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Gene: DRG1 (developmentally regulated GTP binding protein 1) Homo sapiens

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Symbol:

DRG1

Name:

developmentally regulated GTP binding protein 1

RGD ID:

1312753

HGNC Page

HGNC:3029

Description:

Enables several functions, including GTPase activity; identical protein binding activity; and potassium ion binding activity. Involved in positive regulation of microtubule polymerization and regulation of mitotic spindle assembly. Located in cytosol and nuclear body.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

developmentally regulated GTP-binding protein 1; developmentally-regulated GTP-binding protein 1; DKFZp434N1827; DRG-1; NEDD-3; NEDD3; neural precursor cell expressed developmentally down-regulated protein 3; neural precursor cell expressed, developmentally down-regulated 3; TANALS; TRAFAC GTPase DRG1; translation factor GTPase DRG1

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Related Pseudogenes:

DRG1P1 DRG1P2

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	22	31,399,604 - 31,434,452 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	22	31,399,604 - 31,528,740 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	22	31,795,590 - 31,830,438 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	22	30,125,539 - 30,160,172 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	22	30,120,092 - 30,154,725	NCBI
Celera	22	15,596,029 - 15,630,660 (+)	NCBI		Celera
Cytogenetic Map	22	q12.2	NCBI
HuRef	22	14,757,243 - 14,784,270 (+)	NCBI		HuRef
CHM1_1	22	31,755,375 - 31,789,984 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	22	31,864,208 - 31,899,052 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

Contracture (IAGP)

Neurodevelopmental Disorders (IAGP)

TAN-ALMURSHEDI SYNDROME (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

17alpha-ethynylestradiol (ISO)

17beta-estradiol (ISO)

2,2',4,4'-Tetrabromodiphenyl ether (EXP)

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

3,3',5,5'-tetrabromobisphenol A (EXP)

actinomycin D (EXP)

amitrole (ISO)

arsenite(3-) (EXP)

benzo[a]pyrene (ISO)

beta-lapachone (EXP)

bis(2-ethylhexyl) phthalate (ISO)

bisphenol A (EXP,ISO)

bisphenol AF (EXP)

bisphenol F (EXP)

cisplatin (EXP)

copper(II) sulfate (EXP)

Dibutyl phosphate (EXP)

dicrotophos (EXP)

enzyme inhibitor (EXP)

ethanol (ISO)

flutamide (ISO)

folic acid (ISO)

indole-3-methanol (ISO)

irinotecan (EXP)

ivermectin (EXP)

methimazole (ISO)

Nutlin-3 (EXP)

ozone (EXP)

perfluorooctanoic acid (EXP)

pregnenolone 16alpha-carbonitrile (ISO)

SB 431542 (EXP)

Se-methyl-L-selenocysteine (EXP)

Se-methylselenocysteine (EXP)

sodium arsenite (EXP)

temozolomide (EXP)

thiram (EXP)

titanium dioxide (ISO)

valproic acid (ISO)

vinclozolin (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

cytoplasmic translation (IBA)

positive regulation of microtubule polymerization (IMP)

regulation of mitotic spindle assembly (IMP)

Cellular Component

cytoplasm (IBA,IDA,IEA)

cytosol (IDA,TAS)

membrane (HDA)

nuclear body (IDA)

nucleoplasm (IDA)

nucleus (IDA,IEA)

Molecular Function

GTP binding (IBA,IEA)

GTPase activity (IDA,IEA)

hydrolase activity (IEA)

identical protein binding (IPI)

metal ion binding (IEA)

microtubule binding (IDA)

potassium ion binding (IDA)

protein binding (IPI)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Autoimmune hemolytic anemia (IAGP)

Autosomal recessive inheritance (IAGP)

Brachycephaly (IAGP)

Camptodactyly (IAGP)

Congenital onset (IAGP)

Dry skin (IAGP)

Eczematoid dermatitis (IAGP)

Everted lower lip vermilion (IAGP)

Failure to thrive (IAGP)

Flexion contracture (IAGP)

Increased circulating antibody concentration (IAGP)

Intrauterine growth retardation (IAGP)

Low-set ears (IAGP)

Microcephaly (IAGP)

Myelomeningocele (IAGP)

Neurodevelopmental delay (IAGP)

Posteriorly rotated ears (IAGP)

Prominent forehead (IAGP)

Proportionate short stature (IAGP)

Recurrent infections (IAGP)

Seizure (IAGP)

Short eyelashes (IAGP)

Short palpebral fissure (IAGP)

Spasticity (IAGP)

Talipes equinovarus (IAGP)

Underdeveloped supraorbital ridges (IAGP)

Wide nasal bridge (IAGP)

Widely spaced teeth (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:1280421	PMID:1449490	PMID:7929244	PMID:8649774	PMID:9824680	PMID:10591208	PMID:10760581	PMID:12477932	PMID:12702552	PMID:15184886	PMID:15461802	PMID:15489334
PMID:15676025	PMID:16169070	PMID:16189514	PMID:17178897	PMID:17361185	PMID:17709345	PMID:18029348	PMID:18184589	PMID:19058789	PMID:19380743	PMID:19738201	PMID:19819225
PMID:19946888	PMID:20467437	PMID:21081503	PMID:21516116	PMID:21873635	PMID:21907836	PMID:21988832	PMID:22623428	PMID:22990118	PMID:23125841	PMID:23455922	PMID:23602568
PMID:23711155	PMID:24163370	PMID:24550385	PMID:24625528	PMID:24711643	PMID:25416956	PMID:25852190	PMID:25921289	PMID:25944354	PMID:25993655	PMID:26186194	PMID:26344197
PMID:26496610	PMID:26673895	PMID:26972000	PMID:27025967	PMID:27142060	PMID:27173435	PMID:27591049	PMID:27626498	PMID:28416769	PMID:28514442	PMID:28515276	PMID:28855639
PMID:29053956	PMID:29229926	PMID:29509190	PMID:29802200	PMID:29845934	PMID:29915238	PMID:30194290	PMID:30196744	PMID:30463901	PMID:30884312	PMID:30940648	PMID:30948266
PMID:30997501	PMID:31059266	PMID:31073040	PMID:31091453	PMID:31324722	PMID:31527615	PMID:31586073	PMID:31665637	PMID:31685992	PMID:31753913	PMID:31980649	PMID:31985874
PMID:32129710	PMID:32235678	PMID:32266933	PMID:32296183	PMID:32460013	PMID:32687490	PMID:32707033	PMID:32801337	PMID:32807901	PMID:32905556	PMID:32971831	PMID:33022573
PMID:33306668	PMID:33471252	PMID:33545068	PMID:33658012	PMID:33660365	PMID:33731348	PMID:33742100	PMID:33957083	PMID:33961781	PMID:34029587	PMID:34079125	PMID:34189442
PMID:34244565	PMID:34349018	PMID:34591612	PMID:34650049	PMID:34664086	PMID:34709727	PMID:35013218	PMID:35032548	PMID:35156780	PMID:35256949	PMID:35271311	PMID:35446349
PMID:35509820	PMID:35563538	PMID:35696571	PMID:35777956	PMID:35790840	PMID:35831314	PMID:35915203	PMID:35944360	PMID:36012204	PMID:36057605	PMID:36114006	PMID:36180891
PMID:36215168	PMID:36244648	PMID:36273042	PMID:36449624	PMID:36517590	PMID:36526897	PMID:36597993	PMID:36610398	PMID:36634849	PMID:36652389	PMID:37167062	PMID:37179472
PMID:37314180	PMID:37314216	PMID:37317656	PMID:37689310	PMID:37827155	PMID:38113892	PMID:38697112	PMID:39147351

Genomics

Comparative Map Data

DRG1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	22	31,399,604 - 31,434,452 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	22	31,399,604 - 31,528,740 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	22	31,795,590 - 31,830,438 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	22	30,125,539 - 30,160,172 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	22	30,120,092 - 30,154,725	NCBI
Celera	22	15,596,029 - 15,630,660 (+)	NCBI		Celera
Cytogenetic Map	22	q12.2	NCBI
HuRef	22	14,757,243 - 14,784,270 (+)	NCBI		HuRef
CHM1_1	22	31,755,375 - 31,789,984 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	22	31,864,208 - 31,899,052 (+)	NCBI		T2T-CHM13v2.0

Drg1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	11	3,199,907 - 3,221,882 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	11	3,137,360 - 3,216,415 (-)	Ensembl		GRCm39 Ensembl
GRCm38	11	3,249,907 - 3,266,464 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	11	3,187,360 - 3,266,415 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	11	3,149,925 - 3,166,389 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	11	3,149,925 - 3,166,389 (-)	NCBI		MGSCv36	mm8
Celera	11	3,741,153 - 3,757,517 (-)	NCBI		Celera
Cytogenetic Map	11	A1	NCBI
cM Map	11	2.23	NCBI

Drg1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	14	82,328,320 - 82,344,416 (-)	NCBI		GRCr8
mRatBN7.2	14	78,103,876 - 78,119,976 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	14	78,103,876 - 78,119,953 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	14	82,545,654 - 82,561,686 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	14	83,785,762 - 83,801,794 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	14	80,231,501 - 80,247,531 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	14	83,460,540 - 83,476,568 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	14	83,460,540 - 83,476,568 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	14	84,148,278 - 84,164,306 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	14	83,855,894 - 83,871,922 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	14	83,866,172 - 83,882,201 (-)	NCBI
Celera	14	77,019,064 - 77,035,075 (-)	NCBI		Celera
Cytogenetic Map	14	q21	NCBI

Drg1
(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_004955455	5,588,313 - 5,610,964 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955455	5,588,313 - 5,608,091 (+)	NCBI	ChiLan1.0	ChiLan1.0

DRG1
(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	23	41,353,822 - 41,388,587 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	22	44,054,293 - 44,089,035 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	22	12,424,080 - 12,458,810 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	22	30,283,745 - 30,317,458 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	22	30,283,745 - 30,317,458 (+)	Ensembl	panpan1.1		panPan2

DRG1
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	26	24,327,714 - 24,350,782 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	26	24,327,739 - 24,350,659 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	26	24,197,255 - 24,219,666 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	26	24,710,964 - 24,733,978 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	26	24,710,995 - 24,735,944 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	26	24,413,968 - 24,436,345 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	26	24,675,939 - 24,698,308 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	26	24,737,518 - 24,759,907 (+)	NCBI		UU_Cfam_GSD_1.0

Drg1
(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_024405118	117,300,259 - 117,325,599 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936755	557,903 - 583,192 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936755	557,862 - 583,204 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

DRG1
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	14	48,126,863 - 48,157,906 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	14	48,126,807 - 48,153,103 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	14	51,288,040 - 51,313,823 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

DRG1
(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	19	14,287,537 - 14,322,216 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	19	14,287,564 - 14,321,998 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666045	111,790,836 - 111,827,627 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Drg1
(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_004624747	7,869,570 - 7,895,220 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624747	7,869,544 - 7,895,231 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in DRG1
14 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 22q11.21-12.3(chr22:18178957-31821193)x3	copy number gain	See cases [RCV000050768]	Chr22:18178957..31821193 [GRCh38] Chr22:18661724..32217179 [GRCh37] Chr22:17041724..30547179 [NCBI36] Chr22:22q11.21-12.3	pathogenic
GRCh38/hg38 22q12.1-12.3(chr22:26979579-33992220)x3	copy number gain	See cases [RCV000050553]	Chr22:26979579..33992220 [GRCh38] Chr22:27375542..34388209 [GRCh37] Chr22:25705542..32718209 [NCBI36] Chr22:22q12.1-12.3	pathogenic
GRCh38/hg38 22q12.1-12.2(chr22:28278805-31742328)x1	copy number loss	See cases [RCV000052870]	Chr22:28278805..31742328 [GRCh38] Chr22:28674793..32138314 [GRCh37] Chr22:27004793..30468314 [NCBI36] Chr22:22q12.1-12.2	pathogenic
GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3	copy number gain	See cases [RCV000133646]	Chr22:16916608..50739836 [GRCh38] Chr22:17397498..51178264 [GRCh37] Chr22:15777498..49525130 [NCBI36] Chr22:22q11.1-13.33	pathogenic
GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3	copy number gain	See cases [RCV000134730]	Chr22:16916743..50739785 [GRCh38] Chr22:17397633..51178213 [GRCh37] Chr22:15777633..49525079 [NCBI36] Chr22:22q11.1-13.33	pathogenic
GRCh38/hg38 22q11.23-12.3(chr22:23279231-36247369)x3	copy number gain	See cases [RCV000138172]	Chr22:23279231..36247369 [GRCh38] Chr22:23621418..36643415 [GRCh37] Chr22:21951418..34973361 [NCBI36] Chr22:22q11.23-12.3	pathogenic
GRCh38/hg38 22q11.21-12.3(chr22:20907226-37187347)x3	copy number gain	See cases [RCV000137926]	Chr22:20907226..37187347 [GRCh38] Chr22:21261514..37583387 [GRCh37] Chr22:19591514..35913333 [NCBI36] Chr22:22q11.21-12.3	pathogenic
GRCh38/hg38 22q12.1-12.2(chr22:26451042-31451926)x1	copy number loss	See cases [RCV000143415]	Chr22:26451042..31451926 [GRCh38] Chr22:26847008..31847912 [GRCh37] Chr22:25177008..30177912 [NCBI36] Chr22:22q12.1-12.2	pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3	copy number gain	See cases [RCV000240091]	Chr22:16054691..51237518 [GRCh37] Chr22:22q11.1-13.33	pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3	copy number gain	See cases [RCV000446956]	Chr22:16054691..51220902 [GRCh37] Chr22:22q11.1-13.33	pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3	copy number gain	See cases [RCV000448847]	Chr22:16054691..51237463 [GRCh37] Chr22:22q11.1-13.33	pathogenic
GRCh37/hg19 22q12.1-12.3(chr22:28349854-33013062)x3	copy number gain	See cases [RCV000510523]	Chr22:28349854..33013062 [GRCh37] Chr22:22q12.1-12.3	likely pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)	copy number gain	See cases [RCV000510873]	Chr22:16888900..51197838 [GRCh37] Chr22:22q11.1-13.33	pathogenic
GRCh37/hg19 22q11.23-12.3(chr22:23637907-36614412)x3	copy number gain	See cases [RCV000511098]	Chr22:23637907..36614412 [GRCh37] Chr22:22q11.23-12.3	pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3	copy number gain	See cases [RCV000512333]	Chr22:16888900..51197838 [GRCh37] Chr22:22q11.1-13.33	pathogenic
GRCh37/hg19 22q11.22-12.3(chr22:22460754-35198232)x3	copy number gain	not provided [RCV000684530]	Chr22:22460754..35198232 [GRCh37] Chr22:22q11.22-12.3	pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054667-51243435)x3	copy number gain	not provided [RCV000741689]	Chr22:16054667..51243435 [GRCh37] Chr22:22q11.1-13.33	pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51195728)x3	copy number gain	not provided [RCV000741691]	Chr22:16114244..51195728 [GRCh37] Chr22:22q11.1-13.33	pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51211392)x3	copy number gain	not provided [RCV000741692]	Chr22:16114244..51211392 [GRCh37] Chr22:22q11.1-13.33	pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3	copy number gain	not provided [RCV000846344]	Chr22:16888899..51197838 [GRCh37] Chr22:22q11.1-13.33	pathogenic
NM_004147.4(DRG1):c.118C>T (p.Arg40Ter)	single nucleotide variant	Flexion contracture [RCV001007813]	Chr22:31400695 [GRCh38] Chr22:31796681 [GRCh37] Chr22:22q12.2	likely pathogenic
GRCh37/hg19 22q12.2-12.3(chr22:31748161-32659394)x3	copy number gain	not provided [RCV000846837]	Chr22:31748161..32659394 [GRCh37] Chr22:22q12.2-12.3	uncertain significance
GRCh37/hg19 22q12.2-13.33(chr22:30654764-51197838)x3	copy number gain	not provided [RCV001007181]	Chr22:30654764..51197838 [GRCh37] Chr22:22q12.2-13.33	pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3	copy number gain	See cases [RCV001263056]	Chr22:16197005..51224252 [GRCh37] Chr22:22q11.1-13.33	pathogenic
GRCh37/hg19 22q12.2(chr22:31565901-32105115)x1	copy number loss	not provided [RCV001258779]	Chr22:31565901..32105115 [GRCh37] Chr22:22q12.2	uncertain significance
NM_004147.4(DRG1):c.43-1G>T	single nucleotide variant	Neurodevelopmental disorder [RCV001262401]	Chr22:31400619 [GRCh38] Chr22:31796605 [GRCh37] Chr22:22q12.2	uncertain significance
NC_000022.10:g.(?_29083885)_(34046674_?)dup	duplication	not provided [RCV001979643]	Chr22:29083885..34046674 [GRCh37] Chr22:22q12.1-12.3	uncertain significance
NM_004147.4(DRG1):c.1000A>G (p.Lys334Glu)	single nucleotide variant	not specified [RCV004146900]	Chr22:31427178 [GRCh38] Chr22:31823164 [GRCh37] Chr22:22q12.2	uncertain significance
NM_004147.4(DRG1):c.127A>G (p.Ile43Val)	single nucleotide variant	not specified [RCV004119518]	Chr22:31400704 [GRCh38] Chr22:31796690 [GRCh37] Chr22:22q12.2	uncertain significance
NM_004147.4(DRG1):c.668G>A (p.Ser223Asn)	single nucleotide variant	not specified [RCV004346870]	Chr22:31423365 [GRCh38] Chr22:31819351 [GRCh37] Chr22:22q12.2	uncertain significance
NM_004147.4(DRG1):c.160G>T (p.Gly54Ter)	single nucleotide variant	Tan-Almurshedi syndrome [RCV003447450]	Chr22:31400737 [GRCh38] Chr22:31796723 [GRCh37] Chr22:22q12.2	pathogenic\|likely pathogenic
NM_004147.4(DRG1):c.418C>T (p.Arg140Ter)	single nucleotide variant	Tan-Almurshedi syndrome [RCV003447453]	Chr22:31420261 [GRCh38] Chr22:31816247 [GRCh37] Chr22:22q12.2	pathogenic\|likely pathogenic
NM_004147.4(DRG1):c.742_743inv (p.Asn248Phe)	inversion	Tan-Almurshedi syndrome [RCV003447451]	Chr22:31426643..31426644 [GRCh38] Chr22:31822629..31822630 [GRCh37] Chr22:22q12.2	pathogenic\|likely pathogenic
NM_004147.4(DRG1):c.787A>T (p.Lys263Ter)	single nucleotide variant	Tan-Almurshedi syndrome [RCV003447452]	Chr22:31426688 [GRCh38] Chr22:31822674 [GRCh37] Chr22:22q12.2	pathogenic\|likely pathogenic
NM_004147.4(DRG1):c.197G>A (p.Arg66Gln)	single nucleotide variant	not specified [RCV004377126]	Chr22:31403059 [GRCh38] Chr22:31799045 [GRCh37] Chr22:22q12.2	uncertain significance
NM_004147.4(DRG1):c.943A>G (p.Arg315Gly)	single nucleotide variant	not specified [RCV004377129]	Chr22:31427121 [GRCh38] Chr22:31823107 [GRCh37] Chr22:22q12.2	uncertain significance
NM_004147.4(DRG1):c.598C>A (p.Leu200Met)	single nucleotide variant	not specified [RCV004377127]	Chr22:31423295 [GRCh38] Chr22:31819281 [GRCh37] Chr22:22q12.2	uncertain significance
NM_004147.4(DRG1):c.146G>C (p.Gly49Ala)	single nucleotide variant	not specified [RCV004619859]	Chr22:31400723 [GRCh38] Chr22:31796709 [GRCh37] Chr22:22q12.2	uncertain significance
NM_004147.4(DRG1):c.442G>A (p.Val148Ile)	single nucleotide variant	not specified [RCV004619860]	Chr22:31420285 [GRCh38] Chr22:31816271 [GRCh37] Chr22:22q12.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	818
Count of miRNA genes:	579
Interacting mature miRNAs:	657
Transcripts:	ENST00000331457, ENST00000416465, ENST00000433341, ENST00000469673, ENST00000486584, ENST00000548143
Prediction methods:	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.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597104215	GWAS1200289_H	neutrophil count QTL GWAS1200289 (human)		6e-17	neutrophil quantity (VT:0000222)	blood neutrophil count (CMO:0000030)	22	31417072	31417073	Human
1581529	BP71_H	Blood pressure QTL 71 (human)	2	0.001	Blood pressure	pulse pressure	22	11094966	37094966	Human
597083573	GWAS1179647_H	myeloid white cell count QTL GWAS1179647 (human)		2e-18	myeloid white cell count	white blood cell count (CMO:0000027)	22	31417072	31417073	Human
407008791	GWAS657767_H	neutrophil count QTL GWAS657767 (human)		1e-21	neutrophil quantity (VT:0000222)	blood neutrophil count (CMO:0000030)	22	31417072	31417073	Human
2289428	BW313_H	Body weight QTL 313 (human)	2.09	0.0015	Body weight	BMI	22	11344284	37344284	Human
406971561	GWAS620537_H	neutrophil count QTL GWAS620537 (human)		8e-09	neutrophil quantity (VT:0000222)	blood neutrophil count (CMO:0000030)	22	31417072	31417073	Human
597048190	GWAS1144264_H	leukocyte count QTL GWAS1144264 (human)		2e-14	leukocyte quantity (VT:0000217)	white blood cell count (CMO:0000027)	22	31425733	31425734	Human
597301830	GWAS1397904_H	neutrophil count QTL GWAS1397904 (human)		2e-09	neutrophil quantity (VT:0000222)	blood neutrophil count (CMO:0000030)	22	31417072	31417073	Human
406977132	GWAS626108_H	neutrophil count, basophil count QTL GWAS626108 (human)		5e-09	basophil quantity (VT:0002607)	blood granulocyte count (CMO:0000111)	22	31417072	31417073	Human

Markers in Region

STS-R96070

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,829,902 - 31,830,098	UniSTS	GRCh37
Build 36	22	30,159,902 - 30,160,098	RGD	NCBI36
Celera	22	15,630,390 - 15,630,586	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	17	31,591,060 - 31,591,256	UniSTS
GeneMap99-GB4 RH Map	22	85.75	UniSTS

stbK210G9SP6

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,807,327 - 31,807,409	UniSTS	GRCh37
Build 36	22	30,137,327 - 30,137,409	RGD	NCBI36
Celera	22	15,607,818 - 15,607,900	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,768,399 - 14,768,481	UniSTS

ECD02880

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,829,640 - 31,830,454	UniSTS	GRCh37
Build 36	22	30,159,640 - 30,160,454	RGD	NCBI36
Celera	22	15,630,128 - 15,630,942	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	17	31,590,704 - 31,591,518	UniSTS

ECD07666

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,816,017 - 31,816,692	UniSTS	GRCh37
Build 36	22	30,146,017 - 30,146,692	RGD	NCBI36
Celera	22	15,616,507 - 15,617,182	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,777,119 - 14,777,794	UniSTS

ECD11561

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,822,399 - 31,822,967	UniSTS	GRCh37
Build 36	22	30,152,399 - 30,152,967	RGD	NCBI36
Celera	22	15,622,890 - 15,623,458	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,783,501 - 14,784,069	UniSTS

ECD12710

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,823,015 - 31,823,551	UniSTS	GRCh37
Build 36	22	30,153,015 - 30,153,551	RGD	NCBI36
Celera	22	15,623,506 - 15,624,042	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,784,117 - 14,784,653	UniSTS

ECD17655

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,819,089 - 31,819,478	UniSTS	GRCh37
Build 36	22	30,149,089 - 30,149,478	RGD	NCBI36
Celera	22	15,619,579 - 15,619,968	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,780,191 - 14,780,580	UniSTS

ECD18199

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,806,815 - 31,807,184	UniSTS	GRCh37
Build 36	22	30,136,815 - 30,137,184	RGD	NCBI36
Celera	22	15,607,306 - 15,607,675	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,767,887 - 14,768,256	UniSTS

ECD19700

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,821,080 - 31,821,392	UniSTS	GRCh37
Build 36	22	30,151,080 - 30,151,392	RGD	NCBI36
Celera	22	15,621,571 - 15,621,883	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,782,182 - 14,782,494	UniSTS

ECD20351

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,827,717 - 31,828,004	UniSTS	GRCh37
Build 36	22	30,157,717 - 30,158,004	RGD	NCBI36
Celera	22	15,628,205 - 15,628,492	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,788,817 - 14,789,104	UniSTS

ECD21512

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,804,787 - 31,805,034	UniSTS	GRCh37
Build 36	22	30,134,787 - 30,135,034	RGD	NCBI36
Celera	22	15,605,278 - 15,605,525	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,765,859 - 14,766,106	UniSTS

ECD21513

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,828,926 - 31,829,173	UniSTS	GRCh37
Build 36	22	30,158,926 - 30,159,173	RGD	NCBI36
Celera	22	15,629,414 - 15,629,661	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	17	31,591,985 - 31,592,232	UniSTS

REN73839

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,804,245 - 31,804,484	UniSTS	GRCh37
Build 36	22	30,134,245 - 30,134,484	RGD	NCBI36
Celera	22	15,604,735 - 15,604,974	RGD
Cytogenetic Map	22	q12.2	UniSTS

REN73840

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,804,778 - 31,805,002	UniSTS	GRCh37
Build 36	22	30,134,778 - 30,135,002	RGD	NCBI36
Celera	22	15,605,269 - 15,605,493	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,765,850 - 14,766,074	UniSTS

REN73841

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,804,938 - 31,805,177	UniSTS	GRCh37
Build 36	22	30,134,938 - 30,135,177	RGD	NCBI36
Celera	22	15,605,429 - 15,605,668	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,766,010 - 14,766,249	UniSTS

REN73842

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,805,122 - 31,805,347	UniSTS	GRCh37
Build 36	22	30,135,122 - 30,135,347	RGD	NCBI36
Celera	22	15,605,613 - 15,605,838	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,766,194 - 14,766,419	UniSTS

REN73843

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,805,330 - 31,805,590	UniSTS	GRCh37
Build 36	22	30,135,330 - 30,135,590	RGD	NCBI36
Celera	22	15,605,821 - 15,606,081	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,766,402 - 14,766,662	UniSTS

REN73844

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,805,561 - 31,805,818	UniSTS	GRCh37
Build 36	22	30,135,561 - 30,135,818	RGD	NCBI36
Celera	22	15,606,052 - 15,606,309	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,766,633 - 14,766,890	UniSTS

REN73845

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,805,793 - 31,806,040	UniSTS	GRCh37
Build 36	22	30,135,793 - 30,136,040	RGD	NCBI36
Celera	22	15,606,284 - 15,606,531	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,766,865 - 14,767,112	UniSTS

REN73846

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,805,878 - 31,806,127	UniSTS	GRCh37
Build 36	22	30,135,878 - 30,136,127	RGD	NCBI36
Celera	22	15,606,369 - 15,606,618	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,766,950 - 14,767,199	UniSTS

REN73847

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,806,104 - 31,806,358	UniSTS	GRCh37
Build 36	22	30,136,104 - 30,136,358	RGD	NCBI36
Celera	22	15,606,595 - 15,606,849	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,767,176 - 14,767,430	UniSTS

REN73848

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,806,216 - 31,806,454	UniSTS	GRCh37
Build 36	22	30,136,216 - 30,136,454	RGD	NCBI36
Celera	22	15,606,707 - 15,606,945	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,767,288 - 14,767,526	UniSTS

REN73849

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,806,615 - 31,806,840	UniSTS	GRCh37
Build 36	22	30,136,615 - 30,136,840	RGD	NCBI36
Celera	22	15,607,106 - 15,607,331	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,767,687 - 14,767,912	UniSTS

REN73850

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,806,815 - 31,807,067	UniSTS	GRCh37
Build 36	22	30,136,815 - 30,137,067	RGD	NCBI36
Celera	22	15,607,306 - 15,607,558	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,767,887 - 14,768,139	UniSTS

REN73851

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,807,056 - 31,807,305	UniSTS	GRCh37
Build 36	22	30,137,056 - 30,137,305	RGD	NCBI36
Celera	22	15,607,547 - 15,607,796	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,768,128 - 14,768,377	UniSTS

REN73852

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,807,280 - 31,807,504	UniSTS	GRCh37
Build 36	22	30,137,280 - 30,137,504	RGD	NCBI36
Celera	22	15,607,771 - 15,607,995	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,768,352 - 14,768,576	UniSTS

REN73853

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,807,473 - 31,807,740	UniSTS	GRCh37
Build 36	22	30,137,473 - 30,137,740	RGD	NCBI36
Celera	22	15,607,964 - 15,608,231	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,768,545 - 14,768,812	UniSTS

REN73854

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,807,650 - 31,807,881	UniSTS	GRCh37
Build 36	22	30,137,650 - 30,137,881	RGD	NCBI36
Celera	22	15,608,141 - 15,608,372	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,768,722 - 14,768,953	UniSTS

REN73855

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,807,763 - 31,807,987	UniSTS	GRCh37
Build 36	22	30,137,763 - 30,137,987	RGD	NCBI36
Celera	22	15,608,254 - 15,608,478	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,768,835 - 14,769,059	UniSTS

REN73856

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,808,655 - 31,808,894	UniSTS	GRCh37
Build 36	22	30,138,655 - 30,138,894	RGD	NCBI36
Celera	22	15,609,146 - 15,609,385	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,769,723 - 14,769,962	UniSTS

REN73857

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,808,762 - 31,809,011	UniSTS	GRCh37
Build 36	22	30,138,762 - 30,139,011	RGD	NCBI36
Celera	22	15,609,253 - 15,609,502	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,769,830 - 14,770,079	UniSTS

REN73858

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,808,993 - 31,809,218	UniSTS	GRCh37
Build 36	22	30,138,993 - 30,139,218	RGD	NCBI36
Celera	22	15,609,484 - 15,609,709	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,770,061 - 14,770,286	UniSTS

REN73859

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,809,185 - 31,809,449	UniSTS	GRCh37
Build 36	22	30,139,185 - 30,139,449	RGD	NCBI36
Celera	22	15,609,676 - 15,609,940	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,770,253 - 14,770,517	UniSTS

REN73860

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,809,436 - 31,809,687	UniSTS	GRCh37
Build 36	22	30,139,436 - 30,139,687	RGD	NCBI36
Celera	22	15,609,927 - 15,610,178	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,770,504 - 14,770,756	UniSTS

REN73861

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,809,453 - 31,809,716	UniSTS	GRCh37
Build 36	22	30,139,453 - 30,139,716	RGD	NCBI36
Celera	22	15,609,944 - 15,610,207	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,770,521 - 14,770,785	UniSTS

REN73862

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,809,694 - 31,809,952	UniSTS	GRCh37
Build 36	22	30,139,694 - 30,139,952	RGD	NCBI36
Celera	22	15,610,185 - 15,610,443	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,770,763 - 14,771,021	UniSTS

REN73863

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,809,929 - 31,810,175	UniSTS	GRCh37
Build 36	22	30,139,929 - 30,140,175	RGD	NCBI36
Celera	22	15,610,420 - 15,610,666	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,770,998 - 14,771,244	UniSTS

REN73864

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,810,106 - 31,810,357	UniSTS	GRCh37
Build 36	22	30,140,106 - 30,140,357	RGD	NCBI36
Celera	22	15,610,597 - 15,610,848	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,771,175 - 14,771,426	UniSTS

REN73865

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,810,323 - 31,810,586	UniSTS	GRCh37
Build 36	22	30,140,323 - 30,140,586	RGD	NCBI36
Celera	22	15,610,814 - 15,611,077	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,771,392 - 14,771,655	UniSTS

REN73866

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,810,571 - 31,810,809	UniSTS	GRCh37
Build 36	22	30,140,571 - 30,140,809	RGD	NCBI36
Celera	22	15,611,062 - 15,611,300	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,771,640 - 14,771,878	UniSTS

REN73867

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,810,743 - 31,810,982	UniSTS	GRCh37
Build 36	22	30,140,743 - 30,140,982	RGD	NCBI36
Celera	22	15,611,234 - 15,611,473	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,771,812 - 14,772,051	UniSTS

REN73868

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,810,904 - 31,811,133	UniSTS	GRCh37
Build 36	22	30,140,904 - 30,141,133	RGD	NCBI36
Celera	22	15,611,395 - 15,611,624	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,771,973 - 14,772,202	UniSTS

REN73869

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,811,104 - 31,811,359	UniSTS	GRCh37
Build 36	22	30,141,104 - 30,141,359	RGD	NCBI36
Celera	22	15,611,595 - 15,611,850	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,772,173 - 14,772,428	UniSTS

REN73870

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,811,340 - 31,811,586	UniSTS	GRCh37
Build 36	22	30,141,340 - 30,141,586	RGD	NCBI36
Celera	22	15,611,831 - 15,612,077	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,772,409 - 14,772,655	UniSTS

REN73871

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,811,558 - 31,811,816	UniSTS	GRCh37
Build 36	22	30,141,558 - 30,141,816	RGD	NCBI36
Celera	22	15,612,049 - 15,612,307	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,772,627 - 14,772,885	UniSTS

REN73872

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,811,808 - 31,812,032	UniSTS	GRCh37
Build 36	22	30,141,808 - 30,142,032	RGD	NCBI36
Celera	22	15,612,299 - 15,612,523	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,772,877 - 14,773,101	UniSTS

REN73873

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,812,001 - 31,812,226	UniSTS	GRCh37
Build 36	22	30,142,001 - 30,142,226	RGD	NCBI36
Celera	22	15,612,492 - 15,612,717	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,773,070 - 14,773,295	UniSTS

REN73874

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,812,195 - 31,812,440	UniSTS	GRCh37
Build 36	22	30,142,195 - 30,142,440	RGD	NCBI36
Celera	22	15,612,686 - 15,612,931	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,773,264 - 14,773,509	UniSTS

REN73875

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,812,432 - 31,812,692	UniSTS	GRCh37
Build 36	22	30,142,432 - 30,142,692	RGD	NCBI36
Celera	22	15,612,923 - 15,613,183	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,773,501 - 14,773,761	UniSTS

REN73876

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,812,666 - 31,812,934	UniSTS	GRCh37
Build 36	22	30,142,666 - 30,142,934	RGD	NCBI36
Celera	22	15,613,157 - 15,613,424	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,773,735 - 14,774,002	UniSTS

REN73877

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,812,821 - 31,813,053	UniSTS	GRCh37
Build 36	22	30,142,821 - 30,143,053	RGD	NCBI36
Celera	22	15,613,312 - 15,613,543	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,773,890 - 14,774,121	UniSTS

REN73878

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	50,377,707 - 50,378,095	UniSTS	GRCh37
GRCh37	22	31,813,023 - 31,813,250	UniSTS	GRCh37
Build 36	14	49,447,457 - 49,447,845	RGD	NCBI36
Celera	14	30,244,836 - 30,245,224	RGD
Celera	22	15,613,513 - 15,613,740	UniSTS
HuRef	14	30,502,256 - 30,502,644	UniSTS
HuRef	12	56,640,195 - 56,640,697	UniSTS
HuRef	22	14,774,091 - 14,774,318	UniSTS

REN73879

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,813,229 - 31,813,492	UniSTS	GRCh37
Build 36	22	30,143,229 - 30,143,492	RGD	NCBI36
Celera	22	15,613,719 - 15,613,982	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,774,297 - 14,774,560	UniSTS

REN73880

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,813,906 - 31,814,150	UniSTS	GRCh37
Build 36	22	30,143,906 - 30,144,150	RGD	NCBI36
Celera	22	15,614,396 - 15,614,640	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,774,974 - 14,775,218	UniSTS

REN73881

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,814,131 - 31,814,355	UniSTS	GRCh37
Build 36	22	30,144,131 - 30,144,355	RGD	NCBI36
Celera	22	15,614,621 - 15,614,845	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,775,199 - 14,775,423	UniSTS

REN73882

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,814,471 - 31,814,704	UniSTS	GRCh37
Build 36	22	30,144,471 - 30,144,704	RGD	NCBI36
Celera	22	15,614,961 - 15,615,194	RGD
Cytogenetic Map	22	q12.2	UniSTS

REN73883

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,815,094 - 31,815,346	UniSTS	GRCh37
Build 36	22	30,145,094 - 30,145,346	RGD	NCBI36
Celera	22	15,615,584 - 15,615,836	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,776,126 - 14,776,378	UniSTS

REN73884

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,815,272 - 31,815,537	UniSTS	GRCh37
Build 36	22	30,145,272 - 30,145,537	RGD	NCBI36
Celera	22	15,615,762 - 15,616,027	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,776,304 - 14,776,569	UniSTS

REN73885

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,815,526 - 31,815,754	UniSTS	GRCh37
Build 36	22	30,145,526 - 30,145,754	RGD	NCBI36
Celera	22	15,616,016 - 15,616,244	RGD
Cytogenetic Map	22	q12.2	UniSTS

REN73886

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,815,618 - 31,815,869	UniSTS	GRCh37
Build 36	22	30,145,618 - 30,145,869	RGD	NCBI36
Celera	22	15,616,108 - 15,616,359	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,776,720 - 14,776,971	UniSTS

REN73887

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,815,844 - 31,816,070	UniSTS	GRCh37
Build 36	22	30,145,844 - 30,146,070	RGD	NCBI36
Celera	22	15,616,334 - 15,616,560	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,776,946 - 14,777,172	UniSTS

REN73888

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,816,049 - 31,816,287	UniSTS	GRCh37
Build 36	22	30,146,049 - 30,146,287	RGD	NCBI36
Celera	22	15,616,539 - 15,616,777	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,777,151 - 14,777,389	UniSTS

REN73889

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,816,246 - 31,816,500	UniSTS	GRCh37
Build 36	22	30,146,246 - 30,146,500	RGD	NCBI36
Celera	22	15,616,736 - 15,616,990	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,777,348 - 14,777,602	UniSTS

REN73890

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,816,449 - 31,816,697	UniSTS	GRCh37
Build 36	22	30,146,449 - 30,146,697	RGD	NCBI36
Celera	22	15,616,939 - 15,617,187	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,777,551 - 14,777,799	UniSTS

REN73891

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,816,686 - 31,816,937	UniSTS	GRCh37
Build 36	22	30,146,686 - 30,146,937	RGD	NCBI36
Celera	22	15,617,176 - 15,617,427	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,777,788 - 14,778,039	UniSTS

REN73892

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,816,936 - 31,817,195	UniSTS	GRCh37
Build 36	22	30,146,936 - 30,147,195	RGD	NCBI36
Celera	22	15,617,426 - 15,617,685	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,778,038 - 14,778,297	UniSTS

REN73893

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,817,120 - 31,817,359	UniSTS	GRCh37
Build 36	22	30,147,120 - 30,147,359	RGD	NCBI36
Celera	22	15,617,610 - 15,617,849	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,778,222 - 14,778,461	UniSTS

REN73894

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,817,331 - 31,817,562	UniSTS	GRCh37
Build 36	22	30,147,331 - 30,147,562	RGD	NCBI36
Celera	22	15,617,821 - 15,618,052	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,778,433 - 14,778,664	UniSTS

REN73895

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,817,549 - 31,817,799	UniSTS	GRCh37
Build 36	22	30,147,549 - 30,147,799	RGD	NCBI36
Celera	22	15,618,039 - 15,618,289	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,778,651 - 14,778,901	UniSTS

REN73896

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,817,776 - 31,818,028	UniSTS	GRCh37
Build 36	22	30,147,776 - 30,148,028	RGD	NCBI36
Celera	22	15,618,266 - 15,618,518	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,778,878 - 14,779,130	UniSTS

REN73897

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,818,289 - 31,818,515	UniSTS	GRCh37
Build 36	22	30,148,289 - 30,148,515	RGD	NCBI36
Celera	22	15,618,779 - 15,619,005	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,779,391 - 14,779,617	UniSTS

REN73898

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,818,506 - 31,818,746	UniSTS	GRCh37
Build 36	22	30,148,506 - 30,148,746	RGD	NCBI36
Celera	22	15,618,996 - 15,619,236	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,779,608 - 14,779,848	UniSTS

REN73899

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,818,744 - 31,818,995	UniSTS	GRCh37
Build 36	22	30,148,744 - 30,148,995	RGD	NCBI36
Celera	22	15,619,234 - 15,619,485	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,779,846 - 14,780,097	UniSTS

REN73900

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,818,984 - 31,819,214	UniSTS	GRCh37
Build 36	22	30,148,984 - 30,149,214	RGD	NCBI36
Celera	22	15,619,474 - 15,619,704	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,780,086 - 14,780,316	UniSTS

REN73901

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,819,185 - 31,819,419	UniSTS	GRCh37
Build 36	22	30,149,185 - 30,149,419	RGD	NCBI36
Celera	22	15,619,675 - 15,619,909	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,780,287 - 14,780,521	UniSTS

REN73902

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,819,244 - 31,819,483	UniSTS	GRCh37
Build 36	22	30,149,244 - 30,149,483	RGD	NCBI36
Celera	22	15,619,734 - 15,619,973	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,780,346 - 14,780,585	UniSTS

REN73903

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,821,003 - 31,821,236	UniSTS	GRCh37
Build 36	22	30,151,003 - 30,151,236	RGD	NCBI36
Celera	22	15,621,494 - 15,621,727	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,782,105 - 14,782,338	UniSTS

REN73904

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,821,160 - 31,821,388	UniSTS	GRCh37
Build 36	22	30,151,160 - 30,151,388	RGD	NCBI36
Celera	22	15,621,651 - 15,621,879	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,782,262 - 14,782,490	UniSTS

REN73905

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,821,365 - 31,821,629	UniSTS	GRCh37
Build 36	22	30,151,365 - 30,151,629	RGD	NCBI36
Celera	22	15,621,856 - 15,622,120	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,782,467 - 14,782,731	UniSTS

REN73906

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,821,607 - 31,821,874	UniSTS	GRCh37
Build 36	22	30,151,607 - 30,151,874	RGD	NCBI36
Celera	22	15,622,098 - 15,622,365	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,782,709 - 14,782,976	UniSTS

REN73907

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,821,857 - 31,822,107	UniSTS	GRCh37
Build 36	22	30,151,857 - 30,152,107	RGD	NCBI36
Celera	22	15,622,348 - 15,622,598	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,782,959 - 14,783,209	UniSTS

REN73908

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,822,082 - 31,822,312	UniSTS	GRCh37
Build 36	22	30,152,082 - 30,152,312	RGD	NCBI36
Celera	22	15,622,573 - 15,622,803	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,783,184 - 14,783,414	UniSTS

REN73909

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,822,276 - 31,822,505	UniSTS	GRCh37
Build 36	22	30,152,276 - 30,152,505	RGD	NCBI36
Celera	22	15,622,767 - 15,622,996	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,783,378 - 14,783,607	UniSTS

REN73910

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,822,478 - 31,822,725	UniSTS	GRCh37
Build 36	22	30,152,478 - 30,152,725	RGD	NCBI36
Celera	22	15,622,969 - 15,623,216	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,783,580 - 14,783,827	UniSTS

REN73911

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,822,710 - 31,822,951	UniSTS	GRCh37
Build 36	22	30,152,710 - 30,152,951	RGD	NCBI36
Celera	22	15,623,201 - 15,623,442	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,783,812 - 14,784,053	UniSTS

REN73912

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,822,935 - 31,823,191	UniSTS	GRCh37
Build 36	22	30,152,935 - 30,153,191	RGD	NCBI36
Celera	22	15,623,426 - 15,623,682	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,784,037 - 14,784,293	UniSTS

REN73913

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,823,182 - 31,823,435	UniSTS	GRCh37
Build 36	22	30,153,182 - 30,153,435	RGD	NCBI36
Celera	22	15,623,673 - 15,623,926	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,784,284 - 14,784,537	UniSTS

REN73914

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,823,412 - 31,823,645	UniSTS	GRCh37
Build 36	22	30,153,412 - 30,153,645	RGD	NCBI36
Celera	22	15,623,903 - 15,624,136	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,784,514 - 14,784,747	UniSTS

REN73915

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,823,491 - 31,823,719	UniSTS	GRCh37
Build 36	22	30,153,491 - 30,153,719	RGD	NCBI36
Celera	22	15,623,982 - 15,624,210	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,784,593 - 14,784,821	UniSTS

REN73916

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,824,493 - 31,824,717	UniSTS	GRCh37
Build 36	22	30,154,493 - 30,154,717	RGD	NCBI36
Celera	22	15,624,984 - 15,625,208	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,785,595 - 14,785,819	UniSTS

REN73917

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,824,714 - 31,824,953	UniSTS	GRCh37
Build 36	22	30,154,714 - 30,154,953	RGD	NCBI36
Celera	22	15,625,205 - 15,625,444	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,785,816 - 14,786,055	UniSTS

REN73918

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,824,916 - 31,825,159	UniSTS	GRCh37
Build 36	22	30,154,916 - 30,155,159	RGD	NCBI36
Celera	22	15,625,407 - 15,625,650	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,786,018 - 14,786,261	UniSTS

REN73919

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,825,138 - 31,825,396	UniSTS	GRCh37
Build 36	22	30,155,138 - 30,155,396	RGD	NCBI36
Celera	22	15,625,629 - 15,625,887	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,786,240 - 14,786,498	UniSTS

REN73920

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,825,373 - 31,825,617	UniSTS	GRCh37
Build 36	22	30,155,373 - 30,155,617	RGD	NCBI36
Celera	22	15,625,864 - 15,626,108	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,786,475 - 14,786,719	UniSTS

REN73921

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,825,590 - 31,825,852	UniSTS	GRCh37
Build 36	22	30,155,590 - 30,155,852	RGD	NCBI36
Celera	22	15,626,081 - 15,626,343	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,786,692 - 14,786,954	UniSTS

REN73922

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,825,823 - 31,826,053	UniSTS	GRCh37
Build 36	22	30,155,823 - 30,156,053	RGD	NCBI36
Celera	22	15,626,314 - 15,626,544	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,786,925 - 14,787,155	UniSTS

REN73923

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,826,030 - 31,826,297	UniSTS	GRCh37
Build 36	22	30,156,030 - 30,156,297	RGD	NCBI36
Celera	22	15,626,521 - 15,626,788	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,787,132 - 14,787,399	UniSTS

REN73924

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,826,156 - 31,826,380	UniSTS	GRCh37
Build 36	22	30,156,156 - 30,156,380	RGD	NCBI36
Celera	22	15,626,647 - 15,626,871	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,787,258 - 14,787,482	UniSTS

REN73925

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,826,755 - 31,826,998	UniSTS	GRCh37
Build 36	22	30,156,755 - 30,156,998	RGD	NCBI36
Celera	22	15,627,246 - 15,627,489	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,787,857 - 14,788,100	UniSTS

REN73926

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,827,359 - 31,827,591	UniSTS	GRCh37
Build 36	22	30,157,359 - 30,157,591	RGD	NCBI36
Celera	22	15,627,847 - 15,628,079	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,788,459 - 14,788,691	UniSTS

REN73927

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,827,583 - 31,827,822	UniSTS	GRCh37
Build 36	22	30,157,583 - 30,157,822	RGD	NCBI36
Celera	22	15,628,071 - 15,628,310	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,788,683 - 14,788,922	UniSTS

REN73928

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,827,769 - 31,828,015	UniSTS	GRCh37
Build 36	22	30,157,769 - 30,158,015	RGD	NCBI36
Celera	22	15,628,257 - 15,628,503	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,788,869 - 14,789,115	UniSTS

REN73929

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,827,996 - 31,828,265	UniSTS	GRCh37
Build 36	22	30,157,996 - 30,158,265	RGD	NCBI36
Celera	22	15,628,484 - 15,628,753	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,789,096 - 14,789,364	UniSTS

REN73930

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,828,166 - 31,828,395	UniSTS	GRCh37
Build 36	22	30,158,166 - 30,158,395	RGD	NCBI36
Celera	22	15,628,654 - 15,628,883	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	22	14,789,265 - 14,789,494	UniSTS

REN73931

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,828,837 - 31,829,086	UniSTS	GRCh37
Build 36	22	30,158,837 - 30,159,086	RGD	NCBI36
Celera	22	15,629,325 - 15,629,574	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	17	31,592,072 - 31,592,321	UniSTS

REN73932

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,829,003 - 31,829,258	UniSTS	GRCh37
Build 36	22	30,159,003 - 30,159,258	RGD	NCBI36
Celera	22	15,629,491 - 15,629,746	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	17	31,591,900 - 31,592,155	UniSTS

REN73933

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,829,234 - 31,829,492	UniSTS	GRCh37
Build 36	22	30,159,234 - 30,159,492	RGD	NCBI36
Celera	22	15,629,722 - 15,629,980	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	17	31,591,666 - 31,591,924	UniSTS

REN73934

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,829,490 - 31,829,737	UniSTS	GRCh37
Build 36	22	30,159,490 - 30,159,737	RGD	NCBI36
Celera	22	15,629,978 - 15,630,225	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	17	31,591,421 - 31,591,668	UniSTS

REN73935

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,829,718 - 31,829,968	UniSTS	GRCh37
Build 36	22	30,159,718 - 30,159,968	RGD	NCBI36
Celera	22	15,630,206 - 15,630,456	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	17	31,591,190 - 31,591,440	UniSTS

REN73936

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,829,956 - 31,830,204	UniSTS	GRCh37
Build 36	22	30,159,956 - 30,160,204	RGD	NCBI36
Celera	22	15,630,444 - 15,630,692	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	17	31,590,954 - 31,591,202	UniSTS

REN73937

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,830,180 - 31,830,404	UniSTS	GRCh37
Build 36	22	30,160,180 - 30,160,404	RGD	NCBI36
Celera	22	15,630,668 - 15,630,892	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	17	31,590,754 - 31,590,978	UniSTS

REN73938

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,830,376 - 31,830,628	UniSTS	GRCh37
Build 36	22	30,160,376 - 30,160,628	RGD	NCBI36
Celera	22	15,630,864 - 15,631,116	RGD
Cytogenetic Map	22	q12.2	UniSTS
HuRef	17	31,590,530 - 31,590,782	UniSTS

stSG602020

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,804,786 - 31,806,038	UniSTS	GRCh37
Build 36	22	30,134,786 - 30,136,038	RGD	NCBI36
Celera	22	15,605,277 - 15,606,529	RGD
HuRef	22	14,765,858 - 14,767,110	UniSTS

stSG602021

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,806,018 - 31,807,066	UniSTS	GRCh37
Build 36	22	30,136,018 - 30,137,066	RGD	NCBI36
Celera	22	15,606,509 - 15,607,557	RGD
HuRef	22	14,767,090 - 14,768,138	UniSTS

stSG602022

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,807,073 - 31,808,312	UniSTS	GRCh37
Build 36	22	30,137,073 - 30,138,312	RGD	NCBI36
Celera	22	15,607,564 - 15,608,803	RGD
HuRef	22	14,768,145 - 14,769,384	UniSTS

stSG602023

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,808,296 - 31,808,933	UniSTS	GRCh37
Build 36	22	30,138,296 - 30,138,933	RGD	NCBI36
Celera	22	15,608,787 - 15,609,424	RGD
HuRef	22	14,769,368 - 14,770,001	UniSTS

stSG602024

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,810,741 - 31,811,873	UniSTS	GRCh37
Build 36	22	30,140,741 - 30,141,873	RGD	NCBI36
Celera	22	15,611,232 - 15,612,364	RGD
HuRef	22	14,771,810 - 14,772,942	UniSTS

stSG602027

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,816,357 - 31,816,694	UniSTS	GRCh37
Build 36	22	30,146,357 - 30,146,694	RGD	NCBI36
Celera	22	15,616,847 - 15,617,184	RGD
HuRef	22	14,777,459 - 14,777,796	UniSTS

stSG602028

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,819,089 - 31,820,470	UniSTS	GRCh37
GRCh37	22	31,819,089 - 31,819,846	UniSTS	GRCh37
Build 36	22	30,149,089 - 30,150,470	RGD	NCBI36
Celera	22	15,619,579 - 15,620,336	UniSTS
Celera	22	15,619,579 - 15,620,960	RGD
HuRef	22	14,780,191 - 14,781,570	UniSTS
HuRef	22	14,780,191 - 14,780,948	UniSTS

stSG602029

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,820,452 - 31,821,879	UniSTS	GRCh37
Build 36	22	30,150,452 - 30,151,879	RGD	NCBI36
Celera	22	15,620,942 - 15,622,370	RGD
HuRef	22	14,781,552 - 14,782,981	UniSTS

stSG602030

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,821,864 - 31,823,125	UniSTS	GRCh37
Build 36	22	30,151,864 - 30,153,125	RGD	NCBI36
Celera	22	15,622,355 - 15,623,616	RGD
HuRef	22	14,782,966 - 14,784,227	UniSTS

stSG602031

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,822,521 - 31,823,551	UniSTS	GRCh37
Build 36	22	30,152,521 - 30,153,551	RGD	NCBI36
Celera	22	15,623,012 - 15,624,042	RGD
HuRef	22	14,783,623 - 14,784,653	UniSTS

stSG602032

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,827,771 - 31,828,949	UniSTS	GRCh37
Build 36	22	30,157,771 - 30,158,949	RGD	NCBI36
Celera	22	15,628,259 - 15,629,437	RGD

stSG602033

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	22	31,829,002 - 31,830,032	UniSTS	GRCh37
Build 36	22	30,159,002 - 30,160,032	RGD	NCBI36
Celera	22	15,629,490 - 15,630,520	RGD
HuRef	17	31,591,126 - 31,592,156	UniSTS

Expression

RNA-SEQ Expression

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	nervous system	renal system	reproductive system	respiratory system	sensory system
2408	4430	5572	4392	8976	2840	3404	776	2366	452	3936	11556	11200	7088	1022	2790	2462	324

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_004147	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AF078103	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ005940	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK098576	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK315659	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL096701	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL096702	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL133085	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC019285	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC020803	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BT007237	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU584654	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471095	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068256	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR456488	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR542059	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000331457 ⟹ ENSP00000329715

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	22	31,399,604 - 31,434,452 (+)	Ensembl

Ensembl Acc Id:

ENST00000416465 ⟹ ENSP00000408091

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	22	31,399,610 - 31,423,319 (+)	Ensembl

Ensembl Acc Id:

ENST00000433341

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	22	31,399,617 - 31,423,346 (+)	Ensembl

Ensembl Acc Id:

ENST00000469673

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	22	31,426,513 - 31,434,155 (+)	Ensembl

Ensembl Acc Id:

ENST00000486584

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	22	31,399,633 - 31,411,060 (+)	Ensembl

Ensembl Acc Id:

ENST00000548143 ⟹ ENSP00000448252

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	22	31,426,741 - 31,528,740 (+)	Ensembl

Ensembl Acc Id:

ENST00000629688 ⟹ ENSP00000485935

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	22	31,508,285 - 31,530,634 (+)	Ensembl

RefSeq Acc Id:

NM_004147 ⟹ NP_004138

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	22	31,399,604 - 31,434,452 (+)	NCBI
GRCh37	22	31,795,539 - 31,830,172 (+)	RGD
Build 36	22	30,125,539 - 30,160,172 (+)	NCBI Archive
Celera	22	15,596,029 - 15,630,660 (+)	RGD
HuRef	22	14,757,243 - 14,784,270 (+)	NCBI
CHM1_1	22	31,755,375 - 31,789,984 (+)	NCBI
T2T-CHM13v2.0	22	31,864,208 - 31,899,052 (+)	NCBI

Sequence:

show sequence

AGTAGCGCCTGGTGGCGGTGGCAGTTTGCCCGCGGGTGTGTGAAGGGAGACAGTGTGGAGGCCA
CAGGGTACTCGCCACGATGAGCAGCACCTTAGCTAAGATCGCGGAGATAGAAGCAGAGATGGCT
CGGACTCAAAAGAACAAGGCCACAGCACACCACTTAGGGCTGCTTAAGGCTCGTCTTGCTAAGC
TTCGTCGAGAACTCATTACTCCAAAGGGTGGTGGTGGTGGAGGTCCAGGAGAAGGTTTTGATGT
GGCCAAGACAGGTGATGCTCGAATTGGATTTGTTGGTTTTCCATCTGTGGGGAAGTCAACACTG
CTTAGTAACCTGGCAGGGGTATATTCTGAGGTGGCAGCCTATGAATTCACTACTCTGACCACTG
TGCCTGGTGTCATCAGATACAAAGGTGCCAAGATCCAGCTCCTGGATCTCCCAGGTATCATTGA
AGGTGCCAAGGATGGGAAAGGTAGAGGTCGTCAAGTCATTGCAGTGGCCCGAACCTGTAACTTG
ATCTTGATTGTTCTGGATGTCCTGAAACCTTTGGGACATAAGAAGATAATTGAAAATGAGCTGG
AAGGCTTTGGCATTCGCTTGAACAGCAAACCCCCCAACATTGGCTTTAAGAAGAAGGACAAGGG
AGGCATTAATCTCACAGCCACTTGCCCCCAGAGTGAGCTGGATGCTGAAACTGTGAAGAGCATT
CTGGCTGAATACAAGATTCATAATGCCGATGTGACTCTACGTAGTGATGCTACAGCTGATGACC
TCATTGATGTGGTGGAAGGAAACAGAGTTTATATCCCCTGTATCTATGTGTTAAATAAGATTGA
CCAAATCTCCATTGAGGAATTGGATATCATCTATAAGGTGCCTCACTGTGTACCCATCTCTGCC
CATCACCGCTGGAATTTTGATGACCTATTGGAAAAGATCTGGGACTATCTGAAACTAGTGAGAA
TTTACACCAAACCCAAAGGCCAGTTACCAGATTACACATCCCCAGTGGTGCTTCCTTACTCCAG
GACCACAGTGGAGGATTTCTGCATGAAGATTCACAAAAATCTTATCAAAGAATTTAAATATGCT
CTGGTCTGGGGTCTCTCTGTGAAACACAATCCTCAGAAAGTGGGTAAAGACCATACGTTGGAGG
ATGAGGATGTCATTCAAATTGTGAAGAAGTGAAACCTTTCCCTTTTCCCATCTGCCGGACGAAC
CACAACAGCGTTCCCCATGATCAAGCACCCTACCCCAGTTCTTTCTGGTTTTGGCAGTCACTGG
ATCAGGATCCAGGGGAGGGAGATGGAGGCACCCAAACTGGAACTTCATTTGTCTTACCTTGGTG
TCACCTTGTATGTCGAACTGCATAAAAGATCTGGTAGGCTGGTCAGCTACATGCAGCTCATGTG
TCATTGTCAGAATTTGTTTTGGGATGGGCTGAATGAGGAAGGGTATATACGGTGAAGCAGCTAC
AGAAGGGATCCTTGGGAACTTCATCTTGAGTGTGAAATGGATAAAAATATGACATGCTGCATCT
TACTTGATGTTTACTTATGGGAACCCCTTCCAAACTAGATATGGCTTTCAGTCCTTTCAAGTAG
TCTTTCCCACATGATACTGGAGAGAGGAAGGACTTTATGTAAGTTAATTGATCACTCCCCGCAA
G

hide sequence

Protein Sequences


Protein RefSeqs	NP_004138	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAD12240	(Get FASTA)	NCBI Sequence Viewer
	AAH19285	(Get FASTA)	NCBI Sequence Viewer
	AAH20803	(Get FASTA)	NCBI Sequence Viewer
	AAP35901	(Get FASTA)	NCBI Sequence Viewer
	BAG38025	(Get FASTA)	NCBI Sequence Viewer
	CAA06775	(Get FASTA)	NCBI Sequence Viewer
	CAB61403	(Get FASTA)	NCBI Sequence Viewer
	CAG30374	(Get FASTA)	NCBI Sequence Viewer
	CAG46856	(Get FASTA)	NCBI Sequence Viewer
	EAW59974	(Get FASTA)	NCBI Sequence Viewer
	EAW59975	(Get FASTA)	NCBI Sequence Viewer
	EAW59976	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000329715
	ENSP00000329715.4
	ENSP00000408091.1
	ENSP00000448252.1
GenBank Protein	Q9Y295	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_004138 ⟸ NM_004147

- UniProtKB:

Q9Y295 (UniProtKB/Swiss-Prot), Q8WW69 (UniProtKB/Swiss-Prot), Q6FGP8 (UniProtKB/Swiss-Prot), B2RDS8 (UniProtKB/Swiss-Prot), Q9UGF2 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MSSTLAKIAEIEAEMARTQKNKATAHHLGLLKARLAKLRRELITPKGGGGGGPGEGFDVAKTGD
ARIGFVGFPSVGKSTLLSNLAGVYSEVAAYEFTTLTTVPGVIRYKGAKIQLLDLPGIIEGAKDG
KGRGRQVIAVARTCNLILIVLDVLKPLGHKKIIENELEGFGIRLNSKPPNIGFKKKDKGGINLT
ATCPQSELDAETVKSILAEYKIHNADVTLRSDATADDLIDVVEGNRVYIPCIYVLNKIDQISIE
ELDIIYKVPHCVPISAHHRWNFDDLLEKIWDYLKLVRIYTKPKGQLPDYTSPVVLPYSRTTVED
FCMKIHKNLIKEFKYALVWGLSVKHNPQKVGKDHTLEDEDVIQIVKK

hide sequence

Ensembl Acc Id:

ENSP00000329715 ⟸ ENST00000331457

Ensembl Acc Id:

ENSP00000408091 ⟸ ENST00000416465

Ensembl Acc Id:

ENSP00000448252 ⟸ ENST00000548143

Ensembl Acc Id:

ENSP00000485935 ⟸ ENST00000629688

Protein Domains

OBG-type G TGS

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9Y295-F1-model_v2	AlphaFold	Q9Y295	1-367	view protein structure

Promoters

RGD ID:

6799831

Promoter ID:

HG_KWN:42403

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4

Transcripts:

OTTHUMT00000075680, OTTHUMT00000129109, OTTHUMT00000145209, OTTHUMT00000319107

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	22	30,125,304 - 30,125,804 (+)	MPROMDB

RGD ID:

6851542

Promoter ID:

EP73572

Type:

initiation region

Name:

HS_DRG1

Description:

Developmentally regulated GTP binding protein 1.

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

NEDO full length human cDNA sequencing project.; Oligo-capping

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	22	30,125,590 - 30,125,650	EPD

RGD ID:

6799832

Promoter ID:

HG_KWN:42404

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

OTTHUMT00000129110, OTTHUMT00000317344, OTTHUMT00000317872

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	22	30,152,141 - 30,152,641 (+)	MPROMDB

RGD ID:

13603764

Promoter ID:

EPDNEW_H28067

Type:

initiation region

Name:

DRG1_1

Description:

developmentally regulated GTP binding protein 1

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	22	31,399,604 - 31,399,664	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:3029	AgrOrtholog
COSMIC	DRG1	COSMIC
Ensembl Genes	ENSG00000185721	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000331457	ENTREZGENE
	ENST00000331457.9	UniProtKB/Swiss-Prot
	ENST00000416465.5	UniProtKB/TrEMBL
	ENST00000548143.1	UniProtKB/TrEMBL
Gene3D-CATH	3.10.20.30	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	6.10.140.1070	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000185721	GTEx
HGNC ID	HGNC:3029	ENTREZGENE
Human Proteome Map	DRG1	Human Proteome Map
InterPro	Beta-grasp_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	DRG	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_OBG	UniProtKB/Swiss-Prot
	GTP-binding_2	UniProtKB/Swiss-Prot
	GTP1-OBG_CS	UniProtKB/Swiss-Prot
	GTP_binding_domain	UniProtKB/Swiss-Prot
	P-loop_NTPase	UniProtKB/Swiss-Prot
	Small_GTP-bd_dom	UniProtKB/Swiss-Prot
	TGS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	TGS-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:4733	UniProtKB/Swiss-Prot
NCBI Gene	4733	ENTREZGENE
OMIM	603952	OMIM
PANTHER	PTHR43127	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	MMR_HSR1	UniProtKB/Swiss-Prot
	MMR_HSR1_Xtn	UniProtKB/Swiss-Prot
	TGS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA27483	PharmGKB
PRINTS	GTP1OBG	UniProtKB/Swiss-Prot
PROSITE	G_OBG	UniProtKB/Swiss-Prot
	GTP1_OBG	UniProtKB/Swiss-Prot
	TGS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF52540	UniProtKB/Swiss-Prot
	SSF81271	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	B2RDS8	ENTREZGENE
	DRG1_HUMAN	UniProtKB/Swiss-Prot
	F8WEE0_HUMAN	UniProtKB/TrEMBL
	H0YI06_HUMAN	UniProtKB/TrEMBL
	Q6FGP8	ENTREZGENE
	Q8WW69	ENTREZGENE
	Q9UGF2	ENTREZGENE
	Q9Y295	ENTREZGENE
UniProt Secondary	B2RDS8	UniProtKB/Swiss-Prot
	Q6FGP8	UniProtKB/Swiss-Prot
	Q8WW69	UniProtKB/Swiss-Prot
	Q9UGF2	UniProtKB/Swiss-Prot

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

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

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

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Imported Disease Annotations - ClinVar

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Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - OMIM

Imported Human Phenotype Annotations - HPO

Imported Human Phenotype Annotations - ClinVar