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Gene: MARCHF10 (membrane associated ring-CH-type finger 10) Homo sapiens

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Symbol:

MARCHF10

Name:

membrane associated ring-CH-type finger 10

RGD ID:

1601818

HGNC Page

HGNC:26655

Description:

Predicted to enable transferase activity and zinc ion binding activity. Predicted to be involved in protein ubiquitination.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FLJ35757; MARCH-X; MARCH10; membrane associated ring finger 10; membrane-associated ring finger (C3HC4) 10, E3 ubiquitin protein ligase; membrane-associated RING finger protein 10; membrane-associated RING-CH protein X; probable E3 ubiquitin-protein ligase MARCH10; probable E3 ubiquitin-protein ligase MARCHF10; ring finger protein 190; RING-type E3 ubiquitin transferase MARCH10; RING-type E3 ubiquitin transferase MARCHF10; RNF190; testis secretory sperm-binding protein Li 228n

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	17	62,701,314 - 62,808,314 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	62,701,314 - 62,808,344 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	60,778,675 - 60,885,675 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	58,132,407 - 58,239,437 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	17	55,166,551 - 55,273,592 (-)	NCBI		Celera
Cytogenetic Map	17	q23.2	NCBI
HuRef	17	56,145,700 - 56,254,053 (-)	NCBI		HuRef
CHM1_1	17	60,842,970 - 60,949,946 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	17	63,571,227 - 63,678,377 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
MARCHF10	Human	1,2-dimethylhydrazine	decreases expression	ISO	RGD:1617043	6480464	1,2-Dimethylhydrazine results in decreased expression of MARCHF10 mRNA	CTD	PMID:22206623
MARCHF10	Human	17alpha-ethynylestradiol	affects expression	ISO	RGD:1617043	6480464	Ethinyl Estradiol affects the expression of MARCHF10 mRNA	CTD	PMID:17555576
MARCHF10	Human	17beta-estradiol 3-benzoate	decreases methylation	ISO	RGD:1311692	6480464	estradiol 3-benzoate results in decreased methylation of MARCHF10 promoter	CTD	PMID:27415467
MARCHF10	Human	benzo[a]pyrene	affects methylation	EXP		6480464	Benzo(a)pyrene affects the methylation of MARCHF10 5' UTR	CTD	PMID:27901495
MARCHF10	Human	benzo[a]pyrene	decreases methylation	EXP		6480464	Benzo(a)pyrene results in decreased methylation of MARCHF10 promoter	CTD	PMID:27901495
MARCHF10	Human	benzo[a]pyrene	increases methylation	EXP		6480464	Benzo(a)pyrene results in increased methylation of MARCHF10 3' UTR	CTD	PMID:27901495
MARCHF10	Human	benzo[e]pyrene	increases methylation	EXP		6480464	benzo(e)pyrene results in increased methylation of MARCHF10 exon	CTD	PMID:30157460
MARCHF10	Human	bisphenol A	decreases expression	ISO	RGD:1311692	6480464	bisphenol A results in decreased expression of MARCHF10 mRNA	CTD	PMID:25181051
MARCHF10	Human	chlorpyrifos	decreases expression	ISO	RGD:1617043	6480464	Chlorpyrifos results in decreased expression of MARCHF10 mRNA	CTD	PMID:37019170
MARCHF10	Human	ethylparaben	decreases expression	EXP		6480464	ethyl-p-hydroxybenzoate results in decreased expression of MARCHF10 mRNA	CTD	PMID:37690743
MARCHF10	Human	fenvalerate	increases expression	ISO	RGD:1311692	6480464	fenvalerate results in increased expression of MARCHF10 mRNA	CTD	PMID:30307764
MARCHF10	Human	furan	increases methylation	ISO	RGD:1311692	6480464	furan results in increased methylation of MARCHF10 gene	CTD	PMID:22079235
MARCHF10	Human	gentamycin	increases expression	ISO	RGD:1311692	6480464	Gentamicins results in increased expression of MARCHF10 mRNA	CTD	PMID:33387578
MARCHF10	Human	methapyrilene	increases methylation	EXP		6480464	Methapyrilene results in increased methylation of MARCHF10 exon	CTD	PMID:30157460
MARCHF10	Human	sodium arsenite	increases expression	EXP		6480464	sodium arsenite results in increased expression of MARCHF10 mRNA	CTD	PMID:29301061
MARCHF10	Human	titanium dioxide	decreases expression	ISO	RGD:1617043	6480464	titanium dioxide results in decreased expression of MARCHF10 mRNA	CTD	PMID:29264374
MARCHF10	Human	trichloroethene	increases expression	ISO	RGD:1311692	6480464	Trichloroethylene results in increased expression of MARCHF10 mRNA	CTD	PMID:33387578
MARCHF10	Human	vancomycin	increases expression	ISO	RGD:1617043	6480464	Vancomycin results in increased expression of MARCHF10 mRNA	CTD	PMID:18930951

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)
MARCHF10	Human	protein ubiquitination	involved_in	IEA	UniPathway:UPA00143	150520179		UniProt	GO_REF:0000041

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)
MARCHF10	Human	metal ion binding	enables	IEA	UniProtKB-KW:KW-0479	150520179		UniProt	GO_REF:0000043
MARCHF10	Human	protein binding	enables	IPI	UniProtKB:Q96HA8\|UniProtKB:Q9H3U1\|UniProtKB:Q9NQW6-2	150520179	PMID:25416956	IntAct	PMID:25416956
MARCHF10	Human	protein binding	enables	IPI	UniProtKB:O43464\|UniProtKB:Q7Z699\|UniProtKB:Q8WXH2	150520179	PMID:32814053	IntAct	PMID:32814053
MARCHF10	Human	protein binding	enables	IPI	UniProtKB:Q9H3U1	150520179	PMID:31515488, PMID:32296183	IntAct	PMID:31515488\|PMID:32296183
MARCHF10	Human	transferase activity	enables	IEA	UniProtKB-KW:KW-0808	150520179		UniProt	GO_REF:0000043
MARCHF10	Human	zinc ion binding	enables	IEA	InterPro:IPR011016	150520179		InterPro	GO_REF:0000002
MARCHF10	Human	zinc ion binding	enables	IEA	UniProtKB-KW:KW-0863	150520179		UniProt	GO_REF:0000043

#	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

PMID:12477932	PMID:14702039	PMID:15489334	PMID:17604280	PMID:19549727	PMID:19724895	PMID:19851296	PMID:20198315	PMID:21658281	PMID:21832049	PMID:21873635	PMID:23602568
PMID:23686814	PMID:24722188	PMID:25416956	PMID:27107014	PMID:31515488	PMID:32296183	PMID:32814053

MARCHF10
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	17	62,701,314 - 62,808,314 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	62,701,314 - 62,808,344 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	60,778,675 - 60,885,675 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	58,132,407 - 58,239,437 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	17	55,166,551 - 55,273,592 (-)	NCBI		Celera
Cytogenetic Map	17	q23.2	NCBI
HuRef	17	56,145,700 - 56,254,053 (-)	NCBI		HuRef
CHM1_1	17	60,842,970 - 60,949,946 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	17	63,571,227 - 63,678,377 (-)	NCBI		T2T-CHM13v2.0

Marchf10
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	11	105,251,624 - 105,348,527 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	11	105,251,624 - 105,347,561 (-)	Ensembl		GRCm39 Ensembl
GRCm38	11	105,360,798 - 105,457,701 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	11	105,360,798 - 105,456,735 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	11	105,469,840 - 105,499,479 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	11	105,217,744 - 105,272,814 (-)	NCBI		MGSCv36	mm8
Celera	11	117,094,272 - 117,123,876 (-)	NCBI		Celera
Cytogenetic Map	11	E1	NCBI
cM Map	11	68.73	NCBI

Marchf10
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	10	90,832,647 - 90,975,700 (-)	NCBI		GRCr8
mRatBN7.2	10	90,332,783 - 90,423,109 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	10	90,332,784 - 90,421,588 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	10	95,382,178 - 95,471,096 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	10	94,845,350 - 94,934,268 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	10	90,263,550 - 90,352,488 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	10	93,591,187 - 93,681,507 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	10	93,591,188 - 93,679,974 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	10	93,350,038 - 93,439,947 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	10	94,762,789 - 94,855,777 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	10	94,777,159 - 94,870,147 (-)	NCBI
Celera	10	89,015,563 - 89,104,950 (-)	NCBI		Celera
Cytogenetic Map	10	q32.1	NCBI

Marchf10
(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_004955478	8,931,191 - 9,018,656 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955478	8,931,511 - 9,024,645 (+)	NCBI	ChiLan1.0	ChiLan1.0

MARCHF10
(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	19	78,856,475 - 79,129,525 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	17	83,674,996 - 83,947,072 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	17	56,765,318 - 57,005,576 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	17	61,914,713 - 62,027,464 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	17	61,914,713 - 62,027,464 (-)	Ensembl	panpan1.1		panPan2

MARCHF10
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	9	10,880,225 - 10,968,991 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	9	10,880,226 - 10,961,157 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	9	11,905,886 - 11,994,600 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	9	12,541,972 - 12,630,777 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	9	12,541,973 - 12,622,742 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	9	11,490,017 - 11,578,452 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	9	15,954,881 - 16,043,271 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	9	15,958,697 - 16,047,459 (+)	NCBI		UU_Cfam_GSD_1.0

Marchf10
(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_024405602	15,612,955 - 15,699,910 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936541	3,494,464 - 3,618,580 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936541	3,494,590 - 3,581,621 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

MARCHF10
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	12	15,969,769 - 16,052,680 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	12	15,969,915 - 16,052,445 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	12	15,861,982 - 15,944,352 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

MARCHF10
(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	16	58,466,882 - 58,574,222 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666077	29,099,127 - 29,210,962 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Marchf10
(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_004624849	220,875 - 316,789 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624849	224,553 - 454,822 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in MARCHF10
89 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3	copy number gain	See cases [RCV000050957]	Chr17:36449220..68170214 [GRCh38] Chr17:48563237..65936105 [GRCh37] Chr17:45918236..63677950 [NCBI36] Chr17:17q21.33-24.2	pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]\|See cases [RCV000052483]	Chr17:36449220..83086677 [GRCh38] Chr17:58617905..81044553 [GRCh37] Chr17:55972687..78637842 [NCBI36] Chr17:17q23.2-25.3	pathogenic
GRCh37/hg19 17q23-24(chr17:59209629-64222315)x3	copy number gain	See cases [RCV000052485]	Chr17:59209629..64222315 [GRCh37] Chr17:56564411..61652777 [NCBI36] Chr17:17q23-24	pathogenic
NM_001100875.2(MARCH10):c.877G>A (p.Glu293Lys)	single nucleotide variant	Malignant melanoma [RCV000071595]	Chr17:62736991 [GRCh38] Chr17:60814352 [GRCh37] Chr17:58168084 [NCBI36] Chr17:17q23.2	not provided
NM_001100875.2(MARCH10):c.211-5694C>A	single nucleotide variant	Lung cancer [RCV000100594]	Chr17:62765700 [GRCh38] Chr17:60843061 [GRCh37] Chr17:17q23.2	uncertain significance
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3	copy number gain	See cases [RCV000137437]	Chr17:36449220..75053130 [GRCh38] Chr17:57595736..73049225 [GRCh37] Chr17:54950518..70560820 [NCBI36] Chr17:17q23.1-25.1	pathogenic
GRCh38/hg38 17q23.2-23.3(chr17:61631101-63219455)x1	copy number loss	See cases [RCV000140458]	Chr17:61631101..63219455 [GRCh38] Chr17:59708462..61296816 [GRCh37] Chr17:57063244..58650548 [NCBI36] Chr17:17q23.2-23.3	likely pathogenic\|uncertain significance
GRCh38/hg38 17q23.2(chr17:62039036-62927189)x3	copy number gain	See cases [RCV000141715]	Chr17:62039036..62927189 [GRCh38] Chr17:60116397..61004550 [GRCh37] Chr17:57471179..58358282 [NCBI36] Chr17:17q23.2	likely pathogenic\|uncertain significance
GRCh37/hg19 17q22-23.3(chr17:56321134-62080001)x3	copy number gain	See cases [RCV000240364]	Chr17:56321134..62080001 [GRCh37] Chr17:17q22-23.3	pathogenic
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3	copy number gain	See cases [RCV000447823]	Chr17:42580684..81085615 [GRCh37] Chr17:17q21.31-25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	copy number gain	See cases [RCV000511439]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
NM_152598.4(MARCHF10):c.979G>C (p.Ala327Pro)	single nucleotide variant	not specified [RCV004287550]	Chr17:62736889 [GRCh38] Chr17:60814250 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.347A>T (p.Lys116Ile)	single nucleotide variant	not specified [RCV004294449]	Chr17:62759870 [GRCh38] Chr17:60837231 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1267G>A (p.Asp423Asn)	single nucleotide variant	not specified [RCV004303068]	Chr17:62736601 [GRCh38] Chr17:60813962 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.287T>A (p.Leu96His)	single nucleotide variant	not specified [RCV004297041]	Chr17:62759930 [GRCh38] Chr17:60837291 [GRCh37] Chr17:17q23.2	uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	copy number gain	See cases [RCV000512441]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3	copy number gain	not provided [RCV000739325]	Chr17:12344..81057996 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3	copy number gain	not provided [RCV000739324]	Chr17:8547..81060040 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3	copy number gain	not provided [RCV000739320]	Chr17:7214..81058310 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17q23.2-24.2(chr17:59597348-64886364)x3	copy number gain	not provided [RCV000752158]	Chr17:59597348..64886364 [GRCh37] Chr17:17q23.2-24.2	pathogenic
GRCh37/hg19 17q22-24.2(chr17:57357088-66306668)	copy number gain	not provided [RCV000767764]	Chr17:57357088..66306668 [GRCh37] Chr17:17q22-24.2	pathogenic
GRCh37/hg19 17q23.1-24.2(chr17:57869604-67078443)x3	copy number gain	not provided [RCV000845965]	Chr17:57869604..67078443 [GRCh37] Chr17:17q23.1-24.2	pathogenic
NM_152598.4(MARCHF10):c.2367T>C (p.Asn789=)	single nucleotide variant	not provided [RCV001171800]	Chr17:62705543 [GRCh38] Chr17:60782904 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.262T>G (p.Ser88Ala)	single nucleotide variant	not specified [RCV004292589]	Chr17:62759955 [GRCh38] Chr17:60837316 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.2014C>T (p.Pro672Ser)	single nucleotide variant	not specified [RCV004298104]	Chr17:62725028 [GRCh38] Chr17:60802389 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.464C>T (p.Pro155Leu)	single nucleotide variant	not specified [RCV004291162]	Chr17:62744447 [GRCh38] Chr17:60821808 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.781G>A (p.Val261Ile)	single nucleotide variant	not specified [RCV004320822]	Chr17:62737087 [GRCh38] Chr17:60814448 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1957G>A (p.Glu653Lys)	single nucleotide variant	not specified [RCV004282188]	Chr17:62725085 [GRCh38] Chr17:60802446 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.406T>C (p.Leu136=)	single nucleotide variant	not provided [RCV001171801]	Chr17:62744505 [GRCh38] Chr17:60821866 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.455C>T (p.Ser152Leu)	single nucleotide variant	not specified [RCV004256521]	Chr17:62744456 [GRCh38] Chr17:60821817 [GRCh37] Chr17:17q23.2	likely benign
GRCh37/hg19 17q23.2(chr17:60695522-60809245)x1	copy number loss	not provided [RCV002473441]	Chr17:60695522..60809245 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1547T>C (p.Ile516Thr)	single nucleotide variant	not specified [RCV004318329]	Chr17:62736321 [GRCh38] Chr17:60813682 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1279G>T (p.Val427Leu)	single nucleotide variant	not specified [RCV004333240]	Chr17:62736589 [GRCh38] Chr17:60813950 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.988A>C (p.Lys330Gln)	single nucleotide variant	not specified [RCV004285190]	Chr17:62736880 [GRCh38] Chr17:60814241 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1576G>A (p.Glu526Lys)	single nucleotide variant	not specified [RCV004250855]	Chr17:62736292 [GRCh38] Chr17:60813653 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.865G>A (p.Asp289Asn)	single nucleotide variant	not specified [RCV004262252]	Chr17:62737003 [GRCh38] Chr17:60814364 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.677C>A (p.Pro226His)	single nucleotide variant	not specified [RCV004260775]	Chr17:62737191 [GRCh38] Chr17:60814552 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.182G>A (p.Arg61Gln)	single nucleotide variant	not specified [RCV004275438]	Chr17:62788508 [GRCh38] Chr17:60865869 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.2025G>T (p.Glu675Asp)	single nucleotide variant	not specified [RCV004253219]	Chr17:62725017 [GRCh38] Chr17:60802378 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1282G>A (p.Glu428Lys)	single nucleotide variant	not specified [RCV004273854]	Chr17:62736586 [GRCh38] Chr17:60813947 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1798C>T (p.Pro600Ser)	single nucleotide variant	not specified [RCV004270365]	Chr17:62736070 [GRCh38] Chr17:60813431 [GRCh37] Chr17:17q23.2	uncertain significance
GRCh37/hg19 17q23.2-23.3(chr17:60705832-61417743)x1	copy number loss	Intellectual developmental disorder with autistic features and language delay, with or without seizures [RCV003329501]	Chr17:60705832..61417743 [GRCh37] Chr17:17q23.2-23.3	uncertain significance
NM_152598.4(MARCHF10):c.1048A>G (p.Ser350Gly)	single nucleotide variant	not specified [RCV004334705]	Chr17:62736820 [GRCh38] Chr17:60814181 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.716T>C (p.Phe239Ser)	single nucleotide variant	not specified [RCV004351429]	Chr17:62737152 [GRCh38] Chr17:60814513 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1299C>T (p.Thr433=)	single nucleotide variant	MARCHF10-related disorder [RCV003939442]	Chr17:62736569 [GRCh38] Chr17:60813930 [GRCh37] Chr17:17q23.2	likely benign
GRCh37/hg19 17q23.2-23.3(chr17:58596397-62540700)x3	copy number gain	See cases [RCV004442795]	Chr17:58596397..62540700 [GRCh37] Chr17:17q23.2-23.3	uncertain significance
NM_152598.4(MARCHF10):c.1679C>T (p.Thr560Ile)	single nucleotide variant	MARCHF10-related disorder [RCV003972285]	Chr17:62736189 [GRCh38] Chr17:60813550 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.2372-4C>T	single nucleotide variant	MARCHF10-related disorder [RCV003904009]	Chr17:62701762 [GRCh38] Chr17:60779123 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.91-15GTT[2]	microsatellite	MARCHF10-related disorder [RCV003969109]	Chr17:62788606..62788608 [GRCh38] Chr17:60865967..60865969 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.2031C>T (p.Cys677=)	single nucleotide variant	MARCHF10-related disorder [RCV003919663]	Chr17:62725011 [GRCh38] Chr17:60802372 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.1285C>T (p.His429Tyr)	single nucleotide variant	MARCHF10-related disorder [RCV003979362]	Chr17:62736583 [GRCh38] Chr17:60813944 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.365C>T (p.Pro122Leu)	single nucleotide variant	MARCHF10-related disorder [RCV003959127]	Chr17:62759852 [GRCh38] Chr17:60837213 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.956T>C (p.Phe319Ser)	single nucleotide variant	MARCHF10-related disorder [RCV003974566]	Chr17:62736912 [GRCh38] Chr17:60814273 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.241C>T (p.Pro81Ser)	single nucleotide variant	MARCHF10-related disorder [RCV003927291]	Chr17:62759976 [GRCh38] Chr17:60837337 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.2329-9T>G	single nucleotide variant	MARCHF10-related disorder [RCV003963859]	Chr17:62705590 [GRCh38] Chr17:60782951 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.2404A>G (p.Ile802Val)	single nucleotide variant	MARCHF10-related disorder [RCV003921476]	Chr17:62701726 [GRCh38] Chr17:60779087 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.1674A>C (p.Leu558=)	single nucleotide variant	MARCHF10-related disorder [RCV003969581]	Chr17:62736194 [GRCh38] Chr17:60813555 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.1759G>A (p.Gly587Ser)	single nucleotide variant	MARCHF10-related disorder [RCV003936904]	Chr17:62736109 [GRCh38] Chr17:60813470 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.669G>A (p.Pro223=)	single nucleotide variant	MARCHF10-related disorder [RCV003924733]	Chr17:62737199 [GRCh38] Chr17:60814560 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.1275T>C (p.Ile425=)	single nucleotide variant	MARCHF10-related disorder [RCV003937063]	Chr17:62736593 [GRCh38] Chr17:60813954 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.383-2335T>C	single nucleotide variant	MARCHF10-related disorder [RCV003979567]	Chr17:62746863 [GRCh38] Chr17:60824224 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.1464C>T (p.Asp488=)	single nucleotide variant	MARCHF10-related disorder [RCV003904178]	Chr17:62736404 [GRCh38] Chr17:60813765 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.370G>A (p.Glu124Lys)	single nucleotide variant	MARCHF10-related disorder [RCV003951625]	Chr17:62759847 [GRCh38] Chr17:60837208 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.1602C>T (p.Asn534=)	single nucleotide variant	MARCHF10-related disorder [RCV003974339]	Chr17:62736266 [GRCh38] Chr17:60813627 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.725A>C (p.Lys242Thr)	single nucleotide variant	MARCHF10-related disorder [RCV003904130]	Chr17:62737143 [GRCh38] Chr17:60814504 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.309A>G (p.Ser103=)	single nucleotide variant	MARCHF10-related disorder [RCV003904135]	Chr17:62759908 [GRCh38] Chr17:60837269 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.1985G>A (p.Cys662Tyr)	single nucleotide variant	MARCHF10-related disorder [RCV003971769]	Chr17:62725057 [GRCh38] Chr17:60802418 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.1478C>T (p.Ser493Leu)	single nucleotide variant	MARCHF10-related disorder [RCV003971783]	Chr17:62736390 [GRCh38] Chr17:60813751 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.617C>T (p.Ser206Leu)	single nucleotide variant	MARCHF10-related disorder [RCV003944429]	Chr17:62737251 [GRCh38] Chr17:60814612 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.1247A>G (p.Asn416Ser)	single nucleotide variant	MARCHF10-related disorder [RCV003904000]	Chr17:62736621 [GRCh38] Chr17:60813982 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.801A>G (p.Ala267=)	single nucleotide variant	MARCHF10-related disorder [RCV003904066]	Chr17:62737067 [GRCh38] Chr17:60814428 [GRCh37] Chr17:17q23.2	benign
NM_152598.4(MARCHF10):c.1430T>C (p.Met477Thr)	single nucleotide variant	not specified [RCV004408779]	Chr17:62736438 [GRCh38] Chr17:60813799 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1052A>G (p.His351Arg)	single nucleotide variant	not specified [RCV004408776]	Chr17:62736816 [GRCh38] Chr17:60814177 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1074T>G (p.Asn358Lys)	single nucleotide variant	not specified [RCV004408777]	Chr17:62736794 [GRCh38] Chr17:60814155 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1367C>A (p.Ser456Tyr)	single nucleotide variant	not specified [RCV004408778]	Chr17:62736501 [GRCh38] Chr17:60813862 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1801T>C (p.Phe601Leu)	single nucleotide variant	not specified [RCV004408784]	Chr17:62736067 [GRCh38] Chr17:60813428 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1612G>A (p.Glu538Lys)	single nucleotide variant	not specified [RCV004408780]	Chr17:62736256 [GRCh38] Chr17:60813617 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1619C>T (p.Ala540Val)	single nucleotide variant	not specified [RCV004408781]	Chr17:62736249 [GRCh38] Chr17:60813610 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1702G>A (p.Gly568Ser)	single nucleotide variant	not specified [RCV004408782]	Chr17:62736166 [GRCh38] Chr17:60813527 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.1979G>A (p.Arg660His)	single nucleotide variant	not specified [RCV004408785]	Chr17:62725063 [GRCh38] Chr17:60802424 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.2002T>C (p.Ser668Pro)	single nucleotide variant	not specified [RCV004408786]	Chr17:62725040 [GRCh38] Chr17:60802401 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.2097A>G (p.Ile699Met)	single nucleotide variant	not specified [RCV004408787]	Chr17:62724945 [GRCh38] Chr17:60802306 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.261A>G (p.Ile87Met)	single nucleotide variant	not specified [RCV004408791]	Chr17:62759956 [GRCh38] Chr17:60837317 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.2116G>A (p.Gly706Ser)	single nucleotide variant	not specified [RCV004408788]	Chr17:62722586 [GRCh38] Chr17:60799947 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.2179A>G (p.Met727Val)	single nucleotide variant	not specified [RCV004408789]	Chr17:62722523 [GRCh38] Chr17:60799884 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.2407T>G (p.Ser803Ala)	single nucleotide variant	not specified [RCV004408790]	Chr17:62701723 [GRCh38] Chr17:60779084 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.570C>A (p.Asn190Lys)	single nucleotide variant	not specified [RCV004408792]	Chr17:62737298 [GRCh38] Chr17:60814659 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.572C>G (p.Thr191Ser)	single nucleotide variant	not specified [RCV004408793]	Chr17:62737296 [GRCh38] Chr17:60814657 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.668C>T (p.Pro223Leu)	single nucleotide variant	not specified [RCV004408794]	Chr17:62737200 [GRCh38] Chr17:60814561 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.840G>T (p.Leu280Phe)	single nucleotide variant	not specified [RCV004408795]	Chr17:62737028 [GRCh38] Chr17:60814389 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.916C>T (p.Arg306Cys)	single nucleotide variant	not specified [RCV004408796]	Chr17:62736952 [GRCh38] Chr17:60814313 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.922C>T (p.Pro308Ser)	single nucleotide variant	not specified [RCV004408797]	Chr17:62736946 [GRCh38] Chr17:60814307 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.926G>A (p.Cys309Tyr)	single nucleotide variant	not specified [RCV004408798]	Chr17:62736942 [GRCh38] Chr17:60814303 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1096C>T (p.Arg366Trp)	single nucleotide variant	not specified [RCV004643042]	Chr17:62736772 [GRCh38] Chr17:60814133 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.1144A>G (p.Arg382Gly)	single nucleotide variant	not specified [RCV004643044]	Chr17:62736724 [GRCh38] Chr17:60814085 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.1931A>C (p.Gln644Pro)	single nucleotide variant	not specified [RCV004643043]	Chr17:62735937 [GRCh38] Chr17:60813298 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.2156T>C (p.Leu719Pro)	single nucleotide variant	not specified [RCV004940691]	Chr17:62722546 [GRCh38] Chr17:60799907 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1187C>G (p.Ala396Gly)	single nucleotide variant	not specified [RCV004940685]	Chr17:62736681 [GRCh38] Chr17:60814042 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1044G>T (p.Glu348Asp)	single nucleotide variant	not specified [RCV004940687]	Chr17:62736824 [GRCh38] Chr17:60814185 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1513T>A (p.Ser505Thr)	single nucleotide variant	not specified [RCV004940688]	Chr17:62736355 [GRCh38] Chr17:60813716 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.2183T>C (p.Ile728Thr)	single nucleotide variant	not specified [RCV004940689]	Chr17:62722519 [GRCh38] Chr17:60799880 [GRCh37] Chr17:17q23.2	likely benign
NM_152598.4(MARCHF10):c.1438G>A (p.Ala480Thr)	single nucleotide variant	not specified [RCV004940690]	Chr17:62736430 [GRCh38] Chr17:60813791 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.1216A>G (p.Lys406Glu)	single nucleotide variant	not specified [RCV004940692]	Chr17:62736652 [GRCh38] Chr17:60814013 [GRCh37] Chr17:17q23.2	uncertain significance
GRCh37/hg19 17q23.2-24.1(chr17:58773496-62757149)x3	copy number gain	not provided [RCV004819317]	Chr17:58773496..62757149 [GRCh37] Chr17:17q23.2-24.1	pathogenic
NM_152598.4(MARCHF10):c.368G>A (p.Ser123Asn)	single nucleotide variant	not specified [RCV004940684]	Chr17:62759849 [GRCh38] Chr17:60837210 [GRCh37] Chr17:17q23.2	uncertain significance
NM_152598.4(MARCHF10):c.77A>C (p.Asp26Ala)	single nucleotide variant	not specified [RCV004940686]	Chr17:62801659 [GRCh38] Chr17:60879020 [GRCh37] Chr17:17q23.2	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	2600
Count of miRNA genes:	833
Interacting mature miRNAs:	979
Transcripts:	ENST00000311269, ENST00000456609, ENST00000544856, ENST00000578346, ENST00000579620, ENST00000580520, ENST00000582358, ENST00000582568, ENST00000583600, ENST00000583803
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.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597208860	GWAS1304934_H	neuroticism measurement QTL GWAS1304934 (human)		4e-08	depressive symptom measurement		17	62717713	62717714	Human
597273806	GWAS1369880_H	physical activity measurement QTL GWAS1369880 (human)		9e-11	wellness/fitness trait (VT:1000152)	voluntary body mobility/immobility measurement (CMO:0000954)	17	62774198	62774199	Human
597203265	GWAS1299339_H	wellbeing measurement QTL GWAS1299339 (human)		3e-08	wellness/fitness trait (VT:1000152)		17	62717713	62717714	Human
597323024	GWAS1419098_H	educational attainment QTL GWAS1419098 (human)		0.0000001	educational attainment		17	62761292	62761293	Human
407128938	GWAS777914_H	sudden cardiac arrest QTL GWAS777914 (human)		0.0000004	sudden cardiac arrest		17	62701571	62701572	Human

D17S794

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	60,817,253 - 60,817,484	UniSTS	GRCh37
GRCh37	17	60,817,252 - 60,817,543	UniSTS	GRCh37
Build 36	17	58,170,984 - 58,171,275	RGD	NCBI36
Celera	17	55,205,129 - 55,205,360	UniSTS
Celera	17	55,205,128 - 55,205,419	RGD
Cytogenetic Map	17	q23.2	UniSTS
HuRef	17	56,184,206 - 56,184,437	UniSTS
HuRef	17	56,184,205 - 56,184,496	UniSTS
Marshfield Genetic Map	17	83.4	UniSTS
Marshfield Genetic Map	17	83.4	RGD
Genethon Genetic Map	17	84.2	UniSTS
TNG Radiation Hybrid Map	17	26693.0	UniSTS
deCODE Assembly Map	17	92.02	UniSTS
Stanford-G3 RH Map	17	2666.0	UniSTS
GeneMap99-GB4 RH Map	17	394.04	UniSTS
Whitehead-RH Map	17	451.6	UniSTS
Whitehead-YAC Contig Map	17		UniSTS
NCBI RH Map	17	670.6	UniSTS
GeneMap99-G3 RH Map	17	3167.0	UniSTS

SHGC-84552

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	60,784,902 - 60,785,231	UniSTS	GRCh37
Build 36	17	58,138,634 - 58,138,963	RGD	NCBI36
Celera	17	55,172,778 - 55,173,107	RGD
Cytogenetic Map	17	q23.2	UniSTS
HuRef	17	56,151,927 - 56,152,256	UniSTS
TNG Radiation Hybrid Map	17	26684.0	UniSTS

SHGC-105257

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	60,821,673 - 60,821,966	UniSTS	GRCh37
Build 36	17	58,175,405 - 58,175,698	RGD	NCBI36
Celera	17	55,209,549 - 55,209,842	RGD
Cytogenetic Map	17	q23.2	UniSTS
HuRef	17	56,188,626 - 56,188,919	UniSTS

AU048752

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	17	q23.2	UniSTS
HuRef	17	56,182,785 - 56,184,407	UniSTS

D17S794

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	17	q23.2	UniSTS
TNG Radiation Hybrid Map	17	26693.0	UniSTS
Stanford-G3 RH Map	17	2666.0	UniSTS
GeneMap99-GB4 RH Map	17	394.04	UniSTS
NCBI RH Map	17	671.3	UniSTS
GeneMap99-G3 RH Map	17	3167.0	UniSTS

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

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system
1009	2224	2110	1703	4657	1189	1787	3	309	1188	155	1999	4937	4900	12	3607	757	1642	1367	163


RefSeq Transcripts	NM_001100875	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001288779	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001288780	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_152598	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005257095	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005257096	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005257097	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005257098	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005257100	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005257102	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005257103	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005257106	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011524435	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011524436	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011524437	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315255	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315256	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315257	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315258	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315260	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315263	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315265	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315266	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008484791	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_934406	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC005821	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC068512	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC080038	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI223162	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI262871	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK093076	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK097506	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK122947	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AW138484	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AW263642	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AW473122	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC035021	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX105355	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX648705	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471109	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HC007264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HM005641	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY007336	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY010920	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF456303	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459572	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000311269 ⟹ ENSP00000311496

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	62,701,314 - 62,808,314 (-)	Ensembl

Ensembl Acc Id:

ENST00000456609 ⟹ ENSP00000416177

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	62,701,314 - 62,806,653 (-)	Ensembl

Ensembl Acc Id:

ENST00000544856 ⟹ ENSP00000443746

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	62,704,948 - 62,808,290 (-)	Ensembl

Ensembl Acc Id:

ENST00000578346

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	62,780,940 - 62,808,325 (-)	Ensembl

Ensembl Acc Id:

ENST00000579620

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	62,701,314 - 62,736,517 (-)	Ensembl

Ensembl Acc Id:

ENST00000580520 ⟹ ENSP00000464220

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	62,701,314 - 62,744,514 (-)	Ensembl

Ensembl Acc Id:

ENST00000582358

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	62,701,314 - 62,703,432 (-)	Ensembl

Ensembl Acc Id:

ENST00000582568 ⟹ ENSP00000463572

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	62,749,976 - 62,759,991 (-)	Ensembl

Ensembl Acc Id:

ENST00000583600 ⟹ ENSP00000463080

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	62,701,315 - 62,808,344 (-)	Ensembl

Ensembl Acc Id:

ENST00000583803 ⟹ ENSP00000463029

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	62,788,507 - 62,806,640 (-)	Ensembl

RefSeq Acc Id:

NM_001100875 ⟹ NP_001094345

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,806,640 (-)	NCBI
GRCh37	17	60,778,675 - 60,885,705 (-)	RGD
Build 36	17	58,132,407 - 58,237,743 (-)	NCBI Archive
Celera	17	55,166,551 - 55,273,592 (-)	RGD
HuRef	17	56,145,700 - 56,254,090 (-)	NCBI
CHM1_1	17	60,842,970 - 60,948,255 (-)	NCBI
T2T-CHM13v2.0	17	63,571,227 - 63,676,703 (-)	NCBI

Sequence:

show sequence

ATTACTCGCTCTTGCTTTCAGCAAGGCAGGACCCCCTCCTTCCTTCTCCACCTGCCTCCAACTCCCTCCTCCTTTCTCTCTCCCTACTTAATATGGCTTCTTATGTTGATTTCTAAAGCACAGATTTG
GCACAAGACATTATCACCAGAAAGACTTAAAACAGAAGTGTGCATAACCATGAGTGGGTTTTAAATTAAGAAGCAGTTCAAAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAGA
AGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTCTGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGGG
CAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAGGATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCAA
ACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGAGAAAGTGGACCCCAGCGAACCCTCTCCAGCAGACCAAGCACCAATGGTTTTATTAAGAA
AGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAACAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAA
GTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACAGCCAATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCC
GAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGTTCTCGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAA
AGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAGGAAACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCC
TGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGCTGAAAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCA
TGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGCTGCCTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTG
AAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGGAGTGATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCT
GAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATATCTCCAAGATCATCAGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTC
TGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGTTTCATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCAT
TTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTAACAAGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTA
AATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTCTGGGTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTC
TCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGGCAGACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGG
AGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGCGGCTGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAA
AAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGTTGACCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCA
GCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCAGAGGTTTGCAGAACTCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGTTGT
CAAGAAATTACCCACAACCCAGAACAGAGGAAAATGAAAATTCGGAGTTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGAAGCCAACTGTGGAGCTCGGCGGAGACC
TCTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCTCCCTCCTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGTGCCACTCTCTTTTGGGGTCTGGCTTGA
GCATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAGCACAGGTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCCTTAGCCCAGAAGCCCTGCCAGGTCCAG
TGGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCACTCCACCCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

NM_001288779 ⟹ NP_001275708

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,808,314 (-)	NCBI
HuRef	17	56,145,700 - 56,254,090 (-)	NCBI
CHM1_1	17	60,842,970 - 60,949,983 (-)	NCBI
T2T-CHM13v2.0	17	63,571,227 - 63,678,377 (-)	NCBI

Sequence:

show sequence

AGCCGCCCCCACCGCCTCCGCCCCAGGCAAGGCCGGCCGGCGCCGCGGAAAGCAGCCTCGGGGAAGGAGGAGGAAGAGGGGCAGGTGTAGGGAGTGAAGAAGCAAAAAGAGGAGGAGGAAGAGGAGCT
CAGGGCCGTCCCCGCGCAATTAATGGGCGGCTCCTGCGCCCTGGACCGGCCCGCCCGCCCAGCCCCTCGACCCCTGTAGCCCCGGCAGGGGAGGAAGGGCAGACCCACAGGTCAGGGATTAGGAATCA
TGTTGCATGACGCAAGGGACAGGCAGAAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTCTGAGACGACAGGAATATAGAAGAGACCCAAAT
GAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAGGATGCTCTAACTGAACCAAGGTCATCTATCAA
GATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGAGAAAGTGGACCCCAGCGAACCCTCTCCAGCAG
AGTCAGAGCCGACTTGGTGGAATAAACCGGAAACAGACCTCGGAGGACCTTCTGGCTGGTGCAGTCTGGGGAAGAAAGGTCCCATGAGCAGAAGCATCCCTCCCTGTGAAGCAGACCAAGCACCAATG
GTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAACAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAG
GGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACAGCCAATGACTGAGAACGCCCCTGATAGAGCCA
AAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGTTCTCGGGGCCACCACTCACACCCACCACTGTA
GGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAGGAAACCCAGTCTGAAGAATGTCTGTGGGTTGG
TGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGCTGAAAATTGCAGAGGTCATTCTTCAAGAAGAA
GTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGCTGCCTGATAGGGAATCTGCTACAGAGAAGGAC
AGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGGAGTGATTGTATTTCTGTGGAACATAGGCCTGG
CACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATATCTCCAAGATCATCAGTGAATTCATCCTATAACCCTCCTGCAT
CATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGTTTCATGTTTGCCAACCACTGTCTCCCATTAGA
AATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTAACAAGCCAGCCTCAGGGGGCTCCACTATATAC
AGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTCTGGGTCTCTGCAAGAAAATACACCATTTACTT
TCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGGCAGACCCTGAGAAACTCAAGAAATTGCAAGAA
AGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGCGGCTGTGTGGGAAGCCTGCAGTTTGTTCATCA
AGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGTTGACCTGGGTGACTTTAACATGATTGAGTTCT
ACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCAGAGGTTTGCAGAACTCATGAGGCTCAACCACAACCAGGTGGAA
AGAGAGAGGTTGTCAAGAAATTACCCACAACCCAGAACAGAGGAAAATGAAAATTCGGAGTTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGAAGCCAACTGTGGAG
CTCGGCGGAGACCTCTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCTCCCTCCTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGTGCCACTCTCTTTTG
GGGTCTGGCTTGAGCATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAGCACAGGTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCCTTAGCCCAGAAGCC
CTGCCAGGTCCAGTGGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCACTCCACCCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

NM_001288780 ⟹ NP_001275709

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,704,905 - 62,808,314 (-)	NCBI
HuRef	17	56,145,700 - 56,254,090 (-)	NCBI
CHM1_1	17	60,846,561 - 60,949,983 (-)	NCBI
T2T-CHM13v2.0	17	63,574,818 - 63,678,377 (-)	NCBI

Sequence:

show sequence

AGCCGCCCCCACCGCCTCCGCCCCAGGCAAGGCCGGCCGGCGCCGCGGAAAGCAGCCTCGGGGAAGGAGGAGGAAGAGGGGCAGGTGTAGGGAGTGAAGAAGCAAAAAGAGGAGGAGGAAGAGGAGCT
CAGGGCCGTCCCCGCGCAATTAATGGGCGGCTCCTGCGCCCTGGACCGGCCCGCCCGCCCAGCCCCTCGACCCCTGTAGCCCCGGCAGGGGAGGAAGGGCAGACCCACAGGGCCAGATGATAAACCAT
GTGAGATTTCATAACTACCAGACCAGACGCTGGGTCACCATGAGTCCGGGGCGGCCTGACTCTGCCAATATCTGCACAACTGAATAAACAGGAGGAGCGAGGGAATGCCGCAGAACGTATACACCTGA
AGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAGAAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTCTGAGACGACAGG
AATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAGGATGCTCTAACT
GAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGAGAAAGTGGACCC
CAGCGAACCCTCTCCAGACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAAC
AGCAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACAG
CCAATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGTT
CTCGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAGG
AAACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGCT
GAAAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGCT
GCCTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGGA
GTGATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATATCTCCAAGATCA
TCAGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGTT
TCATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTAA
CAAGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTCT
GGGTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGGC
AGACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGCG
GCTGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGTT
GACCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCAGAGGTTTGCAGA
ACTCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGTTGTCAAGAAATTACCCACAACCCAGAACAGAGGAAAATGAAAGTAGGTTTTGGGGGCCAGTCCTGCCATTTTGAGGGTGTTTGCTAA
ATTACTCTTTTTCTGTGACTGTGTGGAACCAAATGCCATGGAAGGAAGGAATGACCACCACCCAGAGGCAAAAATAACCCCGCAAAGCTTGGGAAAGTCAGCCGCAGCAAACAATCAGGAAGGCGAGG
CCAAGTTCACTGGATGCAGAGCAGATAAGAATTTTAATTCATCCTGAACGCAAGGAAAGGCGCCAACAAAGGGAAGAGGTTATCTTCCGGCATGAGATAAGATTTGTTCCTTTTCCTTGCTGGGATTC
TCCAGCGTCCAGCACTTGGAGAGTTTGGGGGTTGGTTTTTTTACTGCCAGGATTCCTCTAGGAAAACCCTCCCCAAGCCCTGGCAGGGGCTGTCTGGCCCTTACCTGAAGGGACCACATTCACTCACA
AGCTAGTGGCCTTGGTGGATTTGGGGTCTGCTGAATTCAGAGGTTGAACAAAGCAAACAGGTCTCCCAAGAAAGGGCCCTCAAAGCGGGCAAGACGGCTCTCTGCAAACAGGTTCGAGAAAAGCCTTC
TCCCTGTTCCTTTTTCCATTAAAAAAAAAAAAAAACGACTGGAGAAAAACGTGCTTAATAAAGCAGGCGGGCTCGAA

hide sequence

RefSeq Acc Id:

NM_152598 ⟹ NP_689811

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,808,314 (-)	NCBI
GRCh37	17	60,778,675 - 60,885,705 (-)	RGD
Build 36	17	58,132,407 - 58,239,437 (-)	NCBI Archive
Celera	17	55,166,551 - 55,273,592 (-)	RGD
HuRef	17	56,145,700 - 56,254,090 (-)	NCBI
CHM1_1	17	60,842,970 - 60,949,983 (-)	NCBI
T2T-CHM13v2.0	17	63,571,227 - 63,678,377 (-)	NCBI

Sequence:

show sequence

AGCCGCCCCCACCGCCTCCGCCCCAGGCAAGGCCGGCCGGCGCCGCGGAAAGCAGCCTCGGGGAAGGAGGAGGAAGAGGGGCAGGTGTAGGGAGTGAAGAAGCAAAAAGAGGAGGAGGAAGAGGAGCT
CAGGGCCGTCCCCGCGCAATTAATGGGCGGCTCCTGCGCCCTGGACCGGCCCGCCCGCCCAGCCCCTCGACCCCTGTAGCCCCGGCAGGGGAGGAAGGGCAGACCCACAGGTCAGGGATTAGGAATCA
TGTTGCATGACGCAAGGGACAGGCAGAAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTCTGAGACGACAGGAATATAGAAGAGACCCAAAT
GAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAGGATGCTCTAACTGAACCAAGGTCATCTATCAA
GATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGAGAAAGTGGACCCCAGCGAACCCTCTCCAGCAG
ACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAACAGCAGTGGCCTGCAAAG
GTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACAGCCAATGACTGAGAACGC
CCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGTTCTCGGGGCCACCACTCA
CACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAGGAAACCCAGTCTGAAGAA
TGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGCTGAAAATTGCAGAGGTCA
TTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGCTGCCTGATAGGGAATCTG
CTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGGAGTGATTGTATTTCTGTG
GAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATATCTCCAAGATCATCAGTGAATTCATCCTA
TAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGTTTCATGTTTGCCAACCAC
TGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTAACAAGCCAGCCTCAGGGG
GCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTCTGGGTCTCTGCAAGAAAA
TACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGGCAGACCCTGAGAAACTCA
AGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGCGGCTGTGTGGGAAGCCTG
CAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGTTGACCTGGGTGACTTTAA
CATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCAGAGGTTTGCAGAACTCATGAGGCTCAACC
ACAACCAGGTGGAAAGAGAGAGGTTGTCAAGAAATTACCCACAACCCAGAACAGAGGAAAATGAAAATTCGGAGTTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGA
AGCCAACTGTGGAGCTCGGCGGAGACCTCTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCTCCCTCCTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGT
GCCACTCTCTTTTGGGGTCTGGCTTGAGCATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAGCACAGGTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCC
TTAGCCCAGAAGCCCTGCCAGGTCCAGTGGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCACTCCACCCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

XM_005257095 ⟹ XP_005257152

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,808,314 (-)	NCBI
GRCh37	17	60,778,675 - 60,885,705 (-)	NCBI

Sequence:

show sequence

GCGGTTGCTAGGGAAACCGGAGGACGCCCGGTAGCCGCCCCCACCGCCTCCGCCCCAGGCAAGGCCGGCCGGCGCCGCGGAAAGCAGCCTCGGGGAAGGAGGAGGAAGAGGGGCAGGTGTAGGGAGTG
AAGAAGCAAAAAGAGGAGGAGGAAGAGGAGCTCAGGGCCGTCCCCGCGCAATTAATGGGCGGCTCCTGCGCCCTGGACCGGCCCGCCCGCCCAGCCCCTCGACCCCTGTAGCCCCGGCAGGGGAGGAA
GGGCAGACCCACAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAGAAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTC
TGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAG
GATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGA
GAAAGTGGACCCCAGCGAACCCTCTCCAGCAGAGTCAGAGCCGACTTGGTGGAATAAACCGGAAACAGACCTCGGAGGACCTTCTGGCTGGTGCAGTCTGGGGAAGAAAGGTCCCATGAGCAGAAGCA
TCCCTCCCTGTGAAGCAGACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAA
CAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACA
GCCAATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGT
TCTCGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAG
GAAACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGC
TGAAAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGC
TGCCTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGG
AGTGATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATATCTCCAAGATC
ATCAGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGT
TTCATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTA
ACAAGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTC
TGGGTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGG
CAGACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGC
GGCTGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGT
TGACCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCAGAGGTTTGCAG
AACTCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGATTCGGAGTTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGAAGCCAACTGTGGAGCTCGGCGGAGA
CCTCTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCTCCCTCCTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGTGCCACTCTCTTTTGGGGTCTGGCTT
GAGCATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAGCACAGGTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCCTTAGCCCAGAAGCCCTGCCAGGTCC
AGTGGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCACTCCACCCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

XM_005257096 ⟹ XP_005257153

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,806,640 (-)	NCBI
GRCh37	17	60,778,675 - 60,885,705 (-)	NCBI

Sequence:

show sequence

AATTACTCGCTCTTGCTTTCAGCAAGGCAGGACCCCCTCCTTCCTTCTCCACCTGCCTCCAACTCCCTCCTCCTTTCTCTCTCCCTACTTAATATGGCTTCTTATGTTGATTTCTAAAGCACAGATTT
GGCACAAGACATTATCACCAGAAAGACTTAAAACAGAAGTGTGCATAACCATGAGTGGGTTTTAAATTAAGAAGCAGTTCAAAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAG
AAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTCTGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGG
GCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAGGATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCA
AACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGAGAAAGTGGACCCCAGCGAACCCTCTCCAGCAGAGTCAGAGCCGACTTGGTGGAATAAA
CCGGAAACAGACCTCGGAGGACCTTCTGGCTGGTGCAGTCTGGGGAAGAAAGGTCCCATGAGCAGAAGCATCCCTCCCTGTGAAGCAGACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAA
CCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAACAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAG
AAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACAGCCAATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCC
CAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGTTCTCGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAG
GTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAGGAAACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCC
ATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGCTGAAAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGA
ATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGCTGCCTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAA
GAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGGAGTGATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGA
AAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATATCTCCAAGATCATCAGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGAT
GATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGTTTCATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGA
AAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTAACAAGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCA
ATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTCTGGGTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAAT
CAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGGCAGACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGA
GGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGCGGCTGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAG
TGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGTTGACCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGCA
CAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCAGAGGTTTGCAGAACTCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGATTCGGAGTTGGGAGAT
GGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGAAGCCAACTGTGGAGCTCGGCGGAGACCTCTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCTCCCTCCTCCTCTTT
ACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGTGCCACTCTCTTTTGGGGTCTGGCTTGAGCATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAGCACAGGTCAAGCAG
CGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCCTTAGCCCAGAAGCCCTGCCAGGTCCAGTGGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCACTCCACCCTGAATGG
ACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

XM_005257097 ⟹ XP_005257154

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,806,640 (-)	NCBI
GRCh37	17	60,778,675 - 60,885,705 (-)	NCBI

Sequence:

show sequence

ATTACTCGCTCTTGCTTTCAGCAAGGCAGGACCCCCTCCTTCCTTCTCCACCTGCCTCCAACTC
CCTCCTCCTTTCTCTCTCCCTACTTAATATGGCTTCTTATGTTGATTTCTAAAGCACAGATTTGGCACAAGACATTATCACCAGAAAGACTTAAAACAGAAGTGTGCATAACCATGAGTGGGTTTTAA
ATTAAGAAGCAGTTCAAAGGGCCAGATGATAAACCATGTGAGATTTCATAACTACCAGACCAGACGCTGGGTCACCATGAGTCCGGGGCGGCCTGACTCTGCCAATATCTGCACAACTGAATAAACAG
GAGGAGCGAGGGAATGCCGCAGAACGTATACACCTGAAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAGAAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAG
GTGGACTCTGAGTATCAGGCTTGTCTGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATC
TTCCAAACAGAGTTCTAGTGAGGAGGATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAA
GTACCATGACTGTAAGGAAAGCAGAGAAAGTGGACCCCAGCGAACCCTCTCCAGCAGAGTCAGAGCCGACTTGGTGGAATAAACCGGAAACAGACCTCGGAGGACCTTCTGGCTGGTGCAGTCTGGGG
AAGAAAGGTCCCATGAGCAGAAGCATCCCTCCCTGTGAAGCAGACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGC
ATCTGGGGACAGAAGCAGACAGAAACAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGA
GAAGAAACTTGGTCCCATCGTCACAGCCAATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAA
AATAGTCCTCAAGTATTGAGTGAGTTCTCGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAG
AAGAGAAAGCGATGACACTGAAGAGGAAACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCA
AAAATAAAAATTTTGAAGAAAATGCTGAAAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGG
CAAAGGTTGTCCCAAGACCCCGGGCTGCCTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGT
TGGTGTCAATGCTGAAAATGTATGGAGTGATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTT
CTGGCAGACCAATATCTCCAAGATCATCAGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGC
TCAGACTCAGAGGGAAACTCAGGGTTTCATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGT
CAGGGAAGCAGAAGATACTACTTTAACAAGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGA
ACTCAGAAGGCCATTTGCATGTGTCTGGGTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGAT
GAAAAGGAAACCAGTAAGATAAAGGCAGACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCC
AAGCAACCCCCTCCTGGAGCCTTGCGGCTGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTG
AGATGTGTAAGCAAGGCCTGCTGGTTGACCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTT
CACCTCTATGAGCAGAGGTTTGCAGAACTCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGATTCGGAGTTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGA
AGCCAACTGTGGAGCTCGGCGGAGACCTCTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCTCCCTCCTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGT
GCCACTCTCTTTTGGGGTCTGGCTTGAGCATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAGCACAGGTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCC
TTAGCCCAGAAGCCCTGCCAGGTCCAGTGGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCACTCCACCCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

XM_005257098 ⟹ XP_005257155

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,808,314 (-)	NCBI
GRCh37	17	60,778,675 - 60,885,705 (-)	NCBI

Sequence:

show sequence

GCGGTTGCTAGGGAAACCGGAGGACGCCCGGTAGCCGCCCCCACCGCCTCCGCCCCAGGCAAGGCCGGCCGGCGCCGCGGAAAGCAGCCTCGGGGAAGGAGGAGGAAGAGGGGCAGGTGTAGGGAGTG
AAGAAGCAAAAAGAGGAGGAGGAAGAGGAGCTCAGGGCCGTCCCCGCGCAATTAATGGGCGGCTCCTGCGCCCTGGACCGGCCCGCCCGCCCAGCCCCTCGACCCCTGTAGCCCCGGCAGGGGAGGAA
GGGCAGACCCACAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAGAAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTC
TGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAG
GATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGA
GAAAGTGGACCCCAGCGAACCCTCTCCAGAGTCAGAGCCGACTTGGTGGAATAAACCGGAAACAGACCTCGGAGGACCTTCTGGCTGGTGCAGTCTGGGGAAGAAAGGTCCCATGAGCAGAAGCATCC
CTCCCTGTGAAGCAGACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAACAG
CAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACAGCC
AATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGTTCT
CGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAGGAA
ACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGCTGA
AAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGCTGC
CTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGGAGT
GATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATATCTCCAAGATCATC
AGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGTTTC
ATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTAACA
AGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTCTGG
GTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGGCAG
ACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGCGGC
TGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGTTGA
CCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCAGAGGTTTGCAGAAC
TCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGATTCGGAGTTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGAAGCCAACTGTGGAGCTCGGCGGAGACCT
CTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCTCCCTCCTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGTGCCACTCTCTTTTGGGGTCTGGCTTGAG
CATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAGCACAGGTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCCTTAGCCCAGAAGCCCTGCCAGGTCCAGT
GGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCACTCCACCCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

XM_005257100 ⟹ XP_005257157

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,808,314 (-)	NCBI
GRCh37	17	60,778,675 - 60,885,705 (-)	NCBI

Sequence:

show sequence

GCGGTTGCTAGGGAAACCGGAGGACGCCCGGTAGCCGCCCCCACCGCCTCCGCCCCAGGCAAGGCCGGCCGGCGCCGCGGAAAGCAGCCTCGGGGAAGGAGGAGGAAGAGGGGCAGGTGTAGGGAGTG
AAGAAGCAAAAAGAGGAGGAGGAAGAGGAGCTCAGGGCCGTCCCCGCGCAATTAATGGGCGGCTCCTGCGCCCTGGACCGGCCCGCCCGCCCAGCCCCTCGACCCCTGTAGCCCCGGCAGGGGAGGAA
GGGCAGACCCACAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAGAAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTC
TGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAG
GATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGA
GAAAGTGGACCCCAGCGAACCCTCTCCAGCAGACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACA
GAAGCAGACAGAAACAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTG
GTCCCATCGTCACAGCCAATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCA
AGTATTGAGTGAGTTCTCGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCG
ATGACACTGAAGAGGAAACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAAT
TTTGAAGAAAATGCTGAAAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTC
CCAAGACCCCGGGCTGCCTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATG
CTGAAAATGTATGGAGTGATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCA
ATATCTCCAAGATCATCAGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGA
GGGAAACTCAGGGTTTCATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAG
AAGATACTACTTTAACAAGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGC
CATTTGCATGTGTCTGGGTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAAC
CAGTAAGATAAAGGCAGACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCC
TCCTGGAGCCTTGCGGCTGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAG
CAAGGCCTGCTGGTTGACCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGA
GCAGAGGTTTGCAGAACTCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGATTCGGAGTTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGAAGCCAACTGTG
GAGCTCGGCGGAGACCTCTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCTCCCTCCTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGTGCCACTCTCTT
TTGGGGTCTGGCTTGAGCATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAGCACAGGTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCCTTAGCCCAGAA
GCCCTGCCAGGTCCAGTGGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCACTCCACCCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

XM_005257102 ⟹ XP_005257159

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,808,314 (-)	NCBI
GRCh37	17	60,778,675 - 60,885,705 (-)	NCBI

Sequence:

show sequence

GCGGTTGCTAGGGAAACCGGAGGACGCCCGGTAGCCGCCCCCACCGCCTCCGCCCCAGGCAAGGCCGGCCGGCGCCGCGGAAAGCAGCCTCGGGGAAGGAGGAGGAAGAGGGGCAGGTGTAGGGAGTG
AAGAAGCAAAAAGAGGAGGAGGAAGAGGAGCTCAGGGCCGTCCCCGCGCAATTAATGGGCGGCTCCTGCGCCCTGGACCGGCCCGCCCGCCCAGCCCCTCGACCCCTGTAGCCCCGGCAGGGGAGGAA
GGGCAGACCCACAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAGAAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTC
TGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAG
GATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGA
GAAAGTGGACCCCAGCGAACCCTCTCCAGACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAA
GCAGACAGAAACAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTC
CCATCGTCACAGCCAATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGT
ATTGAGTGAGTTCTCGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATG
ACACTGAAGAGGAAACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTT
GAAGAAAATGCTGAAAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCA
AGACCCCGGGCTGCCTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTG
AAAATGTATGGAGTGATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATA
TCTCCAAGATCATCAGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGG
AAACTCAGGGTTTCATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAG
ATACTACTTTAACAAGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCAT
TTGCATGTGTCTGGGTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAG
TAAGATAAAGGCAGACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCC
TGGAGCCTTGCGGCTGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAA
GGCCTGCTGGTTGACCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCA
GAGGTTTGCAGAACTCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGATTCGGAGTTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGAAGCCAACTGTGGAG
CTCGGCGGAGACCTCTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCTCCCTCCTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGTGCCACTCTCTTTTG
GGGTCTGGCTTGAGCATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAGCACAGGTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCCTTAGCCCAGAAGCC
CTGCCAGGTCCAGTGGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCACTCCACCCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

XM_005257103 ⟹ XP_005257160

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,704,905 - 62,808,314 (-)	NCBI
GRCh37	17	60,778,675 - 60,885,705 (-)	NCBI

Sequence:

show sequence

GCGGTTGCTAGGGAAACCGGAGGACGCCCGGTAGCCGCCCCCACCGCCTCCGCCCCAGGCAAGGCCGGCCGGCGCCGCGGAAAGCAGCCTCGGGGAAGGAGGAGGAAGAGGGGCAGGTGTAGGGAGTG
AAGAAGCAAAAAGAGGAGGAGGAAGAGGAGCTCAGGGCCGTCCCCGCGCAATTAATGGGCGGCTCCTGCGCCCTGGACCGGCCCGCCCGCCCAGCCCCTCGACCCCTGTAGCCCCGGCAGGGGAGGAA
GGGCAGACCCACAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAGAAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTC
TGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAG
GATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGA
GAAAGTGGACCCCAGCGAACCCTCTCCAGACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAA
GCAGACAGAAACAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTC
CCATCGTCACAGCCAATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGT
ATTGAGTGAGTTCTCGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATG
ACACTGAAGAGGAAACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTT
GAAGAAAATGCTGAAAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCA
AGACCCCGGGCTGCCTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTG
AAAATGTATGGAGTGATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATA
TCTCCAAGATCATCAGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGG
AAACTCAGGGTTTCATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAG
ATACTACTTTAACAAGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCAT
TTGCATGTGTCTGGGTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAG
TAAGATAAAGGCAGACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCC
TGGAGCCTTGCGGCTGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAA
GGCCTGCTGGTTGACCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCA
GAGGTTTGCAGAACTCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGTTGTCAAGAAATTACCCACAACCCAGAACAGAGGAAAATGAAAGTAGGTTTTGGGGGCCAGTCCTGCCATTTTGAG
GGTGTTTGCTAAATTACTCTTTTTCTGTGACTGTGTGGAACCAAATGCCATGGAAGGAAGGAATGACCACCACCCAGAGGCAAAAATAACCCCGCAAAGCTTGGGAAAGTCAGCCGCAGCAAACAATC
AGGAAGGCGAGGCCAAGTTCACTGGATGCAGAGCAGATAAGAATTTTAATTCATCCTGAACGCAAGGAAAGGCGCCAACAAAGGGAAGAGGTTATCTTCCGGCATGAGATAAGATTTGTTCCTTTTCC
TTGCTGGGATTCTCCAGCGTCCAGCACTTGGAGAGTTTGGGGGTTGGTTTTTTTACTGCCAGGATTCCTCTAGGAAAACCCTCCCCAAGCCCTGGCAGGGGCTGTCTGGCCCTTACCTGAAGGGACCA
CATTCACTCACAAGCTAGTGGCCTTGGTGGATTTGGGGTCTGCTGAATTCAGAGGTTGAACAAAGCAAACAGGTCTCCCAAGAAAGGGCCCTCAAAGCGGGCAAGACGGCTCTCTGCAAACAGGTTCG
AGAAAAGCCTTCTCCCTGTTCCTTTTTCCATT

hide sequence

RefSeq Acc Id:

XM_005257106 ⟹ XP_005257163

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,795,044 (-)	NCBI
GRCh37	17	60,778,675 - 60,885,705 (-)	NCBI

Sequence:

show sequence

ATTCTCCTCCTGGCTCACCTTTGAGGCTTGTCTGAGACGACAGGAATATAGAAGAGACCCAAAT
GAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAGGATGCTCTAACTGAACCAAGGTCATCTATCAA
GATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGAGAAAGTGGACCCCAGCGAACCCTCTCCAGCAG
AGTCAGAGCCGACTTGGTGGAATAAACCGGAAACAGACCTCGGAGGACCTTCTGGCTGGTGCAGTCTGGGGAAGAAAGGTCCCATGAGCAGAAGCATCCCTCCCTGTGAAGCAGACCAAGCACCAATG
GTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAACAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAG
GGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACAGCCAATGACTGAGAACGCCCCTGATAGAGCCA
AAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGTTCTCGGGGCCACCACTCACACCCACCACTGTA
GGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAGGAAACCCAGTCTGAAGAATGTCTGTGGGTTGG
TGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGCTGAAAATTGCAGAGGTCATTCTTCAAGAAGAA
GTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGCTGCCTGATAGGGAATCTGCTACAGAGAAGGAC
AGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGGAGTGATTGTATTTCTGTGGAACATAGGCCTGG
CACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATATCTCCAAGATCATCAGTGAATTCATCCTATAACCCTCCTGCAT
CATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGTTTCATGTTTGCCAACCACTGTCTCCCATTAGA
AATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTAACAAGCCAGCCTCAGGGGGCTCCACTATATAC
AGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTCTGGGTCTCTGCAAGAAAATACACCATTTACTT
TCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGGCAGACCCTGAGAAACTCAAGAAATTGCAAGAA
AGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGCGGCTGTGTGGGAAGCCTGCAGTTTGTTCATCA
AGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGTTGACCTGGGTGACTTTAACATGATTGAGTTCT
ACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCAGAGGTTTGCAGAACTCATGAGGCTCAACCACAACCAGGTGGAA
AGAGAGAGGATTCGGAGTTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGAAGCCAACTGTGGAGCTCGGCGGAGACCTCTCCCGCCAGCCCTTCTTTCTACGTCCCC
AAGTGCCTCCCTCCCTCCTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGTGCCACTCTCTTTTGGGGTCTGGCTTGAGCATCTATGGGCAGCCACAGCGACCAGTCT
AGTCCCAGACAGCACAGGTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCCTTAGCCCAGAAGCCCTGCCAGGTCCAGTGGCCTGGGGTCCCACTGCTGAGGGCACCT
GCCAGGCCTCACTCCACCCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

XM_011524435 ⟹ XP_011522737

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,808,314 (-)	NCBI

Sequence:

show sequence

GCGGTTGCTAGGGAAACCGGAGGACGCCCGGTAGCCGCCCCCACCGCCTCCGCCCCAGGCAAGGCCGGCCGGCGCCGCGGAAAGCAGCCTCGGGGAAGGAGGAGGAAGAGGGGCAGGTGTAGGGAGTG
AAGAAGCAAAAAGAGGAGGAGGAAGAGGAGCTCAGGGCCGTCCCCGCGCAATTAATGGGCGGCTCCTGCGCCCTGGACCGGCCCGCCCGCCCAGCCCCTCGACCCCTGTAGCCCCGGCAGGGGAGGAA
GGGCAGACCCACAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAGAAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTC
TGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAG
GATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGA
GAAAGTGGACCCCAGCGAACCCTCTCCAGCAGAGTCAGAGCCGACTTGGTGGAATAAACCGGAAACAGACCTCGGAGGACCTTCTGGCTGGTGCAGTCTGGGGAAGAAAGGTCCCATGAGCAGAAGCA
TCCCTCCCTGTGAAGACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAACAG
CAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACAGCC
AATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGTTCT
CGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAGGAA
ACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGCTGA
AAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGCTGC
CTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGGAGT
GATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATATCTCCAAGATCATC
AGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGTTTC
ATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTAACA
AGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTCTGG
GTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGGCAG
ACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGCGGC
TGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGTTGA
CCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCAGAGGTTTGCAGAAC
TCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGATTCGGAGTTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGAAGCCAACTGTGGAGCTCGGCGGAGACCT
CTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCTCCCTCCTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGTGCCACTCTCTTTTGGGGTCTGGCTTGAG
CATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAGCACAGGTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCCTTAGCCCAGAAGCCCTGCCAGGTCCAGT
GGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCACTCCACCCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

XM_011524436 ⟹ XP_011522738

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,806,640 (-)	NCBI

Sequence:

show sequence

AATTACTCGCTCTTGCTTTCAGCAAGGCAGGACCCCCTCCTTCCTTCTCCACCTGCCTCCAACTCCCTCCTCCTTTCTCTCTCCCTACTTAATATGGCTTCTTATGTTGATTTCTAAAGCACAGATTT
GGCACAAGACATTATCACCAGAAAGACTTAAAACAGAAGTGTGCATAACCATGAGTGGGTTTTAAATTAAGAAGCAGTTCAAAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAG
AAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTCTGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGG
GCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAGGATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCA
AACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGAGAAAGTGGACCCCAGCGAACCCTCTCCAGCAGACCAAGCACCAATGGTTTTATTAAGA
AAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAACAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCA
AGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACAGCCAATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACC
CGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGTTCTCGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGA
AAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAGGAAACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACC
CTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGCTGAAAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTC
ATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGCTGCCTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGT
GAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGGAGTGATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTC
TGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATATCTCCAAGATCATCAGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATT
CTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGTTTCATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCA
TTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTAACAAGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACT
AAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTCTGGGTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGT
CTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGGCAGACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAG
GAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGCGGCTGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAA
AAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGTTGACCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACC
AGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGGTGCTGCTGCTTCACCTCTATGAGCAGAGGTTTGCAGAACTCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGATT
CGGAGTTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGAAGCCAACTGTGGAGCTCGGCGGAGACCTCTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCT
CCCTCCTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGTGCCACTCTCTTTTGGGGTCTGGCTTGAGCATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAG
CACAGGTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCCTTAGCCCAGAAGCCCTGCCAGGTCCAGTGGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCAC
TCCACCCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCCA

hide sequence

RefSeq Acc Id:

XM_011524437 ⟹ XP_011522739

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,701,314 - 62,806,640 (-)	NCBI

Sequence:

show sequence

ATTACTCGCTCTTGCTTTCAGCAAGGCAGGACCCCCTCCTTCCTTCTCCACCTGCCTCCAACTC
CCTCCTCCTTTCTCTCTCCCTACTTAATATGGCTTCTTATGTTGATTTCTAAAGCACAGATTTGGCACAAGACATTATCACCAGAAAGACTTAAAACAGAAGTGTGCATAACCATGAGTGGGTTTTAA
ATTAAGAAGCAGTTCAAAGGGCCAGATGATAAACCATGTGAGATTTCATAACTACCAGACCAGACGCTGGGTCACCATGAGTCCGGGGCGGCCTGACTCTGCCAATATCTGCACAACTGAATAAACAG
GAGGAGCGAGGGAATGCCGCAGAACGTATACACCTGAAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAGAAGTTCTTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAG
GTGGACTCTGAGTATCAGGCTTGTCTGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGGGCAAGAGACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATC
TTCCAAACAGAGTTCTAGTGAGGAGGATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCAAACTTCCAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAA
GTACCATGACTGTAAGGAAAGCAGAGAAAGTGGACCCCAGCGAACCCTCTCCAGACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAACCTGAGGAGATTTACAGTCAGCCCAGAATCGCAC
AGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAACAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAGAAGGCCTGATGTGTAACACTAAGCTGAAGAGGCC
AAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACAGCCAATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCCCAGAGTGAGCTGCATCCAGCCCTGTCCCAGGCCT
TCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGTTCTCGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAGGTTCCGAGATGAAGACTTTTATTCCATTTTGTCA
TTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAGGAAACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCCATCACAAAAGAAGTAGATTTGGGGGGACATCGAC
CCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGCTGAAAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGAATAAGCAATGCAATGGAGCCAGCAACAGAGCGGC
CTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGCTGCCTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAAGAGCCCTCTTTCGTGGGACACCAAATCCGAGCCC
AGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGGAGTGATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGAAAGACTATTTAAACAGTTCTCAAAATTCTCTTGA
CTACTTTATTTCTGGCAGACCAATATCTCCAAGATCATCAGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGATGATATTCCAGTAGACTTGTCAATGTCATCGACTT
CAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGTTTCATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGAAAACCATAATTATTTCCCAGTAAACAGTGCACAC
GAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTAACAAGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCAATTTGTCCTTAGTGGATTCTTCCAGCTCCTCTCC
ATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTCTGGGTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAATCAAAATGATAATGGGAGCAGGATGGCAGCCTCTG
GTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGGCAGACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGAGGAGGGAGACTTGTGTCGCATCTGTCAGATAGCC
GGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGCGGCTGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAATAACATCAGGAGCAGATCTTGGTGCCGT
GAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGTTGACCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGCACAAAACGAGCTGATGAATTCAGGCTTGTACCTGG
TGCTGCTGCTTCACCTCTATGAGCAGAGGTTTGCAGAACTCATGAGGCTCAACCACAACCAGGTGGAAAGAGAGAGGTTGTCAAGAAATTACCCACAACCCAGAACAGAGGAAAATGAAAATTCGGAG
TTGGGAGATGGAAATGAAGGCAGCATTTCTCAAAGCCAGGTCGTCTAGCAAGGAAGCCAACTGTGGAGCTCGGCGGAGACCTCTCCCGCCAGCCCTTCTTTCTACGTCCCCAAGTGCCTCCCTCCCTC
CTCCTCTTTACTGAAACTGAAACCAAAGCGTTCACAGTTAGATTTTCACCTCGTGCCACTCTCTTTTGGGGTCTGGCTTGAGCATCTATGGGCAGCCACAGCGACCAGTCTAGTCCCAGACAGCACAG
GTCAAGCAGCGTGGGACTGTGGAGCCCCTGGCAGGCTGGCCTGGTGCTGCCCCCTTAGCCCAGAAGCCCTGCCAGGTCCAGTGGCCTGGGGTCCCACTGCTGAGGGCACCTGCCAGGCCTCACTCCAC
CCTGAATGGACTCGAGCCATGTATTCATTCAGTAAACTGACATTATTCTCCC

hide sequence

RefSeq Acc Id:

XM_054315255 ⟹ XP_054171230

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,571,227 - 63,678,377 (-)	NCBI

RefSeq Acc Id:

XM_054315256 ⟹ XP_054171231

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,571,227 - 63,676,703 (-)	NCBI

RefSeq Acc Id:

XM_054315257 ⟹ XP_054171232

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,571,227 - 63,676,703 (-)	NCBI

RefSeq Acc Id:

XM_054315258 ⟹ XP_054171233

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,571,227 - 63,678,377 (-)	NCBI

RefSeq Acc Id:

XM_054315259 ⟹ XP_054171234

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,571,227 - 63,678,377 (-)	NCBI

RefSeq Acc Id:

XM_054315260 ⟹ XP_054171235

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,571,227 - 63,678,377 (-)	NCBI

RefSeq Acc Id:

XM_054315261 ⟹ XP_054171236

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,571,227 - 63,676,703 (-)	NCBI

RefSeq Acc Id:

XM_054315262 ⟹ XP_054171237

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,571,227 - 63,678,377 (-)	NCBI

RefSeq Acc Id:

XM_054315263 ⟹ XP_054171238

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,571,227 - 63,676,703 (-)	NCBI

RefSeq Acc Id:

XM_054315264 ⟹ XP_054171239

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,575,409 - 63,678,377 (-)	NCBI

RefSeq Acc Id:

XM_054315265 ⟹ XP_054171240

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,571,227 - 63,665,107 (-)	NCBI

RefSeq Acc Id:

XM_054315266 ⟹ XP_054171241

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,620,036 - 63,678,377 (-)	NCBI

RefSeq Acc Id:

XM_054315267 ⟹ XP_054171242

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,620,036 - 63,676,703 (-)	NCBI

RefSeq Acc Id:

XR_008484791

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	63,581,617 - 63,678,377 (-)	NCBI

RefSeq Acc Id:

XR_934406

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	62,711,704 - 62,808,314 (-)	NCBI

Sequence:

show sequence

GCGGTTGCTAGGGAAACCGGAGGACGCCCGGTAGCCGCCCCCACCGCCTCCGCCCCAGGCAAGG
CCGGCCGGCGCCGCGGAAAGCAGCCTCGGGGAAGGAGGAGGAAGAGGGGCAGGTGTAGGGAGTGAAGAAGCAAAAAGAGGAGGAGGAAGAGGAGCTCAGGGCCGTCCCCGCGCAATTAATGGGCGGCT
CCTGCGCCCTGGACCGGCCCGCCCGCCCAGCCCCTCGACCCCTGTAGCCCCGGCAGGGGAGGAAGGGCAGACCCACAGGTCAGGGATTAGGAATCATGTTGCATGACGCAAGGGACAGGCAGAAGTTC
TTCAGCGATGTTCAGTATCTGCGGGACATGCAGCATAAGGTGGACTCTGAGTATCAGGCTTGTCTGAGACGACAGGAATATAGAAGAGACCCAAATGAGAAGAAACGCGATCAGTTTTGGGGGCAAGA
GACAAGTTTTGAGAGATCCCGGTTTTCTAGCAGGTCATCTTCCAAACAGAGTTCTAGTGAGGAGGATGCTCTAACTGAACCAAGGTCATCTATCAAGATATCTGCATTTAAGTGTGACTCCAAACTTC
CAGCAATTGACCAAACATCAGTCAAGCAGAAACATAAAAGTACCATGACTGTAAGGAAAGCAGAGAAAGTGGACCCCAGCGAACCCTCTCCAGCAGAGTCAGAGCCGACTTGGTGGAATAAACCGGAA
ACAGACCTCGGAGGACCTTCTGGCTGGTGCAGTCTGGGGAAGAAAGGTCCCATGAGCAGAAGCATCCCTCCCTGTGAAGCAGACCAAGCACCAATGGTTTTATTAAGAAAGAGGAAGCCAAACCTGAG
GAGATTTACAGTCAGCCCAGAATCGCACAGCCCGAGAGCATCTGGGGACAGAAGCAGACAGAAACAGCAGTGGCCTGCAAAGGTGCCGGTTCCCAGGGGAGCAGATCAAGTAGTTCAACAAGAAGGCC
TGATGTGTAACACTAAGCTGAAGAGGCCAAATCAAGAGAGAAGAAACTTGGTCCCATCGTCACAGCCAATGACTGAGAACGCCCCTGATAGAGCCAAAAAAGGAGACCCGAGTGCTCCTTCCCAGAGT
GAGCTGCATCCAGCCCTGTCCCAGGCCTTCCAAGGAAAAAATAGTCCTCAAGTATTGAGTGAGTTCTCGGGGCCACCACTCACACCCACCACTGTAGGAGGGCCAAGAAAGGCATCATTTAGGTTCCG
AGATGAAGACTTTTATTCCATTTTGTCATTGAACAGCAGAAGAGAAAGCGATGACACTGAAGAGGAAACCCAGTCTGAAGAATGTCTGTGGGTTGGTGTGCGCTCACCCTGTTCTCCTTCCCATCACA
AAAGAAGTAGATTTGGGGGGACATCGACCCCTCAGGCCAAAAATAAAAATTTTGAAGAAAATGCTGAAAATTGCAGAGGTCATTCTTCAAGAAGAAGTGAGCCCAGTCATGGCTCATTGAGAATAAGC
AATGCAATGGAGCCAGCAACAGAGCGGCCTTCTGCTGGGCAAAGGTTGTCCCAAGACCCCGGGCTGCCTGATAGGGAATCTGCTACAGAGAAGGACAGAGGTGGCAGTGAAAATGCGAAAAAGAGCCC
TCTTTCGTGGGACACCAAATCCGAGCCCAGACAAGAGGTTGGTGTCAATGCTGAAAATGTATGGAGTGATTGTATTTCTGTGGAACATAGGCCTGGCACCCATGATTCTGAAGGATACTGGAAAGACT
ATTTAAACAGTTCTCAAAATTCTCTTGACTACTTTATTTCTGGCAGACCAATATCTCCAAGATCATCAGTGAATTCATCCTATAACCCTCCTGCATCATTCATGCATTCTGCTCTGAGAGATGATATT
CCAGTAGACTTGTCAATGTCATCGACTTCAGTTCACAGCTCAGACTCAGAGGGAAACTCAGGGTTTCATGTTTGCCAACCACTGTCTCCCATTAGAAATAGGACTCCATTTGCCAGTGCCGAAAACCA
TAATTATTTCCCAGTAAACAGTGCACACGAATTTGCTGTCAGGGAAGCAGAAGATACTACTTTAACAAGCCAGCCTCAGGGGGCTCCACTATATACAGATCTCTTACTAAATCCACAGGGCAATTTGT
CCTTAGTGGATTCTTCCAGCTCCTCTCCATCAAGAATGAACTCAGAAGGCCATTTGCATGTGTCTGGGTCTCTGCAAGAAAATACACCATTTACTTTCTTTGCAGTGTCTCATTTCCCAAATCAAAAT
GATAATGGGAGCAGGATGGCAGCCTCTGGTTTCACAGATGAAAAGGAAACCAGTAAGATAAAGGCAGACCCTGAGAAACTCAAGAAATTGCAAGAAAGTCTCCTGGAGGAGGACTCCGAGGAGGAGGG
AGACTTGTGTCGCATCTGTCAGATAGCCGGGGGTTCCCCAAGCAACCCCCTCCTGGAGCCTTGCGGCTGTGTGGGAAGCCTGCAGTTTGTTCATCAAGAGTGCCTGAAAAAGTGGCTGAAAGTGAAAA
TAACATCAGGAGCAGATCTTGGTGCCGTGAAGACCTGTGAGATGTGTAAGCAAGGCCTGCTGGTTGACCTGGGTGACTTTAACATGATTGAGTTCTACCAGAAGCACCAGCAATCTCAGGATGTGTTG
GTGTTGCGAGATCCCATATATTAGCTCACTTTACTATCATGCTTTGAGGAAACAGGCAGAACAGAGGTTACTTCCCTTCCATTACAAATTGAGTCCCTTTGGTCCTGCACAGTTAAAACTCTGCCTAA
AGTCACAGTGTCCGGTGGCCCTGCACTGCCCACCTTAGCCGGCAGCGCTTTCCAGGCCAAGGTCAGCAGAGCACAAAAAACACGACCAAAGGCTAAAAATAGGAGGCTAACTGCTAAGGACAGAGGAC
TGGGGCCTTCGAAGATGGATCTGTAGAATGGTGGAGAGGCCTGCAGCAGTGATCTCAGGGCCGGCTGTCACCAAGATCCAGAGTTGGCCCTGATTCAGAAGGAAGAGCATATCAATCCTTGCTCAACT
TCTGTGCCTTTTCTGGCAGCTGCTTGGTCCTGGGAGAGGTGGGTTCTGTGCCAACCTCCTGAGCTGCCCTGGATCTAATGAGAACAGGAAGATGTGGCACCCGCGCTGCTGCAGGAAGAAGGCAGATG
AGACACTGAGTGCTCACTGTGTCATTCATGCCCACGCATCGTTATCCTGGGCCGACAGAGTCACAGTTGCAAGCTTTCCCAAGGGTGACGGAAGGGGCCATGCCCTCTGCTGGGGACTCTATTCCCCG
GGGGCTGGGTGGCTTTGTGAGCACAGCCTGGCCCATCCCAAGACCCCCACTCAAGGGAAAGATGGGGACTGAAAGGGCCTTCCCCTCCTTCCCCTATAGAGGGATAGGAGTAGTTGTTACTAATACCA
CTGATTTATGGAAGGTCTGTGAAAGGTCTAGAGTGAGCACAGCCACTCTTGGCAGCAAAGCCCAAGTGCTAAGGACAGAGAAGTGCCATGGGCAGCCAGACCATCACATCCTCCCTGTGTAGCGCCTG
TTCTGAGCACCAGCGAGAAAAAAAGCACAGCCCACTCCTCAAGAGAAAGCGGAAACGTTAACAAGTGCAAAAGGTGATATGCAAGATCAAGACGAATGCTTAGGGACTGGGAAGCAAAGGAATGATGG
GGGCAAAGGAGGCTCCTCAGGAAGCCTTTCACAAGGGGACATCTGTGACTGCTGAGAACGTTATGGACAAGGCCTGGTGCATCTCTGTTGTAGCACCCGACACATCCAGCTTGTACTGGAGCTGTTTA
CCGATGAAGCTCTCTCCCCCACACCAGGTGATCGG

hide sequence


Protein RefSeqs	NP_001094345	(Get FASTA)	NCBI Sequence Viewer
	NP_001275708	(Get FASTA)	NCBI Sequence Viewer
	NP_001275709	(Get FASTA)	NCBI Sequence Viewer
	NP_689811	(Get FASTA)	NCBI Sequence Viewer
	XP_005257152	(Get FASTA)	NCBI Sequence Viewer
	XP_005257153	(Get FASTA)	NCBI Sequence Viewer
	XP_005257154	(Get FASTA)	NCBI Sequence Viewer
	XP_005257155	(Get FASTA)	NCBI Sequence Viewer
	XP_005257157	(Get FASTA)	NCBI Sequence Viewer
	XP_005257159	(Get FASTA)	NCBI Sequence Viewer
	XP_005257160	(Get FASTA)	NCBI Sequence Viewer
	XP_005257163	(Get FASTA)	NCBI Sequence Viewer
	XP_011522737	(Get FASTA)	NCBI Sequence Viewer
	XP_011522738	(Get FASTA)	NCBI Sequence Viewer
	XP_011522739	(Get FASTA)	NCBI Sequence Viewer
	XP_054171230	(Get FASTA)	NCBI Sequence Viewer
	XP_054171231	(Get FASTA)	NCBI Sequence Viewer
	XP_054171232	(Get FASTA)	NCBI Sequence Viewer
	XP_054171233	(Get FASTA)	NCBI Sequence Viewer
	XP_054171234	(Get FASTA)	NCBI Sequence Viewer
	XP_054171235	(Get FASTA)	NCBI Sequence Viewer
	XP_054171236	(Get FASTA)	NCBI Sequence Viewer
	XP_054171237	(Get FASTA)	NCBI Sequence Viewer
	XP_054171238	(Get FASTA)	NCBI Sequence Viewer
	XP_054171239	(Get FASTA)	NCBI Sequence Viewer
	XP_054171240	(Get FASTA)	NCBI Sequence Viewer
	XP_054171241	(Get FASTA)	NCBI Sequence Viewer
	XP_054171242	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH35021	(Get FASTA)	NCBI Sequence Viewer
	AEE61238	(Get FASTA)	NCBI Sequence Viewer
	BAC04044	(Get FASTA)	NCBI Sequence Viewer
	BAC05079	(Get FASTA)	NCBI Sequence Viewer
	BAG53812	(Get FASTA)	NCBI Sequence Viewer
	CBH19437	(Get FASTA)	NCBI Sequence Viewer
	EAW94337	(Get FASTA)	NCBI Sequence Viewer
	EAW94338	(Get FASTA)	NCBI Sequence Viewer
	EAW94339	(Get FASTA)	NCBI Sequence Viewer
	EAW94340	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000311496
	ENSP00000311496.5
	ENSP00000416177
	ENSP00000416177.2
	ENSP00000443746
	ENSP00000463080
	ENSP00000464220
GenBank Protein	Q8NA82	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_689811 ⟸ NM_152598
- Peptide Label:	isoform 1
- UniProtKB:	Q8IYS7 (UniProtKB/Swiss-Prot), D3DU09 (UniProtKB/Swiss-Prot), Q8N7Z7 (UniProtKB/Swiss-Prot), Q8NA82 (UniProtKB/Swiss-Prot), A0A140VKA1 (UniProtKB/TrEMBL), B3KVK0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLHDARDRQKFFSDVQYLRDMQHKVDSEYQACLRRQEYRRDPNEKKRDQFWGQETSFERSRFSSRSSSKQSSSEEDALTEPRSSIKISAFKCDSKLPAIDQTSVKQKHKSTMTVRKAEKVDPSEPSPA DQAPMVLLRKRKPNLRRFTVSPESHSPRASGDRSRQKQQWPAKVPVPRGADQVVQQEGLMCNTKLKRPNQERRNLVPSSQPMTENAPDRAKKGDPSAPSQSELHPALSQAFQGKNSPQVLSEFSGPPL TPTTVGGPRKASFRFRDEDFYSILSLNSRRESDDTEEETQSEECLWVGVRSPCSPSHHKRSRFGGTSTPQAKNKNFEENAENCRGHSSRRSEPSHGSLRISNAMEPATERPSAGQRLSQDPGLPDRES ATEKDRGGSENAKKSPLSWDTKSEPRQEVGVNAENVWSDCISVEHRPGTHDSEGYWKDYLNSSQNSLDYFISGRPISPRSSVNSSYNPPASFMHSALRDDIPVDLSMSSTSVHSSDSEGNSGFHVCQP LSPIRNRTPFASAENHNYFPVNSAHEFAVREAEDTTLTSQPQGAPLYTDLLLNPQGNLSLVDSSSSSPSRMNSEGHLHVSGSLQENTPFTFFAVSHFPNQNDNGSRMAASGFTDEKETSKIKADPEKL KKLQESLLEEDSEEEGDLCRICQIAGGSPSNPLLEPCGCVGSLQFVHQECLKKWLKVKITSGADLGAVKTCEMCKQGLLVDLGDFNMIEFYQKHQQSQAQNELMNSGLYLVLLLHLYEQRFAELMRLN HNQVERERLSRNYPQPRTEENENSELGDGNEGSISQSQVV hide sequence

RefSeq Acc Id:	NP_001094345 ⟸ NM_001100875
- Peptide Label:	isoform 1
- UniProtKB:	Q8IYS7 (UniProtKB/Swiss-Prot), D3DU09 (UniProtKB/Swiss-Prot), Q8N7Z7 (UniProtKB/Swiss-Prot), Q8NA82 (UniProtKB/Swiss-Prot), A0A140VKA1 (UniProtKB/TrEMBL), B3KVK0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLHDARDRQKFFSDVQYLRDMQHKVDSEYQACLRRQEYRRDPNEKKRDQFWGQETSFERSRFSS RSSSKQSSSEEDALTEPRSSIKISAFKCDSKLPAIDQTSVKQKHKSTMTVRKAEKVDPSEPSPADQAPMVLLRKRKPNLRRFTVSPESHSPRASGDRSRQKQQWPAKVPVPRGADQVVQQEGLMCNTK LKRPNQERRNLVPSSQPMTENAPDRAKKGDPSAPSQSELHPALSQAFQGKNSPQVLSEFSGPPLTPTTVGGPRKASFRFRDEDFYSILSLNSRRESDDTEEETQSEECLWVGVRSPCSPSHHKRSRFG GTSTPQAKNKNFEENAENCRGHSSRRSEPSHGSLRISNAMEPATERPSAGQRLSQDPGLPDRESATEKDRGGSENAKKSPLSWDTKSEPRQEVGVNAENVWSDCISVEHRPGTHDSEGYWKDYLNSSQ NSLDYFISGRPISPRSSVNSSYNPPASFMHSALRDDIPVDLSMSSTSVHSSDSEGNSGFHVCQPLSPIRNRTPFASAENHNYFPVNSAHEFAVREAEDTTLTSQPQGAPLYTDLLLNPQGNLSLVDSS SSSPSRMNSEGHLHVSGSLQENTPFTFFAVSHFPNQNDNGSRMAASGFTDEKETSKIKADPEKLKKLQESLLEEDSEEEGDLCRICQIAGGSPSNPLLEPCGCVGSLQFVHQECLKKWLKVKITSGAD LGAVKTCEMCKQGLLVDLGDFNMIEFYQKHQQSQAQNELMNSGLYLVLLLHLYEQRFAELMRLNHNQVERERLSRNYPQPRTEENENSELGDGNEGSISQSQVV hide sequence

RefSeq Acc Id:	XP_005257159 ⟸ XM_005257102
- Peptide Label:	isoform X5
- UniProtKB:	B3KVK0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLHDARDRQKFFSDVQYLRDMQHKVDSEYQACLRRQEYRRDPNEKKRDQFWGQETSFERSRFSSRSSSKQSSSEEDALTEPRSSIKISAFKCDSKLPAIDQTSVKQKHKSTMTVRKAEKVDPSEPSPD QAPMVLLRKRKPNLRRFTVSPESHSPRASGDRSRQKQQWPAKVPVPRGADQVVQQEGLMCNTKLKRPNQERRNLVPSSQPMTENAPDRAKKGDPSAPSQSELHPALSQAFQGKNSPQVLSEFSGPPLT PTTVGGPRKASFRFRDEDFYSILSLNSRRESDDTEEETQSEECLWVGVRSPCSPSHHKRSRFGGTSTPQAKNKNFEENAENCRGHSSRRSEPSHGSLRISNAMEPATERPSAGQRLSQDPGLPDRESA TEKDRGGSENAKKSPLSWDTKSEPRQEVGVNAENVWSDCISVEHRPGTHDSEGYWKDYLNSSQNSLDYFISGRPISPRSSVNSSYNPPASFMHSALRDDIPVDLSMSSTSVHSSDSEGNSGFHVCQPL SPIRNRTPFASAENHNYFPVNSAHEFAVREAEDTTLTSQPQGAPLYTDLLLNPQGNLSLVDSSSSSPSRMNSEGHLHVSGSLQENTPFTFFAVSHFPNQNDNGSRMAASGFTDEKETSKIKADPEKLK KLQESLLEEDSEEEGDLCRICQIAGGSPSNPLLEPCGCVGSLQFVHQECLKKWLKVKITSGADLGAVKTCEMCKQGLLVDLGDFNMIEFYQKHQQSQAQNELMNSGLYLVLLLHLYEQRFAELMRLNH NQVERERIRSWEMEMKAAFLKARSSSKEANCGARRRPLPPALLSTSPSASLPPPLY hide sequence

RefSeq Acc Id:	XP_005257157 ⟸ XM_005257100
- Peptide Label:	isoform X4
- UniProtKB:	B3KVK0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLHDARDRQKFFSDVQYLRDMQHKVDSEYQACLRRQEYRRDPNEKKRDQFWGQETSFERSRFSS RSSSKQSSSEEDALTEPRSSIKISAFKCDSKLPAIDQTSVKQKHKSTMTVRKAEKVDPSEPSPADQAPMVLLRKRKPNLRRFTVSPESHSPRASGDRSRQKQQWPAKVPVPRGADQVVQQEGLMCNTK LKRPNQERRNLVPSSQPMTENAPDRAKKGDPSAPSQSELHPALSQAFQGKNSPQVLSEFSGPPLTPTTVGGPRKASFRFRDEDFYSILSLNSRRESDDTEEETQSEECLWVGVRSPCSPSHHKRSRFG GTSTPQAKNKNFEENAENCRGHSSRRSEPSHGSLRISNAMEPATERPSAGQRLSQDPGLPDRESATEKDRGGSENAKKSPLSWDTKSEPRQEVGVNAENVWSDCISVEHRPGTHDSEGYWKDYLNSSQ NSLDYFISGRPISPRSSVNSSYNPPASFMHSALRDDIPVDLSMSSTSVHSSDSEGNSGFHVCQPLSPIRNRTPFASAENHNYFPVNSAHEFAVREAEDTTLTSQPQGAPLYTDLLLNPQGNLSLVDSS SSSPSRMNSEGHLHVSGSLQENTPFTFFAVSHFPNQNDNGSRMAASGFTDEKETSKIKADPEKLKKLQESLLEEDSEEEGDLCRICQIAGGSPSNPLLEPCGCVGSLQFVHQECLKKWLKVKITSGAD LGAVKTCEMCKQGLLVDLGDFNMIEFYQKHQQSQAQNELMNSGLYLVLLLHLYEQRFAELMRLNHNQVERERIRSWEMEMKAAFLKARSSSKEANCGARRRPLPPALLSTSPSASLPPPLY hide sequence

RefSeq Acc Id:	XP_005257155 ⟸ XM_005257098
- Peptide Label:	isoform X2
- UniProtKB:	B3KVK0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLHDARDRQKFFSDVQYLRDMQHKVDSEYQACLRRQEYRRDPNEKKRDQFWGQETSFERSRFSSRSSSKQSSSEEDALTEPRSSIKISAFKCDSKLPAIDQTSVKQKHKSTMTVRKAEKVDPSEPSPE SEPTWWNKPETDLGGPSGWCSLGKKGPMSRSIPPCEADQAPMVLLRKRKPNLRRFTVSPESHSPRASGDRSRQKQQWPAKVPVPRGADQVVQQEGLMCNTKLKRPNQERRNLVPSSQPMTENAPDRAK KGDPSAPSQSELHPALSQAFQGKNSPQVLSEFSGPPLTPTTVGGPRKASFRFRDEDFYSILSLNSRRESDDTEEETQSEECLWVGVRSPCSPSHHKRSRFGGTSTPQAKNKNFEENAENCRGHSSRRS EPSHGSLRISNAMEPATERPSAGQRLSQDPGLPDRESATEKDRGGSENAKKSPLSWDTKSEPRQEVGVNAENVWSDCISVEHRPGTHDSEGYWKDYLNSSQNSLDYFISGRPISPRSSVNSSYNPPAS FMHSALRDDIPVDLSMSSTSVHSSDSEGNSGFHVCQPLSPIRNRTPFASAENHNYFPVNSAHEFAVREAEDTTLTSQPQGAPLYTDLLLNPQGNLSLVDSSSSSPSRMNSEGHLHVSGSLQENTPFTF FAVSHFPNQNDNGSRMAASGFTDEKETSKIKADPEKLKKLQESLLEEDSEEEGDLCRICQIAGGSPSNPLLEPCGCVGSLQFVHQECLKKWLKVKITSGADLGAVKTCEMCKQGLLVDLGDFNMIEFY QKHQQSQAQNELMNSGLYLVLLLHLYEQRFAELMRLNHNQVERERIRSWEMEMKAAFLKARSSSKEANCGARRRPLPPALLSTSPSASLPPPLY hide sequence

Protein Domains

RING-CH-type

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q8NA82-F1-model_v2	AlphaFold	Q8NA82	1-808	view protein structure

RGD ID:

7235933

Promoter ID:

EPDNEW_H23712

Type:

initiation region

Name:

MARCH10_1

Description:

membrane associated ring-CH-type finger 10

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	17	62,808,290 - 62,808,350	EPDNEW

Database	Acc Id	Source(s)
COSMIC	MARCHF10	COSMIC
Ensembl Genes	ENSG00000173838	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000311269	ENTREZGENE
	ENST00000311269.10	UniProtKB/Swiss-Prot
	ENST00000456609	ENTREZGENE
	ENST00000456609.6	UniProtKB/Swiss-Prot
	ENST00000544856	ENTREZGENE
	ENST00000580520	ENTREZGENE
	ENST00000583600	ENTREZGENE
Gene3D-CATH	3.30.40.10	UniProtKB/Swiss-Prot
GTEx	ENSG00000173838	GTEx
HGNC ID	HGNC:26655	ENTREZGENE
Human Proteome Map	MARCHF10	Human Proteome Map
InterPro	MARCH10_RING_CH-C4HC3	UniProtKB/Swiss-Prot
	RING-CH-type_E3_ubiq-ligase	UniProtKB/Swiss-Prot
	Znf_RING-CH	UniProtKB/Swiss-Prot
	Znf_RING/FYVE/PHD	UniProtKB/Swiss-Prot
KEGG Report	hsa:162333	UniProtKB/Swiss-Prot
NCBI Gene	162333	ENTREZGENE
OMIM	613337	OMIM
PANTHER	E3 UBIQUITIN-PROTEIN LIGASE MARCHF10-RELATED	UniProtKB/Swiss-Prot
	MARCH7/10 E3 UBIQUITIN PROTEIN LIGASE FAMILY MEMBER	UniProtKB/Swiss-Prot
Pfam	RINGv	UniProtKB/Swiss-Prot
PharmGKB	PA166351956	PharmGKB
PROSITE	ZF_RING_CH	UniProtKB/Swiss-Prot
SMART	RINGv	UniProtKB/Swiss-Prot
Superfamily-SCOP	RING/U-box	UniProtKB/Swiss-Prot
UniProt	A0A140VKA1	ENTREZGENE, UniProtKB/TrEMBL
	B3KVK0	ENTREZGENE, UniProtKB/TrEMBL
	D3DU09	ENTREZGENE
	G3V1Q5	ENTREZGENE, UniProtKB/TrEMBL
	J3KTK3_HUMAN	UniProtKB/TrEMBL
	J3KTN9	ENTREZGENE, UniProtKB/TrEMBL
	J3QLJ2_HUMAN	UniProtKB/TrEMBL
	J3QRH7	ENTREZGENE, UniProtKB/TrEMBL
	MARHA_HUMAN	UniProtKB/Swiss-Prot
	Q8IYS7	ENTREZGENE
	Q8N7Z7	ENTREZGENE
	Q8NA82	ENTREZGENE
UniProt Secondary	D3DU09	UniProtKB/Swiss-Prot
	Q8IYS7	UniProtKB/Swiss-Prot
	Q8N7Z7	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2019-07-16	MARCHF10	membrane associated ring-CH-type finger 10	MARCH10	membrane associated ring-CH-type finger 10	Symbol and/or name change	5135510	APPROVED
2015-12-01	MARCH10	membrane associated ring-CH-type finger 10	MARCH10	membrane-associated ring finger (C3HC4) 10, E3 ubiquitin protein ligase	Symbol and/or name change	5135510	APPROVED
2012-03-01	MARCH10	membrane-associated ring finger (C3HC4) 10, E3 ubiquitin protein ligase	MARCH10	membrane-associated ring finger (C3HC4) 10	Symbol and/or name change	5135510	APPROVED

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


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


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