCG
CCTCATCCTCTTCAAGGGTGCCCGCTACTACGTGCTGGCCCGAGGGGGACTGCAAGTGGAGCCC
TACTACCCCCGAAGTCTGCAGGACTGGGGAGGCATCCCTGAGGAGGTCAGCGGCGCCCTGCCGA
GGCCCGATGGCTCCATCATCTTCTTCCGAGATGACCGCTACTGGCGCCTCGACCAGGCCAAACT
GCAGGCAACCACCTCGGGCCGCTGGGCCACCGAGCTGCCCTGGATGGGCTGCTGGCATGCCAAC
TCGGGGAGCGCCCTGTTCTGAAGGCACCTCCTCACCTCAGAAACTGGTGGTGCTCTCAGGGCAA
AATCATGTTCCCCACCCCCGGGGCAGAACCCCTCTTAGAAGCCTCTGAGTCCCTCTGCAGAAGA
CCGGGCAGCAAAGCCTCCATCTGGAAGTCTGTCTGCCTTTGTTCCTTGAAGAATGCAGCATTGT
CTTTGTCTGTCCCCACCACATGGAGGTGGGGGTGGGATCAATCTTAGGAAAAGCAAAAAAGGGT
CCCAGATCCCTTGGCCCTTTCCTCCGAGGACTTCTATCCTCCCCAGGCCTTTGTTTCTTCGGCT
AAAGGTACAGTTCCTTTCAAGAGGTAACAGCACTGGGATCCAAGCAGGGGGATGAAAAACTCAG
CAGAGAAATTCGAGACCATTTTGCAAGACTGTGCCCTTCTCCTCAGGACCCCCTGGCTCAGTTC
TTGAAAAACGGTGTCATATTTAGTCAGAGGCCCCACCCCCAGGAAGCATGGATGGGGATGAAGG
CACAGGCGTCTCCAACCTCAGAGGCCCTTTGTGGGGTCAGGACACAGAGTGGGAGGGAGACTGA
TGCAGGCCTACCAGTCCCTGGCTTTTTGTCTGGGGCTGGAATAAAGAGGTGCCTTCAGCTGGTG
GGCCGAGAGGCAGGAAGCAGCCTT

hide sequence

RefSeq Acc Id:

XM_011525227 ⟹ XP_011523529

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,765,865 - 35,795,260 (-)	NCBI

Sequence:

show sequence

TACCTGGCGGAGAGCGGAGGAAACTGAGGCATGAAAAATGCCTCACAGAAGAGGGTTAGGGACA
CCTCCAGGAGCAGAGGGAGTTTCAACCCCACCACCTCCTCACCCGGGAAGTTGGATCTGCCTCC
ACTCCACAGAATGTGAGAGCACCCAGCCCTGACAGCATTAAGGAGCCCCTTCCTGCATTCCTAG
AGAAGTACGGATACCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGATGC
CATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACCCTG
CGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTGAGA
GGATCAGTGACTTGTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAAGCA
AGGTAACAAATGGTACAAGCAGCACCTCTCCTACCGCCTGGTGAACTGGCCTGAGCATCTGCCG
GAGCCGGCAGTTCGGGGCGCCGTGCGCGCCGCCTTCCAGTTGTGGAGCAACGTCTCAGCGCTGG
AGTTCTGGGAGGCCCCAGCCACAGGCCCCGCTGACATCCGGCTCACCTTCTTCCAAGGGGACCA
CAACGATGGGCTGGGCAATGCCTTTGATGGCCCAGGGGGCGCCCTGGCGCACGCCTTCCTGCCC
CGCCGCGGCGAAGCGCACTTCGACCAAGATGAGCGCTGGTCCCTGAGCCGCCGCCGCGGGCGCA
ACCTGTTCGTGGTGCTGGCGCACGAGATCGGTCACACGCTTGGCCTCACCCACTCGCCCGCGCC
GCGCGCGCTCATGGCGCCCTACTACAAGAGGCTGGGCCGCGACGCGCTGCTCAGCTGGGACGAC
GTGCTGGCCGTGCAGAGCCTGTATGGGAAGCCCCTAGGGGGCTCAGTGGCCGTCCAGCTCCCAG
GAAAGCTGTTCACTGACTTTGAGACCTGGGACTCCTACAGCCCCCAAGGAAGGCGCCCTGAAAC
GCAGGGCCCTAAATACTGCCACTCTTCCTTCGATGCCATCACTGTAGACAGGCAACAGCAACTG
TACATTTTTAAAGGGAGCCATTTCTGGGAGGTGGCAGCTGATGGCAACGTCTCAGAGCCCCGTC
CACTGCAGGAAAGATGGGTCGGGCTGCCCCCCAACATTGAGGCTGCGGCAGTGTCATTGAATGA
TGGAGATTTCTACTTCTTCAAAGGGGGTCGATGCTGGAGGTTCCGGGGCCCCAAGCCAGTGTGG
GGTCTCCCACAGCTGTGCCGGGCAGGGGGCCTGCCCCGCCATCCTGACGCCGCCCTCTTCTTCC
CTCCTCTGCGCCGCCTCATCCTCTTCAAGGGTGCCCGCTACTACGTGCTGGCCCGAGGGGGACT
GCAAGTGGAGCCCTACTACCCCCGAAGTCTGCAGGACTGGGGAGGCATCCCTGAGGAGGTCAGC
GGCGCCCTGCCGAGGCCCGATGGCTCCATCATCTTCTTCCGAGATGACCGCTACTGGCGCCTCG
ACCAGGCCAAACTGCAGGCAACCACCTCGGGCCGCTGGGCCACCGAGCTGCCCTGGATGGGCTG
CTGGCATGCCAACTCGGGGAGCGCCCTGTTCTGAAGGCACCTCCTCACCTCAGAAACTGGTGGT
GCTCTCAGGGCAAAATCATGTTCCCCACCCCCGGGGCAGAACCCCTCTTAGAAGCCTCTGAGTC
CCTCTGCAGAAGACCGGGCAGCAAAGCCTCCATCTGGAAGTCTGTCTGCCTTTGTTCCTTGAAG
AATGCAGCATTGTCTTTGTCTGTCCCCACCACATGGAGGTGGGGGTGGGATCAATCTTAGGAAA
AGCAAAAAAGGGTCCCAGATCCCTTGGCCCTTTCCTCCGAGGACTTCTATCCTCCCCAGGCCTT
TGTTTCTTCGGCTAAAGGTACAGTTCCTTTCAAGAGGTAACAGCACTGGGATCCAAGCAGGGGG
ATGAAAAACTCAGCAGAGAAATTCGAGACCATTTTGCAAGACTGTGCCCTTCTCCTCAGGACCC
CCTGGCTCAGTTCTTGAAAAACGGTGTCATATTTAGTCAGAGGCCCCACCCCCAGGAAGCATGG
ATGGGGATGAAGGCACAGGCGTCTCCAACCTCAGAGGCCCTTTGTGGGGTCAGGACACAGAGTG
GGAGGGAGACTGATGCAGGCCTACCAGTCCCTGGCTTTTTGTCTGGGGCTGGAATAAAGAGGTG
CCTTCAGCTGGTGGGCCGAGAGGCAGGAAGCAGCCTT

hide sequence

RefSeq Acc Id:

XM_011525229 ⟹ XP_011523531

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,765,865 - 35,795,263 (-)	NCBI

Sequence:

show sequence

ACGCCGTGTGTACCTGGCGGAGAGCGGTGCGTGTGCTTGAGACCTGTCAGAACTCGGCAGTCAG
GCCACCCGGCAGTCCCCTGCATTCCTAGAGAAGTACGGATACCTCAATGAACAGGTCCCCAAAG
CTCCCACCTCCACTCGATTCAGCGATGCCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGT
CAGCGGCGTGTTGGACCGCGCCACCCTGCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGAT
ACCAACAGTTATGCGGCCTGGGCTGAGAGGATCAGTGACTTGTTTGCTAGACACCGGACCAAAA
TGAGGCGTAAGAAACGCTTTGCAAAGCAAGGTAACAAATGGTACAAGCAGCACCTCTCCTACCG
CCTGGTGAACTGGCCTGAGCATCTGCCGGAGCCGGCAGTTCGGGGCGCCGTGCGCGCCGCCTTC
CAGTTGTGGAGCAACGTCTCAGCGCTGGAGTTCTGGGAGGCCCCAGCCACAGGCCCCGCTGACA
TCCGGCTCACCTTCTTCCAAGGGGACCACAACGATGGGCTGGGCAATGCCTTTGATGGCCCAGG
GGGCGCCCTGGCGCACGCCTTCCTGCCCCGCCGCGGCGAAGCGCACTTCGACCAAGATGAGCGC
TGGTCCCTGAGCCGCCGCCGCGGGCGCAACCTGTTCGTGGTGCTGGCGCACGAGATCGGTCACA
CGCTTGGCCTCACCCACTCGCCCGCGCCGCGCGCGCTCATGGCGCCCTACTACAAGAGGCTGGG
CCGCGACGCGCTGCTCAGCTGGGACGACGTGCTGGCCGTGCAGAGCCTGTATGGGAAGCCCCTA
GGGGGCTCAGTGGCCGTCCAGCTCCCAGGAAAGCTGTTCACTGACTTTGAGACCTGGGACTCCT
ACAGCCCCCAAGGAAGGCGCCCTGAAACGCAGGGCCCTAAATACTGCCACTCTTCCTTCGATGC
CATCACTGTAGACAGGCAACAGCAACTGTACATTTTTAAAGGGAGCCATTTCTGGGAGGTGGCA
GCTGATGGCAACGTCTCAGAGCCCCGTCCACTGCAGGAAAGATGGGTCGGGCTGCCCCCCAACA
TTGAGGCTGCGGCAGTGTCATTGAATGATGGAGATTTCTACTTCTTCAAAGGGGGTCGATGCTG
GAGGTTCCGGGGCCCCAAGCCAGTGTGGGGTCTCCCACAGCTGTGCCGGGCAGGGGGCCTGCCC
CGCCATCCTGACGCCGCCCTCTTCTTCCCTCCTCTGCGCCGCCTCATCCTCTTCAAGGGTGCCC
GCTACTACGTGCTGGCCCGAGGGGGACTGCAAGTGGAGCCCTACTACCCCCGAAGTCTGCAGGA
CTGGGGAGGCATCCCTGAGGAGGTCAGCGGCGCCCTGCCGAGGCCCGATGGCTCCATCATCTTC
TTCCGAGATGACCGCTACTGGCGCCTCGACCAGGCCAAACTGCAGGCAACCACCTCGGGCCGCT
GGGCCACCGAGCTGCCCTGGATGGGCTGCTGGCATGCCAACTCGGGGAGCGCCCTGTTCTGAAG
GCACCTCCTCACCTCAGAAACTGGTGGTGCTCTCAGGGCAAAATCATGTTCCCCACCCCCGGGG
CAGAACCCCTCTTAGAAGCCTCTGAGTCCCTCTGCAGAAGACCGGGCAGCAAAGCCTCCATCTG
GAAGTCTGTCTGCCTTTGTTCCTTGAAGAATGCAGCATTGTCTTTGTCTGTCCCCACCACATGG
AGGTGGGGGTGGGATCAATCTTAGGAAAAGCAAAAAAGGGTCCCAGATCCCTTGGCCCTTTCCT
CCGAGGACTTCTATCCTCCCCAGGCCTTTGTTTCTTCGGCTAAAGGTACAGTTCCTTTCAAGAG
GTAACAGCACTGGGATCCAAGCAGGGGGATGAAAAACTCAGCAGAGAAATTCGAGACCATTTTG
CAAGACTGTGCCCTTCTCCTCAGGACCCCCTGGCTCAGTTCTTGAAAAACGGTGTCATATTTAG
TCAGAGGCCCCACCCCCAGGAAGCATGGATGGGGATGAAGGCACAGGCGTCTCCAACCTCAGAG
GCCCTTTGTGGGGTCAGGACACAGAGTGGGAGGGAGACTGATGCAGGCCTACCAGTCCCTGGCT
TTTTGTCTGGGGCTGGAATAAAGAGGTGCCTTCAGCTGGTGGGCCGAGAGGCAGGAAGCAGCCT
T

hide sequence

RefSeq Acc Id:

XM_011525230 ⟹ XP_011523532

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,765,865 - 35,795,641 (-)	NCBI

Sequence:

show sequence

AGCAGCGGCGCGGGGTGGGTGGGGCGGGAGTGCCGGGCCTCCGCCCCCTCCGCCTGCCTTTCCT
TCCTCCCTCCCTCGGTCCCCGGGGCCGGCGGACCCGCGGGCAGGCACTGCCCGGGCTGGACGAC
GTCTGGCCGGCTCCCGGCGAAGGGCAGCGGAGGAGCGGCCCAGAGCGCGCAGCTAGGGCACTGG
CGAAACCCCGGGACAGTCCCTCTCCGTGCGGGGGCGGCGCAGAGCAGTCCCATCCCCGGGGTCC
CGGGCGCGGCTGACTGCCGGCTGGTTCCCTGCGCGCAGTAGCTCCCCGAGCCGGGCTGCACCGG
AGGCGGCGAGATGGTCGCGCGCGTCGGCCTCCTGCTGCGCGCCCTGCAGCTGCTACTGTGGGGC
CACCTGGACGCCCAGCCCGCGGAGCGCGGAGGCCAGGAGCTGCGCAAGGAGGCGGAGGCATTCC
TAGAGAAGTACGGATACCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGA
TGCCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACC
CTGCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTG
AGAGGATCAGTGACTTGTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAA
GCAAGGTAACAAATGGTACAAGCAGCACCTCTCCTACCGCCTGGTGAACTGGCCTGAGCATCTG
CCGGAGCCGGCAGTTCGGGGCGCCGTGCGCGCCGCCTTCCAGTTGTGGAGCAACGTCTCAGCGC
TGGAGTTCTGGGAGGCCCCAGCCACAGGCCCCGCTGACATCCGGCTCACCTTCTTCCAAGGGGA
CCACAACGATGGGCTGGGCAATGCCTTTGATGGCCCAGGGGGCGCCCTGGCGCACGCCTTCCTG
CCCCGCCGCGGCGAAGCGCACTTCGACCAAGATGAGCGCTGGTCCCTGAGCCGCCGCCGCGGGC
GCAACCTGTTCGTGGTGCTGGCGCACGAGATCGGTCACACGCTTGGCCTCACCCACTCGCCCGC
GCCGCGCGCGCTCATGGCGCCCTACTACAAGAGGCTGGGCCGCGACGCGCTGCTCAGCTGGGAC
GACGTGCTGGCCGTGCAGAGCCTGTATGGGAAGCCCCTAGGGGGCTCAGTGGCCGTCCAGCTCC
CAGGAAAGCTGTTCACTGACTTTGAGACCTGGGACTCCTACAGCCCCCAAGGAAGGCGCCCTGA
AACGCAGGGCCCTAAATACTGCCACTCTTCCTTCGATGCCATCACTGTAGACAGGCAACAGCAA
CTGTACATTTTTAAAGGGAGCCATTTCTGGGAGGTGGCAGCTGATGGCAACGTCTCAGAGCCCC
GTCCACTGCAGGAAAGATGGGTCGGGCTGCCCCCCAACATTGAGGCTGCGGCAGTGTCATTGAA
TGATGGAGATTTCTACTTCTTCAAAGGGTGCCCGCTACTACGTGCTGGCCCGAGGGGGACTGCA
AGTGGAGCCCTACTACCCCCGAAGTCTGCAGGACTGGGGAGGCATCCCTGAGGAGGTCAGCGGC
GCCCTGCCGAGGCCCGATGGCTCCATCATCTTCTTCCGAGATGACCGCTACTGGCGCCTCGACC
AGGCCAAACTGCAGGCAACCACCTCGGGCCGCTGGGCCACCGAGCTGCCCTGGATGGGCTGCTG
GCATGCCAACTCGGGGAGCGCCCTGTTCTGAAGGCACCTCCTCACCTCAGAAACTGGTGGTGCT
CTCAGGGCAAAATCATGTTCCCCACCCCCGGGGCAGAACCCCTCTTAGAAGCCTCTGAGTCCCT
CTGCAGAAGACCGGGCAGCAAAGCCTCCATCTGGAAGTCTGTCTGCCTTTGTTCCTTGAAGAAT
GCAGCATTGTCTTTGTCTGTCCCCACCACATGGAGGTGGGGGTGGGATCAATCTTAGGAAAAGC
AAAAAAGGGTCCCAGATCCCTTGGCCCTTTCCTCCGAGGACTTCTATCCTCCCCAGGCCTTTGT
TTCTTCGGCTAAAGGTACAGTTCCTTTCAAGAGGTAACAGCACTGGGATCCAAGCAGGGGGATG
AAAAACTCAGCAGAGAAATTCGAGACCATTTTGCAAGACTGTGCCCTTCTCCTCAGGACCCCCT
GGCTCAGTTCTTGAAAAACGGTGTCATATTTAGTCAGAGGCCCCACCCCCAGGAAGCATGGATG
GGGATGAAGGCACAGGCGTCTCCAACCTCAGAGGCCCTTTGTGGGGTCAGGACACAGAGTGGGA
GGGAGACTGATGCAGGCCTACCAGTCCCTGGCTTTTTGTCTGGGGCTGGAATAAAGAGGTGCCT
TCAGCTGGTGGGCCGAGAGGCAGGAAGCAGCCTT

hide sequence

RefSeq Acc Id:

XM_011525231 ⟹ XP_011523533

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,756,249 - 35,795,641 (-)	NCBI

Sequence:

show sequence

AGCAGCGGCGCGGGGTGGGTGGGGCGGGAGTGCCGGGCCTCCGCCCCCTCCGCCTGCCTTTCCT
TCCTCCCTCCCTCGGTCCCCGGGGCCGGCGGACCCGCGGGCAGGCACTGCCCGGGCTGGACGAC
GTCTGGCCGGCTCCCGGCGAAGGGCAGCGGAGGAGCGGCCCAGAGCGCGCAGCTAGGGCACTGG
CGAAACCCCGGGACAGTCCCTCTCCGTGCGGGGGCGGCGCAGAGCAGTCCCATCCCCGGGGTCC
CGGGCGCGGCTGACTGCCGGCTGGTTCCCTGCGCGCAGTAGCTCCCCGAGCCGGGCTGCACCGG
AGGCGGCGAGATGGTCGCGCGCGTCGGCCTCCTGCTGCGCGCCCTGCAGCTGCTACTGTGGGGC
CACCTGGACGCCCAGCCCGCGGAGCGCGGAGGCCAGGAGCTGCGCAAGGAGGCGGAGGCATTCC
TAGAGAAGTACGGATACCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGA
TGCCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACC
CTGCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTG
AGAGGATCAGTGACTTGTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAA
GCAAGGTAACAAATGGTACAAGCAGCACCTCTCCTACCGCCTGGTGAACTGGCCTGAGCATCTG
CCGGAGCCGGCAGTTCGGGGCGCCGTGCGCGCCGCCTTCCAGTTGTGGAGCAACGTCTCAGCGC
TGGAGTTCTGGGAGGCCCCAGCCACAGGCCCCGCTGACATCCGGCTCACCTTCTTCCAAGGGGA
CCACAACGATGGGCTGGGCAATGCCTTTGATGGCCCAGGGGGCGCCCTGGCGCACGCCTTCCTG
CCCCGCCGCGGCGAAGCGCACTTCGACCAAGATGAGCGCTGGTCCCTGAGCCGCCGCCGCGGGC
GCAACCTGTTCGTGGTGCTGGCGCACGAGATCGGTCACACGCTTGGCCTCACCCACTCGCCCGC
GCCGCGCGCGCTCATGGCGCCCTACTACAAGAGGCTGGGCCGCGACGCGCTGCTCAGCTGGGAC
GACGTGCTGGCCGTGCAGAGCCTGTATGGGAAGCCCCTAGGGGGCTCAGTGGCCGTCCAGCTCC
CAGGAAAGCTGTTCACTGACTTTGAGACCTGGGACTCCTACAGCCCCCAAGGAAGGCGCCCTGA
AACGCAGGGCCCTAAATACTGCCACTCTTCCTTCGATGCCATCACTGTAGACAGGCAACAGCAA
CTGTACATTTTTAAAGGGAGCCATTTCTGGGAGGTGGCAGCTGATGGCAACGTCTCAGAGCCCC
GTCCACTGCAGGAAAGATGGGTCGGGCTGCCCCCCAACATTGAGGCTGCGGCAGTGTCATTGAA
TGATGGAGATTTCTACTTCTTCAAAGCCTGAGGACAAAGTTCTGGGAGATCGGCATTGACTATG
TAAGTAACAACAACGGCCTAAAGAAGCAACAAGAAAGGAACCGAGTGCCTGGAGAACTTCATGG
AGCAGAGCCACTTGCCTACTTTGGATCATCTGTCTCTAAGAGAGGGAAATAAACATTTCTTTTG
TGTGA

hide sequence

RefSeq Acc Id:

XM_011525232 ⟹ XP_011523534

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,765,865 - 35,795,641 (-)	NCBI

Sequence:

show sequence

AGCAGCGGCGCGGGGTGGGTGGGGCGGGAGTGCCGGGCCTCCGCCCCCTCCGCCTGCCTTTCCT
TCCTCCCTCCCTCGGTCCCCGGGGCCGGCGGACCCGCGGGCAGGCACTGCCCGGGCTGGACGAC
GTCTGGCCGGCTCCCGGCGAAGGGCAGCGGAGGAGCGGCCCAGAGCGCGCAGCTAGGGCACTGG
CGAAACCCCGGGACAGTCCCTCTCCGTGCGGGGGCGGCGCAGAGCAGTCCCATCCCCGGGGTCC
CGGGCGCGGCTGACTGCCGGCTGGTTCCCTGCGCGCAGTAGCTCCCCGAGCCGGGCTGCACCGG
AGGCGGCGAGATGGTCGCGCGCGTCGGCCTCCTGCTGCGCGCCCTGCAGCTGCTACTGTGGGGC
CACCTGGACGCCCAGCCCGCGGAGCGCGGAGGCCAGGAGCTGCGCAAGGAGGCGGAGGCATTCC
TAGAGAAGTACGGATACCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGA
TGCCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACC
CTGCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTG
AGAGGATCAGTGACTTGTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAA
GCAAGGTAACAAATGGTACAAGCAGCACCTCTCCTACCGCCTGGTGAACTGGCCTGAGCATCTG
CCGGAGCCGGCAGTTCGGGGCGCCGTGCGCGCCGCCTTCCAGTTGTGGAGCAACGTCTCAGCGC
TGGAGTTCTGGGAGGCCCCAGCCACAGGCCCCGCTGACATCCGGCTCACCTTCTTCCAAGGGGA
CCACAACGATGGGCTGGGCAATGCCTTTGATGGCCCAGGGGGCGCCCTGGCGCACGCCTTCCTG
CCCCGCCGCGGCGAAGCGCACTTCGACCAAGATGAGCGCTGGTCCCTGAGCCGCCGCCGCGGGC
GCAACCTGTTCGTGGTGCTGGCGCACGAGATCGGTCACACGCTTGGCCTCACCCACTCGCCCGC
GCCGCGCGCGCTCATGGCGCCCTACTACAAGAGGCTGGGCCGCGACGCGCTGCTCAGCTGGGAC
GACGTGCTGGCCGTGCAGAGCCTGTATGTGTCTCCAGAGCTGCAGTACAAGTTGGGGGGATGGA
CTGTAAAAGCCAGAAATCCCAAGCCACAAGCACGCTGCAGGCAACAGCAACTGTACATTTTTAA
AGGGAGCCATTTCTGGGAGGTGGCAGCTGATGGCAACGTCTCAGAGCCCCGTCCACTGCAGGAA
AGATGGGTCGGGCTGCCCCCCAACATTGAGGCTGCGGCAGTGTCATTGAATGATGGAGATTTCT
ACTTCTTCAAAGGGGGTCGATGCTGGAGGTTCCGGGGCCCCAAGCCAGTGTGGGGTCTCCCACA
GCTGTGCCGGGCAGGGGGCCTGCCCCGCCATCCTGACGCCGCCCTCTTCTTCCCTCCTCTGCGC
CGCCTCATCCTCTTCAAGGGTGCCCGCTACTACGTGCTGGCCCGAGGGGGACTGCAAGTGGAGC
CCTACTACCCCCGAAGTCTGCAGGACTGGGGAGGCATCCCTGAGGAGGTCAGCGGCGCCCTGCC
GAGGCCCGATGGCTCCATCATCTTCTTCCGAGATGACCGCTACTGGCGCCTCGACCAGGCCAAA
CTGCAGGCAACCACCTCGGGCCGCTGGGCCACCGAGCTGCCCTGGATGGGCTGCTGGCATGCCA
ACTCGGGGAGCGCCCTGTTCTGAAGGCACCTCCTCACCTCAGAAACTGGTGGTGCTCTCAGGGC
AAAATCATGTTCCCCACCCCCGGGGCAGAACCCCTCTTAGAAGCCTCTGAGTCCCTCTGCAGAA
GACCGGGCAGCAAAGCCTCCATCTGGAAGTCTGTCTGCCTTTGTTCCTTGAAGAATGCAGCATT
GTCTTTGTCTGTCCCCACCACATGGAGGTGGGGGTGGGATCAATCTTAGGAAAAGCAAAAAAGG
GTCCCAGATCCCTTGGCCCTTTCCTCCGAGGACTTCTATCCTCCCCAGGCCTTTGTTTCTTCGG
CTAAAGGTACAGTTCCTTTCAAGAGGTAACAGCACTGGGATCCAAGCAGGGGGATGAAAAACTC
AGCAGAGAAATTCGAGACCATTTTGCAAGACTGTGCCCTTCTCCTCAGGACCCCCTGGCTCAGT
TCTTGAAAAACGGTGTCATATTTAGTCAGAGGCCCCACCCCCAGGAAGCATGGATGGGGATGAA
GGCACAGGCGTCTCCAACCTCAGAGGCCCTTTGTGGGGTCAGGACACAGAGTGGGAGGGAGACT
GATGCAGGCCTACCAGTCCCTGGCTTTTTGTCTGGGGCTGGAATAAAGAGGTGCCTTCAGCTGG
TGGGCCGAGAGGCAGGAAGCAGCCTT

hide sequence

RefSeq Acc Id:

XM_017025063 ⟹ XP_016880552

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,766,678 - 35,795,641 (-)	NCBI

Sequence:

show sequence

AGCAGCGGCGCGGGGTGGGTGGGGCGGGAGTGCCGGGCCTCCGCCCCCTCCGCCTGCCTTTCCT
TCCTCCCTCCCTCGGTCCCCGGGGCCGGCGGACCCGCGGGCAGGCACTGCCCGGGCTGGACGAC
GTCTGGCCGGCTCCCGGCGAAGGGCAGCGGAGGAGCGGCCCAGAGCGCGCAGCTAGGGCACTGG
CGAAACCCCGGGACAGTCCCTCTCCGTGCGGGGGCGGCGCAGAGCAGTCCCATCCCCGGGGTCC
CGGGCGCGGCTGACTGCCGGCTGGTTCCCTGCGCGCAGTAGCTCCCCGAGCCGGGCTGCACCGG
AGGCGGCGAGATGGTCGCGCGCGTCGGCCTCCTGCTGCGCGCCCTGCAGCTGCTACTGTGGGGC
CACCTGGACGCCCAGCCCGCGGAGCGCGGAGGCCAGGAGCTGCGCAAGGAGGCGGAGGCATTCC
TAGAGAAGTACGGATACCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGA
TGCCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACC
CTGCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTG
AGAGGATCAGTGACTTGTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAA
GCAAGGTAACAAATGGTACAAGCAGCACCTCTCCTACCGCCTGGTGAACTGGCCTGAGCATCTG
CCGGAGCCGGCAGTTCGGGGCGCCGTGCGCGCCGCCTTCCAGTTGTGGAGCAACGTCTCAGCGC
TGGAGTTCTGGGAGGCCCCAGCCACAGGCCCCGCTGACATCCGGCTCACCTTCTTCCAAGGGGA
CCACAACGATGGGCTGGGCAATGCCTTTGATGGCCCAGGGGGCGCCCTGGCGCACGCCTTCCTG
CCCCGCCGCGGCGAAGCGCACTTCGACCAAGATGAGCGCTGGTCCCTGAGCCGCCGCCGCGGGC
GCAACCTGTTCGTGGTGCTGGCGCACGAGATCGGTCACACGCTTGGCCTCACCCACTCGCCCGC
GCCGCGCGCGCTCATGGCGCCCTACTACAAGAGGCTGGGCCGCGACGCGCTGCTCAGCTGGGAC
GACGTGCTGGCCGTGCAGAGCCTGTATGGGAAGCCCCTAGGGGGCTCAGTGGCCGTCCAGCTCC
CAGGAAAGCTGTTCACTGACTTTGAGACCTGGGACTCCTACAGCCCCCAAGGAAGGCGCCCTGA
AACGCAGGGCCCTAAATACTGCCACTCTTCCTTCGATGCCATCACTGTAGGCAACAGCAACTGT
ACATTTTTAAAGGGAGCCATTTCTGGGAGGTGGCAGCTGATGGCAACGTCTCAGAGCCCCGTCC
ACTGCAGGAAAGATGGGTCGGGCTGCCCCCCAACATTGAGGCTGCGGCAGTGTCATTGAATGAT
GGAGATTTCTACTTCTTCAAAGGGTGCCCGCTACTACGTGCTGGCCCGAGGGGGACTGCAAGTG
GAGCCCTACTACCCCCGAAGTCTGCAGGACTGGGGAGGCAT

hide sequence

RefSeq Acc Id:

XM_017025064 ⟹ XP_016880553

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,756,249 - 35,795,641 (-)	NCBI

Sequence:

show sequence

AGCAGCGGCGCGGGGTGGGTGGGGCGGGAGTGCCGGGCCTCCGCCCCCTCCGCCTGCCTTTCCT
TCCTCCCTCCCTCGGTCCCCGGGGCCGGCGGACCCGCGGGCAGGCACTGCCCGGGCTGGACGAC
GTCTGGCCGGCTCCCGGCGAAGGGCAGCGGAGGAGCGGCCCAGAGCGCGCAGCTAGGGCACTGG
CGAAACCCCGGGACAGTCCCTCTCCGTGCGGGGGCGGCGCAGAGCAGTCCCATCCCCGGGGTCC
CGGGCGCGGCTGACTGCCGGCTGGTTCCCTGCGCGCAGTAGCTCCCCGAGCCGGGCTGCACCGG
AGGCGGCGAGATGGTCGCGCGCGTCGGCCTCCTGCTGCGCGCCCTGCAGCTGCTACTGTGGGGC
CACCTGGACGCCCAGCCCGCGGAGCGCGGAGGCCAGGAGCTGCGCAAGGAGGCGGAGGCATTCC
TAGAGAAGTACGGATACCTCAATGAACAGGTCCCCAAAGCTCCCACCTCCACTCGATTCAGCGA
TGCCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTGTCAGCGGCGTGTTGGACCGCGCCACC
CTGCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGATACCAACAGTTATGCGGCCTGGGCTG
AGAGGATCAGTGACTTGTTTGCTAGACACCGGACCAAAATGAGGCGTAAGAAACGCTTTGCAAA
GCAAGGTAACAAATGGTACAAGCAGCACCTCTCCTACCGCCTGGTGAACTGGCCTGAGCATCTG
CCGGAGCCGGCAGTTCGGGGCGCCGTGCGCGCCGCCTTCCAGTTGTGGAGCAACGTCTCAGCGC
TGGAGTTCTGGGAGGCCCCAGCCACAGGCCCCGCTGACATCCGGCTCACCTTCTTCCAAGGGGA
CCACAACGATGGGCTGGGCAATGCCTTTGATGGCCCAGGGGGCGCCCTGGCGCACGCCTTCCTG
CCCCGCCGCGGCGAAGCGCACTTCGACCAAGATGAGCGCTGGTCCCTGAGCCGCCGCCGCGGGC
GCAACCTGTTCGTGGTGCTGGCGCACGAGATCGGTCACACGCTTGGCCTCACCCACTCGCCCGC
GCCGCGCGCGCTCATGGCGCCCTACTACAAGAGGCTGGGCCGCGACGCGCTGCTCAGCTGGGAC
GACGTGCTGGCCGTGCAGAGCCTGTATGGGAAGCCCCTAGGGGGCTCAGTGGCCGTCCAGCTCC
CAGGAAAGCTGTTCACTGACTTTGAGACCTGGGACTCCTACAGCCCCCAAGGAAGGCGCCCTGA
AACGCAGGGCCCTAAATACTGCCACTCTTCCTTCGATGCCATCACTGTAGGCAACAGCAACTGT
ACATTTTTAAAGGGAGCCATTTCTGGGAGGTGGCAGCTGATGGCAACGTCTCAGAGCCCCGTCC
ACTGCAGGAAAGATGGGTCGGGCTGCCCCCCAACATTGAGGCTGCGGCAGTGTCATTGAATGAT
GGAGATTTCTACTTCTTCAAAGCCTGAGGACAAAGTTCTGGGAGATCGGCATTGACTATGTAAG
TAACAACAACGGCCTAAAGAAGCAACAAGAAAGGAACCGAGTGCCTGGAGAACTTCATGGAGCA
GAGCCACTTGCCTACTTTGGATCATCTGTCTCTAAGAGAGGGAAATAAACATTTCTTTTGTGTG
A

hide sequence

RefSeq Acc Id:

XM_024450943 ⟹ XP_024306711

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,765,865 - 35,780,728 (-)	NCBI

Sequence:

show sequence

AGAGTAGTTGGGACAACAGGCATTCCTAGAGAAGTACGGATACCTCAATGAACAGGTCCCCAAA
GCTCCCACCTCCACTCGATTCAGCGATGCCATCAGAGCGTTTCAGTGGGTGTCCCAGCTACCTG
TCAGCGGCGTGTTGGACCGCGCCACCCTGCGCCAGATGACTCGTCCCCGCTGCGGGGTTACAGA
TACCAACAGTTATGCGGCCTGGGCTGAGAGGATCAGTGACTTGTTTGCTAGACACCGGACCAAA
ATGAGGCGTAAGAAACGCTTTGCAAAGCAAGGTAACAAATGGTACAAGCAGCACCTCTCCTACC
GCCTGGTGAACTGGCCTGAGCATCTGCCGGAGCCGGCAGTTCGGGGCGCCGTGCGCGCCGCCTT
CCAGTTGTGGAGCAACGTCTCAGCGCTGGAGTTCTGGGAGGCCCCAGCCACAGGCCCCGCTGAC
ATCCGGCTCACCTTCTTCCAAGGGGACCACAACGATGGGCTGGGCAATGCCTTTGATGGCCCAG
GGGGCGCCCTGGCGCACGCCTTCCTGCCCCGCCGCGGCGAAGCGCACTTCGACCAAGATGAGCG
CTGGTCCCTGAGCCGCCGCCGCGGGCGCAACCTGTTCGTGGTGCTGGCGCACGAGATCGGTCAC
ACGCTTGGCCTCACCCACTCGCCCGCGCCGCGCGCGCTCATGGCGCCCTACTACAAGAGGCTGG
GCCGCGACGCGCTGCTCAGCTGGGACGACGTGCTGGCCGTGCAGAGCCTGTATGGGAAGCCCCT
AGGGGGCTCAGTGGCCGTCCAGCTCCCAGGAAAGCTGTTCACTGACTTTGAGACCTGGGACTCC
TACAGCCCCCAAGGAAGGCGCCCTGAAACGCAGGGCCCTAAATACTGCCACTCTTCCTTCGATG
CCATCACTGTAGACAGGCAACAGCAACTGTACATTTTTAAAGGGAGCCATTTCTGGGAGGTGGC
AGCTGATGGCAACGTCTCAGAGCCCCGTCCACTGCAGGAAAGATGGGTCGGGCTGCCCCCCAAC
ATTGAGGCTGCGGCAGTGTCATTGAATGATGGAGATTTCTACTTCTTCAAAGGGGGTCGATGCT
GGAGGTTCCGGGGCCCCAAGCCAGTGTGGGGTCTCCCACAGCTGTGCCGGGCAGGGGGCCTGCC
CCGCCATCCTGACGCCGCCCTCTTCTTCCCTCCTCTGCGCCGCCTCATCCTCTTCAAGGGTGCC
CGCTACTACGTGCTGGCCCGAGGGGGACTGCAAGTGGAGCCCTACTACCCCCGAAGTCTGCAGG
ACTGGGGAGGCATCCCTGAGGAGGTCAGCGGCGCCCTGCCGAGGCCCGATGGCTCCATCATCTT
CTTCCGAGATGACCGCTACTGGCGCCTCGACCAGGCCAAACTGCAGGCAACCACCTCGGGCCGC
TGGGCCACCGAGCTGCCCTGGATGGGCTGCTGGCATGCCAACTCGGGGAGCGCCCTGTTCTGAA
GGCACCTCCTCACCTCAGAAACTGGTGGTGCTCTCAGGGCAAAATCATGTTCCCCACCCCCGGG
GCAGAACCCCTCTTAGAAGCCTCTGAGTCCCTCTGCAGAAGACCGGGCAGCAAAGCCTCCATCT
GGAAGTCTGTCTGCCTTTGTTCCTTGAAGAATGCAGCATTGTCTTTGTCTGTCCCCACCACATG
GAGGTGGGGGTGGGATCAATCTTAGGAAAAGCAAAAAAGGGTCCCAGATCCCTTGGCCCTTTCC
TCCGAGGACTTCTATCCTCCCCAGGCCTTTGTTTCTTCGGCTAAAGGTACAGTTCCTTTCAAGA
GGTAACAGCACTGGGATCCAAGCAGGGGGATGAAAAACTCAGCAGAGAAATTCGAGACCATTTT
GCAAGACTGTGCCCTTCTCCTCAGGACCCCCTGGCTCAGTTCTTGAAAAACGGTGTCATATTTA
GTCAGAGGCCCCACCCCCAGGAAGCATGGATGGGGATGAAGGCACAGGCGTCTCCAACCTCAGA
GGCCCTTTGTGGGGTCAGGACACAGAGTGGGAGGGAGACTGATGCAGGCCTACCAGTCCCTGGC
TTTTTGTCTGGGGCTGGAATAAAGAGGTGCCTTCAGCTGGTGGGCCGAGAGGCAGGAAGCAGCC
TT

hide sequence

RefSeq Acc Id:

XM_047436731 ⟹ XP_047292687

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	35,765,865 - 35,795,254 (-)	NCBI

RefSeq Acc Id:

XM_054317173 ⟹ XP_054173148

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	36,713,803 - 36,743,551 (-)	NCBI

RefSeq Acc Id:

XM_054317174 ⟹ XP_054173149

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	36,713,803 - 36,743,551 (-)	NCBI

RefSeq Acc Id:

XM_054317175 ⟹ XP_054173150

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	36,713,803 - 36,743,170 (-)	NCBI

RefSeq Acc Id:

XM_054317176 ⟹ XP_054173151

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	36,713,803 - 36,743,551 (-)	NCBI

RefSeq Acc Id:

XM_054317177 ⟹ XP_054173152

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	36,713,803 - 36,743,164 (-)	NCBI

RefSeq Acc Id:

XM_054317178 ⟹ XP_054173153

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	36,713,803 - 36,743,173 (-)	NCBI

RefSeq Acc Id:

XM_054317179 ⟹ XP_054173154

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	36,713,803 - 36,728,638 (-)	NCBI

RefSeq Acc Id:

XM_054317180 ⟹ XP_054173155

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	36,713,795 - 36,743,551 (-)	NCBI

RefSeq Acc Id:

XM_054317181 ⟹ XP_054173156

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	36,704,182 - 36,743,551 (-)	NCBI

RefSeq Acc Id:

XM_054317182 ⟹ XP_054173157

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	36,714,616 - 36,743,551 (-)	NCBI

RefSeq Acc Id:

XM_054317183 ⟹ XP_054173158

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	36,704,182 - 36,743,551 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001027449	(Get FASTA)	NCBI Sequence Viewer
	NP_077278	(Get FASTA)	NCBI Sequence Viewer
	NP_116568	(Get FASTA)	NCBI Sequence Viewer
	XP_011523527	(Get FASTA)	NCBI Sequence Viewer
	XP_011523528	(Get FASTA)	NCBI Sequence Viewer
	XP_011523529	(Get FASTA)	NCBI Sequence Viewer
	XP_011523531	(Get FASTA)	NCBI Sequence Viewer
	XP_011523532	(Get FASTA)	NCBI Sequence Viewer
	XP_011523533	(Get FASTA)	NCBI Sequence Viewer
	XP_011523534	(Get FASTA)	NCBI Sequence Viewer
	XP_016880552	(Get FASTA)	NCBI Sequence Viewer
	XP_016880553	(Get FASTA)	NCBI Sequence Viewer
	XP_024306711	(Get FASTA)	NCBI Sequence Viewer
	XP_047292687	(Get FASTA)	NCBI Sequence Viewer
	XP_054173148	(Get FASTA)	NCBI Sequence Viewer
	XP_054173149	(Get FASTA)	NCBI Sequence Viewer
	XP_054173150	(Get FASTA)	NCBI Sequence Viewer
	XP_054173151	(Get FASTA)	NCBI Sequence Viewer
	XP_054173152	(Get FASTA)	NCBI Sequence Viewer
	XP_054173153	(Get FASTA)	NCBI Sequence Viewer
	XP_054173154	(Get FASTA)	NCBI Sequence Viewer
	XP_054173155	(Get FASTA)	NCBI Sequence Viewer
	XP_054173156	(Get FASTA)	NCBI Sequence Viewer
	XP_054173157	(Get FASTA)	NCBI Sequence Viewer
	XP_054173158	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAG41981	(Get FASTA)	NCBI Sequence Viewer
	AAH02631	(Get FASTA)	NCBI Sequence Viewer
	AAH11774	(Get FASTA)	NCBI Sequence Viewer
	AAK01480	(Get FASTA)	NCBI Sequence Viewer
	AAK01706	(Get FASTA)	NCBI Sequence Viewer
	AAL15619	(Get FASTA)	NCBI Sequence Viewer
	AAQ89346	(Get FASTA)	NCBI Sequence Viewer
	BAG53618	(Get FASTA)	NCBI Sequence Viewer
	EAW80128	(Get FASTA)	NCBI Sequence Viewer
	EAW80129	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000473853
	ENSP00000473853.1
	ENSP00000479124.1
	ENSP00000481051.1
	ENSP00000482385.1
	ENSP00000483299
	ENSP00000483299.1
	ENSP00000483539
	ENSP00000483539.1
	ENSP00000484430.1
	ENSP00000484562.1
	ENSP00000487783.1
	ENSP00000487847.1
	ENSP00000488096.1
	ENSP00000488159.1
GenBank Protein	Q9H239	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_077278 ⟸ NM_024302
- Peptide Label:	isoform 1 preproprotein
- UniProtKB:	Q96F04 (UniProtKB/Swiss-Prot), Q96TE2 (UniProtKB/Swiss-Prot), Q9H239 (UniProtKB/Swiss-Prot), B3KV06 (UniProtKB/TrEMBL)
- Sequence:	show sequence MVARVGLLLRALQLLLWGHLDAQPAERGGQELRKEAEAFLEKYGYLNEQVPKAPTSTRFSDAIR AFQWVSQLPVSGVLDRATLRQMTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGN KWYKQHLSYRLVNWPEHLPEPAVRGAVRAAFQLWSNVSALEFWEAPATGPADIRLTFFQGDHND GLGNAFDGPGGALAHAFLPRRGEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRA LMAPYYKRLGRDALLSWDDVLAVQSLYGKPLGGSVAVQLPGKLFTDFETWDSYSPQGRRPETQG PKYCHSSFDAITVDRQQQLYIFKGSHFWEVAADGNVSEPRPLQERWVGLPPNIEAAAVSLNDGD FYFFKGGRCWRFRGPKPVWGLPQLCRAGGLPRHPDAALFFPPLRRLILFKGARYYVLARGGLQV EPYYPRSLQDWGGIPEEVSGALPRPDGSIIFFRDDRYWRLDQAKLQATTSGRWATELPWMGCWH ANSGSALF hide sequence

RefSeq Acc Id:	NP_001027449 ⟸ NM_001032278
- Peptide Label:	isoform 3 precursor
- UniProtKB:	Q9H239 (UniProtKB/Swiss-Prot), B3KV06 (UniProtKB/TrEMBL)
- Sequence:	show sequence MVARVGLLLRALQLLLWGHLDAQPAERGGQELRKEAEAFLEKYGYLNEQVPKAPTSTRFSDAIR AFQWVSQLPVSGVLDRATLRQMTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGE HC hide sequence

RefSeq Acc Id:	NP_116568 ⟸ NM_032950
- Peptide Label:	isoform 2 preproprotein
- UniProtKB:	C0H5X0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MVARVGLLLRALQLLLWGHLDAQPAERGGQELRKEAEAFLEKYGYLNEQVPKAPTSTRFSDAIR AFQWVSQLPVSGVLDRATLRQMTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGN KWYKQHLSYRLVNWPEHLPEPAVRGAVRAAFQLWSNVSALEFWEAPATGPADIRLTFFQGDHND GLGNAFDGPGGALAHAFLPRRGEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRA LMAPYYKRLGRDALLSWDDVLAVQSLYGKPLGGSVAVQLPGKLFTDFETWDSYSPQGRRPETQG PKYCHSSFDAITVDRQQQLYIFKGSHFWEVAADGNVSEPRPLQERWVGLPPNIEAAAVSLNDGD FYFFKVQSV hide sequence

RefSeq Acc Id:

XP_011523533 ⟸ XM_011525231

- Peptide Label:

isoform X5

- Sequence:

show sequence

MVARVGLLLRALQLLLWGHLDAQPAERGGQELRKEAEAFLEKYGYLNEQVPKAPTSTRFSDAIR
AFQWVSQLPVSGVLDRATLRQMTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGN
KWYKQHLSYRLVNWPEHLPEPAVRGAVRAAFQLWSNVSALEFWEAPATGPADIRLTFFQGDHND
GLGNAFDGPGGALAHAFLPRRGEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRA
LMAPYYKRLGRDALLSWDDVLAVQSLYGKPLGGSVAVQLPGKLFTDFETWDSYSPQGRRPETQG
PKYCHSSFDAITVDRQQQLYIFKGSHFWEVAADGNVSEPRPLQERWVGLPPNIEAAAVSLNDGD
FYFFKA

hide sequence

RefSeq Acc Id:	XP_011523527 ⟸ XM_011525225
- Peptide Label:	isoform X2
- UniProtKB:	B3KV06 (UniProtKB/TrEMBL)
- Sequence:	show sequence MVARVGLLLRALQLLLWGHLDAQPAERGGQELRKEAEAFLEKYGYLNEQVPKAPTSTRFSDAIR AFQWVSQLPVSGVLDRATLRQMTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGG ALAHAFLPRRGEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRALMAPYYKRLGR DALLSWDDVLAVQSLYGKPLGGSVAVQLPGKLFTDFETWDSYSPQGRRPETQGPKYCHSSFDAI TVDRQQQLYIFKGSHFWEVAADGNVSEPRPLQERWVGLPPNIEAAAVSLNDGDFYFFKGGRCWR FRGPKPVWGLPQLCRAGGLPRHPDAALFFPPLRRLILFKGARYYVLARGGLQVEPYYPRSLQDW GGIPEEVSGALPRPDGSIIFFRDDRYWRLDQAKLQATTSGRWATELPWMGCWHANSGSALF hide sequence

RefSeq Acc Id:

XP_011523532 ⟸ XM_011525230

- Peptide Label:

isoform X4

- Sequence:

show sequence

MVARVGLLLRALQLLLWGHLDAQPAERGGQELRKEAEAFLEKYGYLNEQVPKAPTSTRFSDAIR
AFQWVSQLPVSGVLDRATLRQMTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGN
KWYKQHLSYRLVNWPEHLPEPAVRGAVRAAFQLWSNVSALEFWEAPATGPADIRLTFFQGDHND
GLGNAFDGPGGALAHAFLPRRGEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRA
LMAPYYKRLGRDALLSWDDVLAVQSLYGKPLGGSVAVQLPGKLFTDFETWDSYSPQGRRPETQG
PKYCHSSFDAITVDRQQQLYIFKGSHFWEVAADGNVSEPRPLQERWVGLPPNIEAAAVSLNDGD
FYFFKGCPLLRAGPRGTASGALLPPKSAGLGRHP

hide sequence

RefSeq Acc Id:	XP_011523528 ⟸ XM_011525226
- Peptide Label:	isoform X3
- UniProtKB:	B3KV06 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGNKWYKQHLSYRLVNWPEHLPEP AVRGAVRAAFQLWSNVSALEFWEAPATGPADIRLTFFQGDHNDGLGNAFDGPGGALAHAFLPRR GEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRALMAPYYKRLGRDALLSWDDVL AVQSLYGKPLGGSVAVQLPGKLFTDFETWDSYSPQGRRPETQGPKYCHSSFDAITVDRQQQLYI FKGSHFWEVAADGNVSEPRPLQERWVGLPPNIEAAAVSLNDGDFYFFKGGRCWRFRGPKPVWGL PQLCRAGGLPRHPDAALFFPPLRRLILFKGARYYVLARGGLQVEPYYPRSLQDWGGIPEEVSGA LPRPDGSIIFFRDDRYWRLDQAKLQATTSGRWATELPWMGCWHANSGSALF hide sequence

RefSeq Acc Id:	XP_011523531 ⟸ XM_011525229
- Peptide Label:	isoform X3
- UniProtKB:	B3KV06 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGNKWYKQHLSYRLVNWPEHLPEP AVRGAVRAAFQLWSNVSALEFWEAPATGPADIRLTFFQGDHNDGLGNAFDGPGGALAHAFLPRR GEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRALMAPYYKRLGRDALLSWDDVL AVQSLYGKPLGGSVAVQLPGKLFTDFETWDSYSPQGRRPETQGPKYCHSSFDAITVDRQQQLYI FKGSHFWEVAADGNVSEPRPLQERWVGLPPNIEAAAVSLNDGDFYFFKGGRCWRFRGPKPVWGL PQLCRAGGLPRHPDAALFFPPLRRLILFKGARYYVLARGGLQVEPYYPRSLQDWGGIPEEVSGA LPRPDGSIIFFRDDRYWRLDQAKLQATTSGRWATELPWMGCWHANSGSALF hide sequence

RefSeq Acc Id:	XP_011523529 ⟸ XM_011525227
- Peptide Label:	isoform X3
- UniProtKB:	B3KV06 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGNKWYKQHLSYRLVNWPEHLPEP AVRGAVRAAFQLWSNVSALEFWEAPATGPADIRLTFFQGDHNDGLGNAFDGPGGALAHAFLPRR GEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRALMAPYYKRLGRDALLSWDDVL AVQSLYGKPLGGSVAVQLPGKLFTDFETWDSYSPQGRRPETQGPKYCHSSFDAITVDRQQQLYI FKGSHFWEVAADGNVSEPRPLQERWVGLPPNIEAAAVSLNDGDFYFFKGGRCWRFRGPKPVWGL PQLCRAGGLPRHPDAALFFPPLRRLILFKGARYYVLARGGLQVEPYYPRSLQDWGGIPEEVSGA LPRPDGSIIFFRDDRYWRLDQAKLQATTSGRWATELPWMGCWHANSGSALF hide sequence

RefSeq Acc Id:	XP_011523534 ⟸ XM_011525232
- Peptide Label:	isoform X1
- UniProtKB:	B3KV06 (UniProtKB/TrEMBL)
- Sequence:	show sequence MVARVGLLLRALQLLLWGHLDAQPAERGGQELRKEAEAFLEKYGYLNEQVPKAPTSTRFSDAIR AFQWVSQLPVSGVLDRATLRQMTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGN KWYKQHLSYRLVNWPEHLPEPAVRGAVRAAFQLWSNVSALEFWEAPATGPADIRLTFFQGDHND GLGNAFDGPGGALAHAFLPRRGEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRA LMAPYYKRLGRDALLSWDDVLAVQSLYVSPELQYKLGGWTVKARNPKPQARCRQQQLYIFKGSH FWEVAADGNVSEPRPLQERWVGLPPNIEAAAVSLNDGDFYFFKGGRCWRFRGPKPVWGLPQLCR AGGLPRHPDAALFFPPLRRLILFKGARYYVLARGGLQVEPYYPRSLQDWGGIPEEVSGALPRPD GSIIFFRDDRYWRLDQAKLQATTSGRWATELPWMGCWHANSGSALF hide sequence

RefSeq Acc Id:

XP_016880553 ⟸ XM_017025064

- Peptide Label:

isoform X6

- Sequence:

show sequence

MVARVGLLLRALQLLLWGHLDAQPAERGGQELRKEAEAFLEKYGYLNEQVPKAPTSTRFSDAIR
AFQWVSQLPVSGVLDRATLRQMTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGN
KWYKQHLSYRLVNWPEHLPEPAVRGAVRAAFQLWSNVSALEFWEAPATGPADIRLTFFQGDHND
GLGNAFDGPGGALAHAFLPRRGEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRA
LMAPYYKRLGRDALLSWDDVLAVQSLYGKPLGGSVAVQLPGKLFTDFETWDSYSPQGRRPETQG
PKYCHSSFDAITVGNSNCTFLKGAISGRWQLMATSQSPVHCRKDGSGCPPTLRLRQCH

hide sequence

RefSeq Acc Id:

XP_016880552 ⟸ XM_017025063

- Peptide Label:

isoform X6

- Sequence:

show sequence

MVARVGLLLRALQLLLWGHLDAQPAERGGQELRKEAEAFLEKYGYLNEQVPKAPTSTRFSDAIR
AFQWVSQLPVSGVLDRATLRQMTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGN
KWYKQHLSYRLVNWPEHLPEPAVRGAVRAAFQLWSNVSALEFWEAPATGPADIRLTFFQGDHND
GLGNAFDGPGGALAHAFLPRRGEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRA
LMAPYYKRLGRDALLSWDDVLAVQSLYGKPLGGSVAVQLPGKLFTDFETWDSYSPQGRRPETQG
PKYCHSSFDAITVGNSNCTFLKGAISGRWQLMATSQSPVHCRKDGSGCPPTLRLRQCH

hide sequence

RefSeq Acc Id:	XP_024306711 ⟸ XM_024450943
- Peptide Label:	isoform X3
- UniProtKB:	B3KV06 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTRPRCGVTDTNSYAAWAERISDLFARHRTKMRRKKRFAKQGNKWYKQHLSYRLVNWPEHLPEP AVRGAVRAAFQLWSNVSALEFWEAPATGPADIRLTFFQGDHNDGLGNAFDGPGGALAHAFLPRR GEAHFDQDERWSLSRRRGRNLFVVLAHEIGHTLGLTHSPAPRALMAPYYKRLGRDALLSWDDVL AVQSLYGKPLGGSVAVQLPGKLFTDFETWDSYSPQGRRPETQGPKYCHSSFDAITVDRQQQLYI FKGSHFWEVAADGNVSEPRPLQERWVGLPPNIEAAAVSLNDGDFYFFKGGRCWRFRGPKPVWGL PQLCRAGGLPRHPDAALFFPPLRRLILFKGARYYVLARGGLQVEPYYPRSLQDWGGIPEEVSGA LPRPDGSIIFFRDDRYWRLDQAKLQATTSGRWATELPWMGCWHANSGSALF hide sequence

RefSeq Acc Id:

ENSP00000484562 ⟸ ENST00000612292

RefSeq Acc Id:

ENSP00000483539 ⟸ ENST00000612672

RefSeq Acc Id:

ENSP00000482385 ⟸ ENST00000615317

RefSeq Acc Id:

ENSP00000483299 ⟸ ENST00000615136

RefSeq Acc Id:

ENSP00000481051 ⟸ ENST00000619655

RefSeq Acc Id:

ENSP00000473853 ⟸ ENST00000605424

RefSeq Acc Id:	XP_047292687 ⟸ XM_047436731
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054173158 ⟸ XM_054317183
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054173156 ⟸ XM_054317181
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054173155 ⟸ XM_054317180
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054173149 ⟸ XM_054317174
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054173148 ⟸ XM_054317173
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054173151 ⟸ XM_054317176
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054173153 ⟸ XM_054317178
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054173150 ⟸ XM_054317175
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054173152 ⟸ XM_054317177
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054173154 ⟸ XM_054317179
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054173157 ⟸ XM_054317182
- Peptide Label:	isoform X6

Protein Domains

Peptidase metallopeptidase

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9H239-F1-model_v2	AlphaFold	Q9H239	1-520	view protein structure

Promoters

RGD ID:

6794017

Promoter ID:

HG_KWN:25795

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

HeLa_S3

Transcripts:

ENST00000250144, ENST00000338839, NM_001032278, NM_024302, UC002HJW.1, UC002HJZ.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	17	31,146,391 - 31,146,891 (-)	MPROMDB

RGD ID:

7234675

Promoter ID:

EPDNEW_H23083

Type:

initiation region

Name:

MMP28_1

Description:

matrix metallopeptidase 28

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	17	35,795,614 - 35,795,674	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:14366	AgrOrtholog
COSMIC	MMP28	COSMIC
Ensembl Genes	ENSG00000271447	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ENSG00000278843	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000605424	ENTREZGENE
	ENST00000605424.6	UniProtKB/Swiss-Prot
	ENST00000611911.4	UniProtKB/Swiss-Prot
	ENST00000612292.1	UniProtKB/TrEMBL
	ENST00000612672	ENTREZGENE
	ENST00000612672.1	UniProtKB/Swiss-Prot
	ENST00000613289.2	UniProtKB/TrEMBL
	ENST00000615136	ENTREZGENE
	ENST00000615136.4	UniProtKB/TrEMBL
	ENST00000615317.4	UniProtKB/TrEMBL
	ENST00000619655	ENTREZGENE
	ENST00000619655.4	UniProtKB/TrEMBL
	ENST00000631999.1	UniProtKB/TrEMBL
	ENST00000632360.1	UniProtKB/Swiss-Prot
	ENST00000632913.1	UniProtKB/TrEMBL
	ENST00000634159.1	UniProtKB/TrEMBL
Gene3D-CATH	1.10.101.10	UniProtKB/TrEMBL
	2.110.10.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	3.40.390.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000271447	GTEx
	ENSG00000278843	GTEx
HGNC ID	HGNC:14366	ENTREZGENE
Human Proteome Map	MMP28	Human Proteome Map
InterPro	Hemopexin-like_dom	UniProtKB/Swiss-Prot
	Hemopexin-like_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Hemopexin-like_repeat	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	M10A_MMP	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	MetalloPept_cat_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Pept_M10_metallopeptidase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Pept_M10A	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Peptidase_Metallo	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Peptidoglycan-bd-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PGBD-like_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PGBDSf	UniProtKB/TrEMBL
KEGG Report	hsa:79148	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	79148	ENTREZGENE
OMIM	608417	OMIM
PANTHER	MATRIX METALLOPROTEINASE	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	MATRIX METALLOPROTEINASE-28	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	Hemopexin	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Peptidase_M10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PG_binding_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA30885	PharmGKB
PIRSF	Peptidase_M10A_matrix	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PRINTS	MATRIXIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	HEMOPEXIN_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC_PROTEASE	UniProtKB/Swiss-Prot
SMART	SM00120	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZnMc	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	Metalloproteases ('zincins'), catalytic domain	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF47090	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF50923	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A087WZ56_HUMAN	UniProtKB/TrEMBL
	A0A087X1Y9_HUMAN	UniProtKB/TrEMBL
	A0A0J9YW29_HUMAN	UniProtKB/TrEMBL
	B3KV06	ENTREZGENE, UniProtKB/TrEMBL
	C0H5X0	ENTREZGENE, UniProtKB/TrEMBL
	MMP28_HUMAN	UniProtKB/Swiss-Prot
	Q96F04	ENTREZGENE
	Q96TE2	ENTREZGENE
	Q9H239	ENTREZGENE
UniProt Secondary	Q96F04	UniProtKB/Swiss-Prot
	Q96TE2	UniProtKB/Swiss-Prot

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

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

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

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

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Imported Disease Annotations - ClinVar