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Gene: NECAB3 (N-terminal EF-hand calcium binding protein 3) Homo sapiens

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Symbol:

NECAB3

Name:

N-terminal EF-hand calcium binding protein 3

RGD ID:

1320847

HGNC Page

HGNC:15851

Description:

Predicted to enable calcium ion binding activity. Involved in regulation of amyloid precursor protein biosynthetic process. Located in Golgi cis cisterna and endoplasmic reticulum membrane.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

amyloid beta (A4) precursor protein-binding, family A, member 2 binding protein; amyloid beta A4 protein-binding family A member 2-binding protein; APBA2BP; dJ63M2.4; dJ63M2.5; EF-hand calcium binding protein 3; EFCBP3; N-terminal EF-hand calcium-binding protein 3; Nek2-interacting protein 1; neuronal calcium-binding protein 3; neuronal calcium-binding protein NECAB3; NIP1; STIP3; synaptotagmin interacting protein 2; synaptotagmin interacting protein STIP3; SYTIP2; X11L-binding protein 51; XB51

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	20	33,657,087 - 33,675,348 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	20	33,657,087 - 33,674,463 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	20	32,244,893 - 32,262,234 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	20	31,708,554 - 31,725,925 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	20	31,708,554 - 31,725,923	NCBI
Celera	20	28,997,925 - 29,015,296 (-)	NCBI		Celera
Cytogenetic Map	20	q11.22	NCBI
HuRef	20	29,030,990 - 29,048,237 (-)	NCBI		HuRef
CHM1_1	20	32,145,985 - 32,163,356 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	20	35,383,618 - 35,401,879 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NECAB3	Human	glutathione synthetase deficiency		IAGP	RGD:405874612	8554872	ClinVar Annotator: match by term: PYROGLUTAMIC ACIDURIA	ClinVar	PMID:12638941\|PMID:15717202\|PMID:28492532
NECAB3	Human	glutatione synthetase deficiency with 5-oxoprolinuria		IAGP	RGD:405874612	8554872	ClinVar Annotator: match by term: 5-OXOPROLINURIA DUE TO GLUTATHIONE SYNTHETASE DEFICIENCY	ClinVar	PMID:12638941\|PMID:15717202\|PMID:28492532
NECAB3	Human	hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		IAGP	RGD:405874644	8554872	ClinVar Annotator: match by term: Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase	ClinVar	PMID:15024124\|PMID:20852937\|PMID:28492532
NECAB3	Human	long QT syndrome		IAGP	RGD:13819266\|RGD:13819679	8554872	ClinVar Annotator: match by term: Long QT syndrome	ClinVar	PMID:28492532

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NECAB3	Human	17alpha-ethynylestradiol	multiple interactions	ISO	RGD:1320848	6480464	[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of NECAB3 mRNA	CTD	PMID:17942748
NECAB3	Human	17alpha-ethynylestradiol	increases expression	ISO	RGD:1320848	6480464	Ethinyl Estradiol results in increased expression of NECAB3 mRNA	CTD	PMID:17942748
NECAB3	Human	2,3,7,8-tetrachlorodibenzodioxine	multiple interactions	ISO	RGD:1320848	6480464	[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of NECAB3 mRNA	CTD	PMID:17942748
NECAB3	Human	4,4'-sulfonyldiphenol	decreases expression	ISO	RGD:1320848	6480464	bisphenol S results in decreased expression of NECAB3 mRNA	CTD	PMID:30951980
NECAB3	Human	6-propyl-2-thiouracil	multiple interactions	ISO	RGD:1320848	6480464	[Propylthiouracil co-treated with Iodine deficiency] results in decreased expression of NECAB3 mRNA	CTD	PMID:36706583
NECAB3	Human	acrylamide	decreases expression	EXP		6480464	Acrylamide results in decreased expression of NECAB3 mRNA	CTD	PMID:32763439
NECAB3	Human	antirheumatic drug	increases expression	EXP		6480464	Antirheumatic Agents results in increased expression of NECAB3 mRNA	CTD	PMID:24449571
NECAB3	Human	aristolochic acid A	decreases expression	EXP		6480464	aristolochic acid I results in decreased expression of NECAB3 mRNA	CTD	PMID:33212167
NECAB3	Human	arsane	affects methylation	EXP		6480464	Arsenic affects the methylation of NECAB3 gene	CTD	PMID:25304211
NECAB3	Human	arsenic atom	affects methylation	EXP		6480464	Arsenic affects the methylation of NECAB3 gene	CTD	PMID:25304211
NECAB3	Human	benzo[a]pyrene	decreases expression	EXP		6480464	Benzo(a)pyrene results in decreased expression of NECAB3 mRNA	CTD	PMID:20106945
NECAB3	Human	benzo[a]pyrene	increases methylation	EXP		6480464	Benzo(a)pyrene results in increased methylation of NECAB3 promoter	CTD	PMID:27901495
NECAB3	Human	bisphenol A	decreases methylation	ISO	RGD:1320848	6480464	bisphenol A results in decreased methylation of NECAB3 promoter	CTD	PMID:27312807
NECAB3	Human	bisphenol A	decreases methylation	EXP		6480464	bisphenol A results in decreased methylation of NECAB3 gene	CTD	PMID:31601247
NECAB3	Human	bisphenol A	decreases expression	ISO	RGD:1320848	6480464	bisphenol A results in decreased expression of NECAB3 mRNA	CTD	PMID:35598803
NECAB3	Human	bisphenol F	decreases expression	ISO	RGD:1320848	6480464	bisphenol F results in decreased expression of NECAB3 mRNA	CTD	PMID:30951980
NECAB3	Human	cadmium dichloride	decreases expression	EXP		6480464	Cadmium Chloride results in decreased expression of NECAB3 mRNA	CTD	PMID:38568856
NECAB3	Human	CGP 52608	multiple interactions	EXP		6480464	CGP 52608 promotes the reaction [RORA protein binds to NECAB3 gene]	CTD	PMID:28238834
NECAB3	Human	cisplatin	multiple interactions	EXP		6480464	[Cisplatin co-treated with jinfukang] results in increased expression of NECAB3 mRNA	CTD	PMID:27392435
NECAB3	Human	diiodine	multiple interactions	ISO	RGD:1320848	6480464	[Propylthiouracil co-treated with Iodine deficiency] results in decreased expression of NECAB3 mRNA	CTD	PMID:36706583
NECAB3	Human	doxorubicin	decreases expression	EXP		6480464	Doxorubicin results in decreased expression of NECAB3 mRNA	CTD	PMID:29803840
NECAB3	Human	ethanol	affects splicing	ISO	RGD:1320848	6480464	Ethanol affects the splicing of NECAB3 mRNA	CTD	PMID:30319688
NECAB3	Human	fulvestrant	increases methylation	EXP		6480464	Fulvestrant results in increased methylation of NECAB3 gene	CTD	PMID:31601247
NECAB3	Human	GW 4064	increases expression	ISO	RGD:1320848	6480464	GW 4064 results in increased expression of NECAB3 mRNA	CTD	PMID:26655953
NECAB3	Human	maneb	multiple interactions	ISO	RGD:1320848	6480464	[Maneb co-treated with Paraquat] results in decreased expression of NECAB3 mRNA	CTD	PMID:36117858
NECAB3	Human	methyl methanesulfonate	increases expression	EXP		6480464	Methyl Methanesulfonate results in increased expression of NECAB3 mRNA	CTD	PMID:23649840
NECAB3	Human	paraquat	multiple interactions	ISO	RGD:1320848	6480464	[Maneb co-treated with Paraquat] results in decreased expression of NECAB3 mRNA	CTD	PMID:36117858
NECAB3	Human	sodium arsenite	increases expression	EXP		6480464	sodium arsenite results in increased expression of NECAB3 mRNA	CTD	PMID:38568856
NECAB3	Human	titanium dioxide	decreases methylation	ISO	RGD:1320848	6480464	titanium dioxide results in decreased methylation of NECAB3 gene	CTD	PMID:35295148
NECAB3	Human	triphenyl phosphate	affects expression	EXP		6480464	triphenyl phosphate affects the expression of NECAB3 mRNA	CTD	PMID:37042841
NECAB3	Human	trovafloxacin	decreases expression	ISO	RGD:1320848	6480464	trovafloxacin results in decreased expression of NECAB3 mRNA	CTD	PMID:35537566
NECAB3	Human	urethane	decreases expression	EXP		6480464	Urethane results in decreased expression of NECAB3 mRNA	CTD	PMID:28818685
NECAB3	Human	valproic acid	increases methylation	EXP		6480464	Valproic Acid results in increased methylation of NECAB3 gene	CTD	PMID:29154799

Biological Process

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NECAB3	Human	protein secretion	involved_in	NAS		150520179	PMID:12780348	UniProt	PMID:12780348
NECAB3	Human	regulation of amyloid precursor protein biosynthetic process	involved_in	IDA		150520179	PMID:10833507	UniProt	PMID:10833507
NECAB3	Human	regulation of amyloid precursor protein biosynthetic process	involved_in	IBA	PANTHER:PTN000953129\|UniProtKB:Q96P71	150520179		GO_Central	GO_REF:0000033

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NECAB3	Human	cytoplasm	located_in	IDA		150520179	PMID:10833507	UniProt	PMID:10833507
NECAB3	Human	cytoplasm	is_active_in	IBA	MGI:1861721\|PANTHER:PTN000953129\|UniProtKB:Q8N987\|UniProtKB:Q96P71	150520179		GO_Central	GO_REF:0000033
NECAB3	Human	endoplasmic reticulum	located_in	IEA	UniProtKB:Q9D6J4\|ensembl:ENSMUSP00000000895	150520179		Ensembl	GO_REF:0000107
NECAB3	Human	endoplasmic reticulum	is_active_in	IBA	MGI:1861721\|PANTHER:PTN002638592\|UniProtKB:Q96P71	150520179		GO_Central	GO_REF:0000033
NECAB3	Human	endoplasmic reticulum membrane	located_in	IDA		150520179	PMID:10833507	UniProt	PMID:10833507
NECAB3	Human	Golgi apparatus	located_in	IEA	UniProtKB-KW:KW-0333	150520179		UniProt	GO_REF:0000043
NECAB3	Human	Golgi apparatus	located_in	IDA		150520179		HPA	GO_REF:0000052
NECAB3	Human	Golgi apparatus	located_in	IEA	UniProtKB-SubCell:SL-0132	150520179		UniProt	GO_REF:0000044
NECAB3	Human	Golgi cis cisterna	located_in	IDA		150520179	PMID:10833507	UniProt	PMID:10833507
NECAB3	Human	Golgi cis cisterna	is_active_in	IBA	MGI:1861721\|PANTHER:PTN002638592\|UniProtKB:Q96P71	150520179		GO_Central	GO_REF:0000033
NECAB3	Human	Golgi cis cisterna	located_in	IEA	UniProtKB:Q9D6J4\|ensembl:ENSMUSP00000000895	150520179		Ensembl	GO_REF:0000107
NECAB3	Human	nucleus	located_in	NAS		150520179	PMID:10833507	UniProt	PMID:10833507

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NECAB3	Human	calcium ion binding	enables	IEA	InterPro:IPR002048	150520179		InterPro	GO_REF:0000002
NECAB3	Human	metal ion binding	enables	IEA	UniProtKB-KW:KW-0479	150520179		UniProt	GO_REF:0000043
NECAB3	Human	protein binding	enables	IPI	UniProtKB:O96018	150520179	PMID:26948053, PMID:28514442, PMID:33961781	IntAct	PMID:26948053\|PMID:28514442\|PMID:33961781
NECAB3	Human	protein binding	enables	IPI	UniProtKB:P21917\|UniProtKB:Q14114-3	150520179	PMID:32814053	IntAct	PMID:32814053
NECAB3	Human	protein binding	enables	IPI	UniProtKB:Q99767	150520179	PMID:10833507	UniProt	PMID:10833507

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NECAB3	Human	Prolonged QT interval		IAGP	RGD:126761903	8554872	ClinVar Annotator: match by term: Long QT syndrome	ClinVar
NECAB3	Human	Prolonged QT interval		IAGP	RGD:13819679	8554872	ClinVar Annotator: match by term: Long QT syndrome	ClinVar	PMID:28492532
NECAB3	Human	Prolonged QT interval		IAGP	RGD:13819266	8554872	ClinVar Annotator: match by term: Long QT syndrome	ClinVar	PMID:28492532
NECAB3	Human	Reduced glutathione synthetase level		IAGP	RGD:405874612	8554872	ClinVar Annotator: match by term: Reduced glutathione synthetase level	ClinVar	PMID:12638941\|PMID:15717202\|PMID:28492532

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

PMID:9776767	PMID:10715114	PMID:10833507	PMID:11780052	PMID:12044471	PMID:12477932	PMID:12780348	PMID:14697346	PMID:14702039	PMID:15489334	PMID:18854154	PMID:19035353
PMID:20098747	PMID:20237496	PMID:21048031	PMID:21653829	PMID:21832049	PMID:21873635	PMID:22623531	PMID:26687681	PMID:26948053	PMID:28514442	PMID:28986522	PMID:31267263
PMID:32814053	PMID:33961781	PMID:35914814

NECAB3
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	20	33,657,087 - 33,675,348 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	20	33,657,087 - 33,674,463 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	20	32,244,893 - 32,262,234 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	20	31,708,554 - 31,725,925 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	20	31,708,554 - 31,725,923	NCBI
Celera	20	28,997,925 - 29,015,296 (-)	NCBI		Celera
Cytogenetic Map	20	q11.22	NCBI
HuRef	20	29,030,990 - 29,048,237 (-)	NCBI		HuRef
CHM1_1	20	32,145,985 - 32,163,356 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	20	35,383,618 - 35,401,879 (-)	NCBI		T2T-CHM13v2.0

Necab3
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	154,386,311 - 154,401,326 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	154,386,319 - 154,400,810 (-)	Ensembl		GRCm39 Ensembl
GRCm38	2	154,544,391 - 154,559,406 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	154,544,399 - 154,558,890 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	2	154,370,141 - 154,384,589 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	2	154,235,846 - 154,247,095 (-)	NCBI		MGSCv36	mm8
Celera	2	160,458,609 - 160,473,071 (-)	NCBI		Celera
Cytogenetic Map	2	H1	NCBI
cM Map	2	76.79	NCBI

Necab3
(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_004955422	27,644,916 - 27,659,820 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955422	27,644,913 - 27,660,538 (+)	NCBI	ChiLan1.0	ChiLan1.0

NECAB3
(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	21	39,348,026 - 39,366,136 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	20	39,341,127 - 39,359,237 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	20	29,944,457 - 29,962,566 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	20	31,085,500 - 31,103,274 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	20	31,085,500 - 31,100,871 (-)	Ensembl	panpan1.1		panPan2

NECAB3
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	24	22,877,723 - 22,893,892 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	24	22,878,402 - 22,904,656 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	24	22,522,944 - 22,539,095 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	24	23,564,444 - 23,580,577 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	24	23,564,448 - 23,580,930 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	24	22,856,920 - 22,873,068 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	24	22,950,478 - 22,966,614 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	24	23,381,563 - 23,397,718 (-)	NCBI		UU_Cfam_GSD_1.0

Necab3
(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_024408640	171,830,208 - 171,844,773 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936561	6,906,494 - 6,918,647 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936561	6,905,111 - 6,919,400 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

NECAB3
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	17	37,160,434 - 37,177,278 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	17	37,160,431 - 37,177,272 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	17	42,101,645 - 42,116,052 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

NECAB3
(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	2	37,950,024 - 37,967,314 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666050	88,914,587 - 88,931,846 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Necab3
(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_004624842	5,614,729 - 5,630,838 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624842	5,614,692 - 5,631,566 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in NECAB3
64 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 20p12.2-q12(chr20:9811433-39316956)x3	copy number gain	See cases [RCV000052999]	Chr20:9811433..39316956 [GRCh38] Chr20:9792081..37945599 [GRCh37] Chr20:9740081..37379013 [NCBI36] Chr20:20p12.2-q12	pathogenic
NM_005225.2(E2F1):c.1301C>T (p.Pro434Leu)	single nucleotide variant	Malignant melanoma [RCV000072588]	Chr20:33676745 [GRCh38] Chr20:32264551 [GRCh37] Chr20:31728212 [NCBI36] Chr20:20q11.22	not provided
NM_005225.2(E2F1):c.879C>T (p.Ile293=)	single nucleotide variant	Malignant melanoma [RCV000072589]	Chr20:33677292 [GRCh38] Chr20:32265098 [GRCh37] Chr20:31728759 [NCBI36] Chr20:20q11.22	not provided
GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3	copy number gain	See cases [RCV000135859]	Chr20:99557..64277321 [GRCh38] Chr20:80198..62908674 [GRCh37] Chr20:28198..62379118 [NCBI36] Chr20:20p13-q13.33	pathogenic
GRCh38/hg38 20q11.21-11.23(chr20:33432363-36821881)x1	copy number loss	See cases [RCV000135440]	Chr20:33432363..36821881 [GRCh38] Chr20:32020169..35450284 [GRCh37] Chr20:31483830..34883698 [NCBI36] Chr20:20q11.21-11.23	pathogenic
GRCh38/hg38 20q11.21-11.23(chr20:32062768-35906606)x3	copy number gain	See cases [RCV000141833]	Chr20:32062768..35906606 [GRCh38] Chr20:30650571..34494528 [GRCh37] Chr20:30114232..33957942 [NCBI36] Chr20:20q11.21-11.23	pathogenic
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3	copy number gain	See cases [RCV000510832]	Chr20:61569..62915555 [GRCh37] Chr20:20p13-q13.33	pathogenic
NM_001024675.2(ACTL10):c.185C>T (p.Ala62Val)	single nucleotide variant	not specified [RCV004302580]	Chr20:33667682 [GRCh38] Chr20:32255488 [GRCh37] Chr20:20q11.22	uncertain significance
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)	copy number gain	See cases [RCV000512450]	Chr20:61569..62915555 [GRCh37] Chr20:20p13-q13.33	pathogenic
NC_000020.10:g.(?_31996293)_(33761838_?)del	deletion	Long QT syndrome [RCV000708204]	Chr20:31996293..33761838 [GRCh37] Chr20:20q11.21-11.22	uncertain significance
NC_000020.10:g.(?_31996293)_(33338342_?)del	deletion	Long QT syndrome [RCV000708495]	Chr20:31996293..33338342 [GRCh37] Chr20:20q11.21-11.22	uncertain significance
GRCh37/hg19 20p13-q13.33(chr20:63244-62961294)x3	copy number gain	not provided [RCV000741059]	Chr20:63244..62961294 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20q11.22(chr20:32243830-32255233)x0	copy number loss	not provided [RCV000741172]	Chr20:32243830..32255233 [GRCh37] Chr20:20q11.22	benign
GRCh37/hg19 20q11.22(chr20:32246571-32255643)x1	copy number loss	not provided [RCV000741173]	Chr20:32246571..32255643 [GRCh37] Chr20:20q11.22	benign
GRCh37/hg19 20p13-q13.33(chr20:63244-62912463)x3	copy number gain	not provided [RCV000741057]	Chr20:63244..62912463 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62948788)x3	copy number gain	not provided [RCV000741058]	Chr20:63244..62948788 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20q11.21-11.23(chr20:29833608-35087952)x3	copy number gain	not provided [RCV000849735]	Chr20:29833608..35087952 [GRCh37] Chr20:20q11.21-11.23	pathogenic
NM_031232.4(NECAB3):c.715G>A (p.Glu239Lys)	single nucleotide variant	not specified [RCV004293007]	Chr20:33659661 [GRCh38] Chr20:32247467 [GRCh37] Chr20:20q11.22	uncertain significance
GRCh37/hg19 20q11.21-11.22(chr20:31966407-33169058)x3	copy number gain	not provided [RCV001007091]	Chr20:31966407..33169058 [GRCh37] Chr20:20q11.21-11.22	uncertain significance
NC_000020.10:g.(?_31996293)_(33761838_?)del	deletion	Long QT syndrome [RCV001300227]	Chr20:31996293..33761838 [GRCh37] Chr20:20q11.21-11.22	uncertain significance
GRCh37/hg19 20p11.23-q11.22(chr20:18665879-33903216)x3	copy number gain	not provided [RCV001829151]	Chr20:18665879..33903216 [GRCh37] Chr20:20p11.23-q11.22	likely pathogenic
GRCh37/hg19 20p11.21-q11.22(chr20:25442597-33761550)	copy number gain	not specified [RCV002052709]	Chr20:25442597..33761550 [GRCh37] Chr20:20p11.21-q11.22	pathogenic
NC_000020.10:g.(?_31189994)_(34287210_?)del	deletion	not provided [RCV001956104]	Chr20:31189994..34287210 [GRCh37] Chr20:20q11.21-11.22	pathogenic
NM_031232.4(NECAB3):c.773C>T (p.Pro258Leu)	single nucleotide variant	not specified [RCV004294246]	Chr20:33659603 [GRCh38] Chr20:32247409 [GRCh37] Chr20:20q11.22	likely benign
GRCh37/hg19 20q11.21-11.23(chr20:29833535-34815537)x3	copy number gain	not provided [RCV002474532]	Chr20:29833535..34815537 [GRCh37] Chr20:20q11.21-11.23	likely pathogenic
NM_031232.4(NECAB3):c.586C>G (p.Arg196Gly)	single nucleotide variant	not specified [RCV004210808]	Chr20:33659942 [GRCh38] Chr20:32247748 [GRCh37] Chr20:20q11.22	uncertain significance
NM_080825.4(C20orf144):c.358C>G (p.Arg120Gly)	single nucleotide variant	not specified [RCV004227807]	Chr20:33663763 [GRCh38] Chr20:32251569 [GRCh37] Chr20:20q11.22	uncertain significance
GRCh37/hg19 20q11.21-11.23(chr20:29652122-35603726)x3	copy number gain	not provided [RCV002475651]	Chr20:29652122..35603726 [GRCh37] Chr20:20q11.21-11.23	likely pathogenic
NM_031232.4(NECAB3):c.137G>A (p.Arg46His)	single nucleotide variant	not specified [RCV004216647]	Chr20:33672415 [GRCh38] Chr20:32260221 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.319A>G (p.Ser107Gly)	single nucleotide variant	not specified [RCV004111205]	Chr20:33667816 [GRCh38] Chr20:32255622 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.565G>A (p.Gly189Ser)	single nucleotide variant	not specified [RCV004191058]	Chr20:33659963 [GRCh38] Chr20:32247769 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.101C>A (p.Ala34Glu)	single nucleotide variant	not specified [RCV004240178]	Chr20:33667598 [GRCh38] Chr20:32255404 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.621G>T (p.Trp207Cys)	single nucleotide variant	not specified [RCV004106519]	Chr20:33659907 [GRCh38] Chr20:32247713 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.563G>A (p.Arg188Gln)	single nucleotide variant	not specified [RCV004179636]	Chr20:33668060 [GRCh38] Chr20:32255866 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.583C>T (p.Arg195Cys)	single nucleotide variant	not specified [RCV004175076]	Chr20:33659945 [GRCh38] Chr20:32247751 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.631A>T (p.Thr211Ser)	single nucleotide variant	not specified [RCV004201803]	Chr20:33668128 [GRCh38] Chr20:32255934 [GRCh37] Chr20:20q11.22	uncertain significance
NM_080825.4(C20orf144):c.352T>G (p.Trp118Gly)	single nucleotide variant	not specified [RCV004093681]	Chr20:33663757 [GRCh38] Chr20:32251563 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.158C>G (p.Ser53Trp)	single nucleotide variant	not specified [RCV004143855]	Chr20:33667655 [GRCh38] Chr20:32255461 [GRCh37] Chr20:20q11.22	uncertain significance
NM_080825.4(C20orf144):c.439C>G (p.Arg147Gly)	single nucleotide variant	not specified [RCV004110968]	Chr20:33663844 [GRCh38] Chr20:32251650 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.949C>T (p.Arg317Cys)	single nucleotide variant	not specified [RCV004194433]	Chr20:33658765 [GRCh38] Chr20:32246571 [GRCh37] Chr20:20q11.22	likely benign
NM_080825.4(C20orf144):c.91T>C (p.Ser31Pro)	single nucleotide variant	not specified [RCV004105437]	Chr20:33662436 [GRCh38] Chr20:32250242 [GRCh37] Chr20:20q11.22	likely benign
NM_031232.4(NECAB3):c.673C>T (p.Arg225Trp)	single nucleotide variant	not specified [RCV004082916]	Chr20:33659703 [GRCh38] Chr20:32247509 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.499G>A (p.Gly167Ser)	single nucleotide variant	not specified [RCV004275847]	Chr20:33667996 [GRCh38] Chr20:32255802 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.45C>G (p.Phe15Leu)	single nucleotide variant	not specified [RCV004281273]	Chr20:33667542 [GRCh38] Chr20:32255348 [GRCh37] Chr20:20q11.22	likely benign
NM_031232.4(NECAB3):c.89C>T (p.Ala30Val)	single nucleotide variant	not specified [RCV004281281]	Chr20:33674264 [GRCh38] Chr20:32262070 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.424G>A (p.Ala142Thr)	single nucleotide variant	not specified [RCV004349849]	Chr20:33667921 [GRCh38] Chr20:32255727 [GRCh37] Chr20:20q11.22	likely benign
NM_031232.4(NECAB3):c.589G>A (p.Ala197Thr)	single nucleotide variant	not specified [RCV004356501]	Chr20:33659939 [GRCh38] Chr20:32247745 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.488T>C (p.Val163Ala)	single nucleotide variant	not specified [RCV004428168]	Chr20:33667985 [GRCh38] Chr20:32255791 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.526G>C (p.Ala176Pro)	single nucleotide variant	not specified [RCV004428175]	Chr20:33668023 [GRCh38] Chr20:32255829 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.5C>G (p.Ala2Gly)	single nucleotide variant	not specified [RCV004428184]	Chr20:33667502 [GRCh38] Chr20:32255308 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.190A>C (p.Asn64His)	single nucleotide variant	not specified [RCV004428149]	Chr20:33667687 [GRCh38] Chr20:32255493 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.411G>C (p.Glu137Asp)	single nucleotide variant	not specified [RCV004428158]	Chr20:33667908 [GRCh38] Chr20:32255714 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.625C>T (p.Pro209Ser)	single nucleotide variant	not specified [RCV004480694]	Chr20:33659903 [GRCh38] Chr20:32247709 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.61C>T (p.Pro21Ser)	single nucleotide variant	not specified [RCV004262667]	Chr20:33674292 [GRCh38] Chr20:32262098 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.1130C>T (p.Ala377Val)	single nucleotide variant	not specified [RCV004480663]	Chr20:33657974 [GRCh38] Chr20:32245780 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.166C>T (p.Leu56Phe)	single nucleotide variant	not specified [RCV004480666]	Chr20:33670781 [GRCh38] Chr20:32258587 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.523C>T (p.Arg175Trp)	single nucleotide variant	not specified [RCV004480676]	Chr20:33660260 [GRCh38] Chr20:32248066 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.574C>T (p.Arg192Trp)	single nucleotide variant	not specified [RCV004480683]	Chr20:33659954 [GRCh38] Chr20:32247760 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.686G>C (p.Arg229Pro)	single nucleotide variant	not specified [RCV004428191]	Chr20:33668183 [GRCh38] Chr20:32255989 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.1126C>T (p.Arg376Trp)	single nucleotide variant	not specified [RCV004480660]	Chr20:33657978 [GRCh38] Chr20:32245784 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.558G>C (p.Arg186Ser)	single nucleotide variant	not specified [RCV004641455]	Chr20:33659970 [GRCh38] Chr20:32247776 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.233C>T (p.Thr78Ile)	single nucleotide variant	not specified [RCV004602788]	Chr20:33667730 [GRCh38] Chr20:32255536 [GRCh37] Chr20:20q11.22	uncertain significance
NC_000020.10:g.(?_31368130)_(34287210_?)del	deletion	Glutathione synthetase deficiency with 5-oxoprolinuria [RCV004579432]	Chr20:31368130..34287210 [GRCh37] Chr20:20q11.21-11.22	pathogenic
NC_000020.10:g.(?_31571600)_(33001705_?)del	deletion	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase [RCV004579470]	Chr20:31571600..33001705 [GRCh37] Chr20:20q11.21-11.22	pathogenic
NM_031232.4(NECAB3):c.446C>T (p.Thr149Met)	single nucleotide variant	not specified [RCV004641456]	Chr20:33660337 [GRCh38] Chr20:32248143 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.610G>C (p.Gly204Arg)	single nucleotide variant	not specified [RCV004602796]	Chr20:33668107 [GRCh38] Chr20:32255913 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.224A>G (p.Lys75Arg)	single nucleotide variant	not specified [RCV004602805]	Chr20:33667721 [GRCh38] Chr20:32255527 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.626T>G (p.Val209Gly)	single nucleotide variant	not specified [RCV004602780]	Chr20:33668123 [GRCh38] Chr20:32255929 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.131T>G (p.Val44Gly)	single nucleotide variant	not specified [RCV004829636]	Chr20:33672421 [GRCh38] Chr20:32260227 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.37C>T (p.Arg13Trp)	single nucleotide variant	not specified [RCV004829637]	Chr20:33674316 [GRCh38] Chr20:32262122 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.266A>C (p.Asn89Thr)	single nucleotide variant	not specified [RCV004829641]	Chr20:33669710 [GRCh38] Chr20:32257516 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.715G>C (p.Glu239Gln)	single nucleotide variant	not specified [RCV004829639]	Chr20:33659661 [GRCh38] Chr20:32247467 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.719G>A (p.Cys240Tyr)	single nucleotide variant	not specified [RCV004829640]	Chr20:33659657 [GRCh38] Chr20:32247463 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.512T>A (p.Leu171Gln)	single nucleotide variant	not specified [RCV004892542]	Chr20:33668009 [GRCh38] Chr20:32255815 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.340G>A (p.Val114Ile)	single nucleotide variant	not specified [RCV004903035]	Chr20:33667837 [GRCh38] Chr20:32255643 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.176T>A (p.Leu59Gln)	single nucleotide variant	not specified [RCV004903058]	Chr20:33667673 [GRCh38] Chr20:32255479 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.392G>A (p.Gly131Asp)	single nucleotide variant	not specified [RCV004903063]	Chr20:33667889 [GRCh38] Chr20:32255695 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.212C>T (p.Ala71Val)	single nucleotide variant	not specified [RCV004903070]	Chr20:33667709 [GRCh38] Chr20:32255515 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.229A>G (p.Ile77Val)	single nucleotide variant	not specified [RCV004903033]	Chr20:33667726 [GRCh38] Chr20:32255532 [GRCh37] Chr20:20q11.22	likely benign
NM_001024675.2(ACTL10):c.276G>C (p.Glu92Asp)	single nucleotide variant	not specified [RCV004903074]	Chr20:33667773 [GRCh38] Chr20:32255579 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.701A>C (p.Glu234Ala)	single nucleotide variant	not specified [RCV004903075]	Chr20:33668198 [GRCh38] Chr20:32256004 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.673C>G (p.Arg225Gly)	single nucleotide variant	not specified [RCV004903023]	Chr20:33668170 [GRCh38] Chr20:32255976 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.64G>T (p.Ala22Ser)	single nucleotide variant	not specified [RCV004903040]	Chr20:33667561 [GRCh38] Chr20:32255367 [GRCh37] Chr20:20q11.22	uncertain significance
NM_001024675.2(ACTL10):c.322G>C (p.Val108Leu)	single nucleotide variant	not specified [RCV004903051]	Chr20:33667819 [GRCh38] Chr20:32255625 [GRCh37] Chr20:20q11.22	likely benign
NM_031232.4(NECAB3):c.452G>A (p.Ser151Asn)	single nucleotide variant	not specified [RCV004829638]	Chr20:33660331 [GRCh38] Chr20:32248137 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.425C>T (p.Thr142Met)	single nucleotide variant	not specified [RCV004480671]	Chr20:33660358 [GRCh38] Chr20:32248164 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.703A>G (p.Ile235Val)	single nucleotide variant	not specified [RCV004480701]	Chr20:33659673 [GRCh38] Chr20:32247479 [GRCh37] Chr20:20q11.22	uncertain significance
NM_031232.4(NECAB3):c.795G>C (p.Trp265Cys)	single nucleotide variant	not specified [RCV004480711]	Chr20:33659581 [GRCh38] Chr20:32247387 [GRCh37] Chr20:20q11.22	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	8015
Count of miRNA genes:	1112
Interacting mature miRNAs:	1422
Transcripts:	ENST00000246190, ENST00000375238, ENST00000439478, ENST00000463246, ENST00000473892, ENST00000477778, ENST00000478237, ENST00000480994, ENST00000483813, ENST00000484824, ENST00000485399, ENST00000485976, ENST00000488489, ENST00000493590, ENST00000494174, ENST00000498353, ENST00000606106, ENST00000606525, ENST00000606690, ENST00000606699, ENST00000607055, ENST00000607805
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.

RH12699

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	32,245,001 - 32,245,128	UniSTS	GRCh37
Build 36	20	31,708,662 - 31,708,789	RGD	NCBI36
Celera	20	28,998,033 - 28,998,160	RGD
Cytogenetic Map	20	q11.22	UniSTS
HuRef	20	29,031,098 - 29,031,225	UniSTS
GeneMap99-GB4 RH Map	20	194.28	UniSTS
NCBI RH Map	20	279.4	UniSTS

PMC344741P1

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	32,263,516 - 32,263,912	UniSTS	GRCh37
Build 36	20	31,727,177 - 31,727,573	RGD	NCBI36
Celera	20	29,016,548 - 29,016,944	RGD
Cytogenetic Map	20	q11.2	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
HuRef	20	29,049,490 - 29,049,886	UniSTS

A006D04

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	32,244,977 - 32,245,135	UniSTS	GRCh37
Build 36	20	31,708,638 - 31,708,796	RGD	NCBI36
Celera	20	28,998,009 - 28,998,167	RGD
Cytogenetic Map	20	q11.22	UniSTS
HuRef	20	29,031,074 - 29,031,232	UniSTS
GeneMap99-GB4 RH Map	20	192.65	UniSTS
NCBI RH Map	20	279.4	UniSTS

AF021113

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	32,251,392 - 32,251,581	UniSTS	GRCh37
Build 36	20	31,715,053 - 31,715,242	RGD	NCBI36
Celera	20	29,004,424 - 29,004,613	RGD
Cytogenetic Map	20	q11.22	UniSTS
HuRef	20	29,037,489 - 29,037,678	UniSTS

RH78379

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	32,263,555 - 32,263,708	UniSTS	GRCh37
Build 36	20	31,727,216 - 31,727,369	RGD	NCBI36
Celera	20	29,016,587 - 29,016,740	RGD
Cytogenetic Map	20	q11.2	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
HuRef	20	29,049,529 - 29,049,682	UniSTS
GeneMap99-GB4 RH Map	20	194.39	UniSTS
NCBI RH Map	20	289.8	UniSTS

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2439	2788	2253	4974	1726	2351	6	624	1948	465	2270	7303	6469	53	3734	1	852	1744	1617	175	1


RefSeq Transcripts	NM_031231	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_031232	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005260510	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011528991	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011528992	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017028015	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017028016	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440369	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440370	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323826	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323827	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323828	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323829	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323830	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323831	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_002958502	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB039947	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF193759	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF409141	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK023706	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK124388	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK291895	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK309285	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL121906	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL519842	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC023270	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC047673	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ212085	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ431858	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CD580591	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471077	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068258	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000246190 ⟹ ENSP00000246190

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,087 - 33,674,428 (-)	Ensembl

Ensembl Acc Id:

ENST00000375238 ⟹ ENSP00000364386

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,087 - 33,674,463 (-)	Ensembl

Ensembl Acc Id:

ENST00000439478 ⟹ ENSP00000392064

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,658,523 - 33,674,409 (-)	Ensembl

Ensembl Acc Id:

ENST00000463246

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,945 - 33,662,184 (-)	Ensembl

Ensembl Acc Id:

ENST00000473892 ⟹ ENSP00000476165

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,669,143 - 33,670,765 (-)	Ensembl

Ensembl Acc Id:

ENST00000477778

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,087 - 33,659,547 (-)	Ensembl

Ensembl Acc Id:

ENST00000478237

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,730 - 33,662,237 (-)	Ensembl

Ensembl Acc Id:

ENST00000480994 ⟹ ENSP00000475834

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,962 - 33,666,659 (-)	Ensembl

Ensembl Acc Id:

ENST00000483813

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,564 - 33,662,419 (-)	Ensembl

Ensembl Acc Id:

ENST00000484824

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,669,448 - 33,674,420 (-)	Ensembl

Ensembl Acc Id:

ENST00000485399 ⟹ ENSP00000475369

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,637 - 33,674,389 (-)	Ensembl

Ensembl Acc Id:

ENST00000485976

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,677 - 33,663,719 (-)	Ensembl

Ensembl Acc Id:

ENST00000488489 ⟹ ENSP00000475938

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,088 - 33,674,420 (-)	Ensembl

Ensembl Acc Id:

ENST00000493590 ⟹ ENSP00000475755

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,659,885 - 33,674,366 (-)	Ensembl

Ensembl Acc Id:

ENST00000494174

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,757 - 33,669,428 (-)	Ensembl

Ensembl Acc Id:

ENST00000498353

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,659,659 - 33,662,423 (-)	Ensembl

Ensembl Acc Id:

ENST00000606106

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,659,927 - 33,666,702 (-)	Ensembl

Ensembl Acc Id:

ENST00000606525

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,657,088 - 33,662,778 (-)	Ensembl

Ensembl Acc Id:

ENST00000606690 ⟹ ENSP00000475420

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,658,480 - 33,674,359 (-)	Ensembl

Ensembl Acc Id:

ENST00000606699

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,660,251 - 33,674,420 (-)	Ensembl

Ensembl Acc Id:

ENST00000607055

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,672,034 - 33,674,388 (-)	Ensembl

Ensembl Acc Id:

ENST00000607805 ⟹ ENSP00000476044

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	33,658,527 - 33,674,408 (-)	Ensembl

RefSeq Acc Id:

NM_031231 ⟹ NP_112508

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	33,657,087 - 33,674,428 (-)	NCBI
GRCh37	20	32,244,893 - 32,262,264 (-)	RGD
Build 36	20	31,708,554 - 31,725,925 (-)	NCBI Archive
Celera	20	28,997,925 - 29,015,296 (-)	RGD
HuRef	20	29,030,990 - 29,048,237 (-)	ENTREZGENE
CHM1_1	20	32,145,985 - 32,163,356 (-)	NCBI
T2T-CHM13v2.0	20	35,383,618 - 35,400,959 (-)	NCBI

Sequence:

show sequence

CTCTAGCCACACCGAGTCCGCCGCGGCGTCCAGGGTCGGCAGCAACCGCAGCCGAGCCCGAGCGGGTGGCGGCGCCATGGCGTGCGCGGGGCTGCTCACCGTGTGCCTGCTCCGGCCGCCCGCGCCCC
AGCCCCAGCCCCAGACCCCGCGGCACCCCCAGCTCGCGCCCGACCCGGGGCCCGCCGGACACACGCTCTTCCAGGACGTTTTCCGCAGAGCAGACAAGAATGATGATGGGAAGCTCTCATTTGAGGAA
TTCCAGAATTACTTTGCCGATGGGGTTCTCAGCCTGGGGGAGCTGCAGGAACTGTTCAGCGGCATTGATGGGCATCTCACCGACAATTTAGAAACAGAAAAACTGTGTGACTACTTCTCAGAGCACCT
GGGTGTCTACCGGCCGGTGCTGGCTGCATTGGAATCGCTGAACCGTGCAGTGCTCGCTGCCATGGATGCCACCAAGCTGGAGTACGAGAGGGCCTCCAAAGTGGACCAGTTTGTGACGCGCTTCCTGC
TGCGGGAGACGGTGAGCCAGCTGCAAGCCCTTCAGAGCTCGCTGGAGGGGGCGTCAGATACCCTGGAGGCCCAGGCCCATGGCTGGCGGTCAGATGCAGAGAGCGTGGAGGCGCAGAGCAGGCTCTGC
GGCAGCCGGCGGGCAGGACGCCGAGCCCTGAGGAGTGTCAGCCGGTCATCCACCTGGTCCCCCGGCTCTTCTGACACAGGGCGCAGCTCAGAGGCCGAGATGCAGTGGCGGCTCCAGGTGAACCGCCT
CCAGGAGCTCATCGACCAGCTCGAGTGCAAGGCCCCCCGGCTGGAACCCCTGCGTGAAGAGGACCTGGCCAAGGGGCCTGACTTGCACATCCTCATGGCCCAGAGGCAGGTCCAGGTGGCAGAGGAAG
GCCTGCAGGACTTCCACCGAGCCCTGCGCTGCTATGTGGACTTCACAGGGGCCCAGAGCCATTGTCTGCATGTGTCCGCCCAGAAGATGCTGGACGGTGCCTCCTTCACCCTGTATGAGTTCTGGCAG
GATGAGGCCTCCTGGAGAAGGCACCAGCAGTCGCCTGGCAGCAAGGCCTTCCAGCGCATCCTCATCGACCACCTGCGGGCCCCGGACACCCTCACCACTGTGTTCTTCCCAGCCTCCTGGTGGATAAT
GAATAACAACTGAGCCAGACCTGCACACGCCGAGGGCCCCGGGACCCTGCCTGCCTCCCTCTGGAGCCTTCTGGACTGGCCAGCCCAGCGCAAAGACCAGGACTTGTCTCCTCCTGGACTTGGGCCTG
GTGGAAGGGCTCTCAGCCCAGGGATCAGGGACTGGGCTGCTTGCTTTCTATTTATTATTGATTTATTTATCCCTGTATTTTATTGTTTGTCACTTCAGCCTCCAAGCTACTTTGGCTTCTGCCTGGCT
CAGGAGACCTGGATTCTGGTCCCTGCTGTCCCTGCCTGGCTGAGCGACCCAGGGCAGGTCCCGTCCCTGTCTGGGTGGGCCTCAGGCCATCTGGCCGCCTAGCGAGGGTCCTGCTTTCTTCCTGCTGT
CTTGGGACCAGGCTTCTGCTCCTCCTCAGCCAGCGGCAGAAGCAGGGCTGATGCTCAGGGACCCCCCAACCCTCAAACCTTGCCTCCGAGGCTGGGCCTGAGCTGGGTGCCCCGTCGCCCTCCCAGGC
CACTAGGCTCTGACTCTTCCAGCACCCATGGATGTGCCAGAGGCCTCTGGGTTGGTTTGCATGTCATTTGCATATCGTTTGCATGCCCTCATCCCACCCATTCTCAGGGCAGTATGGGAAGCCCCAAG
GTGACCTGGCCAAGTAGCAATAATTTGGGTCCAGGGTCACCTATTGCCCCCAGAGGCCTCTGAACCCCAGGCTGGGACCCCAGCACAGAGGCAATAAAGGCAGTGGTCCCTTCCA

hide sequence

RefSeq Acc Id:

NM_031232 ⟹ NP_112509

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	33,657,087 - 33,674,428 (-)	NCBI
GRCh37	20	32,244,893 - 32,262,264 (-)	RGD
Build 36	20	31,708,554 - 31,725,925 (-)	NCBI Archive
Celera	20	28,997,925 - 29,015,296 (-)	RGD
HuRef	20	29,030,990 - 29,048,237 (-)	ENTREZGENE
CHM1_1	20	32,145,985 - 32,163,356 (-)	NCBI
T2T-CHM13v2.0	20	35,383,618 - 35,400,959 (-)	NCBI

Sequence:

show sequence

CTCTAGCCACACCGAGTCCGCCGCGGCGTCCAGGGTCGGCAGCAACCGCAGCCGAGCCCGAGCGGGTGGCGGCGCCATGGCGTGCGCGGGGCTGCTCACCGTGTGCCTGCTCCGGCCGCCCGCGCCCC
AGCCCCAGCCCCAGACCCCGCGGCACCCCCAGCTCGCGCCCGACCCGGGGCCCGCCGGACACACGCTCTTCCAGGACGTTTTCCGCAGAGCAGACAAGAATGATGATGGGAAGCTCTCATTTGAGGAA
TTCCAGAATTACTTTGCCGATGGGGTTCTCAGCCTGGGGGAGCTGCAGGAACTGTTCAGCGGCATTGATGGGCATCTCACCGACAATTTAGAAACAGAAAAACTGTGTGACTACTTCTCAGAGCACCT
GGGTGTCTACCGGCCGGTGCTGGCTGCATTGGAATCGCTGAACCGTGCAGTGCTCGCTGCCATGGATGCCACCAAGCTGGAGTACGAGAGGGCCTCCAAAGTGGACCAGTTTGTGACGCGCTTCCTGC
TGCGGGAGACGGTGAGCCAGCTGCAAGCCCTTCAGAGCTCGCTGGAGGGGGCGTCAGATACCCTGGAGGCCCAGGCCCATGGCTGGCGGTCAGATGCAGAGAGCGTGGAGGCGCAGAGCAGGCTCTGC
GGCAGCCGGCGGGCAGGACGCCGAGCCCTGAGGAGTGTCAGCCGGTCATCCACCTGGTCCCCCGGCTCTTCTGACACAGGGCGCAGCTCAGAGGCCGAGATGCAGTGGCGGCTCCAGGTGAACCGCCT
CCAGGAGCTCATCGACCAGCTCGAGTGCAAGGTGAGGGCCGTGGGGCCAGGGCCCCACAAGGGAGGACCCTCCTGGTATCCACCAGAGCCAGGCCCATGCTGGAGGCCCGGCCCACACTCTGTGCCCT
CACAGGCCCCCCGGCTGGAACCCCTGCGTGAAGAGGACCTGGCCAAGGGGCCTGACTTGCACATCCTCATGGCCCAGAGGCAGGTCCAGGTGGCAGAGGAAGGCCTGCAGGACTTCCACCGAGCCCTG
CGCTGCTATGTGGACTTCACAGGGGCCCAGAGCCATTGTCTGCATGTGTCCGCCCAGAAGATGCTGGACGGTGCCTCCTTCACCCTGTATGAGTTCTGGCAGGATGAGGCCTCCTGGAGAAGGCACCA
GCAGTCGCCTGGCAGCAAGGCCTTCCAGCGCATCCTCATCGACCACCTGCGGGCCCCGGACACCCTCACCACTGTGTTCTTCCCAGCCTCCTGGTGGATAATGAATAACAACTGAGCCAGACCTGCAC
ACGCCGAGGGCCCCGGGACCCTGCCTGCCTCCCTCTGGAGCCTTCTGGACTGGCCAGCCCAGCGCAAAGACCAGGACTTGTCTCCTCCTGGACTTGGGCCTGGTGGAAGGGCTCTCAGCCCAGGGATC
AGGGACTGGGCTGCTTGCTTTCTATTTATTATTGATTTATTTATCCCTGTATTTTATTGTTTGTCACTTCAGCCTCCAAGCTACTTTGGCTTCTGCCTGGCTCAGGAGACCTGGATTCTGGTCCCTGC
TGTCCCTGCCTGGCTGAGCGACCCAGGGCAGGTCCCGTCCCTGTCTGGGTGGGCCTCAGGCCATCTGGCCGCCTAGCGAGGGTCCTGCTTTCTTCCTGCTGTCTTGGGACCAGGCTTCTGCTCCTCCT
CAGCCAGCGGCAGAAGCAGGGCTGATGCTCAGGGACCCCCCAACCCTCAAACCTTGCCTCCGAGGCTGGGCCTGAGCTGGGTGCCCCGTCGCCCTCCCAGGCCACTAGGCTCTGACTCTTCCAGCACC
CATGGATGTGCCAGAGGCCTCTGGGTTGGTTTGCATGTCATTTGCATATCGTTTGCATGCCCTCATCCCACCCATTCTCAGGGCAGTATGGGAAGCCCCAAGGTGACCTGGCCAAGTAGCAATAATTT
GGGTCCAGGGTCACCTATTGCCCCCAGAGGCCTCTGAACCCCAGGCTGGGACCCCAGCACAGAGGCAATAAAGGCAGTGGTCCCTTCCA

hide sequence

RefSeq Acc Id:

XM_005260510 ⟹ XP_005260567

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	33,657,087 - 33,674,428 (-)	NCBI
GRCh37	20	32,244,893 - 32,262,264 (-)	NCBI

Sequence:

show sequence

CTCTAGCCACACCGAGTCCGCCGCGGCGTCCAGGGTCGGCAGCAACCGCAGCCGAGCCCGAGCGGGTGGCGGCGCCATGGCGTGCGCGGGGCTGCTCACCGTGTGCCTGCTCCGGCCGCCCGCGCCCC
AGCCCCAGCCCCAGACCCCGCGGCACCCCCAGCTCGCGCCCGACCCGGGGCCCGCCGGACACACGCTCTTCCAGGACGTTTTCCGCAGAGCAGACAAGAATGATGATGGGAAGCTCTCATTTGAGGAA
TTCCAGAATTACTTTGCCGATGGGGTTCTCAGCCTGGGGGAGCTGCAGGAACTGTTCAGCGGCATTGATGGGCATCTCACCGACAATTTAGAAACAGAAAAACTGTGTGACTACTTCTCAGAGCACCT
GGGTGTCTACCGGCCGGTGCTGGCTGCATTGGAATCGCTGAACCGTGCAGTGCTCGCTGCCATGGATGCCACCAAGCTGGAGTACGAGAGGGCCTCCAAAGTGGACCAGTTTGTGACGCGCTTCCTGC
TGCGGGAGACGGTGAGCCAGCTGCAAGCCCTTCAGAGCTCGCTGGAGGGGGCGTCAGATACCCTGGAGGCCCAGGCCCATGGCTGGCGGTCAGATGCAGAGAGCGTGGAGGCGCAGAGCAGGCTCTGC
GGCAGCCGGCGGGCAGGACGCCGAGCCCTGAGGAGTGTCAGCCGGTCATCCACCTGGTCCCCCGGCTCTTCTGACACAGGGCGCAGCTCAGAGGCCGAGATGCAGTGGCGGCTCCAGGTGAACCGCCT
CCAGGAGCTCATCGACCAGCTCGAGTGCAAGCACATCCTCATGGCCCAGAGGCAGGTCCAGGTGGCAGAGGAAGGCCTGCAGGACTTCCACCGAGCCCTGCGCTGCTATGTGGACTTCACAGGGGCCC
AGAGCCATTGTCTGCATGTGTCCGCCCAGAAGATGCTGGACGGTGCCTCCTTCACCCTGTATGAGTTCTGGCAGGATGAGGCCTCCTGGAGAAGGCACCAGCAGTCGCCTGGCAGCAAGGCCTTCCAG
CGCATCCTCATCGACCACCTGCGGGCCCCGGACACCCTCACCACTGTGTTCTTCCCAGCCTCCTGGTGGATAATGAATAACAACTGAGCCAGACCTGCACACGCCGAGGGCCCCGGGACCCTGCCTGC
CTCCCTCTGGAGCCTTCTGGACTGGCCAGCCCAGCGCAAAGACCAGGACTTGTCTCCTCCTGGACTTGGGCCTGGTGGAAGGGCTCTCAGCCCAGGGATCAGGGACTGGGCTGCTTGCTTTCTATTTA
TTATTGATTTATTTATCCCTGTATTTTATTGTTTGTCACTTCAGCCTCCAAGCTACTTTGGCTTCTGCCTGGCTCAGGAGACCTGGATTCTGGTCCCTGCTGTCCCTGCCTGGCTGAGCGACCCAGGG
CAGGTCCCGTCCCTGTCTGGGTGGGCCTCAGGCCATCTGGCCGCCTAGCGAGGGTCCTGCTTTCTTCCTGCTGTCTTGGGACCAGGCTTCTGCTCCTCCTCAGCCAGCGGCAGAAGCAGGGCTGATGC
TCAGGGACCCCCCAACCCTCAAACCTTGCCTCCGAGGCTGGGCCTGAGCTGGGTGCCCCGTCGCCCTCCCAGGCCACTAGGCTCTGACTCTTCCAGCACCCATGGATGTGCCAGAGGCCTCTGGGTTG
GTTTGCATGTCATTTGCATATCGTTTGCATGCCCTCATCCCACCCATTCTCAGGGCAGTATGGGAAGCCCCAAGGTGACCTGGCCAAGTAGCAATAATTTGGGTCCAGGGTCACCTATTGCCCCCAGA
GGCCTCTGAACCCCAGGCTGGGACCCCAGCACAGAGGCAATAAAGGCAGTGGTCCCTTCCA

hide sequence

RefSeq Acc Id:

XM_011528991 ⟹ XP_011527293

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	33,657,087 - 33,663,716 (-)	NCBI

Sequence:

show sequence

TCTGCCCCCTGGGCCCTGGCAACATTGTGACCTCACGGGCTGACCTCACCAATTGCAGGCTCTG
AGCACCGCCTTCCAGGGCCCACAGGAGTACGAGAGGGCCTCCAAAGTGGACCAGTTTGTGACGCGCTTCCTGCTGCGGGAGACGGTGAGCCAGCTGCAAGCCCTTCAGAGCTCGCTGGAGGGGGCGTC
AGATACCCTGGAGGCCCAGGCCCATGGCTGGCGTCCTCGGCCCTGTGAGCCTCACTTCCTCTAGGTCAGATGCAGAGAGCGTGGAGGCGCAGAGCAGGCTCTGCGGCAGCCGGCGGGCAGGACGCCGA
GCCCTGAGGAGTGTCAGCCGGTCATCCACCTGGTCCCCCGGCTCTTCTGACACAGGGCGCAGCTCAGAGGCCGAGATGCAGTGGCGGCTCCAGGTGAACCGCCTCCAGGAGCTCATCGACCAGCTCGA
GTGCAAGGCCCCCCGGCTGGAACCCCTGCGTGAAGAGGACCTGGCCAAGGGGCCTGACTTGCACATCCTCATGGCCCAGAGGCAGGTCCAGGTGGCAGAGGAAGGCCTGCAGGACTTCCACCGAGCCC
TGCGCTGCTATGTGGACTTCACAGGGGCCCAGAGCCATTGTCTGCATGTGTCCGCCCAGAAGATGCTGGACGGTGCCTCCTTCACCCTGTATGAGTTCTGGCAGGATGAGGCCTCCTGGAGAAGGCAC
CAGCAGTCGCCTGGCAGCAAGGCCTTCCAGCGCATCCTCATCGACCACCTGCGGGCCCCGGACACCCTCACCACTGTGTTCTTCCCAGCCTCCTGGTGGATAATGAATAACAACTGAGCCAGACCTGC
ACACGCCGAGGGCCCCGGGACCCTGCCTGCCTCCCTCTGGAGCCTTCTGGACTGGCCAGCCCAGCGCAAAGACCAGGACTTGTCTCCTCCTGGACTTGGGCCTGGTGGAAGGGCTCTCAGCCCAGGGA
TCAGGGACTGGGCTGCTTGCTTTCTATTTATTATTGATTTATTTATCCCTGTATTTTATTGTTTGTCACTTCAGCCTCCAAGCTACTTTGGCTTCTGCCTGGCTCAGGAGACCTGGATTCTGGTCCCT
GCTGTCCCTGCCTGGCTGAGCGACCCAGGGCAGGTCCCGTCCCTGTCTGGGTGGGCCTCAGGCCATCTGGCCGCCTAGCGAGGGTCCTGCTTTCTTCCTGCTGTCTTGGGACCAGGCTTCTGCTCCTC
CTCAGCCAGCGGCAGAAGCAGGGCTGATGCTCAGGGACCCCCCAACCCTCAAACCTTGCCTCCGAGGCTGGGCCTGAGCTGGGTGCCCCGTCGCCCTCCCAGGCCACTAGGCTCTGACTCTTCCAGCA
CCCATGGATGTGCCAGAGGCCTCTGGGTTGGTTTGCATGTCATTTGCATATCGTTTGCATGCCCTCATCCCACCCATTCTCAGGGCAGTATGGGAAGCCCCAAGGTGACCTGGCCAAGTAGCAATAAT
TTGGGTCCAGGGTCACCTATTGCCCCCAGAGGCCTCTGAACCCCAGGCTGGGACCCCAGCACAGAGGCAATAAAGGCAGTGGTCCCTTCCA

hide sequence

RefSeq Acc Id:

XM_011528992 ⟹ XP_011527294

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	33,659,915 - 33,674,428 (-)	NCBI

Sequence:

show sequence

CTCTAGCCACACCGAGTCCGCCGCGGCGTCCAGGGTCGGCAGCAACCGCAGCCGAGCCCGAGCGGGTGGCGGCGCCATGGCGTGCGCGGGGCTGCTCACCGTGTGCCTGCTCCGGCCGCCCGCGCCCC
AGCCCCAGCCCCAGACCCCGCGGCACCCCCAGCTCGCGCCCGACCCGGGGCCCGCCGGACACACGCTCTTCCAGGACGTTTTCCGCAGAGCAGACAAGAATGATGATGGGAAGCTCTCATTTGAGGAA
TTCCAGAATTACTTTGCCGATGGGGTTCTCAGCCTGGGGGAGCTGCAGGAACTGTTCAGCGGCATTGATGGGCATCTCACCGACAATTTAGAAACAGAAAAACTGTGTGACTACTTCTCAGAGCACCT
GGGTGTCTACCGGCCGGTGCTGGCTGCATTGGAATCGCTGAACCGTGCAGTGCTCGCTGCCATGGATGCCACCAAGCTGGAGTACGAGAGGGCCTCCAAAGTGGACCAGTTTGTGACGCGCTTCCTGC
TGCGGGAGACGGTGAGCCAGCTGCAAGCCCTTCAGAGCTCGCTGGAGGGGGCGTCAGATACCCTGGAGGCCCAGGCCCATGGCTGGCGTCCTCGGCCCTGTGAGCCTCACTTCCTCTAGGTCAGATGC
AGAGAGCGTGGAGGCGCAGAGCAGGCTCTGCGGCAGCCGGCGGGCAGGACGCCGAGCCCTGAGGAGTGTCAGCCGGTCATCCACC

hide sequence

RefSeq Acc Id:

XM_017028016 ⟹ XP_016883505

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	33,657,087 - 33,662,181 (-)	NCBI

Sequence:

show sequence

AGGCAATGCATGTAAGGAGTACGAGAGGGCCTCCAAAGTGGACCAGTTTGTGACGCGCTTCCTGCTGCGGGAGACGGTGAGCCAGCTGCAAGCCCTTCAGAGCTCGCTGGAGGGGGCGTCAGATACCC
TGGAGGCCCAGGCCCATGGCTGGCGTCCTCGGCCCTGTGAGCCTCACTTCCTCTAGGTCAGATGCAGAGAGCGTGGAGGCGCAGAGCAGGCTCTGCGGCAGCCGGCGGGCAGGACGCCGAGCCCTGAG
GAGTGTCAGCCGGTCATCCACCTGGTCCCCCGGCTCTTCTGACACAGGGCGCAGCTCAGAGGCCGAGATGCAGTGGCGGCTCCAGGTGAACCGCCTCCAGGAGCTCATCGACCAGCTCGAGTGCAAGG
CCCCCCGGCTGGAACCCCTGCGTGAAGAGGACCTGGCCAAGGGGCCTGACTTGCACATCCTCATGGCCCAGAGGCAGGTCCAGGTGGCAGAGGAAGGCCTGCAGGACTTCCACCGAGCCCTGCGCTGC
TATGTGGACTTCACAGGGGCCCAGAGCCATTGTCTGCATGTGTCCGCCCAGAAGATGCTGGACGGTGCCTCCTTCACCCTGTATGAGTTCTGGCAGGATGAGGCCTCCTGGAGAAGGCACCAGCAGTC
GCCTGGCAGCAAGGCCTTCCAGCGCATCCTCATCGACCACCTGCGGGCCCCGGACACCCTCACCACTGTGTTCTTCCCAGCCTCCTGGTGGATAATGAATAACAACTGAGCCAGACCTGCACACGCCG
AGGGCCCCGGGACCCTGCCTGCCTCCCTCTGGAGCCTTCTGGACTGGCCAGCCCAGCGCAAAGACCAGGACTTGTCTCCTCCTGGACTTGGGCCTGGTGGAAGGGCTCTCAGCCCAGGGATCAGGGAC
TGGGCTGCTTGCTTTCTATTTATTATTGATTTATTTATCCCTGTATTTTATTGTTTGTCACTTCAGCCTCCAAGCTACTTTGGCTTCTGCCTGGCTCAGGAGACCTGGATTCTGGTCCCTGCTGTCCC
TGCCTGGCTGAGCGACCCAGGGCAGGTCCCGTCCCTGTCTGGGTGGGCCTCAGGCCATCTGGCCGCCTAGCGAGGGTCCTGCTTTCTTCCTGCTGTCTTGGGACCAGGCTTCTGCTCCTCCTCAGCCA
GCGGCAGAAGCAGGGCTGATGCTCAGGGACCCCCCAACCCTCAAACCTTGCCTCCGAGGCTGGGCCTGAGCTGGGTGCCCCGTCGCCCTCCCAGGCCACTAGGCTCTGACTCTTCCAGCACCCATGGA
TGTGCCAGAGGCCTCTGGGTTGGTTTGCATGTCATTTGCATATCGTTTGCATGCCCTCATCCCACCCATTCTCAGGGCAGTATGGGAAGCCCCAAGGTGACCTGGCCAAGTAGCAATAATTTGGGTCC
AGGGTCACCTATTGCCCCCAGAGGCCTCTGAACCCCAGGCTGGGACCCCAGCACAGAGGCAATAAAGGCAGTGGTCCCTTCCA

hide sequence

RefSeq Acc Id:

XM_047440369 ⟹ XP_047296325

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	33,657,087 - 33,675,348 (-)	NCBI

RefSeq Acc Id:

XM_047440370 ⟹ XP_047296326

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	33,657,087 - 33,675,348 (-)	NCBI

RefSeq Acc Id:

XM_054323826 ⟹ XP_054179801

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	35,383,618 - 35,400,959 (-)	NCBI

RefSeq Acc Id:

XM_054323827 ⟹ XP_054179802

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	35,383,618 - 35,401,879 (-)	NCBI

RefSeq Acc Id:

XM_054323828 ⟹ XP_054179803

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	35,383,618 - 35,401,879 (-)	NCBI

RefSeq Acc Id:

XM_054323829 ⟹ XP_054179804

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	35,383,618 - 35,388,867 (-)	NCBI

RefSeq Acc Id:

XM_054323830 ⟹ XP_054179805

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	35,383,618 - 35,388,712 (-)	NCBI

RefSeq Acc Id:

XM_054323831 ⟹ XP_054179806

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	35,386,453 - 35,400,959 (-)	NCBI


Protein RefSeqs	NP_112508	(Get FASTA)	NCBI Sequence Viewer
	NP_112509	(Get FASTA)	NCBI Sequence Viewer
	XP_005260567	(Get FASTA)	NCBI Sequence Viewer
	XP_011527293	(Get FASTA)	NCBI Sequence Viewer
	XP_011527294	(Get FASTA)	NCBI Sequence Viewer
	XP_016883505	(Get FASTA)	NCBI Sequence Viewer
	XP_047296325	(Get FASTA)	NCBI Sequence Viewer
	XP_047296326	(Get FASTA)	NCBI Sequence Viewer
	XP_054179801	(Get FASTA)	NCBI Sequence Viewer
	XP_054179802	(Get FASTA)	NCBI Sequence Viewer
	XP_054179803	(Get FASTA)	NCBI Sequence Viewer
	XP_054179804	(Get FASTA)	NCBI Sequence Viewer
	XP_054179805	(Get FASTA)	NCBI Sequence Viewer
	XP_054179806	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAG28415	(Get FASTA)	NCBI Sequence Viewer
	AAH47673	(Get FASTA)	NCBI Sequence Viewer
	AAL01118	(Get FASTA)	NCBI Sequence Viewer
	BAB14649	(Get FASTA)	NCBI Sequence Viewer
	BAB16413	(Get FASTA)	NCBI Sequence Viewer
	BAF84584	(Get FASTA)	NCBI Sequence Viewer
	EAW76301	(Get FASTA)	NCBI Sequence Viewer
	EAW76302	(Get FASTA)	NCBI Sequence Viewer
	EAW76303	(Get FASTA)	NCBI Sequence Viewer
	EAW76304	(Get FASTA)	NCBI Sequence Viewer
	EAW76305	(Get FASTA)	NCBI Sequence Viewer
	EAW76306	(Get FASTA)	NCBI Sequence Viewer
	EAW76307	(Get FASTA)	NCBI Sequence Viewer
	EAW76308	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000246190
	ENSP00000246190.6
	ENSP00000364386
	ENSP00000364386.4
	ENSP00000392064
	ENSP00000475369
GenBank Protein	Q96P71	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_112509 ⟸ NM_031232
- Peptide Label:	isoform 2
- UniProtKB:	Q9HBW7 (UniProtKB/Swiss-Prot), Q9H8G8 (UniProtKB/Swiss-Prot), Q9H433 (UniProtKB/Swiss-Prot), Q86VV1 (UniProtKB/Swiss-Prot), Q5JWF7 (UniProtKB/Swiss-Prot), Q5JWF6 (UniProtKB/Swiss-Prot), Q5JWF5 (UniProtKB/Swiss-Prot), E1P5N2 (UniProtKB/Swiss-Prot), A8K780 (UniProtKB/Swiss-Prot), Q9HCQ9 (UniProtKB/Swiss-Prot), Q96P71 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MACAGLLTVCLLRPPAPQPQPQTPRHPQLAPDPGPAGHTLFQDVFRRADKNDDGKLSFEEFQNYFADGVLSLGELQELFSGIDGHLTDNLETEKLCDYFSEHLGVYRPVLAALESLNRAVLAAMDATK LEYERASKVDQFVTRFLLRETVSQLQALQSSLEGASDTLEAQAHGWRSDAESVEAQSRLCGSRRAGRRALRSVSRSSTWSPGSSDTGRSSEAEMQWRLQVNRLQELIDQLECKVRAVGPGPHKGGPSW YPPEPGPCWRPGPHSVPSQAPRLEPLREEDLAKGPDLHILMAQRQVQVAEEGLQDFHRALRCYVDFTGAQSHCLHVSAQKMLDGASFTLYEFWQDEASWRRHQQSPGSKAFQRILIDHLRAPDTLTTV FFPASWWIMNNN hide sequence

RefSeq Acc Id:	NP_112508 ⟸ NM_031231
- Peptide Label:	isoform 1
- UniProtKB:	U3KQ06 (UniProtKB/TrEMBL)
- Sequence:	show sequence MACAGLLTVCLLRPPAPQPQPQTPRHPQLAPDPGPAGHTLFQDVFRRADKNDDGKLSFEEFQNY FADGVLSLGELQELFSGIDGHLTDNLETEKLCDYFSEHLGVYRPVLAALESLNRAVLAAMDATKLEYERASKVDQFVTRFLLRETVSQLQALQSSLEGASDTLEAQAHGWRSDAESVEAQSRLCGSRR AGRRALRSVSRSSTWSPGSSDTGRSSEAEMQWRLQVNRLQELIDQLECKAPRLEPLREEDLAKGPDLHILMAQRQVQVAEEGLQDFHRALRCYVDFTGAQSHCLHVSAQKMLDGASFTLYEFWQDEAS WRRHQQSPGSKAFQRILIDHLRAPDTLTTVFFPASWWIMNNN hide sequence

RefSeq Acc Id:	XP_005260567 ⟸ XM_005260510
- Peptide Label:	isoform X1
- UniProtKB:	U3KQ06 (UniProtKB/TrEMBL)
- Sequence:	show sequence MACAGLLTVCLLRPPAPQPQPQTPRHPQLAPDPGPAGHTLFQDVFRRADKNDDGKLSFEEFQNY FADGVLSLGELQELFSGIDGHLTDNLETEKLCDYFSEHLGVYRPVLAALESLNRAVLAAMDATKLEYERASKVDQFVTRFLLRETVSQLQALQSSLEGASDTLEAQAHGWRSDAESVEAQSRLCGSRR AGRRALRSVSRSSTWSPGSSDTGRSSEAEMQWRLQVNRLQELIDQLECKHILMAQRQVQVAEEGLQDFHRALRCYVDFTGAQSHCLHVSAQKMLDGASFTLYEFWQDEASWRRHQQSPGSKAFQRILI DHLRAPDTLTTVFFPASWWIMNNN hide sequence

RefSeq Acc Id:

XP_011527293 ⟸ XM_011528991

- Peptide Label:

isoform X4

- Sequence:

show sequence

MAGVLGPVSLTSSRSDAESVEAQSRLCGSRRAGRRALRSVSRSSTWSPGSSDTGRSSEAEMQWR
LQVNRLQELIDQLECKAPRLEPLREEDLAKGPDLHILMAQRQVQVAEEGLQDFHRALRCYVDFTGAQSHCLHVSAQKMLDGASFTLYEFWQDEASWRRHQQSPGSKAFQRILIDHLRAPDTLTTVFFP
ASWWIMNNN

hide sequence

RefSeq Acc Id:	XP_011527294 ⟸ XM_011528992
- Peptide Label:	isoform X5
- UniProtKB:	U3KPZ3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MACAGLLTVCLLRPPAPQPQPQTPRHPQLAPDPGPAGHTLFQDVFRRADKNDDGKLSFEEFQNY FADGVLSLGELQELFSGIDGHLTDNLETEKLCDYFSEHLGVYRPVLAALESLNRAVLAAMDATKLEYERASKVDQFVTRFLLRETVSQLQALQSSLEGASDTLEAQAHGWRPRPCEPHFL hide sequence

Protein Domains

ABM EF-hand

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96P71-F1-model_v2	AlphaFold	Q96P71	1-396	view protein structure

RGD ID:

6798864

Promoter ID:

HG_KWN:39090

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

HeLa_S3, K562

Transcripts:

OTTHUMT00000078716

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	20	31,710,821 - 31,711,972 (-)	MPROMDB

RGD ID:

6798866

Promoter ID:

HG_KWN:39091

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

OTTHUMT00000078721, OTTHUMT00000078722, OTTHUMT00000078727, UC002WZL.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	20	31,713,671 - 31,715,237 (-)	MPROMDB

RGD ID:

6798869

Promoter ID:

HG_KWN:39093

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

OTTHUMT00000078728

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	20	31,715,001 - 31,716,147 (-)	MPROMDB

RGD ID:

6798865

Promoter ID:

HG_KWN:39094

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:

OTTHUMT00000078720

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	20	31,718,301 - 31,719,037 (-)	MPROMDB

RGD ID:

6798863

Promoter ID:

HG_KWN:39095

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562, Lymphoblastoid

Transcripts:

OTTHUMT00000078715

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	20	31,720,536 - 31,721,777 (-)	MPROMDB

RGD ID:

6799202

Promoter ID:

HG_KWN:39097

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_031232, OTTHUMT00000078717, OTTHUMT00000078718, OTTHUMT00000078725, OTTHUMT00000078726, OTTHUMT00000078730, UC002WZO.2, UC002WZP.2, UC002WZQ.2, UC002WZR.2, UC010GEO.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	20	31,725,901 - 31,726,487 (-)	MPROMDB

RGD ID:

13206703

Promoter ID:

EPDNEW_H26932

Type:

initiation region

Name:

NECAB3_1

Description:

N-terminal EF-hand calcium binding protein 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	20	33,674,428 - 33,674,488	EPDNEW

Database	Acc Id	Source(s)
COSMIC	NECAB3	COSMIC
Ensembl Genes	ENSG00000125967	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000246190	ENTREZGENE
	ENST00000246190.11	UniProtKB/Swiss-Prot
	ENST00000375238	ENTREZGENE
	ENST00000375238.8	UniProtKB/Swiss-Prot
	ENST00000439478	ENTREZGENE
	ENST00000485399	ENTREZGENE
Gene3D-CATH	3.30.70.100	UniProtKB/Swiss-Prot
	EF-hand	UniProtKB/Swiss-Prot
GTEx	ENSG00000125967	GTEx
HGNC ID	HGNC:15851	ENTREZGENE
Human Proteome Map	NECAB3	Human Proteome Map
InterPro	ABM_dom	UniProtKB/Swiss-Prot
	Dimeric_a/b-barrel	UniProtKB/Swiss-Prot
	EF-hand-dom_pair	UniProtKB/Swiss-Prot
	EF_Hand_1_Ca_BS	UniProtKB/Swiss-Prot
	EF_hand_dom	UniProtKB/Swiss-Prot
	NECAB1/2/3	UniProtKB/Swiss-Prot
KEGG Report	hsa:63941	UniProtKB/Swiss-Prot
NCBI Gene	63941	ENTREZGENE
OMIM	612478	OMIM
PANTHER	N-TERMINAL EF-HAND CALCIUM-BINDING PROTEIN 3	UniProtKB/Swiss-Prot
	PTHR12178	UniProtKB/Swiss-Prot
Pfam	ABM	UniProtKB/Swiss-Prot
	EF-hand_5	UniProtKB/Swiss-Prot
PharmGKB	PA24871	PharmGKB
PROSITE	ABM	UniProtKB/Swiss-Prot
	EF_HAND_1	UniProtKB/Swiss-Prot
	EF_HAND_2	UniProtKB/Swiss-Prot
SMART	EFh	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF47473	UniProtKB/Swiss-Prot
	SSF54909	UniProtKB/Swiss-Prot
UniProt	A8K780	ENTREZGENE
	E1P5N2	ENTREZGENE
	NECA3_HUMAN	UniProtKB/Swiss-Prot
	Q5JWF5	ENTREZGENE
	Q5JWF6	ENTREZGENE
	Q5JWF7	ENTREZGENE
	Q86VV1	ENTREZGENE
	Q96P71	ENTREZGENE
	Q9H433	ENTREZGENE
	Q9H8G8	ENTREZGENE
	Q9HBW7	ENTREZGENE
	Q9HCQ9	ENTREZGENE
	U3KPZ3	ENTREZGENE, UniProtKB/TrEMBL
	U3KQ06	ENTREZGENE, UniProtKB/TrEMBL
	U3KQC6_HUMAN	UniProtKB/TrEMBL
	U3KQF5_HUMAN	UniProtKB/TrEMBL
	U3KQJ7_HUMAN	UniProtKB/TrEMBL
	U3KQM7_HUMAN	UniProtKB/TrEMBL
	U3KQR6_HUMAN	UniProtKB/TrEMBL
	X6RCW6_HUMAN	UniProtKB/TrEMBL
UniProt Secondary	A8K780	UniProtKB/Swiss-Prot
	E1P5N2	UniProtKB/Swiss-Prot
	Q5JWF5	UniProtKB/Swiss-Prot
	Q5JWF6	UniProtKB/Swiss-Prot
	Q5JWF7	UniProtKB/Swiss-Prot
	Q86VV1	UniProtKB/Swiss-Prot
	Q9H433	UniProtKB/Swiss-Prot
	Q9H8G8	UniProtKB/Swiss-Prot
	Q9HBW7	UniProtKB/Swiss-Prot
	Q9HCQ9	UniProtKB/Swiss-Prot

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


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


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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Imported Disease Annotations - ClinVar

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