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Gene: HROB (homologous recombination factor with OB-fold) Homo sapiens

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Symbol:

HROB

Name:

homologous recombination factor with OB-fold

RGD ID:

1602101

HGNC Page

HGNC:28460

Description:

Predicted to enable single-stranded DNA binding activity. Involved in DNA synthesis involved in DNA repair and interstrand cross-link repair. Located in site of DNA damage.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C17orf53; chromosome 17 open reading frame 53; FLJ11594; homologous recombincation factor with OB-fold; hypothetical protein LOC78995; MCM8-9-Interacting Protein); MCM8IP; MGC3130; ODG11; uncharacterized protein C17orf53

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	44,141,930 - 44,162,476 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	44,141,906 - 44,162,476 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	42,219,298 - 42,239,844 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	39,574,852 - 39,595,369 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	17	38,927,986 - 38,948,557 (+)	NCBI		Celera
Cytogenetic Map	17	q21.31	NCBI
HuRef	17	37,983,300 - 38,003,871 (+)	NCBI		HuRef
CHM1_1	17	42,454,660 - 42,475,226 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
HROB	Human	GRN-related frontotemporal lobar degeneration with TDP43 inclusions		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: GRN-related frontotemporal lobar degeneration with Tdp43 inclusions	ClinVar	PMID:28492532
HROB	Human	hereditary breast ovarian cancer syndrome		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Breast-ovarian cancer more ...	ClinVar	PMID:38922859
HROB	Human	Ovarian Dysgenesis 11		IAGP	(Homo sapiens) and (Homo sapiens)	8554872	ClinVar Annotator: match by term: Ovarian dysgenesis 11	ClinVar	PMID:38105698
HROB	Human	Ovarian Dysgenesis 11		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Ovarian dysgenesis 11	ClinVar	PMID:34707299
HROB	Human	primary ovarian insufficiency		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Premature ovarian insufficiency	ClinVar	PMID:34707299

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
HROB	Human	Ovarian Dysgenesis 11		IAGP		7240710		OMIM

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
HROB	Human	17beta-estradiol	multiple interactions	ISO	Hrob (Rattus norvegicus)	6480464	[estradiol 3-benzoate co-treated with [Testosterone co-treated with Estradiol]] results in increased expression of HROB mRNA	CTD	PMID:32741896
HROB	Human	17beta-estradiol 3-benzoate	multiple interactions	ISO	Hrob (Rattus norvegicus)	6480464	[estradiol 3-benzoate co-treated with [Testosterone co-treated with Estradiol]] results in increased expression of HROB mRNA	CTD	PMID:32741896
HROB	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	Hrob (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin results in increased expression of HROB mRNA	CTD	PMID:33387578
HROB	Human	acrylamide	decreases expression	EXP		6480464	Acrylamide results in decreased expression of HROB mRNA	CTD	PMID:32763439
HROB	Human	aflatoxin B1	increases expression	EXP		6480464	Aflatoxin B1 results in increased expression of HROB mRNA	CTD	PMID:22100608
HROB	Human	all-trans-retinoic acid	decreases expression	EXP		6480464	Tretinoin results in decreased expression of HROB mRNA	CTD	PMID:33167477
HROB	Human	aristolochic acid A	increases expression	EXP		6480464	aristolochic acid I results in increased expression of HROB mRNA	CTD	PMID:33212167
HROB	Human	arsane	multiple interactions	EXP		6480464	[sodium arsenate results in increased abundance of Arsenic] which results in increased expression of HROB mRNA	CTD	PMID:32525701
HROB	Human	arsenic atom	multiple interactions	EXP		6480464	[sodium arsenate results in increased abundance of Arsenic] which results in increased expression of HROB mRNA	CTD	PMID:32525701
HROB	Human	benzo[a]pyrene	affects methylation	EXP		6480464	Benzo(a)pyrene affects the methylation of HROB promoter	CTD	PMID:27901495
HROB	Human	benzo[a]pyrene	increases expression	EXP		6480464	Benzo(a)pyrene results in increased expression of HROB mRNA	CTD	PMID:32234424
HROB	Human	bisphenol A	decreases expression	ISO	Hrob (Rattus norvegicus)	6480464	bisphenol A results in decreased expression of HROB mRNA	CTD	PMID:25181051
HROB	Human	bisphenol A	increases expression	EXP		6480464	bisphenol A results in increased expression of HROB mRNA	CTD	PMID:36232920
HROB	Human	bisphenol A	increases expression	ISO	Hrob (Rattus norvegicus)	6480464	bisphenol A results in increased expression of HROB mRNA	CTD	PMID:32145629
HROB	Human	bisphenol A	multiple interactions	ISO	Hrob (Rattus norvegicus)	6480464	[bisphenol A co-treated with tributyltin] results in decreased expression of HROB mRNA	CTD	PMID:31129395
HROB	Human	bisphenol A	decreases expression	EXP		6480464	bisphenol A results in decreased expression of HROB mRNA	CTD	PMID:27685785 and PMID:29275510
HROB	Human	cadmium dichloride	decreases expression	ISO	Hrob (Rattus norvegicus)	6480464	Cadmium Chloride results in decreased expression of HROB mRNA	CTD	PMID:33453195
HROB	Human	calcitriol	multiple interactions	EXP		6480464	[Testosterone co-treated with Calcitriol] results in decreased expression of HROB mRNA	CTD	PMID:21592394
HROB	Human	calcitriol	decreases expression	EXP		6480464	Calcitriol results in decreased expression of HROB mRNA	CTD	PMID:21592394
HROB	Human	cannabidiol	increases expression	EXP		6480464	Cannabidiol results in increased expression of HROB mRNA	CTD	PMID:27918106
HROB	Human	cisplatin	increases expression	EXP		6480464	Cisplatin results in increased expression of HROB mRNA	CTD	PMID:27392435
HROB	Human	cisplatin	multiple interactions	EXP		6480464	[Cisplatin co-treated with jinfukang] results in increased expression of HROB mRNA	CTD	PMID:27392435
HROB	Human	copper(II) sulfate	decreases expression	EXP		6480464	Copper Sulfate results in decreased expression of HROB mRNA	CTD	PMID:19549813
HROB	Human	diquat	decreases expression	ISO	Hrob (Mus musculus)	6480464	Diquat results in decreased expression of HROB mRNA	CTD	PMID:36851058
HROB	Human	doxorubicin	decreases expression	EXP		6480464	Doxorubicin results in decreased expression of HROB mRNA	CTD	PMID:29803840
HROB	Human	FR900359	increases phosphorylation	EXP		6480464	FR900359 results in increased phosphorylation of HROB protein	CTD	PMID:37730182
HROB	Human	gentamycin	increases expression	ISO	Hrob (Rattus norvegicus)	6480464	Gentamicins results in increased expression of HROB mRNA	CTD	PMID:33387578
HROB	Human	methyl methanesulfonate	increases expression	EXP		6480464	Methyl Methanesulfonate results in increased expression of HROB mRNA	CTD	PMID:23649840
HROB	Human	N-methyl-4-phenylpyridinium	decreases expression	EXP		6480464	1-Methyl-4-phenylpyridinium results in decreased expression of HROB mRNA	CTD	PMID:24810058
HROB	Human	ozone	multiple interactions	ISO	Hrob (Mus musculus)	6480464	[Air Pollutants results in increased abundance of [Ozone co-treated with Soot]] which results in increased expression of HROB mRNA and [Air Pollutants results in increased abundance of Ozone] which results in increased expression of HROB mRNA	CTD	PMID:34911549
HROB	Human	paracetamol	increases expression	EXP		6480464	Acetaminophen results in increased expression of HROB mRNA	CTD	PMID:22230336
HROB	Human	paracetamol	increases expression	ISO	Hrob (Rattus norvegicus)	6480464	Acetaminophen results in increased expression of HROB mRNA	CTD	PMID:33387578
HROB	Human	paracetamol	decreases expression	EXP		6480464	Acetaminophen results in decreased expression of HROB mRNA	CTD	PMID:29067470
HROB	Human	potassium chromate	increases expression	EXP		6480464	potassium chromate(VI) results in increased expression of HROB mRNA	CTD	PMID:22714537
HROB	Human	silicon dioxide	increases expression	ISO	Hrob (Mus musculus)	6480464	Silicon Dioxide results in increased expression of HROB mRNA	CTD	PMID:29341224
HROB	Human	sodium arsenate	multiple interactions	EXP		6480464	[sodium arsenate results in increased abundance of Arsenic] which results in increased expression of HROB mRNA	CTD	PMID:32525701
HROB	Human	sodium arsenite	decreases expression	EXP		6480464	sodium arsenite results in decreased expression of HROB mRNA	CTD	PMID:38568856
HROB	Human	sunitinib	decreases expression	EXP		6480464	Sunitinib results in decreased expression of HROB mRNA	CTD	PMID:31533062
HROB	Human	testosterone	decreases expression	EXP		6480464	Testosterone results in decreased expression of HROB mRNA	CTD	PMID:21592394
HROB	Human	testosterone	multiple interactions	ISO	Hrob (Rattus norvegicus)	6480464	[estradiol 3-benzoate co-treated with [Testosterone co-treated with Estradiol]] results in increased expression of HROB mRNA	CTD	PMID:32741896
HROB	Human	testosterone	multiple interactions	EXP		6480464	[Testosterone co-treated with Calcitriol] results in decreased expression of HROB mRNA	CTD	PMID:21592394
HROB	Human	tributylstannane	multiple interactions	ISO	Hrob (Rattus norvegicus)	6480464	[bisphenol A co-treated with tributyltin] results in decreased expression of HROB mRNA	CTD	PMID:31129395
HROB	Human	trichloroethene	increases expression	ISO	Hrob (Rattus norvegicus)	6480464	Trichloroethylene results in increased expression of HROB mRNA	CTD	PMID:33387578

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)
HROB	Human	DNA biosynthetic process	involved_in	IEA	UniProtKB-KW:KW-0237	150520179		UniProt	GO_REF:0000043
HROB	Human	DNA damage response	involved_in	IMP		150520179	PMID:31467087	UniProt	PMID:31467087
HROB	Human	DNA damage response	involved_in	IEA	UniProtKB-KW:KW-0227	150520179		UniProt	GO_REF:0000043
HROB	Human	DNA recombination	involved_in	IEA	UniProtKB-KW:KW-0233	150520179		UniProt	GO_REF:0000043
HROB	Human	DNA repair	involved_in	IEA	UniProtKB-KW:KW-0234	150520179		UniProt	GO_REF:0000043
HROB	Human	DNA synthesis involved in DNA repair	involved_in	IMP		150520179	PMID:31467087	UniProt	PMID:31467087
HROB	Human	female gamete generation	involved_in	ISS	UniProtKB:Q32P12	150520179		UniProt	GO_REF:0000024
HROB	Human	female gamete generation	involved_in	IEA	UniProtKB:Q32P12 and ensembl:ENSMUSP00000097961	150520179		Ensembl	GO_REF:0000107
HROB	Human	interstrand cross-link repair	involved_in	IMP		150520179	PMID:31467087	UniProt	PMID:31467087
HROB	Human	male gamete generation	involved_in	IEA	UniProtKB:Q32P12 and ensembl:ENSMUSP00000097961	150520179		Ensembl	GO_REF:0000107
HROB	Human	male gamete generation	involved_in	ISS	UniProtKB:Q32P12	150520179		UniProt	GO_REF:0000024
HROB	Human	recombinational repair	involved_in	IEA	InterPro:IPR028045	150520179		InterPro	GO_REF:0000002

Cellular Component

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
HROB	Human	chromosome	located_in	IEA	UniProtKB-SubCell:SL-0468	150520179		UniProt	GO_REF:0000044
HROB	Human	chromosome	located_in	IEA	UniProtKB-KW:KW-0158	150520179		UniProt	GO_REF:0000043
HROB	Human	nucleus	located_in	IEA	UniProtKB-SubCell:SL-0191	150520179		UniProt	GO_REF:0000044
HROB	Human	nucleus	located_in	IEA	UniProtKB-KW:KW-0539	150520179		UniProt	GO_REF:0000043
HROB	Human	site of DNA damage	located_in	IMP		150520179	PMID:31467087	UniProt	PMID:31467087

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)
HROB	Human	DNA binding	enables	IEA	UniProtKB-KW:KW-0238	150520179		UniProt	GO_REF:0000043
HROB	Human	protein binding	enables	IPI	UniProtKB:Q9UJA3	150520179	PMID:31467087	UniProt	PMID:31467087
HROB	Human	protein binding	enables	IPI	UniProtKB:Q9UPY8	150520179	PMID:32296183	IntAct	PMID:32296183
HROB	Human	single-stranded DNA binding	enables	IEA	UniProtKB:Q32P12 and ensembl:ENSMUSP00000097961	150520179		Ensembl	GO_REF:0000107
HROB	Human	single-stranded DNA binding	enables	ISS	UniProtKB:Q32P12	150520179		UniProt	GO_REF:0000024

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
HROB	Human	Aplasia of the ovary		IAGP		8699517		HPO	MIM:620897
HROB	Human	Autosomal recessive inheritance		IAGP		8699517		HPO	MIM:620897
HROB	Human	Decreased circulating antimullerian hormone circulation		IAGP		8699517		HPO	MIM:620897
HROB	Human	Decreased serum estradiol		IAGP		8699517		HPO	MIM:620897
HROB	Human	Delayed menarche		IAGP		8699517		HPO	MIM:620897
HROB	Human	Delayed puberty		IAGP		8699517		HPO	MIM:620897
HROB	Human	Early young adult onset		IAGP		8699517		HPO	MIM:620897
HROB	Human	Elevated circulating follicle stimulating hormone level		IAGP		8699517		HPO	MIM:620897
HROB	Human	Elevated circulating luteinizing hormone level		IAGP		8699517		HPO	MIM:620897
HROB	Human	Juvenile onset		IAGP		8699517		HPO	MIM:620897
HROB	Human	Primary amenorrhea		IAGP		8699517		HPO	MIM:620897

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
HROB	Human	Premature ovarian insufficiency		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Premature ovarian insufficiency	ClinVar	PMID:34707299

#	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:19079262	PMID:21873635	PMID:22504420	PMID:23455924	PMID:24163370	PMID:25814554	PMID:26496610	PMID:26673895	PMID:26972000	PMID:27107014
PMID:28514442	PMID:28718761	PMID:29395067	PMID:30370607	PMID:31391242	PMID:31467087	PMID:32296183	PMID:32528060	PMID:32853826	PMID:33961781	PMID:34373451	PMID:34707299
PMID:35271311	PMID:35559673	PMID:37827155	PMID:38360978	PMID:38678026

HROB
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	44,141,906 - 44,162,476 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	42,219,298 - 42,239,844 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	39,574,852 - 39,595,369 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	17	38,927,986 - 38,948,557 (+)	NCBI		Celera
Cytogenetic Map	17	q21.31	NCBI
HuRef	17	37,983,300 - 38,003,871 (+)	NCBI		HuRef
CHM1_1	17	42,454,660 - 42,475,226 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI		T2T-CHM13v2.0

Hrob
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	11	102,139,677 - 102,156,009 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	11	102,139,708 - 102,156,013 (+)	Ensembl		GRCm39 Ensembl
GRCm38	11	102,248,857 - 102,265,183 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	11	102,248,882 - 102,265,187 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	11	102,110,196 - 102,126,497 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	11	102,064,975 - 102,081,268 (+)	NCBI		MGSCv36	mm8
Celera	11	113,955,724 - 113,972,051 (+)	NCBI		Celera
Cytogenetic Map	11	D	NCBI
cM Map	11	66.21	NCBI

Hrob
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	10	87,705,846 - 87,722,635 (+)	NCBI		GRCr8
mRatBN7.2	10	87,206,017 - 87,222,483 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	10	87,206,049 - 87,222,483 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	10	92,235,757 - 92,252,069 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	10	91,707,723 - 91,724,057 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	10	87,101,040 - 87,117,376 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	10	90,192,608 - 90,214,486 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	10	90,192,627 - 90,214,486 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	10	89,978,419 - 90,001,064 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	10	91,329,706 - 91,347,594 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	10	91,344,075 - 91,361,964 (+)	NCBI
Celera	10	85,922,100 - 85,938,261 (+)	NCBI		Celera
Cytogenetic Map	10	q32.1	NCBI

Hrob
(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	NW_004955451	17,256,593 - 17,264,872 (+)	NCBI	ChiLan1.0	ChiLan1.0

HROB
(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	20,744,231 - 20,767,556 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	17	22,708,577 - 22,731,897 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	17	13,233,464 - 13,254,726 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	17	13,395,473 - 13,415,346 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	17	13,395,473 - 13,409,505 (-)	Ensembl	panpan1.1		panPan2

HROB
(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	19,230,345 - 19,245,518 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	9	19,230,399 - 19,245,624 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	9	18,621,143 - 18,636,309 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	9	19,926,089 - 19,941,286 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	9	19,926,137 - 19,941,347 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	9	18,779,466 - 18,794,637 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	9	18,962,526 - 18,977,694 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	9	19,107,482 - 19,122,654 (-)	NCBI		UU_Cfam_GSD_1.0

Hrob
(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	18,559,665 - 18,575,134 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936541	620,754 - 633,499 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936541	619,120 - 633,590 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

HROB
(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	19,044,043 - 19,077,829 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	12	19,044,569 - 19,077,877 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	12	19,338,655 - 19,344,491 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

HROB
(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	62,230,588 - 62,251,090 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	16	62,230,261 - 62,250,734 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666077	32,998,346 - 33,023,368 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Hrob
(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 1.0	NW_004624795	799,533 - 806,876 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in HROB
8 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
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
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 17q12-21.31(chr17:39199873-45629579)x3	copy number gain	See cases [RCV000052479]	Chr17:39199873..45629579 [GRCh38] Chr17:37356126..43706945 [GRCh37] Chr17:34609652..41062728 [NCBI36] Chr17:17q12-21.31	pathogenic
GRCh38/hg38 17q21.31(chr17:43570878-44762377)x1	copy number loss	See cases [RCV000053429]	Chr17:43570878..44762377 [GRCh38] Chr17:41648246..42839745 [GRCh37] Chr17:39003772..40195271 [NCBI36] Chr17:17q21.31	pathogenic
NM_001171251.1(C17orf53):c.54+17G>A	single nucleotide variant	Lung cancer [RCV000100472]	Chr17:44145270 [GRCh38] Chr17:42222638 [GRCh37] Chr17:17q21.31	uncertain significance
GRCh38/hg38 17q21.31(chr17:43934167-44854025)x1	copy number loss	See cases [RCV000134949]	Chr17:43934167..44854025 [GRCh38] Chr17:42011535..42931393 [GRCh37] Chr17:39367061..40286919 [NCBI36] Chr17:17q21.31	pathogenic
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
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
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(chr17:8547-81060040)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 17p13.3-q25.3(chr17:12344-81057996)x3	copy number gain	not provided [RCV000739325]	Chr17:12344..81057996 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
NC_000017.11:g.(?_44027807)_(44352876_?)dup	duplication	GRN-related frontotemporal lobar degeneration with Tdp43 inclusions [RCV001032594]	Chr17:42105175..42430244 [GRCh37] Chr17:17q21.31	uncertain significance
GRCh37/hg19 17q21.31(chr17:42085508-42361563)x3	copy number gain	not provided [RCV001836539]	Chr17:42085508..42361563 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001171251.3(HROB):c.421del (p.Glu141fs)	deletion	Ovarian dysgenesis 11 [RCV004595619]\|Premature ovarian insufficiency [RCV001839427]	Chr17:44148224 [GRCh38] Chr17:42225592 [GRCh37] Chr17:17q21.31	pathogenic\|likely pathogenic\|not provided
NM_001171251.3(HROB):c.1189C>T (p.Arg397Cys)	single nucleotide variant	not specified [RCV004402341]	Chr17:44148992 [GRCh38] Chr17:42226360 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001171251.3(HROB):c.190C>T (p.His64Tyr)	single nucleotide variant	not specified [RCV004402342]	Chr17:44147993 [GRCh38] Chr17:42225361 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001171251.3(HROB):c.527G>T (p.Cys176Phe)	single nucleotide variant	not specified [RCV004402343]	Chr17:44148330 [GRCh38] Chr17:42225698 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001171251.3(HROB):c.718C>T (p.Arg240Ter)	single nucleotide variant	Ovarian dysgenesis 11 [RCV004595818]	Chr17:44148521 [GRCh38] Chr17:42225889 [GRCh37] Chr17:17q21.31	pathogenic\|not provided
NM_001171251.3(HROB):c.1351C>T (p.Arg451Ter)	single nucleotide variant	Ovarian dysgenesis 11 [RCV004595819]	Chr17:44152679 [GRCh38] Chr17:42230047 [GRCh37] Chr17:17q21.31	pathogenic\|not provided
GRCh37/hg19 17q12-22(chr17:41196270-41277589)	copy number loss	Breast-ovarian cancer, familial, susceptibility to, 1 [RCV004759419]	Chr17:41196270..41277589 [GRCh37] Chr17:17q12-22	pathogenic
Single allele	deletion	Breast-ovarian cancer, familial, susceptibility to, 1 [RCV004759420]	Chr17:41231503..41277589 [GRCh37] Chr17:17q21.31-22	pathogenic

Predicted Target Of

	Summary Value
Count of predictions:	1761
Count of miRNA genes:	617
Interacting mature miRNAs:	701
Transcripts:	ENST00000245382, ENST00000319977, ENST00000585683, ENST00000588073, ENST00000588434
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
597337193	GWAS1433267_H	sexual dimorphism measurement QTL GWAS1433267 (human)		6e-10	sexual dimorphism measurement		17	44156835	44156836	Human
597514745	GWAS1610819_H	anthropometric measurement QTL GWAS1610819 (human)		3e-08	anthropometric measurement	body morphological measurement (CMO:0000021)	17	44162193	44162194	Human
407045480	GWAS694456_H	femoral neck bone mineral density QTL GWAS694456 (human)		3e-24	bone mineralization trait (VT:0002896)	bone mineral density (CMO:0001226)	17	44148179	44148180	Human
597616914	GWAS1673774_H	osteoporosis QTL GWAS1673774 (human)		4e-11	osteoporosis		17	44143542	44143543	Human

MARC_17439-17440:1022701360:3

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	42,232,264 - 42,232,736	UniSTS	GRCh37
Build 36	17	39,587,790 - 39,588,262	RGD	NCBI36
Celera	17	38,940,976 - 38,941,448	RGD
HuRef	17	37,996,290 - 37,996,762	UniSTS

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2438	2787	2250	4964	1725	2351	6	623	1950	465	2269	7298	6465	53	3726	1	850	1740	1616	173	1


RefSeq Transcripts	NM_001171251	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001321310	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001321311	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_024032	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525187	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525188	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525189	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525190	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525191	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525192	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525193	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525194	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525195	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525197	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436676	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436677	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436678	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436679	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436680	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436681	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436682	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436683	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436684	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436685	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436686	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436687	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436688	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436689	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436690	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436691	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436692	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436693	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436694	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317091	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317092	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317093	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317094	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317095	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317096	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317097	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317098	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317099	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317100	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317101	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317102	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317103	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317104	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317105	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317106	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317107	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317108	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317109	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317110	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317111	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317112	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317113	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317114	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317115	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317116	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317117	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317118	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317119	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_002958064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_934545	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC004596	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK021656	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK291924	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL834295	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC000121	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI829278	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471178	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC350778	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY032119	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000245382 ⟹ ENSP00000245382

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	44,142,022 - 44,162,476 (+)	Ensembl

Ensembl Acc Id:

ENST00000319977 ⟹ ENSP00000313500

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	44,141,906 - 44,162,476 (+)	Ensembl

Ensembl Acc Id:

ENST00000585683 ⟹ ENSP00000466618

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	44,141,930 - 44,162,476 (+)	Ensembl

Ensembl Acc Id:

ENST00000588073

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	44,154,360 - 44,162,004 (+)	Ensembl

Ensembl Acc Id:

ENST00000588434

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	44,147,771 - 44,152,767 (+)	Ensembl

RefSeq Acc Id:

NM_001171251 ⟹ NP_001164722

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI
GRCh37	17	42,219,274 - 42,239,844 (+)	RGD
Celera	17	38,927,986 - 38,948,557 (+)	RGD
HuRef	17	37,983,300 - 38,003,871 (+)	ENTREZGENE
CHM1_1	17	42,454,656 - 42,475,226 (+)	NCBI
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

Sequence:

show sequence

AGTGGCGGCGTCTTCGAATGCGGCCTAAGGCGCCTGCCGCCAGTCTCCTGGCGACTTTCCCTATATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCC
ACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGCCGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGT
TTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCCTGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCC
TCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACCTCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCC
CCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAAGTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCC
AACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAGCATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATC
CTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTGGATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGA
GTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGTCACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGC
AACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCCTCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCAT
TTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTATTTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCC
AAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACTGCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCC
CTGGCCCAGCTGGGATCCTGCCTCACCAGCAGAGTGGGAGAAGTCTGGAGGACATCATGGTTTCCGCGCCCCAAACTCCAACCCATGGTGCTCTGGCTAAATTCCAGACAGAGATTGTTGCTAGTTCC
CAGGCATCTGTGGAGGAGGATTTTGGGCGAGGGCCCTGGCTGACCATGAAATCCACGCTAGGCCTGGATGAGAGAGACCCTAGCTGCTTCCTCTGTACCTACAGCATTGTCATGGTGCTGCGCAAGGC
AGCCCTGAAGCAGCTTCCTAGGAACAAGGTCCCCAACATGGCGGTGATGATCAAGTCCCTGACTCGGAGCACAATGGACGCCAGTGTGGTTTTCAAGGACCCCACGGGAGAGATGCAGGGGACGGTGC
ACAGGTTGCTGCTGGAGACGTGCCAGAATGAGCTGAAGCCTGGCTCAGTGCTGCTGCTGAAGCAGATTGGAGTGTTTTCTCCTTCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTGGTC
CATATTTACAGCCCGGATTCTGGGGATGGGAGCTTCCTCAAGCCATCTCAGCCCTTCCCCAAGGATTCAGGGAGCTTCCAGCATGATGTGGCTGCAAAGCCCGAGGAAGGCTTCAGAACAGCACAGAA
CCTAGAGGCAGAGGCGTCCCCTGAGGAAGAACTCCCAGAAGCAGATGACCTGGATGGACTCCTGAGTGAGCTTCCTGAAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAAC
CCACCATGAGCAGGCAGCTCTGGGCATGTGTCTGGTCACATCCAAGGGGGAGAAGAAGGCCAGCATGATTGGAGAGTGGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCT
GAGAGCCCCCTCATCTCTGCGCTGCCCTCACTTTGGGCCTTCCTTTGCCGTTGGCACCAGAATCCGGCCGGAGACTGGCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCT
CCTGCCTCAGCTTAATTTTAGAGGATATTGGGCCTGGTTTTCTTGTCCCTTCATACCCTAGTCCCTGGACAGCTGAGGAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGG
GGAGAAGCACGCTCAGGCTTCCTCTGCTTTGTCTCTTCAGACCTGTGGTTGCTCTGCTCATCCATGCCCAAGGTTCCCAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCA
TCTCCTGCTT

hide sequence

RefSeq Acc Id:

NM_001321310 ⟹ NP_001308239

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI
CHM1_1	17	42,454,656 - 42,475,226 (+)	NCBI
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

Sequence:

show sequence

AGTGGCGGCGTCTTCGAATGCGGCCTAAGGCGCCTGCCGCCAGTCTCCTGGCGACTTTCCCTAT
ATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCCACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGC
CGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGTTTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCC
TGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCCTCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACC
TCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCCCCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAA
GTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCCAACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAG
CATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATCCTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTG
GATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGAGTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGT
CACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGCAACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCC
TCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCATTTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTAT
TTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCCAAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACT
GCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCCCTGGCCCAGCTGGGATCCTGCCTCACCAGGCAGCCCTGAAGCAGCTTCCTAGGAACAAGGTCCC
CAACATGGCGGTGATGATCAAGTCCCTGACTCGGAGCACAATGGACGCCAGTGTGGTTTTCAAGGACCCCACGGGAGAGATGCAGGGGACGGTGCACAGGTTGCTGCTGGAGACGTGCCAGAATGAGC
TGAAGCCTGGCTCAGTGCTGCTGCTGAAGCAGATTGGAGTGTTTTCTCCTTCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTGGTCCATATTTACAGCCCGGATTCTGGGGATGGGAGC
TTCCTCAAGCCATCTCAGCCCTTCCCCAAGATGACCTGGATGGACTCCTGAGTGAGCTTCCTGAAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAACCCACCATGAGCAGG
CAGCTCTGGGCATGTGTCTGGTCACATCCAAGGGGGAGAAGAAGGCCAGCATGATTGGAGAGTGGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCTGAGAGCCCCCTCAT
CTCTGCGCTGCCCTCACTTTGGGCCTTCCTTTGCCGTTGGCACCAGAATCCGGCCGGAGACTGGCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCTCCTGCCTCAGCTTA
ATTTTAGAGGATATTGGGCCTGGTTTTCTTGTCCCTTCATACCCTAGTCCCTGGACAGCTGAGGAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGGGGAGAAGCACGCTC
AGGCTTCCTCTGCTTTGTCTCTTCAGACCTGTGGTTGCTCTGCTCATCCATGCCCAAGGTTCCCAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCATCTCCTGCTT

hide sequence

RefSeq Acc Id:

NM_001321311 ⟹ NP_001308240

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI
CHM1_1	17	42,454,656 - 42,475,226 (+)	NCBI
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

Sequence:

show sequence

AGTGGCGGCGTCTTCGAATGCGGCCTAAGGCGCCTGCCGCCAGTCTCCTGGCGACTTTCCCTATATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCC
ACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGCCGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGT
TTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCCTGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCC
TCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACCTCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCC
CCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAAGTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCC
AACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAGCATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATC
CTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTGGATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGA
GTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGTCACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGC
AACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCCTCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCAT
TTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTATTTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCC
AAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACTGCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCC
CTGGCCCAGCTGGGATCCTGCCTCACCAGAGTGGGAGAAGTCTGGAGGACATCATGGTTTCCGCGCCCCAAACTCCAACCCATGGTGCTCTGGCTAAATTCCAGACAGAGATTGTTGCTAGTTCCCAG
GCATCTGTGGAGGAGGATTTTGGGCGAGGGCCCTGGCTGACCATGAAATCCACGCTAGGCCTGGATGAGAGAGACCCTAGCTGCTTCCTCTGTACCTACAGCATTGTCATGGTGCTGCGCAAGGCAGC
CCTGAAGCAGCTTCCTAGGAACAAGGTCCCCAACATGGCGGTGATGATCAAGTCCCTGACTCGGAGCACAATGGACGCCAGTGTGGTTTTCAAGGACCCCACGGGAGAGATGCAGGGGACGGTGCACA
GGTTGCTGCTGGAGACGTGCCAGAATGAGCTGAAGCCTGGCTCAGTGCTGCTGCTGAAGCAGATTGGAGTGTTTTCTCCTTCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTGGTCCAT
ATTTACAGCCCGGATTCTGGGGATGGGAGCTTCCTCAAGCCATCTCAGCCCTTCCCCAAGGATTCAGGGAGCTTCCAGCATGATGTGGCTGCAAAGCCCGAGGAAGGCTTCAGAACAGCACAGAACCT
AGAGGCAGAGGCGTCCCCTGAGGAAGAACTCCCAGAAGCAGATGACCTGGATGGACTCCTGAGTGAGCTTCCTGAAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAACCCA
CCATGAGCAGGCAGCTCTGGGCATGTGTCTGGTCACATCCAAGGGGGAGAAGAAGGCCAGCATGATTGGAGAGTGGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCTGAG
AGCCCCCTCATCTCTGCGCTGCCCTCACTTTGGGCCTTCCTTTGCCGTTGGCACCAGAATCCGGCCGGAGACTGGCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCTCCT
GCCTCAGCTTAATTTTAGAGGATATTGGGCCTGGTTTTCTTGTCCCTTCATACCCTAGTCCCTGGACAGCTGAGGAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGGGGA
GAAGCACGCTCAGGCTTCCTCTGCTTTGTCTCTTCAGACCTGTGGTTGCTCTGCTCATCCATGCCCAAGGTTCCCAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCATCT
CCTGCTT

hide sequence

RefSeq Acc Id:

NM_024032 ⟹ NP_076937

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI
GRCh37	17	42,219,274 - 42,239,844 (+)	RGD
Build 36	17	39,574,852 - 39,595,369 (+)	NCBI Archive
Celera	17	38,927,986 - 38,948,557 (+)	RGD
HuRef	17	37,983,300 - 38,003,871 (+)	ENTREZGENE
CHM1_1	17	42,454,656 - 42,475,226 (+)	NCBI
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

Sequence:

show sequence

AGTGGCGGCGTCTTCGAATGCGGCCTAAGGCGCCTGCCGCCAGTCTCCTGGCGACTTTCCCTAT
ATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCCACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGC
CGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGTTTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCC
TGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCCTCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACC
TCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCCCCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAA
GTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCCAACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAG
CATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATCCTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTG
GATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGAGTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGT
CACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGCAACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCC
TCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCATTTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTAT
TTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCCAAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACT
GCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCCCTGGCCCAGCTGGGATCCTGCCTCACCAGCAGAGTGGGAGAAGTCTGGAGGACATCATGGTTTC
CGCGCCCCAAACTCCAACCCATGGTGCTCTGGCTAAATTCCAGACAGAGATTGTTGCTAGTTCCCAGGCATCTGTGGAGGAGGATTTTGGGCGAGGGCCCTGGCTGACCATGAAATCCACGCTAGGCC
TGGATGAGAGAGACCCTAGCTGCTTCCTCTGTACCTACAGCATTGTCATGGTGCTGCGCAAGCAGGCAGCCCTGAAGCAGCTTCCTAGGAACAAGGTCCCCAACATGGCGGTGATGATCAAGTCCCTG
ACTCGGAGCACAATGGACGCCAGTGTGGTTTTCAAGGACCCCACGGGAGAGATGCAGGGGACGGTGCACAGGTTGCTGCTGGAGACGTGCCAGAATGAGCTGAAGCCTGGCTCAGTGCTGCTGCTGAA
GCAGATTGGAGTGTTTTCTCCTTCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTGGTCCATATTTACAGCCCGGATTCTGGGGATGGGAGCTTCCTCAAGCCATCTCAGCCCTTCCCCA
AGGATTCAGGGAGCTTCCAGCATGATGTGGCTGCAAAGCCCGAGGAAGGCTTCAGAACAGCACAGAACCTAGAGGCAGAGGCGTCCCCTGAGGAAGAACTCCCAGAAGCAGATGACCTGGATGGACTC
CTGAGTGAGCTTCCTGAAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAACCCACCATGAGCAGGCAGCTCTGGGCATGTGTCTGGTCACATCCAAGGGGGAGAAGAAGGCC
AGCATGATTGGAGAGTGGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCTGAGAGCCCCCTCATCTCTGCGCTGCCCTCACTTTGGGCCTTCCTTTGCCGTTGGCACCAGA
ATCCGGCCGGAGACTGGCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCTCCTGCCTCAGCTTAATTTTAGAGGATATTGGGCCTGGTTTTCTTGTCCCTTCATACCCTAG
TCCCTGGACAGCTGAGGAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGGGGAGAAGCACGCTCAGGCTTCCTCTGCTTTGTCTCTTCAGACCTGTGGTTGCTCTGCTCAT
CCATGCCCAAGGTTCCCAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCATCTCCTGCTT

hide sequence

RefSeq Acc Id:

XM_011525187 ⟹ XP_011523489

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

Sequence:

show sequence

ATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCCACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGC
CGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGTTTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCC
TGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCCTCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACC
TCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCCCCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAA
GTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCCAACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAG
CATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATCCTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTG
GATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGAGTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGT
CACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGCAACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCC
TCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCATTTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTAT
TTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCCAAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACT
GCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCCCTGGCCCAGCTGGGATCCTGCCTCACCAGAGTGGGAGAAGTCTGGAGGACATCATGGTTTCCGC
GCCCCAAACTCCAACCCATGGTGCTCTGGCTAAATTCCAGACAGAGATTGTTGCTAGTTCCCAGGCATCTGTGGAGGAGGATTTTGGGCGAGGGCCCTGGCTGACCATGAAATCCACGCTAGGCCTGG
ATGAGAGAGACCCTAGCTGCTTCCTCTGTACCTACAGCATTGTCATGGTGCTGCGCAAGCAGGCAGCCCTGAAGCAGCTTCCTAGGAACAAGGTCCCCAACATGGCGGTGATGATCAAGTCCCTGACT
CGGAGCACAATGGACGCCAGTGTGGTTTTCAAGGACCCCACGGGAGAGATGCAGGGGACGGTGCACAGGTTGCTGCTGGAGACGTGCCAGAATGAGCTGAAGCCTGGCTCAGTGCTGCTGCTGAAGCA
GATTGGAGTGTTTTCTCCTTCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTGGTCCATATTTACAGCCCGGATTCTGGGGATGGGAGCTTCCTCAAGCCATCTCAGCCCTTCCCCAAGG
ATTCAGGGAGCTTCCAGCATGATGTGGCTGCAAAGCCCGAGGAAGGCTTCAGAACAGCACAGAACCTAGAGGCAGAGGCGTCCCCTGAGGAAGAACTCCCAGAAGCAGATGACCTGGATGGACTCCTG
AGTGAGCTTCCTGAAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAACCCACCATGAGCAGGCAGCTCTGGGCATGTGTCTGGTCACATCCAAGGGGGAGAAGAAGGCCAGC
ATGATTGGAGAGTGGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCTGAGAGCCCCCTCATCTCTGCGCTGCCCTCACTTTGGGCCTTCCTTTGCCGTTGGCACCAGAATC
CGGCCGGAGACTGGCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCTCCTGCCTCAGCTTAATTTTAGAGGATATTGGGCCTGGTTTTCTTGTCCCTTCATACCCTAGTCC
CTGGACAGCTGAGGAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGGGGAGAAGCACGCTCAGGCTTCCTCTGCTTTGTCTCTTCAGACCTGTGGTTGCTCTGCTCATCCA
TGCCCAAGGTTCCCAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCATCTCCTGCTTC

hide sequence

RefSeq Acc Id:

XM_011525188 ⟹ XP_011523490

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

Sequence:

show sequence

ATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCCACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGC
CGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGTTTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCC
TGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCCTCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACC
TCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCCCCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAA
GTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCCAACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAG
CATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATCCTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTG
GATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGAGTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGT
CACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGCAACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCC
TCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCATTTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTAT
TTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCCAAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACT
GCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCCCTGGCCCAGCTGGGATCCTGCCTCACCAGATTGTTGCTAGTTCCCAGGCATCTGTGGAGGAGGA
TTTTGGGCGAGGGCCCTGGCTGACCATGAAATCCACGCTAGGCCTGGATGAGAGAGACCCTAGCTGCTTCCTCTGTACCTACAGCATTGTCATGGTGCTGCGCAAGCAGGCAGCCCTGAAGCAGCTTC
CTAGGAACAAGGTCCCCAACATGGCGGTGATGATCAAGTCCCTGACTCGGAGCACAATGGACGCCAGTGTGGTTTTCAAGGACCCCACGGGAGAGATGCAGGGGACGGTGCACAGGTTGCTGCTGGAG
ACGTGCCAGAATGAGCTGAAGCCTGGCTCAGTGCTGCTGCTGAAGCAGATTGGAGTGTTTTCTCCTTCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTGGTCCATATTTACAGCCCGGA
TTCTGGGGATGGGAGCTTCCTCAAGCCATCTCAGCCCTTCCCCAAGGATTCAGGGAGCTTCCAGCATGATGTGGCTGCAAAGCCCGAGGAAGGCTTCAGAACAGCACAGAACCTAGAGGCAGAGGCGT
CCCCTGAGGAAGAACTCCCAGAAGCAGATGACCTGGATGGACTCCTGAGTGAGCTTCCTGAAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAACCCACCATGAGCAGGCAG
CTCTGGGCATGTGTCTGGTCACATCCAAGGGGGAGAAGAAGGCCAGCATGATTGGAGAGTGGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCTGAGAGCCCCCTCATCTC
TGCGCTGCCCTCACTTTGGGCCTTCCTTTGCCGTTGGCACCAGAATCCGGCCGGAGACTGGCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCTCCTGCCTCAGCTTAATT
TTAGAGGATATTGGGCCTGGTTTTCTTGTCCCTTCATACCCTAGTCCCTGGACAGCTGAGGAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGGGGAGAAGCACGCTCAGG
CTTCCTCTGCTTTGTCTCTTCAGACCTGTGGTTGCTCTGCTCATCCATGCCCAAGGTTCCCAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCATCTCCTGCTTC

hide sequence

RefSeq Acc Id:

XM_011525189 ⟹ XP_011523491

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

Sequence:

show sequence

ATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCCACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGC
CGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGTTTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCC
TGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCCTCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACC
TCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCCCCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAA
GTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCCAACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAG
CATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATCCTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTG
GATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGAGTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGT
CACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGCAACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCC
TCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCATTTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTAT
TTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCCAAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACT
GCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCCCTGGCCCAGCTGGGATCCTGCCTCACCAGCAGAGTGGGAGAAGTCTGGAGGACATCATGGTTTC
CGCGCCCCAAACTCCAACCCATGGTGCTCTGGCTAAATTCCAGACAGAGCAGGCAGCCCTGAAGCAGCTTCCTAGGAACAAGGTCCCCAACATGGCGGTGATGATCAAGTCCCTGACTCGGAGCACAA
TGGACGCCAGTGTGGTTTTCAAGGACCCCACGGGAGAGATGCAGGGGACGGTGCACAGGTTGCTGCTGGAGACGTGCCAGAATGAGCTGAAGCCTGGCTCAGTGCTGCTGCTGAAGCAGATTGGAGTG
TTTTCTCCTTCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTGGTCCATATTTACAGCCCGGATTCTGGGGATGGGAGCTTCCTCAAGCCATCTCAGCCCTTCCCCAAGGATTCAGGGAG
CTTCCAGCATGATGTGGCTGCAAAGCCCGAGGAAGGCTTCAGAACAGCACAGAACCTAGAGGCAGAGGCGTCCCCTGAGGAAGAACTCCCAGAAGCAGATGACCTGGATGGACTCCTGAGTGAGCTTC
CTGAAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAACCCACCATGAGCAGGCAGCTCTGGGCATGTGTCTGGTCACATCCAAGGGGGAGAAGAAGGCCAGCATGATTGGAG
AGTGGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCTGAGAGCCCCCTCATCTCTGCGCTGCCCTCACTTTGGGCCTTCCTTTGCCGTTGGCACCAGAATCCGGCCGGAGA
CTGGCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCTCCTGCCTCAGCTTAATTTTAGAGGATATTGGGCCTGGTTTTCTTGTCCCTTCATACCCTAGTCCCTGGACAGCT
GAGGAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGGGGAGAAGCACGCTCAGGCTTCCTCTGCTTTGTCTCTTCAGACCTGTGGTTGCTCTGCTCATCCATGCCCAAGGT
TCCCAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCATCTCCTGCTTC

hide sequence

RefSeq Acc Id:

XM_011525190 ⟹ XP_011523492

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

Sequence:

show sequence

ATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCCACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGC
CGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGTTTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCC
TGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCCTCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACC
TCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCCCCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAA
GTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCCAACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAG
CATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATCCTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTG
GATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGAGTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGT
CACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGCAACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCC
TCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCATTTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTAT
TTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCCAAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACT
GCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCCCTGGCCCAGCTGGGATCCTGCCTCACCAGCAGAGTGGGAGAAGTCTGGAGGACATCATGGTTTC
CGCGCCCCAAACTCCAACCCATGGTGCTCTGGCTAAATTCCAGACAGAGGCAGCCCTGAAGCAGCTTCCTAGGAACAAGGTCCCCAACATGGCGGTGATGATCAAGTCCCTGACTCGGAGCACAATGG
ACGCCAGTGTGGTTTTCAAGGACCCCACGGGAGAGATGCAGGGGACGGTGCACAGGTTGCTGCTGGAGACGTGCCAGAATGAGCTGAAGCCTGGCTCAGTGCTGCTGCTGAAGCAGATTGGAGTGTTT
TCTCCTTCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTGGTCCATATTTACAGCCCGGATTCTGGGGATGGGAGCTTCCTCAAGCCATCTCAGCCCTTCCCCAAGGATTCAGGGAGCTT
CCAGCATGATGTGGCTGCAAAGCCCGAGGAAGGCTTCAGAACAGCACAGAACCTAGAGGCAGAGGCGTCCCCTGAGGAAGAACTCCCAGAAGCAGATGACCTGGATGGACTCCTGAGTGAGCTTCCTG
AAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAACCCACCATGAGCAGGCAGCTCTGGGCATGTGTCTGGTCACATCCAAGGGGGAGAAGAAGGCCAGCATGATTGGAGAGT
GGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCTGAGAGCCCCCTCATCTCTGCGCTGCCCTCACTTTGGGCCTTCCTTTGCCGTTGGCACCAGAATCCGGCCGGAGACTG
GCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCTCCTGCCTCAGCTTAATTTTAGAGGATATTGGGCCTGGTTTTCTTGTCCCTTCATACCCTAGTCCCTGGACAGCTGAG
GAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGGGGAGAAGCACGCTCAGGCTTCCTCTGCTTTGTCTCTTCAGACCTGTGGTTGCTCTGCTCATCCATGCCCAAGGTTCC
CAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCATCTCCTGCTTC

hide sequence

RefSeq Acc Id:

XM_011525191 ⟹ XP_011523493

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

Sequence:

show sequence

ATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCC
ACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGCCGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGT
TTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCCTGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCC
TCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACCTCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCC
CCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAAGTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCC
AACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAGCATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATC
CTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTGGATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGA
GTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGTCACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGC
AACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCCTCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCAT
TTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTATTTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCC
AAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACTGCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCC
CTGGCCCAGCTGGGATCCTGCCTCACCAGCAGAGTGGGAGAAGTCTGGAGGACATCATGGTTTCCGCGCCCCAAACTCCAACCCATGGTGCTCTGGCTAAATTCCAGACAGAGATTGTTGCTAGTTCC
CAGGCATCTGTGGAGGAGGATTTTGGGCGAGGGCCCTGGCTGACCATGAAATCCACGCTAGGCCTGGATGAGAGAGACCCTAGCTGCTTCCTCTGTACCTACAGCATTGTCATGGTGCTGCGCAAGCA
GGCAGCCCTGAAGCAGCTTCCTAGGAACAAGGTCCCCAACATGGCGGTGATGATCAAGTCCCTGACTCGGAGCACAATGGACGCCAGTGTGGTTTTCAAGGACCCCACGGGAGAGATGCAGGGGACGG
TGCACAGGTTGCTGCTGGAGACGTGCCAGAATGAGCTGAAGCCTGGCTCAGTGCTGCTGCTGAAGCAGATTGGAGTGTTTTCTCCTTCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTG
GTCCATATTTACAGCCCGGATTCTGGGGATGGGAGCTTCCTCAAGCCATCTCAGCCCTTCCCCAAGATGACCTGGATGGACTCCTGAGTGAGCTTCCTGAAGACTTCTTCTGTGGGACCAGTAGTTGA
GACTGCCCCAACGCAGGACAACCCACCATGAGCAGGCAGCTCTGGGCATGTGTCTGGTCA

hide sequence

RefSeq Acc Id:

XM_011525192 ⟹ XP_011523494

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

Sequence:

show sequence

ATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCC
ACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGCCGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGT
TTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCCTGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCC
TCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACCTCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCC
CCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAAGTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCC
AACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAGCATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATC
CTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTGGATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGA
GTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGTCACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGC
AACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCCTCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCAT
TTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTATTTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCC
AAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACTGCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCC
CTGGCCCAGCTGGGATCCTGCCTCACCAGCAGAGTGGGAGAAGTCTGGAGGACATCATGGTTTCCGCGCCCCAAACTCCAACCCATGGTGCTCTGGCTAAATTCCAGACAGAGATTGTTGCTAGTTCC
CAGGCATCTGTGGAGGAGGATTTTGGGCGAGGGCCCTGGCTGACCATGAAATCCACGCTAGGCCTGGATGAGAGAGACCCTAGCTGCTTCCTCTGTACCTACAGCATTGTCATGGTGCTGCGCAAGCA
GGCAGCCCTGAAGCAGCTTCCTAGGAACAAGGTCCCCAACATGGCGGTGATGATCAAGTCCCTGACTCGGAGCACAATGGACGCCAGTGTGGTTTTCAAGGACCCCACGGATTGGAGTGTTTTCTCCT
TCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTGGTCCATATTTACAGCCCGGATTCTGGGGATGGGAGCTTCCTCAAGCCATCTCAGCCCTTCCCCAAGATGACCTGGATGGACTCCTG
AGTGAGCTTCCTGAAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAACCCACCATGAGCAGGCAGCTCTGGGCATGTGTCTGGTCACATCCAAGGGGGAGAAGAAGGCCAGC
ATGATTGGAGAGTGGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCTGAGAGCCCCCTCATCTCTGCGCTGCCCTCACTTTGGGCCTTCCTTTGCCGTTGGCACCAGAATC
CGGCCGGAGACTGGCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCTCCTGCCTCAGCTTAATTTTAGAGGATATTGGGCCTGGTTTTCTTGTCCCTTCATACCCTAGTCC
CTGGACAGCTGAGGAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGGGGAGAAGCACGCTCAGGCTTCCTCTGCTTTGTCTCTTCAGACCTGTGGTTGCTCTGCTCATCCA
TGCCCAAGGTTCCCAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCATCTCCTGCTTC

hide sequence

RefSeq Acc Id:

XM_011525193 ⟹ XP_011523495

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

Sequence:

show sequence

ATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCCACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGC
CGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGTTTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCC
TGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCCTCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACC
TCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCCCCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAA
GTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCCAACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAG
CATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATCCTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTG
GATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGAGTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGT
CACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGCAACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCC
TCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCATTTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTAT
TTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCCAAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACT
GCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCCCTGGCCCAGCTGGGATCCTGCCTCACCAGGCAGCCCTGAAGCAGCTTCCTAGGAACAAGGTCCC
CAACATGGCGGTGATGATCAAGTCCCTGACTCGGAGCACAATGGACGCCAGTGTGGTTTTCAAGGACCCCACGGGAGAGATGCAGGGGACGGTGCACAGGTTGCTGCTGGAGACGTGCCAGAATGAGC
TGAAGCCTGGCTCAGTGCTGCTGCTGAAGCAGATTGGAGTGTTTTCTCCTTCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTGGTCCATATTTACAGCCCGGATTCTGGGGATGGGAGC
TTCCTCAAGCCATCTCAGCCCTTCCCCAAGGATTCAGGGAGCTTCCAGCATGATGTGGCTGCAAAGCCCGAGGAAGGCTTCAGAACAGCACAGAACCTAGAGGCAGAGGCGTCCCCTGAGGAAGAACT
CCCAGAAGCAGATGACCTGGATGGACTCCTGAGTGAGCTTCCTGAAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAACCCACCATGAGCAGGCAGCTCTGGGCATGTGTCT
GGTCACATCCAAGGGGGAGAAGAAGGCCAGCATGATTGGAGAGTGGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCTGAGAGCCCCCTCATCTCTGCGCTGCCCTCACTT
TGGGCCTTCCTTTGCCGTTGGCACCAGAATCCGGCCGGAGACTGGCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCTCCTGCCTCAGCTTAATTTTAGAGGATATTGGGC
CTGGTTTTCTTGTCCCTTCATACCCTAGTCCCTGGACAGCTGAGGAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGGGGAGAAGCACGCTCAGGCTTCCTCTGCTTTGTC
TCTTCAGACCTGTGGTTGCTCTGCTCATCCATGCCCAAGGTTCCCAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCATCTCCTGCTTC

hide sequence

RefSeq Acc Id:

XM_011525194 ⟹ XP_011523496

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,154,846 (+)	NCBI

Sequence:

show sequence

ATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCCACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGC
CGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGTTTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCC
TGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCCTCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACC
TCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCCCCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAA
GTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCCAACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAG
CATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATCCTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTG
GATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGAGTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGT
CACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGCAACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCC
TCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCATTTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTAT
TTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCCAAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACT
GCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCCCTGGCCCAGCTGGGATCCTGCCTCACCAGCAGAGTGGGAGAAGTCTGGAGGACATCATGGTTTC
CGCGCCCCAAACTCCAACCCATGGTGCTCTGGCTAAATTCCAGACAGAGATTGTTGCTAGTTCCCAGGCATCTGTGGAGGAGGATTTTGGGCGAGGGCCCTGGCTGACCATGAAATCCACGCTAGGCC
TGGATGAGAGAGACCCTAGCTGCTTCCTCTGTACCTACAGCATTGTCATGGTGCTGCGCAAGCAGGCAGCCCTGAAGCAGCTTCCTAGGAACAAGGTCCCCAACATGGCGGTGATGATCAAGTCCCTG
ACTCGGAGCACAATGGACGCCAGTGTGGTTTTCAAGGACCCCACGGACAGGAAAACTGAGGCAGTGAGCAGCCCACTTCCCAGCCAGGGCCCATACCAGTCGCTGTGCTGCCCTTGACCCCGAGACTG
ATGGGCCATGTGGTAT

hide sequence

RefSeq Acc Id:

XM_011525195 ⟹ XP_011523497

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

Sequence:

show sequence

ATCGCAGAGACTCATCCCTCTGACCCCAGCCCGGAAGCACTGTCCCTCGGAGTCCGAGACTTCC
ACCTGGGTCGTGTCCAAGGCCCCGGCGACTCCCCGGACTCGGGGTGCCGGGCCAACCTCCCCGCCGAGGCCCACCCGCCGTCGCTATGGCGTGCAGTTTGCAGAAGCTGTTTGCTGTGGAAGAGGAGT
TTGAAGATGAGGATTTCTTGTCTGCTGTGGAGGATGCAGAGAACCGGTTTACTGGCTCACTGCCTGTGAATGCTGGGCGCCTGAGACCTGTCTCTTCTAGGCCACAGGAGACTGTGCAGGCACAGTCC
TCCAGGCTGCTGCTGTTACACCCCACTGCTCCCTCAGAGGCTTTGGGCCTGCCAGACTTGGACCTCTGCCTCCCTGCCTCCAGCACGCCCAGTGCTGACAGCCGTCCATCATGCATAGGAGCAGCTCC
CCTAAGGCCTGTCTCTACTTCCAGCAGCTGGATTGGCAATCAGAGAAGAGTGACAGTGACAGAAGTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCCCTACTCACCTTTGAGAGCC
AACAGCAGCAAGTTGGTGGCTTTGAGGGGCCTGAACAAGACGAATTTGATAAAGTCCTGGCAAGCATGGAGTTGGAGGAGCCTGGCATGGAGCTGGAATGTGGAGTCAGCAGTGAGGCCATACCAATC
CTGCCTGCCCAGCAGCGGGAGGGTTCAGTATTGGCTAAAAAAGCCCGGGTAGTTGATCTGAGTGGATCTTGCCAGAAGGGGCCTGTGCCTGCCATCCACAAAGCGGGTATCATGTCCGCCCAGGATGA
GTCTCTAGATCCTGTCATCCAATGTAGGACTCCACGACCCCCCTTGAGACCTGGTGCTGTGGGTCACCTTCCTGTTCCAACTGCCTTAACAGTTCCCACTCAGCAACTCCACTGGGAAGTCTGTCCGC
AACGCTCCCCTGTTCAAGCACTTCAGCCTCTCCAAGCTGCTAGAGGGACCATTCAGAGCAGCCCTCAAAATCGTTTCCCTTGTCAGCCATTCCAGTCTCCAAGTTCCTGGTTAAGTGGCAAAGCTCAT
TTACCCAGACCTCGAACTCCCAACTCAAGCTGTTCTACTCCCTCAAGGACTAGCTCTGGATTATTTCCTCGGATACCCTTACAACCGCAAGCTCCAGTGTCTTCCATTGGGTCTCCTGTTGGTACCCC
AAAAGGTCCCCAGGGAGCTCTGCAGACACCCATAGTCACCAACCACCTGGTGCAGCTAGTCACTGCTGCCAGCCGGACACCCCAGCAGCCCACCCATCCCTCCACCCGAGCCAAAACTCGCCGTTTCC
CTGGCCCAGCTGGGATCCTGCCTCACCAGCAGAGTGGGAGAAGTCTGGAGGACATCATGGTTTCCGCGCCCCAAACTCCAACCCATGGTGCTCTGGCTAAATTCCAGACAGAGATTGTTGCTAGTTCC
CAGGCATCTGTGGAGGAGGATTTTGGGCGAGGGCCCTGGCTGACCATGAAATCCACGCTAGGCCTGGATGAGAGAGACCCTAGCTGCTTCCTCTGTACCTACAGCATTGTCATGGTGCTGCGCAAGGA
TTCAGGGAGCTTCCAGCATGATGTGGCTGCAAAGCCCGAGGAAGGCTTCAGAACAGCACAGAACCTAGAGGCAGAGGCGTCCCCTGAGGAAGAACTCCCAGAAGCAGATGACCTGGATGGACTCCTGA
GTGAGCTTCCTGAAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAACCCACCATGAGCAGGCAGCTCTGGGCATGTGTCTGGTCACATCCAAGGGGGAGAAGAAGGCCAGCA
TGATTGGAGAGTGGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCTGAGAGCCCCCTCATCTCTGCGCTGCCCTCACTTTGGGCCTTCCTTTGCCGTTGGCACCAGAATCC
GGCCGGAGACTGGCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCTCCTGCCTCAGCTTAATTTTAGAGGATATTGGGCCTGGTTTTCTTGTCCCTTCATACCCTAGTCCC
TGGACAGCTGAGGAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGGGGAGAAGCACGCTCAGGCTTCCTCTGCTTTGTCTCTTCAGACCTGTGGTTGCTCTGCTCATCCAT
GCCCAAGGTTCCCAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCATCTCCTGCTTC

hide sequence

RefSeq Acc Id:

XM_011525197 ⟹ XP_011523499

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,151,051 - 44,162,476 (+)	NCBI

Sequence:

show sequence

TATGCAAATGTTAACTTTCTGGGTGTGATTTGAGAGTGAGGGGCGTCCCTGTGTGTTTCAGGAGTTAAGAATCAAGAGCTGATGCTGCTAGGCCTGTTTGCTGGTGTCACACACTAAAAGGCATTTGA
GGCAGGTAGTTGGGGGAGGCAGCAATTTTACTGGCATTAAGTGAGGCCTGTCCTGGTGCCAGGTAGGTATTATCTGATGCCATGGGTCCAGCCTTCTTTCCCATCTAAGAAATAAAGGCCCAGCTAGC
TCCAGCTTCCCCTGGGGGAGGAGACTGTGATAAGTATTATGAGATTGTGTCTCAGGAGCCCTTCCTCTCAGGTTTCTGAGAACTGAGCTGGGAAGGATCTGCCTTCTCTTGCCTTTGCTGGGTTCCCT
TTGGTGGGTGAGACCCTGCTTCCCTTCTCCTTGGGGTTCTGGTTGACCTGCTCTGCCCTCAAACCCAGTTTTGCTTTTAATTCTCCCCAGTATTTTTTCTCTGCTGTAGCTCCGCAGATCTGCCAGTC
CATTTCAGATCCAAAGCAGCAGATACTCTCTGGATTCAAAGCATGTATTAATATTGTTGCTAGTTCCCAGGCATCTGTGGAGGAGGATTTTGGGCGAGGGCCCTGGCTGACCATGAAATCCACGCTAG
GCCTGGATGAGAGAGACCCTAGCTGCTTCCTCTGTACCTACAGCATTGTCATGGTGCTGCGCAAGCAGGCAGCCCTGAAGCAGCTTCCTAGGAACAAGGTCCCCAACATGGCGGTGATGATCAAGTCC
CTGACTCGGAGCACAATGGACGCCAGTGTGGTTTTCAAGGACCCCACGGGAGAGATGCAGGGGACGGTGCACAGGTTGCTGCTGGAGACGTGCCAGAATGAGCTGAAGCCTGGCTCAGTGCTGCTGCT
GAAGCAGATTGGAGTGTTTTCTCCTTCACTTCGAAATCACTACCTCAACGTGACACCCAACAACCTGGTCCATATTTACAGCCCGGATTCTGGGGATGGGAGCTTCCTCAAGCCATCTCAGCCCTTCC
CCAAGGATTCAGGGAGCTTCCAGCATGATGTGGCTGCAAAGCCCGAGGAAGGCTTCAGAACAGCACAGAACCTAGAGGCAGAGGCGTCCCCTGAGGAAGAACTCCCAGAAGCAGATGACCTGGATGGA
CTCCTGAGTGAGCTTCCTGAAGACTTCTTCTGTGGGACCAGTAGTTGAGACTGCCCCAACGCAGGACAACCCACCATGAGCAGGCAGCTCTGGGCATGTGTCTGGTCACATCCAAGGGGGAGAAGAAG
GCCAGCATGATTGGAGAGTGGACACAGCCGGGGGGCTTCTGTGGTTGCTCCCACCCTGGGTGTTTTCCCTGAGAGCCCCCTCATCTCTGCGCTGCCCTCACTTTGGGCCTTCCTTTGCCGTTGGCACC
AGAATCCGGCCGGAGACTGGCTCTCCAGCCAACAAGAAAGGCCTGTCACCCTCGCCTTGGGTGTCCCTCTCCTGCCTCAGCTTAATTTTAGAGGATATTGGGCCTGGTTTTCTTGTCCCTTCATACCC
TAGTCCCTGGACAGCTGAGGAGATGAAAGGAGCCACACCACAACAATGGCGGCCTGCCCCTCCACACAGGGGAGAAGCACGCTCAGGCTTCCTCTGCTTTGTCTCTTCAGACCTGTGGTTGCTCTGCT
CATCCATGCCCAAGGTTCCCAGGTGCAGGACAGAGGTGTGGCCTATTGTACCTTGTTCTGAAATAAAGCATCTCCTGCTTC

hide sequence

RefSeq Acc Id:

XM_047436676 ⟹ XP_047292632

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436677 ⟹ XP_047292633

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436678 ⟹ XP_047292634

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436679 ⟹ XP_047292635

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436680 ⟹ XP_047292636

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436681 ⟹ XP_047292637

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436682 ⟹ XP_047292638

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436683 ⟹ XP_047292639

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,157,935 (+)	NCBI

RefSeq Acc Id:

XM_047436684 ⟹ XP_047292640

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436685 ⟹ XP_047292641

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436686 ⟹ XP_047292642

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436687 ⟹ XP_047292643

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436688 ⟹ XP_047292644

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,154,846 (+)	NCBI

RefSeq Acc Id:

XM_047436689 ⟹ XP_047292645

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436690 ⟹ XP_047292646

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436691 ⟹ XP_047292647

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436692 ⟹ XP_047292648

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436693 ⟹ XP_047292649

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,141,930 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_047436694 ⟹ XP_047292650

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	44,142,504 - 44,162,476 (+)	NCBI

RefSeq Acc Id:

XM_054317091 ⟹ XP_054173066

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317092 ⟹ XP_054173067

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317093 ⟹ XP_054173068

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317094 ⟹ XP_054173069

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317095 ⟹ XP_054173070

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317096 ⟹ XP_054173071

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317097 ⟹ XP_054173072

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317098 ⟹ XP_054173073

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317099 ⟹ XP_054173074

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317100 ⟹ XP_054173075

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317101 ⟹ XP_054173076

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317102 ⟹ XP_054173077

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317103 ⟹ XP_054173078

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317104 ⟹ XP_054173079

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317105 ⟹ XP_054173080

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,011,035 (+)	NCBI

RefSeq Acc Id:

XM_054317106 ⟹ XP_054173081

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317107 ⟹ XP_054173082

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317108 ⟹ XP_054173083

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317109 ⟹ XP_054173084

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317110 ⟹ XP_054173085

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,007,946 (+)	NCBI

RefSeq Acc Id:

XM_054317111 ⟹ XP_054173086

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,007,946 (+)	NCBI

RefSeq Acc Id:

XM_054317112 ⟹ XP_054173087

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317113 ⟹ XP_054173088

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317114 ⟹ XP_054173089

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317115 ⟹ XP_054173090

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317116 ⟹ XP_054173091

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317117 ⟹ XP_054173092

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,027 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317118 ⟹ XP_054173093

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	44,995,601 - 45,015,576 (+)	NCBI

RefSeq Acc Id:

XM_054317119 ⟹ XP_054173094

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	45,004,151 - 45,015,576 (+)	NCBI


Protein RefSeqs	NP_001164722	(Get FASTA)	NCBI Sequence Viewer
	NP_001308239	(Get FASTA)	NCBI Sequence Viewer
	NP_001308240	(Get FASTA)	NCBI Sequence Viewer
	NP_076937	(Get FASTA)	NCBI Sequence Viewer
	XP_011523489	(Get FASTA)	NCBI Sequence Viewer
	XP_011523490	(Get FASTA)	NCBI Sequence Viewer
	XP_011523491	(Get FASTA)	NCBI Sequence Viewer
	XP_011523492	(Get FASTA)	NCBI Sequence Viewer
	XP_011523493	(Get FASTA)	NCBI Sequence Viewer
	XP_011523494	(Get FASTA)	NCBI Sequence Viewer
	XP_011523495	(Get FASTA)	NCBI Sequence Viewer
	XP_011523496	(Get FASTA)	NCBI Sequence Viewer
	XP_011523497	(Get FASTA)	NCBI Sequence Viewer
	XP_011523499	(Get FASTA)	NCBI Sequence Viewer
	XP_047292632	(Get FASTA)	NCBI Sequence Viewer
	XP_047292633	(Get FASTA)	NCBI Sequence Viewer
	XP_047292634	(Get FASTA)	NCBI Sequence Viewer
	XP_047292635	(Get FASTA)	NCBI Sequence Viewer
	XP_047292636	(Get FASTA)	NCBI Sequence Viewer
	XP_047292637	(Get FASTA)	NCBI Sequence Viewer
	XP_047292638	(Get FASTA)	NCBI Sequence Viewer
	XP_047292639	(Get FASTA)	NCBI Sequence Viewer
	XP_047292640	(Get FASTA)	NCBI Sequence Viewer
	XP_047292641	(Get FASTA)	NCBI Sequence Viewer
	XP_047292642	(Get FASTA)	NCBI Sequence Viewer
	XP_047292643	(Get FASTA)	NCBI Sequence Viewer
	XP_047292644	(Get FASTA)	NCBI Sequence Viewer
	XP_047292645	(Get FASTA)	NCBI Sequence Viewer
	XP_047292646	(Get FASTA)	NCBI Sequence Viewer
	XP_047292647	(Get FASTA)	NCBI Sequence Viewer
	XP_047292648	(Get FASTA)	NCBI Sequence Viewer
	XP_047292649	(Get FASTA)	NCBI Sequence Viewer
	XP_047292650	(Get FASTA)	NCBI Sequence Viewer
	XP_054173066	(Get FASTA)	NCBI Sequence Viewer
	XP_054173067	(Get FASTA)	NCBI Sequence Viewer
	XP_054173068	(Get FASTA)	NCBI Sequence Viewer
	XP_054173069	(Get FASTA)	NCBI Sequence Viewer
	XP_054173070	(Get FASTA)	NCBI Sequence Viewer
	XP_054173071	(Get FASTA)	NCBI Sequence Viewer
	XP_054173072	(Get FASTA)	NCBI Sequence Viewer
	XP_054173073	(Get FASTA)	NCBI Sequence Viewer
	XP_054173074	(Get FASTA)	NCBI Sequence Viewer
	XP_054173075	(Get FASTA)	NCBI Sequence Viewer
	XP_054173076	(Get FASTA)	NCBI Sequence Viewer
	XP_054173077	(Get FASTA)	NCBI Sequence Viewer
	XP_054173078	(Get FASTA)	NCBI Sequence Viewer
	XP_054173079	(Get FASTA)	NCBI Sequence Viewer
	XP_054173080	(Get FASTA)	NCBI Sequence Viewer
	XP_054173081	(Get FASTA)	NCBI Sequence Viewer
	XP_054173082	(Get FASTA)	NCBI Sequence Viewer
	XP_054173083	(Get FASTA)	NCBI Sequence Viewer
	XP_054173084	(Get FASTA)	NCBI Sequence Viewer
	XP_054173085	(Get FASTA)	NCBI Sequence Viewer
	XP_054173086	(Get FASTA)	NCBI Sequence Viewer
	XP_054173087	(Get FASTA)	NCBI Sequence Viewer
	XP_054173088	(Get FASTA)	NCBI Sequence Viewer
	XP_054173089	(Get FASTA)	NCBI Sequence Viewer
	XP_054173090	(Get FASTA)	NCBI Sequence Viewer
	XP_054173091	(Get FASTA)	NCBI Sequence Viewer
	XP_054173092	(Get FASTA)	NCBI Sequence Viewer
	XP_054173093	(Get FASTA)	NCBI Sequence Viewer
	XP_054173094	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH00121	(Get FASTA)	NCBI Sequence Viewer
	BAB13867	(Get FASTA)	NCBI Sequence Viewer
	BAF84613	(Get FASTA)	NCBI Sequence Viewer
	CAD38968	(Get FASTA)	NCBI Sequence Viewer
	EAW51629	(Get FASTA)	NCBI Sequence Viewer
	EAW51630	(Get FASTA)	NCBI Sequence Viewer
	EAW51631	(Get FASTA)	NCBI Sequence Viewer
	EAW51632	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000245382
	ENSP00000245382.5
	ENSP00000313500
	ENSP00000313500.4
	ENSP00000466618
	ENSP00000466618.1
GenBank Protein	Q8N3J3	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001164722 ⟸ NM_001171251
- Peptide Label:	isoform 2
- UniProtKB:	Q8N3J3 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MACSLQKLFAVEEEFEDEDFLSAVEDAENRFTGSLPVNAGRLRPVSSRPQETVQAQSSRLLLLHPTAPSEALGLPDLDLCLPASSTPSADSRPSCIGAAPLRPVSTSSSWIGNQRRVTVTEVLRETAR PQSSALHPLLTFESQQQQVGGFEGPEQDEFDKVLASMELEEPGMELECGVSSEAIPILPAQQREGSVLAKKARVVDLSGSCQKGPVPAIHKAGIMSAQDESLDPVIQCRTPRPPLRPGAVGHLPVPTA LTVPTQQLHWEVCPQRSPVQALQPLQAARGTIQSSPQNRFPCQPFQSPSSWLSGKAHLPRPRTPNSSCSTPSRTSSGLFPRIPLQPQAPVSSIGSPVGTPKGPQGALQTPIVTNHLVQLVTAASRTPQ QPTHPSTRAKTRRFPGPAGILPHQQSGRSLEDIMVSAPQTPTHGALAKFQTEIVASSQASVEEDFGRGPWLTMKSTLGLDERDPSCFLCTYSIVMVLRKAALKQLPRNKVPNMAVMIKSLTRSTMDAS VVFKDPTGEMQGTVHRLLLETCQNELKPGSVLLLKQIGVFSPSLRNHYLNVTPNNLVHIYSPDSGDGSFLKPSQPFPKDSGSFQHDVAAKPEEGFRTAQNLEAEASPEEELPEADDLDGLLSELPEDF FCGTSS hide sequence

RefSeq Acc Id:	NP_076937 ⟸ NM_024032
- Peptide Label:	isoform 1
- UniProtKB:	Q9BWM9 (UniProtKB/Swiss-Prot), A8K7A9 (UniProtKB/Swiss-Prot), Q9HAI1 (UniProtKB/Swiss-Prot), Q8N3J3 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MACSLQKLFAVEEEFEDEDFLSAVEDAENRFTGSLPVNAGRLRPVSSRPQETVQAQSSRLLLLH PTAPSEALGLPDLDLCLPASSTPSADSRPSCIGAAPLRPVSTSSSWIGNQRRVTVTEVLRETARPQSSALHPLLTFESQQQQVGGFEGPEQDEFDKVLASMELEEPGMELECGVSSEAIPILPAQQRE GSVLAKKARVVDLSGSCQKGPVPAIHKAGIMSAQDESLDPVIQCRTPRPPLRPGAVGHLPVPTALTVPTQQLHWEVCPQRSPVQALQPLQAARGTIQSSPQNRFPCQPFQSPSSWLSGKAHLPRPRTP NSSCSTPSRTSSGLFPRIPLQPQAPVSSIGSPVGTPKGPQGALQTPIVTNHLVQLVTAASRTPQQPTHPSTRAKTRRFPGPAGILPHQQSGRSLEDIMVSAPQTPTHGALAKFQTEIVASSQASVEED FGRGPWLTMKSTLGLDERDPSCFLCTYSIVMVLRKQAALKQLPRNKVPNMAVMIKSLTRSTMDASVVFKDPTGEMQGTVHRLLLETCQNELKPGSVLLLKQIGVFSPSLRNHYLNVTPNNLVHIYSPD SGDGSFLKPSQPFPKDSGSFQHDVAAKPEEGFRTAQNLEAEASPEEELPEADDLDGLLSELPEDFFCGTSS hide sequence

RefSeq Acc Id:

XP_011523494 ⟸ XM_011525192

- Peptide Label:

isoform X11

- Sequence:

show sequence

MACSLQKLFAVEEEFEDEDFLSAVEDAENRFTGSLPVNAGRLRPVSSRPQETVQAQSSRLLLLHPTAPSEALGLPDLDLCLPASSTPSADSRPSCIGAAPLRPVSTSSSWIGNQRRVTVTEVLRETAR
PQSSALHPLLTFESQQQQVGGFEGPEQDEFDKVLASMELEEPGMELECGVSSEAIPILPAQQREGSVLAKKARVVDLSGSCQKGPVPAIHKAGIMSAQDESLDPVIQCRTPRPPLRPGAVGHLPVPTA
LTVPTQQLHWEVCPQRSPVQALQPLQAARGTIQSSPQNRFPCQPFQSPSSWLSGKAHLPRPRTPNSSCSTPSRTSSGLFPRIPLQPQAPVSSIGSPVGTPKGPQGALQTPIVTNHLVQLVTAASRTPQ
QPTHPSTRAKTRRFPGPAGILPHQQSGRSLEDIMVSAPQTPTHGALAKFQTEIVASSQASVEEDFGRGPWLTMKSTLGLDERDPSCFLCTYSIVMVLRKQAALKQLPRNKVPNMAVMIKSLTRSTMDA
SVVFKDPTDWSVFSFTSKSLPQRDTQQPGPYLQPGFWGWELPQAISALPQDDLDGLLSELPEDFFCGTSS

hide sequence

RefSeq Acc Id:

XP_011523497 ⟸ XM_011525195

- Peptide Label:

isoform X22

- Sequence:

show sequence

MACSLQKLFAVEEEFEDEDFLSAVEDAENRFTGSLPVNAGRLRPVSSRPQETVQAQSSRLLLLHPTAPSEALGLPDLDLCLPASSTPSADSRPSCIGAAPLRPVSTSSSWIGNQRRVTVTEVLRETAR
PQSSALHPLLTFESQQQQVGGFEGPEQDEFDKVLASMELEEPGMELECGVSSEAIPILPAQQREGSVLAKKARVVDLSGSCQKGPVPAIHKAGIMSAQDESLDPVIQCRTPRPPLRPGAVGHLPVPTA
LTVPTQQLHWEVCPQRSPVQALQPLQAARGTIQSSPQNRFPCQPFQSPSSWLSGKAHLPRPRTPNSSCSTPSRTSSGLFPRIPLQPQAPVSSIGSPVGTPKGPQGALQTPIVTNHLVQLVTAASRTPQ
QPTHPSTRAKTRRFPGPAGILPHQQSGRSLEDIMVSAPQTPTHGALAKFQTEIVASSQASVEEDFGRGPWLTMKSTLGLDERDPSCFLCTYSIVMVLRKDSGSFQHDVAAKPEEGFRTAQNLEAEASP
EEELPEADDLDGLLSELPEDFFCGTSS

hide sequence

RefSeq Acc Id:

XP_011523491 ⟸ XM_011525189

- Peptide Label:

isoform X4

- Sequence:

show sequence

MACSLQKLFAVEEEFEDEDFLSAVEDAENRFTGSLPVNAGRLRPVSSRPQETVQAQSSRLLLLH
PTAPSEALGLPDLDLCLPASSTPSADSRPSCIGAAPLRPVSTSSSWIGNQRRVTVTEVLRETARPQSSALHPLLTFESQQQQVGGFEGPEQDEFDKVLASMELEEPGMELECGVSSEAIPILPAQQRE
GSVLAKKARVVDLSGSCQKGPVPAIHKAGIMSAQDESLDPVIQCRTPRPPLRPGAVGHLPVPTALTVPTQQLHWEVCPQRSPVQALQPLQAARGTIQSSPQNRFPCQPFQSPSSWLSGKAHLPRPRTP
NSSCSTPSRTSSGLFPRIPLQPQAPVSSIGSPVGTPKGPQGALQTPIVTNHLVQLVTAASRTPQQPTHPSTRAKTRRFPGPAGILPHQQSGRSLEDIMVSAPQTPTHGALAKFQTEQAALKQLPRNKV
PNMAVMIKSLTRSTMDASVVFKDPTGEMQGTVHRLLLETCQNELKPGSVLLLKQIGVFSPSLRNHYLNVTPNNLVHIYSPDSGDGSFLKPSQPFPKDSGSFQHDVAAKPEEGFRTAQNLEAEASPEEE
LPEADDLDGLLSELPEDFFCGTSS

hide sequence

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q8N3J3-F1-model_v2	AlphaFold	Q8N3J3	1-647	view protein structure

RGD ID:

6793799

Promoter ID:

HG_KWN:26298

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000245382, ENST00000253405, NM_001171251, NM_024032

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	17	39,574,616 - 39,575,116 (+)	MPROMDB

RGD ID:

7235237

Promoter ID:

EPDNEW_H23364

Type:

initiation region

Name:

C17orf53_1

Description:

chromosome 17 open reading frame 53

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	44,141,930 - 44,141,990	EPDNEW

Database	Acc Id	Source(s)
COSMIC	HROB	COSMIC
Ensembl Genes	ENSG00000125319	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000245382	ENTREZGENE
	ENST00000245382.6	UniProtKB/Swiss-Prot
	ENST00000319977	ENTREZGENE
	ENST00000319977.8	UniProtKB/Swiss-Prot
	ENST00000585683	ENTREZGENE
	ENST00000585683.6	UniProtKB/Swiss-Prot
GTEx	ENSG00000125319	GTEx
HGNC ID	HGNC:28460	ENTREZGENE
Human Proteome Map	HROB	Human Proteome Map
InterPro	DUF4539	UniProtKB/Swiss-Prot
KEGG Report	hsa:78995	UniProtKB/Swiss-Prot
NCBI Gene	78995	ENTREZGENE
OMIM	618611	OMIM
PANTHER	HOMOLOGOUS RECOMBINATION OB-FOLD PROTEIN	UniProtKB/Swiss-Prot
	PTHR14523	UniProtKB/Swiss-Prot
Pfam	DUF4539	UniProtKB/Swiss-Prot
PharmGKB	PA166351920	PharmGKB
UniProt	A8K7A9	ENTREZGENE
	CQ053_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
	Q9BWM9	ENTREZGENE
	Q9HAI1	ENTREZGENE
UniProt Secondary	A8K7A9	UniProtKB/Swiss-Prot
	Q9BWM9	UniProtKB/Swiss-Prot
	Q9HAI1	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2019-09-10	HROB	homologous recombination factor with OB-fold	C17orf53	chromosome 17 open reading frame 53	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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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

Imported Disease Annotations - ClinVar

Imported Disease Annotations - OMIM

Imported Human Phenotype Annotations - HPO

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - OMIM

Imported Human Phenotype Annotations - HPO

Imported Human Phenotype Annotations - ClinVar