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Gene: DPEP2 (dipeptidase 2) Homo sapiens

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Symbol:

DPEP2

Name:

dipeptidase 2

RGD ID:

1313962

HGNC Page

HGNC:23028

Description:

Enables dipeptidase activity. Involved in leukotriene D4 catabolic process. Predicted to be located in membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

MBD2

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Dpep2 (dipeptidase 2)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Rattus norvegicus (Norway rat):	Dpep2 (dipeptidase 2)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Pan paniscus (bonobo/pygmy chimpanzee):	DPEP2 (dipeptidase 2)	NCBI	Ortholog
Canis lupus familiaris (dog):	DPEP2 (dipeptidase 2)	HGNC	EggNOG, Ensembl, HomoloGene, OMA, OrthoDB, Panther
Sus scrofa (pig):	DPEP2 (dipeptidase 2)	HGNC	Ensembl, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	DPEP2 (dipeptidase 2)	NCBI	Ortholog
Other homologs ²
Mus musculus (house mouse):	Dpep3 (dipeptidase 3)	HGNC	OrthoDB, OrthoMCL
Rattus norvegicus (Norway rat):	Dpep3 (dipeptidase 3)	HGNC	OrthoDB
Rattus norvegicus (Norway rat):	Kbtbd8 (kelch repeat and BTB domain containing 8)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Dpep2 (dipeptidase 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|SonicParanoid)
Mus musculus (house mouse):	Dpep2 (dipeptidase 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|SonicParanoid)
Danio rerio (zebrafish):	dpep2 (dipeptidase 2)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Drosophila melanogaster (fruit fly):	CG6154	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|OrthoFinder\|OrthoInspector\|PANTHER)
Drosophila melanogaster (fruit fly):	CG42750	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|OrthoInspector\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	CG44837	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|OrthoInspector\|PANTHER)
Drosophila melanogaster (fruit fly):	CG5282	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PANTHER)
Xenopus tropicalis (tropical clawed frog):	dpep2	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	16	67,987,390 - 68,000,619 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	67,987,394 - 68,000,586 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	68,021,293 - 68,034,522 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	66,578,798 - 66,590,857 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	16	66,578,800 - 66,590,857	NCBI
Celera	16	52,529,750 - 52,541,821 (-)	NCBI		Celera
Cytogenetic Map	16	q22.1	NCBI
HuRef	16	53,894,885 - 53,907,048 (-)	NCBI		HuRef
CHM1_1	16	69,429,363 - 69,441,488 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	16	73,783,178 - 73,796,408 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
DPEP2	Human	autosomal dominant dyskeratosis congenita 6		IAGP	RGD:156450340	8554872	ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal dominant 6	ClinVar	PMID:28492532
DPEP2	Human	Chromosome 16q12 Duplication Syndrome		IAGP	RGD:407429775	8554872	ClinVar Annotator: match by term: Chromosome 16q12 duplication syndrome	ClinVar	PMID:25741868

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
DPEP2	Human	17beta-estradiol	increases expression	EXP		6480464	Estradiol results in increased expression of DPEP2 mRNA	CTD	PMID:19619570
DPEP2	Human	17beta-estradiol	multiple interactions	ISO	RGD:1305746	6480464	[estradiol 3-benzoate co-treated with [Testosterone co-treated with Estradiol]] results in increased expression of DPEP2 mRNA	CTD	PMID:32741896
DPEP2	Human	17beta-estradiol	multiple interactions	EXP		6480464	[Estradiol co-treated with Tetrachlorodibenzodioxin] results in increased expression of DPEP2 mRNA	CTD	PMID:19619570
DPEP2	Human	17beta-estradiol 3-benzoate	multiple interactions	ISO	RGD:1305746	6480464	[estradiol 3-benzoate co-treated with [Testosterone co-treated with Estradiol]] results in increased expression of DPEP2 mRNA	CTD	PMID:32741896
DPEP2	Human	2,3,7,8-tetrachlorodibenzodioxine	multiple interactions	EXP		6480464	[Estradiol co-treated with Tetrachlorodibenzodioxin] results in increased expression of DPEP2 mRNA	CTD	PMID:19619570
DPEP2	Human	2,3,7,8-tetrachlorodibenzodioxine	affects expression	ISO	RGD:1313963	6480464	Tetrachlorodibenzodioxin affects the expression of DPEP2 mRNA	CTD	PMID:26377647
DPEP2	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	EXP		6480464	Tetrachlorodibenzodioxin results in increased expression of DPEP2 mRNA	CTD	PMID:19619570
DPEP2	Human	2,4-dibromophenyl 2,4,5-tribromophenyl ether	affects expression	ISO	RGD:1313963	6480464	2,2',4,4',5-brominated diphenyl ether affects the expression of DPEP2 mRNA	CTD	PMID:38648751
DPEP2	Human	3,3',4,4',5-pentachlorobiphenyl	increases expression	ISO	RGD:1305746	6480464	3,4,5,3',4'-pentachlorobiphenyl results in increased expression of DPEP2 mRNA	CTD	PMID:23196670
DPEP2	Human	3,4-methylenedioxymethamphetamine	increases expression	ISO	RGD:1313963	6480464	N-Methyl-3,4-methylenedioxyamphetamine results in increased expression of DPEP2 mRNA	CTD	PMID:26251327
DPEP2	Human	4,4'-sulfonyldiphenol	multiple interactions	EXP		6480464	[bisphenol S co-treated with Fulvestrant] results in decreased methylation of DPEP2 gene	CTD	PMID:31601247
DPEP2	Human	acetamide	increases expression	ISO	RGD:1305746	6480464	acetamide results in increased expression of DPEP2 mRNA	CTD	PMID:31881176
DPEP2	Human	acrylamide	decreases expression	ISO	RGD:1305746	6480464	Acrylamide results in decreased expression of DPEP2 mRNA	CTD	PMID:28959563
DPEP2	Human	aldehydo-D-glucose	increases expression	ISO	RGD:1313963	6480464	Glucose results in increased expression of DPEP2 mRNA	CTD	PMID:31525975
DPEP2	Human	amphetamine	increases expression	ISO	RGD:1305746	6480464	Amphetamine results in increased expression of DPEP2 mRNA	CTD	PMID:30779732
DPEP2	Human	Azoxymethane	multiple interactions	ISO	RGD:1313963	6480464	[titanium dioxide co-treated with Azoxymethane co-treated with Dextran Sulfate] results in decreased expression of DPEP2 more ...	CTD	PMID:29950665
DPEP2	Human	benzo[a]pyrene	increases expression	ISO	RGD:1313963	6480464	Benzo(a)pyrene results in increased expression of DPEP2 mRNA	CTD	PMID:22228805
DPEP2	Human	benzo[a]pyrene	decreases expression	ISO	RGD:1305746	6480464	Benzo(a)pyrene results in decreased expression of DPEP2 mRNA	CTD	PMID:30085273
DPEP2	Human	benzo[a]pyrene	affects methylation	EXP		6480464	Benzo(a)pyrene affects the methylation of DPEP2 promoter	CTD	PMID:27901495
DPEP2	Human	benzo[b]fluoranthene	increases expression	ISO	RGD:1313963	6480464	benzo(b)fluoranthene results in increased expression of DPEP2 mRNA	CTD	PMID:26377693
DPEP2	Human	bisphenol A	decreases expression	ISO	RGD:1305746	6480464	bisphenol A results in decreased expression of DPEP2 mRNA	CTD	PMID:25181051\|PMID:34947998
DPEP2	Human	bisphenol A	multiple interactions	ISO	RGD:1313963	6480464	[Dextran Sulfate co-treated with bisphenol A] results in decreased expression of DPEP2 protein	CTD	PMID:35999755
DPEP2	Human	bisphenol A	increases expression	ISO	RGD:1305746	6480464	bisphenol A results in increased expression of DPEP2 mRNA	CTD	PMID:30816183\|PMID:32528016
DPEP2	Human	bisphenol A	multiple interactions	ISO	RGD:1305746	6480464	[bisphenol A co-treated with tributyltin] results in decreased expression of DPEP2 mRNA	CTD	PMID:31129395
DPEP2	Human	cadmium atom	multiple interactions	ISO	RGD:1313963	6480464	[Cadmium Chloride results in increased abundance of Cadmium] which results in increased expression of DPEP2 more ...	CTD	PMID:37325564
DPEP2	Human	cadmium dichloride	multiple interactions	ISO	RGD:1313963	6480464	[Cadmium Chloride results in increased abundance of Cadmium] which results in increased expression of DPEP2 more ...	CTD	PMID:37325564
DPEP2	Human	carbon nanotube	increases expression	ISO	RGD:1313963	6480464	Nanotubes, Carbon analog results in increased expression of DPEP2 mRNA; Nanotubes, Carbon results in increased more ...	CTD	PMID:25554681
DPEP2	Human	CGP 52608	multiple interactions	EXP		6480464	CGP 52608 promotes the reaction [RORA protein binds to DPEP2 gene]	CTD	PMID:28238834
DPEP2	Human	D-glucose	increases expression	ISO	RGD:1313963	6480464	Glucose results in increased expression of DPEP2 mRNA	CTD	PMID:31525975
DPEP2	Human	dextran sulfate	multiple interactions	ISO	RGD:1313963	6480464	[Dextran Sulfate co-treated with bisphenol A] results in decreased expression of DPEP2 protein; [titanium dioxide more ...	CTD	PMID:29950665\|PMID:35999755
DPEP2	Human	Dibutyl phosphate	affects expression	EXP		6480464	di-n-butylphosphoric acid affects the expression of DPEP2 mRNA	CTD	PMID:37042841
DPEP2	Human	diuron	decreases expression	EXP		6480464	Diuron results in decreased expression of DPEP2 mRNA	CTD	PMID:35967413
DPEP2	Human	fulvestrant	multiple interactions	EXP		6480464	[bisphenol S co-treated with Fulvestrant] results in decreased methylation of DPEP2 gene	CTD	PMID:31601247
DPEP2	Human	gentamycin	decreases expression	ISO	RGD:1305746	6480464	Gentamicins results in decreased expression of DPEP2 mRNA	CTD	PMID:22061828\|PMID:33387578
DPEP2	Human	glucose	increases expression	ISO	RGD:1313963	6480464	Glucose results in increased expression of DPEP2 mRNA	CTD	PMID:31525975
DPEP2	Human	GSK-J4	decreases expression	EXP		6480464	GSK-J4 results in decreased expression of DPEP2 mRNA	CTD	PMID:29301935
DPEP2	Human	lidocaine	increases expression	ISO	RGD:1305746	6480464	Lidocaine results in increased expression of DPEP2 mRNA	CTD	PMID:35283115
DPEP2	Human	manganese(II) chloride	increases expression	ISO	RGD:1305746	6480464	manganese chloride results in increased expression of DPEP2 mRNA	CTD	PMID:28801915
DPEP2	Human	mono(2-ethylhexyl) phthalate	decreases expression	ISO	RGD:1313963	6480464	mono-(2-ethylhexyl)phthalate results in decreased expression of DPEP2 mRNA	CTD	PMID:22401849
DPEP2	Human	N-methyl-4-phenylpyridinium	increases expression	ISO	RGD:1305746	6480464	1-Methyl-4-phenylpyridinium results in increased expression of DPEP2 mRNA	CTD	PMID:28801915
DPEP2	Human	nickel atom	increases expression	EXP		6480464	Nickel results in increased expression of DPEP2 mRNA	CTD	PMID:25583101
DPEP2	Human	oxaliplatin	decreases expression	ISO	RGD:1305746	6480464	oxaliplatin results in decreased expression of DPEP2 mRNA	CTD	PMID:25729387
DPEP2	Human	oxaliplatin	multiple interactions	ISO	RGD:1305746	6480464	[oxaliplatin co-treated with Topotecan] results in decreased expression of DPEP2 mRNA	CTD	PMID:25729387
DPEP2	Human	ozone	multiple interactions	EXP		6480464	[Air Pollutants results in increased abundance of Ozone] which affects the expression of DPEP2 mRNA	CTD	PMID:35430440
DPEP2	Human	paracetamol	decreases expression	ISO	RGD:1305746	6480464	Acetaminophen results in decreased expression of DPEP2 mRNA	CTD	PMID:33387578
DPEP2	Human	sodium arsenite	increases expression	EXP		6480464	sodium arsenite results in increased expression of DPEP2 mRNA	CTD	PMID:38568856
DPEP2	Human	sodium arsenite	decreases expression	ISO	RGD:1313963	6480464	sodium arsenite results in decreased expression of DPEP2 mRNA	CTD	PMID:37682722
DPEP2	Human	testosterone	multiple interactions	ISO	RGD:1305746	6480464	[estradiol 3-benzoate co-treated with [Testosterone co-treated with Estradiol]] results in increased expression of DPEP2 mRNA	CTD	PMID:32741896
DPEP2	Human	thiram	increases expression	EXP		6480464	Thiram results in increased expression of DPEP2 mRNA	CTD	PMID:38568856
DPEP2	Human	titanium dioxide	multiple interactions	ISO	RGD:1313963	6480464	[titanium dioxide co-treated with Azoxymethane co-treated with Dextran Sulfate] results in decreased expression of DPEP2 more ...	CTD	PMID:29950665
DPEP2	Human	topotecan	decreases expression	ISO	RGD:1305746	6480464	Topotecan results in decreased expression of DPEP2 mRNA	CTD	PMID:25729387
DPEP2	Human	topotecan	multiple interactions	ISO	RGD:1305746	6480464	[oxaliplatin co-treated with Topotecan] results in decreased expression of DPEP2 mRNA	CTD	PMID:25729387
DPEP2	Human	tributylstannane	multiple interactions	ISO	RGD:1305746	6480464	[bisphenol A co-treated with tributyltin] results in decreased expression of DPEP2 mRNA	CTD	PMID:31129395
DPEP2	Human	triphenyl phosphate	affects expression	EXP		6480464	triphenyl phosphate affects the expression of DPEP2 mRNA	CTD	PMID:37042841
DPEP2	Human	triptonide	increases expression	ISO	RGD:1313963	6480464	triptonide results in increased expression of DPEP2 mRNA	CTD	PMID:33045310
DPEP2	Human	urethane	increases expression	EXP		6480464	Urethane results in increased expression of DPEP2 mRNA	CTD	PMID:28818685

Biological Process

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
DPEP2	Human	leukotriene D4 catabolic process	involved_in	IDA		150520179	PMID:32325220	UniProt	PMID:32325220
DPEP2	Human	leukotriene metabolic process	involved_in	ISS	UniProtKB:Q8C255	150520179		UniProt	GO_REF:0000024
DPEP2	Human	lipid metabolic process	involved_in	IEA	UniProtKB-KW:KW-0443	150520179		UniProt	GO_REF:0000043
DPEP2	Human	proteolysis	involved_in	IEA	InterPro:IPR000180\|InterPro:IPR008257	150520179		InterPro	GO_REF:0000002
DPEP2	Human	proteolysis	involved_in	IEA	UniProtKB-KW:KW-0645	150520179		UniProt	GO_REF:0000043

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
DPEP2	Human	membrane	located_in	IEA	UniRule:UR000100391	150520179		UniProt	GO_REF:0000104
DPEP2	Human	membrane	located_in	IEA	UniProtKB-KW:KW-0472	150520179		UniProt	GO_REF:0000043
DPEP2	Human	membrane	located_in	ISS	UniProtKB:Q8C255	150520179		UniProt	GO_REF:0000024
DPEP2	Human	membrane	located_in	IEA	UniProtKB-SubCell:SL-0162	150520179		UniProt	GO_REF:0000044
DPEP2	Human	side of membrane	located_in	IEA	UniProtKB-KW:KW-0336	150520179		UniProt	GO_REF:0000043

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
DPEP2	Human	dipeptidase activity	enables	IDA		150520179	PMID:32325220	UniProt	PMID:32325220
DPEP2	Human	dipeptidase activity	enables	IEA	EC:3.4.13.19	150520179		UniProt	GO_REF:0000003
DPEP2	Human	dipeptidase activity	enables	IEA	ARBA:ARBA00026909	150520179		UniProt	GO_REF:0000117
DPEP2	Human	dipeptidase activity	enables	IEA	UniProtKB-KW:KW-0224	150520179		UniProt	GO_REF:0000043
DPEP2	Human	dipeptidase activity	enables	ISS	UniProtKB:Q8C255	150520179		UniProt	GO_REF:0000024
DPEP2	Human	exopeptidase activity	enables	ISO	RGD:1313963	9068941	PMID:12738806	MGI	PMID:12738806
DPEP2	Human	hydrolase activity	enables	IEA	UniProtKB-KW:KW-0378	150520179		UniProt	GO_REF:0000043
DPEP2	Human	metal ion binding	enables	IEA	UniRule:UR000100391	150520179		UniProt	GO_REF:0000104
DPEP2	Human	metal ion binding	enables	IEA	UniProtKB-KW:KW-0479	150520179		UniProt	GO_REF:0000043
DPEP2	Human	metallodipeptidase activity	enables	IEA	InterPro:IPR000180\|InterPro:IPR008257	150520179		InterPro	GO_REF:0000002
DPEP2	Human	metallopeptidase activity	enables	IEA	UniProtKB-KW:KW-0482	150520179		UniProt	GO_REF:0000043
DPEP2	Human	peptidase activity	enables	IEA	UniProtKB-KW:KW-0645	150520179		UniProt	GO_REF:0000043

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
DPEP2	Human	Immunodeficiency		IAGP	RGD:151815659	8554872	ClinVar Annotator: match by term: Immunodeficiency	ClinVar

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

PMID:12477932	PMID:12738806	PMID:12975309	PMID:14702039	PMID:15342556	PMID:15489334	PMID:16335952	PMID:16344560	PMID:18193043	PMID:21555454	PMID:25056061	PMID:25464930
PMID:26186194	PMID:28514442	PMID:32325220	PMID:33961781	PMID:36629882	PMID:37449493	PMID:39823405

DPEP2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	67,987,390 - 68,000,619 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	67,987,394 - 68,000,586 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	68,021,293 - 68,034,522 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	66,578,798 - 66,590,857 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	16	66,578,800 - 66,590,857	NCBI
Celera	16	52,529,750 - 52,541,821 (-)	NCBI		Celera
Cytogenetic Map	16	q22.1	NCBI
HuRef	16	53,894,885 - 53,907,048 (-)	NCBI		HuRef
CHM1_1	16	69,429,363 - 69,441,488 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	16	73,783,178 - 73,796,408 (-)	NCBI		T2T-CHM13v2.0

Dpep2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	8	106,711,577 - 106,732,658 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	8	106,711,577 - 106,723,055 (-)	Ensembl		GRCm39 Ensembl
GRCm39 Ensembl	8	106,711,576 - 106,718,391 (-)	Ensembl		GRCm39 Ensembl
GRCm38	8	105,984,945 - 106,006,026 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	8	105,984,944 - 105,991,759 (-)	Ensembl	GRCm38		mm10	GRCm38
GRCm38.p6 Ensembl	8	105,984,945 - 105,996,423 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	8	108,508,957 - 108,520,323 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	8	108,874,186 - 108,885,552 (-)	NCBI		MGSCv36	mm8
Celera	8	110,213,109 - 110,224,474 (-)	NCBI		Celera
Cytogenetic Map	8	D3	NCBI
cM Map	8	53.07	NCBI

Dpep2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	19	50,795,322 - 50,806,320 (-)	NCBI		GRCr8
mRatBN7.2	19	33,883,557 - 33,896,487 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	19	33,885,478 - 33,891,954 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	19	40,701,008 - 40,707,443 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	19	41,354,322 - 41,360,757 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	19	43,653,038 - 43,659,469 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	19	37,964,098 - 37,975,154 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	19	37,964,105 - 37,970,537 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	19	48,831,084 - 48,851,920 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	19	35,832,224 - 35,838,659 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	19	35,837,105 - 35,843,540 (-)	NCBI
Celera	19	33,313,021 - 33,319,456 (-)	NCBI		Celera
Cytogenetic Map	19	q12	NCBI

DPEP2
(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	18	77,510,359 - 77,526,862 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	16	83,421,784 - 83,438,196 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	16	48,328,281 - 48,341,510 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	16	67,715,805 - 67,729,164 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	16	67,715,805 - 67,729,164 (-)	Ensembl	panpan1.1		panPan2

DPEP2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	5	81,506,635 - 81,511,282 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	5	81,506,330 - 81,511,175 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	5	81,495,291 - 81,501,196 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	5	81,940,443 - 81,946,361 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	5	81,940,034 - 81,946,254 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	5	81,766,906 - 81,772,812 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	5	81,449,218 - 81,455,110 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	5	82,091,144 - 82,097,061 (+)	NCBI		UU_Cfam_GSD_1.0

DPEP2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	6	28,593,546 - 28,599,051 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	6	28,593,542 - 28,599,076 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	6	26,020,128 - 26,025,817 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

DPEP2
(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	5	59,439,237 - 59,447,400 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	5	59,440,951 - 59,447,698 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666047	22,172,991 - 22,187,738 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Variants in DPEP2
51 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 16q13-22.2(chr16:56883592-71279975)x3	copy number gain	See cases [RCV000052405]	Chr16:56883592..71279975 [GRCh38] Chr16:56917504..71313878 [GRCh37] Chr16:55475005..69871379 [NCBI36] Chr16:16q13-22.2	pathogenic
GRCh38/hg38 16q21-23.1(chr16:58456122-74708723)x3	copy number gain	See cases [RCV000052408]	Chr16:58456122..74708723 [GRCh38] Chr16:58490026..74742621 [GRCh37] Chr16:57047527..73300122 [NCBI36] Chr16:16q21-23.1	pathogenic
GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3	copy number gain	See cases [RCV000052421]	Chr16:65313395..90081985 [GRCh38] Chr16:65347298..90148393 [GRCh37] Chr16:63904799..88675894 [NCBI36] Chr16:16q21-24.3	pathogenic
GRCh38/hg38 16q21-22.1(chr16:63318997-70555249)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053334]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053334]\|See cases [RCV000053334]	Chr16:63318997..70555249 [GRCh38] Chr16:63352901..70589152 [GRCh37] Chr16:61910402..69146653 [NCBI36] Chr16:16q21-22.1	pathogenic
GRCh38/hg38 16q21-22.1(chr16:64311275-68062011)x1	copy number loss	See cases [RCV000053335]	Chr16:64311275..68062011 [GRCh38] Chr16:64345179..68095914 [GRCh37] Chr16:62902680..66653415 [NCBI36] Chr16:16q21-22.1	pathogenic
NM_022355.3(DPEP2):c.1438C>T (p.Pro480Ser)	single nucleotide variant	Malignant melanoma [RCV000071190]	Chr16:67987529 [GRCh38] Chr16:68021432 [GRCh37] Chr16:66578933 [NCBI36] Chr16:16q22.1	not provided
GRCh38/hg38 16q21-24.1(chr16:62925929-84585795)x3	copy number gain	See cases [RCV000135863]	Chr16:62925929..84585795 [GRCh38] Chr16:62959833..84619401 [GRCh37] Chr16:61517334..83176902 [NCBI36] Chr16:16q21-24.1	pathogenic
GRCh38/hg38 16q21-24.3(chr16:65511483-90096995)x3	copy number gain	See cases [RCV000139426]	Chr16:65511483..90096995 [GRCh38] Chr16:65545386..90163403 [GRCh37] Chr16:64102887..88690904 [NCBI36] Chr16:16q21-24.3	pathogenic
GRCh38/hg38 16q21-24.3(chr16:64389378-90081985)x3	copy number gain	See cases [RCV000142578]	Chr16:64389378..90081985 [GRCh38] Chr16:64423281..90148393 [GRCh37] Chr16:62980782..88675894 [NCBI36] Chr16:16q21-24.3	pathogenic\|likely pathogenic
GRCh38/hg38 16q12.2-24.3(chr16:52899183-90088654)x3	copy number gain	See cases [RCV000143425]	Chr16:52899183..90088654 [GRCh38] Chr16:52933095..90155062 [GRCh37] Chr16:51490596..88682563 [NCBI36] Chr16:16q12.2-24.3	pathogenic
GRCh38/hg38 16q12.1-22.1(chr16:49685521-68401712)x3	copy number gain	See cases [RCV000143752]	Chr16:49685521..68401712 [GRCh38] Chr16:49719432..68435615 [GRCh37] Chr16:48276933..66993116 [NCBI36] Chr16:16q12.1-22.1	pathogenic
GRCh38/hg38 16q21-23.3(chr16:65957829-83611443)x3	copy number gain	See cases [RCV000143742]	Chr16:65957829..83611443 [GRCh38] Chr16:65991732..83645048 [GRCh37] Chr16:64549233..82202549 [NCBI36] Chr16:16q21-23.3	pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46615804-90142285)x1	copy number loss	Breast ductal adenocarcinoma [RCV000207138]	Chr16:46615804..90142285 [GRCh37] Chr16:16q11.2-24.3	uncertain significance
GRCh37/hg19 16q12.2-22.2(chr16:55359026-70884455)x1	copy number loss	Breast ductal adenocarcinoma [RCV000207067]	Chr16:55359026..70884455 [GRCh37] Chr16:16q12.2-22.2	likely pathogenic\|uncertain significance
Single allele	complex	Breast ductal adenocarcinoma [RCV000207314]	Chr16:56368689..90141355 [GRCh37] Chr16:16q12.2-24.3	uncertain significance
GRCh37/hg19 16q22.1(chr16:67654566-68404073)x1	copy number loss	See cases [RCV000449234]	Chr16:67654566..68404073 [GRCh37] Chr16:16q22.1	likely pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46464488-90155062)x3	copy number gain	See cases [RCV000446110]	Chr16:46464488..90155062 [GRCh37] Chr16:16q11.2-24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3	copy number gain	See cases [RCV000446684]	Chr16:69193..90274381 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3	copy number gain	See cases [RCV000511622]	Chr16:9273328..89548493 [GRCh37] Chr16:16p13.2-q24.3	uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46497599-90354753)x1	copy number loss	Poly (ADP-Ribose) polymerase inhibitor response [RCV000626429]	Chr16:46497599..90354753 [GRCh37] Chr16:16q11.2-24.3	drug response
NM_022355.4(DPEP2):c.175G>A (p.Ala59Thr)	single nucleotide variant	not specified [RCV004317389]	Chr16:67993038 [GRCh38] Chr16:68026941 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3	copy number gain	See cases [RCV000512138]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16q13-24.3(chr16:57051473-89797669)x3	copy number gain	See cases [RCV000512511]	Chr16:57051473..89797669 [GRCh37] Chr16:16q13-24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)	copy number gain	See cases [RCV000511296]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46455960-90354753)x1	copy number loss	Poly (ADP-Ribose) polymerase inhibitor response [RCV000626435]	Chr16:46455960..90354753 [GRCh37] Chr16:16q11.2-24.3	drug response
GRCh37/hg19 16q12.2-22.2(chr16:54416050-72453266)x3	copy number gain	not provided [RCV000683820]	Chr16:54416050..72453266 [GRCh37] Chr16:16q12.2-22.2	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3	copy number gain	not provided [RCV000738918]	Chr16:88165..90274695 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3	copy number gain	not provided [RCV000738915]	Chr16:61451..90294632 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3	copy number gain	not provided [RCV000738917]	Chr16:88165..90163275 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16q21-22.1(chr16:65669673-70180183)x1	copy number loss	not provided [RCV001006797]	Chr16:65669673..70180183 [GRCh37] Chr16:16q21-22.1	pathogenic
GRCh37/hg19 16q22.1(chr16:67132790-68166320)	copy number loss	not provided [RCV000767617]	Chr16:67132790..68166320 [GRCh37] Chr16:16q22.1	pathogenic
NM_022355.4(DPEP2):c.802C>T (p.Arg268Trp)	single nucleotide variant	not specified [RCV004300251]	Chr16:67990928 [GRCh38] Chr16:68024831 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q21-24.3(chr16:61524229-90155062)x3	copy number gain	not provided [RCV001249359]	Chr16:61524229..90155062 [GRCh37] Chr16:16q21-24.3	not provided
GRCh37/hg19 16q22.1(chr16:67765964-68246270)x1	copy number loss	not provided [RCV001259860]	Chr16:67765964..68246270 [GRCh37] Chr16:16q22.1	uncertain significance
NC_000016.9:g.(?_66545871)_(72146396_?)dup	duplication	Dyskeratosis congenita, autosomal dominant 6 [RCV001900384]\|Immunodeficiency [RCV001900385]\|not provided [RCV001900386]	Chr16:66545871..72146396 [GRCh37] Chr16:16q21-22.2	uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46503968-90155062)x3	copy number gain	not provided [RCV002221458]	Chr16:46503968..90155062 [GRCh37] Chr16:16q11.2-24.3	pathogenic
NC_000016.9:g.(?_65821800)_(72146396_?)del	deletion	Dyskeratosis congenita, autosomal dominant 6 [RCV003122496]	Chr16:65821800..72146396 [GRCh37] Chr16:16q21-22.2	uncertain significance
NM_022355.4(DPEP2):c.1396T>C (p.Ser466Pro)	single nucleotide variant	not specified [RCV004302882]	Chr16:67987571 [GRCh38] Chr16:68021474 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.892G>T (p.Asp298Tyr)	single nucleotide variant	not specified [RCV004163680]	Chr16:67990838 [GRCh38] Chr16:68024741 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.959A>C (p.Gln320Pro)	single nucleotide variant	not specified [RCV004244424]	Chr16:67990082 [GRCh38] Chr16:68023985 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.376C>G (p.Leu126Val)	single nucleotide variant	not specified [RCV004203253]	Chr16:67992524 [GRCh38] Chr16:68026427 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.1162G>A (p.Val388Ile)	single nucleotide variant	not specified [RCV004123196]	Chr16:67987896 [GRCh38] Chr16:68021799 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.470G>A (p.Arg157His)	single nucleotide variant	not specified [RCV004118938]	Chr16:67992114 [GRCh38] Chr16:68026017 [GRCh37] Chr16:16q22.1	likely benign
NM_022355.4(DPEP2):c.803G>A (p.Arg268Gln)	single nucleotide variant	not specified [RCV004174556]	Chr16:67990927 [GRCh38] Chr16:68024830 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.190C>T (p.Leu64Phe)	single nucleotide variant	not specified [RCV004126451]	Chr16:67993023 [GRCh38] Chr16:68026926 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.158C>G (p.Thr53Ser)	single nucleotide variant	not specified [RCV004113072]	Chr16:67993055 [GRCh38] Chr16:68026958 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.826G>A (p.Ala276Thr)	single nucleotide variant	not specified [RCV004227535]	Chr16:67990904 [GRCh38] Chr16:68024807 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.1184G>A (p.Arg395Gln)	single nucleotide variant	not specified [RCV004077953]	Chr16:67987874 [GRCh38] Chr16:68021777 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.814G>A (p.Glu272Lys)	single nucleotide variant	not specified [RCV004173137]	Chr16:67990916 [GRCh38] Chr16:68024819 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.275T>C (p.Leu92Pro)	single nucleotide variant	not specified [RCV004173978]	Chr16:67992625 [GRCh38] Chr16:68026528 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.833T>A (p.Val278Glu)	single nucleotide variant	not specified [RCV004219039]	Chr16:67990897 [GRCh38] Chr16:68024800 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.230G>A (p.Arg77Gln)	single nucleotide variant	not specified [RCV004261510]	Chr16:67992983 [GRCh38] Chr16:68026886 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.1285G>A (p.Asp429Asn)	single nucleotide variant	not specified [RCV004256100]	Chr16:67987682 [GRCh38] Chr16:68021585 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.712G>A (p.Gly238Arg)	single nucleotide variant	not specified [RCV004254065]	Chr16:67991135 [GRCh38] Chr16:68025038 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.848C>T (p.Ser283Leu)	single nucleotide variant	not specified [RCV004358130]	Chr16:67990882 [GRCh38] Chr16:68024785 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.1295G>A (p.Arg432His)	single nucleotide variant	not specified [RCV004339337]	Chr16:67987672 [GRCh38] Chr16:68021575 [GRCh37] Chr16:16q22.1	likely benign
GRCh37/hg19 16q22.1(chr16:67498380-68754276)x3	copy number gain	not provided [RCV003485117]	Chr16:67498380..68754276 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.510C>T (p.Thr170=)	single nucleotide variant	not provided [RCV003426749]	Chr16:67992074 [GRCh38] Chr16:68025977 [GRCh37] Chr16:16q22.1	likely benign
GRCh37/hg19 16q22.1(chr16:67583728-69977397)x3	copy number gain	not specified [RCV003987175]	Chr16:67583728..69977397 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.38G>C (p.Gly13Ala)	single nucleotide variant	not specified [RCV004384280]	Chr16:67993175 [GRCh38] Chr16:68027078 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.1406T>C (p.Met469Thr)	single nucleotide variant	not specified [RCV004384276]	Chr16:67987561 [GRCh38] Chr16:68021464 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.233C>T (p.Ala78Val)	single nucleotide variant	not specified [RCV004384278]	Chr16:67992980 [GRCh38] Chr16:68026883 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.440G>A (p.Arg147His)	single nucleotide variant	not specified [RCV004384281]	Chr16:67992144 [GRCh38] Chr16:68026047 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.817G>A (p.Val273Met)	single nucleotide variant	not specified [RCV004384282]	Chr16:67990913 [GRCh38] Chr16:68024816 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.1149A>C (p.Glu383Asp)	single nucleotide variant	not specified [RCV004384272]	Chr16:67987909 [GRCh38] Chr16:68021812 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.1292C>T (p.Ser431Leu)	single nucleotide variant	not specified [RCV004384274]	Chr16:67987675 [GRCh38] Chr16:68021578 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.1298T>C (p.Leu433Pro)	single nucleotide variant	not specified [RCV004384275]	Chr16:67987669 [GRCh38] Chr16:68021572 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.1253C>T (p.Pro418Leu)	single nucleotide variant	not specified [RCV004384273]	Chr16:67987714 [GRCh38] Chr16:68021617 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.261C>G (p.Asp87Glu)	single nucleotide variant	not specified [RCV004384279]	Chr16:67992952 [GRCh38] Chr16:68026855 [GRCh37] Chr16:16q22.1	uncertain significance
NC_000016.9:g.(?_48799549)_(70756330_?)dup	duplication	Chromosome 16q12 duplication syndrome [RCV004595820]	Chr16:48799549..70756330 [GRCh37] Chr16:16q12.1-22.1	likely pathogenic
NM_022355.4(DPEP2):c.635C>T (p.Thr212Met)	single nucleotide variant	not specified [RCV004624659]	Chr16:67991865 [GRCh38] Chr16:68025768 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.116C>T (p.Pro39Leu)	single nucleotide variant	not specified [RCV004624660]	Chr16:67993097 [GRCh38] Chr16:68027000 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.254T>A (p.Leu85His)	single nucleotide variant	not specified [RCV004624661]	Chr16:67992959 [GRCh38] Chr16:68026862 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.107C>A (p.Thr36Lys)	single nucleotide variant	not specified [RCV004624662]	Chr16:67993106 [GRCh38] Chr16:68027009 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.473G>A (p.Arg158His)	single nucleotide variant	not specified [RCV004912110]	Chr16:67992111 [GRCh38] Chr16:68026014 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.1158G>C (p.Gln386His)	single nucleotide variant	not specified [RCV004912111]	Chr16:67987900 [GRCh38] Chr16:68021803 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.122G>C (p.Arg41Thr)	single nucleotide variant	not specified [RCV004912115]	Chr16:67993091 [GRCh38] Chr16:68026994 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.635C>G (p.Thr212Arg)	single nucleotide variant	not specified [RCV004912112]	Chr16:67991865 [GRCh38] Chr16:68025768 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.769G>A (p.Val257Ile)	single nucleotide variant	not specified [RCV004912108]	Chr16:67990961 [GRCh38] Chr16:68024864 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.47C>T (p.Pro16Leu)	single nucleotide variant	not specified [RCV004912114]	Chr16:67993166 [GRCh38] Chr16:68027069 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q21-24.1(chr16:62746020-84485022)x3	copy number gain	not provided [RCV004819314]	Chr16:62746020..84485022 [GRCh37] Chr16:16q21-24.1	pathogenic
NM_022355.4(DPEP2):c.1300C>T (p.Arg434Cys)	single nucleotide variant	not specified [RCV004912107]	Chr16:67987667 [GRCh38] Chr16:68021570 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.767T>C (p.Met256Thr)	single nucleotide variant	not specified [RCV004912113]	Chr16:67990963 [GRCh38] Chr16:68024866 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.596T>C (p.Ile199Thr)	single nucleotide variant	not specified [RCV004912116]	Chr16:67991904 [GRCh38] Chr16:68025807 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.254T>C (p.Leu85Pro)	single nucleotide variant	not specified [RCV004920255]	Chr16:67992959 [GRCh38] Chr16:68026862 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.856C>T (p.Arg286Trp)	single nucleotide variant	not specified [RCV004920256]	Chr16:67990874 [GRCh38] Chr16:68024777 [GRCh37] Chr16:16q22.1	uncertain significance
NM_022355.4(DPEP2):c.139G>A (p.Gly47Ser)	single nucleotide variant	not specified [RCV004920257]	Chr16:67993074 [GRCh38] Chr16:68026977 [GRCh37] Chr16:16q22.1	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	2470
Count of miRNA genes:	921
Interacting mature miRNAs:	1115
Transcripts:	ENST00000268795, ENST00000393847, ENST00000412757, ENST00000572624, ENST00000572888, ENST00000573808, ENST00000574316, ENST00000574865, ENST00000575203, ENST00000575510
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.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
596972244	GWAS1091763_H	phospholipids:total lipids ratio QTL GWAS1091763 (human)		1e-10	phospholipids:total lipids ratio		16	67991092	67991093	Human
597526044	GWAS1622118_H	phospholipids:total lipids ratio QTL GWAS1622118 (human)		1e-10	phospholipids:total lipids ratio		16	67991092	67991093	Human
597459999	GWAS1556073_H	phospholipids:total lipids ratio, high density lipoprotein cholesterol measurement QTL GWAS1556073 (human)		2e-15	phospholipids:total lipids ratio, high density lipoprotein cholesterol measurement	blood high density lipoprotein cholesterol level (CMO:0000052)	16	67991092	67991093	Human
407100487	GWAS749463_H	alkaline phosphatase measurement QTL GWAS749463 (human)		1e-13	alkaline phosphatase measurement		16	67991092	67991093	Human
597499929	GWAS1596003_H	high density lipoprotein cholesterol measurement QTL GWAS1596003 (human)		8e-17	high density lipoprotein cholesterol measurement	blood high density lipoprotein cholesterol level (CMO:0000052)	16	67995836	67995837	Human
597450842	GWAS1546916_H	high density lipoprotein cholesterol measurement QTL GWAS1546916 (human)		2e-68	high density lipoprotein cholesterol measurement	blood high density lipoprotein cholesterol level (CMO:0000052)	16	67991092	67991093	Human
407099083	GWAS748059_H	high density lipoprotein cholesterol measurement QTL GWAS748059 (human)		0.0000001	high density lipoprotein cholesterol measurement		16	67991092	67991093	Human
597424919	GWAS1520993_H	apolipoprotein A 1 measurement QTL GWAS1520993 (human)		4e-60	apolipoprotein A 1 measurement	blood apolipoprotein AI level (CMO:0000520)	16	67991092	67991093	Human
596951323	GWAS1070842_H	high density lipoprotein cholesterol measurement QTL GWAS1070842 (human)		2e-68	high density lipoprotein cholesterol measurement		16	67991092	67991093	Human
596988698	GWAS1108217_H	cholesteryl esters:total lipids ratio, high density lipoprotein cholesterol measurement QTL GWAS1108217 (human)		4e-08	cholesteryl esters:total lipids ratio, high density lipoprotein cholesterol measurement		16	67995836	67995837	Human
597450445	GWAS1546519_H	total cholesterol measurement QTL GWAS1546519 (human)		5e-11	total cholesterol measurement	blood total cholesterol level (CMO:0000051)	16	67991092	67991093	Human
407104923	GWAS753899_H	apolipoprotein A 1 measurement QTL GWAS753899 (human)		4e-60	apolipoprotein A 1 measurement		16	67991092	67991093	Human
407104351	GWAS753327_H	total cholesterol measurement QTL GWAS753327 (human)		5e-11	total cholesterol measurement		16	67991092	67991093	Human
596972616	GWAS1092135_H	phospholipids:total lipids ratio, high density lipoprotein cholesterol measurement QTL GWAS1092135 (human)		2e-15	phospholipids:total lipids ratio, high density lipoprotein cholesterol measurement		16	67991092	67991093	Human
596987447	GWAS1106966_H	high density lipoprotein cholesterol measurement QTL GWAS1106966 (human)		8e-17	high density lipoprotein cholesterol measurement		16	67995836	67995837	Human
407023271	GWAS672247_H	phospholipids:total lipids ratio QTL GWAS672247 (human)		1e-10	phospholipids:total lipids ratio		16	67991092	67991093	Human
407087141	GWAS736117_H	phospholipids:total lipids ratio, high density lipoprotein cholesterol measurement QTL GWAS736117 (human)		2e-15	phospholipids:total lipids ratio, high density lipoprotein cholesterol measurement		16	67991092	67991093	Human
407096554	GWAS745530_H	high density lipoprotein cholesterol measurement QTL GWAS745530 (human)		3e-13	high density lipoprotein cholesterol measurement		16	67991092	67991093	Human
597404213	GWAS1500287_H	high density lipoprotein cholesterol measurement QTL GWAS1500287 (human)		3e-13	high density lipoprotein cholesterol measurement	blood high density lipoprotein cholesterol level (CMO:0000052)	16	67991092	67991093	Human
597435944	GWAS1532018_H	cholesteryl esters:total lipids ratio, high density lipoprotein cholesterol measurement QTL GWAS1532018 (human)		4e-08	cholesteryl esters:total lipids ratio, high density lipoprotein cholesterol measurement	blood high density lipoprotein cholesterol level (CMO:0000052)	16	67995836	67995837	Human
597526312	GWAS1622386_H	dipeptidase 2 measurement QTL GWAS1622386 (human)		3e-22	dipeptidase 2 measurement		16	67995972	67995973	Human
596951468	GWAS1070987_H	apolipoprotein A 1 measurement QTL GWAS1070987 (human)		4e-60	apolipoprotein A 1 measurement		16	67991092	67991093	Human
597421411	GWAS1517485_H	alkaline phosphatase measurement QTL GWAS1517485 (human)		1e-13	alkaline phosphatase measurement	blood alkaline phosphatase activity level (CMO:0000576)	16	67991092	67991093	Human
597461540	GWAS1557614_H	high density lipoprotein cholesterol measurement QTL GWAS1557614 (human)		3e-19	high density lipoprotein cholesterol measurement	blood high density lipoprotein cholesterol level (CMO:0000052)	16	67995836	67995837	Human
596951470	GWAS1070989_H	total cholesterol measurement QTL GWAS1070989 (human)		5e-11	total cholesterol measurement		16	67991092	67991093	Human
407105656	GWAS754632_H	high density lipoprotein cholesterol measurement QTL GWAS754632 (human)		2e-68	high density lipoprotein cholesterol measurement		16	67991092	67991093	Human
597378919	GWAS1474993_H	high density lipoprotein cholesterol measurement QTL GWAS1474993 (human)		0.0000001	high density lipoprotein cholesterol measurement	blood high density lipoprotein cholesterol level (CMO:0000052)	16	67991092	67991093	Human
596951467	GWAS1070986_H	alkaline phosphatase measurement QTL GWAS1070986 (human)		1e-13	alkaline phosphatase measurement		16	67991092	67991093	Human

SHGC-60842

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	68,021,321 - 68,021,576	UniSTS	GRCh37
Build 36	16	66,578,822 - 66,579,077	RGD	NCBI36
Celera	16	52,529,778 - 52,530,033	RGD
Cytogenetic Map	16	q22.1	UniSTS
HuRef	16	53,894,913 - 53,895,168	UniSTS
GeneMap99-GB4 RH Map	16	406.22	UniSTS
Whitehead-RH Map	16	306.4	UniSTS
NCBI RH Map	16	508.6	UniSTS

SHGC-60762

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	68,021,301 - 68,021,451	UniSTS	GRCh37
Build 36	16	66,578,802 - 66,578,952	RGD	NCBI36
Celera	16	52,529,758 - 52,529,908	RGD
Cytogenetic Map	16	q22.1	UniSTS
HuRef	16	53,894,893 - 53,895,043	UniSTS
GeneMap99-GB4 RH Map	16	404.61	UniSTS
Whitehead-RH Map	16	304.7	UniSTS
NCBI RH Map	16	508.6	UniSTS

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	2351	2788	2246	4672	1703	2177	5	610	1929	450	2037	7153	6428	18	3653	1	806	1663	1461	170	1


RefSeq Transcripts	NM_001324159	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001369657	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_022355	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_136706	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005256090	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011523266	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011523268	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011523271	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011523272	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011523273	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011523274	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017023542	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017023543	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017023544	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017023545	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017023547	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450372	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450373	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450374	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450376	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047434459	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047434460	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047434461	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047434462	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047434463	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047434464	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047434465	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313622	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313623	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313624	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313625	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313626	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313627	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313628	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313629	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313630	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313631	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313632	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313633	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313634	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313635	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313636	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313637	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313638	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313639	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054313640	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008484713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008484714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_243420	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_933389	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_933390	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_933391	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_933392	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA404265	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC040162	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ295149	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK092884	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK298003	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK315090	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY358454	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC024021	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP299049	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CB528462	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471092	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA677374	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB038910	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KC877614	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000268795

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,991,643 - 68,000,581 (-)	Ensembl

Ensembl Acc Id:

ENST00000393847 ⟹ ENSP00000377430

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,987,394 - 67,999,484 (-)	Ensembl

Ensembl Acc Id:

ENST00000572624 ⟹ ENSP00000460169

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,992,173 - 67,999,518 (-)	Ensembl

Ensembl Acc Id:

ENST00000572888 ⟹ ENSP00000458977

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,987,506 - 67,993,863 (-)	Ensembl

Ensembl Acc Id:

ENST00000573808 ⟹ ENSP00000463604

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,990,898 - 67,999,512 (-)	Ensembl

Ensembl Acc Id:

ENST00000574316

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,992,817 - 68,000,568 (-)	Ensembl

Ensembl Acc Id:

ENST00000574865 ⟹ ENSP00000461250

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,992,557 - 67,994,328 (-)	Ensembl

Ensembl Acc Id:

ENST00000575203 ⟹ ENSP00000459375

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,987,397 - 68,000,586 (-)	Ensembl

Ensembl Acc Id:

ENST00000575510 ⟹ ENSP00000462652

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,990,049 - 68,000,564 (-)	Ensembl

RefSeq Acc Id:

NM_001324159 ⟹ NP_001311088

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,394 - 67,994,291 (-)	NCBI
CHM1_1	16	69,429,363 - 69,436,264 (-)	NCBI
T2T-CHM13v2.0	16	73,783,182 - 73,790,079 (-)	NCBI

Sequence:

show sequence

GGAGTGTGGCTGCAGAACCCAGGTGGCAGGGCTTTCCTCAGGCCCCTTACTCCTGACCTGGACGAGGCCGGGGCTTCCTCAAGGAGTTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGAT
GCCCTGCGCCTCACCCTGGAGCAGATTGACCTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGT
AGAGGGTGGCCACTCGCTGGACAATAGCCTCTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCC
ACTCCTTCTACAACAACATCAGCGGGCTGACTGACTTTGGTGAGAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAA
GTGTCACAGGCACCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTC
CATGGGAGTAATACAGTGCAACCCATCAGCCAATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAAT
TCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAGTTGCTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGGGTCTTCAGACAAGTG
GAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGACTTCAGGCCA
GGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTATTCTGTGGC
TCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAA

hide sequence

RefSeq Acc Id:

NM_001369657 ⟹ NP_001356586

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,993,394 (-)	NCBI
T2T-CHM13v2.0	16	73,783,178 - 73,789,182 (-)	NCBI

Sequence:

show sequence

GGTGCCGCCGCTCTCCGCACATCCTTCGCGGGGCCCTGTGACTTCGTTACCCTCCTCTTGAGGCCACGCCGCCAGGTGGCCTGAATCGAGGGTCGGGACTCCATCGTCGCGCTCTGCCCCTCGCCCGC
CCCTCTCAGGCTCTCTGACTGCCACCCCTGCCTGCCTGCCCGGCCCTGCACAACATGCAGCCCTCCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCTGCTGAGTCTGCTGCTCCTGCTGCT
GCTGCTCCAGCCTGTAACCTGTGCCTACACCACGCCAGGCCCCCCCAGAGCCCTCACCACGCTGGGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTCCCTCGACCACACTCAGTAGTCCCA
GCACCCAGGGCCTGCAAGAGCAGGCACGGGCCCTGATGCGGGACTTCCCGCTCGTGGACGGCCACAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAAGGGCTACAGGATGTTAACCTGCGC
AATTTCAGCTACGGCCAGACCAGCCTGGACAGGCTTAGAGATGGCCTCGTGGGCGCCCAGTTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGAT
TGACCTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATA
GCCTCTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGG
CTGACTGACTTTGGTGAGAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTC
CCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCCAT
CAGCCAATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAATTCCCTCAGGGGCTGGAAGACGTGTCC
ACATACCCGGTCCTGATAGAGGAGTTGCTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGGGTCTTCAGACAAGTGGAAAAGGTACAGGAAGAAAACAAATG
GCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGACTTCAGGCCAGGAACTCACTGAGATTCCCATACACT
GGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTATTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAG
ATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAACAGA

hide sequence

RefSeq Acc Id:

NM_022355 ⟹ NP_071750

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,394 - 67,999,484 (-)	NCBI
GRCh37	16	68,021,293 - 68,034,493 (-)	NCBI
Build 36	16	66,578,798 - 66,590,857 (-)	NCBI Archive
Celera	16	52,529,750 - 52,541,821 (-)	RGD
HuRef	16	53,894,885 - 53,907,048 (-)	NCBI
CHM1_1	16	69,429,363 - 69,441,488 (-)	NCBI
T2T-CHM13v2.0	16	73,783,182 - 73,795,272 (-)	NCBI

Sequence:

show sequence

ACACACTAGTGAAATCTTGTCTTAGTGTGTCCGGAATTGGTGGGTTCTTGGTCTCACTGAGTTCTAGAATGAAGCTGCAGACCCTCGCAGTGAGTGTTACAGCTCTTAAGGCTCTCTGACTGCCACCC
CTGCCTGCCTGCCCGGCCCTGCACAACATGCAGCCCTCCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCTGCTGAGTCTGCTGCTCCTGCTGCTGCTGCTCCAGCCTGTAACCTGTGCCTA
CACCACGCCAGGCCCCCCCAGAGCCCTCACCACGCTGGGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTCCCTCGACCACACTCAGTAGTCCCAGCACCCAGGGCCTGCAAGAGCAGGCAC
GGGCCCTGATGCGGGACTTCCCGCTCGTGGACGGCCACAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAAGGGCTACAGGATGTTAACCTGCGCAATTTCAGCTACGGCCAGACCAGCCTG
GACAGGCTTAGAGATGGCCTCGTGGGCGCCCAGTTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGATTGACCTCATACGCCGCATGTGTGCCTC
CTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATAGCCTCTCCATCTTACGTACCTTCTACA
TGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGGCTGACTGACTTTGGTGAGAAGGTGGTG
GCAGAAATGAACCGCCTGGGCATGATGGTAGACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTGCAA
CAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCCATCAGCCAATGTGTCCACTGTGGCAGATC
ACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAATTCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAGTTG
CTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGGGTCTTCAGACAAGTGGAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCC
GGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGACTTCAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGT
CAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTATTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACC
CCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAA

hide sequence

RefSeq Acc Id:

NR_136706

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,394 - 68,000,619 (-)	NCBI
CHM1_1	16	69,429,363 - 69,442,556 (-)	NCBI
T2T-CHM13v2.0	16	73,783,182 - 73,796,407 (-)	NCBI

Sequence:

show sequence

GTCTACAGTGGCCAGGCTGCTTTCTGGCTTGGAAGACTATTGTTTCTTGGGAATTGTCTGTATC
AGACATCATGGGAGCAGATCCAGGGCGACATCAAAGGGAAGCATGAGTCTCCAGGACCAGAGGGGCTTGGATGCAGATGATCATCATCTGGGCACTGCTGGATACTGAAGTTCTCATTATGTTGCCTA
GACTGGTCTCAAACCTCCGGCTTCAAGAGATCCTCTCACCTCGACCTTCAAATTACTGGGATTACAGGCATGAGCCACCATGTCCTACCAGACTTTGTTAAAAGAGGAACAGGCCAGGCATCGTGGGC
TCACATGAACACTCATGCCCCAGAAGTAAACAAGTGTTAGCCAACCAGGAGGCCTATCCTCCCCCTAACCTCACCCAAAGCCATCTCTGTGCCCTCCCCCTTGCAGGGGAAACAGCACACACTAGTGA
AATCTTGTCTTAGTGTGTCCGGAATTGGTGGGTTCTTGGTCTCACTGAGTTCTAGAATGAAGCTGCAGACCCTCGCAGTGAGTGTTACAGCTCTTAAGGTAGCGCGTCTGGAGTTTGTTTCTTTTGAT
GTTTGGATGTTTGGAGTTTCTTCCTTCTGGTGGGTTTGTGGTCTTGTTGGCTCAGGAGTGAAGCTGCAGACCTTCGTGGCTCTCTGACTGCCACCCCTGCCTGCCTGCCCGGCCCTGCACAACATGCA
GCCCTCCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCTGCTGAGTCTGCTGCTCCTGCTGCTGCTGCTCCAGCCTGTAACCTGTGCCTACACCACGCCAGGCCCCCCCAGAGCCCTCACCA
CGCTGGGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTCCCTCGACCACACTCAGTAGTCCCAGCACCCAGGGCCTGCAAGAGCAGGCACGGGCCCTGATGCGGGACTTCCCGCTCGTGGAC
GGCCACAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAAGGGCTACAGGATGTTAACCTGCGCAATTTCAGCTACGGCCAGACCAGCCTGGACAGGCTTAGAGATGGCCTCGTGGGCGCCCA
GTTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGATTGACCTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTA
AAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATAGCCTCTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCAC
ACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGGCTGACTGACTTTGGTGAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCT
GTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACA
GTGCAACCCATCAGCCAATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAACCCTGGACTGTGGTTC
TGAGTCATGATCAGGGAATCAGGTCTGAAACCCACTAGCTGGTGGCCACACAGATTCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAGTTGCTGAGTCGTGGCTGGAGTGA
GGAAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGGGTCTTCAGACAAGTGGAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTT
CCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGACTTCAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCC
CACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTATTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGT
GCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAA

hide sequence

RefSeq Acc Id:

XM_005256090 ⟹ XP_005256147

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,993,394 (-)	NCBI
GRCh37	16	68,021,293 - 68,034,493 (-)	NCBI

Sequence:

show sequence

GGTGCCGCCGCTCTCCGCACATCCTTCGCGGGGCCCTGTGACTTCGTTACCCTCCTCTTGAGGC
CACGCCGCCAGGTGGCCTGAATCGAGGGTCGGGACTCCATCGTCGCGCTCTGCCCCTCGCCCGCCCCTCTCAGGCTCTCTGACTGCCACCCCTGCCTGCCTGCCCGGCCCTGCACAACATGCAGCCCT
CCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCTGCTGAGTCTGCTGCTCCTGCTGCTGCTGCTCCAGCCTGTAACCTGTGCCTACACCACGCCAGGCCCCCCCAGAGCCCTCACCACGCTG
GGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTCCCTCGACCACACTCAGTAGTCCCAGCACCCAGGGCCTGCAAGAGCAGGCACGGGCCCTGATGCGGGACTTCCCGCTCGTGGACGGCCA
CAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAAGGGCTACAGGATGTTAACCTGCGCAATTTCAGCTACGGCCAGACCAGCCTGGACAGGCTTAGAGATGGCCTCGTGGGCGCCCAGTTCT
GGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGATTGACCTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCT
CTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATAGCCTCTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTG
CAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGGCTGACTGACTTTGGTGAGAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTAT
CCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTT
CTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCCATCAGCCAATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTT
CATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCT
GCGTCAGAGACAGAGTCTGACTTCAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTG
TGGCCACCTTCCCAGTCCTTATTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATA
AATGTTTTGGACATAGAAACAGA

hide sequence

RefSeq Acc Id:

XM_011523266 ⟹ XP_011521568

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,999,484 (-)	NCBI

Sequence:

show sequence

AGTGTGTCCGGAATTGGTGGGTTCTTGGTCTCACTGAGTTCTAGAATGAAGCTGCAGACCCTCG
CAGTGAGTGTTACAGCTCTTAAGGCTCTCTGACTGCCACCCCTGCCTGCCTGCCCGGCCCTGCACAACATGCAGCCCTCCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCTGCTGAGTCTG
CTGCTCCTGCTGCTGCTGCTCCAGCCTGTAACCTGTGCCTACACCACGCCAGGCCCCCCCAGAGCCCTCACCACGCTGGGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTCCCTCGACCAC
ACTCAGTAGTCCCAGCACCCAGGGCCTGCAAGAGCAGGCACGGGCCCTGATGCGGGACTTCCCGCTCGTGGACGGCCACAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAAGGGCTACAGG
ATGTTAACCTGCGCAATTTCAGCTACGGCCAGACCAGCCTGGACAGGCTTAGAGATGGCCTCGTGGGCGCCCAGTTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTC
ACCCTGGAGCAGATTGACCTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCA
CTCGCTGGACAATAGCCTCTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACA
ACAACATCAGCGGGCTGACTGACTTTGGTGAGAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCA
CCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAAT
ACAGTGCAACCCATCAGCCAATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAGGAATCAGGTCTGA
AACCCACTAGCTGGTGGCCACACAGATTCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAGTTGCTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGTCCTTCGTGGA
AACCTGCTGCGGGTCTTCAGACAAGTGGAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCG
TCAGAGACAGAGTCTGACTTCAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGG
CCACCTTCCCAGTCCTTATTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAAT
GTTTTGGACATAGAAACAGA

hide sequence

RefSeq Acc Id:

XM_011523268 ⟹ XP_011521570

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,993,394 (-)	NCBI

Sequence:

show sequence

GGTGCCGCCGCTCTCCGCACATCCTTCGCGGGGCCCTGTGACTTCGTTACCCTCCTCTTGAGGC
CACGCCGCCAGGTGGCCTGAATCGAGGGTCGGGACTCCATCGTCGCGCTCTGCCCCTCGCCCGCCCCTCTCAGGCTCTCTGACTGCCACCCCTGCCTGCCTGCCCGGCCCTGCACAACATGCAGCCCT
CCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCTGCTGAGTCTGCTGCTCCTGCTGCTGCTGCTCCAGCCTGTAACCTGTGCCTACACCACGCCAGGCCCCCCCAGAGCCCTCACCACGCTG
GGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTCCCTCGACCACACTCAGTAGTCCCAGCACCCAGGGCCTGCAAGAGCAGGCACGGGCCCTGATGCGGGACTTCCCGCTCGTGGACGGCCA
CAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAAGGGCTACAGGATGTTAACCTGCGCAATTTCAGCTACGGCCAGACCAGCCTGGACAGGCTTAGAGATGGCCTCGTGGGCGCCCAGTTCT
GGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGATTGACCTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCT
CTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATAGCCTCTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTG
CAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGGCTGACTGACTTTGGTGAGAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTAT
CCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTT
CTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCCATCAGCCAATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTT
CATCGGGATTGGTGGAGATTATGATGGGGCCGGCAACTGGTGGCCACACAGATTCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAGTTGCTGAGTCGTGGCTGGAGTGAGG
AAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGGGTCTTCAGACAAGTGGAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTTCC
TGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGACTTCAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCCCA
CATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTATTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGTGC
AGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAACAGA

hide sequence

RefSeq Acc Id:

XM_011523271 ⟹ XP_011521573

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,993,394 (-)	NCBI

Sequence:

show sequence

GGTGCCGCCGCTCTCCGCACATCCTTCGCGGGGCCCTGTGACTTCGTTACCCTCCTCTTGAGGC
CACGCCGCCAGGTGGCCTGAATCGAGGGTCGGGACTCCATCGTCGCGCTCTGCCCCTCGCCCGCCCCTCTCAGGCTCTCTGACTGCCACCCCTGCCTGCCTGCCCGGCCCTGCACAACATGCAGCCCT
CCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCTGCTGAGTCTGCTGCTCCTGCTGCTGCTGCTCCAGCCTGTAACCTGTGCCTACACCACGCCAGGCCCCCCCAGAGCCCTCACCACGCTG
GGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTCCCTCGACCACACTCAGTAGTCCCAGCACCCAGGGCCTGCAAGAGCAGGCACGGGCCCTGATGCGGGACTTCCCGCTCGTGGACGGCCA
CAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAAGGGCTACAGGATGTTAACCTGCGCAATTTCAGCTACGGCCAGACCAGCCTGGACAGGCTTAGAGATGGCCTCGTGGGCGCCCAGTTCT
GGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGATTGACCTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCT
CTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATAGCCTCTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTG
CAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGGCTGACTGACTTTGGTGAGAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTAT
CCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTT
CTGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGG
ATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGACTTCAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCA
GTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTATTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCC
ACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAACAGA

hide sequence

RefSeq Acc Id:

XM_011523273 ⟹ XP_011521575

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 68,000,619 (-)	NCBI

Sequence:

show sequence

GAGGATGTTTGTCTACAGTGGCCAGGCTGCTTTCTGGCTTGGAAGACTATTGTTTCTTGGGAATTGTCTGTATCAGACATCATGGGAGCAGATCCAGGGCGACATCAAAGGGAAGCATGAGTCTCCAG
GACCAGAGGGGCTTGGATGCAGATGATCATCATCTGGGCACTGCTGGATACTGATTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGATTGACCT
CATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATAGCCTCT
CCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGGCTGACT
GACTTTGGTGAGAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCACTC
GGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCCATCAGCCA
ATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAGGAATCAGGTCTGAAACCCACTAGCTGGTGGCCA
CACAGATTCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAGTTGCTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGGGTCTTCAG
ACAAGTGGAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGACTT
CAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTATT
CTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAACAGA

hide sequence

RefSeq Acc Id:

XM_011523274 ⟹ XP_011521576

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 68,000,619 (-)	NCBI

Sequence:

show sequence

TGGAGGATGTTTGTCTACAGTGGCCAGGCTGCTTTCTGGCTTGGAAGACTATTGTTTCTTGGGAATTGTCTGTATCAGACATCATGGGAGCAGATCCAGGGCGACATCAAAGGGAAGCATGAGTCTCC
AGGACCAGAGGGGCTTGGATGCAGATGATCATCATCTGGGCACTGCTGGATACTGAGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGGCTGACTGACTTTGGTGAGAA
GGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTG
TGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCCATCAGCCAATGTGTCCACTGTG
GCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAGGAATCAGGTCTGAAACCCACTAGCTGGTGGCCACACAGATTCCCTCA
GGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAGTTGCTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGGGTCTTCAGACAAGTGGAAAAGG
TACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGACTTCAGGCCAGGAACTC
ACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTATTCTGTGGCTCTGATG
ACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAACAGA

hide sequence

RefSeq Acc Id:

XM_017023545 ⟹ XP_016879034

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,994,291 (-)	NCBI

Sequence:

show sequence

TGAGCCAAGATTGTGCCACTACCCTCTAGCCTGGGCAACAAAGTGAGACTCTGTCTCAAAACAAACAAAAAAAGACCCCCTTCGGCAGCAGTAGACGTGACAGTTAACCCACCTCGAGCACTCGGCCA
TCGATCTGCCTTCCTCCTGGACAGCAGACACTGGGCAACATCAAGTGTGCAGTCCCTAAAATACATCAAAGCTGGGATCACTTCCCCTCCTGGGTAGCTTGGGACCTCCAGTCCCTTTGGAAGAGTTG
GTTCATTTTCTTTTTAGGAGGCCTTCTTGAATCTCTAGTCGTCGTCAGGCTTAGGTCACACTACCCATGCACTGATCAGCCCTGCCACGTGGGGGAGGCTCCAAAAAATGAAGCGGTTCCAGGGGTGC
CAAGGTTCAGAGCAGAGTCTTGAGAGCCTGAGGGGCAGGAGGAGGCAAAGGTCTCTGAGGACGAAGGGGTTTGGCCACAGTCCCGGAAGATCTCAGGTCGTGGGGCTTCTGTGAGCGGGCACATCCCC
TGTGCCTGTGTGATTGTGAGCTTGTGTGCTTGTGTGGTTGGGGGTCCTTCCTGGAGGAGGCATCTAGGTTGAGGGCCCCAGGCCGGGAATGGGGTGGGGCCTGTCGTCAAGGAAGGGACTCAGCCCTG
GAGGTTTCTGTGAGAGCTCAAGCCACAGGAGCCACAAGATAAGAGGAGTGTGGCTGCAGAACCCAGGTGGCAGGGCTTTCCTCAGGCCCCTTACTCCTGACCTGGACGAGGCCGGGGCTTCCTCAAGG
AGTTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGATTGACCTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCT
AAAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATAGCCTCTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCA
CACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGGCTGACTGACTTTGGTGAGAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAG
ACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTG
CAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCCATCAGCCAATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATC
CAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAGGAATCAGGTCTGAAACCCACTAGCTGGTGGCCACACAGATTCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAG
AGGAGTTGCTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGGGTCTTCAGACAAGTGGAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGAC
AAGTTCCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGACTTCAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGC
CAAGTGGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTATTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCA
CAGACACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAACAGA

hide sequence

RefSeq Acc Id:

XM_017023547 ⟹ XP_016879036

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 68,000,619 (-)	NCBI

Sequence:

show sequence

TGGGCACTGCTGGATACTGAAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTC
TCCCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCC
ATCAGCCAATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAGGAATCAGGTCTGAAACCCACTAGCT
GGTGGCCACACAGATTCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAGTTGCTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGG
GTCTTCAGACAAGTGGAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAG
TCTGACTTCAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAG
TCCTTATTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATA
GAAACAGA

hide sequence

RefSeq Acc Id:

XM_024450372 ⟹ XP_024306140

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,994,291 (-)	NCBI

Sequence:

show sequence

ACAAGATAAGAGGAGTGTGGCTGCAGAACCCAGGTGGCAGGGCTTTCCTCAGGCCCCTTACTCC
TGACCTGGACGAGGCCGGGGCTTCCTCAAGGAGGCTCTCTGACTGCCACCCCTGCCTGCCTGCCCGGCCCTGCACAACATGCAGCCCTCCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCT
GCTGAGTCTGCTGCTCCTGCTGCTGCTGCTCCAGCCTGTAACCTGTGCCTACACCACGCCAGGCCCCCCCAGAGCCCTCACCACGCTGGGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTC
CCTCGACCACACTCAGTAGTCCCAGCACCCAGGGCCTGCAAGAGCAGGCACGGGCCCTGATGCGGGACTTCCCGCTCGTGGACGGCCACAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAA
GGGCTACAGGATGTTAACCTGCGCAATTTCAGCTACGGCCAGACCAGCCTGGACAGGCTTAGAGATGGCCTCGTGGGCGCCCAGTTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGC
CCTGCGCCTCACCCTGGAGCAGATTGACCTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAG
AGGGTGGCCACTCGCTGGACAATAGCCTCTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCAC
TCCTTCTACAACAACATCAGCGGGCTGACTGACTTTGGTGAGAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGT
GTCACAGGCACCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCA
TGGGAGTAATACAGTGCAACCCATCAGCCAATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAGGAA
TCAGGTCTGAAACCCACTAGCTGGTGGCCACACAGATTCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAGTTGCTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGT
CCTTCGTGGAAACCTGCTGCGGGTCTTCAGACAAGTGGAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCT
CACGTCTGCGTCAGAGACAGAGTCTGACTTCAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTT
GCAGTTGTGGCCACCTTCCCAGTCCTTATTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCC
TGAAATAAATGTTTTGGACATAGAAACAGA

hide sequence

RefSeq Acc Id:

XM_024450373 ⟹ XP_024306141

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 68,000,619 (-)	NCBI

Sequence:

show sequence

TCAGCTTGGTGATTGGAGGATGTTTGTCTACAGTGGCCAGGCTGCTTTCTGGCTTGGAAGACTA
TTGTTTCTTGGGAATTGTCTGTATCAGACATCATGGGAGCAGATCCAGGGCGACATCAAAGGGAAGCATGAGTCTCCAGGACCAGAGGGGCTTGGATGCAGATGATCATCATCTGGGCACTGCTGGAT
ACTGAGCTCTCTGACTGCCACCCCTGCCTGCCTGCCCGGCCCTGCACAACATGCAGCCCTCCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCTGCTGAGTCTGCTGCTCCTGCTGCTGCTG
CTCCAGCCTGTAACCTGTGCCTACACCACGCCAGGCCCCCCCAGAGCCCTCACCACGCTGGGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTCCCTCGACCACACTCAGTAGTCCCAGCAC
CCAGGGCCTGCAAGAGCAGGCACGGGCCCTGATGCGGGACTTCCCGCTCGTGGACGGCCACAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAAGGGCTACAGGATGTTAACCTGCGCAATT
TCAGCTACGGCCAGACCAGCCTGGACAGGCTTAGAGATGGCCTCGTGGGCGCCCAGTTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGATTGAC
CTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATAGCCT
CTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGGCTGA
CTGACTTTGGTGAGAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCAC
TCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCCATCAGC
CAATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAGGAATCAGGTCTGAAACCCACTAGCTGGTGGC
CACACAGATTCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAGTTGCTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGGGTCTTC
AGACAAGTGGAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGAC
TTCAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTA
TTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAACA
GA

hide sequence

RefSeq Acc Id:

XM_024450374 ⟹ XP_024306142

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,999,484 (-)	NCBI

Sequence:

show sequence

AAACCTCCGGCTTCAAGAGATCCTCTCACCTCGACCTTCAAATTACTGGGATTACAGGCATGAG
CCACCATGTCCTACCAGACTTTGTTAAAAGAGGAACAGGCCAGGCATCGTGGGCTCACATGAACACTCATGCCCCAGAAGTAAACAAGTGTTAGCCAACCAGGAGGCCTATCCTCCCCCTAACCTCAC
CCAAAGCCATCTCTGTGCCCTCCCCCTTGCAGGGGAAACAGCACACACTAGTGAAATCTTGTCTTAGTGTGTCCGGAATTGGTGGGTTCTTGGTCTCACTGAGTTCTAGAATGAAGCTGCAGACCCTC
GCAGCTCTCTGACTGCCACCCCTGCCTGCCTGCCCGGCCCTGCACAACATGCAGCCCTCCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCTGCTGAGTCTGCTGCTCCTGCTGCTGCTGCT
CCAGCCTGTAACCTGTGCCTACACCACGCCAGGCCCCCCCAGAGCCCTCACCACGCTGGGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTCCCTCGACCACACTCAGTAGTCCCAGCACCC
AGGGCCTGCAAGAGCAGGCACGGGCCCTGATGCGGGACTTCCCGCTCGTGGACGGCCACAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAAGGGCTACAGGATGTTAACCTGCGCAATTTC
AGCTACGGCCAGACCAGCCTGGACAGGCTTAGAGATGGCCTCGTGGGCGCCCAGTTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGATTGACCT
CATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATAGCCTCT
CCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGGCTGACT
GACTTTGGTGAGAAGGTGGTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCACTC
GGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCCATCAGCCA
ATGTGTCCACTGTGGCAGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAGGAATCAGGTCTGAAACCCACTAGCTGGTGGCCA
CACAGATTCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAGTTGCTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGGGTCTTCAG
ACAAGTGGAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTTCCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGACTT
CAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGTGGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTATT
CTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGACACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAACAGA

hide sequence

RefSeq Acc Id:

XM_024450376 ⟹ XP_024306144

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 68,000,619 (-)	NCBI

Sequence:

show sequence

GGATGTTTGTCTACAGTGGCCAGGCTGCTTTCTGGCTTGGAAGACTATTGTTTCTTGGGAATTGTCTGTATCAGACATCATGGGAGCAGATCCAGGGCGACATCAAAGGGAAGCATGAGTCTCCAGGA
CCAGAGGGGCTTGGATGCAGATGATCATCATCTGGGCACTGCTGGATACTGAGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGGCTGACTGACTTTGGTGAGAAGGTG
GTGGCAGAAATGAACCGCCTGGGCATGATGGTAGACTTATCCCATGTCTCAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTG
CAACAGTGCTCGGAATGTTCCTGATGACATCCTGCAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCCATCAGCCAATGTGTCCACTGTGGCAG
ATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAAATTCCCTCAGGGGCTGGAAGACGTGTCCACATACCCGGTCCTGATAGAGGAG
TTGCTGAGTCGTGGCTGGAGTGAGGAAGAGCTTCAGGGTGTCCTTCGTGGAAACCTGCTGCGGGTCTTCAGACAAGTGGAAAAGGTACAGGAAGAAAACAAATGGCAAAGCCCCTTGGAGGACAAGTT
CCCGGATGAGCAGCTGAGCAGTTCCTGCCACTCCGACCTCTCACGTCTGCGTCAGAGACAGAGTCTGACTTCAGGCCAGGAACTCACTGAGATTCCCATACACTGGACAGCCAAGTTACCAGCCAAGT
GGTCAGTCTCAGAGTCCTCCCCCCACATGGCCCCAGTCCTTGCAGTTGTGGCCACCTTCCCAGTCCTTATTCTGTGGCTCTGATGACCCAGTTAGTCCTGCCAGATGTCACTGTAGCAAGCCACAGAC
ACCCCACAAAGTTCCCCTGTTGTGCAGGCACAAATATTTCCTGAAATAAATGTTTTGGACATAGAAACAGA

hide sequence

RefSeq Acc Id:

XM_047434459 ⟹ XP_047290415

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,994,975 (-)	NCBI

RefSeq Acc Id:

XM_047434460 ⟹ XP_047290416

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,994,291 (-)	NCBI

RefSeq Acc Id:

XM_047434461 ⟹ XP_047290417

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,999,484 (-)	NCBI

RefSeq Acc Id:

XM_047434462 ⟹ XP_047290418

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,390 - 67,999,484 (-)	NCBI

RefSeq Acc Id:

XM_047434463 ⟹ XP_047290419

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,848 - 67,993,394 (-)	NCBI

RefSeq Acc Id:

XM_047434464 ⟹ XP_047290420

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,848 - 67,993,394 (-)	NCBI

RefSeq Acc Id:

XM_047434465 ⟹ XP_047290421

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,987,848 - 67,993,394 (-)	NCBI

RefSeq Acc Id:

XM_054313622 ⟹ XP_054169597

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,790,079 (-)	NCBI

RefSeq Acc Id:

XM_054313623 ⟹ XP_054169598

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,790,763 (-)	NCBI

RefSeq Acc Id:

XM_054313624 ⟹ XP_054169599

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,796,408 (-)	NCBI

RefSeq Acc Id:

XM_054313625 ⟹ XP_054169600

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,795,503 (-)	NCBI

RefSeq Acc Id:

XM_054313626 ⟹ XP_054169601

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,795,272 (-)	NCBI

RefSeq Acc Id:

XM_054313627 ⟹ XP_054169602

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,789,182 (-)	NCBI

RefSeq Acc Id:

XM_054313628 ⟹ XP_054169603

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,790,079 (-)	NCBI

RefSeq Acc Id:

XM_054313629 ⟹ XP_054169604

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,795,272 (-)	NCBI

RefSeq Acc Id:

XM_054313630 ⟹ XP_054169605

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,789,182 (-)	NCBI

RefSeq Acc Id:

XM_054313631 ⟹ XP_054169606

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,795,503 (-)	NCBI

RefSeq Acc Id:

XM_054313632 ⟹ XP_054169607

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,636 - 73,789,182 (-)	NCBI

RefSeq Acc Id:

XM_054313633 ⟹ XP_054169608

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,789,182 (-)	NCBI

RefSeq Acc Id:

XM_054313634 ⟹ XP_054169609

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,636 - 73,789,182 (-)	NCBI

RefSeq Acc Id:

XM_054313635 ⟹ XP_054169610

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,796,404 (-)	NCBI

RefSeq Acc Id:

XM_054313636 ⟹ XP_054169611

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,790,079 (-)	NCBI

RefSeq Acc Id:

XM_054313637 ⟹ XP_054169612

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,636 - 73,789,182 (-)	NCBI

RefSeq Acc Id:

XM_054313638 ⟹ XP_054169613

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,796,405 (-)	NCBI

RefSeq Acc Id:

XM_054313639 ⟹ XP_054169614

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,796,402 (-)	NCBI

RefSeq Acc Id:

XM_054313640 ⟹ XP_054169615

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,783,178 - 73,796,404 (-)	NCBI

RefSeq Acc Id:

XR_008484713

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,785,835 - 73,789,182 (-)	NCBI

RefSeq Acc Id:

XR_008484714

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,785,113 - 73,789,182 (-)	NCBI

RefSeq Acc Id:

XR_243420

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,990,047 - 67,993,394 (-)	NCBI
GRCh37	16	68,021,293 - 68,034,493 (-)	NCBI

Sequence:

show sequence

GGTGCCGCCGCTCTCCGCACATCCTTCGCGGGGCCCTGTGACTTCGTTACCCTCCTCTTGAGGCCACGCCGCCAGGTGGCCTGAATCGAGGGTCGGGACTCCATCGTCGCGCTCTGCCCCTCGCCCGC
CCCTCTCAGGCTCTCTGACTGCCACCCCTGCCTGCCTGCCCGGCCCTGCACAACATGCAGCCCTCCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCTGCTGAGTCTGCTGCTCCTGCTGCT
GCTGCTCCAGCCTGTAACCTGTGCCTACACCACGCCAGGCCCCCCCAGAGCCCTCACCACGCTGGGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTCCCTCGACCACACTCAGTAGTCCCA
GCACCCAGGGCCTGCAAGAGCAGGCACGGGCCCTGATGCGGGACTTCCCGCTCGTGGACGGCCACAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAAGGGCTACAGGATGTTAACCTGCGC
AATTTCAGCTACGGCCAGACCAGCCTGGACAGGCTTAGAGATGGCCTCGTGGGCGCCCAGTTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGAT
TGACCTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATA
GCCTCTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGG
CTGACTGACTTTGGTGAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTG
CAGCTTCTGAAGAAGAACGGTGGCGTCGTGATGGTGTCTTTGTCCATGGGAGTAATACAGTGCAACCCATCAGCCAATGTGTCCACTGTGGCAG

hide sequence

RefSeq Acc Id:

XR_933392

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,989,325 - 67,993,394 (-)	NCBI

Sequence:

show sequence

GGTGCCGCCGCTCTCCGCACATCCTTCGCGGGGCCCTGTGACTTCGTTACCCTCCTCTTGAGGCCACGCCGCCAGGTGGCCTGAATCGAGGGTCGGGACTCCATCGTCGCGCTCTGCCCCTCGCCCGC
CCCTCTCAGGCTCTCTGACTGCCACCCCTGCCTGCCTGCCCGGCCCTGCACAACATGCAGCCCTCCGGCCTCGAGGGTCCCGGCACGTTTGGTCGGTGGCCTCTGCTGAGTCTGCTGCTCCTGCTGCT
GCTGCTCCAGCCTGTAACCTGTGCCTACACCACGCCAGGCCCCCCCAGAGCCCTCACCACGCTGGGCGCCCCCAGAGCCCACACCATGCCGGGCACCTACGCTCCCTCGACCACACTCAGTAGTCCCA
GCACCCAGGGCCTGCAAGAGCAGGCACGGGCCCTGATGCGGGACTTCCCGCTCGTGGACGGCCACAACGACCTGCCCCTGGTCCTAAGGCAGGTTTACCAGAAAGGGCTACAGGATGTTAACCTGCGC
AATTTCAGCTACGGCCAGACCAGCCTGGACAGGCTTAGAGATGGCCTCGTGGGCGCCCAGTTCTGGTCAGCCTATGTGCCATGCCAGACCCAGGACCGGGATGCCCTGCGCCTCACCCTGGAGCAGAT
TGACCTCATACGCCGCATGTGTGCCTCCTATTCTGAGCTGGAGCTTGTGACCTCGGCTAAAGCTCTGAACGACACTCAGAAATTGGCCTGCCTCATCGGTGTAGAGGGTGGCCACTCGCTGGACAATA
GCCTCTCCATCTTACGTACCTTCTACATGCTGGGAGTGCGCTACCTGACGCTCACCCACACCTGCAACACACCCTGGGCAGAGAGCTCCGCTAAGGGCGTCCACTCCTTCTACAACAACATCAGCGGG
CTGACTGACTTTGGTGAGATGCTGTGGCACGGCGGGCCCTGGAAGTGTCACAGGCACCTGTGATCTTCTCCCACTCGGCTGCCCGGGGTGTGTGCAACAGTGCTCGGAATGTTCCTGATGACATCCTG
CAGCTTCTGATCACTTCGACCACATCAAGGCTGTCATTGGATCCAAGTTCATCGGGATTGGTGGAGATTATGATGGGGCCGGCAA

hide sequence


Protein RefSeqs	NP_001311088	(Get FASTA)	NCBI Sequence Viewer
	NP_001356586	(Get FASTA)	NCBI Sequence Viewer
	NP_071750	(Get FASTA)	NCBI Sequence Viewer
	XP_005256147	(Get FASTA)	NCBI Sequence Viewer
	XP_011521568	(Get FASTA)	NCBI Sequence Viewer
	XP_011521570	(Get FASTA)	NCBI Sequence Viewer
	XP_011521573	(Get FASTA)	NCBI Sequence Viewer
	XP_011521575	(Get FASTA)	NCBI Sequence Viewer
	XP_011521576	(Get FASTA)	NCBI Sequence Viewer
	XP_016879034	(Get FASTA)	NCBI Sequence Viewer
	XP_016879036	(Get FASTA)	NCBI Sequence Viewer
	XP_024306140	(Get FASTA)	NCBI Sequence Viewer
	XP_024306141	(Get FASTA)	NCBI Sequence Viewer
	XP_024306142	(Get FASTA)	NCBI Sequence Viewer
	XP_024306144	(Get FASTA)	NCBI Sequence Viewer
	XP_047290415	(Get FASTA)	NCBI Sequence Viewer
	XP_047290416	(Get FASTA)	NCBI Sequence Viewer
	XP_047290417	(Get FASTA)	NCBI Sequence Viewer
	XP_047290418	(Get FASTA)	NCBI Sequence Viewer
	XP_047290419	(Get FASTA)	NCBI Sequence Viewer
	XP_047290420	(Get FASTA)	NCBI Sequence Viewer
	XP_047290421	(Get FASTA)	NCBI Sequence Viewer
	XP_054169597	(Get FASTA)	NCBI Sequence Viewer
	XP_054169598	(Get FASTA)	NCBI Sequence Viewer
	XP_054169599	(Get FASTA)	NCBI Sequence Viewer
	XP_054169600	(Get FASTA)	NCBI Sequence Viewer
	XP_054169601	(Get FASTA)	NCBI Sequence Viewer
	XP_054169602	(Get FASTA)	NCBI Sequence Viewer
	XP_054169603	(Get FASTA)	NCBI Sequence Viewer
	XP_054169604	(Get FASTA)	NCBI Sequence Viewer
	XP_054169605	(Get FASTA)	NCBI Sequence Viewer
	XP_054169606	(Get FASTA)	NCBI Sequence Viewer
	XP_054169607	(Get FASTA)	NCBI Sequence Viewer
	XP_054169608	(Get FASTA)	NCBI Sequence Viewer
	XP_054169609	(Get FASTA)	NCBI Sequence Viewer
	XP_054169610	(Get FASTA)	NCBI Sequence Viewer
	XP_054169611	(Get FASTA)	NCBI Sequence Viewer
	XP_054169612	(Get FASTA)	NCBI Sequence Viewer
	XP_054169613	(Get FASTA)	NCBI Sequence Viewer
	XP_054169614	(Get FASTA)	NCBI Sequence Viewer
	XP_054169615	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH24021	(Get FASTA)	NCBI Sequence Viewer
	AAQ88819	(Get FASTA)	NCBI Sequence Viewer
	BAG37555	(Get FASTA)	NCBI Sequence Viewer
	BAG52621	(Get FASTA)	NCBI Sequence Viewer
	BAG60309	(Get FASTA)	NCBI Sequence Viewer
	CAC14667	(Get FASTA)	NCBI Sequence Viewer
	EAW83200	(Get FASTA)	NCBI Sequence Viewer
	EAW83201	(Get FASTA)	NCBI Sequence Viewer
	EAW83202	(Get FASTA)	NCBI Sequence Viewer
	EAW83203	(Get FASTA)	NCBI Sequence Viewer
	EAW83204	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000377430
	ENSP00000377430.1
	ENSP00000458977
	ENSP00000458977.1
	ENSP00000459375.1
GenBank Protein	Q9H4A9	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_071750 ⟸ NM_022355
- Peptide Label:	isoform 1 precursor
- UniProtKB:	Q6UX92 (UniProtKB/Swiss-Prot), I3L248 (UniProtKB/Swiss-Prot), B3KS59 (UniProtKB/Swiss-Prot), B2RCF8 (UniProtKB/Swiss-Prot), Q8TC95 (UniProtKB/Swiss-Prot), Q9H4A9 (UniProtKB/Swiss-Prot), A0A024R6Y5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MQPSGLEGPGTFGRWPLLSLLLLLLLLQPVTCAYTTPGPPRALTTLGAPRAHTMPGTYAPSTTLSSPSTQGLQEQARALMRDFPLVDGHNDLPLVLRQVYQKGLQDVNLRNFSYGQTSLDRLRDGLVG AQFWSAYVPCQTQDRDALRLTLEQIDLIRRMCASYSELELVTSAKALNDTQKLACLIGVEGGHSLDNSLSILRTFYMLGVRYLTLTHTCNTPWAESSAKGVHSFYNNISGLTDFGEKVVAEMNRLGMM VDLSHVSDAVARRALEVSQAPVIFSHSAARGVCNSARNVPDDILQLLKKNGGVVMVSLSMGVIQCNPSANVSTVADHFDHIKAVIGSKFIGIGGDYDGAGKFPQGLEDVSTYPVLIEELLSRGWSEEE LQGVLRGNLLRVFRQVEKVQEENKWQSPLEDKFPDEQLSSSCHSDLSRLRQRQSLTSGQELTEIPIHWTAKLPAKWSVSESSPHMAPVLAVVATFPVLILWL hide sequence

RefSeq Acc Id:

XP_005256147 ⟸ XM_005256090

- Peptide Label:

isoform X5

- Sequence:

show sequence

MQPSGLEGPGTFGRWPLLSLLLLLLLLQPVTCAYTTPGPPRALTTLGAPRAHTMPGTYAPSTTLSSPSTQGLQEQARALMRDFPLVDGHNDLPLVLRQVYQKGLQDVNLRNFSYGQTSLDRLRDGLVG
AQFWSAYVPCQTQDRDALRLTLEQIDLIRRMCASYSELELVTSAKALNDTQKLACLIGVEGGHSLDNSLSILRTFYMLGVRYLTLTHTCNTPWAESSAKGVHSFYNNISGLTDFGEKVVAEMNRLGMM
VDLSHVSDAVARRALEVSQAPVIFSHSAARGVCNSARNVPDDILQLLKKNGGVVMVSLSMGVIQCNPSANVSTVADHFDHIKAVIGSKFIGIGGDYDGAGKYRKKTNGKAPWRTSSRMSS

hide sequence

RefSeq Acc Id:

XP_011521576 ⟸ XM_011523274

- Peptide Label:

isoform X12

- Sequence:

show sequence

MQMIIIWALLDTEAESSAKGVHSFYNNISGLTDFGEKVVAEMNRLGMMVDLSHVSDAVARRALEVSQAPVIFSHSAARGVCNSARNVPDDILQLLKKNGGVVMVSLSMGVIQCNPSANVSTVADHFDH
IKAVIGSKFIGIGGDYDGAGKESGLKPTSWWPHRFPQGLEDVSTYPVLIEELLSRGWSEEELQGVLRGNLLRVFRQVEKVQEENKWQSPLEDKFPDEQLSSSCHSDLSRLRQRQSLTSGQELTEIPIH
WTAKLPAKWSVSESSPHMAPVLAVVATFPVLILWL

hide sequence

RefSeq Acc Id:

XP_011521575 ⟸ XM_011523273

- Peptide Label:

isoform X10

- Sequence:

show sequence

MCASYSELELVTSAKALNDTQKLACLIGVEGGHSLDNSLSILRTFYMLGVRYLTLTHTCNTPWA
ESSAKGVHSFYNNISGLTDFGEKVVAEMNRLGMMVDLSHVSDAVARRALEVSQAPVIFSHSAARGVCNSARNVPDDILQLLKKNGGVVMVSLSMGVIQCNPSANVSTVADHFDHIKAVIGSKFIGIGG
DYDGAGKESGLKPTSWWPHRFPQGLEDVSTYPVLIEELLSRGWSEEELQGVLRGNLLRVFRQVEKVQEENKWQSPLEDKFPDEQLSSSCHSDLSRLRQRQSLTSGQELTEIPIHWTAKLPAKWSVSES
SPHMAPVLAVVATFPVLILWL

hide sequence

RefSeq Acc Id:

XP_011521568 ⟸ XM_011523266

- Peptide Label:

isoform X1

- Sequence:

show sequence

MQPSGLEGPGTFGRWPLLSLLLLLLLLQPVTCAYTTPGPPRALTTLGAPRAHTMPGTYAPSTTL
SSPSTQGLQEQARALMRDFPLVDGHNDLPLVLRQVYQKGLQDVNLRNFSYGQTSLDRLRDGLVGAQFWSAYVPCQTQDRDALRLTLEQIDLIRRMCASYSELELVTSAKALNDTQKLACLIGVEGGHS
LDNSLSILRTFYMLGVRYLTLTHTCNTPWAESSAKGVHSFYNNISGLTDFGEKVVAEMNRLGMMVDLSHVSDAVARRALEVSQAPVIFSHSAARGVCNSARNVPDDILQLLKKNGGVVMVSLSMGVIQ
CNPSANVSTVADHFDHIKAVIGSKFIGIGGDYDGAGKESGLKPTSWWPHRFPQGLEDVSTYPVLIEELLSRGWSEEELQGVLRGNLLRVFRQVEKVQEENKWQSPLEDKFPDEQLSSSCHSDLSRLRQ
RQSLTSGQELTEIPIHWTAKLPAKWSVSESSPHMAPVLAVVATFPVLILWL

hide sequence

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9H4A9-F1-model_v2	AlphaFold	Q9H4A9	1-486	view protein structure

RGD ID:

6793039

Promoter ID:

HG_KWN:24071

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

ENST00000322384, UC002EVD.2, UC010CEY.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	16	66,584,684 - 66,585,184 (-)	MPROMDB

RGD ID:

6792976

Promoter ID:

HG_KWN:24072

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell_12Hour, Lymphoblastoid, NB4

Transcripts:

NM_022355

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	16	66,590,756 - 66,591,747 (-)	MPROMDB

RGD ID:

7232617

Promoter ID:

EPDNEW_H22054

Type:

initiation region

Name:

DPEP2_3

Description:

dipeptidase 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H22055 EPDNEW_H22056

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,994,302 - 67,994,362	EPDNEW

RGD ID:

7232619

Promoter ID:

EPDNEW_H22055

Type:

initiation region

Name:

DPEP2_1

Description:

dipeptidase 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H22054 EPDNEW_H22056

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,999,484 - 67,999,544	EPDNEW

RGD ID:

7232621

Promoter ID:

EPDNEW_H22056

Type:

initiation region

Name:

DPEP2_2

Description:

dipeptidase 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H22054 EPDNEW_H22055

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	68,000,586 - 68,000,646	EPDNEW

Database	Acc Id	Source(s)
COSMIC	DPEP2	COSMIC
Ensembl Genes	ENSG00000167261	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000393847	ENTREZGENE
	ENST00000393847.6	UniProtKB/Swiss-Prot
	ENST00000572888	ENTREZGENE
	ENST00000572888.5	UniProtKB/Swiss-Prot
	ENST00000575203	ENTREZGENE
	ENST00000575203.5	UniProtKB/Swiss-Prot
Gene3D-CATH	Metal-dependent hydrolases	UniProtKB/Swiss-Prot
GTEx	ENSG00000167261	GTEx
HGNC ID	HGNC:23028	ENTREZGENE
Human Proteome Map	DPEP2	Human Proteome Map
InterPro	Dipep_AS	UniProtKB/Swiss-Prot
	Metal_Hydrolase	UniProtKB/Swiss-Prot
	Pept_M19	UniProtKB/Swiss-Prot
KEGG Report	hsa:64174	UniProtKB/Swiss-Prot
NCBI Gene	64174	ENTREZGENE
OMIM	609925	OMIM
PANTHER	DIPEPTIDASE 2	UniProtKB/Swiss-Prot
	PTHR10443	UniProtKB/Swiss-Prot
Pfam	Peptidase_M19	UniProtKB/Swiss-Prot
PharmGKB	PA134985997	PharmGKB
PROSITE	RENAL_DIPEPTIDASE_1	UniProtKB/Swiss-Prot
	RENAL_DIPEPTIDASE_2	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF51556	UniProtKB/Swiss-Prot
UniProt	A0A024R6Y5	ENTREZGENE
	B2RCF8	ENTREZGENE
	B3KS59	ENTREZGENE
	DPEP2_HUMAN	UniProtKB/Swiss-Prot
	I3L248	ENTREZGENE
	I3L348_HUMAN	UniProtKB/TrEMBL
	I3L4H3_HUMAN	UniProtKB/TrEMBL
	J3KSU4_HUMAN	UniProtKB/TrEMBL
	J3QLL2_HUMAN	UniProtKB/TrEMBL
	Q6UX92	ENTREZGENE
	Q8TC95	ENTREZGENE
	Q9H4A9	ENTREZGENE
UniProt Secondary	A0A024R6Y5	UniProtKB/Swiss-Prot
	B2RCF8	UniProtKB/Swiss-Prot
	B3KS59	UniProtKB/Swiss-Prot
	I3L248	UniProtKB/Swiss-Prot
	Q6UX92	UniProtKB/Swiss-Prot
	Q8TC95	UniProtKB/Swiss-Prot

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


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


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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Imported Disease Annotations - ClinVar

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