CALCR (calcitonin receptor) - Rat Genome Database

Name: CALCR
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

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Gene: CALCR (calcitonin receptor) Homo sapiens

Analyze

Symbol:

CALCR

Name:

calcitonin receptor

RGD ID:

731272

HGNC Page

HGNC:1440

Description:

Enables calcitonin binding activity and calcitonin family receptor activity. Involved in several processes, including G protein-coupled receptor signaling pathway; positive regulation of intracellular signal transduction; and positive regulation of macromolecule metabolic process. Part of amylin receptor complex 1; amylin receptor complex 2; and amylin receptor complex 3. Implicated in osteoporosis.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

CRT; CT-R; CTR; CTR1

RGD Orthologs

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Calcr (calcitonin receptor)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Rattus norvegicus (Norway rat):	Calcr (calcitonin receptor)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Calcr (calcitonin receptor)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	CALCR (calcitonin receptor)	NCBI	Ortholog
Canis lupus familiaris (dog):	CALCR (calcitonin receptor)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Calcr (calcitonin receptor)	NCBI	Ortholog
Sus scrofa (pig):	CALCR (calcitonin receptor)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	CALCR (calcitonin receptor)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Calcr (calcitonin receptor)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Calcrl (calcitonin receptor like receptor)	HGNC	OrthoDB
Mus musculus (house mouse):	Calcrl (calcitonin receptor-like)	HGNC	OrthoDB
Canis lupus familiaris (dog):	CALCRL (calcitonin receptor like receptor)	HGNC	OrthoDB
Sus scrofa (pig):	CALCRL (calcitonin receptor like receptor)	HGNC	OrthoDB
Alliance orthologs ³
Mus musculus (house mouse):	Calcr (calcitonin receptor)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Rattus norvegicus (Norway rat):	Calcr (calcitonin receptor)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	calcr (calcitonin receptor)	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|ZFIN)
Drosophila melanogaster (fruit fly):	Dh31-R	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|SonicParanoid)
Caenorhabditis elegans (roundworm):	pdfr-1	Alliance	DIOPT (InParanoid\|OMA\|OrthoInspector\|SonicParanoid)
Drosophila melanogaster (fruit fly):	hec	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER)
Xenopus tropicalis (tropical clawed frog):	calcr	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	calcr.L	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	calcr.S	Alliance	DIOPT (Xenbase)

Allele / Splice:

See ClinVar data

Candidate Gene For:

BMD1_H

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	7	93,424,486 - 93,574,724 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	7	93,424,486 - 93,574,730 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	7	93,053,798 - 93,204,036 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	7	92,891,735 - 93,041,686 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	7	92,698,449 - 92,848,401	NCBI
Celera	7	87,758,299 - 87,908,414 (-)	NCBI		Celera
Cytogenetic Map	7	q21.3	NCBI
HuRef	7	87,664,656 - 87,814,674 (-)	NCBI		HuRef
CHM1_1	7	92,983,802 - 93,134,094 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	7	94,666,953 - 94,817,060 (-)	NCBI		T2T-CHM13v2.0
CRA_TCAGchr7v2	7	92,383,112 - 92,533,218 (-)	NCBI

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

genetic disease (IAGP)

Herpes Simplex Encephalitis (ISO)

hypercalcemia (EXP)

osteoporosis (EXP,IAGP)

pleomorphic xanthoastrocytoma (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,1-dichloroethene (ISO)

17beta-estradiol (EXP)

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

2-aminopurine (ISO)

afimoxifene (EXP)

aflatoxin B1 (EXP)

ammonium chloride (ISO)

amphetamine (ISO)

benzo[a]pyrene (EXP,ISO)

benzo[b]fluoranthene (ISO)

bis(2-chloroethyl) sulfide (ISO)

bisphenol A (EXP,ISO)

chlorpromazine (ISO)

coumestrol (EXP)

cytarabine (EXP)

dibenz[a,h]anthracene (ISO)

ethanol (ISO)

fenvalerate (ISO)

flavonoids (ISO)

fulvestrant (EXP)

gamma-aminobutyric acid (ISO)

genistein (ISO)

GW 4064 (ISO)

kaempferol (ISO)

KN-93 (ISO)

lipopolysaccharide (EXP)

mangiferin (ISO)

naringin (ISO)

paraquat (ISO)

quercetin (ISO)

resveratrol (EXP)

rubiadin (ISO)

silicon dioxide (EXP)

sulforaphane (ISO)

tacrolimus hydrate (ISO)

tetraphene (ISO)

triptonide (ISO)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

adenylate cyclase-activating G protein-coupled receptor signaling pathway (IBA,IDA,IEA,IGI,ISO,NAS)

adenylate cyclase-modulating G protein-coupled receptor signaling pathway (IEA,ISO)

amylin receptor signaling pathway (IDA,IGI)

cell surface receptor signaling pathway (IEA)

cellular response to transforming growth factor beta stimulus (ISO)

cellular response to tumor necrosis factor (ISO)

G protein-coupled receptor signaling pathway (IEA)

mononuclear cell differentiation (ISO)

negative regulation of ossification (IEA,ISO)

ossification (IEA,ISO)

osteoclast differentiation (IEA,ISO)

positive regulation of calcium-mediated signaling (IGI)

positive regulation of cAMP-mediated signaling (IDA)

positive regulation of cytosolic calcium ion concentration (IBA,IDA,IEA,ISO)

positive regulation of ERK1 and ERK2 cascade (IGI)

positive regulation of gene expression (IGI)

positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction (IGI)

positive regulation of protein kinase A signaling (IGI)

regulation of bone resorption (ISO)

regulation of mRNA stability (IEA,ISO)

response to amyloid-beta (IGI)

response to glucocorticoid (IDA)

signal transduction (IEA)

Cellular Component

acrosomal vesicle (IEA)

amylin receptor complex 1 (IDA)

amylin receptor complex 2 (IDA)

amylin receptor complex 3 (IDA)

axon (IBA,ISO)

cilium (IEA)

membrane (IEA)

neuronal cell body (ISO)

plasma membrane (IBA,IEA,NAS,TAS)

Molecular Function

amylin receptor activity (IBA,IGI,IPI)

amyloid-beta binding (IDA)

calcitonin binding (IDA,IPI,ISO)

calcitonin gene-related peptide receptor activity (IPI)

calcitonin receptor activity (IBA,IDA,IEA,ISO)

G protein-coupled receptor activity (IEA)

protein binding (IPI)

transmembrane signaling receptor activity (IEA)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Autosomal dominant inheritance (IAGP)

Osteoporosis (IAGP)

Pleomorphic xanthoastrocytoma (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	The calcitonin receptor gene is a candidate for regulation of susceptibility to herpes simplex type 1 neuronal infection leading to encephalitis in rat.	Abdelmagid N, etal., PLoS Pathog. 2012;8(6):e1002753. doi: 10.1371/journal.ppat.1002753. Epub 2012 Jun 28.
2.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
3.	OMIM Disease Annotation Pipeline	OMIM Disease Annotation Pipeline
4.	Online Mendelian Inheritance in Man, OMIM (TM).	Online Mendelian Inheritance in Man, OMIM (TM).
5.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
6.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
7.	Association between osteoporosis and polymorphisms of the bone Gla protein, estrogen receptor 1, collagen 1-A1 and calcitonin receptor genes in Turkish postmenopausal women.	Tural S, etal., Gene. 2013 Feb 15;515(1):167-72. doi: 10.1016/j.gene.2012.10.041. Epub 2012 Nov 5.

Additional References at PubMed

PMID:1331173	PMID:4961748	PMID:7588285	PMID:7619207	PMID:7720653	PMID:7733946	PMID:7769107	PMID:7789182	PMID:7961748	PMID:8078488	PMID:8143880	PMID:9571205
PMID:9817931	PMID:10385705	PMID:10570950	PMID:10865224	PMID:10882736	PMID:11136533	PMID:11250927	PMID:11298188	PMID:11353946	PMID:11464063	PMID:11560994	PMID:11858573
PMID:12016463	PMID:12036966	PMID:12147682	PMID:12375338	PMID:12397072	PMID:12477932	PMID:12517415	PMID:12531889	PMID:12565884	PMID:12690205	PMID:12771454	PMID:12821648
PMID:12853948	PMID:12905735	PMID:14583624	PMID:14614653	PMID:14722252	PMID:15086532	PMID:15155765	PMID:15279076	PMID:15489334	PMID:15490304	PMID:15563840	PMID:15670850
PMID:15856322	PMID:15860547	PMID:15929987	PMID:15966503	PMID:16280328	PMID:16363366	PMID:16412323	PMID:16713399	PMID:17487556	PMID:17709929	PMID:17714780	PMID:18240029
PMID:18622089	PMID:18676680	PMID:19170196	PMID:19255718	PMID:19445988	PMID:19447889	PMID:19453261	PMID:19625176	PMID:19692168	PMID:19903822	PMID:19913121	PMID:19946674
PMID:20424473	PMID:20654748	PMID:20869948	PMID:20961463	PMID:21033393	PMID:21462477	PMID:21873635	PMID:22335784	PMID:22500019	PMID:23202124	PMID:23820954	PMID:24296906
PMID:24522475	PMID:24643196	PMID:25055932	PMID:25402775	PMID:26895962	PMID:28428082	PMID:28435134	PMID:28437792	PMID:28614667	PMID:29507222	PMID:31626518	PMID:33823567
PMID:34312771	PMID:34417812	PMID:35090891	PMID:35202609	PMID:36088585	PMID:36834780

Genomics

Comparative Map Data

CALCR
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	7	93,424,486 - 93,574,724 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	7	93,424,486 - 93,574,730 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	7	93,053,798 - 93,204,036 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	7	92,891,735 - 93,041,686 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	7	92,698,449 - 92,848,401	NCBI
Celera	7	87,758,299 - 87,908,414 (-)	NCBI		Celera
Cytogenetic Map	7	q21.3	NCBI
HuRef	7	87,664,656 - 87,814,674 (-)	NCBI		HuRef
CHM1_1	7	92,983,802 - 93,134,094 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	7	94,666,953 - 94,817,060 (-)	NCBI		T2T-CHM13v2.0
CRA_TCAGchr7v2	7	92,383,112 - 92,533,218 (-)	NCBI

Calcr
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	6	3,685,678 - 3,764,713 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	6	3,685,680 - 3,764,714 (-)	Ensembl		GRCm39 Ensembl
GRCm38	6	3,685,678 - 3,764,713 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	6	3,685,680 - 3,764,714 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	6	3,635,720 - 3,714,713 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	6	3,635,734 - 3,718,616 (-)	NCBI		MGSCv36	mm8
Celera	6	3,838,106 - 3,917,223 (-)	NCBI		Celera
Cytogenetic Map	6	A1	NCBI
cM Map	6	1.81	NCBI

Calcr
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
mRatBN7.2	4	31,661,270 - 31,736,392 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	4	31,661,273 - 31,736,392 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	4	36,633,979 - 36,709,091 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	4	32,560,089 - 32,635,205 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	4	30,919,584 - 30,995,051 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	4	28,627,439 - 28,702,559 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	4	28,627,442 - 28,702,559 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	4	28,532,077 - 28,607,201 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	4	28,486,176 - 28,561,296 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	4	28,501,581 - 28,574,979 (-)	NCBI
Celera	4	27,047,821 - 27,123,526 (-)	NCBI		Celera
Cytogenetic Map	4	q13	NCBI

Calcr
(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_004955432	10,309,263 - 10,391,141 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955432	10,310,776 - 10,391,029 (-)	NCBI	ChiLan1.0	ChiLan1.0

CALCR
(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	7	159,534,252 - 159,684,366 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	7	85,382,167 - 85,532,562 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	7	98,975,906 - 99,125,841 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	7	98,975,906 - 99,047,162 (-)	Ensembl	panpan1.1		panPan2

CALCR
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	14	18,923,116 - 19,074,904 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	14	18,923,116 - 19,074,904 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	14	18,482,050 - 18,633,756 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	14	18,730,002 - 18,888,306 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	14	18,729,945 - 18,888,301 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	14	18,889,119 - 19,040,277 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	14	18,624,883 - 18,776,465 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	14	18,875,566 - 19,033,608 (-)	NCBI		UU_Cfam_GSD_1.0

Calcr
(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	32,331,279 - 32,443,389 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936803	422,890 - 466,730 (+)	Ensembl	SpeTri2.0
SpeTri2.0	NW_004936803	423,558 - 466,762 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

CALCR
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	9	73,279,879 - 73,403,436 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	9	73,279,874 - 73,403,516 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	9	80,112,418 - 80,234,372 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3
Pig Cytomap	9	q11-q12	NCBI

CALCR
(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	21	55,433,438 - 55,585,608 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	21	55,523,412 - 55,583,735 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666042	48,721,181 - 48,873,559 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Calcr
(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_004624813	233,042 - 357,396 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624813	233,117 - 357,507 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in CALCR
75 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_001742.4(CALCR):c.1340T>C (p.Leu447Pro)	single nucleotide variant	Bone mineral density quantitative trait locus 15 [RCV000019203]\|not provided [RCV001642229]	Chr7:93426441 [GRCh38] Chr7:93055753 [GRCh37] Chr7:7q21.3	risk factor\|benign
GRCh37/hg19 7q21.2-22.1(chr7:92445452-99686985)x1	copy number loss	Split hand-foot malformation 1 [RCV000656540]	Chr7:92445452..99686985 [GRCh37] Chr7:7q21.2-22.1	pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1	copy number loss	See cases [RCV000052250]	Chr7:53985..159282531 [GRCh38] Chr7:53985..159075220 [GRCh37] Chr7:149068..158767981 [NCBI36] Chr7:7p22.3-q36.3	pathogenic
NM_001164737.1(CALCR):c.520C>T (p.His174Tyr)	single nucleotide variant	Malignant melanoma [RCV000068010]	Chr7:93468770 [GRCh38] Chr7:93098082 [GRCh37] Chr7:92936018 [NCBI36] Chr7:7q21.3	not provided
NM_001164737.1(CALCR):c.418C>T (p.Pro140Ser)	single nucleotide variant	Malignant melanoma [RCV000068011]	Chr7:93472440 [GRCh38] Chr7:93101752 [GRCh37] Chr7:92939688 [NCBI36] Chr7:7q21.3	not provided
NM_001164737.1(CALCR):c.1488C>T (p.Ile496=)	single nucleotide variant	Malignant melanoma [RCV000061700]	Chr7:93426395 [GRCh38] Chr7:93055707 [GRCh37] Chr7:92893643 [NCBI36] Chr7:7q21.3	not provided
NM_001164737.1(CALCR):c.355G>T (p.Asp119Tyr)	single nucleotide variant	Malignant melanoma [RCV000061701]	Chr7:93477573 [GRCh38] Chr7:93106885 [GRCh37] Chr7:92944821 [NCBI36] Chr7:7q21.3	not provided
NM_001164737.1(CALCR):c.1032+143G>A	single nucleotide variant	Lung cancer [RCV000106662]	Chr7:93437917 [GRCh38] Chr7:93067229 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001164737.1(CALCR):c.905-485G>C	single nucleotide variant	Lung cancer [RCV000106663]	Chr7:93438755 [GRCh38] Chr7:93068067 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001164737.1(CALCR):c.751-4817T>A	single nucleotide variant	Lung cancer [RCV000106664]	Chr7:93448574 [GRCh38] Chr7:93077886 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001164737.1(CALCR):c.-43-13764A>G	single nucleotide variant	Lung cancer [RCV000106665]	Chr7:93509738 [GRCh38] Chr7:93139050 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001164737.1(CALCR):c.-44+34332G>T	single nucleotide variant	Lung cancer [RCV000106666]	Chr7:93539957 [GRCh38] Chr7:93169269 [GRCh37] Chr7:7q21.3	uncertain significance
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	copy number loss	See cases [RCV000135401]	Chr7:54185..159282390 [GRCh38] Chr7:54185..159075079 [GRCh37] Chr7:149268..158767840 [NCBI36] Chr7:7p22.3-q36.3	pathogenic
GRCh38/hg38 7q21.3(chr7:93410151-93604672)x1	copy number loss	See cases [RCV000135731]	Chr7:93410151..93604672 [GRCh38] Chr7:93039463..93233984 [GRCh37] Chr7:92877399..93071920 [NCBI36] Chr7:7q21.3	uncertain significance
GRCh38/hg38 7q21.2-21.3(chr7:92945146-94512098)x1	copy number loss	See cases [RCV000137564]	Chr7:92945146..94512098 [GRCh38] Chr7:92574460..94141410 [GRCh37] Chr7:92412396..93979346 [NCBI36] Chr7:7q21.2-21.3	likely pathogenic
GRCh38/hg38 7q21.2-21.3(chr7:92759144-97568646)x1	copy number loss	See cases [RCV000141756]	Chr7:92759144..97568646 [GRCh38] Chr7:92388458..97197958 [GRCh37] Chr7:92226394..97035894 [NCBI36] Chr7:7q21.2-21.3	pathogenic
GRCh38/hg38 7q21.11-21.3(chr7:84002634-95228883)x1	copy number loss	See cases [RCV000143271]	Chr7:84002634..95228883 [GRCh38] Chr7:83631950..94858195 [GRCh37] Chr7:83469886..94696131 [NCBI36] Chr7:7q21.11-21.3	pathogenic
GRCh38/hg38 7q21.3(chr7:93410151-93604672)x1	copy number loss	See cases [RCV000149543]	Chr7:93410151..93604672 [GRCh38] Chr7:93039463..93233984 [GRCh37] Chr7:92877399..93071920 [NCBI36] Chr7:7q21.3	uncertain significance
TMEM106B-BRAF fusion	deletion	Pleomorphic xanthoastrocytoma [RCV000454357]	Chr7:12258147..140494267 [GRCh37] Chr7:7p21.3-q34	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1	copy number loss	See cases [RCV000446044]	Chr7:43360..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)	copy number gain	See cases [RCV000510686]	Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3	copy number gain	See cases [RCV000511549]	Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
NM_001742.4(CALCR):c.179A>G (p.Gln60Arg)	single nucleotide variant	Inborn genetic diseases [RCV003257553]	Chr7:93479380 [GRCh38] Chr7:93108692 [GRCh37] Chr7:7q21.3	uncertain significance
Single allele	deletion	not provided [RCV000677988]	Chr7:73591993..93683437 [GRCh37] Chr7:7q11.23-21.3	uncertain significance
GRCh37/hg19 7q21.3(chr7:93006562-93511541)x3	copy number gain	not provided [RCV000682852]	Chr7:93006562..93511541 [GRCh37] Chr7:7q21.3	uncertain significance
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv	inversion	Childhood apraxia of speech [RCV000234948]	Chr7:21001537..114528369 [GRCh37] Chr7:7p15.3-q31.1	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3	copy number gain	not provided [RCV000746280]	Chr7:44935..159126310 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3	copy number gain	not provided [RCV000746278]	Chr7:10704..159122532 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
NM_001742.4(CALCR):c.1149+138A>T	single nucleotide variant	not provided [RCV001540257]	Chr7:93435814 [GRCh38] Chr7:93065126 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.430-29GTTT[5]	microsatellite	not provided [RCV001708622]	Chr7:93468823..93468824 [GRCh38] Chr7:93098135..93098136 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1150-108dup	duplication	not provided [RCV001648204]	Chr7:93434389..93434390 [GRCh38] Chr7:93063701..93063702 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1149+72A>G	single nucleotide variant	not provided [RCV001679150]	Chr7:93435880 [GRCh38] Chr7:93065192 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.522-1472C>G	single nucleotide variant	not provided [RCV001680677]	Chr7:93462419 [GRCh38] Chr7:93091731 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.430-29GTTT[6]	microsatellite	not provided [RCV001535122]	Chr7:93468823..93468824 [GRCh38] Chr7:93098135..93098136 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.429+37T>C	single nucleotide variant	not provided [RCV001669257]	Chr7:93472338 [GRCh38] Chr7:93101650 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.-26-8791A>G	single nucleotide variant	not provided [RCV001692518]	Chr7:93495798 [GRCh38] Chr7:93125110 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.648+124C>A	single nucleotide variant	not provided [RCV001679322]	Chr7:93460697 [GRCh38] Chr7:93090009 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.765G>A (p.Glu255=)	single nucleotide variant	not provided [RCV000967058]	Chr7:93443641 [GRCh38] Chr7:93072953 [GRCh37] Chr7:7q21.3	benign
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3	copy number gain	not provided [RCV000848126]	Chr7:10365..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
NM_001742.4(CALCR):c.206-3C>T	single nucleotide variant	not provided [RCV000967059]	Chr7:93477671 [GRCh38] Chr7:93106983 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1285G>T (p.Ala429Ser)	single nucleotide variant	not provided [RCV000906274]	Chr7:93426496 [GRCh38] Chr7:93055808 [GRCh37] Chr7:7q21.3	likely benign
NM_001742.4(CALCR):c.1265C>G (p.Ser422Cys)	single nucleotide variant	Inborn genetic diseases [RCV003290220]	Chr7:93426516 [GRCh38] Chr7:93055828 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.931-189_931-187del	deletion	not provided [RCV001614746]	Chr7:93436357..93436359 [GRCh38] Chr7:93065669..93065671 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.51+105C>T	single nucleotide variant	not provided [RCV001610822]	Chr7:93486826 [GRCh38] Chr7:93116138 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.206-113T>G	single nucleotide variant	not provided [RCV001597985]	Chr7:93477781 [GRCh38] Chr7:93107093 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.802+245C>A	single nucleotide variant	not provided [RCV001674829]	Chr7:93443359 [GRCh38] Chr7:93072671 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.205+182C>T	single nucleotide variant	not provided [RCV001678653]	Chr7:93479172 [GRCh38] Chr7:93108484 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.317-192A>G	single nucleotide variant	not provided [RCV001714912]	Chr7:93472679 [GRCh38] Chr7:93101991 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.-26-78dup	duplication	not provided [RCV001614395]	Chr7:93487079..93487080 [GRCh38] Chr7:93116391..93116392 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.903C>A (p.Ile301=)	single nucleotide variant	not provided [RCV000967057]	Chr7:93438087 [GRCh38] Chr7:93067399 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.127G>A (p.Val43Ile)	single nucleotide variant	not provided [RCV000890734]	Chr7:93479432 [GRCh38] Chr7:93108744 [GRCh37] Chr7:7q21.3	likely benign
NM_001742.4(CALCR):c.649-78G>C	single nucleotide variant	not provided [RCV001659548]	Chr7:93443835 [GRCh38] Chr7:93073147 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1150-216C>T	single nucleotide variant	not provided [RCV001643974]	Chr7:93434510 [GRCh38] Chr7:93063822 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.-26-9245G>T	single nucleotide variant	not provided [RCV001682187]	Chr7:93496252 [GRCh38] Chr7:93125564 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.522-979C>T	single nucleotide variant	not provided [RCV001689163]	Chr7:93461926 [GRCh38] Chr7:93091238 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1150-301del	deletion	not provided [RCV001671414]	Chr7:93434595 [GRCh38] Chr7:93063907 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1191+167C>A	single nucleotide variant	not provided [RCV001596841]	Chr7:93434086 [GRCh38] Chr7:93063398 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1150-238T>A	single nucleotide variant	not provided [RCV001655255]	Chr7:93434532 [GRCh38] Chr7:93063844 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.429+266C>T	single nucleotide variant	not provided [RCV001641807]	Chr7:93472109 [GRCh38] Chr7:93101421 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1149+125A>T	single nucleotide variant	not provided [RCV001614290]	Chr7:93435827 [GRCh38] Chr7:93065139 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.522-1328A>C	single nucleotide variant	not provided [RCV001616803]	Chr7:93462275 [GRCh38] Chr7:93091587 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.931-271G>T	single nucleotide variant	not provided [RCV001635600]	Chr7:93436441 [GRCh38] Chr7:93065753 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.522-1329G>A	single nucleotide variant	not provided [RCV001637825]	Chr7:93462276 [GRCh38] Chr7:93091588 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.316+326A>G	single nucleotide variant	not provided [RCV001654232]	Chr7:93477232 [GRCh38] Chr7:93106544 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1149+149C>G	single nucleotide variant	not provided [RCV001635854]	Chr7:93435803 [GRCh38] Chr7:93065115 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.649-303A>C	single nucleotide variant	not provided [RCV001657160]	Chr7:93444060 [GRCh38] Chr7:93073372 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1150-311_1150-310dup	duplication	not provided [RCV001599042]	Chr7:93434594..93434595 [GRCh38] Chr7:93063906..93063907 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.521+53C>T	single nucleotide variant	not provided [RCV001708405]	Chr7:93468662 [GRCh38] Chr7:93097974 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1358del (p.Asn453fs)	deletion	not specified [RCV001532989]	Chr7:93426423 [GRCh38] Chr7:93055735 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.930+37del	deletion	not provided [RCV001614389]	Chr7:93438023 [GRCh38] Chr7:93067335 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.522-1226A>G	single nucleotide variant	not provided [RCV001696367]	Chr7:93462173 [GRCh38] Chr7:93091485 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1149+104TATT[5]	microsatellite	not provided [RCV001672319]	Chr7:93435825..93435828 [GRCh38] Chr7:93065137..93065140 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1149+123_1149+124insA	insertion	not provided [RCV001648385]	Chr7:93435828..93435829 [GRCh38] Chr7:93065140..93065141 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.-6T>C	single nucleotide variant	not provided [RCV001679189]	Chr7:93486987 [GRCh38] Chr7:93116299 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1150-108_1150-105dup	duplication	not provided [RCV001680443]	Chr7:93434389..93434390 [GRCh38] Chr7:93063701..93063702 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.430-77T>G	single nucleotide variant	not provided [RCV001613593]	Chr7:93468883 [GRCh38] Chr7:93098195 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.52-264A>T	single nucleotide variant	not provided [RCV001708998]	Chr7:93479771 [GRCh38] Chr7:93109083 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.648G>A (p.Pro216=)	single nucleotide variant	not provided [RCV001708131]	Chr7:93460821 [GRCh38] Chr7:93090133 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1192-326T>C	single nucleotide variant	not provided [RCV001714031]	Chr7:93426915 [GRCh38] Chr7:93056227 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.430-120T>C	single nucleotide variant	not provided [RCV001651612]	Chr7:93468926 [GRCh38] Chr7:93098238 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.522-327A>G	single nucleotide variant	not provided [RCV001613733]	Chr7:93461274 [GRCh38] Chr7:93090586 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.317-282del	deletion	not provided [RCV001641968]	Chr7:93472769 [GRCh38] Chr7:93102081 [GRCh37] Chr7:7q21.3	benign
GRCh37/hg19 7q21.12-22.1(chr7:87477185-100333327)	copy number gain	Isolated Pierre-Robin syndrome [RCV001352649]	Chr7:87477185..100333327 [GRCh37] Chr7:7q21.12-22.1	pathogenic
NM_001742.4(CALCR):c.52-250GT[4]	microsatellite	not provided [RCV001538195]	Chr7:93479751..93479752 [GRCh38] Chr7:93109063..93109064 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.*18C>T	single nucleotide variant	not provided [RCV001614978]	Chr7:93426338 [GRCh38] Chr7:93055650 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.522-1229G>A	single nucleotide variant	not provided [RCV001684242]	Chr7:93462176 [GRCh38] Chr7:93091488 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.522-1355C>T	single nucleotide variant	not provided [RCV001654478]	Chr7:93462302 [GRCh38] Chr7:93091614 [GRCh37] Chr7:7q21.3	benign
NM_001742.4(CALCR):c.1150-108_1150-107dup	duplication	not provided [RCV001685220]	Chr7:93434389..93434390 [GRCh38] Chr7:93063701..93063702 [GRCh37] Chr7:7q21.3	benign
GRCh37/hg19 7q21.2-21.3(chr7:92044792-93320149)	copy number loss	not specified [RCV002053709]	Chr7:92044792..93320149 [GRCh37] Chr7:7q21.2-21.3	uncertain significance
GRCh37/hg19 7q21.11-21.3(chr7:77821356-93340137)	copy number gain	not specified [RCV002053701]	Chr7:77821356..93340137 [GRCh37] Chr7:7q21.11-21.3	pathogenic
Single allele	complex	Ring chromosome 7 [RCV002280646]	Chr7:43360..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1	copy number loss	See cases [RCV002287832]	Chr7:56604613..96692931 [GRCh37] Chr7:7p22.3-q36.3	uncertain significance
NM_001742.4(CALCR):c.427A>G (p.Lys143Glu)	single nucleotide variant	Inborn genetic diseases [RCV003286665]	Chr7:93472377 [GRCh38] Chr7:93101689 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.1349A>G (p.Glu450Gly)	single nucleotide variant	Inborn genetic diseases [RCV002902315]	Chr7:93426432 [GRCh38] Chr7:93055744 [GRCh37] Chr7:7q21.3	uncertain significance
GRCh37/hg19 7q21.2-22.1(chr7:92721627-98311537)x1	copy number loss	not provided [RCV002474498]	Chr7:92721627..98311537 [GRCh37] Chr7:7q21.2-22.1	pathogenic
NM_001742.4(CALCR):c.449A>G (p.Tyr150Cys)	single nucleotide variant	Inborn genetic diseases [RCV002817275]	Chr7:93468787 [GRCh38] Chr7:93098099 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.149A>G (p.Asp50Gly)	single nucleotide variant	Inborn genetic diseases [RCV002992682]	Chr7:93479410 [GRCh38] Chr7:93108722 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.149A>C (p.Asp50Ala)	single nucleotide variant	Inborn genetic diseases [RCV002865558]	Chr7:93479410 [GRCh38] Chr7:93108722 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.553A>G (p.Lys185Glu)	single nucleotide variant	Inborn genetic diseases [RCV002731932]	Chr7:93460916 [GRCh38] Chr7:93090228 [GRCh37] Chr7:7q21.3	uncertain significance
GRCh37/hg19 7q21.3(chr7:93024221-93276286)x1	copy number loss	not provided [RCV002475724]	Chr7:93024221..93276286 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.1226T>C (p.Phe409Ser)	single nucleotide variant	Inborn genetic diseases [RCV002794274]	Chr7:93426555 [GRCh38] Chr7:93055867 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.1247G>A (p.Arg416His)	single nucleotide variant	Inborn genetic diseases [RCV002661140]	Chr7:93426534 [GRCh38] Chr7:93055846 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.193T>G (p.Tyr65Asp)	single nucleotide variant	Inborn genetic diseases [RCV002893351]	Chr7:93479366 [GRCh38] Chr7:93108678 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.851A>T (p.Tyr284Phe)	single nucleotide variant	Inborn genetic diseases [RCV002767773]	Chr7:93438222 [GRCh38] Chr7:93067534 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.23G>A (p.Arg8Gln)	single nucleotide variant	Inborn genetic diseases [RCV003004014]	Chr7:93486959 [GRCh38] Chr7:93116271 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.434C>T (p.Ala145Val)	single nucleotide variant	Inborn genetic diseases [RCV002934582]	Chr7:93468802 [GRCh38] Chr7:93098114 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.173G>A (p.Arg58Gln)	single nucleotide variant	Inborn genetic diseases [RCV003185488]	Chr7:93479386 [GRCh38] Chr7:93108698 [GRCh37] Chr7:7q21.3	uncertain significance
NM_001742.4(CALCR):c.638G>A (p.Arg213Gln)	single nucleotide variant	Inborn genetic diseases [RCV003212386]	Chr7:93460831 [GRCh38] Chr7:93090143 [GRCh37] Chr7:7q21.3	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	3047
Count of miRNA genes:	720
Interacting mature miRNAs:	811
Transcripts:	ENST00000359558, ENST00000360249, ENST00000394441, ENST00000415529, ENST00000421592, ENST00000423724, ENST00000426151
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

G59766

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	93,194,868 - 93,194,982	UniSTS	GRCh37
Build 36	7	93,032,804 - 93,032,918	RGD	NCBI36
Celera	7	87,899,249 - 87,899,363	RGD
Cytogenetic Map	7	q21.3	UniSTS
HuRef	7	87,805,504 - 87,805,618	UniSTS
CRA_TCAGchr7v2	7	92,524,053 - 92,524,167	UniSTS

SHGC-144374

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	93,182,335 - 93,182,624	UniSTS	GRCh37
Build 36	7	93,020,271 - 93,020,560	RGD	NCBI36
Celera	7	87,886,725 - 87,887,014	RGD
Cytogenetic Map	7	q21.3	UniSTS
HuRef	7	87,792,974 - 87,793,263	UniSTS
CRA_TCAGchr7v2	7	92,511,529 - 92,511,818	UniSTS

CALCR

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	93,054,250 - 93,054,316	UniSTS	GRCh37
GRCh37	7	93,065,303 - 93,065,403	UniSTS	GRCh37
Build 36	7	92,892,186 - 92,892,252	RGD	NCBI36
Celera	7	87,758,750 - 87,758,816	RGD
Celera	7	87,769,804 - 87,769,904	UniSTS
Cytogenetic Map	7	q21.3	UniSTS
HuRef	7	87,665,107 - 87,665,173	UniSTS
CRA_TCAGchr7v2	7	92,394,617 - 92,394,717	UniSTS
CRA_TCAGchr7v2	7	92,383,563 - 92,383,629	UniSTS

CALCR_3944

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	93,053,675 - 93,054,545	UniSTS	GRCh37
Build 36	7	92,891,611 - 92,892,481	RGD	NCBI36
Celera	7	87,758,175 - 87,759,045	RGD
HuRef	7	87,664,532 - 87,665,402	UniSTS
CRA_TCAGchr7v2	7	92,382,988 - 92,383,858	UniSTS

GDB:1317942

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	93,133,603 - 93,133,748	UniSTS	GRCh37
Build 36	7	92,971,539 - 92,971,684	RGD	NCBI36
Celera	7	87,838,108 - 87,838,253	RGD
Cytogenetic Map	7	q21.3	UniSTS
HuRef	7	87,744,379 - 87,744,524	UniSTS
CRA_TCAGchr7v2	7	92,462,913 - 92,463,058	UniSTS

GDB:1317880

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	93,133,502 - 93,133,682	UniSTS	GRCh37
Build 36	7	92,971,438 - 92,971,618	RGD	NCBI36
Celera	7	87,838,007 - 87,838,187	RGD
Cytogenetic Map	7	q21.3	UniSTS
HuRef	7	87,744,278 - 87,744,458	UniSTS
CRA_TCAGchr7v2	7	92,462,812 - 92,462,992	UniSTS

D7S2736

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	93,055,472 - 93,055,595	UniSTS	GRCh37
Build 36	7	92,893,408 - 92,893,531	RGD	NCBI36
Celera	7	87,759,972 - 87,760,095	RGD
Cytogenetic Map	7	q21.3	UniSTS
HuRef	7	87,666,329 - 87,666,452	UniSTS
CRA_TCAGchr7v2	7	92,384,785 - 92,384,908	UniSTS
Stanford-G3 RH Map	7	4343.0	UniSTS
GeneMap99-G3 RH Map	7	4343.0	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

Low

309

407

224

359

122

Below cutoff

1507

1675

950

274

496

162

3098

1487

2517

122

591

1048

117

994

2163

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NG_013005	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001164737	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001164738	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001742	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB022177	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB022178	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC003078	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC005024	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AH007368	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ831406	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ831407	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK313996	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY430048	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC069611	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC075028	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH236949	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471091	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068271	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	FN994993	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	FN994994	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	FN994995	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	FN994996	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	L00587	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	S77789	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	U26553	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	U26554	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X69920	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X82466	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000359558 ⟹ ENSP00000352561

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	93,424,487 - 93,574,730 (-)	Ensembl

RefSeq Acc Id:

ENST00000360249 ⟹ ENSP00000353385

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	93,426,310 - 93,487,013 (-)	Ensembl

RefSeq Acc Id:

ENST00000394441 ⟹ ENSP00000377959

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	93,426,323 - 93,559,810 (-)	Ensembl

RefSeq Acc Id:

ENST00000415529 ⟹ ENSP00000413179

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	93,426,356 - 93,486,981 (-)	Ensembl

RefSeq Acc Id:

ENST00000423724 ⟹ ENSP00000391369

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	93,426,356 - 93,486,981 (-)	Ensembl

RefSeq Acc Id:

ENST00000426151 ⟹ ENSP00000389295

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	93,424,486 - 93,574,724 (-)	Ensembl

RefSeq Acc Id:

ENST00000649521 ⟹ ENSP00000497687

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	93,424,539 - 93,574,730 (-)	Ensembl

RefSeq Acc Id:

NM_001164737 ⟹ NP_001158209

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	93,424,486 - 93,574,724 (-)	NCBI
GRCh37	7	93,053,799 - 93,204,042 (-)	ENTREZGENE
HuRef	7	87,664,656 - 87,814,674 (-)	ENTREZGENE
CHM1_1	7	92,983,802 - 93,134,094 (-)	NCBI
T2T-CHM13v2.0	7	94,666,953 - 94,817,060 (-)	NCBI
CRA_TCAGchr7v2	7	92,383,112 - 92,533,218 (-)	ENTREZGENE

Sequence:

show sequence

ACAGCTGGGAGAGCGCAGGAAGGCGCCGGGAAGGAAAGCCAGCCCACCAGCGTCTGGGTGGGCT
GCGCCGCGCGGCTGGCGGACCTTCCCGGGTTGGAGAAGTGCGCACGTCCGCACCTCACCCTGCG
GCTGACATCTCCTGCCCAGGAGATGGGCGCTGAAGCTTGAGCGCCTGAGTCCCTGGAGCCACAC
CTGCGAACACCCTTTGCTTCTATTGAGCTGTGCCCAGCCGCCCAGTGACAGAATTCCAGAATAA
ATGATTCCCACTGATCCACCCACTTTTGCCACCCCAGGATGCAATTTTCTGGAGAGAAGATTAG
TGGACAAAGAGATCTTCAAAAATCAAAAATGAGGTTCACATTTACAAGCCGGTGCTTGGCACTG
TTTCTTCTTCTAAATCACCCAACCCCAATTCTTCCTGCCTTTTCAAATCAAACCTATCCAACAA
TAGAGCCCAAGCCATTTCTTTACGTCGTAGGACGAAAGAAGATGATGGATGCACAGTACAAATG
CTATGACCGAATGCAGCAGTTACCCGCATACCAAGGAGAAGGTCCATATTGCAATCGCACCTGG
GATGGATGGCTGTGCTGGGATGACACACCGGCTGGAGTATTGTCCTATCAGTTCTGCCCAGATT
ATTTTCCGGATTTTGATCCATCAGAAAAGGTTACAAAATACTGTGATGAAAAAGGTGTTTGGTT
TAAACATCCTGAAAACAATCGAACCTGGTCCAACTATACTATGTGCAATGCTTTCACTCCTGAG
AAACTGAAGAATGCATATGTTCTGTACTATTTGGCTATTGTGGGTCATTCTTTGTCAATTTTCA
CCCTAGTGATTTCCCTGGGGATTTTCGTGTTTTTCAGAAAATTGACAACTATTTTTCCTTTGAA
TTGGAAATATAGGAAGGCATTGAGCCTTGGCTGCCAAAGGGTAACCCTGCACAAGAACATGTTT
CTTACTTACATTCTGAATTCTATGATTATCATCATCCACCTGGTTGAAGTAGTACCCAATGGAG
AGCTCGTGCGAAGGGACCCGGTGAGCTGCAAGATTTTGCATTTTTTCCACCAGTACATGATGGC
CTGCAACTATTTCTGGATGCTCTGTGAAGGGATCTATCTTCATACACTCATTGTCGTGGCTGTG
TTTACTGAGAAGCAACGCTTGCGGTGGTATTATCTCTTGGGCTGGGGGTTCCCGCTGGTGCCAA
CCACTATCCATGCTATTACCAGGGCCGTGTACTTCAATGACAACTGCTGGCTGAGTGTGGAAAC
CCATTTGCTTTACATAATCCATGGACCTGTCATGGCGGCACTTGTGGTCAATTTCTTCTTTTTG
CTCAACATTGTCCGGGTGCTTGTGACCAAAATGAGGGAAACCCATGAGGCGGAATCCCACATGT
ACCTGAAGGCTGTGAAGGCCACCATGATCCTTGTGCCCCTGCTGGGAATCCAGTTTGTCGTCTT
TCCCTGGAGACCTTCCAACAAGATGCTTGGGAAGATATATGATTACGTGATGCACTCTCTGATT
CATTTCCAGGGCTTCTTTGTTGCGACCATCTACTGCTTCTGCAACAATGAGGTCCAAACCACCG
TGAAGCGCCAATGGGCCCAATTCAAAATTCAGTGGAACCAGCGTTGGGGGAGGCGCCCCTCCAA
CCGCTCTGCTCGCGCTGCAGCCGCTGCTGCGGAGGCTGGCGACATCCCAATTTACATCTGCCAT
CAGGAGCTGAGGAATGAACCAGCCAACAACCAAGGCGAGGAGAGTGCTGAGATCATCCCTTTGA
ATATCATAGAGCAAGAGTCATCTGCTTGAATGTGAAGCAAACACAGCATCGTGATCACTGAGCC
ATCATTTCCTGGGAGAAAGACCATGCATTTAAAGTATTCTCCATCCTCCCAGGAACCGAACATA
TCATTTGTGAAGAATTATTCAGTGAATTTGTCCATTGTAAATCTGAAGAAAGTTATTCTTGGTA
CTGTTGCTTTGGGAGACAGTCTAGGAATGGAGTCTCCCACTGCAACTTGTGAACTCCATCATTC
ATCCAGGACTGAGATGCAAATGTCACAGTAATGCAAGCAAAGTATCAAAGAAAAACAATGAAAT
TGACCTAGTTCAGATACAGGGTGCTCCTTGTCAATACTGAGCCATTTATACCTTTGAAATATTA
AAATCACTGTCAATATTTTTATTTTTAACTCTGGATTTTGAATTAGATTATTTCTGTATTTGGC
TATGGATCTGATTTTTAATTTTTTTAAATTTCAGTCAATTCTGATGTTACTGAGATGTTTTACC
ATCCTTACAATGTAAACCACATGAACTACGTGACCTCTGCAAGACAAAGCGGCTTTCTAATAGA
GAGATTAGTAAATATGTGAAGAAAAAGACCTGCATTTGGCAGGAAGATGTATGCTTTGAATGCA
AAAGAAATTTAGAGTCAATTTGCTGAAAACATTACATGCTCAGCTTGGTTTTGGACAAGCCTGT
CCATTGGGCAGGACCTAGCTGTTGTAAAGAATTGGTCTTAATGTTGAATGTATTTTGGTTGCTG
ATGTTTATAAACTGAGAGGTCACAAAGAATCTATCACTAAAAATTTTTACAAAACTGCCAAAAA
TATAATTCTTAGTGGAAGACAATACTCCCTTTAAAGAGAGTTTGCCACTCCCCTAAACTCCAGG
ATTTATAAAGCAAATTACTCCAAGGTTTATAAAGCAGATTACCTCTTGCCCTTGGGTGCTATCT
AGCAGTAAAAGATAAATTTGTTGAATATTGGTAATTAAAAGACTCCACATAAGTCCATTAACTG
CTTTCCACCCAGCTTCAAAGCTTAAAAAGAGCTCAGGCTTTTCCAGGAAGATCCAGGAGGGCTA
ATTAGAAATCAACTTGTGGTTGACCGCTTGTTTCTTGTTATTACCAAAACAGGAGGGGAAAAAA
TTAACTGCTCCAAATTTAACCATAAATCAATTCATGTTTAACGTTTCTCATTAAAATCCAGTAT
TATATTATCATATCTCTCTTTACTTCCCAGTATAAGATTTTTGAAAATCCTGAATAAACCAGTA
TCGTTACTGGCACCTGAAATTAATTTGTGAATTTGCAACAGTAATCAGAGTTACCATTATTTAA
TTTGTATGCTAAATGAGGAGGTACATTGAAACCCTCCAAATCTCCAGTCTCATCTATGTCATAT
TTTGCCACTGCCTTTCAGAAGTGATTTAGTTGTGGAAAGATAATAAATTGATTTGTTATGGTTA
CATATTTAGCGCACCCAGAGAAAATTAATTATATTTCTACAGAGAAAATGAATTTGGGATACTA
AAGTAGTTTAAGTCTCCTTTACTGAATGTAAGGGGGGGATCGAAAAGAAGGTATTTTTCCAATC
ACAGTGTTATGTAGTATTGTTCTATTTTTGTTTACAAACATGGAAAACAGAGTATTTCTGGCAG
CTGTGGTACAAATGTGATAATATATTGCTAAAATATTTTAGATGTTATTATGCTAATATAGTAG
GGGTTGAAGAAAACAAAATAGCTTATTATAGAATTGCACATAGTTCTGCCCAAATTATGTGAAA
TGCTTATGCTTGTGTATATGTATAAATTAATACAGAGTACGTTAAAAGCAAAAAGATGTATATT
TGCATATTTTTCTAAAGAAATATATTATTCATCTTTTCATTCA

hide sequence

RefSeq Acc Id:

NM_001164738 ⟹ NP_001158210

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	93,424,486 - 93,559,810 (-)	NCBI
GRCh37	7	93,053,799 - 93,204,042 (-)	ENTREZGENE
HuRef	7	87,664,656 - 87,814,674 (-)	ENTREZGENE
CHM1_1	7	92,983,802 - 93,119,166 (-)	NCBI
T2T-CHM13v2.0	7	94,666,953 - 94,802,148 (-)	NCBI
CRA_TCAGchr7v2	7	92,383,112 - 92,533,218 (-)	ENTREZGENE

Sequence:

show sequence

AGTTATAAGAGACAGGAATACCAGTGAGAAGTATGAGAGAGTGGGTGGGAGATAATGTTTAGAA
TCTCTTTTGCTGCCCGCAATTTATGAAAATGGCTTGAAAATATTTATGGTCAAAGACCGAAATA
TTTCTTCAAAGAAGATTAGCTTTGCTCCATTAAAAGTAATGAGTAGAAATATTAAAAAAAAAAA
AAGTTTTAAGTACCTGAGTATCTTGCCAGCAACTGACCACCACTGCTAAAAGTGAGGAGAGACA
CAGCTTTCATCATTGGGACTGCAGTTTATTTCAGGACAAAGAGATCTTCAAAAATCAAAAATGA
GGTTCACATTTACAAGCCGGTGCTTGGCACTGTTTCTTCTTCTAAATCACCCAACCCCAATTCT
TCCTGCCTTTTCAAATCAAACCTATCCAACAATAGAGCCCAAGCCATTTCTTTACGTCGTAGGA
CGAAAGAAGATGATGGATGCACAGTACAAATGCTATGACCGAATGCAGCAGTTACCCGCATACC
AAGGAGAAGGTCCATATTGCAATCGCACCTGGGATGGATGGCTGTGCTGGGATGACACACCGGC
TGGAGTATTGTCCTATCAGTTCTGCCCAGATTATTTTCCGGATTTTGATCCATCAGAAAAGGTT
ACAAAATACTGTGATGAAAAAGGTGTTTGGTTTAAACATCCTGAAAACAATCGAACCTGGTCCA
ACTATACTATGTGCAATGCTTTCACTCCTGAGAAACTGAAGAATGCATATGTTCTGTACTATTT
GGCTATTGTGGGTCATTCTTTGTCAATTTTCACCCTAGTGATTTCCCTGGGGATTTTCGTGTTT
TTCAGGAGCCTTGGCTGCCAAAGGGTAACCCTGCACAAGAACATGTTTCTTACTTACATTCTGA
ATTCTATGATTATCATCATCCACCTGGTTGAAGTAGTACCCAATGGAGAGCTCGTGCGAAGGGA
CCCGGTGAGCTGCAAGATTTTGCATTTTTTCCACCAGTACATGATGGCCTGCAACTATTTCTGG
ATGCTCTGTGAAGGGATCTATCTTCATACACTCATTGTCGTGGCTGTGTTTACTGAGAAGCAAC
GCTTGCGGTGGTATTATCTCTTGGGCTGGGGGTTCCCGCTGGTGCCAACCACTATCCATGCTAT
TACCAGGGCCGTGTACTTCAATGACAACTGCTGGCTGAGTGTGGAAACCCATTTGCTTTACATA
ATCCATGGACCTGTCATGGCGGCACTTGTGGTCAATTTCTTCTTTTTGCTCAACATTGTCCGGG
TGCTTGTGACCAAAATGAGGGAAACCCATGAGGCGGAATCCCACATGTACCTGAAGGCTGTGAA
GGCCACCATGATCCTTGTGCCCCTGCTGGGAATCCAGTTTGTCGTCTTTCCCTGGAGACCTTCC
AACAAGATGCTTGGGAAGATATATGATTACGTGATGCACTCTCTGATTCATTTCCAGGGCTTCT
TTGTTGCGACCATCTACTGCTTCTGCAACAATGAGGTCCAAACCACCGTGAAGCGCCAATGGGC
CCAATTCAAAATTCAGTGGAACCAGCGTTGGGGGAGGCGCCCCTCCAACCGCTCTGCTCGCGCT
GCAGCCGCTGCTGCGGAGGCTGGCGACATCCCAATTTACATCTGCCATCAGGAGCTGAGGAATG
AACCAGCCAACAACCAAGGCGAGGAGAGTGCTGAGATCATCCCTTTGAATATCATAGAGCAAGA
GTCATCTGCTTGAATGTGAAGCAAACACAGCATCGTGATCACTGAGCCATCATTTCCTGGGAGA
AAGACCATGCATTTAAAGTATTCTCCATCCTCCCAGGAACCGAACATATCATTTGTGAAGAATT
ATTCAGTGAATTTGTCCATTGTAAATCTGAAGAAAGTTATTCTTGGTACTGTTGCTTTGGGAGA
CAGTCTAGGAATGGAGTCTCCCACTGCAACTTGTGAACTCCATCATTCATCCAGGACTGAGATG
CAAATGTCACAGTAATGCAAGCAAAGTATCAAAGAAAAACAATGAAATTGACCTAGTTCAGATA
CAGGGTGCTCCTTGTCAATACTGAGCCATTTATACCTTTGAAATATTAAAATCACTGTCAATAT
TTTTATTTTTAACTCTGGATTTTGAATTAGATTATTTCTGTATTTGGCTATGGATCTGATTTTT
AATTTTTTTAAATTTCAGTCAATTCTGATGTTACTGAGATGTTTTACCATCCTTACAATGTAAA
CCACATGAACTACGTGACCTCTGCAAGACAAAGCGGCTTTCTAATAGAGAGATTAGTAAATATG
TGAAGAAAAAGACCTGCATTTGGCAGGAAGATGTATGCTTTGAATGCAAAAGAAATTTAGAGTC
AATTTGCTGAAAACATTACATGCTCAGCTTGGTTTTGGACAAGCCTGTCCATTGGGCAGGACCT
AGCTGTTGTAAAGAATTGGTCTTAATGTTGAATGTATTTTGGTTGCTGATGTTTATAAACTGAG
AGGTCACAAAGAATCTATCACTAAAAATTTTTACAAAACTGCCAAAAATATAATTCTTAGTGGA
AGACAATACTCCCTTTAAAGAGAGTTTGCCACTCCCCTAAACTCCAGGATTTATAAAGCAAATT
ACTCCAAGGTTTATAAAGCAGATTACCTCTTGCCCTTGGGTGCTATCTAGCAGTAAAAGATAAA
TTTGTTGAATATTGGTAATTAAAAGACTCCACATAAGTCCATTAACTGCTTTCCACCCAGCTTC
AAAGCTTAAAAAGAGCTCAGGCTTTTCCAGGAAGATCCAGGAGGGCTAATTAGAAATCAACTTG
TGGTTGACCGCTTGTTTCTTGTTATTACCAAAACAGGAGGGGAAAAAATTAACTGCTCCAAATT
TAACCATAAATCAATTCATGTTTAACGTTTCTCATTAAAATCCAGTATTATATTATCATATCTC
TCTTTACTTCCCAGTATAAGATTTTTGAAAATCCTGAATAAACCAGTATCGTTACTGGCACCTG
AAATTAATTTGTGAATTTGCAACAGTAATCAGAGTTACCATTATTTAATTTGTATGCTAAATGA
GGAGGTACATTGAAACCCTCCAAATCTCCAGTCTCATCTATGTCATATTTTGCCACTGCCTTTC
AGAAGTGATTTAGTTGTGGAAAGATAATAAATTGATTTGTTATGGTTACATATTTAGCGCACCC
AGAGAAAATTAATTATATTTCTACAGAGAAAATGAATTTGGGATACTAAAGTAGTTTAAGTCTC
CTTTACTGAATGTAAGGGGGGGATCGAAAAGAAGGTATTTTTCCAATCACAGTGTTATGTAGTA
TTGTTCTATTTTTGTTTACAAACATGGAAAACAGAGTATTTCTGGCAGCTGTGGTACAAATGTG
ATAATATATTGCTAAAATATTTTAGATGTTATTATGCTAATATAGTAGGGGTTGAAGAAAACAA
AATAGCTTATTATAGAATTGCACATAGTTCTGCCCAAATTATGTGAAATGCTTATGCTTGTGTA
TATGTATAAATTAATACAGAGTACGTTAAAAGCAAAAAGATGTATATTTGCATATTTTTCTAAA
GAAATATATTATTCATCTTTTCATTCA

hide sequence

RefSeq Acc Id:

NM_001742 ⟹ NP_001733

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	93,424,486 - 93,574,724 (-)	NCBI
GRCh37	7	93,053,799 - 93,204,042 (-)	ENTREZGENE
Build 36	7	92,891,735 - 93,041,686 (-)	NCBI Archive
HuRef	7	87,664,656 - 87,814,674 (-)	ENTREZGENE
CHM1_1	7	92,983,802 - 93,134,094 (-)	NCBI
T2T-CHM13v2.0	7	94,666,953 - 94,817,060 (-)	NCBI
CRA_TCAGchr7v2	7	92,383,112 - 92,533,218 (-)	ENTREZGENE

Sequence:

show sequence

ACAGCTGGGAGAGCGCAGGAAGGCGCCGGGAAGGAAAGCCAGCCCACCAGCGTCTGGGTGGGCT
GCGCCGCGCGGCTGGCGGACCTTCCCGGGTTGGAGAAGTGCGCACGTCCGCACCTCACCCTGCG
GCTGACATCTCCTGCCCAGGAGATGGGCGCTGAAGCTTGAGCGCCTGAGTCCCTGGAGCCACAC
CTGCGAACACCCTTTGCTTCTATTGAGCTGTGCCCAGCCGCCCAGTGACAGAATTCCAGGACAA
AGAGATCTTCAAAAATCAAAAATGAGGTTCACATTTACAAGCCGGTGCTTGGCACTGTTTCTTC
TTCTAAATCACCCAACCCCAATTCTTCCTGCCTTTTCAAATCAAACCTATCCAACAATAGAGCC
CAAGCCATTTCTTTACGTCGTAGGACGAAAGAAGATGATGGATGCACAGTACAAATGCTATGAC
CGAATGCAGCAGTTACCCGCATACCAAGGAGAAGGTCCATATTGCAATCGCACCTGGGATGGAT
GGCTGTGCTGGGATGACACACCGGCTGGAGTATTGTCCTATCAGTTCTGCCCAGATTATTTTCC
GGATTTTGATCCATCAGAAAAGGTTACAAAATACTGTGATGAAAAAGGTGTTTGGTTTAAACAT
CCTGAAAACAATCGAACCTGGTCCAACTATACTATGTGCAATGCTTTCACTCCTGAGAAACTGA
AGAATGCATATGTTCTGTACTATTTGGCTATTGTGGGTCATTCTTTGTCAATTTTCACCCTAGT
GATTTCCCTGGGGATTTTCGTGTTTTTCAGGAGCCTTGGCTGCCAAAGGGTAACCCTGCACAAG
AACATGTTTCTTACTTACATTCTGAATTCTATGATTATCATCATCCACCTGGTTGAAGTAGTAC
CCAATGGAGAGCTCGTGCGAAGGGACCCGGTGAGCTGCAAGATTTTGCATTTTTTCCACCAGTA
CATGATGGCCTGCAACTATTTCTGGATGCTCTGTGAAGGGATCTATCTTCATACACTCATTGTC
GTGGCTGTGTTTACTGAGAAGCAACGCTTGCGGTGGTATTATCTCTTGGGCTGGGGGTTCCCGC
TGGTGCCAACCACTATCCATGCTATTACCAGGGCCGTGTACTTCAATGACAACTGCTGGCTGAG
TGTGGAAACCCATTTGCTTTACATAATCCATGGACCTGTCATGGCGGCACTTGTGGTCAATTTC
TTCTTTTTGCTCAACATTGTCCGGGTGCTTGTGACCAAAATGAGGGAAACCCATGAGGCGGAAT
CCCACATGTACCTGAAGGCTGTGAAGGCCACCATGATCCTTGTGCCCCTGCTGGGAATCCAGTT
TGTCGTCTTTCCCTGGAGACCTTCCAACAAGATGCTTGGGAAGATATATGATTACGTGATGCAC
TCTCTGATTCATTTCCAGGGCTTCTTTGTTGCGACCATCTACTGCTTCTGCAACAATGAGGTCC
AAACCACCGTGAAGCGCCAATGGGCCCAATTCAAAATTCAGTGGAACCAGCGTTGGGGGAGGCG
CCCCTCCAACCGCTCTGCTCGCGCTGCAGCCGCTGCTGCGGAGGCTGGCGACATCCCAATTTAC
ATCTGCCATCAGGAGCTGAGGAATGAACCAGCCAACAACCAAGGCGAGGAGAGTGCTGAGATCA
TCCCTTTGAATATCATAGAGCAAGAGTCATCTGCTTGAATGTGAAGCAAACACAGCATCGTGAT
CACTGAGCCATCATTTCCTGGGAGAAAGACCATGCATTTAAAGTATTCTCCATCCTCCCAGGAA
CCGAACATATCATTTGTGAAGAATTATTCAGTGAATTTGTCCATTGTAAATCTGAAGAAAGTTA
TTCTTGGTACTGTTGCTTTGGGAGACAGTCTAGGAATGGAGTCTCCCACTGCAACTTGTGAACT
CCATCATTCATCCAGGACTGAGATGCAAATGTCACAGTAATGCAAGCAAAGTATCAAAGAAAAA
CAATGAAATTGACCTAGTTCAGATACAGGGTGCTCCTTGTCAATACTGAGCCATTTATACCTTT
GAAATATTAAAATCACTGTCAATATTTTTATTTTTAACTCTGGATTTTGAATTAGATTATTTCT
GTATTTGGCTATGGATCTGATTTTTAATTTTTTTAAATTTCAGTCAATTCTGATGTTACTGAGA
TGTTTTACCATCCTTACAATGTAAACCACATGAACTACGTGACCTCTGCAAGACAAAGCGGCTT
TCTAATAGAGAGATTAGTAAATATGTGAAGAAAAAGACCTGCATTTGGCAGGAAGATGTATGCT
TTGAATGCAAAAGAAATTTAGAGTCAATTTGCTGAAAACATTACATGCTCAGCTTGGTTTTGGA
CAAGCCTGTCCATTGGGCAGGACCTAGCTGTTGTAAAGAATTGGTCTTAATGTTGAATGTATTT
TGGTTGCTGATGTTTATAAACTGAGAGGTCACAAAGAATCTATCACTAAAAATTTTTACAAAAC
TGCCAAAAATATAATTCTTAGTGGAAGACAATACTCCCTTTAAAGAGAGTTTGCCACTCCCCTA
AACTCCAGGATTTATAAAGCAAATTACTCCAAGGTTTATAAAGCAGATTACCTCTTGCCCTTGG
GTGCTATCTAGCAGTAAAAGATAAATTTGTTGAATATTGGTAATTAAAAGACTCCACATAAGTC
CATTAACTGCTTTCCACCCAGCTTCAAAGCTTAAAAAGAGCTCAGGCTTTTCCAGGAAGATCCA
GGAGGGCTAATTAGAAATCAACTTGTGGTTGACCGCTTGTTTCTTGTTATTACCAAAACAGGAG
GGGAAAAAATTAACTGCTCCAAATTTAACCATAAATCAATTCATGTTTAACGTTTCTCATTAAA
ATCCAGTATTATATTATCATATCTCTCTTTACTTCCCAGTATAAGATTTTTGAAAATCCTGAAT
AAACCAGTATCGTTACTGGCACCTGAAATTAATTTGTGAATTTGCAACAGTAATCAGAGTTACC
ATTATTTAATTTGTATGCTAAATGAGGAGGTACATTGAAACCCTCCAAATCTCCAGTCTCATCT
ATGTCATATTTTGCCACTGCCTTTCAGAAGTGATTTAGTTGTGGAAAGATAATAAATTGATTTG
TTATGGTTACATATTTAGCGCACCCAGAGAAAATTAATTATATTTCTACAGAGAAAATGAATTT
GGGATACTAAAGTAGTTTAAGTCTCCTTTACTGAATGTAAGGGGGGGATCGAAAAGAAGGTATT
TTTCCAATCACAGTGTTATGTAGTATTGTTCTATTTTTGTTTACAAACATGGAAAACAGAGTAT
TTCTGGCAGCTGTGGTACAAATGTGATAATATATTGCTAAAATATTTTAGATGTTATTATGCTA
ATATAGTAGGGGTTGAAGAAAACAAAATAGCTTATTATAGAATTGCACATAGTTCTGCCCAAAT
TATGTGAAATGCTTATGCTTGTGTATATGTATAAATTAATACAGAGTACGTTAAAAGCAAAAAG
ATGTATATTTGCATATTTTTCTAAAGAAATATATTATTCATCTTTTCATTCA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001158209	(Get FASTA)	NCBI Sequence Viewer
	NP_001158210	(Get FASTA)	NCBI Sequence Viewer
	NP_001733	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA35640	(Get FASTA)	NCBI Sequence Viewer
	AAB83945	(Get FASTA)	NCBI Sequence Viewer
	AAC50300	(Get FASTA)	NCBI Sequence Viewer
	AAC50301	(Get FASTA)	NCBI Sequence Viewer
	AAD14268	(Get FASTA)	NCBI Sequence Viewer
	AAH69611	(Get FASTA)	NCBI Sequence Viewer
	AAH75028	(Get FASTA)	NCBI Sequence Viewer
	AAR06949	(Get FASTA)	NCBI Sequence Viewer
	BAA86928	(Get FASTA)	NCBI Sequence Viewer
	BAA86929	(Get FASTA)	NCBI Sequence Viewer
	BAG36708	(Get FASTA)	NCBI Sequence Viewer
	CAA49541	(Get FASTA)	NCBI Sequence Viewer
	CAA57849	(Get FASTA)	NCBI Sequence Viewer
	CAH40796	(Get FASTA)	NCBI Sequence Viewer
	CAH40797	(Get FASTA)	NCBI Sequence Viewer
	CBN80565	(Get FASTA)	NCBI Sequence Viewer
	CBN80566	(Get FASTA)	NCBI Sequence Viewer
	CBN80567	(Get FASTA)	NCBI Sequence Viewer
	CBN80568	(Get FASTA)	NCBI Sequence Viewer
	EAL24142	(Get FASTA)	NCBI Sequence Viewer
	EAW76813	(Get FASTA)	NCBI Sequence Viewer
	EAW76814	(Get FASTA)	NCBI Sequence Viewer
	P30988	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001733 ⟸ NM_001742
- Peptide Label:	isoform 2 precursor
- UniProtKB:	Q6DJU8 (UniProtKB/Swiss-Prot), Q659U6 (UniProtKB/Swiss-Prot), Q5ZGL8 (UniProtKB/Swiss-Prot), Q13941 (UniProtKB/Swiss-Prot), O14585 (UniProtKB/Swiss-Prot), F5H605 (UniProtKB/Swiss-Prot), A4D1G6 (UniProtKB/Swiss-Prot), Q6T712 (UniProtKB/Swiss-Prot), P30988 (UniProtKB/Swiss-Prot), A0A0C4DG16 (UniProtKB/TrEMBL), D8MIV1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRFTFTSRCLALFLLLNHPTPILPAFSNQTYPTIEPKPFLYVVGRKKMMDAQYKCYDRMQQLPA YQGEGPYCNRTWDGWLCWDDTPAGVLSYQFCPDYFPDFDPSEKVTKYCDEKGVWFKHPENNRTW SNYTMCNAFTPEKLKNAYVLYYLAIVGHSLSIFTLVISLGIFVFFRSLGCQRVTLHKNMFLTYI LNSMIIIIHLVEVVPNGELVRRDPVSCKILHFFHQYMMACNYFWMLCEGIYLHTLIVVAVFTEK QRLRWYYLLGWGFPLVPTTIHAITRAVYFNDNCWLSVETHLLYIIHGPVMAALVVNFFFLLNIV RVLVTKMRETHEAESHMYLKAVKATMILVPLLGIQFVVFPWRPSNKMLGKIYDYVMHSLIHFQG FFVATIYCFCNNEVQTTVKRQWAQFKIQWNQRWGRRPSNRSARAAAAAAEAGDIPIYICHQELR NEPANNQGEESAEIIPLNIIEQESSA hide sequence

RefSeq Acc Id:	NP_001158209 ⟸ NM_001164737
- Peptide Label:	isoform 1 precursor
- UniProtKB:	A0A0A0MSQ7 (UniProtKB/TrEMBL), D8MIV1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MQFSGEKISGQRDLQKSKMRFTFTSRCLALFLLLNHPTPILPAFSNQTYPTIEPKPFLYVVGRK KMMDAQYKCYDRMQQLPAYQGEGPYCNRTWDGWLCWDDTPAGVLSYQFCPDYFPDFDPSEKVTK YCDEKGVWFKHPENNRTWSNYTMCNAFTPEKLKNAYVLYYLAIVGHSLSIFTLVISLGIFVFFR KLTTIFPLNWKYRKALSLGCQRVTLHKNMFLTYILNSMIIIIHLVEVVPNGELVRRDPVSCKIL HFFHQYMMACNYFWMLCEGIYLHTLIVVAVFTEKQRLRWYYLLGWGFPLVPTTIHAITRAVYFN DNCWLSVETHLLYIIHGPVMAALVVNFFFLLNIVRVLVTKMRETHEAESHMYLKAVKATMILVP LLGIQFVVFPWRPSNKMLGKIYDYVMHSLIHFQGFFVATIYCFCNNEVQTTVKRQWAQFKIQWN QRWGRRPSNRSARAAAAAAEAGDIPIYICHQELRNEPANNQGEESAEIIPLNIIEQESSA hide sequence

RefSeq Acc Id:	NP_001158210 ⟸ NM_001164738
- Peptide Label:	isoform 2 precursor
- UniProtKB:	Q6DJU8 (UniProtKB/Swiss-Prot), Q659U6 (UniProtKB/Swiss-Prot), Q5ZGL8 (UniProtKB/Swiss-Prot), Q13941 (UniProtKB/Swiss-Prot), O14585 (UniProtKB/Swiss-Prot), F5H605 (UniProtKB/Swiss-Prot), A4D1G6 (UniProtKB/Swiss-Prot), Q6T712 (UniProtKB/Swiss-Prot), P30988 (UniProtKB/Swiss-Prot), A0A0C4DG16 (UniProtKB/TrEMBL), D8MIV1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRFTFTSRCLALFLLLNHPTPILPAFSNQTYPTIEPKPFLYVVGRKKMMDAQYKCYDRMQQLPA YQGEGPYCNRTWDGWLCWDDTPAGVLSYQFCPDYFPDFDPSEKVTKYCDEKGVWFKHPENNRTW SNYTMCNAFTPEKLKNAYVLYYLAIVGHSLSIFTLVISLGIFVFFRSLGCQRVTLHKNMFLTYI LNSMIIIIHLVEVVPNGELVRRDPVSCKILHFFHQYMMACNYFWMLCEGIYLHTLIVVAVFTEK QRLRWYYLLGWGFPLVPTTIHAITRAVYFNDNCWLSVETHLLYIIHGPVMAALVVNFFFLLNIV RVLVTKMRETHEAESHMYLKAVKATMILVPLLGIQFVVFPWRPSNKMLGKIYDYVMHSLIHFQG FFVATIYCFCNNEVQTTVKRQWAQFKIQWNQRWGRRPSNRSARAAAAAAEAGDIPIYICHQELR NEPANNQGEESAEIIPLNIIEQESSA hide sequence

RefSeq Acc Id:

ENSP00000352561 ⟸ ENST00000359558

RefSeq Acc Id:

ENSP00000391369 ⟸ ENST00000423724

RefSeq Acc Id:

ENSP00000497687 ⟸ ENST00000649521

RefSeq Acc Id:

ENSP00000389295 ⟸ ENST00000426151

RefSeq Acc Id:

ENSP00000353385 ⟸ ENST00000360249

RefSeq Acc Id:

ENSP00000413179 ⟸ ENST00000415529

RefSeq Acc Id:

ENSP00000377959 ⟸ ENST00000394441

Protein Domains

G-protein coupled receptors family 2 profile

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P30988-F1-model_v2	AlphaFold	P30988	1-474	view protein structure

Promoters

RGD ID:

7211085

Promoter ID:

EPDNEW_H11288

Type:

initiation region

Name:

CALCR_1

Description:

calcitonin receptor

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	7	93,574,724 - 93,574,784	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:1440	AgrOrtholog
COSMIC	CALCR	COSMIC
Ensembl Genes	ENSG00000004948	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein	ENSP00000377959	ENTREZGENE
	ENSP00000377959.1	UniProtKB/Swiss-Prot
	ENSP00000389295	ENTREZGENE
	ENSP00000389295.1	UniProtKB/Swiss-Prot
	ENSP00000391369.1	UniProtKB/Swiss-Prot
	ENSP00000413179.1	UniProtKB/Swiss-Prot
	ENSP00000497687	ENTREZGENE
	ENSP00000497687.1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000394441	ENTREZGENE
	ENST00000394441.5	UniProtKB/Swiss-Prot
	ENST00000415529.2	UniProtKB/Swiss-Prot
	ENST00000423724.5	UniProtKB/Swiss-Prot
	ENST00000426151	ENTREZGENE
	ENST00000426151.7	UniProtKB/Swiss-Prot
	ENST00000649521	ENTREZGENE
	ENST00000649521.1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Gene3D-CATH	4.10.1240.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Rhodopsin 7-helix transmembrane proteins	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000004948	GTEx
HGNC ID	HGNC:1440	ENTREZGENE
Human Proteome Map	CALCR	Human Proteome Map
InterPro	GCPR_2_calcitonin_rcpt_fam	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2_calcitonin_rcpt	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2_extracell_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2_extracellular_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2_secretin-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2_secretin-like_CS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:799	UniProtKB/Swiss-Prot
NCBI Gene	799	ENTREZGENE
OMIM	114131	OMIM
PANTHER	PDF RECEPTOR-LIKE PROTEIN-RELATED	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR45620:SF8	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	7tm_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	HRM	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA26032	PharmGKB
PRINTS	CALCITONINR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	CTRFAMILY	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCRSECRETIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	G_PROTEIN_RECEP_F2_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F2_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F2_3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F2_4	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	HormR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	Family A G protein-coupled receptor-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF111418	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A0A0MSQ7	ENTREZGENE, UniProtKB/TrEMBL
	A0A0C4DG16	ENTREZGENE
	A4D1G6	ENTREZGENE
	CALCR_HUMAN	UniProtKB/Swiss-Prot
	D8MIV0_HUMAN	UniProtKB/TrEMBL
	D8MIV1	ENTREZGENE, UniProtKB/TrEMBL
	F5H605	ENTREZGENE
	O14585	ENTREZGENE
	P30988	ENTREZGENE
	Q13941	ENTREZGENE
	Q5ZGL8	ENTREZGENE
	Q659U6	ENTREZGENE
	Q6DJU8	ENTREZGENE
	Q6T712	ENTREZGENE
UniProt Secondary	A0A0C4DG16	UniProtKB/Swiss-Prot
	A4D1G6	UniProtKB/Swiss-Prot
	F5H605	UniProtKB/Swiss-Prot
	O14585	UniProtKB/Swiss-Prot
	Q13941	UniProtKB/Swiss-Prot
	Q5ZGL8	UniProtKB/Swiss-Prot
	Q659U6	UniProtKB/Swiss-Prot
	Q6DJU8	UniProtKB/Swiss-Prot
	Q6T712	UniProtKB/Swiss-Prot

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

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

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

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

Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

Imported Disease Annotations - OMIM

Manual Human Phenotype Annotations - RGD

Imported Human Phenotype Annotations - HPO

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - OMIM

Manual Human Phenotype Annotations - RGD

Imported Human Phenotype Annotations - HPO

Imported Human Phenotype Annotations - ClinVar