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Gene: NAALAD2 (N-acetylated alpha-linked acidic dipeptidase 2) Homo sapiens

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Symbol:

NAALAD2

Name:

N-acetylated alpha-linked acidic dipeptidase 2

RGD ID:

1314164

HGNC Page

HGNC:14526

Description:

Predicted to enable N-formylglutamate deformylase activity and carboxypeptidase activity. Predicted to be involved in carboxylic acid catabolic process. Predicted to act upstream of or within proteolysis. Predicted to be located in plasma membrane.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

GCP3; GCPIII; glutamate carboxypeptidase III; GPCIII; MGC116996; MGC26353; N-acetylated alpha-linked acidic dipeptidase II; N-acetylated-alpha-linked acidic dipeptidase 2; N-acetylated-alpha-linked acidic dipeptidase II; NAADALASE2; NAALADase II; NAALADASE2

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	90,131,699 - 90,192,894 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	90,131,515 - 90,192,894 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	89,867,831 - 89,926,062 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	89,507,530 - 89,565,424 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	11	89,507,529 - 89,565,418	NCBI
Celera	11	87,168,325 - 87,226,293 (+)	NCBI		Celera
Cytogenetic Map	11	q14.3	NCBI
HuRef	11	85,952,467 - 86,010,505 (+)	NCBI		HuRef
CHM1_1	11	89,750,836 - 89,808,679 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	11	90,051,780 - 90,112,974 (+)	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)
NAALAD2	Human	intellectual disability		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Intellectual disability	ClinVar
NAALAD2	Human	Neurodevelopmental Disorders		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Neurodevelopmental disorder	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)
NAALAD2	Human	(R)-noradrenaline	decreases expression	ISO	Naalad2 (Rattus norvegicus)	6480464	Norepinephrine results in decreased expression of NAALAD2 mRNA	CTD	PMID:14618266
NAALAD2	Human	1,2-dichloroethane	decreases expression	ISO	Naalad2 (Mus musculus)	6480464	ethylene dichloride results in decreased expression of NAALAD2 mRNA	CTD	PMID:28960355
NAALAD2	Human	17alpha-ethynylestradiol	affects expression	ISO	Naalad2 (Mus musculus)	6480464	Ethinyl Estradiol affects the expression of NAALAD2 mRNA	CTD	PMID:17555576
NAALAD2	Human	17alpha-ethynylestradiol	increases expression	ISO	Naalad2 (Mus musculus)	6480464	Ethinyl Estradiol results in increased expression of NAALAD2 mRNA	CTD	PMID:17942748
NAALAD2	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	Naalad2 (Mus musculus)	6480464	Tetrachlorodibenzodioxin results in increased expression of NAALAD2 mRNA	CTD	PMID:28213091
NAALAD2	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	Naalad2 (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin results in increased expression of NAALAD2 mRNA	CTD	PMID:33387578
NAALAD2	Human	4-nonylphenol	multiple interactions	EXP		6480464	[4-tert-octylphenol co-treated with 4-nonylphenol] results in decreased expression of NAALAD2 mRNA	CTD	PMID:23626723
NAALAD2	Human	4-tert-Octylphenol	multiple interactions	EXP		6480464	[4-tert-octylphenol co-treated with 4-nonylphenol] results in decreased expression of NAALAD2 mRNA	CTD	PMID:23626723
NAALAD2	Human	acrylamide	increases expression	EXP		6480464	Acrylamide results in increased expression of NAALAD2 mRNA	CTD	PMID:32763439
NAALAD2	Human	aflatoxin B1	decreases methylation	EXP		6480464	Aflatoxin B1 results in decreased methylation of NAALAD2 gene	CTD	PMID:27153756
NAALAD2	Human	aflatoxin M1	decreases expression	EXP		6480464	Aflatoxin M1 results in decreased expression of NAALAD2 mRNA	CTD	PMID:30928695
NAALAD2	Human	aristolochic acid A	increases expression	EXP		6480464	aristolochic acid I results in increased expression of NAALAD2 mRNA	CTD	PMID:33212167
NAALAD2	Human	arsenite(3-)	increases expression	ISO	Naalad2 (Mus musculus)	6480464	arsenite results in increased expression of NAALAD2 protein	CTD	PMID:37955338
NAALAD2	Human	benzo[a]pyrene	decreases expression	EXP		6480464	Benzo(a)pyrene results in decreased expression of NAALAD2 mRNA	CTD	PMID:20106945
NAALAD2	Human	benzo[a]pyrene	increases methylation	EXP		6480464	Benzo(a)pyrene results in increased methylation of NAALAD2 5' UTR and Benzo(a)pyrene results in increased methylation of NAALAD2 exon	CTD	PMID:27901495
NAALAD2	Human	benzo[a]pyrene	affects methylation	EXP		6480464	Benzo(a)pyrene affects the methylation of NAALAD2 promoter	CTD	PMID:27901495
NAALAD2	Human	beta-naphthoflavone	decreases expression	EXP		6480464	beta-Naphthoflavone results in decreased expression of NAALAD2 mRNA	CTD	PMID:32858204
NAALAD2	Human	bis(2-ethylhexyl) phthalate	decreases expression	EXP		6480464	Diethylhexyl Phthalate results in decreased expression of NAALAD2 mRNA	CTD	PMID:31163220
NAALAD2	Human	bisphenol A	increases methylation	ISO	Naalad2 (Rattus norvegicus)	6480464	bisphenol A results in increased methylation of NAALAD2 gene	CTD	PMID:28505145
NAALAD2	Human	bisphenol A	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in increased methylation of NAALAD2 gene	CTD	PMID:31601247
NAALAD2	Human	CGP 52608	multiple interactions	EXP		6480464	CGP 52608 promotes the reaction [RORA protein binds to NAALAD2 gene]	CTD	PMID:28238834
NAALAD2	Human	clofibrate	increases expression	ISO	Naalad2 (Mus musculus)	6480464	Clofibrate results in increased expression of NAALAD2 mRNA	CTD	PMID:17585979
NAALAD2	Human	copper(II) sulfate	decreases expression	EXP		6480464	Copper Sulfate results in decreased expression of NAALAD2 mRNA	CTD	PMID:19549813
NAALAD2	Human	cyclosporin A	decreases expression	EXP		6480464	Cyclosporine results in decreased expression of NAALAD2 mRNA	CTD	PMID:20106945 and PMID:25562108
NAALAD2	Human	D-mannitol	increases expression	ISO	Naalad2 (Mus musculus)	6480464	Mannitol results in increased expression of NAALAD2 mRNA	CTD	PMID:25270620
NAALAD2	Human	dicrotophos	decreases expression	EXP		6480464	dicrotophos results in decreased expression of NAALAD2 mRNA	CTD	PMID:28302478
NAALAD2	Human	dorsomorphin	multiple interactions	EXP		6480464	[NOG protein co-treated with entinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
NAALAD2	Human	endosulfan	decreases expression	ISO	Naalad2 (Rattus norvegicus)	6480464	Endosulfan results in decreased expression of NAALAD2 mRNA	CTD	PMID:29391264
NAALAD2	Human	entinostat	multiple interactions	EXP		6480464	[NOG protein co-treated with entinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of NAALAD2 mRNA	CTD	PMID:27188386
NAALAD2	Human	entinostat	decreases expression	EXP		6480464	entinostat results in decreased expression of NAALAD2 mRNA	CTD	PMID:26272509
NAALAD2	Human	fenvalerate	increases expression	ISO	Naalad2 (Rattus norvegicus)	6480464	fenvalerate results in increased expression of NAALAD2 protein	CTD	PMID:33656234
NAALAD2	Human	folic acid	decreases expression	EXP		6480464	Folic Acid results in decreased expression of NAALAD2 mRNA	CTD	PMID:21867686
NAALAD2	Human	fulvestrant	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in increased methylation of NAALAD2 gene	CTD	PMID:31601247
NAALAD2	Human	mercury dichloride	multiple interactions	EXP		6480464	[NOG protein co-treated with Mercuric Chloride co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in increased expression of NAALAD2 mRNA	CTD	PMID:27188386
NAALAD2	Human	methylmercury chloride	decreases expression	EXP		6480464	methylmercuric chloride results in decreased expression of NAALAD2 mRNA	CTD	PMID:23179753 more ...
NAALAD2	Human	N,N-diethyl-m-toluamide	multiple interactions	ISO	Naalad2 (Rattus norvegicus)	6480464	[Permethrin co-treated with DEET] results in decreased methylation of NAALAD2 gene	CTD	PMID:33148267
NAALAD2	Human	nickel atom	decreases expression	EXP		6480464	Nickel results in decreased expression of NAALAD2 mRNA	CTD	PMID:25583101
NAALAD2	Human	ozone	multiple interactions	ISO	Naalad2 (Mus musculus)	6480464	[Air Pollutants results in increased abundance of [Ozone co-treated with Soot]] which results in decreased expression of NAALAD2 mRNA	CTD	PMID:34911549
NAALAD2	Human	p-tert-Amylphenol	multiple interactions	EXP		6480464	[4-tert-octylphenol co-treated with 4-nonylphenol] results in decreased expression of NAALAD2 mRNA	CTD	PMID:23626723
NAALAD2	Human	paracetamol	decreases expression	EXP		6480464	Acetaminophen results in decreased expression of NAALAD2 mRNA	CTD	PMID:29067470
NAALAD2	Human	perfluorooctanoic acid	decreases expression	EXP		6480464	perfluorooctanoic acid results in decreased expression of NAALAD2 protein	CTD	PMID:26879310
NAALAD2	Human	permethrin	multiple interactions	ISO	Naalad2 (Rattus norvegicus)	6480464	[Permethrin co-treated with DEET] results in decreased methylation of NAALAD2 gene	CTD	PMID:33148267
NAALAD2	Human	pioglitazone	multiple interactions	ISO	Naalad2 (Mus musculus)	6480464	[N-nitroso-tris-chloroethylurea co-treated with pioglitazone] results in decreased expression of NAALAD2 mRNA	CTD	PMID:27935865
NAALAD2	Human	quercetin	decreases expression	EXP		6480464	Quercetin results in decreased expression of NAALAD2 mRNA	CTD	PMID:21632981
NAALAD2	Human	SB 431542	multiple interactions	EXP		6480464	[NOG protein co-treated with entinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
NAALAD2	Human	silicon dioxide	increases expression	EXP		6480464	Silicon Dioxide results in increased expression of NAALAD2 mRNA	CTD	PMID:25351596
NAALAD2	Human	sodium arsenite	decreases expression	ISO	Naalad2 (Mus musculus)	6480464	sodium arsenite results in decreased expression of NAALAD2 mRNA	CTD	PMID:37682722
NAALAD2	Human	tamoxifen	affects expression	ISO	Naalad2 (Mus musculus)	6480464	Tamoxifen affects the expression of NAALAD2 mRNA	CTD	PMID:17555576
NAALAD2	Human	tetrachloromethane	affects expression	ISO	Naalad2 (Mus musculus)	6480464	Carbon Tetrachloride affects the expression of NAALAD2 mRNA	CTD	PMID:17484886
NAALAD2	Human	trichloroethene	decreases methylation	ISO	Naalad2 (Rattus norvegicus)	6480464	Trichloroethylene results in decreased methylation of NAALAD2 gene	CTD	PMID:27618143
NAALAD2	Human	trichloroethene	decreases expression	ISO	Naalad2 (Rattus norvegicus)	6480464	Trichloroethylene results in decreased expression of NAALAD2 mRNA	CTD	PMID:33387578
NAALAD2	Human	trichostatin A	increases expression	EXP		6480464	trichostatin A results in increased expression of NAALAD2 mRNA	CTD	PMID:24935251
NAALAD2	Human	trichostatin A	multiple interactions	EXP		6480464	[NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of NAALAD2 mRNA	CTD	PMID:27188386
NAALAD2	Human	trichostatin A	decreases expression	EXP		6480464	trichostatin A results in decreased expression of NAALAD2 mRNA	CTD	PMID:24935251 and PMID:26272509
NAALAD2	Human	triphenyl phosphate	affects expression	EXP		6480464	triphenyl phosphate affects the expression of NAALAD2 mRNA	CTD	PMID:37042841
NAALAD2	Human	urethane	decreases expression	EXP		6480464	Urethane results in decreased expression of NAALAD2 mRNA	CTD	PMID:28818685
NAALAD2	Human	valproic acid	decreases expression	EXP		6480464	Valproic Acid results in decreased expression of NAALAD2 mRNA	CTD	PMID:23179753 more ...
NAALAD2	Human	valproic acid	multiple interactions	EXP		6480464	[NOG protein co-treated with Valproic Acid co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of NAALAD2 mRNA	CTD	PMID:27188386
NAALAD2	Human	valproic acid	increases expression	EXP		6480464	Valproic Acid results in increased expression of NAALAD2 mRNA	CTD	PMID:23179753 more ...

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)
NAALAD2	Human	carboxylic acid catabolic process	involved_in	IEA	UniProtKB:Q9CZR2 and ensembl:ENSMUSP00000128674	150520179		Ensembl	GO_REF:0000107
NAALAD2	Human	catabolic process	involved_in	IEA	UniProtKB:Q9CZR2 and ensembl:ENSMUSP00000128674	150520179		Ensembl	GO_REF:0000107
NAALAD2	Human	proteolysis	involved_in	IEA	UniProtKB-KW:KW-0645	150520179		UniProt	GO_REF:0000043
NAALAD2	Human	proteolysis	acts_upstream_of_or_within	IEA	UniProtKB:Q9CZR2 and ensembl:ENSMUSP00000128674	150520179		Ensembl	GO_REF:0000107
NAALAD2	Human	proteolysis	involved_in	NAS		150520179	PMID:10085079	UniProt	PMID:10085079

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)
NAALAD2	Human	membrane	located_in	NAS		150520179	PMID:10085079	UniProt	PMID:10085079
NAALAD2	Human	membrane	located_in	IEA	UniProtKB:Q9CZR2 and ensembl:ENSMUSP00000128674	150520179		Ensembl	GO_REF:0000107
NAALAD2	Human	membrane	located_in	IEA	UniProtKB-KW:KW-0472	150520179		UniProt	GO_REF:0000043
NAALAD2	Human	plasma membrane	located_in	TAS		150520179		Reactome	Reactome:R-HSA-5693783
NAALAD2	Human	plasma membrane	located_in	IEA	UniProtKB-SubCell:SL-0039	150520179		UniProt	GO_REF:0000044
NAALAD2	Human	plasma membrane	located_in	IEA	UniProtKB-KW:KW-1003	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)
NAALAD2	Human	carboxypeptidase activity	enables	NAS		150520179	PMID:10085079	UniProt	PMID:10085079
NAALAD2	Human	carboxypeptidase activity	enables	IEA	UniProtKB:Q9CZR2 and ensembl:ENSMUSP00000128674	150520179		Ensembl	GO_REF:0000107
NAALAD2	Human	carboxypeptidase activity	enables	IBA	MGI:1858193 more ...	150520179		GO_Central	GO_REF:0000033
NAALAD2	Human	carboxypeptidase activity	enables	IEA	UniProtKB-KW:KW-0121	150520179		UniProt	GO_REF:0000043
NAALAD2	Human	catalytic activity	enables	IEA	UniProtKB-KW:KW-0511	150520179		UniProt	GO_REF:0000043
NAALAD2	Human	dipeptidase activity	enables	IEA	UniProtKB-KW:KW-0224	150520179		UniProt	GO_REF:0000043
NAALAD2	Human	dipeptidase activity	enables	NAS		150520179	PMID:10085079	UniProt	PMID:10085079
NAALAD2	Human	dipeptidyl-peptidase activity	enables	NAS		150520179	PMID:10085079	UniProt	PMID:10085079
NAALAD2	Human	hydrolase activity	enables	IEA	UniProtKB-KW:KW-0378	150520179		UniProt	GO_REF:0000043
NAALAD2	Human	metal ion binding	enables	IEA	UniProtKB-KW:KW-0479	150520179		UniProt	GO_REF:0000043
NAALAD2	Human	metallocarboxypeptidase activity	enables	IEA	EC:3.4.17.21	150520179		UniProt	GO_REF:0000003
NAALAD2	Human	metallopeptidase activity	enables	IEA	UniProtKB-KW:KW-0482	150520179		UniProt	GO_REF:0000043
NAALAD2	Human	N-formylglutamate deformylase activity	enables	IEA	UniProtKB:Q9CZR2 and ensembl:ENSMUSP00000128674	150520179		Ensembl	GO_REF:0000107
NAALAD2	Human	peptidase activity	enables	IEA	UniProtKB-KW:KW-0645	150520179		UniProt	GO_REF:0000043
NAALAD2	Human	peptidase activity	enables	IEA	UniProtKB:Q9CZR2 and ensembl:ENSMUSP00000128674	150520179		Ensembl	GO_REF:0000107
NAALAD2	Human	protein binding	enables	IPI	UniProtKB:O76024	150520179	PMID:32814053	IntAct	PMID:32814053
NAALAD2	Human	protein binding	enables	IPI	UniProtKB:B2RUZ4 more ...	150520179	PMID:32296183	IntAct	PMID:32296183
NAALAD2	Human	serine-type peptidase activity	enables	NAS		150520179	PMID:10085079	UniProt	PMID:10085079

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NAALAD2	Human	Intellectual disability		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Intellectual disability	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:10085079	PMID:11352574	PMID:11905994	PMID:12204797	PMID:12477932	PMID:15146197	PMID:16303743	PMID:17160644	PMID:17241121	PMID:19678840	PMID:20379614	PMID:21738478
PMID:21873635	PMID:26186194	PMID:27208881	PMID:28514442	PMID:30844704	PMID:32296183	PMID:32814053	PMID:33961781	PMID:34198725	PMID:34850884

NAALAD2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	90,131,699 - 90,192,894 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	90,131,515 - 90,192,894 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	89,867,831 - 89,926,062 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	89,507,530 - 89,565,424 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	11	89,507,529 - 89,565,418	NCBI
Celera	11	87,168,325 - 87,226,293 (+)	NCBI		Celera
Cytogenetic Map	11	q14.3	NCBI
HuRef	11	85,952,467 - 86,010,505 (+)	NCBI		HuRef
CHM1_1	11	89,750,836 - 89,808,679 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	11	90,051,780 - 90,112,974 (+)	NCBI		T2T-CHM13v2.0

Naalad2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	9	18,233,247 - 18,308,834 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	9	18,233,247 - 18,314,291 (-)	Ensembl		GRCm39 Ensembl
GRCm38	9	18,321,951 - 18,397,538 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	9	18,321,951 - 18,402,995 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	9	18,127,465 - 18,190,372 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	9	18,073,423 - 18,136,330 (-)	NCBI		MGSCv36	mm8
Celera	9	15,606,315 - 15,669,553 (-)	NCBI		Celera
Cytogenetic Map	9	A2	NCBI
cM Map	9	7.02	NCBI

Naalad2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	8	23,682,499 - 23,756,066 (-)	NCBI		GRCr8
mRatBN7.2	8	15,406,119 - 15,479,714 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	8	15,407,043 - 15,479,714 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	8	19,393,338 - 19,465,317 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	8	17,691,135 - 17,763,114 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	8	15,587,180 - 15,659,563 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	8	17,453,198 - 17,525,906 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	8	17,454,122 - 17,525,906 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	8	17,526,567 - 17,599,206 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	8	15,767,908 - 15,842,724 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	8	15,767,911 - 15,836,496 (-)	NCBI
Celera	8	16,835,457 - 16,908,126 (-)	NCBI		Celera
Cytogenetic Map	8	q13	NCBI

Naalad2
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955414	3,728,596 - 3,791,706 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955414	3,728,596 - 3,789,265 (-)	NCBI	ChiLan1.0	ChiLan1.0

NAALAD2
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	9	90,948,253 - 91,006,340 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	11	92,034,951 - 92,093,003 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	11	85,105,296 - 85,163,280 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	11	88,600,918 - 88,658,985 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	11	88,600,918 - 88,658,985 (+)	Ensembl	panpan1.1		panPan2

NAALAD2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	21	10,162,323 - 10,222,990 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	21	10,162,578 - 10,253,015 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	21	10,054,329 - 10,119,513 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	21	10,339,550 - 10,404,777 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	21	10,343,608 - 10,435,065 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	21	10,138,437 - 10,197,311 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	21	10,193,157 - 10,258,556 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	21	10,243,380 - 10,308,589 (-)	NCBI		UU_Cfam_GSD_1.0

Naalad2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024404947	75,689,202 - 75,735,773 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936893	673,030 - 721,588 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936893	672,380 - 716,440 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

NAALAD2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	9	23,111,059 - 23,161,832 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	9	23,106,795 - 23,161,825 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	9	25,890,099 - 25,941,320 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

NAALAD2
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	1	81,259,005 - 81,319,255 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	1	81,259,083 - 81,318,092 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666043	44,430,673 - 44,489,885 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Naalad2
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624845	252,042 - 298,864 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624845	252,172 - 295,263 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in NAALAD2
69 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 11q14.1-22.3(chr11:78232836-106779420)x1	copy number loss	See cases [RCV000052710]	Chr11:78232836..106779420 [GRCh38] Chr11:77943882..106650146 [GRCh37] Chr11:77621530..106155356 [NCBI36] Chr11:11q14.1-22.3	pathogenic
GRCh38/hg38 11q14.1-22.2(chr11:85242847-102920097)x1	copy number loss	See cases [RCV000052711]	Chr11:85242847..102920097 [GRCh38] Chr11:84953891..102738968 [GRCh37] Chr11:84631539..102296037 [NCBI36] Chr11:11q14.1-22.2	pathogenic
NM_005467.3(NAALAD2):c.501G>A (p.Val167=)	single nucleotide variant	Malignant melanoma [RCV000069739]	Chr11:90150499 [GRCh38] Chr11:89883667 [GRCh37] Chr11:89523315 [NCBI36] Chr11:11q14.3	not provided
NM_005467.3(NAALAD2):c.1094G>A (p.Gly365Glu)	single nucleotide variant	Malignant melanoma [RCV000069740]	Chr11:90163328 [GRCh38] Chr11:89896496 [GRCh37] Chr11:89536144 [NCBI36] Chr11:11q14.3	not provided
NM_005467.3(NAALAD2):c.871G>A (p.Asp291Asn)	single nucleotide variant	Malignant melanoma [RCV000062366]	Chr11:90158219 [GRCh38] Chr11:89891387 [GRCh37] Chr11:89531035 [NCBI36] Chr11:11q14.3	not provided
Single allele	deletion	Intellectual disability [RCV001293382]	Chr11:118359328..118372573 [GRCh37] Chr11:11p15.3-q23.3	pathogenic
GRCh38/hg38 11q13.5-22.1(chr11:75941754-98357960)x1	copy number loss	See cases [RCV000133838]	Chr11:75941754..98357960 [GRCh38] Chr11:75652798..98228688 [GRCh37] Chr11:75330446..97733898 [NCBI36] Chr11:11q13.5-22.1	pathogenic
GRCh38/hg38 11q14.3(chr11:90123486-91218361)x3	copy number gain	See cases [RCV000135680]	Chr11:90123486..91218361 [GRCh38] Chr11:89856654..90951529 [GRCh37] Chr11:89496302..90591177 [NCBI36] Chr11:11q14.3	uncertain significance
GRCh38/hg38 11q14.3(chr11:89425778-90689442)x1	copy number loss	See cases [RCV000141934]	Chr11:89425778..90689442 [GRCh38] Chr11:89158946..90422610 [GRCh37] Chr11:88798594..90062258 [NCBI36] Chr11:11q14.3	uncertain significance
GRCh37/hg19 11q14.1-21(chr11:80318996-96116221)x1	copy number loss	See cases [RCV000446395]	Chr11:80318996..96116221 [GRCh37] Chr11:11q14.1-21	pathogenic
GRCh37/hg19 11q14.3(chr11:89540275-89956475)x3	copy number gain	See cases [RCV000448705]	Chr11:89540275..89956475 [GRCh37] Chr11:11q14.3	benign
GRCh37/hg19 11q14.3(chr11:89514122-92745981)x1	copy number loss	See cases [RCV000448827]	Chr11:89514122..92745981 [GRCh37] Chr11:11q14.3	uncertain significance
GRCh37/hg19 11q14.2-14.3(chr11:87099219-91921385)	copy number loss	Abnormal esophagus morphology [RCV000416734]	Chr11:87099219..91921385 [GRCh37] Chr11:11q14.2-14.3	likely benign
GRCh37/hg19 11q14.1-21(chr11:84924674-93574799)x1	copy number loss	See cases [RCV000448436]	Chr11:84924674..93574799 [GRCh37] Chr11:11q14.1-21	likely pathogenic
GRCh37/hg19 11q14.2-22.3(chr11:88152458-109414650)x1	copy number loss	See cases [RCV000510457]	Chr11:88152458..109414650 [GRCh37] Chr11:11q14.2-22.3	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)	copy number gain	See cases [RCV000511729]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3	copy number gain	See cases [RCV000510881]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
NM_005467.4(NAALAD2):c.278T>C (p.Phe93Ser)	single nucleotide variant	not specified [RCV004281672]	Chr11:90147413 [GRCh38] Chr11:89880581 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1040A>G (p.Asn347Ser)	single nucleotide variant	not specified [RCV004298534]	Chr11:90162999 [GRCh38] Chr11:89896167 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.436A>T (p.Asn146Tyr)	single nucleotide variant	not specified [RCV004292394]	Chr11:90149060 [GRCh38] Chr11:89882228 [GRCh37] Chr11:11q14.3	uncertain significance
GRCh37/hg19 11q14.1-14.3(chr11:81771852-90851187)	copy number loss	Intellectual disability [RCV000721939]	Chr11:81771852..90851187 [GRCh37] Chr11:11q14.1-14.3	pathogenic
GRCh37/hg19 11q14.3(chr11:89807945-90050965)x1	copy number loss	not provided [RCV000683319]	Chr11:89807945..90050965 [GRCh37] Chr11:11q14.3	uncertain significance
GRCh37/hg19 11q13.4-23.3(chr11:71588805-116680918)x3	copy number gain	not provided [RCV000683374]	Chr11:71588805..116680918 [GRCh37] Chr11:11q13.4-23.3	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3	copy number gain	not provided [RCV000737348]	Chr11:198510..134934063 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11q14.1-23.2(chr11:80053454-113316236)x1	copy number loss	not provided [RCV000737595]	Chr11:80053454..113316236 [GRCh37] Chr11:11q14.1-23.2	pathogenic
GRCh37/hg19 11q14.3(chr11:89834751-90217015)x3	copy number gain	not provided [RCV000737621]	Chr11:89834751..90217015 [GRCh37] Chr11:11q14.3	benign
GRCh37/hg19 11q14.3(chr11:89883658-90004732)x3	copy number gain	not provided [RCV000737622]	Chr11:89883658..90004732 [GRCh37] Chr11:11q14.3	benign
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3	copy number gain	not provided [RCV000749874]	Chr11:70864..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11q14.1-21(chr11:83179196-94716998)x3	copy number gain	not provided [RCV000750120]	Chr11:83179196..94716998 [GRCh37] Chr11:11q14.1-21	pathogenic
NM_005467.4(NAALAD2):c.1769A>G (p.Tyr590Cys)	single nucleotide variant	not specified [RCV004284436]	Chr11:90178028 [GRCh38] Chr11:89911196 [GRCh37] Chr11:11q14.3	uncertain significance
Single allele	deletion	Neurodevelopmental disorder [RCV000787372]	Chr11:89482692..90933956 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.639A>G (p.Ile213Met)	single nucleotide variant	not specified [RCV004324754]	Chr11:90152327 [GRCh38] Chr11:89885495 [GRCh37] Chr11:11q14.3	uncertain significance
GRCh37/hg19 11q14.1-14.3(chr11:84830143-92029933)x3	copy number gain	not provided [RCV001006426]	Chr11:84830143..92029933 [GRCh37] Chr11:11q14.1-14.3	pathogenic
GRCh37/hg19 11q14.3(chr11:89659554-90697895)x3	copy number gain	not provided [RCV001006433]	Chr11:89659554..90697895 [GRCh37] Chr11:11q14.3	uncertain significance
GRCh37/hg19 11q14.3(chr11:89514122-92745981)	copy number loss	not specified [RCV002052946]	Chr11:89514122..92745981 [GRCh37] Chr11:11q14.3	uncertain significance
GRCh37/hg19 11q14.1-21(chr11:80318996-96116221)	copy number loss	not specified [RCV002052941]	Chr11:80318996..96116221 [GRCh37] Chr11:11q14.1-21	pathogenic
GRCh37/hg19 11q14.1-23.3(chr11:85422071-118022671)x1	copy number loss	not provided [RCV001832892]	Chr11:85422071..118022671 [GRCh37] Chr11:11q14.1-23.3	uncertain significance
GRCh37/hg19 11q14.1-21(chr11:84924674-93574799)	copy number loss	not specified [RCV002052942]	Chr11:84924674..93574799 [GRCh37] Chr11:11q14.1-21	likely pathogenic
GRCh37/hg19 11q14.1-22.1(chr11:77855209-98002445)	copy number loss	not specified [RCV002052940]	Chr11:77855209..98002445 [GRCh37] Chr11:11q14.1-22.1	pathogenic
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3	copy number gain	MISSED ABORTION [RCV002282973]	Chr11:32799481..134938470 [GRCh37] Chr11:11p13-q25	pathogenic
GRCh37/hg19 11q14.3(chr11:89474818-89887082)x1	copy number loss	not provided [RCV002474964]	Chr11:89474818..89887082 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.2219T>C (p.Leu740Ser)	single nucleotide variant	not specified [RCV004104553]	Chr11:90191743 [GRCh38] Chr11:89924911 [GRCh37] Chr11:11q14.3	uncertain significance
GRCh37/hg19 11q14.1-22.3(chr11:81478509-104667040)x1	copy number loss	not provided [RCV002475722]	Chr11:81478509..104667040 [GRCh37] Chr11:11q14.1-22.3	pathogenic
NM_005467.4(NAALAD2):c.2098G>A (p.Asp700Asn)	single nucleotide variant	not specified [RCV004116686]	Chr11:90191622 [GRCh38] Chr11:89924790 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.143G>A (p.Arg48Gln)	single nucleotide variant	not specified [RCV004130690]	Chr11:90135619 [GRCh38] Chr11:89868787 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.2003C>T (p.Pro668Leu)	single nucleotide variant	not specified [RCV004219846]	Chr11:90182978 [GRCh38] Chr11:89916146 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.665C>A (p.Ala222Asp)	single nucleotide variant	not specified [RCV004090149]	Chr11:90152353 [GRCh38] Chr11:89885521 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.356C>T (p.Ser119Leu)	single nucleotide variant	not specified [RCV004137783]	Chr11:90147491 [GRCh38] Chr11:89880659 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.350A>C (p.Tyr117Ser)	single nucleotide variant	not specified [RCV004228999]	Chr11:90147485 [GRCh38] Chr11:89880653 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.2114T>C (p.Ile705Thr)	single nucleotide variant	not specified [RCV004207841]	Chr11:90191638 [GRCh38] Chr11:89924806 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.329C>A (p.Pro110His)	single nucleotide variant	not specified [RCV004117101]	Chr11:90147464 [GRCh38] Chr11:89880632 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1988G>T (p.Arg663Ile)	single nucleotide variant	not specified [RCV004131383]	Chr11:90182963 [GRCh38] Chr11:89916131 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.361G>A (p.Val121Met)	single nucleotide variant	not specified [RCV004173473]	Chr11:90147496 [GRCh38] Chr11:89880664 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1284T>A (p.Asn428Lys)	single nucleotide variant	not specified [RCV004125181]	Chr11:90168934 [GRCh38] Chr11:89902102 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.2147A>G (p.Lys716Arg)	single nucleotide variant	not specified [RCV004122301]	Chr11:90191671 [GRCh38] Chr11:89924839 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1289A>G (p.Lys430Arg)	single nucleotide variant	not specified [RCV004113098]	Chr11:90168939 [GRCh38] Chr11:89902107 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.2109T>A (p.Phe703Leu)	single nucleotide variant	not specified [RCV004153429]	Chr11:90191633 [GRCh38] Chr11:89924801 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1801A>G (p.Ile601Val)	single nucleotide variant	not specified [RCV004090000]	Chr11:90178060 [GRCh38] Chr11:89911228 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.889C>T (p.Arg297Cys)	single nucleotide variant	not specified [RCV004090827]	Chr11:90158237 [GRCh38] Chr11:89891405 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.419G>A (p.Gly140Asp)	single nucleotide variant	not specified [RCV004253483]	Chr11:90149043 [GRCh38] Chr11:89882211 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.26A>G (p.Tyr9Cys)	single nucleotide variant	not specified [RCV004252408]	Chr11:90134784 [GRCh38] Chr11:89867952 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1913A>G (p.Lys638Arg)	single nucleotide variant	not specified [RCV004283026]	Chr11:90181674 [GRCh38] Chr11:89914842 [GRCh37] Chr11:11q14.3	likely benign
NM_005467.4(NAALAD2):c.1300G>A (p.Glu434Lys)	single nucleotide variant	not specified [RCV004265655]	Chr11:90168950 [GRCh38] Chr11:89902118 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.724G>A (p.Ala242Thr)	single nucleotide variant	not specified [RCV004272000]	Chr11:90152412 [GRCh38] Chr11:89885580 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.548G>A (p.Gly183Asp)	single nucleotide variant	not specified [RCV004268566]	Chr11:90150546 [GRCh38] Chr11:89883714 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1998C>T (p.Ile666=)	single nucleotide variant	not provided [RCV003395996]	Chr11:90182973 [GRCh38] Chr11:89916141 [GRCh37] Chr11:11q14.3	likely benign
NM_005467.4(NAALAD2):c.125G>A (p.Arg42His)	single nucleotide variant	not specified [RCV004352663]	Chr11:90135601 [GRCh38] Chr11:89868769 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.124C>T (p.Arg42Cys)	single nucleotide variant	not specified [RCV004350121]	Chr11:90135600 [GRCh38] Chr11:89868768 [GRCh37] Chr11:11q14.3	uncertain significance
GRCh37/hg19 11q14.3(chr11:89602560-90979365)x3	copy number gain	not provided [RCV003484848]	Chr11:89602560..90979365 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.838C>T (p.Pro280Ser)	single nucleotide variant	not specified [RCV004460980]	Chr11:90158186 [GRCh38] Chr11:89891354 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.473G>A (p.Gly158Asp)	single nucleotide variant	not specified [RCV004460951]	Chr11:90149097 [GRCh38] Chr11:89882265 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.487G>C (p.Asp163His)	single nucleotide variant	not specified [RCV004460955]	Chr11:90150485 [GRCh38] Chr11:89883653 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.512G>A (p.Arg171His)	single nucleotide variant	not specified [RCV004460958]	Chr11:90150510 [GRCh38] Chr11:89883678 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.620C>T (p.Ala207Val)	single nucleotide variant	not specified [RCV004460960]	Chr11:90152308 [GRCh38] Chr11:89885476 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.958G>A (p.Gly320Arg)	single nucleotide variant	not specified [RCV004460990]	Chr11:90159306 [GRCh38] Chr11:89892474 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.823G>C (p.Glu275Gln)	single nucleotide variant	not specified [RCV004460973]	Chr11:90158171 [GRCh38] Chr11:89891339 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1172G>A (p.Ser391Asn)	single nucleotide variant	not specified [RCV004458800]	Chr11:90163406 [GRCh38] Chr11:89896574 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1063T>C (p.Ser355Pro)	single nucleotide variant	not specified [RCV004458799]	Chr11:90163022 [GRCh38] Chr11:89896190 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1372C>T (p.Pro458Ser)	single nucleotide variant	not specified [RCV004458823]	Chr11:90170098 [GRCh38] Chr11:89903266 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1270T>C (p.Trp424Arg)	single nucleotide variant	not specified [RCV004458814]	Chr11:90163609 [GRCh38] Chr11:89896777 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.185C>T (p.Ser62Leu)	single nucleotide variant	not specified [RCV004458830]	Chr11:90135661 [GRCh38] Chr11:89868829 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.2200G>C (p.Gly734Arg)	single nucleotide variant	not specified [RCV004641121]	Chr11:90191724 [GRCh38] Chr11:89924892 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.512G>T (p.Arg171Leu)	single nucleotide variant	not specified [RCV004641120]	Chr11:90150510 [GRCh38] Chr11:89883678 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.902G>T (p.Gly301Val)	single nucleotide variant	not specified [RCV004652207]	Chr11:90159250 [GRCh38] Chr11:89892418 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.16G>A (p.Gly6Ser)	single nucleotide variant	not specified [RCV004641122]	Chr11:90134774 [GRCh38] Chr11:89867942 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1687C>A (p.Gln563Lys)	single nucleotide variant	not specified [RCV004652206]	Chr11:90177946 [GRCh38] Chr11:89911114 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1132C>G (p.Pro378Ala)	single nucleotide variant	not specified [RCV004652208]	Chr11:90163366 [GRCh38] Chr11:89896534 [GRCh37] Chr11:11q14.3	uncertain significance
GRCh37/hg19 11q14.1-22.1(chr11:81041448-98151664)x1	copy number loss	not provided [RCV004819372]	Chr11:81041448..98151664 [GRCh37] Chr11:11q14.1-22.1	pathogenic
NM_005467.4(NAALAD2):c.1810C>G (p.Leu604Val)	single nucleotide variant	not specified [RCV004833847]	Chr11:90178069 [GRCh38] Chr11:89911237 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.140T>C (p.Ile47Thr)	single nucleotide variant	not specified [RCV004833850]	Chr11:90135616 [GRCh38] Chr11:89868784 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1393T>G (p.Tyr465Asp)	single nucleotide variant	not specified [RCV004833846]	Chr11:90170119 [GRCh38] Chr11:89903287 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.596T>C (p.Phe199Ser)	single nucleotide variant	not specified [RCV004833848]	Chr11:90150594 [GRCh38] Chr11:89883762 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1000A>G (p.Met334Val)	single nucleotide variant	not specified [RCV004833849]	Chr11:90162959 [GRCh38] Chr11:89896127 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1325C>T (p.Ser442Leu)	single nucleotide variant	not specified [RCV004833852]	Chr11:90168975 [GRCh38] Chr11:89902143 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1922T>C (p.Ile641Thr)	single nucleotide variant	not specified [RCV004251598]	Chr11:90181683 [GRCh38] Chr11:89914851 [GRCh37] Chr11:11q14.3	likely benign
NM_005467.4(NAALAD2):c.1103G>C (p.Arg368Pro)	single nucleotide variant	not specified [RCV004652210]	Chr11:90163337 [GRCh38] Chr11:89896505 [GRCh37] Chr11:11q14.3	uncertain significance
NM_005467.4(NAALAD2):c.1691T>G (p.Leu564Arg)	single nucleotide variant	not specified [RCV004641119]	Chr11:90177950 [GRCh38] Chr11:89911118 [GRCh37] Chr11:11q14.3	likely benign

Predicted Target Of

	Summary Value
Count of predictions:	1828
Count of miRNA genes:	785
Interacting mature miRNAs:	909
Transcripts:	ENST00000321955, ENST00000375944, ENST00000524501, ENST00000525171, ENST00000525497, ENST00000526637, ENST00000527493, ENST00000529090, ENST00000532691, ENST00000534061
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597506076	GWAS1602150_H	beta-citrylglutamate measurement QTL GWAS1602150 (human)		3e-53	beta-citrylglutamate measurement		11	90133547	90133548	Human
596968023	GWAS1087542_H	body mass index QTL GWAS1087542 (human)		1e-09	body mass index		11	90189249	90189250	Human
597381087	GWAS1477161_H	serum metabolite measurement QTL GWAS1477161 (human)		2e-47	serum metabolite measurement		11	90133547	90133548	Human
597137040	GWAS1233114_H	beta-citrylglutamate measurement QTL GWAS1233114 (human)		1e-35	beta-citrylglutamate measurement		11	90147706	90147707	Human
597314576	GWAS1410650_H	uric acid measurement QTL GWAS1410650 (human)		2e-08	uric acid measurement	blood uric acid level (CMO:0000501)	11	90189249	90189250	Human
597067590	GWAS1163664_H	basophil count QTL GWAS1163664 (human)		2e-16	basophil quantity (VT:0002607)	blood basophil count (CMO:0000034)	11	90142269	90142270	Human
597528911	GWAS1624985_H	beta-citrylglutamate measurement QTL GWAS1624985 (human)		2e-32	beta-citrylglutamate measurement		11	90134522	90134523	Human
597528910	GWAS1624984_H	beta-citrylglutamate measurement QTL GWAS1624984 (human)		2e-78	beta-citrylglutamate measurement		11	90133547	90133548	Human
597037443	GWAS1133517_H	body mass index QTL GWAS1133517 (human)		5e-11	body mass index	body mass index (BMI) (CMO:0000105)	11	90189249	90189250	Human
597172302	GWAS1268376_H	body mass index QTL GWAS1268376 (human)		7e-11	body mass index	body mass index (BMI) (CMO:0000105)	11	90189249	90189250	Human
596951683	GWAS1071202_H	body mass index QTL GWAS1071202 (human)		1e-11	body mass index		11	90189249	90189250	Human
597137039	GWAS1233113_H	beta-citrylglutamate measurement QTL GWAS1233113 (human)		1e-44	beta-citrylglutamate measurement		11	90142330	90142331	Human
407027550	GWAS676526_H	basophil count QTL GWAS676526 (human)		2e-09	basophil quantity (VT:0002607)	blood granulocyte count (CMO:0000111)	11	90142269	90142270	Human
597514240	GWAS1610314_H	beta-citrylglutamate measurement QTL GWAS1610314 (human)		5e-167	beta-citrylglutamate measurement		11	90163289	90163290	Human
597329851	GWAS1425925_H	beta-citrylglutamate measurement QTL GWAS1425925 (human)		5e-39	beta-citrylglutamate measurement		11	90163369	90163370	Human
597038005	GWAS1134079_H	body mass index QTL GWAS1134079 (human)		1e-11	body mass index	body mass index (BMI) (CMO:0000105)	11	90189249	90189250	Human
596958975	GWAS1078494_H	body mass index QTL GWAS1078494 (human)		7e-11	body mass index		11	90189249	90189250	Human
597288886	GWAS1384960_H	body mass index QTL GWAS1384960 (human)		3e-11	body mass index	body mass index (BMI) (CMO:0000105)	11	90189249	90189250	Human
597185263	GWAS1281337_H	beta-citrylglutamate measurement QTL GWAS1281337 (human)		4e-47	beta-citrylglutamate measurement		11	90165635	90165636	Human
597529381	GWAS1625455_H	metabolite measurement QTL GWAS1625455 (human)		9e-249	metabolite measurement		11	90133547	90133548	Human
597317728	GWAS1413802_H	body mass index QTL GWAS1413802 (human)		1e-09	body mass index	body mass index (BMI) (CMO:0000105)	11	90189249	90189250	Human
597144685	GWAS1240759_H	body mass index QTL GWAS1240759 (human)		7e-09	body mass index	body mass index (BMI) (CMO:0000105)	11	90189249	90189250	Human
597075563	GWAS1171637_H	intelligence QTL GWAS1171637 (human)		8e-09	intelligence		11	90189062	90189063	Human
597185254	GWAS1281328_H	beta-citrylglutamate measurement QTL GWAS1281328 (human)		2e-102	beta-citrylglutamate measurement		11	90163369	90163370	Human
597344869	GWAS1440943_H	body mass index QTL GWAS1440943 (human)		4e-12	body mass index	body mass index (BMI) (CMO:0000105)	11	90189249	90189250	Human

SHGC-53907

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	89,906,803 - 89,907,061	UniSTS	GRCh37
Build 36	11	89,546,451 - 89,546,709	RGD	NCBI36
Celera	11	87,207,314 - 87,207,572	RGD
Cytogenetic Map	11	q14.3-q21	UniSTS
HuRef	11	85,991,535 - 85,991,793	UniSTS
GeneMap99-G3 RH Map	11	3976.0	UniSTS

RH46277

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	89,906,803 - 89,906,998	UniSTS	GRCh37
Build 36	11	89,546,451 - 89,546,646	RGD	NCBI36
Celera	11	87,207,314 - 87,207,509	RGD
Cytogenetic Map	11	q14.3-q21	UniSTS
HuRef	11	85,991,535 - 85,991,730	UniSTS
GeneMap99-GB4 RH Map	11	307.76	UniSTS
NCBI RH Map	11	759.9	UniSTS

RH92833

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	89,925,835 - 89,926,007	UniSTS	GRCh37
Build 36	11	89,565,483 - 89,565,655	RGD	NCBI36
Celera	11	87,226,349 - 87,226,521	RGD
Cytogenetic Map	11	q14.3-q21	UniSTS
HuRef	11	86,010,561 - 86,010,733	UniSTS
GeneMap99-GB4 RH Map	11	309.52	UniSTS

SHGC-82492

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	89,885,408 - 89,885,683	UniSTS	GRCh37
Build 36	11	89,525,056 - 89,525,331	RGD	NCBI36
Celera	11	87,185,919 - 87,186,194	RGD
Cytogenetic Map	11	q14.3-q21	UniSTS
HuRef	11	85,970,051 - 85,970,326	UniSTS
TNG Radiation Hybrid Map	11	41379.0	UniSTS

SHGC-132875

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	89,906,756 - 89,907,047	UniSTS	GRCh37
Build 36	11	89,546,404 - 89,546,695	RGD	NCBI36
Celera	11	87,207,267 - 87,207,558	RGD
Cytogenetic Map	11	q14.3-q21	UniSTS
HuRef	11	85,991,488 - 85,991,779	UniSTS

NAALAD2__6206

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	89,925,153 - 89,925,865	UniSTS	GRCh37
Build 36	11	89,564,801 - 89,565,513	RGD	NCBI36
Celera	11	87,225,667 - 87,226,379	RGD
HuRef	11	86,009,879 - 86,010,591	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	2383	2788	2252	4946	1713	2301	5	618	1866	458	2253	7139	6378	42	3722	1	824	1715	1577	174	1


RefSeq Transcripts	NM_001300930	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_005467	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017017043	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017017044	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017017045	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017017046	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426168	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054332422	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054332423	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054332424	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054332425	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367343	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367344	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367345	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367346	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001747707	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001747708	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001747709	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001747710	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001747711	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_007062427	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_007062428	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008485770	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008485771	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008488319	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008488320	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AJ012370	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK075390	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL133614	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AP000648	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AX136153	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY010115	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC027594	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC038840	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC067793	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC096316	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC096317	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC096318	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC099646	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU618706	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471065	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CN355388	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CS051189	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000321955 ⟹ ENSP00000320083

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	90,134,712 - 90,192,611 (+)	Ensembl

Ensembl Acc Id:

ENST00000375944 ⟹ ENSP00000365111

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	90,134,738 - 90,191,889 (+)	Ensembl

Ensembl Acc Id:

ENST00000524501

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	90,134,695 - 90,164,201 (+)	Ensembl

Ensembl Acc Id:

ENST00000525171 ⟹ ENSP00000435249

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	90,134,729 - 90,164,201 (+)	Ensembl

Ensembl Acc Id:

ENST00000525497 ⟹ ENSP00000431989

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	90,131,515 - 90,147,400 (+)	Ensembl

Ensembl Acc Id:

ENST00000526637 ⟹ ENSP00000435670

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	90,135,064 - 90,149,107 (+)	Ensembl

Ensembl Acc Id:

ENST00000527493 ⟹ ENSP00000433710

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	90,134,615 - 90,164,350 (+)	Ensembl

Ensembl Acc Id:

ENST00000529090

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	90,134,664 - 90,158,757 (+)	Ensembl

Ensembl Acc Id:

ENST00000532691

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	90,162,492 - 90,169,685 (+)	Ensembl

Ensembl Acc Id:

ENST00000534061 ⟹ ENSP00000432481

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	90,134,663 - 90,192,894 (+)	Ensembl

RefSeq Acc Id:

NM_001300930 ⟹ NP_001287859

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	90,134,663 - 90,192,894 (+)	NCBI
CHM1_1	11	89,750,836 - 89,808,679 (+)	NCBI
T2T-CHM13v2.0	11	90,054,744 - 90,112,974 (+)	NCBI

Sequence:

show sequence

AGAGCTCACAGCCTCCTGCCAGCGCGCTCTCTGTTTCTCTGCAGCCCCGAAGCTCGCGAATGTAGCAGGCGCCCCAAGCTCGGTCCTCAAGAAGCCATGGCGGAATCCAGGGGCCGTCTGTACCTTTG
GATGTGCTTGGCTGCTGCGCTGGCATCTTTCCTGATGGGATTTATGGTGGGCTGGTTTATTAAGCCTCTCAAAGAAACGACCACTTCTGTGCGCTATCATCAAAGTATACGGTGGAAACTGGTATCCG
AAATGAAAGCTGAAAACATCAAATCATTTCTTCGTTCTTTTACAAAGCTTCCTCATCTGGCAGGAACAGAACAAAATTTCTTGCTTGCCAAGAAAATCCAAACCCAGTGGAAGAAATTTGGACTAGAT
TCAGCCAAGTTGGTTCATTATGATGTCCTCTTATCTTACCCCAATGAGACAAATGCCAACTATATATCGATTGTGGATGAACATGAAACTGAGATTTTCAAAACATCATACCTTGAACCACCACCAGA
TGGCTATGAGAATGTTACAAATATTGTGCCACCATATAATGCTTTCTCAGCCCAAGGCATGCCAGAGGGAGATCTTGTATATGTGAACTATGCTCGCACTGAAGACTTTTTCAAACTAGAAAGAGAGA
TGGGCATCAACTGTACTGGGAAGATTGTTATTGCAAGATATGGAAAAATCTTCAGAGGAAATAAAGTTAAAAATGCCATGTTAGCAGGAGCCATAGGAATCATCTTGTACTCAGATCCAGCTGACTAC
TTTGCTCCTGAGGTACAGCCATATCCCAAAGGATGGAATCTTCCTGGAACTGCAGCCCAGAGAGGAAATGTGTTAAATTTGAATGGTGCTGGTGACCCACTCACTCCAGGCTATCCAGCAAAAGAATA
CACTTTCAGACTTGATGTTGAAGAAGGAGTGGGAATCCCCCGAATACCTGTACATCCCATTGGATATAATGATGCAGAAATATTATTACGGAAGGTTAGAATGCATGTTTATAACATCAATAAAATTA
CAAGGATTTACAATGTAGTTGGAACTATCAGAGGATCTGTGGAACCTGACAGGTATGTTATTCTGGGAGGTCACCGGGACTCCTGGGTATTTGGAGCTATTGACCCAACCAGTGGGGTTGCTGTTTTG
CAAGAAATTGCCCGGAGTTTTGGAAAACTGATGAGTAAAGGCTGGAGACCTAGAAGAACTATCATTTTTGCCAGCTGGGATGCAGAAGAATTTGGACTTCTGGGTTCCACAGAATGGGCTGAGGAGAA
TGTCAAAATACTCCAGGAGAGAAGCATTGCTTATATCAACTCGGATTCATCTATAGAAGGCAATTATACTCTCAGAGTTGACTGTACTCCCCTTCTTTACCAATTAGTGTATAAACTGACAAAAGAGA
TCCCCAGCCCTGATGATGGGTTTGAGAGTAAATCACTGTATGAAAGCTGGTTGGAAAAAGACCCTTCACCTGAAAATAAAAATTTGCCTAGAATCAATAAGCTGGGATCTGGAAGTGACTTTGAAGCT
TATTTTCAGAGACTTGGAATTGCTTCAGGCAGAGCCCGTTACACTAAGAATAAGAAAACAGATAAGTACAGCAGCTACCCAGTGTACCACACAATTTATGAGACATTTGAATTGGTAGAGAAATTTTA
TGACCCCACATTTAAAAAACAACTTTCTGTGGCTCAATTACGAGGAGCACTGGTATATGAGCTTGTGGATTCTAAAATCATTCCTTTTAATATTCAAGACTATGCAGAAGCTTTGAAAAACTATGCAG
CAAGTATCTATAATCTATCTAAGAAACATGATCAACAATTGACAGACCATGGAGTATCATTTGACTCCTTATTTTCTGCTGTGAAAAACTTCTCAGAGGCTGCTTCAGATTTTCATAAACGACTTATA
CAAGTTGATCTTAACAATCCCATTGCAGTGAGAATGATGAATGACCAACTGATGCTCCTGGAAAGAGCATTCATCGATCCTCTTGGTTTACCAGGAAAGCTGTTCTATAGGCACATCATATTTGCTCC
AAGTAGCCACAACAAATATGCTGGAGAATCATTTCCTGGAATCTATGATGCTATCTTTGATATTGAAAATAAAGCCAACTCTCGTTTGGCCTGGAAAGAAGTAAAGAAACATATTTCTATTGCAGCTT
TTACAATTCAAGCAGCAGCAGGAACTCTGAAAGAAGTATTATAGAAGGTCTCAAGTGGCTAGCCATTAAAGGTGTTGCTAAAAGTCTGAGGATAAAATTCACCTTTCTGATAACTTATGAAGCCAGGG
TGTTCTAAACTCTTTTCATGTCATGTTTTGATTATAGGCTTTGGTCTTTTCATCTGCAAAGCCTTTTTTTTTTGCTCTTTAAAAGTTAATAATTATATTAGCAAAGTGTTAATCTAATGAAGTAAAAA
ACTCCTGTGTGGCAGAAAGTAAAAGAAAATTCCCTAAATTATAGCAAGGAACATGAATTCTCAGACATTGTGAGTGTGGGAATGTAAAATGGTAAAATCACTTTTGAAAACAGTTTGGCAGTTTCCTA
TAAAGTTAAACATACACTTTTACTTTAGGACTCCAGAATTCCACTTCTAGTTATTTATTCAAGAGAAGGAAAAACAATGATCACAGCAATACTTGTATGCATGTTCATTGCAACTTAAAAGCGTAAAA
ACCCCAAATGTCCATCCACAGACGAATGTATAAACTGTGGTATCCATTACACAATAGACTACTTACTACTCAGCAATAAAAATGAAGTAACTTTCAATAAATGCAATATTATTGGCAGACATTGTTGA
AGGAAAAAAGCCAGACAAACAACTACATAAAATATGTTTCTATTTAGATGAAGTGGCAAACTAATCTGTAGTGTTAAAAATTAGATTAGTGATTGCCTGGGCCAAGTGGCAGGTTGGGGAGGATGGCT
GCAAAGAAGTATGAGGAAACTTTCTCCAATAGATGAGAATTTTCCGTATCTTGATCTGAGTGGCAAATTGTAAACTTAAAATATATATAAAATTTATTGTATGAAAATTAAGCCTCAATAAACGTGAT
TATAAAAAACAAGTCTGCAAGGAAACCAGAATCATATACCTTCTCTTGTGAAATCACCATGAAGTGTGAATGGTCAGGAAAAAGCCAGTAATATTCATACATTTAATAATTTCAGCTCTACTGAATAA
ACATATAAGTCTGATGGGTGATGAAAATAGCTACTACAATCTTCATATTCTAACTCCTATAAAGACTGTATATCAGAATCTGCAAACTTTTATGCAGATCCCAGTGACTCAATTACATGTTCAACTAT
GATTAAAGCTTCAATAAACTTGGTTGTTCATCTACTTCA

hide sequence

RefSeq Acc Id:

NM_005467 ⟹ NP_005458

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	90,134,663 - 90,192,894 (+)	NCBI
GRCh37	11	89,867,772 - 89,926,062 (+)	NCBI
Build 36	11	89,507,530 - 89,565,424 (+)	NCBI Archive
Celera	11	87,168,325 - 87,226,293 (+)	RGD
HuRef	11	85,952,467 - 86,010,505 (+)	ENTREZGENE
CHM1_1	11	89,750,836 - 89,808,679 (+)	NCBI
T2T-CHM13v2.0	11	90,054,744 - 90,112,974 (+)	NCBI

Sequence:

show sequence

AGAGCTCACAGCCTCCTGCCAGCGCGCTCTCTGTTTCTCTGCAGCCCCGAAGCTCGCGAATGTA
GCAGGCGCCCCAAGCTCGGTCCTCAAGAAGCCATGGCGGAATCCAGGGGCCGTCTGTACCTTTGGATGTGCTTGGCTGCTGCGCTGGCATCTTTCCTGATGGGATTTATGGTGGGCTGGTTTATTAAG
CCTCTCAAAGAAACGACCACTTCTGTGCGCTATCATCAAAGTATACGGTGGAAACTGGTATCCGAAATGAAAGCTGAAAACATCAAATCATTTCTTCGTTCTTTTACAAAGCTTCCTCATCTGGCAGG
AACAGAACAAAATTTCTTGCTTGCCAAGAAAATCCAAACCCAGTGGAAGAAATTTGGACTAGATTCAGCCAAGTTGGTTCATTATGATGTCCTCTTATCTTACCCCAATGAGACAAATGCCAACTATA
TATCGATTGTGGATGAACATGAAACTGAGATTTTCAAAACATCATACCTTGAACCACCACCAGATGGCTATGAGAATGTTACAAATATTGTGCCACCATATAATGCTTTCTCAGCCCAAGGCATGCCA
GAGGGAGATCTTGTATATGTGAACTATGCTCGCACTGAAGACTTTTTCAAACTAGAAAGAGAGATGGGCATCAACTGTACTGGGAAGATTGTTATTGCAAGATATGGAAAAATCTTCAGAGGAAATAA
AGTTAAAAATGCCATGTTAGCAGGAGCCATAGGAATCATCTTGTACTCAGATCCAGCTGACTACTTTGCTCCTGAGGTACAGCCATATCCCAAAGGATGGAATCTTCCTGGAACTGCAGCCCAGAGAG
GAAATGTGTTAAATTTGAATGGTGCTGGTGACCCACTCACTCCAGGCTATCCAGCAAAAGAATACACTTTCAGACTTGATGTTGAAGAAGGAGTGGGAATCCCCCGAATACCTGTACATCCCATTGGA
TATAATGATGCAGAAATATTATTACGCTACTTGGGAGGAATTGCTCCACCAGATAAGAGTTGGAAGGGAGCCCTTAATGTGAGTTATAGTATCGGACCTGGCTTTACAGGGAGTGATTCTTTCAGGAA
GGTTAGAATGCATGTTTATAACATCAATAAAATTACAAGGATTTACAATGTAGTTGGAACTATCAGAGGATCTGTGGAACCTGACAGGTATGTTATTCTGGGAGGTCACCGGGACTCCTGGGTATTTG
GAGCTATTGACCCAACCAGTGGGGTTGCTGTTTTGCAAGAAATTGCCCGGAGTTTTGGAAAACTGATGAGTAAAGGCTGGAGACCTAGAAGAACTATCATTTTTGCCAGCTGGGATGCAGAAGAATTT
GGACTTCTGGGTTCCACAGAATGGGCTGAGGAGAATGTCAAAATACTCCAGGAGAGAAGCATTGCTTATATCAACTCGGATTCATCTATAGAAGGCAATTATACTCTCAGAGTTGACTGTACTCCCCT
TCTTTACCAATTAGTGTATAAACTGACAAAAGAGATCCCCAGCCCTGATGATGGGTTTGAGAGTAAATCACTGTATGAAAGCTGGTTGGAAAAAGACCCTTCACCTGAAAATAAAAATTTGCCTAGAA
TCAATAAGCTGGGATCTGGAAGTGACTTTGAAGCTTATTTTCAGAGACTTGGAATTGCTTCAGGCAGAGCCCGTTACACTAAGAATAAGAAAACAGATAAGTACAGCAGCTACCCAGTGTACCACACA
ATTTATGAGACATTTGAATTGGTAGAGAAATTTTATGACCCCACATTTAAAAAACAACTTTCTGTGGCTCAATTACGAGGAGCACTGGTATATGAGCTTGTGGATTCTAAAATCATTCCTTTTAATAT
TCAAGACTATGCAGAAGCTTTGAAAAACTATGCAGCAAGTATCTATAATCTATCTAAGAAACATGATCAACAATTGACAGACCATGGAGTATCATTTGACTCCTTATTTTCTGCTGTGAAAAACTTCT
CAGAGGCTGCTTCAGATTTTCATAAACGACTTATACAAGTTGATCTTAACAATCCCATTGCAGTGAGAATGATGAATGACCAACTGATGCTCCTGGAAAGAGCATTCATCGATCCTCTTGGTTTACCA
GGAAAGCTGTTCTATAGGCACATCATATTTGCTCCAAGTAGCCACAACAAATATGCTGGAGAATCATTTCCTGGAATCTATGATGCTATCTTTGATATTGAAAATAAAGCCAACTCTCGTTTGGCCTG
GAAAGAAGTAAAGAAACATATTTCTATTGCAGCTTTTACAATTCAAGCAGCAGCAGGAACTCTGAAAGAAGTATTATAGAAGGTCTCAAGTGGCTAGCCATTAAAGGTGTTGCTAAAAGTCTGAGGAT
AAAATTCACCTTTCTGATAACTTATGAAGCCAGGGTGTTCTAAACTCTTTTCATGTCATGTTTTGATTATAGGCTTTGGTCTTTTCATCTGCAAAGCCTTTTTTTTTTGCTCTTTAAAAGTTAATAAT
TATATTAGCAAAGTGTTAATCTAATGAAGTAAAAAACTCCTGTGTGGCAGAAAGTAAAAGAAAATTCCCTAAATTATAGCAAGGAACATGAATTCTCAGACATTGTGAGTGTGGGAATGTAAAATGGT
AAAATCACTTTTGAAAACAGTTTGGCAGTTTCCTATAAAGTTAAACATACACTTTTACTTTAGGACTCCAGAATTCCACTTCTAGTTATTTATTCAAGAGAAGGAAAAACAATGATCACAGCAATACT
TGTATGCATGTTCATTGCAACTTAAAAGCGTAAAAACCCCAAATGTCCATCCACAGACGAATGTATAAACTGTGGTATCCATTACACAATAGACTACTTACTACTCAGCAATAAAAATGAAGTAACTT
TCAATAAATGCAATATTATTGGCAGACATTGTTGAAGGAAAAAAGCCAGACAAACAACTACATAAAATATGTTTCTATTTAGATGAAGTGGCAAACTAATCTGTAGTGTTAAAAATTAGATTAGTGAT
TGCCTGGGCCAAGTGGCAGGTTGGGGAGGATGGCTGCAAAGAAGTATGAGGAAACTTTCTCCAATAGATGAGAATTTTCCGTATCTTGATCTGAGTGGCAAATTGTAAACTTAAAATATATATAAAAT
TTATTGTATGAAAATTAAGCCTCAATAAACGTGATTATAAAAAACAAGTCTGCAAGGAAACCAGAATCATATACCTTCTCTTGTGAAATCACCATGAAGTGTGAATGGTCAGGAAAAAGCCAGTAATA
TTCATACATTTAATAATTTCAGCTCTACTGAATAAACATATAAGTCTGATGGGTGATGAAAATAGCTACTACAATCTTCATATTCTAACTCCTATAAAGACTGTATATCAGAATCTGCAAACTTTTAT
GCAGATCCCAGTGACTCAATTACATGTTCAACTATGATTAAAGCTTCAATAAACTTGGTTGTTCATCTACTTCA

hide sequence

RefSeq Acc Id:

XM_017017043 ⟹ XP_016872532

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	90,131,699 - 90,192,894 (+)	NCBI

Sequence:

show sequence

ATAACCTGTTTGAAGGAACTTGAGCTTCAGGGTTACAAAACTGCTTCTGCTATGATGGAGAAGAGGAGGAAAAAATGCTTAGATAAGAGCAATTTAACTTAAATGGAGGAAGTGTGTCTATATTGACA
AAAGTCCAAAGACTTGTTGAGCCAGCTAACTGGGCTTTTTACAATGGCTTTTCAAGATTGCAGATGCCGCCTACAGAGACGACAGTCATATTTGAGCCCCGAAGCTCGCGAATGTAGCAGGCGCCCCA
AGCTCGGTCCTCAAGAAGCCATGGCGGAATCCAGGGGCCGTCTGTACCTTTGGATGTGCTTGGCTGCTGCGCTGGCATCTTTCCTGATGGGATTTATGGTGGGCTGGTTTATTAAGCCTCTCAAAGAA
ACGACCACTTCTGTGCGCTATCATCAAAGTATACGGTGGAAACTGGTATCCGAAATGAAAGCTGAAAACATCAAATCATTTCTTCGTTCTTTTACAAAGCTTCCTCATCTGGCAGGAACAGAACAAAA
TTTCTTGCTTGCCAAGAAAATCCAAACCCAGTGGAAGAAATTTGGACTAGATTCAGCCAAGTTGGTTCATTATGATGTCCTCTTATCTTACCCCAATGAGACAAATGCCAACTATATATCGATTGTGG
ATGAACATGAAACTGAGATTTTCAAAACATCATACCTTGAACCACCACCAGATGGCTATGAGAATGTTACAAATATTGTGCCACCATATAATGCTTTCTCAGCCCAAGGCATGCCAGAGGGAGATCTT
GTATATGTGAACTATGCTCGCACTGAAGACTTTTTCAAACTAGAAAGAGAGATGGGCATCAACTGTACTGGGAAGATTGTTATTGCAAGATATGGAAAAATCTTCAGAGGAAATAAAGTTAAAAATGC
CATGTTAGCAGGAGCCATAGGAATCATCTTGTACTCAGATCCAGCTGACTACTTTGCTCCTGAGGTACAGCCATATCCCAAAGGATGGAATCTTCCTGGAACTGCAGCCCAGAGAGGAAATGTGTTAA
ATTTGAATGGTGCTGGTGACCCACTCACTCCAGGCTATCCAGCAAAAGAATACACTTTCAGACTTGATGTTGAAGAAGGAGTGGGAATCCCCCGAATACCTGTACATCCCATTGGATATAATGATGCA
GAAATATTATTACGCTACTTGGGAGGAATTGCTCCACCAGATAAGAGTTGGAAGGGAGCCCTTAATGTGAGTTATAGTATCGGACCTGGCTTTACAGGGAGTGATTCTTTCAGGAAGGTTAGAATGCA
TGTTTATAACATCAATAAAATTACAAGGATTTACAATGTAGTTGGAACTATCAGAGGATCTGTGGAACCTGACAGGTATGTTATTCTGGGAGGTCACCGGGACTCCTGGGTATTTGGAGCTATTGACC
CAACCAGTGGGGTTGCTGTTTTGCAAGAAATTGCCCGGAGTTTTGGAAAACTGATGAGTAAAGGCTGGAGACCTAGAAGAACTATCATTTTTGCCAGCTGGGATGCAGAAGAATTTGGACTTCTGGGT
TCCACAGAATGGGCTGAGGAGAATGTCAAAATACTCCAGGAGAGAAGCATTGCTTATATCAACTCGGATTCATCTATAGAAGGCAATTATACTCTCAGAGTTGACTGTACTCCCCTTCTTTACCAATT
AGTGTATAAACTGACAAAAGAGATCCCCAGCCCTGATGATGGGTTTGAGAGTAAATCACTGTATGAAAGCTGGTTGGAAAAAGACCCTTCACCTGAAAATAAAAATTTGCCTAGAATCAATAAGCTGG
GATCTGGAAGTGACTTTGAAGCTTATTTTCAGAGACTTGGAATTGCTTCAGGCAGAGCCCGTTACACTAAGAATAAGAAAACAGATAAGTACAGCAGCTACCCAGTGTACCACACAATTTATGAGACA
TTTGAATTGGTAGAGAAATTTTATGACCCCACATTTAAAAAACAACTTTCTGTGGCTCAATTACGAGGAGCACTGGTATATGAGCTTGTGGATTCTAAAATCATTCCTTTTAATATTCAAGACTATGC
AGAAGCTTTGAAAAACTATGCAGCAAGTATCTATAATCTATCTAAGAAACATGATCAACAATTGACAGACCATGGAGTATCATTTGACTCCTTATTTTCTGCTGTGAAAAACTTCTCAGAGGCTGCTT
CAGATTTTCATAAACGACTTATACAAGTTGATCTTAACAATCCCATTGCAGTGAGAATGATGAATGACCAACTGATGCTCCTGGAAAGAGCATTCATCGATCCTCTTGGTTTACCAGGAAAGCTGTTC
TATAGGCACATCATATTTGCTCCAAGTAGCCACAACAAATATGCTGGAGAATCATTTCCTGGAATCTATGATGCTATCTTTGATATTGAAAATAAAGCCAACTCTCGTTTGGCCTGGAAAGAAGTAAA
GAAACATATTTCTATTGCAGCTTTTACAATTCAAGCAGCAGCAGGAACTCTGAAAGAAGTATTATAGAAGGTCTCAAGTGGCTAGCCATTAAAGGTGTTGCTAAAAGTCTGAGGATAAAATTCACCTT
TCTGATAACTTATGAAGCCAGGGTGTTCTAAACTCTTTTCATGTCATGTTTTGATTATAGGCTTTGGTCTTTTCATCTGCAAAGCCTTTTTTTTTTGCTCTTTAAAAGTTAATAATTATATTAGCAAA
GTGTTAATCTAATGAAGTAAAAAACTCCTGTGTGGCAGAAAGTAAAAGAAAATTCCCTAAATTATAGCAAGGAACATGAATTCTCAGACATTGTGAGTGTGGGAATGTAAAATGGTAAAATCACTTTT
GAAAACAGTTTGGCAGTTTCCTATAAAGTTAAACATACACTTTTACTTTAGGACTCCAGAATTCCACTTCTAGTTATTTATTCAAGAGAAGGAAAAACAATGATCACAGCAATACTTGTATGCATGTT
CATTGCAACTTAAAAGCGTAAAAACCCCAAATGTCCATCCACAGACGAATGTATAAACTGTGGTATCCATTACACAATAGACTACTTACTACTCAGCAATAAAAATGAAGTAACTTTCAATAAATGCA
ATATTATTGGCAGACATTGTTGAAGGAAAAAAGCCAGACAAACAACTACATAAAATATGTTTCTATTTAGATGAAGTGGCAAACTAATCTGTAGTGTTAAAAATTAGATTAGTGATTGCCTGGGCCAA
GTGGCAGGTTGGGGAGGATGGCTGCAAAGAAGTATGAGGAAACTTTCTCCAATAGATGAGAATTTTCCGTATCTTGATCTGAGTGGCAAATTGTAAACTTAAAATATATATAAAATTTATTGTATGAA
AATTAAGCCTCAATAAACGTGATTATAAAAAACAAGTCTGCAAGGAAACCAGAATCATATACCTTCTCTTGTGAAATCACCATGAAGTGTGAATGGTCAGGAAAAAGCCAGTAATATTCATACATTTA
ATAATTTCAGCTCTACTGAATAAACATATAAGTCTGATGGGTGATGAAAATAGCTACTACAATCTTCATATTCTAACTCCTATAAAGACTGTATATCAGAATCTGCAAACTTTTATGCAGATCCCAGT
GACTCAATTACATGTTCAACTATGATTAAAGCTTCAATAAACTTGGTTGTTCATCTACTTCACCAAAACGAGTTAAGAATTAAAAATTAGAAGAGCCTTCATAGGCAAGTACAATAACTAAAATAAGA
AATGACAGCTCAAAGCTTAACTACAAGGAAAAACTACCCATTACCCTTGCTCCCAGGCCAACAATACAGTTTAACTTAAAACAGTGGGGGCATTTAGTTTAGGGGCATTTTCTATACATCTCAGTATT
ACTAGAGGGTATTTCACTGATCCCCCACAATAAAATAAGTTGCAAGTATAGCAATGACTCTGTCATCAAGGTAACTTTTAAATATGTTCCATTCCTTCTGCTTAAAGAGGCAATAAGGTGTGCTATTT
ATGAAGTATAAATATACACAATTAAGACTTTTGTAAAAGGGAGTTAACTTTACTACCACGCTACACTACCAAAGTATAACACTTTAACTTTTGCCTTGAAGCACTGTGTTGTAGAAAATATACTGCAT
TAAGACCCATGAATCATACTATCTACTACCCAACTGAGTAGATCACTACGTATCTCTGGGCATCAGTTCCCTCCAACTCTATCATTTCTAAAGGAGACAAAGCACAAAGGTTTAGAAATGTCTTGGGT
GTTCTTCCTACTGGTAGTTTTCCTGAAGACAAATGCGAGCTGCCAGAACAGCATATTTGGTCTGAAATATGAGTTTGGAGTAAAATAGTAATTATTGCAATTTAA

hide sequence

RefSeq Acc Id:

XM_017017045 ⟹ XP_016872534

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	90,134,663 - 90,192,894 (+)	NCBI

Sequence:

show sequence

AAGGTCAGCGGAGGCCACCCAGAGCTCACAGCCTCCTGCCAGCGCGCTCTCTGTTTCTCTGCAGCCCCGAAGCTCGCGAATGTAGCAGGCGCCCCAAGCTCGGTCCTCAAGAAGCCATGGCGGAATCC
AGGGGCCGTCTGTACCTTTGGATGTGCTTGGCTGCTGCGCTGGCATCTTTCCTGATGGGATTTATGGCTGGTTTATTAAGCCTCTCAAAGAAACGACCACTTCTGTGCGCTATCATCAAAGTATACGG
TGGAAACTGGTATCCGAAATGAAAGCTGAAAACATCAAATCATTTCTTCGTTCTTTTACAAAGCTTCCTCATCTGGCAGGAACAGAACAAAATTTCTTGCTTGCCAAGAAAATCCAAACCCAGTGGAA
GAAATTTGGACTAGATTCAGCCAAGTTGGTTCATTATGATGTCCTCTTATCTTACCCCAATGAGACAAATGCCAACTATATATCGATTGTGGATGAACATGAAACTGAGATTTTCAAAACATCATACC
TTGAACCACCACCAGATGGCTATGAGAATGTTACAAATATTGTGCCACCATATAATGCTTTCTCAGCCCAAGGCATGCCAGAGGGAGATCTTGTATATGTGAACTATGCTCGCACTGAAGACTTTTTC
AAACTAGAAAGAGAGATGGGCATCAACTGTACTGGGAAGATTGTTATTGCAAGATATGGAAAAATCTTCAGAGGAAATAAAGTTAAAAATGCCATGTTAGCAGGAGCCATAGGAATCATCTTGTACTC
AGATCCAGCTGACTACTTTGCTCCTGAGGTACAGCCATATCCCAAAGGATGGAATCTTCCTGGAACTGCAGCCCAGAGAGGAAATGTGTTAAATTTGAATGGTGCTGGTGACCCACTCACTCCAGGCT
ATCCAGCAAAAGAATACACTTTCAGACTTGATGTTGAAGAAGGAGTGGGAATCCCCCGAATACCTGTACATCCCATTGGATATAATGATGCAGAAATATTATTACGCTACTTGGGAGGAATTGCTCCA
CCAGATAAGAGTTGGAAGGGAGCCCTTAATGTGAGTTATAGTATCGGACCTGGCTTTACAGGGAGTGATTCTTTCAGGAAGGTTAGAATGCATGTTTATAACATCAATAAAATTACAAGGATTTACAA
TGTAGTTGGAACTATCAGAGGATCTGTGGAACCTGACAGGTATGTTATTCTGGGAGGTCACCGGGACTCCTGGGTATTTGGAGCTATTGACCCAACCAGTGGGGTTGCTGTTTTGCAAGAAATTGCCC
GGAGTTTTGGAAAACTGATGAGTAAAGGCTGGAGACCTAGAAGAACTATCATTTTTGCCAGCTGGGATGCAGAAGAATTTGGACTTCTGGGTTCCACAGAATGGGCTGAGGAGAATGTCAAAATACTC
CAGGAGAGAAGCATTGCTTATATCAACTCGGATTCATCTATAGAAGGCAATTATACTCTCAGAGTTGACTGTACTCCCCTTCTTTACCAATTAGTGTATAAACTGACAAAAGAGATCCCCAGCCCTGA
TGATGGGTTTGAGAGTAAATCACTGTATGAAAGCTGGTTGGAAAAAGACCCTTCACCTGAAAATAAAAATTTGCCTAGAATCAATAAGCTGGGATCTGGAAGTGACTTTGAAGCTTATTTTCAGAGAC
TTGGAATTGCTTCAGGCAGAGCCCGTTACACTAAGAATAAGAAAACAGATAAGTACAGCAGCTACCCAGTGTACCACACAATTTATGAGACATTTGAATTGGTAGAGAAATTTTATGACCCCACATTT
AAAAAACAACTTTCTGTGGCTCAATTACGAGGAGCACTGGTATATGAGCTTGTGGATTCTAAAATCATTCCTTTTAATATTCAAGACTATGCAGAAGCTTTGAAAAACTATGCAGCAAGTATCTATAA
TCTATCTAAGAAACATGATCAACAATTGACAGACCATGGAGTATCATTTGACTCCTTATTTTCTGCTGTGAAAAACTTCTCAGAGGCTGCTTCAGATTTTCATAAACGACTTATACAAGTTGATCTTA
ACAATCCCATTGCAGTGAGAATGATGAATGACCAACTGATGCTCCTGGAAAGAGCATTCATCGATCCTCTTGGTTTACCAGGAAAGCTGTTCTATAGGCACATCATATTTGCTCCAAGTAGCCACAAC
AAATATGCTGGAGAATCATTTCCTGGAATCTATGATGCTATCTTTGATATTGAAAATAAAGCCAACTCTCGTTTGGCCTGGAAAGAAGTAAAGAAACATATTTCTATTGCAGCTTTTACAATTCAAGC
AGCAGCAGGAACTCTGAAAGAAGTATTATAGAAGGTCTCAAGTGGCTAGCCATTAAAGGTGTTGCTAAAAGTCTGAGGATAAAATTCACCTTTCTGATAACTTATGAAGCCAGGGTGTTCTAAACTCT
TTTCATGTCATGTTTTGATTATAGGCTTTGGTCTTTTCATCTGCAAAGCCTTTTTTTTTTGCTCTTTAAAAGTTAATAATTATATTAGCAAAGTGTTAATCTAATGAAGTAAAAAACTCCTGTGTGGC
AGAAAGTAAAAGAAAATTCCCTAAATTATAGCAAGGAACATGAATTCTCAGACATTGTGAGTGTGGGAATGTAAAATGGTAAAATCACTTTTGAAAACAGTTTGGCAGTTTCCTATAAAGTTAAACAT
ACACTTTTACTTTAGGACTCCAGAATTCCACTTCTAGTTATTTATTCAAGAGAAGGAAAAACAATGATCACAGCAATACTTGTATGCATGTTCATTGCAACTTAAAAGCGTAAAAACCCCAAATGTCC
ATCCACAGACGAATGTATAAACTGTGGTATCCATTACACAATAGACTACTTACTACTCAGCAATAAAAATGAAGTAACTTTCAATAAATGCAATATTATTGGCAGACATTGTTGAAGGAAAAAAGCCA
GACAAACAACTACATAAAATATGTTTCTATTTAGATGAAGTGGCAAACTAATCTGTAGTGTTAAAAATTAGATTAGTGATTGCCTGGGCCAAGTGGCAGGTTGGGGAGGATGGCTGCAAAGAAGTATG
AGGAAACTTTCTCCAATAGATGAGAATTTTCCGTATCTTGATCTGAGTGGCAAATTGTAAACTTAAAATATATATAAAATTTATTGTATGAAAATTAAGCCTCAATAAACGTGATTATAAAAAACAAG
TCTGCAAGGAAACCAGAATCATATACCTTCTCTTGTGAAATCACCATGAAGTGTGAATGGTCAGGAAAAAGCCAGTAATATTCATACATTTAATAATTTCAGCTCTACTGAATAAACATATAAGTCTG
ATGGGTGATGAAAATAGCTACTACAATCTTCATATTCTAACTCCTATAAAGACTGTATATCAGAATCTGCAAACTTTTATGCAGATCCCAGTGACTCAATTACATGTTCAACTATGATTAAAGCTTCA
ATAAACTTGGTTGTTCATCTACTTCACCAAAACGAGTTAAGAATTAAAAATTAGAAGAGCCTTCATAGGCAAGTACAATAACTAAAATAAGAAATGACAGCTCAAAGCTTAACTACAAGGAAAAACTA
CCCATTACCCTTGCTCCCAGGCCAACAATACAGTTTAACTTAAAACAGTGGGGGCATTTAGTTTAGGGGCATTTTCTATACATCTCAGTATTACTAGAGGGTATTTCACTGATCCCCCACAATAAAAT
AAGTTGCAAGTATAGCAATGACTCTGTCATCAAGGTAACTTTTAAATATGTTCCATTCCTTCTGCTTAAAGAGGCAATAAGGTGTGCTATTTATGAAGTATAAATATACACAATTAAGACTTTTGTAA
AAGGGAGTTAACTTTACTACCACGCTACACTACCAAAGTATAACACTTTAACTTTTGCCTTGAAGCACTGTGTTGTAGAAAATATACTGCATTAAGACCCATGAATCATACTATCTACTACCCAACTG
AGTAGATCACTACGTATCTCTGGGCATCAGTTCCCTCCAACTCTATCATTTCTAAAGGAGACAAAGCACAAAGGTTTAGAAATGTCTTGGGTGTTCTTCCTACTGGTAGTTTTCCTGAAGACAAATGC
GAGCTGCCAGAACAGCATATTTGGTCTGAAATATGAGTTTGGAGTAAAATAGTAATTATTGCAATTTAA

hide sequence

RefSeq Acc Id:

XM_017017046 ⟹ XP_016872535

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	90,132,096 - 90,163,617 (+)	NCBI

Sequence:

show sequence

CATAACCTGTTTGAAGGAACTTGAGCTTCAGGGTTACAAAACTGCTTCTGCTATGATGGAGAAGAGGAGGAAAAAATGCTTAGATAAGAGCAATTTAACTTAAATGGAGGAAGTGTGTCTATATTGAC
AAAAGTCCAAAGACTTGTTGAGCCAGCTAACTGGGCTTTTTACAATGGCTTTTCAAGATTGCAGATGCCGCCTACAGAGACGACAGTCATATTTGAGCCCCGAAGCTCGCGAATGTAGCAGGCGCCCC
AAGCTCGGTCCTCAAGAAGCCATGGCGGAATCCAGGGGCCGTCTGTACCTTTGGATGTGCTTGGCTGCTGCGCTGGCATCTTTCCTGATGGGATTTATGGTGGGCTGGTTTATTAAGCCTCTCAAAGA
AACGACCACTTCTGTGCGCTATCATCAAAGTATACGGTGGAAACTGGTATCCGAAATGAAAGCTGAAAACATCAAATCATTTCTTCGTTCTTTTACAAAGCTTCCTCATCTGGCAGGAACAGAACAAA
ATTTCTTGCTTGCCAAGAAAATCCAAACCCAGTGGAAGAAATTTGGACTAGATTCAGCCAAGTTGGTTCATTATGATGTCCTCTTATCTTACCCCAATGAGACAAATGCCAACTATATATCGATTGTG
GATGAACATGAAACTGAGATTTTCAAAACATCATACCTTGAACCACCACCAGATGGCTATGAGAATGTTACAAATATTGTGCCACCATATAATGCTTTCTCAGCCCAAGGCATGCCAGAGGGAGATCT
TGTATATGTGAACTATGCTCGCACTGAAGACTTTTTCAAACTAGAAAGAGAGATGGGCATCAACTGTACTGGGAAGATTGTTATTGCAAGATATGGAAAAATCTTCAGAGGAAATAAAGTTAAAAATG
CCATGTTAGCAGGAGCCATAGGAATCATCTTGTACTCAGATCCAGCTGACTACTTTGCTCCTGAGGTACAGCCATATCCCAAAGGATGGAATCTTCCTGGAACTGCAGCCCAGAGAGGAAATGTGTTA
AATTTGAATGGTGCTGGTGACCCACTCACTCCAGGCTATCCAGCAAAAGAATACACTTTCAGACTTGATGTTGAAGAAGGAGTGGGAATCCCCCGAATACCTGTACATCCCATTGGATATAATGATGC
AGAAATATTATTACGCTACTTGGGAGGAATTGCTCCACCAGATAAGAGTTGGAAGGGAGCCCTTAATGTGAGTTATAGTATCGGACCTGGCTTTACAGGGAGTGATTCTTTCAGGAAGGTTAGAATGC
ATGTTTATAACATCAATAAAATTACAAGGATTTACAATGTAGTTGGAACTATCAGAGGATCTGTGGAACCTGGTATGTTATTCTGGGAGGTCACCGGGACTCCTGGGTATTTGGAGCTATTGACCCAA
CCAGTGGGGTTGCTGTTTTGCAAGAAATTGCCCGGAGTTTTGGAAAACTGATGAGTAAAGGCTGGAGACCTAGAAGAACTATCATTTTTGCCAGCTGGGATGCAGAAGAATTTGGACTTCTGGGTTCC
ACAGAATGGGCTGAGGTAAATAAGACAAAGAAGGTTCTTATTATTTTTTTGGTCAACAGGGAACAAATATGTATGTGTCTCAGGATGATCAAAAATATATTCCATTACCTAATATGGTTTTGTTTTGG
AGAATGACTCAAGACAATTTAAGAAATAGTTTATTTTTACTTTCACATCAGTTTGGCAATAACCTTTTAGTACTAGACTGCAGACAGAGTTATTGCCTCTTGTCAAAATATTTTCGTTGCCATTTGCA
TTTGTTTTATAAAAAATAAGAAAAATCAGTAAGCTCAGAAAATAATCAAAATTAATGAGATATTTTTGATGATAATTTACTTATCTAAAAACTGATACAGATGCTTAGAGCTAATTTTCAAGTTTTTG
AAGTTTCTTTAGAGTTCTTCCATCTGAGAAAATATAAGATGTTCTATTAAGATGGCCATATATTGACTATATTTTCACATTGACAGATTCCATTTAAAATGGCAACCATAAGTATACTTTAGCATTTA
CAACAGATATGTGCTTCATTGTTAAGTATAAAGTGATAATTCTGTGAATTGAATTACTTTAATAAATTGACCTGCTTTACAATTTCA

hide sequence

RefSeq Acc Id:

XM_047426168 ⟹ XP_047282124

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	90,132,096 - 90,192,894 (+)	NCBI

RefSeq Acc Id:

XM_054367343 ⟹ XP_054223318

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	90,051,780 - 90,112,974 (+)	NCBI

RefSeq Acc Id:

XM_054367344 ⟹ XP_054223319

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	90,052,177 - 90,112,974 (+)	NCBI

RefSeq Acc Id:

XM_054367345 ⟹ XP_054223320

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	90,054,658 - 90,112,974 (+)	NCBI

RefSeq Acc Id:

XM_054367346 ⟹ XP_054223321

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	90,052,177 - 90,083,696 (+)	NCBI

RefSeq Acc Id:

XR_007062427

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	90,132,094 - 90,183,008 (+)	NCBI

RefSeq Acc Id:

XR_007062428

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	90,132,095 - 90,176,062 (+)	NCBI

RefSeq Acc Id:

XR_008488319

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	90,052,175 - 90,103,088 (+)	NCBI

RefSeq Acc Id:

XR_008488320

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	90,052,176 - 90,096,141 (+)	NCBI


Protein RefSeqs	NP_001287859	(Get FASTA)	NCBI Sequence Viewer
	NP_005458	(Get FASTA)	NCBI Sequence Viewer
	XP_016872532	(Get FASTA)	NCBI Sequence Viewer
	XP_016872534	(Get FASTA)	NCBI Sequence Viewer
	XP_016872535	(Get FASTA)	NCBI Sequence Viewer
	XP_047282124	(Get FASTA)	NCBI Sequence Viewer
	XP_054188397	(Get FASTA)	NCBI Sequence Viewer
	XP_054188398	(Get FASTA)	NCBI Sequence Viewer
	XP_054188399	(Get FASTA)	NCBI Sequence Viewer
	XP_054188400	(Get FASTA)	NCBI Sequence Viewer
	XP_054223318	(Get FASTA)	NCBI Sequence Viewer
	XP_054223319	(Get FASTA)	NCBI Sequence Viewer
	XP_054223320	(Get FASTA)	NCBI Sequence Viewer
	XP_054223321	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH27594	(Get FASTA)	NCBI Sequence Viewer
	AAH38840	(Get FASTA)	NCBI Sequence Viewer
	AAH96316	(Get FASTA)	NCBI Sequence Viewer
	AAH96317	(Get FASTA)	NCBI Sequence Viewer
	AAH96318	(Get FASTA)	NCBI Sequence Viewer
	AAH99646	(Get FASTA)	NCBI Sequence Viewer
	BAG52126	(Get FASTA)	NCBI Sequence Viewer
	CAB39967	(Get FASTA)	NCBI Sequence Viewer
	CAC39719	(Get FASTA)	NCBI Sequence Viewer
	CAI72090	(Get FASTA)	NCBI Sequence Viewer
	EAW66865	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000320083
	ENSP00000365111.3
	ENSP00000432481
	ENSP00000432481.1
	ENSP00000494081.1
	ENSP00000494766.1
GenBank Protein	Q9Y3Q0	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_005458 ⟸ NM_005467
- Peptide Label:	isoform 1
- UniProtKB:	Q4KKV4 (UniProtKB/Swiss-Prot), B3KQR4 (UniProtKB/Swiss-Prot), Q4VAM9 (UniProtKB/Swiss-Prot), Q9Y3Q0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAESRGRLYLWMCLAAALASFLMGFMVGWFIKPLKETTTSVRYHQSIRWKLVSEMKAENIKSFLRSFTKLPHLAGTEQNFLLAKKIQTQWKKFGLDSAKLVHYDVLLSYPNETNANYISIVDEHETEI FKTSYLEPPPDGYENVTNIVPPYNAFSAQGMPEGDLVYVNYARTEDFFKLEREMGINCTGKIVIARYGKIFRGNKVKNAMLAGAIGIILYSDPADYFAPEVQPYPKGWNLPGTAAQRGNVLNLNGAGD PLTPGYPAKEYTFRLDVEEGVGIPRIPVHPIGYNDAEILLRYLGGIAPPDKSWKGALNVSYSIGPGFTGSDSFRKVRMHVYNINKITRIYNVVGTIRGSVEPDRYVILGGHRDSWVFGAIDPTSGVAV LQEIARSFGKLMSKGWRPRRTIIFASWDAEEFGLLGSTEWAEENVKILQERSIAYINSDSSIEGNYTLRVDCTPLLYQLVYKLTKEIPSPDDGFESKSLYESWLEKDPSPENKNLPRINKLGSGSDFE AYFQRLGIASGRARYTKNKKTDKYSSYPVYHTIYETFELVEKFYDPTFKKQLSVAQLRGALVYELVDSKIIPFNIQDYAEALKNYAASIYNLSKKHDQQLTDHGVSFDSLFSAVKNFSEAASDFHKRL IQVDLNNPIAVRMMNDQLMLLERAFIDPLGLPGKLFYRHIIFAPSSHNKYAGESFPGIYDAIFDIENKANSRLAWKEVKKHISIAAFTIQAAAGTLKEVL hide sequence

RefSeq Acc Id:	NP_001287859 ⟸ NM_001300930
- Peptide Label:	isoform 2
- UniProtKB:	J3KNJ3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAESRGRLYLWMCLAAALASFLMGFMVGWFIKPLKETTTSVRYHQSIRWKLVSEMKAENIKSFLRSFTKLPHLAGTEQNFLLAKKIQTQWKKFGLDSAKLVHYDVLLSYPNETNANYISIVDEHETEI FKTSYLEPPPDGYENVTNIVPPYNAFSAQGMPEGDLVYVNYARTEDFFKLEREMGINCTGKIVIARYGKIFRGNKVKNAMLAGAIGIILYSDPADYFAPEVQPYPKGWNLPGTAAQRGNVLNLNGAGD PLTPGYPAKEYTFRLDVEEGVGIPRIPVHPIGYNDAEILLRKVRMHVYNINKITRIYNVVGTIRGSVEPDRYVILGGHRDSWVFGAIDPTSGVAVLQEIARSFGKLMSKGWRPRRTIIFASWDAEEFG LLGSTEWAEENVKILQERSIAYINSDSSIEGNYTLRVDCTPLLYQLVYKLTKEIPSPDDGFESKSLYESWLEKDPSPENKNLPRINKLGSGSDFEAYFQRLGIASGRARYTKNKKTDKYSSYPVYHTI YETFELVEKFYDPTFKKQLSVAQLRGALVYELVDSKIIPFNIQDYAEALKNYAASIYNLSKKHDQQLTDHGVSFDSLFSAVKNFSEAASDFHKRLIQVDLNNPIAVRMMNDQLMLLERAFIDPLGLPG KLFYRHIIFAPSSHNKYAGESFPGIYDAIFDIENKANSRLAWKEVKKHISIAAFTIQAAAGTLKEVL hide sequence

RefSeq Acc Id:

XP_016872535 ⟸ XM_017017046

- Peptide Label:

isoform X4

- Sequence:

show sequence

MAFQDCRCRLQRRQSYLSPEARECSRRPKLGPQEAMAESRGRLYLWMCLAAALASFLMGFMVGWFIKPLKETTTSVRYHQSIRWKLVSEMKAENIKSFLRSFTKLPHLAGTEQNFLLAKKIQTQWKKF
GLDSAKLVHYDVLLSYPNETNANYISIVDEHETEIFKTSYLEPPPDGYENVTNIVPPYNAFSAQGMPEGDLVYVNYARTEDFFKLEREMGINCTGKIVIARYGKIFRGNKVKNAMLAGAIGIILYSDP
ADYFAPEVQPYPKGWNLPGTAAQRGNVLNLNGAGDPLTPGYPAKEYTFRLDVEEGVGIPRIPVHPIGYNDAEILLRYLGGIAPPDKSWKGALNVSYSIGPGFTGSDSFRKVRMHVYNINKITRIYNVV
GTIRGSVEPGMLFWEVTGTPGYLELLTQPVGLLFCKKLPGVLEN

hide sequence

RefSeq Acc Id:

XP_016872532 ⟸ XM_017017043

- Peptide Label:

isoform X1

- Sequence:

show sequence

MAFQDCRCRLQRRQSYLSPEARECSRRPKLGPQEAMAESRGRLYLWMCLAAALASFLMGFMVGW
FIKPLKETTTSVRYHQSIRWKLVSEMKAENIKSFLRSFTKLPHLAGTEQNFLLAKKIQTQWKKFGLDSAKLVHYDVLLSYPNETNANYISIVDEHETEIFKTSYLEPPPDGYENVTNIVPPYNAFSAQ
GMPEGDLVYVNYARTEDFFKLEREMGINCTGKIVIARYGKIFRGNKVKNAMLAGAIGIILYSDPADYFAPEVQPYPKGWNLPGTAAQRGNVLNLNGAGDPLTPGYPAKEYTFRLDVEEGVGIPRIPVH
PIGYNDAEILLRYLGGIAPPDKSWKGALNVSYSIGPGFTGSDSFRKVRMHVYNINKITRIYNVVGTIRGSVEPDRYVILGGHRDSWVFGAIDPTSGVAVLQEIARSFGKLMSKGWRPRRTIIFASWDA
EEFGLLGSTEWAEENVKILQERSIAYINSDSSIEGNYTLRVDCTPLLYQLVYKLTKEIPSPDDGFESKSLYESWLEKDPSPENKNLPRINKLGSGSDFEAYFQRLGIASGRARYTKNKKTDKYSSYPV
YHTIYETFELVEKFYDPTFKKQLSVAQLRGALVYELVDSKIIPFNIQDYAEALKNYAASIYNLSKKHDQQLTDHGVSFDSLFSAVKNFSEAASDFHKRLIQVDLNNPIAVRMMNDQLMLLERAFIDPL
GLPGKLFYRHIIFAPSSHNKYAGESFPGIYDAIFDIENKANSRLAWKEVKKHISIAAFTIQAAAGTLKEVL

hide sequence

RefSeq Acc Id:

XP_016872534 ⟸ XM_017017045

- Peptide Label:

isoform X3

- Sequence:

show sequence

MKAENIKSFLRSFTKLPHLAGTEQNFLLAKKIQTQWKKFGLDSAKLVHYDVLLSYPNETNANYISIVDEHETEIFKTSYLEPPPDGYENVTNIVPPYNAFSAQGMPEGDLVYVNYARTEDFFKLEREM
GINCTGKIVIARYGKIFRGNKVKNAMLAGAIGIILYSDPADYFAPEVQPYPKGWNLPGTAAQRGNVLNLNGAGDPLTPGYPAKEYTFRLDVEEGVGIPRIPVHPIGYNDAEILLRYLGGIAPPDKSWK
GALNVSYSIGPGFTGSDSFRKVRMHVYNINKITRIYNVVGTIRGSVEPDRYVILGGHRDSWVFGAIDPTSGVAVLQEIARSFGKLMSKGWRPRRTIIFASWDAEEFGLLGSTEWAEENVKILQERSIA
YINSDSSIEGNYTLRVDCTPLLYQLVYKLTKEIPSPDDGFESKSLYESWLEKDPSPENKNLPRINKLGSGSDFEAYFQRLGIASGRARYTKNKKTDKYSSYPVYHTIYETFELVEKFYDPTFKKQLSV
AQLRGALVYELVDSKIIPFNIQDYAEALKNYAASIYNLSKKHDQQLTDHGVSFDSLFSAVKNFSEAASDFHKRLIQVDLNNPIAVRMMNDQLMLLERAFIDPLGLPGKLFYRHIIFAPSSHNKYAGES
FPGIYDAIFDIENKANSRLAWKEVKKHISIAAFTIQAAAGTLKEVL

hide sequence

Protein Domains

PA Peptidase M28 Transferrin receptor-like dimerisation

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9Y3Q0-F1-model_v2	AlphaFold	Q9Y3Q0	1-740	view protein structure

RGD ID:

6789143

Promoter ID:

HG_KWN:13930

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

NM_005467, UC001PDD.2, UC001PDE.2, UC009YVX.1, UC009YVY.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	89,507,226 - 89,507,726 (+)	MPROMDB

RGD ID:

7221793

Promoter ID:

EPDNEW_H16642

Type:

initiation region

Name:

NAALAD2_2

Description:

N-acetylated alpha-linked acidic dipeptidase 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H16643

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	90,134,521 - 90,134,581	EPDNEW

RGD ID:

7221795

Promoter ID:

EPDNEW_H16643

Type:

initiation region

Name:

NAALAD2_1

Description:

N-acetylated alpha-linked acidic dipeptidase 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H16642

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	90,134,699 - 90,134,759	EPDNEW

Database	Acc Id	Source(s)
COSMIC	NAALAD2	COSMIC
Ensembl Genes	ENSG00000077616	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
	ENSG00000285516	UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000321955	ENTREZGENE
	ENST00000375944.7	UniProtKB/Swiss-Prot
	ENST00000534061	ENTREZGENE
	ENST00000534061.6	UniProtKB/Swiss-Prot
	ENST00000644696.1	UniProtKB/Swiss-Prot
	ENST00000647397.2	UniProtKB/Swiss-Prot
Gene3D-CATH	1.20.930.40	UniProtKB/Swiss-Prot
	3.50.30.30	UniProtKB/Swiss-Prot
	Zn peptidases	UniProtKB/Swiss-Prot
GTEx	ENSG00000077616	GTEx
	ENSG00000285516	GTEx
HGNC ID	HGNC:14526	ENTREZGENE
Human Proteome Map	NAALAD2	Human Proteome Map
InterPro	PA_dom_sf	UniProtKB/Swiss-Prot
	PA_domain	UniProtKB/Swiss-Prot
	Peptidase_M28	UniProtKB/Swiss-Prot
	Peptidase_M28B	UniProtKB/Swiss-Prot
	TFR-like_dimer_dom	UniProtKB/Swiss-Prot
	TFR-like_dimer_dom_sf	UniProtKB/Swiss-Prot
KEGG Report	hsa:10003	UniProtKB/Swiss-Prot
NCBI Gene	10003	ENTREZGENE
OMIM	611636	OMIM
PANTHER	N-ACETYLATED-ALPHA-LINKED ACIDIC DIPEPTIDASE 2	UniProtKB/Swiss-Prot
	PTHR10404	UniProtKB/Swiss-Prot
Pfam	Peptidase_M28	UniProtKB/Swiss-Prot
	PF02225	UniProtKB/Swiss-Prot
	TFR_dimer	UniProtKB/Swiss-Prot
PharmGKB	PA31430	PharmGKB
Superfamily-SCOP	PA domain	UniProtKB/Swiss-Prot
	SSF47672	UniProtKB/Swiss-Prot
	Zn-dependent exopeptidases	UniProtKB/Swiss-Prot
UniProt	B3KQR4	ENTREZGENE
	E9PII2_HUMAN	UniProtKB/TrEMBL
	E9PJ53_HUMAN	UniProtKB/TrEMBL
	E9PJV2_HUMAN	UniProtKB/TrEMBL
	E9PKX5_HUMAN	UniProtKB/TrEMBL
	J3KNJ3	ENTREZGENE, UniProtKB/TrEMBL
	L8EAF7_HUMAN	UniProtKB/TrEMBL
	NALD2_HUMAN	UniProtKB/Swiss-Prot
	Q4G181_HUMAN	UniProtKB/TrEMBL
	Q4KKV4	ENTREZGENE
	Q4VAM9	ENTREZGENE
	Q9Y3Q0	ENTREZGENE
UniProt Secondary	B3KQR4	UniProtKB/Swiss-Prot
	Q4KKV4	UniProtKB/Swiss-Prot
	Q4VAM9	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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