SCRN3 (secernin 3) - Rat Genome Database

Name: SCRN3
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: SCRN3 (secernin 3) Homo sapiens

Analyze

Symbol:

SCRN3

Name:

secernin 3

RGD ID:

1312871

HGNC Page

HGNC:30382

Description:

Predicted to enable cysteine-type exopeptidase activity and dipeptidase activity. Predicted to be involved in proteolysis.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FLJ23142; MGC149597; secernin-3; SES3

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):	Scrn3 (secernin 3)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Scrn3 (secernin 3)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, OMA, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Scrn3 (secernin 3)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	SCRN3 (secernin 3)	NCBI	Ortholog
Canis lupus familiaris (dog):	SCRN3 (secernin 3)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Scrn3 (secernin 3)	NCBI	Ortholog
Sus scrofa (pig):	SCRN3 (secernin 3)	HGNC	Ensembl, NCBI, OrthoDB, Panther
Chlorocebus sabaeus (green monkey):	SCRN3 (secernin 3)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Scrn3 (secernin 3)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Scrn3 (secernin 3)	Alliance	DIOPT (HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Scrn3 (secernin 3)	Alliance	DIOPT (HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	scrn3 (secernin 3)	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Drosophila melanogaster (fruit fly):	CG10098	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	scrn3.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	scrn3	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	174,395,730 - 174,430,071 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	174,395,730 - 174,429,575 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	175,260,458 - 175,294,303 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	174,968,713 - 175,001,974 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	2	175,085,973 - 175,119,234	NCBI
Celera	2	168,873,893 - 168,907,739 (+)	NCBI		Celera
Cytogenetic Map	2	q31.1	NCBI
HuRef	2	167,140,624 - 167,174,864 (+)	NCBI		HuRef
CHM1_1	2	175,266,645 - 175,300,425 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	174,884,418 - 174,918,718 (+)	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

genetic disease (IAGP)

split hand-foot malformation 5 (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(-)-epigallocatechin 3-gallate (EXP)

(1->4)-beta-D-glucan (ISO)

1,2-dimethylhydrazine (ISO)

1-naphthyl isothiocyanate (ISO)

17beta-estradiol (ISO)

2,6-dinitrotoluene (ISO)

2-butoxyethanol (ISO)

4-hydroxyphenyl retinamide (ISO)

all-trans-retinoic acid (EXP)

antirheumatic drug (EXP)

aristolochic acid A (EXP)

atrazine (ISO)

benzo[a]pyrene (EXP)

bisphenol A (ISO)

cadmium dichloride (ISO)

carbon nanotube (ISO)

cyclosporin A (ISO)

dibutyl phthalate (ISO)

doxorubicin (EXP)

ethanol (ISO)

fipronil (ISO)

formaldehyde (EXP)

gallic acid (EXP)

geldanamycin (EXP)

gentamycin (ISO)

lead diacetate (ISO)

methyl methanesulfonate (EXP)

methylmercury chloride (EXP)

ozone (ISO)

paracetamol (EXP,ISO)

pentanal (EXP)

perfluorooctane-1-sulfonic acid (ISO)

potassium chromate (EXP)

testosterone (EXP)

tetrachloromethane (ISO)

thimerosal (EXP)

trichostatin A (EXP)

vancomycin (ISO)

vinclozolin (ISO)

vorinostat (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

proteolysis (IEA)

Molecular Function

cysteine-type exopeptidase activity (IEA)

dipeptidase activity (IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:8889548	PMID:11238933	PMID:12221138	PMID:12477932	PMID:14702039	PMID:15489334	PMID:15815621	PMID:16344560	PMID:21873635	PMID:21988832	PMID:26186194	PMID:28514442
PMID:28986522	PMID:29513927	PMID:33961781	PMID:35256949	PMID:36215168

Genomics

Comparative Map Data

SCRN3
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	174,395,730 - 174,430,071 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	174,395,730 - 174,429,575 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	175,260,458 - 175,294,303 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	174,968,713 - 175,001,974 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	2	175,085,973 - 175,119,234	NCBI
Celera	2	168,873,893 - 168,907,739 (+)	NCBI		Celera
Cytogenetic Map	2	q31.1	NCBI
HuRef	2	167,140,624 - 167,174,864 (+)	NCBI		HuRef
CHM1_1	2	175,266,645 - 175,300,425 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	174,884,418 - 174,918,718 (+)	NCBI		T2T-CHM13v2.0

Scrn3
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	73,142,980 - 73,168,158 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	73,142,945 - 73,168,162 (+)	Ensembl		GRCm39 Ensembl
GRCm38	2	73,312,650 - 73,337,818 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	73,312,601 - 73,337,818 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	2	73,150,709 - 73,175,864 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	2	73,113,491 - 73,138,646 (+)	NCBI		MGSCv36	mm8
Celera	2	74,999,193 - 75,024,348 (+)	NCBI		Celera
Cytogenetic Map	2	C3	NCBI
cM Map	2	43.57	NCBI

Scrn3
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	3	78,596,330 - 78,621,132 (+)	NCBI		GRCr8
mRatBN7.2	3	58,188,820 - 58,213,623 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	3	58,188,889 - 58,213,623 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	3	61,581,372 - 61,605,914 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	3	70,165,030 - 70,189,572 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	3	67,930,043 - 67,954,585 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	3	60,023,970 - 60,048,746 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	3	60,024,013 - 60,048,746 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	3	66,507,891 - 66,532,659 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	3	55,818,804 - 55,835,967 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	3	55,715,175 - 55,732,338 (+)	NCBI
Celera	3	57,724,365 - 57,741,522 (+)	NCBI		Celera
Cytogenetic Map	3	q23	NCBI

Scrn3
(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_004955449	935,659 - 958,460 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955449	935,061 - 960,514 (-)	NCBI	ChiLan1.0	ChiLan1.0

SCRN3
(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	13	77,060,356 - 77,094,587 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	2B	77,075,335 - 77,109,562 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	2B	61,673,624 - 61,707,934 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	2B	179,127,935 - 179,161,560 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	2B	179,127,961 - 179,161,560 (+)	Ensembl	panpan1.1		panPan2

SCRN3
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	36	18,453,027 - 18,476,122 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	36	18,453,050 - 18,474,047 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	36	18,462,257 - 18,485,153 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	36	18,589,069 - 18,611,852 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	36	18,589,132 - 18,611,833 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	36	18,666,216 - 18,688,988 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	36	18,664,543 - 18,687,532 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	36	18,774,956 - 18,798,269 (+)	NCBI		UU_Cfam_GSD_1.0

Scrn3
(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_024405303	135,618,043 - 135,648,959 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936509	4,171,781 - 4,199,332 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936509	4,172,012 - 4,202,862 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

SCRN3
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	15	80,375,778 - 80,425,093 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	15	80,375,738 - 80,419,647 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	15	89,627,030 - 89,640,258 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

SCRN3
(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	10	59,911,754 - 59,937,394 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	10	59,911,524 - 59,937,053 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666040	139,656,972 - 139,682,577 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Scrn3
(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_004624787	11,624,292 - 11,682,080 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624787	11,624,870 - 11,681,138 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in SCRN3
18 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 2q31.1-31.2(chr2:172779876-177598000)x1	copy number loss	See cases [RCV000050765]	Chr2:172779876..177598000 [GRCh38] Chr2:173644604..178462728 [GRCh37] Chr2:173352850..178170974 [NCBI36] Chr2:2q31.1-31.2	pathogenic
GRCh38/hg38 2q24.3-31.1(chr2:164850117-175559190)x1	copy number loss	See cases [RCV000051201]	Chr2:164850117..175559190 [GRCh38] Chr2:165706627..176423918 [GRCh37] Chr2:165414873..176132164 [NCBI36] Chr2:2q24.3-31.1	pathogenic
GRCh38/hg38 2q31.1(chr2:172366752-176361187)x1	copy number loss	See cases [RCV000052554]	Chr2:172366752..176361187 [GRCh38] Chr2:173231480..177225915 [GRCh37] Chr2:172939726..176934161 [NCBI36] Chr2:2q31.1	pathogenic
GRCh38/hg38 2q31.1-31.2(chr2:173408061-177702487)x1	copy number loss	See cases [RCV000052555]	Chr2:173408061..177702487 [GRCh38] Chr2:174272789..178567215 [GRCh37] Chr2:173981035..178275461 [NCBI36] Chr2:2q31.1-31.2	pathogenic
GRCh38/hg38 2q31.1(chr2:173699279-175586070)x1	copy number loss	See cases [RCV000052556]	Chr2:173699279..175586070 [GRCh38] Chr2:174564007..176450798 [GRCh37] Chr2:174272253..176159044 [NCBI36] Chr2:2q31.1	pathogenic
GRCh38/hg38 2q31.1(chr2:173960458-175924594)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052557]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052557]\|See cases [RCV000052557]	Chr2:173960458..175924594 [GRCh38] Chr2:174825186..176789322 [GRCh37] Chr2:174533432..176497568 [NCBI36] Chr2:2q31.1	pathogenic
GRCh38/hg38 2q24.3-32.1(chr2:163965382-182195062)x1	copy number loss	See cases [RCV000054122]	Chr2:163965382..182195062 [GRCh38] Chr2:164821892..183059789 [GRCh37] Chr2:164530138..182768034 [NCBI36] Chr2:2q24.3-32.1	pathogenic
GRCh38/hg38 2q31.1-32.1(chr2:170407688-186189894)x1	copy number loss	See cases [RCV000054127]	Chr2:170407688..186189894 [GRCh38] Chr2:171264198..187054621 [GRCh37] Chr2:170972444..186762866 [NCBI36] Chr2:2q31.1-32.1	pathogenic
NM_001193528.1(SCRN3):c.414G>A (p.Glu138=)	single nucleotide variant	Malignant melanoma [RCV000065206]	Chr2:174401083 [GRCh38] Chr2:175265811 [GRCh37] Chr2:174974057 [NCBI36] Chr2:2q31.1	not provided
GRCh38/hg38 2q31.1-32.2(chr2:171429233-189179568)x1	copy number loss	See cases [RCV000136850]	Chr2:171429233..189179568 [GRCh38] Chr2:172285743..190044294 [GRCh37] Chr2:171993989..189752539 [NCBI36] Chr2:2q31.1-32.2	pathogenic
GRCh38/hg38 2q31.1(chr2:173713838-175467462)x3	copy number gain	See cases [RCV000138664]	Chr2:173713838..175467462 [GRCh38] Chr2:174578566..176332190 [GRCh37] Chr2:174286812..176040436 [NCBI36] Chr2:2q31.1	uncertain significance\|conflicting data from submitters
GRCh38/hg38 2q31.1(chr2:174343200-174549848)x1	copy number loss	See cases [RCV000139193]	Chr2:174343200..174549848 [GRCh38] Chr2:175207928..175414576 [GRCh37] Chr2:174916174..175122822 [NCBI36] Chr2:2q31.1	uncertain significance
GRCh38/hg38 2q31.1-31.2(chr2:171513047-177854080)x1	copy number loss	See cases [RCV000139646]	Chr2:171513047..177854080 [GRCh38] Chr2:172369557..178718807 [GRCh37] Chr2:172077803..178427053 [NCBI36] Chr2:2q31.1-31.2	pathogenic
GRCh38/hg38 2q24.1-31.1(chr2:154294042-175989372)x3	copy number gain	See cases [RCV000142286]	Chr2:154294042..175989372 [GRCh38] Chr2:155150555..176854100 [GRCh37] Chr2:154858801..176562346 [NCBI36] Chr2:2q24.1-31.1	pathogenic
GRCh38/hg38 2q31.1(chr2:173713838-175467462)x1	copy number loss	See cases [RCV000142878]	Chr2:173713838..175467462 [GRCh38] Chr2:174578566..176332190 [GRCh37] Chr2:174286812..176040436 [NCBI36] Chr2:2q31.1	pathogenic
GRCh38/hg38 2q31.1-31.3(chr2:174236451-181188846)x1	copy number loss	See cases [RCV000143597]	Chr2:174236451..181188846 [GRCh38] Chr2:175101179..182053573 [GRCh37] Chr2:174809425..181761818 [NCBI36] Chr2:2q31.1-31.3	pathogenic
GRCh37/hg19 2q24.1-31.3(chr2:156489430-182921298)x3	copy number gain	See cases [RCV000239848]	Chr2:156489430..182921298 [GRCh37] Chr2:2q24.1-31.3	pathogenic
GRCh37/hg19 2q31.1(chr2:174586724-176423918)x1	copy number loss	See cases [RCV000240261]	Chr2:174586724..176423918 [GRCh37] Chr2:2q31.1	likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3	copy number gain	not provided [RCV000752802]	Chr2:14238..243048760 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q31.1(chr2:174562039-175276727)x1	copy number loss	See cases [RCV000447239]	Chr2:174562039..175276727 [GRCh37] Chr2:2q31.1	uncertain significance
GRCh37/hg19 2q31.1-35(chr2:169829974-215521436)x3	copy number gain	See cases [RCV000448271]	Chr2:169829974..215521436 [GRCh37] Chr2:2q31.1-35	pathogenic
GRCh37/hg19 2q31.1(chr2:174573334-175268147)x1	copy number loss	See cases [RCV000448480]	Chr2:174573334..175268147 [GRCh37] Chr2:2q31.1	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	copy number gain	See cases [RCV000512056]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q31.1(chr2:174783555-176832848)x1	copy number loss	See cases [RCV000510266]	Chr2:174783555..176832848 [GRCh37] Chr2:2q31.1	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	copy number gain	See cases [RCV000511212]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q31.1(chr2:171667051-176832848)x3	copy number gain	not provided [RCV000682159]	Chr2:171667051..176832848 [GRCh37] Chr2:2q31.1	pathogenic
GRCh37/hg19 2q31.1-31.2(chr2:173741558-178416381)x1	copy number loss	not provided [RCV000682153]	Chr2:173741558..178416381 [GRCh37] Chr2:2q31.1-31.2	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3	copy number gain	not provided [RCV000752804]	Chr2:15672..243101834 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q23.3-31.2(chr2:152409978-179325736)x3	copy number gain	not provided [RCV000740654]	Chr2:152409978..179325736 [GRCh37] Chr2:2q23.3-31.2	pathogenic
GRCh37/hg19 2q31.1-31.3(chr2:174238257-181604341)x1	copy number loss	not provided [RCV000740710]	Chr2:174238257..181604341 [GRCh37] Chr2:2q31.1-31.3	pathogenic
GRCh37/hg19 2q31.1-32.3(chr2:174690039-195521582)x1	copy number loss	not provided [RCV001005359]	Chr2:174690039..195521582 [GRCh37] Chr2:2q31.1-32.3	pathogenic
GRCh37/hg19 2q31.1-32.1(chr2:173538954-186401606)x1	copy number loss	not provided [RCV000846537]	Chr2:173538954..186401606 [GRCh37] Chr2:2q31.1-32.1	pathogenic
GRCh37/hg19 2q24.3-32.3(chr2:167329586-192756373)x1	copy number loss	not provided [RCV000848216]	Chr2:167329586..192756373 [GRCh37] Chr2:2q24.3-32.3	pathogenic
GRCh37/hg19 2q31.1(chr2:173865202-175428639)x1	copy number loss	not provided [RCV001005356]	Chr2:173865202..175428639 [GRCh37] Chr2:2q31.1	uncertain significance
GRCh37/hg19 2q24.2-34(chr2:163233162-211927188)x3	copy number gain	not provided [RCV001005349]	Chr2:163233162..211927188 [GRCh37] Chr2:2q24.2-34	pathogenic
NM_024583.5(SCRN3):c.83A>G (p.Asp28Gly)	single nucleotide variant	Inborn genetic diseases [RCV003291287]	Chr2:174398366 [GRCh38] Chr2:175263094 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.1251_1263del (p.Asn417fs)	microsatellite	not provided [RCV000948609]	Chr2:174427853..174427865 [GRCh38] Chr2:175292581..175292593 [GRCh37] Chr2:2q31.1	benign
GRCh37/hg19 2q31.1(chr2:174562000-175276727)x1	copy number loss	not provided [RCV001005358]	Chr2:174562000..175276727 [GRCh37] Chr2:2q31.1	uncertain significance
GRCh37/hg19 2q24.2-31.3(chr2:163078055-182119617)x1	copy number loss	2q24 microdeletion syndrome [RCV001263223]	Chr2:163078055..182119617 [GRCh37] Chr2:2q24.2-31.3	pathogenic
GRCh37/hg19 2q31.1-31.3(chr2:171999572-182774361)	copy number loss	3-4 finger syndactyly [RCV001352646]	Chr2:171999572..182774361 [GRCh37] Chr2:2q31.1-31.3	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	copy number gain	Mosaic trisomy 2 [RCV002280628]	Chr2:1..243199373 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q31.1(chr2:174573334-175268147)	copy number loss	not specified [RCV002053267]	Chr2:174573334..175268147 [GRCh37] Chr2:2q31.1	uncertain significance
GRCh37/hg19 2q31.1(chr2:174562039-175276727)	copy number loss	not specified [RCV002053266]	Chr2:174562039..175276727 [GRCh37] Chr2:2q31.1	uncertain significance
GRCh37/hg19 2q31.1(chr2:174673094-177275625)x3	copy number gain	not provided [RCV001825257]	Chr2:174673094..177275625 [GRCh37] Chr2:2q31.1	not provided
GRCh37/hg19 2q31.1-35(chr2:169829974-215521436)	copy number gain	not specified [RCV002053265]	Chr2:169829974..215521436 [GRCh37] Chr2:2q31.1-35	pathogenic
Single allele	deletion	Split hand-foot malformation 5 [RCV002264898]	Chr2:171524396..178694337 [GRCh37] Chr2:2q31.1-31.2	pathogenic
NM_024583.5(SCRN3):c.413G>A (p.Gly138Asp)	single nucleotide variant	Inborn genetic diseases [RCV003302568]	Chr2:174401061 [GRCh38] Chr2:175265789 [GRCh37] Chr2:2q31.1	uncertain significance
GRCh37/hg19 2q31.1-31.3(chr2:175143352-180999636)x1	copy number loss	not provided [RCV002474570]	Chr2:175143352..180999636 [GRCh37] Chr2:2q31.1-31.3	pathogenic
NM_024583.5(SCRN3):c.1046T>C (p.Leu349Pro)	single nucleotide variant	Inborn genetic diseases [RCV002990807]	Chr2:174424603 [GRCh38] Chr2:175289331 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.202G>A (p.Val68Ile)	single nucleotide variant	Inborn genetic diseases [RCV002733814]	Chr2:174399964 [GRCh38] Chr2:175264692 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.1132G>C (p.Glu378Gln)	single nucleotide variant	Inborn genetic diseases [RCV002749259]	Chr2:174427752 [GRCh38] Chr2:175292480 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.860C>T (p.Pro287Leu)	single nucleotide variant	Inborn genetic diseases [RCV002840062]	Chr2:174422990 [GRCh38] Chr2:175287718 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.592C>T (p.Arg198Trp)	single nucleotide variant	Inborn genetic diseases [RCV002689119]	Chr2:174404153 [GRCh38] Chr2:175268881 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.495G>C (p.Trp165Cys)	single nucleotide variant	Inborn genetic diseases [RCV002779072]	Chr2:174401143 [GRCh38] Chr2:175265871 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.613A>C (p.Asn205His)	single nucleotide variant	Inborn genetic diseases [RCV002980448]	Chr2:174404174 [GRCh38] Chr2:175268902 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.28G>A (p.Val10Met)	single nucleotide variant	Inborn genetic diseases [RCV002742750]	Chr2:174398311 [GRCh38] Chr2:175263039 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.190G>C (p.Glu64Gln)	single nucleotide variant	Inborn genetic diseases [RCV002831284]	Chr2:174399952 [GRCh38] Chr2:175264680 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.683T>C (p.Leu228Pro)	single nucleotide variant	Inborn genetic diseases [RCV002940677]	Chr2:174404244 [GRCh38] Chr2:175268972 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.550C>T (p.Arg184Cys)	single nucleotide variant	Inborn genetic diseases [RCV002941396]	Chr2:174404111 [GRCh38] Chr2:175268839 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.164C>A (p.Thr55Lys)	single nucleotide variant	Inborn genetic diseases [RCV002677485]	Chr2:174399926 [GRCh38] Chr2:175264654 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.167A>G (p.Tyr56Cys)	single nucleotide variant	Inborn genetic diseases [RCV003203005]	Chr2:174399929 [GRCh38] Chr2:175264657 [GRCh37] Chr2:2q31.1	uncertain significance
NM_024583.5(SCRN3):c.692C>T (p.Ala231Val)	single nucleotide variant	Inborn genetic diseases [RCV003344627]	Chr2:174404253 [GRCh38] Chr2:175268981 [GRCh37] Chr2:2q31.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1942
Count of miRNA genes:	818
Interacting mature miRNAs:	971
Transcripts:	ENST00000272732, ENST00000409673, ENST00000424069, ENST00000427038, ENST00000435964, ENST00000437944, ENST00000458563, ENST00000475928, ENST00000488349, ENST00000490927, ENST00000548031, ENST00000548868, ENST00000548921, ENST00000549848
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

G42934

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	175,294,639 - 175,294,788	UniSTS	GRCh37
Build 36	2	175,002,885 - 175,003,034	RGD	NCBI36
Celera	2	168,908,075 - 168,908,224	RGD
Cytogenetic Map	2	q31.1	UniSTS
HuRef	2	167,175,200 - 167,175,349	UniSTS

G43281

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	175,263,572 - 175,263,702	UniSTS	GRCh37
Build 36	2	174,971,818 - 174,971,948	RGD	NCBI36
Celera	2	168,877,013 - 168,877,143	RGD
Cytogenetic Map	2	q31.1	UniSTS
HuRef	2	167,143,745 - 167,143,875	UniSTS

G60089

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	175,263,591 - 175,263,692	UniSTS	GRCh37
Build 36	2	174,971,837 - 174,971,938	RGD	NCBI36
Celera	2	168,877,032 - 168,877,133	RGD
Cytogenetic Map	2	q31.1	UniSTS
HuRef	2	167,143,764 - 167,143,865	UniSTS
TNG Radiation Hybrid Map	2	96896.0	UniSTS

WI-15486

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	175,292,786 - 175,292,889	UniSTS	GRCh37
Build 36	2	175,001,032 - 175,001,135	RGD	NCBI36
Celera	2	168,906,222 - 168,906,325	RGD
Cytogenetic Map	2	q31.1	UniSTS
HuRef	2	167,173,347 - 167,173,450	UniSTS
GeneMap99-GB4 RH Map	2	567.08	UniSTS
Whitehead-RH Map	2	869.3	UniSTS

D2S1626E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	178,371,383 - 178,371,504	UniSTS	GRCh37
GRCh37	2	175,294,647 - 175,294,751	UniSTS	GRCh37
Build 36	2	175,002,893 - 175,002,997	RGD	NCBI36
Celera	2	168,908,083 - 168,908,187	RGD
Celera	4	175,698,542 - 175,698,663	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	4	q34.3	UniSTS
HuRef	4	174,121,604 - 174,121,725	UniSTS
HuRef	2	167,175,208 - 167,175,312	UniSTS
GeneMap99-GB4 RH Map	2	567.39	UniSTS
NCBI RH Map	2	1415.4	UniSTS

G20279

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	175,294,594 - 175,294,699	UniSTS	GRCh37
Build 36	2	175,002,840 - 175,002,945	RGD	NCBI36
Celera	2	168,908,030 - 168,908,135	RGD
Cytogenetic Map	2	q31.1	UniSTS
HuRef	2	167,175,155 - 167,175,260	UniSTS

RH35807

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	175,293,554 - 175,293,702	UniSTS	GRCh37
Build 36	2	175,001,800 - 175,001,948	RGD	NCBI36
Celera	2	168,906,990 - 168,907,138	RGD
Cytogenetic Map	2	q31.1	UniSTS
HuRef	2	167,174,115 - 167,174,263	UniSTS
GeneMap99-GB4 RH Map	2	567.59	UniSTS
NCBI RH Map	2	1345.4	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

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

296

278

687

104

465

656

376

1448

213

390

619

458

Low

2143

2550

1039

520

1346

367

3701

1798

2286

206

1070

994

155

1166

2330

Below cutoff

163

140

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001193528	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001412202	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001412203	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001412204	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001412205	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001412206	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001412207	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001412208	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001412209	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001412210	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001412212	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_024583	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005246856	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA227619	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC018470	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF279776	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK026795	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK057912	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK295357	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK296558	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC031821	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC119684	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC119685	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BG492502	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM725063	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471058	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CK301138	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA760451	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	U61107	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000272732 ⟹ ENSP00000272732

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,395,730 - 174,429,575 (+)	Ensembl

RefSeq Acc Id:

ENST00000409673 ⟹ ENSP00000387142

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,395,745 - 174,428,417 (+)	Ensembl

RefSeq Acc Id:

ENST00000424069 ⟹ ENSP00000402086

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,395,792 - 174,400,103 (+)	Ensembl

RefSeq Acc Id:

ENST00000427038 ⟹ ENSP00000408376

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,395,808 - 174,401,054 (+)	Ensembl

RefSeq Acc Id:

ENST00000435964 ⟹ ENSP00000394024

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,395,752 - 174,398,314 (+)	Ensembl

RefSeq Acc Id:

ENST00000437944 ⟹ ENSP00000400421

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,395,730 - 174,427,864 (+)	Ensembl

RefSeq Acc Id:

ENST00000458563 ⟹ ENSP00000396884

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,395,741 - 174,404,210 (+)	Ensembl

RefSeq Acc Id:

ENST00000475928

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,410,344 - 174,428,035 (+)	Ensembl

RefSeq Acc Id:

ENST00000488349

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,395,795 - 174,397,404 (+)	Ensembl

RefSeq Acc Id:

ENST00000490927

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,395,743 - 174,424,570 (+)	Ensembl

RefSeq Acc Id:

ENST00000548031 ⟹ ENSP00000446727

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,398,195 - 174,404,190 (+)	Ensembl

RefSeq Acc Id:

ENST00000548868 ⟹ ENSP00000447307

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,395,730 - 174,428,317 (+)	Ensembl

RefSeq Acc Id:

ENST00000548921

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,410,037 - 174,428,859 (+)	Ensembl

RefSeq Acc Id:

ENST00000549848

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	174,410,082 - 174,427,895 (+)	Ensembl

RefSeq Acc Id:

NM_001193528 ⟹ NP_001180457

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	174,395,730 - 174,429,575 (+)	NCBI
GRCh37	2	175,260,457 - 175,294,303 (+)	RGD
Celera	2	168,873,893 - 168,907,739 (+)	RGD
HuRef	2	167,140,624 - 167,174,864 (+)	RGD
CHM1_1	2	175,266,645 - 175,300,425 (+)	NCBI
T2T-CHM13v2.0	2	174,884,418 - 174,918,222 (+)	NCBI

Sequence:

show sequence

ATCAAAGGTGACAGCTTCCGGCAACTGATGCCTCCACTGGCCACTCCTCCCTCCGTCCACCTGT
CACTTCGGGTAGCTGGGAGGCCAGATAGACTCTATGATGAAGTACAAGAGGTGGTTTATTTTCC
TGCTGTAGTTCATGATAACCTGGGAGAACGTCTTAAGTGTACATATATAGAAATTGATCAAGTT
CCTGAAACATATGCTGTTGTCCTGAGTCGCCCAGCGTGGTTGTGGGGGGCAGAAATGGGAGCCA
ATGAGCATGGAGTTTGCATTGGGAATGAAGCTGTATGGGGAAGAGAAGAAGTTTGTGATGAAGA
AGCACTATTAGGAATGGACCTTGTCAGACTTGGCCTTGAAAGAGCTGATACAGCTGAAAAAGCC
CTCAATGTCATTGTTGACTTACTAGAAAAATATGGCCAGGGTGGAAATTGCACAGAGGGTAGAA
TGGTATTTAGCTATCACAACAGTTTCCTGATAGCTGATAGGAATGAAGCCTGGATTCTGGAGAC
TGCAGGGAAGTACTGGGCAGCAGAAAAAGTACAAGAGGGAGTTCGTAATATTTCTAATCAACTT
TCCATAACAACCAAGATTGCCCGGGAACACCCAGACATGAGAAACTATGCTAAGCGGAAAGGTT
GGTGGGATGGTAAAAAGGAGTTTGATTTTGCTGCAGCATATTCCTATCTTGACACAGCCAAGAT
GATGACTTCATCAGGCAGATACTGTGAGGGCTACAAGCTTCTAAATAAGCACAAAGGAAATATA
ACTTTTGAAACAATGATGGAAATTCTTCGAGATAAACCAAGTGGCATTAATATGGAGGGAGAAT
TCCTGACCACTGCAAGCATGGTTTCTATTTTACCTCAAGACTCCAGCCTTCCTTGCATTCACTT
CTTTACAGGGACTCCTGATCCTGAGAGATCTGTTTTTAAGCCTTTCATATTTGTGCCACATATT
TCACAACTATTGGATACCAGTTCACCAACATTTGAACTTGAAGATCTAGTTAAAAAGAAATCAC
ATTTTAAGCCTGACAGAAGACACCCACTCTACCAAAAACATCAACAGGCATTGGAAGTAGTAAA
TAATAATGAGGAAAAAGCCAAAATAATGTTGGACAACATGAGGAAACTGGAGAAAGAACTATTC
AGAGAGATGGAATCAATCCTTCAAAACAAGCATCTTGATGTGGAGAAAATTGTTAATCTCTTTC
CTCAGTGTACAAAAGATGAAATTCAAATTTATCAGTCAAATTTATCAGTCAAAGTTAGTTCTTA
GTGATCATATGGTCAGCTAATATTAGTTCTTAGTGATCAGTGGTCAGTAATCTTCAAAGTCAGA
ATCTATCACCTTGGTAAATTATATAAACCTAACTTGAGCAGATCTGATTATTCTTGGATAGTAT
TCAAGTGGTATCTTGACTATTAAACTACGTATAGTGTTGCTGAAATAGAAAGAAAACAGCATTG
GAATTGGATTCATGTATCGTGGGATACAGGTGTTATTTCAGGTGATGTACTTGCATTATTTTCT
TTAGCCATAGTAACTTTTTGTCACAATAACTAAGTATTCAATTATATATAAAGAGTGAAACATT
AAAATGACGCATGGATTTATATTTATTATAATTATGTAGTACCCTCAAATCATTTTGTCAGTTA
CATCAAGAAAGCAGATTTTTCTTTAGTCATGAAAAATATCTCAAGTGGTAAGTTGTTTGTGCTT
TAGGCAAACATTAACCAGCTCTAACAAGAAAAATGTCTAGATTTACACATTGTCAATACAGTAT
ATTAGTTCTGCAAATGCACTTTTGTTAAACTCAAACATGCTCTTTGTCAAGACTTGGCTAACCA
GTGAGCTTGTAGCTCTGATTATCTAGCATTTTTAGGGTCATTCTCCTTAATAGGCTTTTATGTT
AATAAGATATATTTTTAGAAGAGCTTGTTTGGGAGATTAGAGAATAAGATAAAAGAACCAAAAC
CTTAGGATATACTGTTTCTGGGTCTGAAATCTCTCTCATTGTTTACTTCTGTTCACTCAGTGAA
AACAGAAACAAGAATGAGGTAGTGGCAATGAAATAGAATTATTAGTATATTATGAACATTATAA
CATTTTGAACACTATAATGCATTATATATTATGAACTTTTATGAACTTTATACATGAGTAATAG
CTTCCTAAAGTTTATAAAACATTGTTTAGGTTACATAAAGATTACCAAGTAAGACTCAAAATTG
CAAATATAAACAAAAGAAAAATCCAACTGAAAATAACACTAAGTATTTTTGAGTTCCTAGAATG
TCCATTTTGGTATTTGGTTACATTATCATATTTACTAGTCACTATCAGCACAATTAGGTTAATA
AAGAAGTGGGTCATTATATTCAAAGAGTGCTCAGGAAGTTATGTGTTCAAAGTTCTCTCATAAA
TACCATCGTCTGCCTGATACTGCTCTTGTCTAATAGAGGGTTGACATTACAAAAGAAAAGATGT
CTGACTCAAGAACTCAGTTGATTCTGTTTGCCTTAAGTTTGGTTCAGTGATAGGCTGTCTTCTA
ACCCCTATACTCCTCTTCTCTCCTTTAATAGATGAGGAAACTAAGGGCAAACAGTTCGTTACAC
TTACGGGAATCTTATTTCCCTCTCTAGGGGCAGCATGTTTTCACCTTCTCCTTTGCTGCCACCT
TGGCCTAAACTAGCACCGTCTTTTAGCTAGACCATTGCGTTAACTGTTCTCCTACACCCATTTT
TGTTCTTTATTTCCACCCACATGAGTCACTGCAGCCAATCTATTACAAATTTAAATCTGATTAT
GAATTCCCCTCCTAAAACTCTTTTTTAAAAGAGACTTTATTTTTTGGAGCAGTTTTAGGTTCAC
AGCAAAATTGAACAGAAAGTACAGAGTTCCAATACAGCCCCTATCAGCATACATGCATAGCCTC
CCCCACTATCAACATCC

hide sequence

RefSeq Acc Id:

NM_001412202 ⟹ NP_001399131

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	174,395,730 - 174,430,071 (+)	NCBI

RefSeq Acc Id:

NM_001412203 ⟹ NP_001399132

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	174,395,730 - 174,430,071 (+)	NCBI

RefSeq Acc Id:

NM_001412204 ⟹ NP_001399133

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	174,395,730 - 174,430,071 (+)	NCBI

RefSeq Acc Id:

NM_001412205 ⟹ NP_001399134

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	174,395,730 - 174,430,071 (+)	NCBI

RefSeq Acc Id:

NM_001412206 ⟹ NP_001399135

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	174,395,730 - 174,430,071 (+)	NCBI

RefSeq Acc Id:

NM_001412207 ⟹ NP_001399136

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	174,395,730 - 174,430,071 (+)	NCBI

RefSeq Acc Id:

NM_001412208 ⟹ NP_001399137

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	174,395,730 - 174,430,071 (+)	NCBI

RefSeq Acc Id:

NM_001412209 ⟹ NP_001399138

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	174,395,730 - 174,430,071 (+)	NCBI

RefSeq Acc Id:

NM_001412210 ⟹ NP_001399139

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	174,395,730 - 174,430,071 (+)	NCBI

RefSeq Acc Id:

NM_001412212 ⟹ NP_001399141

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	174,884,418 - 174,918,718 (+)	NCBI

RefSeq Acc Id:

NM_024583 ⟹ NP_078859

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	174,395,730 - 174,429,575 (+)	NCBI
GRCh37	2	175,260,457 - 175,294,303 (+)	RGD
Build 36	2	174,968,713 - 175,001,974 (+)	NCBI Archive
Celera	2	168,873,893 - 168,907,739 (+)	RGD
HuRef	2	167,140,624 - 167,174,864 (+)	RGD
CHM1_1	2	175,266,645 - 175,300,425 (+)	NCBI
T2T-CHM13v2.0	2	174,884,418 - 174,918,222 (+)	NCBI

Sequence:

show sequence

ATCAAAGGTGACAGCTTCCGGCAACTGATGCCTCCACTGGCCACTCCTCCCTCCGTCCACCTGT
CACTTCGGGTAGCTGGGAGGCCAGTTAAAAAAAATGGAACCTTTTTCCTGTGACACTTTCGTGG
CATTACCTCCAGCAACAGTCGATAACAGGATTATTTTTGGAAAAAATTCAGATAGACTCTATGA
TGAAGTACAAGAGGTGGTTTATTTTCCTGCTGTAGTTCATGATAACCTGGGAGAACGTCTTAAG
TGTACATATATAGAAATTGATCAAGTTCCTGAAACATATGCTGTTGTCCTGAGTCGCCCAGCGT
GGTTGTGGGGGGCAGAAATGGGAGCCAATGAGCATGGAGTTTGCATTGGGAATGAAGCTGTATG
GGGAAGAGAAGAAGTTTGTGATGAAGAAGCACTATTAGGAATGGACCTTGTCAGACTTGGCCTT
GAAAGAGCTGATACAGCTGAAAAAGCCCTCAATGTCATTGTTGACTTACTAGAAAAATATGGCC
AGGGTGGAAATTGCACAGAGGGTAGAATGGTATTTAGCTATCACAACAGTTTCCTGATAGCTGA
TAGGAATGAAGCCTGGATTCTGGAGACTGCAGGGAAGTACTGGGCAGCAGAAAAAGTACAAGAG
GGAGTTCGTAATATTTCTAATCAACTTTCCATAACAACCAAGATTGCCCGGGAACACCCAGACA
TGAGAAACTATGCTAAGCGGAAAGGTTGGTGGGATGGTAAAAAGGAGTTTGATTTTGCTGCAGC
ATATTCCTATCTTGACACAGCCAAGATGATGACTTCATCAGGCAGATACTGTGAGGGCTACAAG
CTTCTAAATAAGCACAAAGGAAATATAACTTTTGAAACAATGATGGAAATTCTTCGAGATAAAC
CAAGTGGCATTAATATGGAGGGAGAATTCCTGACCACTGCAAGCATGGTTTCTATTTTACCTCA
AGACTCCAGCCTTCCTTGCATTCACTTCTTTACAGGGACTCCTGATCCTGAGAGATCTGTTTTT
AAGCCTTTCATATTTGTGCCACATATTTCACAACTATTGGATACCAGTTCACCAACATTTGAAC
TTGAAGATCTAGTTAAAAAGAAATCACATTTTAAGCCTGACAGAAGACACCCACTCTACCAAAA
ACATCAACAGGCATTGGAAGTAGTAAATAATAATGAGGAAAAAGCCAAAATAATGTTGGACAAC
ATGAGGAAACTGGAGAAAGAACTATTCAGAGAGATGGAATCAATCCTTCAAAACAAGCATCTTG
ATGTGGAGAAAATTGTTAATCTCTTTCCTCAGTGTACAAAAGATGAAATTCAAATTTATCAGTC
AAATTTATCAGTCAAAGTTAGTTCTTAGTGATCATATGGTCAGCTAATATTAGTTCTTAGTGAT
CAGTGGTCAGTAATCTTCAAAGTCAGAATCTATCACCTTGGTAAATTATATAAACCTAACTTGA
GCAGATCTGATTATTCTTGGATAGTATTCAAGTGGTATCTTGACTATTAAACTACGTATAGTGT
TGCTGAAATAGAAAGAAAACAGCATTGGAATTGGATTCATGTATCGTGGGATACAGGTGTTATT
TCAGGTGATGTACTTGCATTATTTTCTTTAGCCATAGTAACTTTTTGTCACAATAACTAAGTAT
TCAATTATATATAAAGAGTGAAACATTAAAATGACGCATGGATTTATATTTATTATAATTATGT
AGTACCCTCAAATCATTTTGTCAGTTACATCAAGAAAGCAGATTTTTCTTTAGTCATGAAAAAT
ATCTCAAGTGGTAAGTTGTTTGTGCTTTAGGCAAACATTAACCAGCTCTAACAAGAAAAATGTC
TAGATTTACACATTGTCAATACAGTATATTAGTTCTGCAAATGCACTTTTGTTAAACTCAAACA
TGCTCTTTGTCAAGACTTGGCTAACCAGTGAGCTTGTAGCTCTGATTATCTAGCATTTTTAGGG
TCATTCTCCTTAATAGGCTTTTATGTTAATAAGATATATTTTTAGAAGAGCTTGTTTGGGAGAT
TAGAGAATAAGATAAAAGAACCAAAACCTTAGGATATACTGTTTCTGGGTCTGAAATCTCTCTC
ATTGTTTACTTCTGTTCACTCAGTGAAAACAGAAACAAGAATGAGGTAGTGGCAATGAAATAGA
ATTATTAGTATATTATGAACATTATAACATTTTGAACACTATAATGCATTATATATTATGAACT
TTTATGAACTTTATACATGAGTAATAGCTTCCTAAAGTTTATAAAACATTGTTTAGGTTACATA
AAGATTACCAAGTAAGACTCAAAATTGCAAATATAAACAAAAGAAAAATCCAACTGAAAATAAC
ACTAAGTATTTTTGAGTTCCTAGAATGTCCATTTTGGTATTTGGTTACATTATCATATTTACTA
GTCACTATCAGCACAATTAGGTTAATAAAGAAGTGGGTCATTATATTCAAAGAGTGCTCAGGAA
GTTATGTGTTCAAAGTTCTCTCATAAATACCATCGTCTGCCTGATACTGCTCTTGTCTAATAGA
GGGTTGACATTACAAAAGAAAAGATGTCTGACTCAAGAACTCAGTTGATTCTGTTTGCCTTAAG
TTTGGTTCAGTGATAGGCTGTCTTCTAACCCCTATACTCCTCTTCTCTCCTTTAATAGATGAGG
AAACTAAGGGCAAACAGTTCGTTACACTTACGGGAATCTTATTTCCCTCTCTAGGGGCAGCATG
TTTTCACCTTCTCCTTTGCTGCCACCTTGGCCTAAACTAGCACCGTCTTTTAGCTAGACCATTG
CGTTAACTGTTCTCCTACACCCATTTTTGTTCTTTATTTCCACCCACATGAGTCACTGCAGCCA
ATCTATTACAAATTTAAATCTGATTATGAATTCCCCTCCTAAAACTCTTTTTTAAAAGAGACTT
TATTTTTTGGAGCAGTTTTAGGTTCACAGCAAAATTGAACAGAAAGTACAGAGTTCCAATACAG
CCCCTATCAGCATACATGCATAGCCTCCCCCACTATCAACATCC

hide sequence

Protein Sequences


Protein RefSeqs	NP_001180457	(Get FASTA)	NCBI Sequence Viewer
	NP_001399131	(Get FASTA)	NCBI Sequence Viewer
	NP_001399132	(Get FASTA)	NCBI Sequence Viewer
	NP_001399133	(Get FASTA)	NCBI Sequence Viewer
	NP_001399134	(Get FASTA)	NCBI Sequence Viewer
	NP_001399135	(Get FASTA)	NCBI Sequence Viewer
	NP_001399136	(Get FASTA)	NCBI Sequence Viewer
	NP_001399137	(Get FASTA)	NCBI Sequence Viewer
	NP_001399138	(Get FASTA)	NCBI Sequence Viewer
	NP_001399139	(Get FASTA)	NCBI Sequence Viewer
	NP_001399141	(Get FASTA)	NCBI Sequence Viewer
	NP_078859	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH31821	(Get FASTA)	NCBI Sequence Viewer
	AAI19685	(Get FASTA)	NCBI Sequence Viewer
	AAI19686	(Get FASTA)	NCBI Sequence Viewer
	AAY24217	(Get FASTA)	NCBI Sequence Viewer
	BAB15555	(Get FASTA)	NCBI Sequence Viewer
	BAG58323	(Get FASTA)	NCBI Sequence Viewer
	BAG59179	(Get FASTA)	NCBI Sequence Viewer
	EAX11140	(Get FASTA)	NCBI Sequence Viewer
	EAX11141	(Get FASTA)	NCBI Sequence Viewer
	EAX11142	(Get FASTA)	NCBI Sequence Viewer
	EAX11143	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000272732
	ENSP00000272732.6
	ENSP00000387142
	ENSP00000387142.3
	ENSP00000394024.1
	ENSP00000396884.1
	ENSP00000400421.1
	ENSP00000402086.1
	ENSP00000408376.1
	ENSP00000446727.1
	ENSP00000447307.1
GenBank Protein	Q0VDG4	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_078859 ⟸ NM_024583
- Peptide Label:	isoform 1
- UniProtKB:	Q7L1C5 (UniProtKB/Swiss-Prot), D3DPE0 (UniProtKB/Swiss-Prot), C9JPC1 (UniProtKB/Swiss-Prot), B4DI11 (UniProtKB/Swiss-Prot), Q9H5R5 (UniProtKB/Swiss-Prot), Q0VDG4 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MEPFSCDTFVALPPATVDNRIIFGKNSDRLYDEVQEVVYFPAVVHDNLGERLKCTYIEIDQVPE TYAVVLSRPAWLWGAEMGANEHGVCIGNEAVWGREEVCDEEALLGMDLVRLGLERADTAEKALN VIVDLLEKYGQGGNCTEGRMVFSYHNSFLIADRNEAWILETAGKYWAAEKVQEGVRNISNQLSI TTKIAREHPDMRNYAKRKGWWDGKKEFDFAAAYSYLDTAKMMTSSGRYCEGYKLLNKHKGNITF ETMMEILRDKPSGINMEGEFLTTASMVSILPQDSSLPCIHFFTGTPDPERSVFKPFIFVPHISQ LLDTSSPTFELEDLVKKKSHFKPDRRHPLYQKHQQALEVVNNNEEKAKIMLDNMRKLEKELFRE MESILQNKHLDVEKIVNLFPQCTKDEIQIYQSNLSVKVSS hide sequence

RefSeq Acc Id:	NP_001180457 ⟸ NM_001193528
- Peptide Label:	isoform 2
- UniProtKB:	Q0VDG4 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MPPLATPPSVHLSLRVAGRPDRLYDEVQEVVYFPAVVHDNLGERLKCTYIEIDQVPETYAVVLS RPAWLWGAEMGANEHGVCIGNEAVWGREEVCDEEALLGMDLVRLGLERADTAEKALNVIVDLLE KYGQGGNCTEGRMVFSYHNSFLIADRNEAWILETAGKYWAAEKVQEGVRNISNQLSITTKIARE HPDMRNYAKRKGWWDGKKEFDFAAAYSYLDTAKMMTSSGRYCEGYKLLNKHKGNITFETMMEIL RDKPSGINMEGEFLTTASMVSILPQDSSLPCIHFFTGTPDPERSVFKPFIFVPHISQLLDTSSP TFELEDLVKKKSHFKPDRRHPLYQKHQQALEVVNNNEEKAKIMLDNMRKLEKELFREMESILQN KHLDVEKIVNLFPQCTKDEIQIYQSNLSVKVSS hide sequence

RefSeq Acc Id:

ENSP00000400421 ⟸ ENST00000437944

RefSeq Acc Id:

ENSP00000402086 ⟸ ENST00000424069

RefSeq Acc Id:

ENSP00000408376 ⟸ ENST00000427038

RefSeq Acc Id:

ENSP00000447307 ⟸ ENST00000548868

RefSeq Acc Id:

ENSP00000446727 ⟸ ENST00000548031

RefSeq Acc Id:

ENSP00000272732 ⟸ ENST00000272732

RefSeq Acc Id:

ENSP00000396884 ⟸ ENST00000458563

RefSeq Acc Id:

ENSP00000387142 ⟸ ENST00000409673

RefSeq Acc Id:

ENSP00000394024 ⟸ ENST00000435964

RefSeq Acc Id:	NP_001399131 ⟸ NM_001412202
- Peptide Label:	isoform 1
- UniProtKB:	Q7L1C5 (UniProtKB/Swiss-Prot), Q0VDG4 (UniProtKB/Swiss-Prot), D3DPE0 (UniProtKB/Swiss-Prot), C9JPC1 (UniProtKB/Swiss-Prot), B4DI11 (UniProtKB/Swiss-Prot), Q9H5R5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001399133 ⟸ NM_001412204
- Peptide Label:	isoform 1
- UniProtKB:	Q7L1C5 (UniProtKB/Swiss-Prot), Q0VDG4 (UniProtKB/Swiss-Prot), D3DPE0 (UniProtKB/Swiss-Prot), C9JPC1 (UniProtKB/Swiss-Prot), B4DI11 (UniProtKB/Swiss-Prot), Q9H5R5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001399137 ⟸ NM_001412208
- Peptide Label:	isoform 1
- UniProtKB:	Q7L1C5 (UniProtKB/Swiss-Prot), Q0VDG4 (UniProtKB/Swiss-Prot), D3DPE0 (UniProtKB/Swiss-Prot), C9JPC1 (UniProtKB/Swiss-Prot), B4DI11 (UniProtKB/Swiss-Prot), Q9H5R5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001399132 ⟸ NM_001412203
- Peptide Label:	isoform 1
- UniProtKB:	Q7L1C5 (UniProtKB/Swiss-Prot), Q0VDG4 (UniProtKB/Swiss-Prot), D3DPE0 (UniProtKB/Swiss-Prot), C9JPC1 (UniProtKB/Swiss-Prot), B4DI11 (UniProtKB/Swiss-Prot), Q9H5R5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001399136 ⟸ NM_001412207
- Peptide Label:	isoform 1
- UniProtKB:	Q7L1C5 (UniProtKB/Swiss-Prot), Q0VDG4 (UniProtKB/Swiss-Prot), D3DPE0 (UniProtKB/Swiss-Prot), C9JPC1 (UniProtKB/Swiss-Prot), B4DI11 (UniProtKB/Swiss-Prot), Q9H5R5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001399139 ⟸ NM_001412210
- Peptide Label:	isoform 4

RefSeq Acc Id:	NP_001399134 ⟸ NM_001412205
- Peptide Label:	isoform 1
- UniProtKB:	Q7L1C5 (UniProtKB/Swiss-Prot), Q0VDG4 (UniProtKB/Swiss-Prot), D3DPE0 (UniProtKB/Swiss-Prot), C9JPC1 (UniProtKB/Swiss-Prot), B4DI11 (UniProtKB/Swiss-Prot), Q9H5R5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001399135 ⟸ NM_001412206
- Peptide Label:	isoform 1
- UniProtKB:	Q7L1C5 (UniProtKB/Swiss-Prot), Q0VDG4 (UniProtKB/Swiss-Prot), D3DPE0 (UniProtKB/Swiss-Prot), C9JPC1 (UniProtKB/Swiss-Prot), B4DI11 (UniProtKB/Swiss-Prot), Q9H5R5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001399138 ⟸ NM_001412209
- Peptide Label:	isoform 3

RefSeq Acc Id:	NP_001399141 ⟸ NM_001412212
- Peptide Label:	isoform 5
- UniProtKB:	Q0VDG5 (UniProtKB/TrEMBL)

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q0VDG4-F1-model_v2	AlphaFold	Q0VDG4	1-424	view protein structure

Promoters

RGD ID:

6862068

Promoter ID:

EPDNEW_H4199

Type:

initiation region

Name:

SCRN3_1

Description:

secernin 3

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	2	174,395,765 - 174,395,825	EPDNEW

RGD ID:

6798153

Promoter ID:

HG_KWN:35987

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000409673, NM_024583, OTTHUMT00000255459, OTTHUMT00000255460, OTTHUMT00000334103, OTTHUMT00000334104, OTTHUMT00000334105, OTTHUMT00000334106, OTTHUMT00000334108, OTTHUMT00000334109, OTTHUMT00000334110, OTTHUMT00000334123, OTTHUMT00000334124, UC002UIO.1, UC002UIP.1, UC002UIR.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	2	174,968,606 - 174,969,287 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:30382	AgrOrtholog
COSMIC	SCRN3	COSMIC
Ensembl Genes	ENSG00000144306	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000272732	ENTREZGENE
	ENST00000272732.11	UniProtKB/Swiss-Prot
	ENST00000409673	ENTREZGENE
	ENST00000409673.7	UniProtKB/Swiss-Prot
	ENST00000424069.5	UniProtKB/TrEMBL
	ENST00000427038.5	UniProtKB/TrEMBL
	ENST00000435964.1	UniProtKB/TrEMBL
	ENST00000437944.5	UniProtKB/TrEMBL
	ENST00000458563.5	UniProtKB/TrEMBL
	ENST00000548031.1	UniProtKB/TrEMBL
	ENST00000548868.5	UniProtKB/TrEMBL
GTEx	ENSG00000144306	GTEx
HGNC ID	HGNC:30382	ENTREZGENE
Human Proteome Map	SCRN3	Human Proteome Map
InterPro	Peptidase_C69	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:79634	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	79634	ENTREZGENE
OMIM	614967	OMIM
PANTHER	PTHR12994	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SECERNIN-3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	Peptidase_C69	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134974313	PharmGKB
UniProt	A0A1D5RMN9_HUMAN	UniProtKB/TrEMBL
	B4DI11	ENTREZGENE
	C9JID8_HUMAN	UniProtKB/TrEMBL
	C9JNS3_HUMAN	UniProtKB/TrEMBL
	C9JPC1	ENTREZGENE
	D3DPE0	ENTREZGENE
	F8W0M9_HUMAN	UniProtKB/TrEMBL
	F8WBX0_HUMAN	UniProtKB/TrEMBL
	H9KVC8_HUMAN	UniProtKB/TrEMBL
	Q0VDG4	ENTREZGENE
	Q0VDG5	ENTREZGENE, UniProtKB/TrEMBL
	Q7L1C5	ENTREZGENE
	Q9H5R5	ENTREZGENE
	SCRN3_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	B4DI11	UniProtKB/Swiss-Prot
	C9JPC1	UniProtKB/Swiss-Prot
	D3DPE0	UniProtKB/Swiss-Prot
	Q7L1C5	UniProtKB/Swiss-Prot
	Q9H5R5	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)

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Imported Disease Annotations - ClinVar