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Gene: RADX (RPA1 related single stranded DNA binding protein, X-linked) Homo sapiens

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Symbol:

RADX

Name:

RPA1 related single stranded DNA binding protein, X-linked

RGD ID:

1605981

HGNC Page

HGNC:25486

Description:

Enables single-stranded DNA binding activity. Involved in negative regulation of double-strand break repair via homologous recombination. Located in nuclear speck and replication fork.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

chromosome X open reading frame 57; CXorf57; FLJ10178; FLJ14191; hypothetical protein LOC55086; RP11-647M7.1; RPA-related and RAD51-antagonist, X-chromosome; RPA-related protein RADX; RPA-related, RAD51-antagonist on X-chromosome; uncharacterized protein CXorf57

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	X	106,611,978 - 106,679,439 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	X	106,611,930 - 106,679,439 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	X	105,855,208 - 105,922,669 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	X	105,741,909 - 105,809,328 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	X	106,326,505 - 106,394,019 (+)	NCBI		Celera
Cytogenetic Map	X	q22.3	NCBI
HuRef	X	95,482,341 - 95,550,832 (+)	NCBI		HuRef
CHM1_1	X	105,765,982 - 105,833,494 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	X	105,048,421 - 105,115,882 (+)	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)
RADX	Human	autistic disorder		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Autism	ClinVar	PMID:21681106 and PMID:30208311
RADX	Human	autosomal hemophilia A		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: AUTOSOMAL HEMOPHILIA A	ClinVar	PMID:31690835
RADX	Human	factor VIII deficiency		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Factor 8 deficiency and congenital	ClinVar	PMID:31690835
RADX	Human	syndromic X-linked intellectual disability Lubs type		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type	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)
RADX	Human	17beta-estradiol	increases expression	ISO	Radx (Mus musculus)	6480464	Estradiol results in increased expression of RADX mRNA	CTD	PMID:39298647
RADX	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	Radx (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin results in increased expression of RADX mRNA	CTD	PMID:33387578
RADX	Human	2-hydroxypropanoic acid	increases expression	EXP		6480464	Lactic Acid results in increased expression of RADX mRNA	CTD	PMID:30851411
RADX	Human	aflatoxin B1	decreases methylation	EXP		6480464	Aflatoxin B1 results in decreased methylation of RADX intron	CTD	PMID:30157460
RADX	Human	arsane	affects methylation	EXP		6480464	Arsenic affects the methylation of RADX gene	CTD	PMID:25304211
RADX	Human	arsenic atom	affects methylation	EXP		6480464	Arsenic affects the methylation of RADX gene	CTD	PMID:25304211
RADX	Human	benzo[a]pyrene	affects methylation	EXP		6480464	Benzo(a)pyrene affects the methylation of RADX exon and Benzo(a)pyrene affects the methylation of RADX promoter	CTD	PMID:27901495
RADX	Human	bisphenol A	decreases expression	ISO	Radx (Rattus norvegicus)	6480464	bisphenol A results in decreased expression of RADX mRNA	CTD	PMID:25181051 more ...
RADX	Human	bisphenol A	decreases expression	EXP		6480464	bisphenol A results in decreased expression of RADX mRNA	CTD	PMID:36232920
RADX	Human	bisphenol F	multiple interactions	EXP		6480464	[bisphenol F co-treated with Fulvestrant] results in increased methylation of RADX gene	CTD	PMID:31601247
RADX	Human	butanal	increases expression	EXP		6480464	butyraldehyde results in increased expression of RADX mRNA	CTD	PMID:26079696
RADX	Human	cadmium dichloride	decreases expression	EXP		6480464	Cadmium Chloride results in decreased expression of RADX mRNA	CTD	PMID:38568856
RADX	Human	calcitriol	increases expression	EXP		6480464	Calcitriol results in increased expression of RADX mRNA	CTD	PMID:16002434
RADX	Human	copper atom	multiple interactions	EXP		6480464	[NSC 689534 binds to Copper] which results in increased expression of RADX mRNA	CTD	PMID:20971185
RADX	Human	copper(0)	multiple interactions	EXP		6480464	[NSC 689534 binds to Copper] which results in increased expression of RADX mRNA	CTD	PMID:20971185
RADX	Human	cyclosporin A	decreases expression	EXP		6480464	Cyclosporine results in decreased expression of RADX mRNA	CTD	PMID:20106945
RADX	Human	cyclosporin A	increases expression	EXP		6480464	Cyclosporine results in increased expression of RADX mRNA	CTD	PMID:25562108
RADX	Human	dimethylarsinic acid	multiple interactions	ISO	Radx (Mus musculus)	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results in decreased expression of RADX mRNA	CTD	PMID:34876320
RADX	Human	dorsomorphin	multiple interactions	EXP		6480464	[NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
RADX	Human	fulvestrant	multiple interactions	EXP		6480464	[bisphenol F co-treated with Fulvestrant] results in increased methylation of RADX gene	CTD	PMID:31601247
RADX	Human	lipopolysaccharide	multiple interactions	EXP		6480464	[S-(1 more ...	CTD	PMID:35811015
RADX	Human	melphalan	decreases expression	EXP		6480464	Melphalan results in decreased expression of RADX mRNA	CTD	PMID:22363485
RADX	Human	methotrexate	increases expression	EXP		6480464	Methotrexate results in increased expression of RADX mRNA	CTD	PMID:24449571
RADX	Human	methyl methanesulfonate	increases expression	EXP		6480464	Methyl Methanesulfonate results in increased expression of RADX mRNA	CTD	PMID:23649840
RADX	Human	methylarsonic acid	multiple interactions	ISO	Radx (Mus musculus)	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results in decreased expression of RADX mRNA	CTD	PMID:34876320
RADX	Human	methylmercury chloride	decreases expression	EXP		6480464	methylmercuric chloride results in decreased expression of RADX mRNA	CTD	PMID:28001369
RADX	Human	ochratoxin A	increases expression	EXP		6480464	ochratoxin A results in increased expression of RADX mRNA	CTD	PMID:30559759
RADX	Human	pentanal	increases expression	EXP		6480464	pentanal results in increased expression of RADX mRNA	CTD	PMID:26079696
RADX	Human	propanal	increases expression	EXP		6480464	propionaldehyde results in increased expression of RADX mRNA	CTD	PMID:26079696
RADX	Human	quercetin	affects expression	EXP		6480464	Quercetin affects the expression of RADX mRNA	CTD	PMID:21632981
RADX	Human	quinolin-8-ol	decreases expression	EXP		6480464	Oxyquinoline results in decreased expression of RADX mRNA	CTD	PMID:21632981
RADX	Human	rac-lactic acid	increases expression	EXP		6480464	Lactic Acid results in increased expression of RADX mRNA	CTD	PMID:30851411
RADX	Human	rotenone	increases expression	EXP		6480464	Rotenone results in increased expression of RADX mRNA	CTD	PMID:29955902
RADX	Human	S-(1,2-dichlorovinyl)-L-cysteine	multiple interactions	EXP		6480464	[S-(1 more ...	CTD	PMID:35811015
RADX	Human	S-(1,2-dichlorovinyl)-L-cysteine	decreases expression	EXP		6480464	S-(1 and 2-dichlorovinyl)cysteine results in decreased expression of RADX mRNA	CTD	PMID:35811015
RADX	Human	SB 431542	multiple interactions	EXP		6480464	[NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
RADX	Human	sodium arsenate	multiple interactions	ISO	Radx (Mus musculus)	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results in decreased expression of RADX mRNA	CTD	PMID:34876320
RADX	Human	sodium arsenite	decreases expression	ISO	Radx (Mus musculus)	6480464	sodium arsenite results in decreased expression of RADX mRNA	CTD	PMID:37682722
RADX	Human	sodium arsenite	multiple interactions	ISO	Radx (Mus musculus)	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results in decreased expression of RADX mRNA	CTD	PMID:34876320
RADX	Human	sunitinib	increases expression	EXP		6480464	Sunitinib results in increased expression of RADX mRNA	CTD	PMID:31533062
RADX	Human	temozolomide	decreases expression	EXP		6480464	Temozolomide results in decreased expression of RADX mRNA	CTD	PMID:31758290
RADX	Human	trichostatin A	increases expression	EXP		6480464	trichostatin A results in increased expression of RADX mRNA	CTD	PMID:24935251 and PMID:26272509
RADX	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 increased expression of RADX mRNA	CTD	PMID:27188386
RADX	Human	triphenyl phosphate	affects expression	EXP		6480464	triphenyl phosphate affects the expression of RADX mRNA	CTD	PMID:37042841
RADX	Human	trovafloxacin	decreases expression	ISO	Radx (Mus musculus)	6480464	trovafloxacin results in decreased expression of RADX mRNA	CTD	PMID:35537566
RADX	Human	valproic acid	decreases methylation	EXP		6480464	Valproic Acid results in decreased methylation of RADX gene	CTD	PMID:29154799
RADX	Human	valproic acid	decreases expression	EXP		6480464	Valproic Acid results in decreased expression of RADX mRNA	CTD	PMID:37505509
RADX	Human	valproic acid	affects expression	EXP		6480464	Valproic Acid affects the expression of RADX mRNA	CTD	PMID:25979313
RADX	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 increased expression of RADX mRNA	CTD	PMID:27188386
RADX	Human	valproic acid	increases expression	EXP		6480464	Valproic Acid results in increased expression of RADX mRNA	CTD	PMID:23179753 more ...
RADX	Human	vorinostat	increases expression	EXP		6480464	vorinostat results in increased expression of RADX mRNA	CTD	PMID:27188386
RADX	Human	zoledronic acid	decreases expression	EXP		6480464	zoledronic acid results in decreased expression of RADX mRNA	CTD	PMID:24714768

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)
RADX	Human	negative regulation of double-strand break repair via homologous recombination	involved_in	IDA		150520179	PMID:28735897	UniProt	PMID:28735897
RADX	Human	regulation of DNA repair	involved_in	IBA	PANTHER:PTN002308646 and UniProtKB:Q6NSI4	150520179		GO_Central	GO_REF:0000033

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)
RADX	Human	chromosome	located_in	IEA	UniProtKB-SubCell:SL-0468	150520179		UniProt	GO_REF:0000044
RADX	Human	chromosome	located_in	IEA	UniProtKB-KW:KW-0158	150520179		UniProt	GO_REF:0000043
RADX	Human	nuclear speck	located_in	IDA		150520179		HPA	GO_REF:0000052
RADX	Human	replication fork	located_in	IDA		150520179	PMID:28735897	UniProt	PMID:28735897
RADX	Human	replication fork	is_active_in	IBA	PANTHER:PTN002308646 and UniProtKB:Q6NSI4	150520179		GO_Central	GO_REF:0000033

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)
RADX	Human	DNA binding	enables	IEA	UniProtKB-KW:KW-0238	150520179		UniProt	GO_REF:0000043
RADX	Human	protein binding	enables	IPI	UniProtKB:P40692	150520179	PMID:21516116 more ...	IntAct	PMID:21516116 more ...
RADX	Human	protein binding	enables	IPI	UniProtKB:Q8IVD9	150520179	PMID:25036637	IntAct	PMID:25036637
RADX	Human	RNA binding	enables	HDA		150520179	PMID:22681889	UniProt	PMID:22681889
RADX	Human	single-stranded DNA binding	enables	IEA	InterPro:IPR040893	150520179		InterPro	GO_REF:0000002
RADX	Human	single-stranded DNA binding	enables	IBA	PANTHER:PTN002308646 and UniProtKB:Q6NSI4	150520179		GO_Central	GO_REF:0000033
RADX	Human	single-stranded DNA binding	enables	IDA		150520179	PMID:28735897	UniProt	PMID:28735897

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
RADX	Human	Autism		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Autism	ClinVar	PMID:21681106 and PMID:30208311

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

PMID:12477932	PMID:14702039	PMID:15489334	PMID:15772651	PMID:16344560	PMID:21516116	PMID:21873635	PMID:22681889	PMID:22990118	PMID:24550385	PMID:25036637	PMID:25416956
PMID:25476789	PMID:26972000	PMID:27173435	PMID:27229929	PMID:28735897	PMID:29021206	PMID:29568061	PMID:29845934	PMID:30021152	PMID:30425250	PMID:31240132	PMID:31300519
PMID:31515488	PMID:31665637	PMID:32296183	PMID:32807901	PMID:32941674	PMID:33060197	PMID:33453169	PMID:33722704	PMID:33961781	PMID:34079125	PMID:34597346	PMID:34672954
PMID:34702444	PMID:35120927	PMID:35140242	PMID:35271311	PMID:35509820	PMID:35915203	PMID:36089195	PMID:36114006	PMID:36538041	PMID:36912080	PMID:37314216	PMID:37317656
PMID:37689310	PMID:37827155	PMID:37848033	PMID:38177924	PMID:38580884

RADX
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	X	106,611,978 - 106,679,439 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	X	106,611,930 - 106,679,439 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	X	105,855,208 - 105,922,669 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	X	105,741,909 - 105,809,328 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	X	106,326,505 - 106,394,019 (+)	NCBI		Celera
Cytogenetic Map	X	q22.3	NCBI
HuRef	X	95,482,341 - 95,550,832 (+)	NCBI		HuRef
CHM1_1	X	105,765,982 - 105,833,494 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	X	105,048,421 - 105,115,882 (+)	NCBI		T2T-CHM13v2.0

Radx
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	X	138,381,116 - 138,455,333 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	X	138,381,116 - 138,455,331 (+)	Ensembl		GRCm39 Ensembl
GRCm38	X	139,480,367 - 139,554,584 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	X	139,480,367 - 139,554,582 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	X	136,014,906 - 136,089,119 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	X	134,826,807 - 134,900,944 (+)	NCBI		MGSCv36	mm8
Celera	X	122,741,905 - 122,816,200 (+)	NCBI		Celera
Cytogenetic Map	X	F1	NCBI
cM Map	X	61.35	NCBI

Radx
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	X	107,877,835 - 107,965,476 (+)	NCBI		GRCr8
mRatBN7.2	X	103,089,284 - 103,176,840 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	X	103,089,284 - 103,176,838 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	X	105,221,800 - 105,309,354 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	X	108,720,548 - 108,808,099 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	X	106,291,959 - 106,382,595 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	X	110,670,037 - 110,782,420 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	X	110,670,119 - 110,782,284 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	X	110,810,982 - 110,822,582 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
Rnor_5.0	X	110,711,917 - 110,792,572 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	X	127,170,527 - 127,215,710 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	X	103,855,291 - 103,941,542 (+)	NCBI		Celera
Cytogenetic Map	X	q32	NCBI

RADX
(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	X	106,097,529 - 106,164,854 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	X	106,101,130 - 106,168,455 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	X	95,714,600 - 95,781,853 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	X	106,092,394 - 106,159,716 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	X	106,092,340 - 106,159,772 (+)	Ensembl	panpan1.1		panPan2

RADX
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	X	80,146,335 - 80,234,732 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	X	80,146,040 - 80,235,739 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	X	66,262,981 - 66,351,404 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	X	81,780,985 - 81,869,803 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	X	81,780,959 - 81,869,801 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	X	79,251,983 - 79,340,421 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	X	80,960,658 - 81,049,418 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	X	80,740,823 - 80,829,269 (+)	NCBI		UU_Cfam_GSD_1.0

Radx
(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	X	79,535,640 - 79,598,991 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936499	8,058,972 - 8,122,287 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936499	8,058,973 - 8,122,332 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

RADX
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	X	87,025,603 - 87,103,501 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	X	87,025,603 - 87,103,503 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	X	101,460,402 - 101,480,736 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

RADX
(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	X	94,454,011 - 94,523,015 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	X	94,453,938 - 94,523,012 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666065	19,528,784 - 19,602,879 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Variants in RADX
9 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003242)x3	copy number gain	See cases [RCV000133911]	ChrX:10701..156003242 [GRCh38] ChrX:60701..155232907 [GRCh37] ChrX:701..154886101 [NCBI36] ChrX:Xp22.33-q28	pathogenic\|likely pathogenic\|conflicting data from submitters
GRCh38/hg38 Xp22.33-q28(chrX:3092486-155699618)x2	copy number gain	See cases [RCV000050889]	ChrX:3092486..155699618 [GRCh38] ChrX:3010527..154929279 [GRCh37] ChrX:3020527..154582473 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20140-155699618)x3	copy number gain	See cases [RCV000050810]	ChrX:20140..155699618 [GRCh38] ChrX:70140..154929279 [GRCh37] ChrX:10140..154582473 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20140-155699618)x1	copy number loss	See cases [RCV000050811]	ChrX:20140..155699618 [GRCh38] ChrX:70140..154929279 [GRCh37] ChrX:10140..154582473 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050385]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050385]\|See cases [RCV000050385]	ChrX:10679..156013167 [GRCh38] ChrX:60679..155242832 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x1	copy number loss	Global developmental delay [RCV000050386]\|See cases [RCV000050386]	ChrX:10679..156013167 [GRCh38] ChrX:60679..155242832 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x3	copy number gain	See cases [RCV000050697]	ChrX:10679..156022206 [GRCh38] ChrX:60679..155251871 [GRCh37] ChrX:679..154905065 [NCBI36] ChrX:Xp22.33-q28	pathogenic\|conflicting interpretations of pathogenicity\|conflicting data from submitters
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x1	copy number loss	See cases [RCV000050699]	ChrX:10679..156022206 [GRCh38] ChrX:60679..155251871 [GRCh37] ChrX:679..154905065 [NCBI36] ChrX:Xp22.33-q28	pathogenic\|conflicting interpretations of pathogenicity\|conflicting data from submitters
GRCh38/hg38 Xp11.21-q28(chrX:57372584-155996431)x1	copy number loss	See cases [RCV000051665]	ChrX:57372584..155996431 [GRCh38] ChrX:57399017..155226096 [GRCh37] ChrX:57415742..154879290 [NCBI36] ChrX:Xp11.21-q28	pathogenic
GRCh38/hg38 Xq11.1-28(chrX:63279794-155939524)x1	copy number loss	See cases [RCV000051666]	ChrX:63279794..155939524 [GRCh38] ChrX:62499671..155169188 [GRCh37] ChrX:62416396..154822382 [NCBI36] ChrX:Xq11.1-28	pathogenic
GRCh38/hg38 Xq21.1-23(chrX:77544283-110500317)x1	copy number loss	See cases [RCV000051668]	ChrX:77544283..110500317 [GRCh38] ChrX:76799762..109743545 [GRCh37] ChrX:76686418..109630201 [NCBI36] ChrX:Xq21.1-23	pathogenic
GRCh38/hg38 Xq22.1-28(chrX:100524562-155669954)x1	copy number loss	See cases [RCV000051713]	ChrX:100524562..155669954 [GRCh38] ChrX:99779559..154785891 [GRCh37] ChrX:99666215..154552809 [NCBI36] ChrX:Xq22.1-28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2790845-155699618)x3	copy number gain	See cases [RCV000052359]	ChrX:2790845..155699618 [GRCh38] ChrX:2708886..154929279 [GRCh37] ChrX:2718886..154582473 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:237659-156022362)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052327]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052327]\|See cases [RCV000052327]	ChrX:237659..156022362 [GRCh38] ChrX:154326..155252027 [GRCh37] ChrX:94326..154905221 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:27245-155996431)x3	copy number gain	See cases [RCV000052324]	ChrX:27245..155996431 [GRCh38] ChrX:77245..155226096 [GRCh37] ChrX:17245..154879290 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26101-155999293)x3	copy number gain	See cases [RCV000052322]	ChrX:26101..155999293 [GRCh38] ChrX:76101..155228958 [GRCh37] ChrX:16101..154882152 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:40704-156022362)x3	copy number gain	See cases [RCV000052325]	ChrX:40704..156022362 [GRCh38] ChrX:90704..155252027 [GRCh37] ChrX:30704..154905221 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xq21.1-25(chrX:81261589-126519353)x3	copy number gain	See cases [RCV000052438]	ChrX:81261589..126519353 [GRCh38] ChrX:80517088..125653336 [GRCh37] ChrX:80403744..125481017 [NCBI36] ChrX:Xq21.1-25	pathogenic
GRCh38/hg38 Xq22.1-22.3(chrX:101620923-107632397)x3	copy number gain	See cases [RCV000052441]	ChrX:101620923..107632397 [GRCh38] ChrX:100875913..106875627 [GRCh37] ChrX:100762569..106762283 [NCBI36] ChrX:Xq22.1-22.3	pathogenic
GRCh38/hg38 Xq22.1-22.3(chrX:102070552-108264804)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051716]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051716]\|See cases [RCV000051716]	ChrX:102070552..108264804 [GRCh38] ChrX:101325524..107508034 [GRCh37] ChrX:101212180..107394690 [NCBI36] ChrX:Xq22.1-22.3	pathogenic
GRCh38/hg38 Xq13.2-27.1(chrX:73008114-140201321)x4	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052418]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052418]\|See cases [RCV000052418]	ChrX:73008114..140201321 [GRCh38] ChrX:72227953..139283477 [GRCh37] ChrX:72144678..139111143 [NCBI36] ChrX:Xq13.2-27.1	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x1	copy number loss	Global developmental delay [RCV000052986]\|Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052987]\|Intellectual functioning disability [RCV000052988]\|Global developmental delay [RCV000052989]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052987]\|See cases [RCV000052986]	ChrX:26102..155996431 [GRCh38] ChrX:76102..155226096 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:14245-155999293)x1	copy number loss	Hypoplastic left heart [RCV000052982]\|See cases [RCV000052982]	ChrX:14245..155999293 [GRCh38] ChrX:64245..155228958 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x3	copy number gain	Global developmental delay [RCV000052984]\|Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052985]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052985]\|See cases [RCV000052984]	ChrX:26102..155996431 [GRCh38] ChrX:76102..155226096 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022826)x4	copy number gain	See cases [RCV000133654]	ChrX:10679..156022826 [GRCh38] ChrX:60679..155252491 [GRCh37] ChrX:679..154905685 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-155978689)x1	copy number loss	See cases [RCV000133792]	ChrX:10701..155978689 [GRCh38] ChrX:60701..155208354 [GRCh37] ChrX:701..154861548 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x3	copy number gain	See cases [RCV000050385]	ChrX:10679..156013167 [GRCh38] ChrX:60679..155242832 [GRCh37] ChrX:679..154896026 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x1	copy number loss	See cases [RCV000050386]	ChrX:10679..156013167 [GRCh38] ChrX:60679..155242832 [GRCh37] ChrX:679..154896026 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x1	copy number loss	See cases [RCV000052986]	ChrX:26102..155996431 [GRCh38] ChrX:76102..155226096 [GRCh37] ChrX:16102..154879290 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x3	copy number gain	See cases [RCV000052984]	ChrX:26102..155996431 [GRCh38] ChrX:76102..155226096 [GRCh37] ChrX:16102..154879290 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:14245-155999293)x1	copy number loss	See cases [RCV000052982]	ChrX:14245..155999293 [GRCh38] ChrX:64245..155228958 [GRCh37] ChrX:4245..154882152 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-155999253)x3	copy number gain	See cases [RCV000134564]	ChrX:20297..155999253 [GRCh38] ChrX:70297..155228918 [GRCh37] ChrX:10297..154882112 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xq21.1-28(chrX:78605009-156016560)x1	copy number loss	See cases [RCV000134570]	ChrX:78605009..156016560 [GRCh38] ChrX:77860506..155246225 [GRCh37] ChrX:77747162..154899419 [NCBI36] ChrX:Xq21.1-28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003242)x1	copy number loss	See cases [RCV000133947]	ChrX:10701..156003242 [GRCh38] ChrX:60701..155232907 [GRCh37] ChrX:701..154886101 [NCBI36] ChrX:Xp22.33-q28	pathogenic\|conflicting interpretations of pathogenicity\|conflicting data from submitters
GRCh38/hg38 Xq11.1-28(chrX:62712230-155978888)x3	copy number gain	See cases [RCV000134025]	ChrX:62712230..155978888 [GRCh38] ChrX:61931700..155208553 [GRCh37] ChrX:61848425..154861747 [NCBI36] ChrX:Xq11.1-28	pathogenic
GRCh38/hg38 Xp21.1-q28(chrX:37076284-156016920)x1	copy number loss	See cases [RCV000135300]	ChrX:37076284..156016920 [GRCh38] ChrX:37094357..155246585 [GRCh37] ChrX:37004278..154899779 [NCBI36] ChrX:Xp21.1-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-156026127)x1	copy number loss	See cases [RCV000135321]	ChrX:20297..156026127 [GRCh38] ChrX:70297..155255792 [GRCh37] ChrX:10297..154908986 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp21.1-q28(chrX:36237706-156022206)x1	copy number loss	See cases [RCV000135552]	ChrX:36237706..156022206 [GRCh38] ChrX:36255823..155251871 [GRCh37] ChrX:36165744..154905065 [NCBI36] ChrX:Xp21.1-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003229)x1	copy number loss	See cases [RCV000136097]	ChrX:10701..156003229 [GRCh38] ChrX:60701..155232894 [GRCh37] ChrX:701..154886088 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:40904-155998166)x1	copy number loss	See cases [RCV000136478]	ChrX:40904..155998166 [GRCh38] ChrX:90904..155227831 [GRCh37] ChrX:30904..154881025 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xq22.1-23(chrX:100597687-111651116)x4	copy number gain	See cases [RCV000136029]	ChrX:100597687..111651116 [GRCh38] ChrX:99852684..110894344 [GRCh37] ChrX:99739340..110781000 [NCBI36] ChrX:Xq22.1-23	pathogenic
GRCh38/hg38 Xp22.33-q25(chrX:10701-128393708)	copy number loss	See cases [RCV000136094]	ChrX:10701..128393708 [GRCh38] ChrX:60701..127527686 [GRCh37] ChrX:701..127355367 [NCBI36] ChrX:Xp22.33-q25	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10001-156030895)x1	copy number loss	See cases [RCV000136005]	ChrX:10001..156030895 [GRCh38] ChrX:60001..155260560 [GRCh37] ChrX:1..154913754 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xq21.1-28(chrX:79093152-156003229)x1	copy number loss	See cases [RCV000136083]	ChrX:79093152..156003229 [GRCh38] ChrX:78348649..155232894 [GRCh37] ChrX:78235305..154886088 [NCBI36] ChrX:Xq21.1-28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2765636-155522304)x3	copy number gain	See cases [RCV000136791]	ChrX:2765636..155522304 [GRCh38] ChrX:2683677..154751965 [GRCh37] ChrX:2693677..154405159 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2782275-155611794)x2	copy number gain	See cases [RCV000136841]	ChrX:2782275..155611794 [GRCh38] ChrX:2700316..154785891 [GRCh37] ChrX:2710316..154494649 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xq22.1-28(chrX:102197284-156003242)x1	copy number loss	See cases [RCV000137415]	ChrX:102197284..156003242 [GRCh38] ChrX:101452257..155232907 [GRCh37] ChrX:101338913..154886101 [NCBI36] ChrX:Xq22.1-28	pathogenic
GRCh38/hg38 Xq13.3-28(chrX:76604011-156022206)x1	copy number loss	See cases [RCV000137138]	ChrX:76604011..156022206 [GRCh38] ChrX:75824420..155251871 [GRCh37] ChrX:75740824..154905065 [NCBI36] ChrX:Xq13.3-28	pathogenic
GRCh38/hg38 Xq21.33-28(chrX:95846285-156003242)x3	copy number gain	See cases [RCV000138020]	ChrX:95846285..156003242 [GRCh38] ChrX:95101284..155232907 [GRCh37] ChrX:94987940..154886101 [NCBI36] ChrX:Xq21.33-28	pathogenic
GRCh38/hg38 Xq22.3-28(chrX:106127173-156003242)x1	copy number loss	See cases [RCV000137887]	ChrX:106127173..156003242 [GRCh38] ChrX:105371166..155232907 [GRCh37] ChrX:105257822..154886101 [NCBI36] ChrX:Xq22.3-28	pathogenic
GRCh38/hg38 Xp22.2-q27.3(chrX:13020141-143473520)x1	copy number loss	See cases [RCV000138678]	ChrX:13020141..143473520 [GRCh38] ChrX:13038260..142561303 [GRCh37] ChrX:12948181..142388969 [NCBI36] ChrX:Xp22.2-q27.3	pathogenic
GRCh38/hg38 Xq22.3-28(chrX:106465610-156003242)x1	copy number loss	See cases [RCV000138541]	ChrX:106465610..156003242 [GRCh38] ChrX:105708840..155232907 [GRCh37] ChrX:105595496..154886101 [NCBI36] ChrX:Xq22.3-28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:1085618-155699644)x1	copy number loss	See cases [RCV000139278]	ChrX:1085618..155699644 [GRCh38] ChrX:1118268..154929305 [GRCh37] ChrX:1038268..154582499 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xq11.1-28(chrX:62712219-156003242)x3	copy number gain	See cases [RCV000139416]	ChrX:62712219..156003242 [GRCh38] ChrX:61931689..155232907 [GRCh37] ChrX:61848414..154886101 [NCBI36] ChrX:Xq11.1-28	pathogenic\|likely benign
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004181)x3	copy number gain	See cases [RCV000139888]	ChrX:251880..156004181 [GRCh38] ChrX:168547..155233846 [GRCh37] ChrX:108547..154887040 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2299223-155992188)x3	copy number gain	See cases [RCV000141400]	ChrX:2299223..155992188 [GRCh38] ChrX:2217264..155221853 [GRCh37] ChrX:2227264..154875047 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-156016920)x3	copy number gain	See cases [RCV000141401]	ChrX:20297..156016920 [GRCh38] ChrX:70297..155246585 [GRCh37] ChrX:10297..154899779 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x4	copy number gain	See cases [RCV000140786]	ChrX:251880..156004066 [GRCh38] ChrX:168547..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x1	copy number loss	See cases [RCV000140787]	ChrX:251880..156004066 [GRCh38] ChrX:168547..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic\|conflicting data from submitters
GRCh38/hg38 Xq21.1-28(chrX:82096719-156004066)x1	copy number loss	See cases [RCV000141825]	ChrX:82096719..156004066 [GRCh38] ChrX:81352168..155233731 [GRCh37] ChrX:81238824..154886925 [NCBI36] ChrX:Xq21.1-28	pathogenic
GRCh38/hg38 Xq21.31-28(chrX:89557622-156004066)x1	copy number loss	See cases [RCV000142016]	ChrX:89557622..156004066 [GRCh38] ChrX:88812621..155233731 [GRCh37] ChrX:88699277..154886925 [NCBI36] ChrX:Xq21.31-28	pathogenic
GRCh38/hg38 Xp11.22-q24(chrX:50289384-119297604)	copy number loss	See cases [RCV000141742]	ChrX:50289384..119297604 [GRCh38] ChrX:50032384..118431567 [GRCh37] ChrX:50049124..118315595 [NCBI36] ChrX:Xp11.22-q24	pathogenic
GRCh38/hg38 Xq21.1-23(chrX:81109470-109442793)x1	copy number loss	See cases [RCV000142372]	ChrX:81109470..109442793 [GRCh38] ChrX:80364969..108686022 [GRCh37] ChrX:80251625..108572678 [NCBI36] ChrX:Xq21.1-23	pathogenic
GRCh38/hg38 Xq21.1-28(chrX:78187188-156004066)x1	copy number loss	See cases [RCV000142337]	ChrX:78187188..156004066 [GRCh38] ChrX:77442685..155233731 [GRCh37] ChrX:77329341..154886925 [NCBI36] ChrX:Xq21.1-28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003229)x3	copy number gain	See cases [RCV000142625]	ChrX:10701..156003229 [GRCh38] ChrX:60701..155232894 [GRCh37] ChrX:701..154886088 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xq13.2-28(chrX:74684615-156004066)x1	copy number loss	See cases [RCV000143424]	ChrX:74684615..156004066 [GRCh38] ChrX:73904450..155233731 [GRCh37] ChrX:73821175..154886925 [NCBI36] ChrX:Xq13.2-28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251879-156004066)x1	copy number loss	See cases [RCV000143441]	ChrX:251879..156004066 [GRCh38] ChrX:168546..155233731 [GRCh37] ChrX:108546..154886925 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251879-156004066)x3	copy number gain	See cases [RCV000143433]	ChrX:251879..156004066 [GRCh38] ChrX:168546..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x3	copy number gain	See cases [RCV000143219]	ChrX:251880..156004066 [GRCh38] ChrX:168547..155233731 [GRCh37] ChrX:108547..154886925 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x3	copy number gain	See cases [RCV000148141]	ChrX:10679..156022206 [GRCh38] ChrX:60679..155251871 [GRCh37] ChrX:679..154905065 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x1	copy number loss	See cases [RCV000148135]	ChrX:10679..156022206 [GRCh38] ChrX:60679..155251871 [GRCh37] ChrX:679..154905065 [NCBI36] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155246643)x3	copy number gain	See cases [RCV000240122]	ChrX:71267..155246643 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq11.1-28(chrX:62063537-155246643)x3	copy number gain	See cases [RCV000240143]	ChrX:62063537..155246643 [GRCh37] ChrX:Xq11.1-28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:176426-155250222)x3	copy number gain	See cases [RCV000239843]	ChrX:176426..155250222 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155255839)x1	copy number loss	See cases [RCV000239832]	ChrX:71267..155255839 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq22.1-24(chrX:99931059-120328627)x1	copy number loss	Premature ovarian failure [RCV000225336]	ChrX:99931059..120328627 [GRCh37] ChrX:Xq22.1-24	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x2	copy number gain	See cases [RCV000240106]	ChrX:150002..155234036 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155224766)x1	copy number loss	See cases [RCV000239902]	ChrX:71267..155224766 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155234036)x2	copy number gain	See cases [RCV000239874]	ChrX:71267..155234036 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:176426-155236656)x3	copy number gain	See cases [RCV000240552]	ChrX:176426..155236656 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x3	copy number gain	See cases [RCV000240314]	ChrX:150002..155234036 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:225816-155234036)x2	copy number gain	See cases [RCV000240464]	ChrX:225816..155234036 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq11.1-28(chrX:62063537-155250222)x3	copy number gain	See cases [RCV000240148]	ChrX:62063537..155250222 [GRCh37] ChrX:Xq11.1-28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:2707626-155250222)x2	copy number gain	See cases [RCV000240541]	ChrX:2707626..155250222 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:61545-155226048)x2	copy number gain	Klinefelter syndrome [RCV002282732]	ChrX:61545..155226048 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x3	copy number gain	See cases [RCV000449330]	ChrX:168546..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792)	copy number loss	See cases [RCV000449461]	ChrX:70297..155255792 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq21.33-28(chrX:94043221-155246585)x1	copy number loss	See cases [RCV000449365]	ChrX:94043221..155246585 [GRCh37] ChrX:Xq21.33-28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-154930047)x3	copy number gain	See cases [RCV000449437]	ChrX:168546..154930047 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60701-155246225)x3	copy number gain	See cases [RCV000446270]	ChrX:60701..155246225 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq13.1-28(chrX:68701338-155233731)x3	copy number gain	See cases [RCV000446471]	ChrX:68701338..155233731 [GRCh37] ChrX:Xq13.1-28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155255792)x1	copy number loss	See cases [RCV000446197]	ChrX:71267..155255792 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:318707-155224707)x1	copy number loss	See cases [RCV000446667]	ChrX:318707..155224707 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:2703632-155233731)x1	copy number loss	See cases [RCV000446712]	ChrX:2703632..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq13.3-28(chrX:74787886-155233731)x1	copy number loss	See cases [RCV000447490]	ChrX:74787886..155233731 [GRCh37] ChrX:Xq13.3-28	pathogenic
GRCh37/hg19 Xp11.1-q28(chrX:58140271-155046703)x3	copy number gain	See cases [RCV000446151]	ChrX:58140271..155046703 [GRCh37] ChrX:Xp11.1-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4	copy number gain	See cases [RCV000446932]	ChrX:168546..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155196888)x3	copy number gain	See cases [RCV000446310]	ChrX:168546..155196888 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155081533)x3	copy number gain	See cases [RCV000447253]	ChrX:168546..155081533 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:553069-155233731)x1	copy number loss	See cases [RCV000446026]	ChrX:553069..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168566-155233731)x1	copy number loss	See cases [RCV000445720]	ChrX:168566..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq22.3-28(chrX:105694656-155224707)x1	copy number loss	See cases [RCV000445891]	ChrX:105694656..155224707 [GRCh37] ChrX:Xq22.3-28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	copy number loss	See cases [RCV000448393]	ChrX:168546..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792)x4	copy number gain	See cases [RCV000448034]	ChrX:70297..155255792 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155246585)x1	copy number loss	See cases [RCV000448652]	ChrX:70297..155246585 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq22.2-23(chrX:103158718-111556067)x2	copy number gain	See cases [RCV000448592]	ChrX:103158718..111556067 [GRCh37] ChrX:Xq22.2-23	pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:55532799-150239235)x1	copy number loss	See cases [RCV000448870]	ChrX:55532799..150239235 [GRCh37] ChrX:Xp11.21-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168547-151304063)x1	copy number loss	See cases [RCV000510382]	ChrX:168547..151304063 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q23(chrX:168547-112474026)x1	copy number loss	See cases [RCV000510419]	ChrX:168547..112474026 [GRCh37] ChrX:Xp22.33-q23	pathogenic
GRCh37/hg19 Xq21.1-28(chrX:79862302-155233731)x1	copy number loss	See cases [RCV000511482]	ChrX:79862302..155233731 [GRCh37] ChrX:Xq21.1-28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168547-155233731)	copy number gain	See cases [RCV000512020]	ChrX:168547..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq21.31-28(chrX:86900388-155233731)x1	copy number loss	See cases [RCV000511490]	ChrX:86900388..155233731 [GRCh37] ChrX:Xq21.31-28	pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:57511767-155233731)x3	copy number gain	See cases [RCV000510826]	ChrX:57511767..155233731 [GRCh37] ChrX:Xp11.21-q28	pathogenic
GRCh37/hg19 Xq21.1-28(chrX:78230501-155233731)x1	copy number loss	See cases [RCV000510820]	ChrX:78230501..155233731 [GRCh37] ChrX:Xq21.1-28	pathogenic
Single allele	duplication	Syndromic X-linked intellectual disability Lubs type [RCV000768455]	ChrX:15323210..153542100 [GRCh37] ChrX:Xp22.2-q28	pathogenic
GRCh37/hg19 Xq21.33-28(chrX:96499476-151870013)x3	copy number gain	See cases [RCV000512365]	ChrX:96499476..151870013 [GRCh37] ChrX:Xq21.33-28	uncertain significance
GRCh37/hg19 Xq22.1-28(chrX:98495811-155233731)x1	copy number loss	See cases [RCV000512372]	ChrX:98495811..155233731 [GRCh37] ChrX:Xq22.1-28	pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:57415659-155233731)x3	copy number gain	See cases [RCV000512173]	ChrX:57415659..155233731 [GRCh37] ChrX:Xp11.21-q28	pathogenic
GRCh37/hg19 Xq21.31-28(chrX:91140025-155233731)x1	copy number loss	not provided [RCV000684357]	ChrX:91140025..155233731 [GRCh37] ChrX:Xq21.31-28	pathogenic
GRCh37/hg19 Xq22.1-28(chrX:99324651-155233731)x1	copy number loss	not provided [RCV000684363]	ChrX:99324651..155233731 [GRCh37] ChrX:Xq22.1-28	pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:54941868-155233731)x1	copy number loss	not provided [RCV000848218]	ChrX:54941868..155233731 [GRCh37] ChrX:Xp11.21-q28	uncertain significance
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	copy number loss	not provided [RCV000848828]	ChrX:168546..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq22.3(chrX:105351445-106074607)x3	copy number gain	not provided [RCV000753698]	ChrX:105351445..106074607 [GRCh37] ChrX:Xq22.3	benign
GRCh37/hg19 Xq22.3(chrX:105807192-105861659)x0	copy number loss	not provided [RCV000753700]	ChrX:105807192..105861659 [GRCh37] ChrX:Xq22.3	benign
GRCh37/hg19 Xp22.33-q28(chrX:60814-155254881)x2	copy number gain	not provided [RCV000753277]	ChrX:60814..155254881 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq13.2-28(chrX:73472626-155254881)x1	copy number loss	not provided [RCV000753606]	ChrX:73472626..155254881 [GRCh37] ChrX:Xq13.2-28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:181779-155171702)x1	copy number loss	not provided [RCV000753278]	ChrX:181779..155171702 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60262-155245765)x3	copy number gain	not provided [RCV000753272]	ChrX:60262..155245765 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60814-155236712)x2	copy number gain	not provided [RCV000753276]	ChrX:60814..155236712 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60262-155245765)x1	copy number loss	not provided [RCV000753271]	ChrX:60262..155245765 [GRCh37] ChrX:Xp22.33-q28	pathogenic
Single allele	duplication	Autism [RCV000754365]	ChrX:1..156040895 [GRCh38] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq11.1-28(chrX:61694576-155254881)x1	copy number loss	not provided [RCV000753556]	ChrX:61694576..155254881 [GRCh37] ChrX:Xq11.1-28	pathogenic
NC_000023.10:g.36649710_136649711del100000002insG	indel	Heterotaxy, visceral, 1, X-linked [RCV000754886]	ChrX:36649710..136649711 [GRCh37] ChrX:Xp21.1-q26.3	pathogenic
GRCh37/hg19 Xq22.1-22.3(chrX:101029649-106702784)x1	copy number loss	Early Onset Neurological Disease Trait [RCV000993775]	ChrX:101029649..106702784 [GRCh37] ChrX:Xq22.1-22.3	pathogenic
NM_018015.6(RADX):c.458T>C (p.Val153Ala)	single nucleotide variant	not provided [RCV000901862]	ChrX:106612538 [GRCh38] ChrX:105855768 [GRCh37] ChrX:Xq22.3	benign
GRCh37/hg19 Xq21.1-28(chrX:84387417-155233731)x1	copy number loss	not provided [RCV001007322]	ChrX:84387417..155233731 [GRCh37] ChrX:Xq21.1-28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4	copy number gain	not provided [RCV000846039]	ChrX:168546..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq22.3-28(chrX:104098124-155233731)x1	copy number loss	not provided [RCV000846958]	ChrX:104098124..155233731 [GRCh37] ChrX:Xq22.3-28	pathogenic
GRCh37/hg19 Xq21.32-28(chrX:92814516-155233731)x1	copy number loss	not provided [RCV000845672]	ChrX:92814516..155233731 [GRCh37] ChrX:Xq21.32-28	pathogenic
GRCh37/hg19 Xp11.1-q28(chrX:58455352-155233731)x1	copy number loss	not provided [RCV000846274]	ChrX:58455352..155233731 [GRCh37] ChrX:Xp11.1-q28	pathogenic
GRCh37/hg19 Xq21.32-23(chrX:91829757-113050225)x1	copy number loss	Xq21.32q23 deletion [RCV001579312]	ChrX:91829757..113050225 [GRCh37] ChrX:Xq21.32-23	pathogenic
NM_018015.6(RADX):c.999A>C (p.Arg333=)	single nucleotide variant	not provided [RCV000888269]	ChrX:106632644 [GRCh38] ChrX:105875874 [GRCh37] ChrX:Xq22.3	benign
GRCh37/hg19 Xq22.3(chrX:105730612-107162289)x3	copy number gain	not provided [RCV002473830]	ChrX:105730612..107162289 [GRCh37] ChrX:Xq22.3	uncertain significance
GRCh37/hg19 Xp22.33-q28(chrX:60000-155234966)x1	copy number loss	not provided [RCV001537933]	ChrX:60000..155234966 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq21.33-28(chrX:94264404-155233731)x1	copy number loss	not provided [RCV001259012]	ChrX:94264404..155233731 [GRCh37] ChrX:Xq21.33-28	pathogenic
GRCh37/hg19 Xq21.1-25(chrX:77514079-127770854)x1	copy number loss	not provided [RCV001259005]	ChrX:77514079..127770854 [GRCh37] ChrX:Xq21.1-25	pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:55507789-155198481)x3	copy number gain	See cases [RCV001263024]	ChrX:55507789..155198481 [GRCh37] ChrX:Xp11.21-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)	copy number loss	Turner syndrome [RCV002280668]	ChrX:1..155270560 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq11.1-28(chrX:62685885-155233731)	copy number loss	Turner syndrome [RCV002280672]	ChrX:62685885..155233731 [GRCh37] ChrX:Xq11.1-28	pathogenic
GRCh37/hg19 Xq21.1-28(chrX:77670699-155233731)x1	copy number loss	See cases [RCV002285075]	ChrX:77670699..155233731 [GRCh37] ChrX:Xq21.1-28	pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:56469080-155233731)x3	copy number gain	not provided [RCV001281359]	ChrX:56469080..155233731 [GRCh37] ChrX:Xp11.21-q28	pathogenic
GRCh37/hg19 Xq22.2-23(chrX:103158718-111556067)	copy number gain	not specified [RCV002053170]	ChrX:103158718..111556067 [GRCh37] ChrX:Xq22.2-23	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x3	copy number gain	not provided [RCV001829212]	ChrX:168546..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq22.3(chrX:105522460-105932964)x3	copy number gain	not provided [RCV001827782]	ChrX:105522460..105932964 [GRCh37] ChrX:Xq22.3	likely benign
GRCh37/hg19 Xq22.1-24(chrX:101982475-116885339)	copy number gain	not specified [RCV002053166]	ChrX:101982475..116885339 [GRCh37] ChrX:Xq22.1-24	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:200855-155240074)	copy number gain	Klinefelter syndrome [RCV003236730]	ChrX:200855..155240074 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)	copy number gain	46,XX sex reversal 1 [RCV002280665]\|Hypotonia [RCV002280667]\|Trisomy X syndrome [RCV002280666]	ChrX:1..155270560 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.2-q28(chrX:11522765-155233731)x1	copy number loss	See cases [RCV002286357]	ChrX:11522765..155233731 [GRCh37] ChrX:Xp22.2-q28	pathogenic
GRCh37/hg19 Xq21.1-24(chrX:76794355-119282836)x3	copy number gain	not provided [RCV002291535]	ChrX:76794355..119282836 [GRCh37] ChrX:Xq21.1-24	pathogenic
GRCh37/hg19 Xq22.3(chrX:105652108-106324639)x3	copy number gain	not provided [RCV002474758]	ChrX:105652108..106324639 [GRCh37] ChrX:Xq22.3	uncertain significance
GRCh37/hg19 Xq21.33-24(chrX:93805850-118913329)x1	copy number loss	not provided [RCV002474518]	ChrX:93805850..118913329 [GRCh37] ChrX:Xq21.33-24	pathogenic
GRCh37/hg19 Xq22.3(chrX:105066840-106486528)	copy number loss	Primary ciliary dyskinesia [RCV003236732]	ChrX:105066840..106486528 [GRCh37] ChrX:Xq22.3	likely pathogenic
GRCh37/hg19 Xq21.31-25(chrX:91274467-126799984)x1	copy number loss	not provided [RCV003483927]	ChrX:91274467..126799984 [GRCh37] ChrX:Xq21.31-25	pathogenic
GRCh37/hg19 Xq21.33-22.3(chrX:96349060-106950847)x3	copy number gain	not provided [RCV003485308]	ChrX:96349060..106950847 [GRCh37] ChrX:Xq21.33-22.3	pathogenic
NM_018015.6(RADX):c.980-8T>C	single nucleotide variant	not provided [RCV003432309]	ChrX:106632617 [GRCh38] ChrX:105875847 [GRCh37] ChrX:Xq22.3	likely benign
NM_018015.6(RADX):c.1842T>C (p.Thr614=)	single nucleotide variant	not provided [RCV003432311]	ChrX:106640659 [GRCh38] ChrX:105883889 [GRCh37] ChrX:Xq22.3	likely benign
NM_018015.6(RADX):c.2099G>A (p.Arg700His)	single nucleotide variant	not provided [RCV003432313]	ChrX:106662135 [GRCh38] ChrX:105905365 [GRCh37] ChrX:Xq22.3	likely benign
NM_018015.6(RADX):c.2411G>A (p.Arg804Gln)	single nucleotide variant	not provided [RCV003432314]	ChrX:106669304 [GRCh38] ChrX:105912534 [GRCh37] ChrX:Xq22.3	likely benign
NM_018015.6(RADX):c.1293T>C (p.Asn431=)	single nucleotide variant	not provided [RCV003432310]	ChrX:106633242 [GRCh38] ChrX:105876472 [GRCh37] ChrX:Xq22.3	likely benign
NM_018015.6(RADX):c.1899T>A (p.Ala633=)	single nucleotide variant	not provided [RCV003432312]	ChrX:106640716 [GRCh38] ChrX:105883946 [GRCh37] ChrX:Xq22.3	likely benign
GRCh37/hg19 Xq12-28(chrX:67292994-155240074)x3	copy number gain	not provided [RCV003885530]	ChrX:67292994..155240074 [GRCh37] ChrX:Xq12-28	pathogenic
NM_018015.6(RADX):c.1829A>G (p.Gln610Arg)	single nucleotide variant	not specified [RCV004445547]	ChrX:106640646 [GRCh38] ChrX:105883876 [GRCh37] ChrX:Xq22.3	uncertain significance
GRCh38/hg38 Xp22.33-q28(chrX:2757837-156030895)x2	copy number gain	Klinefelter syndrome [RCV004579655]	ChrX:2757837..156030895 [GRCh38] ChrX:Xp22.33-q28	pathogenic
NC_000023.10:g.(?_54610638)_(154689386_?)dup	duplication	Hereditary factor VIII deficiency disease [RCV004768478]	ChrX:54610638..154689386 [GRCh37] ChrX:Xp11.22-q28	uncertain significance
GRCh37/hg19 Xq21.31-23(chrX:91004293-111532472)x1	copy number loss	not provided [RCV004819414]	ChrX:91004293..111532472 [GRCh37] ChrX:Xq21.31-23	pathogenic
GRCh37/hg19 Xq21.32-26.1(chrX:92712119-129831493)x1	copy number loss	not provided [RCV004819415]	ChrX:92712119..129831493 [GRCh37] ChrX:Xq21.32-26.1	pathogenic
GRCh37/hg19 Xq22.2-28(chrX:103405294-155233731)	copy number loss	not specified [RCV003986202]	ChrX:103405294..155233731 [GRCh37] ChrX:Xq22.2-28	pathogenic
GRCh38/hg38 Xq21.1-28(chrX:85123740-156022206)x3	copy number gain	See cases [RCV000133744]	ChrX:85123740..156022206 [GRCh38] ChrX:84378746..155251871 [GRCh37] ChrX:84265402..154905065 [NCBI36] ChrX:Xq21.1-28	pathogenic
GRCh38/hg38 Xq21.31-28(chrX:92222680-156016920)x1	copy number loss	See cases [RCV000135307]	ChrX:92222680..156016920 [GRCh38] ChrX:91477679..155246585 [GRCh37] ChrX:91364335..154899779 [NCBI36] ChrX:Xq21.31-28	pathogenic
GRCh38/hg38 Xq13.2-28(chrX:74510116-156022206)x1	copy number loss	See cases [RCV000134958]	ChrX:74510116..156022206 [GRCh38] ChrX:73729951..155251871 [GRCh37] ChrX:73646676..154905065 [NCBI36] ChrX:Xq13.2-28	pathogenic
GRCh38/hg38 Xq21.1-28(chrX:77369933-156013167)x1	copy number loss	See cases [RCV000135454]	ChrX:77369933..156013167 [GRCh38] ChrX:76634813..155242832 [GRCh37] ChrX:76507069..154896026 [NCBI36] ChrX:Xq21.1-28	pathogenic
GRCh38/hg38 Xq21.33-28(chrX:94462929-156001635)x3	copy number gain	See cases [RCV000136552]	ChrX:94462929..156001635 [GRCh38] ChrX:93717928..155231300 [GRCh37] ChrX:93604584..154884494 [NCBI36] ChrX:Xq21.33-28	pathogenic
GRCh38/hg38 Xq13.3-28(chrX:75086417-156022206)x1	copy number loss	See cases [RCV000137113]	ChrX:75086417..156022206 [GRCh38] ChrX:74306252..155251871 [GRCh37] ChrX:74222977..154905065 [NCBI36] ChrX:Xq13.3-28	pathogenic
GRCh38/hg38 Xq11.1-28(chrX:62561604-156003242)x3	copy number gain	See cases [RCV000137553]	ChrX:62561604..156003242 [GRCh38] ChrX:61781074..155232907 [GRCh37] ChrX:61697799..154886101 [NCBI36] ChrX:Xq11.1-28	pathogenic
GRCh38/hg38 Xq21.1-28(chrX:79911061-156003229)x1	copy number loss	See cases [RCV000138787]	ChrX:79911061..156003229 [GRCh38] ChrX:79166568..155232894 [GRCh37] ChrX:79053224..154886088 [NCBI36] ChrX:Xq21.1-28	pathogenic
GRCh38/hg38 Xq21.1-28(chrX:82211310-156003229)x1	copy number loss	See cases [RCV000139400]	ChrX:82211310..156003229 [GRCh38] ChrX:81466759..155232894 [GRCh37] ChrX:81353415..154886088 [NCBI36] ChrX:Xq21.1-28	pathogenic
GRCh38/hg38 Xq21.31-28(chrX:88339926-156003242)x1	copy number loss	See cases [RCV000139351]	ChrX:88339926..156003242 [GRCh38] ChrX:87594927..155232907 [GRCh37] ChrX:87481583..154886101 [NCBI36] ChrX:Xq21.31-28	pathogenic\|likely benign
GRCh38/hg38 Xq21.32-23(chrX:93591590-112530092)x3	copy number gain	See cases [RCV000139204]	ChrX:93591590..112530092 [GRCh38] ChrX:92846589..111773320 [GRCh37] ChrX:92733245..111659976 [NCBI36] ChrX:Xq21.32-23	pathogenic
GRCh38/hg38 Xq21.2-28(chrX:86626431-156004066)x1	copy number loss	See cases [RCV000142037]	ChrX:86626431..156004066 [GRCh38] ChrX:85881434..155233731 [GRCh37] ChrX:85768090..154886925 [NCBI36] ChrX:Xq21.2-28	pathogenic
GRCh38/hg38 Xp22.33-q24(chrX:251879-118847157)x3	copy number gain	See cases [RCV000142134]	ChrX:251879..118847157 [GRCh38] ChrX:168546..117981120 [GRCh37] ChrX:108546..117865148 [NCBI36] ChrX:Xp22.33-q24	pathogenic
GRCh38/hg38 Xp11.22-q28(chrX:53144751-156003242)x1	copy number loss	See cases [RCV000143349]	ChrX:53144751..156003242 [GRCh38] ChrX:53321095..155232907 [GRCh37] ChrX:53190658..154886101 [NCBI36] ChrX:Xp11.22-q28	pathogenic
GRCh38/hg38 Xq13.3-28(chrX:76557425-156004066)x1	copy number loss	See cases [RCV000143132]	ChrX:76557425..156004066 [GRCh38] ChrX:75777833..155233731 [GRCh37] ChrX:75694237..154886925 [NCBI36] ChrX:Xq13.3-28	pathogenic
GRCh37/hg19 Xp22.2-q28(chrX:13147668-155250222)x3	copy number gain	See cases [RCV000239798]	ChrX:13147668..155250222 [GRCh37] ChrX:Xp22.2-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60701-155246271)x3	copy number gain	See cases [RCV000239989]	ChrX:60701..155246271 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255839)x3	copy number gain	See cases [RCV000239934]	ChrX:70297..155255839 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xp22.2-q25(chrX:11692290-121187337)x2	copy number gain	not provided [RCV000488046]	ChrX:11692290..121187337 [GRCh37] ChrX:Xp22.2-q25	uncertain significance
GRCh37/hg19 Xq21.33-26.1(chrX:95498487-129063677)x3	copy number gain	See cases [RCV000446318]	ChrX:95498487..129063677 [GRCh37] ChrX:Xq21.33-26.1	pathogenic
GRCh37/hg19 Xq13.2-27.1(chrX:72224362-139262228)x4	copy number gain	See cases [RCV000448394]	ChrX:72224362..139262228 [GRCh37] ChrX:Xq13.2-27.1	pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:55000501-155230750)x3	copy number gain	See cases [RCV000511787]	ChrX:55000501..155230750 [GRCh37] ChrX:Xp11.21-q28	pathogenic
GRCh37/hg19 Xq21.31-23(chrX:86776682-114054291)x1	copy number loss	See cases [RCV000511514]	ChrX:86776682..114054291 [GRCh37] ChrX:Xq21.31-23	pathogenic\|uncertain significance
GRCh37/hg19 Xp21.2-q28(chrX:31088082-155233731)x1	copy number loss	See cases [RCV000511413]	ChrX:31088082..155233731 [GRCh37] ChrX:Xp21.2-q28	pathogenic\|uncertain significance
GRCh37/hg19 Xp11.21-q28(chrX:56457791-155233731)x3	copy number gain	See cases [RCV000511307]	ChrX:56457791..155233731 [GRCh37] ChrX:Xp11.21-q28	pathogenic
GRCh37/hg19 Xq13.3-24(chrX:74560735-116609286)	copy number loss	See cases [RCV000510947]	ChrX:74560735..116609286 [GRCh37] ChrX:Xq13.3-24	pathogenic
GRCh37/hg19 Xq21.1-28(chrX:78444738-155233731)x1	copy number loss	not provided [RCV001007318]	ChrX:78444738..155233731 [GRCh37] ChrX:Xq21.1-28	pathogenic
GRCh37/hg19 Xq22.3-23(chrX:104782507-112949573)x2	copy number gain	not provided [RCV001795543]	ChrX:104782507..112949573 [GRCh37] ChrX:Xq22.3-23	likely pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	copy number loss	not provided [RCV001834509]	ChrX:168546..155233731 [GRCh37] ChrX:Xp22.33-q28	pathogenic
GRCh37/hg19 Xq21.1-24(chrX:77212972-118576590)x3	copy number gain	not provided [RCV003485304]	ChrX:77212972..118576590 [GRCh37] ChrX:Xq21.1-24	pathogenic

Predicted Target Of

	Summary Value
Count of predictions:	2576
Count of miRNA genes:	872
Interacting mature miRNAs:	1015
Transcripts:	ENST00000372544, ENST00000372548, ENST00000421550, ENST00000461251, ENST00000478395, ENST00000497124
Prediction methods:	Microtar, Miranda, Pita, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597065317	GWAS1161391_H	alcoholic pancreatitis QTL GWAS1161391 (human)		0.000005	alcoholic pancreatitis		X	106631560	106631561	Human
597349456	GWAS1445530_H	triiodothyronine measurement QTL GWAS1445530 (human)		3e-09	blood triiodothyronine amount (VT:0005476)	blood triiodothyronine level (CMO:0001291)	X	106614655	106614656	Human

SHGC-53457

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	X	105,922,455 - 105,922,571	UniSTS	GRCh37
Build 36	X	105,809,111 - 105,809,227	RGD	NCBI36
Celera	X	106,393,801 - 106,393,917	RGD
Cytogenetic Map	X	q22.3	UniSTS
HuRef	X	95,550,614 - 95,550,730	UniSTS

L18426

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	18	q12.1-q21.1	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	2	q37	UniSTS
Cytogenetic Map	5	q31.3	UniSTS
Cytogenetic Map	20	q13.1	UniSTS
Cytogenetic Map	14	q21	UniSTS
Cytogenetic Map	6	p21.33	UniSTS
Cytogenetic Map	10	p11	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	2	q37.1	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	14	q21.3	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	3	q13.31	UniSTS
Cytogenetic Map	15	q22.2	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	9	p13.2	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	9	q34.1	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	1	p22.1	UniSTS
Cytogenetic Map	19	q13.31	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	19	p13.1-p12	UniSTS
Cytogenetic Map	18	p11.31-p11.21	UniSTS
Cytogenetic Map	2	p23.1	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	6	q25.3	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	11	q14	UniSTS
Cytogenetic Map	9	q21.32	UniSTS
Cytogenetic Map	1	p34-p33	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	17	q21.1	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	2	q12.3	UniSTS
Cytogenetic Map	20	q11.2-q13.2	UniSTS
Cytogenetic Map	15	q26.3	UniSTS
Cytogenetic Map	8	p23-p22	UniSTS
Cytogenetic Map	13	q32.3	UniSTS
Cytogenetic Map	17	q21-q22	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	5	p13	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	12	q21.1	UniSTS
Cytogenetic Map	3	q26.32	UniSTS
Cytogenetic Map	13	q11	UniSTS
Cytogenetic Map	1	p35.3	UniSTS
Cytogenetic Map	7	p12.3	UniSTS
Cytogenetic Map	17	p12	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	13	q14.11	UniSTS
Cytogenetic Map	3	p25.1	UniSTS
Cytogenetic Map	X	p22	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	17	q11.2-q12	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	2	p25	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	7	p22	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	1	p21.3	UniSTS
Cytogenetic Map	19	q13.13	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	20	q13.3	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	6	p22.3-p22.1	UniSTS
Cytogenetic Map	1	p35-p34.3	UniSTS
Cytogenetic Map	5	q35.1	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	12	p13.3	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	X	p11	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	2	q32.3	UniSTS
Cytogenetic Map	4	q22.1-q23	UniSTS
Cytogenetic Map	1	q22	UniSTS
Cytogenetic Map	17	q22-q23.2	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	18	q22.3	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	12	q24.1-q24.3	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	1	p34.1	UniSTS
Cytogenetic Map	22	q13	UniSTS
Cytogenetic Map	12	q22	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	X	q22.3	UniSTS
Cytogenetic Map	3	q13.13	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	3	q27.3	UniSTS
Cytogenetic Map	17	q21.32	UniSTS
Cytogenetic Map	2	q35	UniSTS
Cytogenetic Map	9	p24.2	UniSTS
Cytogenetic Map	14	q32.11	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	15	q23	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	3	p22.1	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	1	p31.3	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	14	q23	UniSTS
Cytogenetic Map	1	q42.1-q43	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	1	p32	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	6	q25.1-q26	UniSTS
Cytogenetic Map	5	q13	UniSTS
Cytogenetic Map	12	q13.11-q14.3	UniSTS
Cytogenetic Map	7	p11	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	17	q23.1	UniSTS
Cytogenetic Map	X	q13-q21	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	10	q22.1	UniSTS
Cytogenetic Map	1	q41	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	3	q28-q29	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	1	q41-q42.2	UniSTS
Cytogenetic Map	12	q24.2-q24.31	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	11	p11.11	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	1	q43	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	10	q11.21	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	8	q11.2	UniSTS
Cytogenetic Map	15	q11-q13	UniSTS
Cytogenetic Map	13	q12-q14	UniSTS
Cytogenetic Map	18	q21.1	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	22	q13.31	UniSTS
Cytogenetic Map	14	q24.1	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	1	q44	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	10	q26.3	UniSTS
Cytogenetic Map	13	q32.2	UniSTS
Cytogenetic Map	5	q11.2	UniSTS
Cytogenetic Map	11	p15.1	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	2	q23.3	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	10	q25.3	UniSTS
Cytogenetic Map	14	q31	UniSTS
Cytogenetic Map	8	p12-p11	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	8	p11.2	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	15	q26.1	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	17	q23.2	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	21	q22.1	UniSTS
Cytogenetic Map	4	q25-q27	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	3	q25.31	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	1	p36.22	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	3	p22-p21.3	UniSTS
Cytogenetic Map	2	p15-p13	UniSTS
Cytogenetic Map	X	p11.4	UniSTS
Cytogenetic Map	20	p11	UniSTS
Cytogenetic Map	3	p14.1	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	13	q11-q12	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	7	q21.13	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	3	q12	UniSTS
Cytogenetic Map	2	p25.1-p24.1	UniSTS
Cytogenetic Map	16	p13.11	UniSTS
Cytogenetic Map	6	q16.1	UniSTS
Cytogenetic Map	13	q14.13	UniSTS
Cytogenetic Map	5	p13.1	UniSTS
Cytogenetic Map	4	q28-q32	UniSTS
Cytogenetic Map	11	p15	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	1	p32-p31	UniSTS
Cytogenetic Map	1	p21	UniSTS
Cytogenetic Map	7	p14.2	UniSTS
Cytogenetic Map	6	q25	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	18	p11.22	UniSTS
Cytogenetic Map	9	p24.3	UniSTS
Cytogenetic Map	2	p25.3	UniSTS
Cytogenetic Map	1	q42.3	UniSTS
Cytogenetic Map	1	q22-q23	UniSTS
Cytogenetic Map	4	q21.22	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
Cytogenetic Map	2	q24.3	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	9	q31-q33	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	10	p11.21	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	3	q21.1	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	9	q22.1-q22.2	UniSTS
Cytogenetic Map	4	q26	UniSTS
Cytogenetic Map	4	q28.1	UniSTS
Cytogenetic Map	9	q31.3	UniSTS
Cytogenetic Map	6	p22.3	UniSTS
Cytogenetic Map	21	q21.1	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	15	q26.2	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	12	p12.3	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	20	q11.23	UniSTS
Cytogenetic Map	12	q13.11	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	5	q33.3	UniSTS
Cytogenetic Map	5	p13.2	UniSTS
Cytogenetic Map	4	q35.2	UniSTS
Cytogenetic Map	4	q28.2	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	12	q23.1	UniSTS
Cytogenetic Map	11	q24.3	UniSTS
Cytogenetic Map	10	q24.32	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	20	q13.2	UniSTS
Cytogenetic Map	8	q23.3	UniSTS
Cytogenetic Map	16	q23.2	UniSTS
Cytogenetic Map	3	p22.2	UniSTS
Cytogenetic Map	X	p21.1	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	X	p11.23	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	5	p15.3	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	22	q12	UniSTS
Cytogenetic Map	4	q22	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	19	q13.1-q13.2	UniSTS
Cytogenetic Map	1	p36.3	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	2	q32.1	UniSTS
Cytogenetic Map	7	q31.3	UniSTS
Cytogenetic Map	5	q33.1	UniSTS
Cytogenetic Map	13	q13.1	UniSTS
Cytogenetic Map	8	p23.1	UniSTS
Cytogenetic Map	15	q	UniSTS
Cytogenetic Map	3	p26	UniSTS
Cytogenetic Map	1	p13-p12	UniSTS
Cytogenetic Map	21	q22.11	UniSTS
Cytogenetic Map	14	q32.2	UniSTS
Cytogenetic Map	15	q24.1	UniSTS
Cytogenetic Map	4	p16.1	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	3	p25.2	UniSTS
Cytogenetic Map	7	p22.3	UniSTS
Cytogenetic Map	10	q21.1	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	1	p36	UniSTS
Cytogenetic Map	1	q25	UniSTS
Cytogenetic Map	15	q24	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	20	p11.21	UniSTS
Cytogenetic Map	12	q24.1	UniSTS
Cytogenetic Map	5	q31.2	UniSTS
Cytogenetic Map	2	p25.2	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	4	q12	UniSTS
Cytogenetic Map	1	q12	UniSTS
Cytogenetic Map	22	q11.22	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	14	q32.3	UniSTS
Cytogenetic Map	7	q32	UniSTS
Cytogenetic Map	5	q14.1	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	14	q23.3	UniSTS
Cytogenetic Map	1	q24	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	5	p15.33	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	16	p13.13-p13.12	UniSTS
Cytogenetic Map	12	p13.31	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	3	q27	UniSTS
Cytogenetic Map	6	q22	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	15	q15	UniSTS
Cytogenetic Map	1	p13.1	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	16	q13	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	13	q34	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	13	q14.3	UniSTS
Cytogenetic Map	14	q24	UniSTS
Cytogenetic Map	14	q22-q24	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	X	p22.2	UniSTS
Cytogenetic Map	8	q13.1	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	12	p12.1	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	4	q35.1	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	1	p22	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	10	q11	UniSTS
Cytogenetic Map	8	p11.21	UniSTS
Cytogenetic Map	8	q24.11	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	9	q22.33	UniSTS
Cytogenetic Map	9	q22.31	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	20	q12	UniSTS
Cytogenetic Map	2	q13	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	12	q21.31	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	19	q12	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	11	q14.2	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	X	q21.1	UniSTS
Cytogenetic Map	9	p21.1	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	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2425	2788	2244	4958	1720	2335	5	620	1884	463	2269	7211	6398	50	3719	839	1706	1602	172	1


RefSeq Transcripts	NG_021317	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001184782	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_018015	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047442233	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054327345	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001755707	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AK001040	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK024253	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK291730	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL590808	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL606833	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC011483	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC033709	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC047503	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC054032	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC070110	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471120	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068255	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB065928	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000372544 ⟹ ENSP00000361623

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	X	106,611,930 - 106,679,437 (+)	Ensembl

Ensembl Acc Id:

ENST00000372548 ⟹ ENSP00000361628

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	X	106,611,978 - 106,679,439 (+)	Ensembl

Ensembl Acc Id:

ENST00000421550 ⟹ ENSP00000405866

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	X	106,612,657 - 106,679,437 (+)	Ensembl

Ensembl Acc Id:

ENST00000461251 ⟹ ENSP00000432238

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	X	106,611,975 - 106,638,678 (+)	Ensembl

Ensembl Acc Id:

ENST00000478395

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	X	106,639,294 - 106,640,582 (+)	Ensembl

Ensembl Acc Id:

ENST00000497124

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	X	106,640,455 - 106,669,212 (+)	Ensembl

RefSeq Acc Id:

NM_001184782 ⟹ NP_001171711

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	X	106,611,978 - 106,679,439 (+)	NCBI
GRCh37	X	105,855,160 - 105,922,673 (+)	RGD
Celera	X	106,326,505 - 106,394,019 (+)	RGD
HuRef	X	95,482,341 - 95,550,832 (+)	RGD
CHM1_1	X	105,765,982 - 105,833,494 (+)	NCBI
T2T-CHM13v2.0	X	105,048,421 - 105,115,882 (+)	NCBI

Sequence:

show sequence

GGCAGAGTAGCGATCGTCGCCAAAGCGCGCGGTTTTATTTCTCTCCGCTTTGGACGGGGCAAACTAGCTTTTGGGAGTGAAGCGGGTACGCAGTTATCCAACAATGTCTGGTGAGTCAGGACAGCCTG
AGGCTGGTCCCTCACATGCAGGGCTAGATTGGCCGAACCCTGAGAGGAATCGGGCTGGGGTCCCGGGAGGGGTGATCCGAAGAGCTGGTTCCCAAGGGCCCAGGTCCTGGATCCAAAAGGTTCTTGAG
CAGATTATGGACTCACCTCGCCAGTGTGTCACCCCCTCGGAGGTGGTGCCTGTAACTGTGCTGGCCGTCCAGAGGTACCTGTTAGAGGATGAGCCACGCGACACGGTGCCCAAGCCTCCCCTTTATTG
CTATGATGTGACGATCTCAGATGGGGTGTACCAGGAGAAGTGCTACCTGGACCCCAGCTTGAACTCTCTCGTATATCAAAATATTCTTAAAGTTGGCATTCAAATGAGAATTTCCAGGGTCTCATGTC
TTTACAATGAGAAAAGGATAGGCCAGGGGATCCTGTGCATAGATAACGTCCACTGTGGGGAGACTTCAGACAGTATTTCTTTAGAAACTCCCTTCAGAAATAGAGCGCACCAGGAGAAACCAGAGAGG
CCTTTAAGAGGCGGGAAGAGTCATTACCTGGCGCTGTGGAATAACGAAGATCCCTATGGAGATATCTGGTTAACAGACAAGCAACCTGAGGAACACAACTTTAGCGATACCAAAATAATTTCCCTTTC
TCATCTTGAAATGACCTGGACTAACAGAAGAAATTTTCCTGCATTGCTTGTGAGGATCTTACATAAATCAAAACTGCGATACTATGGAAAACCTGATAAAAAGATGATTGAACCATATCAGACCTTTT
TGGAAGTTGCTGACAGTTCAGGCACAGTGTCAGTGATTATGTGGAATGCCCTGTGTCCTGAGTGGTATAAAAGTTTGCGGGTTGGTTTAGTTCTTCTGCTTCAAGACTATTCTGTTAAAAAGAGTTAT
CCATTCAGAATACAGCCTGTCCCCGTGGATCCACAGATCAAACTAATTTCTACAATGGAAATCTGCCTGAATCTTCGAGATCCCCCAACAAATATAATTATCATTCCAGAAAAGCAGGTGAAACCAGA
ATGGAGACTGCCAAAGCTAAATCACCGATTTACCACAAGGTCAGAACTGGATGATATGCCAGAAAATTGCATCTGTGATGTTATTGGCCTTTTAGTTTTTGTAGGAAGGGTCCAGCGGTCAAAAAAGA
AAGAAAACCGTGAAGATTTTTGGTCATATCGCTGGATTCACATTGCTGACGGTACTTCAGAACAACCATTTATAGTGGAACTGTTTTCAACATCGCAGCCAGAAATCTTTGAAAATATTTACCCAATG
GCATATTTTGTGTGTACACAGTTGAAAGTTGTCAGAAATGACAATCAAGTACCTAAGCTGCTTTACCTCACCACTACAAATGAGAGTGGAGTGTTTATTACTGGTCATAGAGGCCAGCCGTATACGTA
TGATGCCAAGAATGCTAACAGACCCTCGACCTCTCAAGCAGCTAGAGTAGAAATTCAAGAAAGAAATGGTAAACGGCATCAAGATGATGAGCCTGTGAATTCTCAGTATTTCCAAACTACATCTACAA
ATTTAAGTCTGAGCAATAAAATAAGAATTCTTCAAGGCCCACACGCTAATCCAGTTGCTGTACCTCAACCAGGAGCTTCTGTACAAACAAAGGGAATTAAACCGGGCATGCCAAGCATCTTCAACCGT
CGAGCAAATATAAATGCTAATCTGCAAGGGAAAGCCAGAAAAACTATAAGTGATAGGTGGGAGAGTCAGCTGTGGAGAGAGAAAAAGTTTGGCTTAATAGATCACCTACACTACAGCCGTGTTTATCC
TGAAAGTATTCCACGGAAATTTATGTTTGAACACAGAAAGTTTCTTAGTGACCAGTATAATTCTCAGCCTGCGAAATATGTACCACCAGAAGGAAGGCCCCCAAAACTTGATGATTTTAAGAGCGCCC
GAAGCCTTGGACATTTTGAAGTAACCATACTAGGTCTGAACCATGAGATAGCAATCGATGTTGCTTTCCTACCCATGTATTGTCCAGAAGATATTCGAACATCTCAAATAGACACACTGTTGACCTCC
ATGAATTACAGCTGTGCATATCCACAGGACACAACTGGAAATGACCGATTGCCAGGTCCAAGAGCGGTTGCAGGTGATATTATAAAAGCAGCAACTGAACTGGATAGAGTGCATATCGTCGGTATCTT
GGATATCTGTAATTTGGGTAATAATAAAGTGGAAGTCTATTTGCACAAGATTTATAGTCCAGAGAATACTTCTTAAAAGTTAGCAAATGAAATTATTACAGATTATACGAGTGTACTGCTTTAAAGAT
ATTCCATCATTTTGCTGGTAATTTCAGTAACTGTTTTCAGCAAGAATATTACATGAGCTCTAAAGTTATTAAGCAGTTTTATGTTCGTTTTGTGTTTAGGGAGCTTTTTAAAACACTTCATTTCAGAT
TCATTATTGAAAAAGGTCATCAAAATAATTTTTGTGTATAAGGGAATTTACCTTGCTTACCTTACTAGTATGACTATTATCTTGACTTCTGGTAATTTATGTTCACTATTCCATTTGTGAAGTGTACT
TTCATTCTAAAGCCTCAGTATAAGGCATCCTAACTTACAAGAGTAACTTTCCATGGACATTTAACATCCTTCCAATTTTATTCACATATAATGGGAAATTTTGAATTGCCAGTTTGAAGACTGTTCTC
CTAAAGTGTTCAACCTGCACTTCTTACAACCAAGGTAGTTTGTATCATTTTCAAAAGTACACATTATTAGGGTCTAGTTGCCCCTGGTCCTTAGCTTGCTCAGCTGCAAAATAAGCGTGCTAAATTAA
ATTGTCTTAAGGTTTTTCCACTTCATTTTGTGACTTTGTGTGGTTCGAATTTCTCAGTATTTTAACCAGTGTGTTGATGTTAAAGTCAAAGGCTGCAGTATGTCTATATTCTTGCTGTACTCATTGGT
AGTTTCAGTATATGTAATGTGAGTTTAAATAGTGAAATTGTATCTCATATTAACATTTCAAATGCTCATATTGAAAATGGAAAATAGTAAACACGGGAATTGATTTTATTCTGGTTGTCTATAATACT
TCATTTTAAATGTAAATGGCCACTCTGCATTTGCAAGGCCCGGTGGTTGACATCTGTGTGGTTTGTTAGATGAGACAAAATGACCATTAAATGAGTTTATAGATTATTCTGTATCAAGATAAATCTGA
TTCCAGTTAAGCTATAAACTTGTGGGATTTTCTTGTAGCCCTATAGTTCTGTGACTTCATTTGCTATACGCTTTAAATGTGTTGAGCAGCCTATGAACCTAAAGACATACTGCAGTTTGTTCATAAAT
GTATTCAGTCTTTTATTCTTTATAATTGTGTGTAAATGTTAACTAAACAGTGGATTCCTCTCGTGTTACAGTTTTGAGTGAATTATTAAAGAAGTTAAAATGCAA

hide sequence

RefSeq Acc Id:

NM_018015 ⟹ NP_060485

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	X	106,611,978 - 106,679,439 (+)	NCBI
GRCh37	X	105,855,160 - 105,922,673 (+)	RGD
Build 36	X	105,741,909 - 105,809,328 (+)	NCBI Archive
Celera	X	106,326,505 - 106,394,019 (+)	RGD
HuRef	X	95,482,341 - 95,550,832 (+)	RGD
CHM1_1	X	105,765,982 - 105,833,494 (+)	NCBI
T2T-CHM13v2.0	X	105,048,421 - 105,115,882 (+)	NCBI

Sequence:

show sequence

GGCAGAGTAGCGATCGTCGCCAAAGCGCGCGGTTTTATTTCTCTCCGCTTTGGACGGGGCAAACTAGCTTTTGGGAGTGAAGCGGGTACGCAGTTATCCAACAATGTCTGGTGAGTCAGGACAGCCTG
AGGCTGGTCCCTCACATGCAGGGCTAGATTGGCCGAACCCTGAGAGGAATCGGGCTGGGGTCCCGGGAGGGGTGATCCGAAGAGCTGGTTCCCAAGGGCCCAGGTCCTGGATCCAAAAGGTTCTTGAG
CAGATTATGGACTCACCTCGCCAGTGTGTCACCCCCTCGGAGGTGGTGCCTGTAACTGTGCTGGCCGTCCAGAGGTACCTGTTAGAGGATGAGCCACGCGACACGGTGCCCAAGCCTCCCCTTTATTG
CTATGATGTGACGATCTCAGATGGGGTGTACCAGGAGAAGTGCTACCTGGACCCCAGCTTGAACTCTCTCGTATATCAAAATATTCTTAAAGTTGGCATTCAAATGAGAATTTCCAGGGTCTCATGTC
TTTACAATGAGAAAAGGATAGGCCAGGGGATCCTGTGCATAGATAACGTCCACTGTGGGGAGACTTCAGACAGTATTTCTTTAGAAACTCCCTTCAGAAATAGAGCGCACCAGGAGAAACCAGAGAGG
CCTTTAAGAGGCGGGAAGAGTCATTACCTGGCGCTGTGGAATAACGAAGATCCCTATGGAGATATCTGGTTAACAGACAAGCAACCTGAGGAACACAACTTTAGCGATACCAAAATAATTTCCCTTTC
TCATCTTGAAATGACCTGGACTAACAGAAGAAATTTTCCTGCATTGCTTGTGAGGATCTTACATAAATCAAAACTGCGATACTATGGAAAACCTGATAAAAAGATGATTGAACCATATCAGACCTTTT
TGGAAGTTGCTGACAGTTCAGGCACAGTGTCAGTGATTATGTGGAATGCCCTGTGTCCTGAGTGGTATAAAAGTTTGCGGGTTGGTTTAGTTCTTCTGCTTCAAGACTATTCTGTTAAAAAGAGTTAT
CCATTCAGAATACAGCCTGTCCCCGTGGATCCACAGATCAAACTAATTTCTACAATGGAAATCTGCCTGAATCTTCGAGATCCCCCAACAAATATAATTATCATTCCAGAAAAGCAGGTGAAACCAGA
ATGGAGACTGCCAAAGCTAAATCACCGATTTACCACAAGGTCAGAACTGGATGATATGCCAGAAAATTGCATCTGTGATGTTATTGGCCTTTTAGTTTTTGTAGGAAGGGTCCAGCGGTCAAAAAAGA
AAGAAAACCGTGAAGATTTTTGGTCATATCGCTGGATTCACATTGCTGACGGTACTTCAGAACAACCATTTATAGTGGAACTGTTTTCAACATCGCAGCCAGAAATCTTTGAAAATATTTACCCAATG
GCATATTTTGTGTGTACACAGTTGAAAGTTGTCAGAAATGACAATCAAGTACCTAAGCTGCTTTACCTCACCACTACAAATGAGAGTGGAGTGTTTATTACTGGTCATAGAGGCCAGCCGTATACGTA
TGATGCCAAGGTAAAAAACTTTATTCAATGGATTAGAACAAAGTCTGATTCCGGGGAACAGAAGAATATGGTTATTGGTGGATATTACCCCTATCCACCAGTGCCAGAGACATTTTCCAAGTATAGTA
GTTCTATTAAAGTTGAGTCGCTCTTGACAGCTATAAGTGAAGTCAGGAAGGAGATTGAAGACTTGCAGTATAGGGAACAAAAGCGCATTGCAATTCAGGGGATAATTACTGCTATAAAGTATATCCCC
CATAGCAGTGCGACTGAAAGTGCCTCAGCATCAGAAACACTTCGGAATGCTAACAGACCCTCGACCTCTCAAGCAGCTAGAGTAGAAATTCAAGAAAGAAATGGTAAACGGCATCAAGATGATGAGCC
TGTGAATTCTCAGTATTTCCAAACTACATCTACAAATTTAAGTCTGAGCAATAAAATAAGAATTCTTCAAGGCCCACACGCTAATCCAGTTGCTGTACCTCAACCAGGAGCTTCTGTACAAACAAAGG
GAATTAAACCGGGCATGCCAAGCATCTTCAACCGTCGAGCAAATATAAATGCTAATCTGCAAGGGAAAGCCAGAAAAACTATAAGTGATAGGTGGGAGAGTCAGCTGTGGAGAGAGAAAAAGTTTGGC
TTAATAGATCACCTACACTACAGCCGTGTTTATCCTGAAAGTATTCCACGGAAATTTATGTTTGAACACAGAAAGTTTCTTAGTGACCAGTATAATTCTCAGCCTGCGAAATATGTACCACCAGAAGG
AAGGCCCCCAAAACTTGATGATTTTAAGAGCGCCCGAAGCCTTGGACATTTTGAAGTAACCATACTAGGTCTGAACCATGAGATAGCAATCGATGTTGCTTTCCTACCCATGTATTGTCCAGAAGATA
TTCGAACATCTCAAATAGACACACTGTTGACCTCCATGAATTACAGCTGTGCATATCCACAGGACACAACTGGAAATGACCGATTGCCAGGTCCAAGAGCGGTTGCAGGTGATATTATAAAAGCAGCA
ACTGAACTGGATAGAGTGCATATCGTCGGTATCTTGGATATCTGTAATTTGGGTAATAATAAAGTGGAAGTCTATTTGCACAAGATTTATAGTCCAGAGAATACTTCTTAAAAGTTAGCAAATGAAAT
TATTACAGATTATACGAGTGTACTGCTTTAAAGATATTCCATCATTTTGCTGGTAATTTCAGTAACTGTTTTCAGCAAGAATATTACATGAGCTCTAAAGTTATTAAGCAGTTTTATGTTCGTTTTGT
GTTTAGGGAGCTTTTTAAAACACTTCATTTCAGATTCATTATTGAAAAAGGTCATCAAAATAATTTTTGTGTATAAGGGAATTTACCTTGCTTACCTTACTAGTATGACTATTATCTTGACTTCTGGT
AATTTATGTTCACTATTCCATTTGTGAAGTGTACTTTCATTCTAAAGCCTCAGTATAAGGCATCCTAACTTACAAGAGTAACTTTCCATGGACATTTAACATCCTTCCAATTTTATTCACATATAATG
GGAAATTTTGAATTGCCAGTTTGAAGACTGTTCTCCTAAAGTGTTCAACCTGCACTTCTTACAACCAAGGTAGTTTGTATCATTTTCAAAAGTACACATTATTAGGGTCTAGTTGCCCCTGGTCCTTA
GCTTGCTCAGCTGCAAAATAAGCGTGCTAAATTAAATTGTCTTAAGGTTTTTCCACTTCATTTTGTGACTTTGTGTGGTTCGAATTTCTCAGTATTTTAACCAGTGTGTTGATGTTAAAGTCAAAGGC
TGCAGTATGTCTATATTCTTGCTGTACTCATTGGTAGTTTCAGTATATGTAATGTGAGTTTAAATAGTGAAATTGTATCTCATATTAACATTTCAAATGCTCATATTGAAAATGGAAAATAGTAAACA
CGGGAATTGATTTTATTCTGGTTGTCTATAATACTTCATTTTAAATGTAAATGGCCACTCTGCATTTGCAAGGCCCGGTGGTTGACATCTGTGTGGTTTGTTAGATGAGACAAAATGACCATTAAATG
AGTTTATAGATTATTCTGTATCAAGATAAATCTGATTCCAGTTAAGCTATAAACTTGTGGGATTTTCTTGTAGCCCTATAGTTCTGTGACTTCATTTGCTATACGCTTTAAATGTGTTGAGCAGCCTA
TGAACCTAAAGACATACTGCAGTTTGTTCATAAATGTATTCAGTCTTTTATTCTTTATAATTGTGTGTAAATGTTAACTAAACAGTGGATTCCTCTCGTGTTACAGTTTTGAGTGAATTATTAAAGAA
GTTAAAATGCAA

hide sequence

RefSeq Acc Id:

XM_047442233 ⟹ XP_047298189

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	X	106,611,978 - 106,640,634 (+)	NCBI

RefSeq Acc Id:

XM_054327345 ⟹ XP_054183320

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	X	105,048,421 - 105,077,078 (+)	NCBI


Protein RefSeqs	NP_001171711	(Get FASTA)	NCBI Sequence Viewer
	NP_060485	(Get FASTA)	NCBI Sequence Viewer
	XP_047298189	(Get FASTA)	NCBI Sequence Viewer
	XP_054183320	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH11483	(Get FASTA)	NCBI Sequence Viewer
	AAH33709	(Get FASTA)	NCBI Sequence Viewer
	AAH54032	(Get FASTA)	NCBI Sequence Viewer
	AAH70110	(Get FASTA)	NCBI Sequence Viewer
	BAB14859	(Get FASTA)	NCBI Sequence Viewer
	BAF84419	(Get FASTA)	NCBI Sequence Viewer
	EAX02738	(Get FASTA)	NCBI Sequence Viewer
	EAX02739	(Get FASTA)	NCBI Sequence Viewer
	EAX02740	(Get FASTA)	NCBI Sequence Viewer
	EAX02741	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000361623
	ENSP00000361623.2
	ENSP00000361628
	ENSP00000361628.4
	ENSP00000432238
	ENSP00000432238.1
GenBank Protein	Q6NSI4	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_060485 ⟸ NM_018015
- Peptide Label:	isoform 1
- UniProtKB:	Q9H7W5 (UniProtKB/Swiss-Prot), Q6PJU8 (UniProtKB/Swiss-Prot), Q6PII9 (UniProtKB/Swiss-Prot), Q6PHY5 (UniProtKB/Swiss-Prot), Q5JRF9 (UniProtKB/Swiss-Prot), Q5JQS1 (UniProtKB/Swiss-Prot), Q4G0L7 (UniProtKB/Swiss-Prot), H7BY89 (UniProtKB/Swiss-Prot), Q9NWA6 (UniProtKB/Swiss-Prot), Q6NSI4 (UniProtKB/Swiss-Prot), A8K6R5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MSGESGQPEAGPSHAGLDWPNPERNRAGVPGGVIRRAGSQGPRSWIQKVLEQIMDSPRQCVTPSEVVPVTVLAVQRYLLEDEPRDTVPKPPLYCYDVTISDGVYQEKCYLDPSLNSLVYQNILKVGIQ MRISRVSCLYNEKRIGQGILCIDNVHCGETSDSISLETPFRNRAHQEKPERPLRGGKSHYLALWNNEDPYGDIWLTDKQPEEHNFSDTKIISLSHLEMTWTNRRNFPALLVRILHKSKLRYYGKPDKK MIEPYQTFLEVADSSGTVSVIMWNALCPEWYKSLRVGLVLLLQDYSVKKSYPFRIQPVPVDPQIKLISTMEICLNLRDPPTNIIIIPEKQVKPEWRLPKLNHRFTTRSELDDMPENCICDVIGLLVFV GRVQRSKKKENREDFWSYRWIHIADGTSEQPFIVELFSTSQPEIFENIYPMAYFVCTQLKVVRNDNQVPKLLYLTTTNESGVFITGHRGQPYTYDAKVKNFIQWIRTKSDSGEQKNMVIGGYYPYPPV PETFSKYSSSIKVESLLTAISEVRKEIEDLQYREQKRIAIQGIITAIKYIPHSSATESASASETLRNANRPSTSQAARVEIQERNGKRHQDDEPVNSQYFQTTSTNLSLSNKIRILQGPHANPVAVPQ PGASVQTKGIKPGMPSIFNRRANINANLQGKARKTISDRWESQLWREKKFGLIDHLHYSRVYPESIPRKFMFEHRKFLSDQYNSQPAKYVPPEGRPPKLDDFKSARSLGHFEVTILGLNHEIAIDVAF LPMYCPEDIRTSQIDTLLTSMNYSCAYPQDTTGNDRLPGPRAVAGDIIKAATELDRVHIVGILDICNLGNNKVEVYLHKIYSPENTS hide sequence

RefSeq Acc Id:	NP_001171711 ⟸ NM_001184782
- Peptide Label:	isoform 2
- UniProtKB:	A8K6R5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MSGESGQPEAGPSHAGLDWPNPERNRAGVPGGVIRRAGSQGPRSWIQKVLEQIMDSPRQCVTPSEVVPVTVLAVQRYLLEDEPRDTVPKPPLYCYDVTISDGVYQEKCYLDPSLNSLVYQNILKVGIQ MRISRVSCLYNEKRIGQGILCIDNVHCGETSDSISLETPFRNRAHQEKPERPLRGGKSHYLALWNNEDPYGDIWLTDKQPEEHNFSDTKIISLSHLEMTWTNRRNFPALLVRILHKSKLRYYGKPDKK MIEPYQTFLEVADSSGTVSVIMWNALCPEWYKSLRVGLVLLLQDYSVKKSYPFRIQPVPVDPQIKLISTMEICLNLRDPPTNIIIIPEKQVKPEWRLPKLNHRFTTRSELDDMPENCICDVIGLLVFV GRVQRSKKKENREDFWSYRWIHIADGTSEQPFIVELFSTSQPEIFENIYPMAYFVCTQLKVVRNDNQVPKLLYLTTTNESGVFITGHRGQPYTYDAKNANRPSTSQAARVEIQERNGKRHQDDEPVNS QYFQTTSTNLSLSNKIRILQGPHANPVAVPQPGASVQTKGIKPGMPSIFNRRANINANLQGKARKTISDRWESQLWREKKFGLIDHLHYSRVYPESIPRKFMFEHRKFLSDQYNSQPAKYVPPEGRPP KLDDFKSARSLGHFEVTILGLNHEIAIDVAFLPMYCPEDIRTSQIDTLLTSMNYSCAYPQDTTGNDRLPGPRAVAGDIIKAATELDRVHIVGILDICNLGNNKVEVYLHKIYSPENTS hide sequence

Ensembl Acc Id:

ENSP00000361623 ⟸ ENST00000372544

Ensembl Acc Id:

ENSP00000361628 ⟸ ENST00000372548

Ensembl Acc Id:

ENSP00000405866 ⟸ ENST00000421550

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q6NSI4-F1-model_v2	AlphaFold	Q6NSI4	1-855	view protein structure

RGD ID:

6808606

Promoter ID:

HG_KWN:67674

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_018015, OTTHUMT00000057799, UC004EMH.2, UC004EMJ.2

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	X	105,741,679 - 105,742,179 (+)	MPROMDB

RGD ID:

6808807

Promoter ID:

HG_KWN:67675

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Jurkat

Transcripts:

ENST00000408286, OTTHUMT00000057802

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	X	105,768,731 - 105,769,231 (+)	MPROMDB

RGD ID:

13627778

Promoter ID:

EPDNEW_H29164

Type:

initiation region

Name:

CXorf57_1

Description:

chromosome X open reading frame 57

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	X	106,611,981 - 106,612,041	EPDNEW

Database	Acc Id	Source(s)
COSMIC	RADX	COSMIC
Ensembl Genes	ENSG00000147231	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000372544	ENTREZGENE
	ENST00000372544.6	UniProtKB/Swiss-Prot
	ENST00000372548	ENTREZGENE
	ENST00000372548.9	UniProtKB/Swiss-Prot
	ENST00000461251	ENTREZGENE
	ENST00000461251.5	UniProtKB/Swiss-Prot
Gene3D-CATH	2.40.50.140	UniProtKB/Swiss-Prot
GTEx	ENSG00000147231	GTEx
HGNC ID	HGNC:25486	ENTREZGENE
Human Proteome Map	RADX	Human Proteome Map
InterPro	NA-bd_OB-fold	UniProtKB/Swiss-Prot
	RADX	UniProtKB/Swiss-Prot
KEGG Report	hsa:55086	UniProtKB/Swiss-Prot
NCBI Gene	55086	ENTREZGENE
PANTHER	PTHR14944	UniProtKB/Swiss-Prot
	RPA-RELATED PROTEIN RADX	UniProtKB/Swiss-Prot
Pfam	DUF5521	UniProtKB/Swiss-Prot
PharmGKB	PA145149058	PharmGKB
Superfamily-SCOP	SSF50249	UniProtKB/Swiss-Prot
UniProt	A8K6R5	ENTREZGENE, UniProtKB/TrEMBL
	B1AQ74_HUMAN	UniProtKB/TrEMBL
	H7BY89	ENTREZGENE
	Q4G0L7	ENTREZGENE
	Q5JQS1	ENTREZGENE
	Q5JRF9	ENTREZGENE
	Q6NSI4	ENTREZGENE
	Q6PHY5	ENTREZGENE
	Q6PII9	ENTREZGENE
	Q6PJU8	ENTREZGENE
	Q9H7W5	ENTREZGENE
	Q9NWA6	ENTREZGENE
	RADX_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	H7BY89	UniProtKB/Swiss-Prot
	Q4G0L7	UniProtKB/Swiss-Prot
	Q5JQS1	UniProtKB/Swiss-Prot
	Q5JRF9	UniProtKB/Swiss-Prot
	Q6PHY5	UniProtKB/Swiss-Prot
	Q6PII9	UniProtKB/Swiss-Prot
	Q6PJU8	UniProtKB/Swiss-Prot
	Q9H7W5	UniProtKB/Swiss-Prot
	Q9NWA6	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2018-09-11	RADX	RPA1 related single stranded DNA binding protein, X-linked	CXorf57	chromosome X open reading frame 57	Symbol and/or name change	5135510	APPROVED

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

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