ZBTB17 (zinc finger and BTB domain containing 17)

Gene: ZBTB17 (zinc finger and BTB domain containing 17) Homo sapiens

Analyze

Symbol:

ZBTB17

Name:

zinc finger and BTB domain containing 17

RGD ID:

1347626

HGNC Page

HGNC:12936

Description:

Enables several functions, including DNA-binding transcription activator activity, RNA polymerase II-specific; transcription cis-regulatory region binding activity; and transcription coactivator binding activity. Involved in negative regulation of cell population proliferation and positive regulation of transcription by RNA polymerase II. Acts upstream of with a negative effect on G1 to G0 transition. Part of protein-DNA complex.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

MIZ-1; myc-interacting zinc finger protein 1; Myc-interacting Zn finger protein-1; pHZ-67; zinc finger and BTB domain-containing protein 17; zinc finger protein 151 (pHZ-67); zinc finger protein 60; ZNF151; ZNF60

RGD Orthologs

Alliance Genes

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	1	15,941,869 - 15,976,101 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	1	15,941,869 - 15,976,132 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	1	16,268,364 - 16,302,596 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	1	16,140,951 - 16,175,101 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	1	16,013,671 - 16,047,820	NCBI
Celera	1	14,748,238 - 14,782,515 (-)	NCBI		Celera
Cytogenetic Map	1	p36.13	NCBI
HuRef	1	14,787,372 - 14,821,661 (-)	NCBI		HuRef
CHM1_1	1	16,066,899 - 16,101,159 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	1	15,383,149 - 15,417,408 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

chromosome 1p36 deletion syndrome (IAGP)

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1-chloro-2,4-dinitrobenzene (EXP)

2,2',4,4'-Tetrabromodiphenyl ether (ISO)

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

2,4-dinitrotoluene (ISO)

2,6-dinitrotoluene (ISO)

6-propyl-2-thiouracil (ISO)

aflatoxin B1 (EXP,ISO)

amitrole (ISO)

aristolochic acid A (EXP)

benzo[a]pyrene (EXP,ISO)

bisphenol A (EXP,ISO)

bisphenol F (EXP)

calciol (ISO)

carmustine (EXP)

cobalt dichloride (EXP)

copper atom (EXP)

copper(0) (EXP)

coumarin (EXP)

cylindrospermopsin (EXP)

diazinon (ISO)

dibutyl phthalate (ISO)

dieldrin (ISO)

eugenol (EXP)

fenthion (ISO)

FR900359 (EXP)

fulvestrant (EXP)

gentamycin (ISO)

methidathion (ISO)

methimazole (ISO)

nickel sulfate (EXP)

ozone (EXP)

paracetamol (ISO)

phenobarbital (EXP)

PhIP (ISO)

pirinixic acid (EXP,ISO)

pregnenolone 16alpha-carbonitrile (ISO)

sulfadimethoxine (ISO)

tetrachloroethene (ISO)

thioacetamide (ISO)

troglitazone (ISO)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

ectoderm development (IEA,ISO)

G1 to G0 transition (IDA)

gastrulation with mouth forming second (IEA,ISO)

negative regulation of cell cycle (TAS)

negative regulation of cell population proliferation (IDA)

negative regulation of transcription by RNA polymerase II (IBA)

positive regulation of DNA-templated transcription (IEA,ISO)

positive regulation of transcription by RNA polymerase II (IDA,IMP)

regulation of cytokine production (IBA)

regulation of immune system process (IBA)

regulation of transcription by RNA polymerase II (IEA)

Cellular Component

nucleoplasm (IBA,TAS)

nucleus (IEA)

protein-containing complex (IDA)

protein-DNA complex (IMP)

Molecular Function

core promoter sequence-specific DNA binding (IDA)

DNA binding (IEA)

DNA-binding transcription activator activity, RNA polymerase II-specific (IDA,IMP)

DNA-binding transcription factor activity (IDA,IEA)

DNA-binding transcription factor binding (IPI)

DNA-binding transcription repressor activity, RNA polymerase II-specific (IBA)

metal ion binding (IEA)

organic cyclic compound binding (IEA)

protein binding (IPI)

RNA polymerase II cis-regulatory region sequence-specific DNA binding (IBA,IEA,IMP)

transcription coactivator binding (IPI)

Molecular Pathway Annotations Click to see Annotation Detail View

cell cycle pathway, mitotic (IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	KEGG Annotation Import Pipeline	Pipeline to import KEGG annotations from KEGG into RGD
3.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:1505991	PMID:1946370	PMID:7557990	PMID:8125298	PMID:9256341	PMID:9308237	PMID:9312026	PMID:11068878	PMID:11283613	PMID:11545736	PMID:12244100	PMID:12356872
PMID:12408820	PMID:12477932	PMID:12545156	PMID:12840021	PMID:12904288	PMID:14739298	PMID:15095404	PMID:15231747	PMID:15489334	PMID:15616584	PMID:15752756	PMID:15856024
PMID:16142238	PMID:16167342	PMID:16269333	PMID:16344560	PMID:16352593	PMID:16537485	PMID:16710414	PMID:17006541	PMID:17050536	PMID:17082179	PMID:17418410	PMID:17880999
PMID:17947461	PMID:18451802	PMID:18923429	PMID:19160485	PMID:19164764	PMID:19274049	PMID:19419955	PMID:19549844	PMID:19786833	PMID:19815509	PMID:19901969	PMID:20308430
PMID:20426839	PMID:20493880	PMID:20697356	PMID:21123453	PMID:21459883	PMID:21804610	PMID:21811581	PMID:21873635	PMID:21908575	PMID:22099967	PMID:22184250	PMID:22939624
PMID:23082233	PMID:23570452	PMID:24296348	PMID:24618291	PMID:24912190	PMID:24983942	PMID:25245946	PMID:25277244	PMID:25484205	PMID:25558878	PMID:26212014	PMID:26766587
PMID:26972249	PMID:27109891	PMID:27339797	PMID:27527891	PMID:27859590	PMID:28035002	PMID:28539603	PMID:29137325	PMID:29445930	PMID:29844126	PMID:30804502	PMID:31391242
PMID:32296183	PMID:32814053	PMID:33057331	PMID:33660365	PMID:33914337	PMID:33961781	PMID:34145038	PMID:34305888	PMID:34373451	PMID:35205757	PMID:35563538	PMID:36538983
PMID:37040844

Genomics

Comparative Map Data

ZBTB17
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	1	15,941,869 - 15,976,101 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	1	15,941,869 - 15,976,132 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	1	16,268,364 - 16,302,596 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	1	16,140,951 - 16,175,101 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	1	16,013,671 - 16,047,820	NCBI
Celera	1	14,748,238 - 14,782,515 (-)	NCBI		Celera
Cytogenetic Map	1	p36.13	NCBI
HuRef	1	14,787,372 - 14,821,661 (-)	NCBI		HuRef
CHM1_1	1	16,066,899 - 16,101,159 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	1	15,383,149 - 15,417,408 (-)	NCBI		T2T-CHM13v2.0

Zbtb17
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	4	141,171,984 - 141,195,248 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	4	141,171,965 - 141,195,241 (+)	Ensembl		GRCm39 Ensembl
GRCm38	4	141,444,673 - 141,467,937 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	4	141,444,654 - 141,467,930 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	4	141,000,588 - 141,023,852 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	4	140,716,760 - 140,739,305 (+)	NCBI		MGSCv36	mm8
Celera	4	143,261,157 - 143,285,202 (+)	NCBI		Celera
Cytogenetic Map	4	D3	NCBI
cM Map	4	74.17	NCBI

Zbtb17
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	5	159,036,482 - 159,057,580 (+)	NCBI		GRCr8
mRatBN7.2	5	153,753,508 - 153,774,613 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	5	153,753,569 - 153,774,609 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	5	156,440,859 - 156,461,960 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	5	158,214,147 - 158,235,248 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	5	158,203,320 - 158,224,423 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	5	159,993,799 - 160,014,899 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	5	159,993,799 - 160,014,895 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	5	163,713,685 - 163,734,715 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	5	160,337,988 - 160,359,060 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	5	160,348,175 - 160,369,246 (+)	NCBI
Celera	5	152,113,183 - 152,134,155 (+)	NCBI		Celera
Cytogenetic Map	5	q36	NCBI

Zbtb17
(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_004955527	2,252,074 - 2,282,787 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955527	2,252,118 - 2,278,127 (+)	NCBI	ChiLan1.0	ChiLan1.0

ZBTB17
(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	1	210,944,784 - 210,977,584 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	1	210,193,373 - 210,226,193 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	1	15,080,880 - 15,113,676 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	1	16,074,005 - 16,106,709 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	1	16,074,005 - 16,106,700 (-)	Ensembl	panpan1.1		panPan2

ZBTB17
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	2	81,652,015 - 81,682,647 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	2	81,652,157 - 81,682,660 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	2	78,188,685 - 78,220,088 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	2	82,297,860 - 82,329,775 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	2	82,297,873 - 82,329,761 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	2	79,051,015 - 79,083,027 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	2	80,069,989 - 80,101,528 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	2	81,136,103 - 81,167,412 (+)	NCBI		UU_Cfam_GSD_1.0

Zbtb17
(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_024405058	37,712,259 - 37,738,912 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936474	3,537,043 - 3,563,770 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936474	3,535,351 - 3,563,664 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZBTB17
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	6	75,107,427 - 75,144,069 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	6	75,108,728 - 75,144,103 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1

ZBTB17
(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	20	116,324,794 - 116,358,600 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666054	19,851,110 - 19,885,521 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Zbtb17
(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_004624764	2,144,878 - 2,174,545 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624764	2,144,555 - 2,174,177 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ZBTB17
33 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 1p36.21-36.12(chr1:15385267-20980349)x1	copy number loss	See cases [RCV000051146]	Chr1:15385267..20980349 [GRCh38] Chr1:15711763..21306842 [GRCh37] Chr1:15584350..21179429 [NCBI36] Chr1:1p36.21-36.12	pathogenic
GRCh38/hg38 1p36.31-36.13(chr1:6853513-17326813)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051795]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051795]\|See cases [RCV000051795]	Chr1:6853513..17326813 [GRCh38] Chr1:6913573..17685411 [GRCh37] Chr1:6836160..17557998 [NCBI36] Chr1:1p36.31-36.13	pathogenic
GRCh38/hg38 1p36.21-36.12(chr1:13110797-20670207)x3	copy number gain	See cases [RCV000051797]	Chr1:13110797..20670207 [GRCh38] Chr1:13178269..20996700 [GRCh37] Chr1:13100856..20869287 [NCBI36] Chr1:1p36.21-36.12	pathogenic
GRCh38/hg38 1p36.21-36.13(chr1:13619979-18466172)x3	copy number gain	See cases [RCV000051799]	Chr1:13619979..18466172 [GRCh38] Chr1:13946474..18792666 [GRCh37] Chr1:13819061..18665253 [NCBI36] Chr1:1p36.21-36.13	pathogenic
GRCh38/hg38 1p36.32-36.13(chr1:3006193-17688934)x1	copy number loss	See cases [RCV000053714]	Chr1:3006193..17688934 [GRCh38] Chr1:2922757..18015429 [GRCh37] Chr1:2912617..17888016 [NCBI36] Chr1:1p36.32-36.13	pathogenic
GRCh38/hg38 1p36.22-36.12(chr1:10556797-22557907)x1	copy number loss	See cases [RCV000053760]	Chr1:10556797..22557907 [GRCh38] Chr1:10616854..22884400 [GRCh37] Chr1:10539441..22756987 [NCBI36] Chr1:1p36.22-36.12	pathogenic
GRCh38/hg38 1p36.22-36.13(chr1:10621776-16520709)x1	copy number loss	See cases [RCV000053763]	Chr1:10621776..16520709 [GRCh38] Chr1:10681833..16847204 [GRCh37] Chr1:10604420..16719791 [NCBI36] Chr1:1p36.22-36.13	pathogenic
GRCh38/hg38 1p36.22-36.13(chr1:10809039-16422500)x1	copy number loss	See cases [RCV000053765]	Chr1:10809039..16422500 [GRCh38] Chr1:10869096..16748995 [GRCh37] Chr1:10791683..16621582 [NCBI36] Chr1:1p36.22-36.13	pathogenic
GRCh38/hg38 1p36.22-36.13(chr1:11121625-16324498)x1	copy number loss	See cases [RCV000053766]	Chr1:11121625..16324498 [GRCh38] Chr1:11181682..16650993 [GRCh37] Chr1:11104269..16523580 [NCBI36] Chr1:1p36.22-36.13	pathogenic
GRCh38/hg38 1p36.21-36.13(chr1:15173497-18242678)x1	copy number loss	See cases [RCV000053769]	Chr1:15173497..18242678 [GRCh38] Chr1:15499993..18569172 [GRCh37] Chr1:15372580..18441759 [NCBI36] Chr1:1p36.21-36.13	pathogenic
GRCh38/hg38 1p36.21-36.13(chr1:15173497-17019576)x1	copy number loss	See cases [RCV000053771]	Chr1:15173497..17019576 [GRCh38] Chr1:15499993..17346071 [GRCh37] Chr1:15372580..17218658 [NCBI36] Chr1:1p36.21-36.13	pathogenic
GRCh38/hg38 1p36.23-36.13(chr1:9034671-16441465)x1	copy number loss	See cases [RCV000053756]	Chr1:9034671..16441465 [GRCh38] Chr1:9094730..16767960 [GRCh37] Chr1:9017317..16640547 [NCBI36] Chr1:1p36.23-36.13	pathogenic
NM_003443.3(ZBTB17):c.709CAAGAGGAG[3] (p.237QEE[3])	microsatellite	Primary dilated cardiomyopathy [RCV001293158]	Chr1:15945137..15945138 [GRCh38] Chr1:16271632..16271633 [GRCh37] Chr1:1p36.13	uncertain significance
GRCh38/hg38 1p36.21-36.13(chr1:15052047-16499873)x1	copy number loss	See cases [RCV000135597]	Chr1:15052047..16499873 [GRCh38] Chr1:15378543..16826368 [GRCh37] Chr1:15251130..16698955 [NCBI36] Chr1:1p36.21-36.13	likely pathogenic\|uncertain significance
GRCh38/hg38 1p36.21-36.13(chr1:12724785-16034788)x1	copy number loss	See cases [RCV000137720]	Chr1:12724785..16034788 [GRCh38] Chr1:12784752..16361283 [GRCh37] Chr1:12707339..16233870 [NCBI36] Chr1:1p36.21-36.13	pathogenic
GRCh38/hg38 1p36.21-36.13(chr1:15681812-19662339)x1	copy number loss	See cases [RCV000138070]	Chr1:15681812..19662339 [GRCh38] Chr1:16008307..19988832 [GRCh37] Chr1:15880894..19861419 [NCBI36] Chr1:1p36.21-36.13	pathogenic
GRCh38/hg38 1p36.31-36.13(chr1:6554885-16056011)x3	copy number gain	See cases [RCV000142906]	Chr1:6554885..16056011 [GRCh38] Chr1:6614945..16382506 [GRCh37] Chr1:6537532..16255093 [NCBI36] Chr1:1p36.31-36.13	pathogenic
GRCh38/hg38 1p36.31-36.13(chr1:5363826-18360302)x1	copy number loss	See cases [RCV000142771]	Chr1:5363826..18360302 [GRCh38] Chr1:5423886..18686796 [GRCh37] Chr1:5323746..18559383 [NCBI36] Chr1:1p36.31-36.13	pathogenic
Single allele	complex	Breast ductal adenocarcinoma [RCV000207058]	Chr1:909238..24706269 [GRCh37] Chr1:1p36.33-36.11	uncertain significance
chr1:909238-16736132 complex variant	complex	Breast ductal adenocarcinoma [RCV000207094]	Chr1:909238..16736132 [GRCh37] Chr1:1p36.33-36.13	uncertain significance
GRCh37/hg19 1p36.32-36.12(chr1:2749920-22564787)x1	copy number loss	See cases [RCV000446470]	Chr1:2749920..22564787 [GRCh37] Chr1:1p36.32-36.12	pathogenic
GRCh37/hg19 1p36.21-36.13(chr1:13178371-19961858)x1	copy number loss	See cases [RCV000447987]	Chr1:13178371..19961858 [GRCh37] Chr1:1p36.21-36.13	pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3	copy number gain	See cases [RCV000510383]	Chr1:849467..249224684 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)	copy number gain	See cases [RCV000510926]	Chr1:849467..249224684 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p36.23-36.13(chr1:8850514-16272383)x1	copy number loss	See cases [RCV000512226]	Chr1:8850514..16272383 [GRCh37] Chr1:1p36.23-36.13	likely pathogenic
GRCh37/hg19 1p36.13(chr1:16217579-16496902)x3	copy number gain	not provided [RCV000684552]	Chr1:16217579..16496902 [GRCh37] Chr1:1p36.13	uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3	copy number gain	not provided [RCV000736295]	Chr1:47851..249228449 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3	copy number gain	not provided [RCV000736305]	Chr1:82154..249218992 [GRCh37] Chr1:1p36.33-q44	pathogenic
NM_003443.3(ZBTB17):c.1698-48G>A	single nucleotide variant	not provided [RCV001708395]	Chr1:15943242 [GRCh38] Chr1:16269737 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.2022C>G (p.Ala674=)	single nucleotide variant	not provided [RCV000945623]	Chr1:15942545 [GRCh38] Chr1:16269040 [GRCh37] Chr1:1p36.13	benign
GRCh37/hg19 1p36.21-36.13(chr1:16096742-16725355)x1	copy number loss	not provided [RCV000847705]	Chr1:16096742..16725355 [GRCh37] Chr1:1p36.21-36.13	uncertain significance
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3	copy number gain	Global developmental delay [RCV000787285]	Chr1:103343285..103455144 [GRCh37] Chr1:1p36.22-21.1	uncertain significance
NM_003443.3(ZBTB17):c.1371+112_1371+127del	deletion	not provided [RCV001667287]	Chr1:15944173..15944188 [GRCh38] Chr1:16270668..16270683 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.1070+12A>G	single nucleotide variant	not provided [RCV001689365]	Chr1:15944685 [GRCh38] Chr1:16271180 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.621T>C (p.Ala207=)	single nucleotide variant	not provided [RCV001667664]	Chr1:15945755 [GRCh38] Chr1:16272250 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.1070+36G>T	single nucleotide variant	not provided [RCV001665976]	Chr1:15944661 [GRCh38] Chr1:16271156 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.1002C>T (p.Phe334=)	single nucleotide variant	not provided [RCV001688675]	Chr1:15944765 [GRCh38] Chr1:16271260 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.*21TTTA[1]	microsatellite	not provided [RCV001639682]	Chr1:15941941..15941944 [GRCh38] Chr1:16268436..16268439 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.-2-60G>A	single nucleotide variant	not provided [RCV001710757]	Chr1:15948557 [GRCh38] Chr1:16275052 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.1070+25C>T	single nucleotide variant	not provided [RCV001637682]	Chr1:15944672 [GRCh38] Chr1:16271167 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.536-74G>A	single nucleotide variant	not provided [RCV001617925]	Chr1:15945914 [GRCh38] Chr1:16272409 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.205+17G>A	single nucleotide variant	not provided [RCV001650719]	Chr1:15948274 [GRCh38] Chr1:16274769 [GRCh37] Chr1:1p36.13	benign
GRCh37/hg19 1p36.21-36.12(chr1:16041431-21295864)x1	copy number loss	not provided [RCV001259568]	Chr1:16041431..21295864 [GRCh37] Chr1:1p36.21-36.12	pathogenic
NM_003443.3(ZBTB17):c.1828+76dup	duplication	not provided [RCV001541672]	Chr1:15942982..15942983 [GRCh38] Chr1:16269477..16269478 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.395-144T>G	single nucleotide variant	not provided [RCV001649575]	Chr1:15946438 [GRCh38] Chr1:16272933 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.2129-37G>A	single nucleotide variant	not provided [RCV001686655]	Chr1:15942289 [GRCh38] Chr1:16268784 [GRCh37] Chr1:1p36.13	benign
GRCh37/hg19 1p36.33-36.13(chr1:849466-17525065)x1	copy number loss	not provided [RCV001832902]	Chr1:849466..17525065 [GRCh37] Chr1:1p36.33-36.13	pathogenic
NC_000001.10:g.(?_16096904)_(16271697_?)del	deletion	not provided [RCV003119472]	Chr1:16096904..16271697 [GRCh37] Chr1:1p36.21-36.13	pathogenic
NM_003443.3(ZBTB17):c.1702G>A (p.Val568Ile)	single nucleotide variant	Inborn genetic diseases [RCV003254383]	Chr1:15943190 [GRCh38] Chr1:16269685 [GRCh37] Chr1:1p36.13	uncertain significance
NC_000001.10:g.4481271_20530242del	deletion	Chromosome 1p36 deletion syndrome [RCV003159574]	Chr1:4481271..20530242 [GRCh37] Chr1:1p36.32-36.12	pathogenic
NC_000001.11:g.10115497_16283149dup	duplication	not specified [RCV002286386]	Chr1:10115497..16283149 [GRCh38] Chr1:1p36.22-36.13	likely pathogenic
GRCh37/hg19 1p36.31-36.13(chr1:6758933-19287770)x1	copy number loss	not provided [RCV002474779]	Chr1:6758933..19287770 [GRCh37] Chr1:1p36.31-36.13	pathogenic
NM_003443.3(ZBTB17):c.417G>C (p.Glu139Asp)	single nucleotide variant	Inborn genetic diseases [RCV002882972]	Chr1:15946272 [GRCh38] Chr1:16272767 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.631G>A (p.Glu211Lys)	single nucleotide variant	Inborn genetic diseases [RCV002973989]	Chr1:15945745 [GRCh38] Chr1:16272240 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.1625C>T (p.Ala542Val)	single nucleotide variant	Inborn genetic diseases [RCV002864246]	Chr1:15943471 [GRCh38] Chr1:16269966 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.490G>A (p.Asp164Asn)	single nucleotide variant	Inborn genetic diseases [RCV002849507]	Chr1:15946199 [GRCh38] Chr1:16272694 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.335A>T (p.Lys112Met)	single nucleotide variant	Inborn genetic diseases [RCV002738503]	Chr1:15946994 [GRCh38] Chr1:16273489 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.578C>T (p.Pro193Leu)	single nucleotide variant	Inborn genetic diseases [RCV002848645]	Chr1:15945798 [GRCh38] Chr1:16272293 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.1166G>A (p.Arg389His)	single nucleotide variant	Inborn genetic diseases [RCV002762052]	Chr1:15944505 [GRCh38] Chr1:16271000 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.511G>A (p.Gly171Ser)	single nucleotide variant	Inborn genetic diseases [RCV002887536]	Chr1:15946178 [GRCh38] Chr1:16272673 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.1872C>A (p.Asn624Lys)	single nucleotide variant	Inborn genetic diseases [RCV002848514]	Chr1:15942695 [GRCh38] Chr1:16269190 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.2135A>G (p.Asn712Ser)	single nucleotide variant	Inborn genetic diseases [RCV002757795]	Chr1:15942246 [GRCh38] Chr1:16268741 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.2030A>G (p.Gln677Arg)	single nucleotide variant	Inborn genetic diseases [RCV002986208]	Chr1:15942537 [GRCh38] Chr1:16269032 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.1328A>G (p.Asp443Gly)	single nucleotide variant	Inborn genetic diseases [RCV002891855]	Chr1:15944343 [GRCh38] Chr1:16270838 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.817G>A (p.Gly273Ser)	single nucleotide variant	Inborn genetic diseases [RCV002936325]	Chr1:15945047 [GRCh38] Chr1:16271542 [GRCh37] Chr1:1p36.13	likely benign
NM_003443.3(ZBTB17):c.1597G>C (p.Val533Leu)	single nucleotide variant	Inborn genetic diseases [RCV003194636]	Chr1:15943499 [GRCh38] Chr1:16269994 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.1660G>A (p.Gly554Arg)	single nucleotide variant	Inborn genetic diseases [RCV003195154]	Chr1:15943436 [GRCh38] Chr1:16269931 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.2222C>T (p.Ala741Val)	single nucleotide variant	Inborn genetic diseases [RCV003209948]	Chr1:15942159 [GRCh38] Chr1:16268654 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.563C>T (p.Ala188Val)	single nucleotide variant	Inborn genetic diseases [RCV003180450]	Chr1:15945813 [GRCh38] Chr1:16272308 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.404A>G (p.Lys135Arg)	single nucleotide variant	Inborn genetic diseases [RCV003302638]	Chr1:15946285 [GRCh38] Chr1:16272780 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.505C>T (p.Arg169Cys)	single nucleotide variant	Inborn genetic diseases [RCV003361457]	Chr1:15946184 [GRCh38] Chr1:16272679 [GRCh37] Chr1:1p36.13	uncertain significance
NM_003443.3(ZBTB17):c.1013A>G (p.Glu338Gly)	single nucleotide variant	Inborn genetic diseases [RCV003376267]	Chr1:15944754 [GRCh38] Chr1:16271249 [GRCh37] Chr1:1p36.13	uncertain significance
GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3	copy number gain	Trisomy 12p [RCV003447845]	Chr1:99125..34026935 [GRCh38] Chr1:1p36.33-35.1	pathogenic
GRCh37/hg19 1p36.21-36.12(chr1:16194137-20561434)x1	copy number loss	not specified [RCV003986551]	Chr1:16194137..20561434 [GRCh37] Chr1:1p36.21-36.12	pathogenic
NM_003443.3(ZBTB17):c.395-17C>T	single nucleotide variant	ZBTB17-related condition [RCV003919870]	Chr1:15946311 [GRCh38] Chr1:16272806 [GRCh37] Chr1:1p36.13	benign
NM_003443.3(ZBTB17):c.507C>T (p.Arg169=)	single nucleotide variant	ZBTB17-related condition [RCV003914282]	Chr1:15946182 [GRCh38] Chr1:16272677 [GRCh37] Chr1:1p36.13	likely benign
NM_003443.3(ZBTB17):c.395-30A>G	single nucleotide variant	ZBTB17-related condition [RCV003934626]	Chr1:15946324 [GRCh38] Chr1:16272819 [GRCh37] Chr1:1p36.13	likely benign
NM_003443.3(ZBTB17):c.432C>T (p.Thr144=)	single nucleotide variant	ZBTB17-related condition [RCV003904129]	Chr1:15946257 [GRCh38] Chr1:16272752 [GRCh37] Chr1:1p36.13	likely benign
NM_003443.3(ZBTB17):c.2232G>A (p.Leu744=)	single nucleotide variant	ZBTB17-related condition [RCV003974204]	Chr1:15942149 [GRCh38] Chr1:16268644 [GRCh37] Chr1:1p36.13	likely benign
NM_003443.3(ZBTB17):c.1372-4A>G	single nucleotide variant	ZBTB17-related condition [RCV003964377]	Chr1:15943899 [GRCh38] Chr1:16270394 [GRCh37] Chr1:1p36.13	likely benign
NM_003443.3(ZBTB17):c.2128+9G>A	single nucleotide variant	ZBTB17-related condition [RCV003941810]	Chr1:15942322 [GRCh38] Chr1:16268817 [GRCh37] Chr1:1p36.13	likely benign
NM_003443.3(ZBTB17):c.624A>G (p.Ala208=)	single nucleotide variant	ZBTB17-related condition [RCV003934365]	Chr1:15945752 [GRCh38] Chr1:16272247 [GRCh37] Chr1:1p36.13	likely benign

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	5457
Count of miRNA genes:	1046
Interacting mature miRNAs:	1328
Transcripts:	ENST00000375733, ENST00000375743, ENST00000440560, ENST00000444358, ENST00000448462, ENST00000462525, ENST00000464719, ENST00000471805, ENST00000472658, ENST00000474511, ENST00000479282, ENST00000487785, ENST00000488008, ENST00000490899, ENST00000492834, ENST00000494020, ENST00000537142
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

Markers in Region

SHGC-31102

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	16,280,445 - 16,280,594	UniSTS	GRCh37
Build 36	1	16,153,032 - 16,153,181	RGD	NCBI36
Celera	1	14,760,319 - 14,760,468	RGD
Cytogenetic Map	1	p36.13	UniSTS
HuRef	1	14,799,453 - 14,799,602	UniSTS
TNG Radiation Hybrid Map	1	23511.0	UniSTS
GeneMap99-GB4 RH Map	1	56.67	UniSTS
Whitehead-RH Map	1	55.1	UniSTS
GeneMap99-G3 RH Map	1	816.0	UniSTS

D1S1336

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	16,288,006 - 16,288,197	UniSTS	GRCh37
Build 36	1	16,160,593 - 16,160,784	RGD	NCBI36
Celera	1	14,767,880 - 14,768,071	RGD
Cytogenetic Map	1	p36.13	UniSTS
HuRef	1	14,807,018 - 14,807,209	UniSTS

ZBTB17_8746

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	16,268,169 - 16,268,742	UniSTS	GRCh37
Build 36	1	16,140,756 - 16,141,329	RGD	NCBI36
Celera	1	14,748,043 - 14,748,616	RGD
HuRef	1	14,787,177 - 14,787,750	UniSTS

SHGC-74246

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	16,268,372 - 16,268,498	UniSTS	GRCh37
Build 36	1	16,140,959 - 16,141,085	RGD	NCBI36
Celera	1	14,748,246 - 14,748,372	RGD
Cytogenetic Map	1	p36.13	UniSTS
HuRef	1	14,787,380 - 14,787,506	UniSTS
TNG Radiation Hybrid Map	1	23529.0	UniSTS
GeneMap99-GB4 RH Map	1	56.57	UniSTS

A005O01

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	16,268,372 - 16,268,498	UniSTS	GRCh37
Build 36	1	16,140,959 - 16,141,085	RGD	NCBI36
Celera	1	14,748,246 - 14,748,372	RGD
Cytogenetic Map	1	p36.13	UniSTS
HuRef	1	14,787,380 - 14,787,506	UniSTS
GeneMap99-GB4 RH Map	1	56.87	UniSTS

RH64190

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	16,268,369 - 16,268,497	UniSTS	GRCh37
Build 36	1	16,140,956 - 16,141,084	RGD	NCBI36
Celera	1	14,748,243 - 14,748,371	RGD
Cytogenetic Map	1	p36.13	UniSTS
HuRef	1	14,787,377 - 14,787,505	UniSTS
GeneMap99-GB4 RH Map	1	56.67	UniSTS

RH70580

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	16,268,600 - 16,268,884	UniSTS	GRCh37
Build 36	1	16,141,187 - 16,141,471	RGD	NCBI36
Celera	1	14,748,474 - 14,748,758	RGD
Cytogenetic Map	1	p36.13	UniSTS
HuRef	1	14,787,608 - 14,787,892	UniSTS
GeneMap99-GB4 RH Map	1	54.76	UniSTS

STS-AA013259

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	16,270,260 - 16,270,881	UniSTS	GRCh37
Celera	1	14,750,134 - 14,750,755	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
HuRef	1	14,789,268 - 14,789,889	UniSTS
GeneMap99-GB4 RH Map	1	56.57	UniSTS

Expression

RNA-SEQ Expression

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

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

2361

2220

1369

272

1769

120

4059

1545

2926

278

1433

1576

165

1180

2509

Low

769

356

351

181

345

297

651

807

140

279

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001242884	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001287603	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001287604	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001324137	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001324138	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_003443	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005245986	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005245987	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011542085	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011542086	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011542087	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011542088	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017002242	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429978	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054338630	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054338631	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054338632	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054338633	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001737399	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AK223618	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK226168	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK294796	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK299820	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK301896	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302610	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK303823	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK309081	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK311083	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK315201	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL034555	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL355994	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC126163	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC143965	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC143968	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ575263	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU634371	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471167	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068277	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB064089	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M88369	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	U20647	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	Y09723	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000375733 ⟹ ENSP00000364885

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,941,871 - 15,976,132 (-)	Ensembl

RefSeq Acc Id:

ENST00000375743 ⟹ ENSP00000364895

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,941,869 - 15,976,101 (-)	Ensembl

RefSeq Acc Id:

ENST00000440560 ⟹ ENSP00000400827

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,941,869 - 15,943,089 (-)	Ensembl

RefSeq Acc Id:

ENST00000444358 ⟹ ENSP00000408483

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,942,407 - 15,944,428 (-)	Ensembl

RefSeq Acc Id:

ENST00000462525

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,941,869 - 15,942,722 (-)	Ensembl

RefSeq Acc Id:

ENST00000464719

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,945,721 - 15,947,292 (-)	Ensembl

RefSeq Acc Id:

ENST00000471805

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,943,240 - 15,944,358 (-)	Ensembl

RefSeq Acc Id:

ENST00000472658

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,943,257 - 15,943,926 (-)	Ensembl

RefSeq Acc Id:

ENST00000474511

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,943,429 - 15,944,393 (-)	Ensembl

RefSeq Acc Id:

ENST00000479282

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,945,846 - 15,976,104 (-)	Ensembl

RefSeq Acc Id:

ENST00000487785

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,943,599 - 15,944,403 (-)	Ensembl

RefSeq Acc Id:

ENST00000488008

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,942,756 - 15,943,384 (-)	Ensembl

RefSeq Acc Id:

ENST00000490899

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,944,988 - 15,947,105 (-)	Ensembl

RefSeq Acc Id:

ENST00000492834

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,944,417 - 15,946,084 (-)	Ensembl

RefSeq Acc Id:

ENST00000494020

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,945,933 - 15,952,973 (-)	Ensembl

RefSeq Acc Id:

ENST00000537142 ⟹ ENSP00000438529

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	15,941,871 - 15,976,079 (-)	Ensembl

RefSeq Acc Id:

NM_001242884 ⟹ NP_001229813

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	15,941,869 - 15,976,101 (-)	NCBI
GRCh37	1	16,268,364 - 16,302,627 (-)	NCBI
HuRef	1	14,787,372 - 14,821,661 (-)	ENTREZGENE
CHM1_1	1	16,066,899 - 16,101,159 (-)	NCBI
T2T-CHM13v2.0	1	15,383,149 - 15,417,408 (-)	NCBI

Sequence:

show sequence

GAGGTCGGTTCCGCCCGACTCTAACATGGCGGCGCCCTTTGTCTGCTCTGGAGTGCCGTCCCCG
GCCTTCTCGCGGCCGTGATGCACCTCCCTCTGCGGTGGGGTCCGGGACATGGCAGGTAATGAGC
CGGACGAGGGGAGCCAAGCTGGAGTTTACACAGGCAAACTGTCAGAAAAGAGTAGCCTGGGCTG
TCTGGAAATCTGAGGCCTGGGGCAGGTGCTGGAGTTTATGTACACGGCCAAGCTGAGCCTGAGC
CCTGAGAACGTGGATGATGTGCTGGCCGTGGCCACTTTCCTCCAAATGCAGGACATCATCACGG
CCTGCCATGCCCTCAAGTCACTTGCTGAGCCGGCTACCAGCCCTGGGGGAAATGCGGAGGCCTT
GGCCACAGAAGGTCTGCCCTGTTCCATCTCCAGGAGGGGACAAGAGAGCCAAAGAGGAGAAGGT
GGCCACCAGCACGCTGAGCAGGCTGGAGCAGGCAGGACGCAGCACACCCATAGGCCCCAGCAGG
GACCTCAAGGAGGAGCGCGGCGGTCAGGCCCAGAGTGCGGCCAGCGGTGCAGAGCAGACAGAGA
AAGCCGATGCGCCCCGGGAGCCGCCGCCTGTGGAGCTCAAGCCAGACCCCACGAGTGGCATGGC
TGCTGCAGAAGCTGAGGCCGCTTTGTCCGAGAGCTCGGAGCAAGAAATGGAGGTGGAGCCCGCC
CGGAAAGGGGAAGAGGAGCAAAAGGAGCAAGAGGAGCAAGAGGAGGAGGGCGCAGGGCCAGCTG
AGGTCAAGGAGGAGGGTTCCCAGCTGGAGAACGGAGAGGCCCCCGAGGAGAACGAGAATGAGGA
GTCAGCGGGCACAGACTCGGGGCAGGAGCTCGGCTCCGAGGCCCGGGGCCTGCGCTCAGGCACC
TACGGCGACCGCACGGAGTCCAAGGCCTACGGCTCCGTCATCCACAAGTGCGAGGACTGTGGGA
AGGAGTTCACGCACACGGGGAACTTCAAGCGGCACATCCGCATCCACACGGGGGAGAAGCCCTT
CTCGTGCCGGGAGTGCAGCAAGGCCTTTTCCGACCCGGCCGCGTGCAAGGCCCATGAGAAGACG
CACAGCCCTCTGAAGCCCTACGGCTGCGAGGAGTGCGGGAAGAGCTACCGCCTCATCAGCCTGC
TGAACCTGCACAAGAAGCGGCACTCGGGCGAGGCGCGCTACCGCTGCGAGGACTGCGGCAAGCT
CTTCACCACCTCGGGCAACCTCAAGCGCCACCAGCTGGTGCACAGCGGCGAGAAGCCCTACCAG
TGCGACTACTGCGGCCGCTCCTTCTCCGACCCCACTTCCAAGATGCGCCACCTGGAGACCCACG
ACACGGACAAGGAGCACAAGTGCCCACACTGCGACAAGAAGTTCAACCAGGTAGGGAACCTGAA
GGCCCACCTGAAGATCCACATCGCTGACGGGCCCCTCAAGTGCCGAGAGTGTGGGAAGCAGTTC
ACCACCTCAGGGAACCTGAAGCGGCACCTTCGGATCCACAGCGGGGAGAAGCCCTACGTGTGCA
TCCACTGCCAGCGACAGTTTGCAGACCCCGGCGCTCTGCAGCGGCACGTCCGCATTCACACAGG
TGAGAAGCCATGCCAGTGTGTGATGTGCGGTAAGGCCTTCACCCAGGCCAGCTCCCTCATCGCC
CACGTGCGCCAGCACACCGGGGAGAAGCCCTACGTCTGCGAGCGCTGCGGCAAGAGATTCGTCC
AGTCCAGCCAGTTGGCCAATCATATTCGCCACCACGACAACATCCGCCCACACAAGTGCAGCGT
GTGCAGCAAGGCCTTCGTGAACGTGGGGGACCTGTCCAAGCACATCATCATTCACACTGGAGAG
AAGCCTTACCTGTGTGATAAGTGTGGGCGTGGCTTCAACCGGGTAGACAACCTGCGCTCCCACG
TGAAGACCGTGCACCAGGGCAAGGCAGGCATCAAGATCCTGGAGCCCGAGGAGGGCAGTGAGGT
CAGCGTGGTCACTGTGGATGACATGGTCACGCTGGCTACCGAGGCACTGGCAGCGACAGCCGTC
ACTCAGCTCACAGTGGTGCCGGTGGGAGCTGCAGTGACAGCCGATGAGACGGAAGTCCTGAAGG
CCGAGATCAGCAAAGCTGTGAAGCAAGTGCAGGAAGAAGACCCCAACACTCACATCCTCTACGC
CTGTGACTCCTGTGGGGACAAGTTTCTGGATGCCAACAGCCTGGCTCAGCATGTGCGAATCCAC
ACAGCCCAGGCACTGGTCATGTTCCAGACAGACGCGGACTTCTATCAGCAGTATGGGCCAGGTG
GCACGTGGCCTGCCGGGCAGGTGCTGCAGGCTGGGGAGCTGGTCTTCCGCCCTCGCGACGGGGC
TGAGGGCCAGCCCGCACTGGCAGAGACCTCCCCTACAGCTCCTGAATGTCCCCCGCCTGCCGAG
TGAGCTGGCGGCCCTTCTGACTGTTTATTTAAGGATGGATGGCACCCTGGAACCGGGAAGGGTG
GCCTGTTCCCTAGAGAGAATAAATTGGATTATTTTCTAA

hide sequence

RefSeq Acc Id:

NM_001287603 ⟹ NP_001274532

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	15,941,869 - 15,976,101 (-)	NCBI
HuRef	1	14,787,372 - 14,821,661 (-)	NCBI
CHM1_1	1	16,066,899 - 16,101,159 (-)	NCBI
T2T-CHM13v2.0	1	15,383,149 - 15,417,408 (-)	NCBI

Sequence:

show sequence

GAGGTCGGTTCCGCCCGACTCTAACATGGCGGCGCCCTTTGTCTGCTCTGGAGTGCCGTCCCCG
GCCTTCTCGCGGCCGTGATGCACCTCCCTCTGCGGTGGGGTCCGGGACATGGCAGGTAATGAGC
CGGACGAGGGGAGCCAAGCTGGAGTTTACACAGGCAAACTGTCAGAAAAGAGTAGCCTGGGCTG
TCTGGAAATCTGAGCCATGGACTTTCCCCAGCACAGCCAGCATGTCTTGGAACAGCTGAACCAG
CAGCGGCAGCTGGGGCTTCTCTGTGACTGCACCTTTGTGGTGGACGGTGTTCACTTTAAGGCTC
ATAAAGCAGTGCTGGCGGCCTGCAGCGAGTACTTCAAGATGCTCTTCGTGGACCAGAAGGACGT
GGTGCACCTGGACATCAGTAACGCGGCAGGCCTGGGGCAGGTGCTGGAGTTTATGTACACGGCC
AAGCTGAGCCTGAGCCCTGAGAACGTGGATGATGTGCTGGCCGTGGCCACTTTCCTCCAAATGC
AGGACATCATCACGGCCTGCCATGCCCTCAAGTCACTTGCTGAGCCGGCTACCAGCCCTGGGGG
AAATGCGGAGGCCTTGGCCACAGAAGGAGGGGACAAGAGAGCCAAAGAGGAGAAGGTGGCCACC
AGCACGCTGAGCAGGCTGGAGCAGGCAGGACGCAGCACACCCATAGGCCCCAGCAGGGACCTCA
AGGAGGAGCGCGGCGGTCAGGCCCAGAGTGCGGCCAGCGGTGCAGAGCAGACAGAGAAAGCCGA
TGCGCCCCGGGAGCCGCCGCCTGTGGAGCTCAAGCCAGACCCCACGAGTGGCATGGCTGCTGCA
GAAGCTGAGGCCGCTTTGTCCGAGAGCTCGGAGCAAGAAATGGAGGTGGAGCCCGCCCGGAAAG
GGGAAGAGGAGCAAAAGGAGCAAGAGGAGCAAGAGGAGGAGGGCGCAGGGCCAGCTGAGGTCAA
GGAGGAGGGTTCCCAGCTGGAGAACGGAGAGGCCCCCGAGGAGAACGAGAATGAGGAGTCAGCG
GGCACAGACTCGGGGCAGGAGCTCGGCTCCGAGGCCCGGGGCCTGCGCTCAGGCACCTACGGCG
ACCGCACGGAGTCCAAGGCCTACGGCTCCGTCATCCACAAGTGCGAGGACTGTGGGAAGGAGTT
CACGCACACGGGGAACTTCAAGCGGCACATCCGCATCCACACGGGGGAGAAGCCCTTCTCGTGC
CGGGAGTGCAGCAAGGCCTTTTCCGACCCGGCCGCGTGCAAGGCCCATGAGAAGACGCACAGCC
CTCTGAAGCCCTACGGCTGCGAGGAGTGCGGGAAGAGCTACCGCCTCATCAGCCTGCTGAACCT
GCACAAGAAGCGGCACTCGGGCGAGGCGCGCTACCGCTGCGAGGACTGCGGCAAGCTCTTCACC
ACCTCGGGCAACCTCAAGCGCCACCAGCTGGTGCACAGCGGCGAGAAGCCCTACCAGTGCGACT
ACTGCGGCCGCTCCTTCTCCGACCCCACTTCCAAGATGCGCCACCTGGAGACCCACGACACGGA
CAAGGAGCACAAGTGCCCACACTGCGACAAGAAGTTCAACCAGGTAGGGAACCTGAAGGCCCAC
CTGAAGATCCACATCGCTGACGGGCCCCTCAAGTGCCGAGAGTGTGGGAAGCAGTTCACCACCT
CAGGGAACCTGAAGCGGCACCTTCGGATCCACAGCGGGGAGAAGCCCTACGTGTGCATCCACTG
CCAGCGACAGTTTGCAGACCCCGGCGCTCTGCAGCGGCACGTCCGCATTCACACAGGTGAGAAG
CCATGCCAGTGTGTGATGTGCGGTAAGGCCTTCACCCAGGCCAGCTCCCTCATCGCCCACGTGC
GCCAGCACACCGGGGAGAAGCCCTACGTCTGCGAGCGCTGCGGCAAGAGATTCGTCCAGTCCAG
CCAGTTGGCCAATCATATTCGCCACCACGACAACATCCGCCCACACAAGTGCAGCGTGTGCAGC
AAGGCCTTCGTGAACGTGGGGGACCTGTCCAAGCACATCATCATTCACACTGGAGAGAAGCCTT
ACCTGTGTGATAAGTGTGGGCGTGGCTTCAACCGGGTAGACAACCTGCGCTCCCACGTGAAGAC
CGTGCACCAGGGCAAGGCAGGCATCAAGATCCTGGAGCCCGAGGAGGGCAGTGAGGTCAGCGTG
GTCACTGTGGATGACATGGTCACGCTGGCTACCGAGGCACTGGCAGCGACAGCCGTCACTCAGC
TCACAGGCCCTGCGACTCTGCCCGCAGTGGTGCCGGTGGGAGCTGCAGTGACAGCCGATGAGAC
GGAAGTCCTGAAGGCCGAGATCAGCAAAGCTGTGAAGCAAGTGCAGGAAGAAGACCCCAACACT
CACATCCTCTACGCCTGTGACTCCTGTGGGGACAAGTTTCTGGATGCCAACAGCCTGGCTCAGC
ATGTGCGAATCCACACAGCCCAGGCACTGGTCATGTTCCAGACAGACGCGGACTTCTATCAGCA
GTATGGGCCAGGTGGCACGTGGCCTGCCGGGCAGGTGCTGCAGGCTGGGGAGCTGGTCTTCCGC
CCTCGCGACGGGGCTGAGGGCCAGCCCGCACTGGCAGAGACCTCCCCTACAGCTCCTGAATGTC
CCCCGCCTGCCGAGTGAGCTGGCGGCCCTTCTGACTGTTTATTTAAGGATGGATGGCACCCTGG
AACCGGGAAGGGTGGCCTGTTCCCTAGAGAGAATAAATTGGATTATTTTCTAA

hide sequence

RefSeq Acc Id:

NM_001287604 ⟹ NP_001274533

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	15,941,869 - 15,976,101 (-)	NCBI
HuRef	1	14,787,372 - 14,821,661 (-)	NCBI
CHM1_1	1	16,066,899 - 16,101,159 (-)	NCBI
T2T-CHM13v2.0	1	15,383,149 - 15,417,408 (-)	NCBI

Sequence:

show sequence

GAGGTCGGTTCCGCCCGACTCTAACATGGCGGCGCCCTTTGTCTGCTCTGGAGTGCCGTCCCCG
GCCTTCTCGCGGCCGTGATGCACCTCCCTCTGCGGTGGGGTCCGGGACATGGCAGGTAATGAGC
CGGACGAGGGGAGCCAAGCTGGAGTTTACACAGGCAAACTGTCAGAAAAGAGTAGCCTGGGCTG
TCTGGAAATCTGAGCCATGGACTTTCCCCAGCACAGCCAGCATGTCTTGGAACAGCTGAACCAG
CAGCGGCAGCTGGGGCTTCTCTGTGACTGCACCTTTGTGGTGGACGGTGTTCACTTTAAGGCTC
ATAAAGCAGTGCTGGCGGCCTGCAGCGAGTACTTCAAGATGCTCTTCGTGGACCAGAAGGACGT
GGTGCACCTGGACATCAGTAACGCGGCCTGGGGCAGGTGCTGGAGTTTATGTACACGGCCAAGC
TGAGCCTGAGCCCTGAGAACGTGGATGATGTGCTGGCCGTGGCCACTTTCCTCCAAATGCAGGA
CATCATCACGGCCTGCCATGCCCTCAAGTCACTTGCTGAGCCGGCTACCAGCCCTGGGGGAAAT
GCGGAGGCCTTGGCCACAGAAGGAGGGGACAAGAGAGCCAAAGAGGAGAAGGTGGCCACCAGCA
CGCTGAGCAGGCTGGAGCAGGCAGGACGCAGCACACCCATAGGCCCCAGCAGGGACCTCAAGGA
GGAGCGCGGCGGTCAGGCCCAGAGTGCGGCCAGCGGTGCAGAGCAGACAGAGAAAGCCGATGCG
CCCCGGGAGCCGCCGCCTGTGGAGCTCAAGCCAGACCCCACGAGTGGCATGGCTGCTGCAGAAG
CTGAGGCCGCTTTGTCCGAGAGCTCGGAGCAAGAAATGGAGGTGGAGCCCGCCCGGAAAGGGGA
AGAGGAGCAAAAGGAGCAAGAGGAGCAAGAGGAGGAGGGCGCAGGGCCAGCTGAGGTCAAGGAG
GAGGGTTCCCAGCTGGAGAACGGAGAGGCCCCCGAGGAGAACGAGAATGAGGAGTCAGCGGGCA
CAGACTCGGGGCAGGAGCTCGGCTCCGAGGCCCGGGGCCTGCGCTCAGGCACCTACGGCGACCG
CACGGAGTCCAAGGCCTACGGCTCCGTCATCCACAAGTGCGAGGACTGTGGGAAGGAGTTCACG
CACACGGGGAACTTCAAGCGGCACATCCGCATCCACACGGGGGAGAAGCCCTTCTCGTGCCGGG
AGTGCAGCAAGGCCTTTTCCGACCCGGCCGCGTGCAAGGCCCATGAGAAGACGCACAGCCCTCT
GAAGCCCTACGGCTGCGAGGAGTGCGGGAAGAGCTACCGCCTCATCAGCCTGCTGAACCTGCAC
AAGAAGCGGCACTCGGGCGAGGCGCGCTACCGCTGCGAGGACTGCGGCAAGCTCTTCACCACCT
CGGGCAACCTCAAGCGCCACCAGCTGGTGCACAGCGGCGAGAAGCCCTACCAGTGCGACTACTG
CGGCCGCTCCTTCTCCGACCCCACTTCCAAGATGCGCCACCTGGAGACCCACGACACGGACAAG
GAGCACAAGTGCCCACACTGCGACAAGAAGTTCAACCAGGTAGGGAACCTGAAGGCCCACCTGA
AGATCCACATCGCTGACGGGCCCCTCAAGTGCCGAGAGTGTGGGAAGCAGTTCACCACCTCAGG
GAACCTGAAGCGGCACCTTCGGATCCACAGCGGGGAGAAGCCCTACGTGTGCATCCACTGCCAG
CGACAGTTTGCAGACCCCGGCGCTCTGCAGCGGCACGTCCGCATTCACACAGGTGAGAAGCCAT
GCCAGTGTGTGATGTGCGGTAAGGCCTTCACCCAGGCCAGCTCCCTCATCGCCCACGTGCGCCA
GCACACCGGGGAGAAGCCCTACGTCTGCGAGCGCTGCGGCAAGAGATTCGTCCAGTCCAGCCAG
TTGGCCAATCATATTCGCCACCACGACAACATCCGCCCACACAAGTGCAGCGTGTGCAGCAAGG
CCTTCGTGAACGTGGGGGACCTGTCCAAGCACATCATCATTCACACTGGAGAGAAGCCTTACCT
GTGTGATAAGTGTGGGCGTGGCTTCAACCGGGTAGACAACCTGCGCTCCCACGTGAAGACCGTG
CACCAGGGCAAGGCAGGCATCAAGATCCTGGAGCCCGAGGAGGGCAGTGAGGTCAGCGTGGTCA
CTGTGGATGACATGGTCACGCTGGCTACCGAGGCACTGGCAGCGACAGCCGTCACTCAGCTCAC
AGTGGTGCCGGTGGGAGCTGCAGTGACAGCCGATGAGACGGAAGTCCTGAAGGCCGAGATCAGC
AAAGCTGTGAAGCAAGTGCAGGAAGAAGACCCCAACACTCACATCCTCTACGCCTGTGACTCCT
GTGGGGACAAGTTTCTGGATGCCAACAGCCTGGCTCAGCATGTGCGAATCCACACAGCCCAGGC
ACTGGTCATGTTCCAGACAGACGCGGACTTCTATCAGCAGTATGGGCCAGGTGGCACGTGGCCT
GCCGGGCAGGTGCTGCAGGCTGGGGAGCTGGTCTTCCGCCCTCGCGACGGGGCTGAGGGCCAGC
CCGCACTGGCAGAGACCTCCCCTACAGCTCCTGAATGTCCCCCGCCTGCCGAGTGAGCTGGCGG
CCCTTCTGACTGTTTATTTAAGGATGGATGGCACCCTGGAACCGGGAAGGGTGGCCTGTTCCCT
AGAGAGAATAAATTGGATTATTTTCTAA

hide sequence

RefSeq Acc Id:

NM_001324137 ⟹ NP_001311066

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	15,941,869 - 15,976,101 (-)	NCBI
CHM1_1	1	16,066,899 - 16,101,159 (-)	NCBI
T2T-CHM13v2.0	1	15,383,149 - 15,417,408 (-)	NCBI

Sequence:

show sequence

GAGGTCGGTTCCGCCCGACTCTAACATGGCGGCGCCCTTTGTCTGCTCTGGAGTGCCGTCCCCG
GCCTTCTCGCGGCCGTGATGCACCTCCCTCTGCGGTGGGGTCCGGGACATGGCAGGTAATGAGC
CGGACGAGGGGAGCCAAGCTGGAGTTTACACAGGCAAACTGTCAGAAAAGAGTAGCCTGGGCTG
TCTGGAAATCTGAGGCCTGGGGCAGGTGCTGGAGTTTATGTACACGGCCAAGCTGAGCCTGAGC
CCTGAGAACGTGGATGATGTGCTGGCCGTGGCCACTTTCCTCCAAATGCAGGACATCATCACGG
CCTGCCATGCCCTCAAGTCACTTGCTGAGCCGGCTACCAGCCCTGGGGGAAATGCGGAGGCCTT
GGCCACAGAAGGAGGGGACAAGAGAGCCAAAGAGGAGAAGGTGGCCACCAGCACGCTGAGCAGG
CTGGAGCAGGCAGGACGCAGCACACCCATAGGCCCCAGCAGGGACCTCAAGGAGGAGCGCGGCG
GTCAGGCCCAGAGTGCGGCCAGCGGTGCAGAGCAGACAGAGAAAGCCGATGCGCCCCGGGAGCC
GCCGCCTGTGGAGCTCAAGCCAGACCCCACGAGTGGCATGGCTGCTGCAGAAGCTGAGGCCGCT
TTGTCCGAGAGCTCGGAGCAAGAAATGGAGGTGGAGCCCGCCCGGAAAGGGGAAGAGGAGCAAA
AGGAGCAAGAGGAGCAAGAGGAGGAGGGCGCAGGGCCAGCTGAGGTCAAGGAGGAGGGTTCCCA
GCTGGAGAACGGAGAGGCCCCCGAGGAGAACGAGAATGAGGAGTCAGCGGGCACAGACTCGGGG
CAGGAGCTCGGCTCCGAGGCCCGGGGCCTGCGCTCAGGCACCTACGGCGACCGCACGGAGTCCA
AGGCCTACGGCTCCGTCATCCACAAGTGCGAGGACTGTGGGAAGGAGTTCACGCACACGGGGAA
CTTCAAGCGGCACATCCGCATCCACACGGGGGAGAAGCCCTTCTCGTGCCGGGAGTGCAGCAAG
GCCTTTTCCGACCCGGCCGCGTGCAAGGCCCATGAGAAGACGCACAGCCCTCTGAAGCCCTACG
GCTGCGAGGAGTGCGGGAAGAGCTACCGCCTCATCAGCCTGCTGAACCTGCACAAGAAGCGGCA
CTCGGGCGAGGCGCGCTACCGCTGCGAGGACTGCGGCAAGCTCTTCACCACCTCGGGCAACCTC
AAGCGCCACCAGCTGGTGCACAGCGGCGAGAAGCCCTACCAGTGCGACTACTGCGGCCGCTCCT
TCTCCGACCCCACTTCCAAGATGCGCCACCTGGAGACCCACGACACGGACAAGGAGCACAAGTG
CCCACACTGCGACAAGAAGTTCAACCAGGTAGGGAACCTGAAGGCCCACCTGAAGATCCACATC
GCTGACGGGCCCCTCAAGTGCCGAGAGTGTGGGAAGCAGTTCACCACCTCAGGGAACCTGAAGC
GGCACCTTCGGATCCACAGCGGGGAGAAGCCCTACGTGTGCATCCACTGCCAGCGACAGTTTGC
AGACCCCGGCGCTCTGCAGCGGCACGTCCGCATTCACACAGGTGAGAAGCCATGCCAGTGTGTG
ATGTGCGGTAAGGCCTTCACCCAGGCCAGCTCCCTCATCGCCCACGTGCGCCAGCACACCGGGG
AGAAGCCCTACGTCTGCGAGCGCTGCGGCAAGAGATTCGTCCAGTCCAGCCAGTTGGCCAATCA
TATTCGCCACCACGACAACATCCGCCCACACAAGTGCAGCGTGTGCAGCAAGGCCTTCGTGAAC
GTGGGGGACCTGTCCAAGCACATCATCATTCACACTGGAGAGAAGCCTTACCTGTGTGATAAGT
GTGGGCGTGGCTTCAACCGGGTAGACAACCTGCGCTCCCACGTGAAGACCGTGCACCAGGGCAA
GGCAGGCATCAAGATCCTGGAGCCCGAGGAGGGCAGTGAGGTCAGCGTGGTCACTGTGGATGAC
ATGGTCACGCTGGCTACCGAGGCACTGGCAGCGACAGCCGTCACTCAGCTCACAGTGGTGCCGG
TGGGAGCTGCAGTGACAGCCGATGAGACGGAAGTCCTGAAGGCCGAGATCAGCAAAGCTGTGAA
GCAAGTGCAGGAAGAAGACCCCAACACTCACATCCTCTACGCCTGTGACTCCTGTGGGGACAAG
TTTCTGGATGCCAACAGCCTGGCTCAGCATGTGCGAATCCACACAGCCCAGGCACTGGTCATGT
TCCAGACAGACGCGGACTTCTATCAGCAGTATGGGCCAGGTGGCACGTGGCCTGCCGGGCAGGT
GCTGCAGGCTGGGGAGCTGGTCTTCCGCCCTCGCGACGGGGCTGAGGGCCAGCCCGCACTGGCA
GAGACCTCCCCTACAGCTCCTGAATGTCCCCCGCCTGCCGAGTGAGCTGGCGGCCCTTCTGACT
GTTTATTTAAGGATGGATGGCACCCTGGAACCGGGAAGGGTGGCCTGTTCCCTAGAGAGAATAA
ATTGGATTATTTTCTAA

hide sequence

RefSeq Acc Id:

NM_001324138 ⟹ NP_001311067

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	15,941,869 - 15,976,101 (-)	NCBI
CHM1_1	1	16,066,899 - 16,101,159 (-)	NCBI
T2T-CHM13v2.0	1	15,383,149 - 15,417,408 (-)	NCBI

Sequence:

show sequence

GAGGTCGGTTCCGCCCGACTCTAACATGGCGGCGCCCTTTGTCTGCTCTGGAGTGCCGTCCCCG
GCCTTCTCGCGGCCGTGATGCACCTCCCTCTGCGGTGGGGTCCGGGACATGGCAGGTAATGAGC
CGGACGAGGGGAGCCAAGCTGGAGTTTACACAGGCAAACTGTCAGAAAAGAGTAGCCTGGGCTG
TCTGGAAATCTGAGCCATGGACTTTCCCCAGCACAGCCAGCATGTCTTGGAACAGCTGAACCAG
CAGCGGCAGCTGGGGCTTCTCTGTGACTGCACCTTTGTGGTGGACGGTGTTCACTTTAAGGCTC
ATAAAGCAGTGCTGGCGGCCTGCAGCGAGTACTTCAAGATGCTCTTCGTGGACCAGAAGGACGT
GGTGCACCTGGACATCAGTAACGCGGCAGGAGGGGACAAGAGAGCCAAAGAGGAGAAGGTGGCC
ACCAGCACGCTGAGCAGGCTGGAGCAGGCAGGACGCAGCACACCCATAGGCCCCAGCAGGGACC
TCAAGGAGGAGCGCGGCGGTCAGGCCCAGAGTGCGGCCAGCGGTGCAGAGCAGACAGAGAAAGC
CGATGCGCCCCGGGAGCCGCCGCCTGTGGAGCTCAAGCCAGACCCCACGAGTGGCATGGCTGCT
GCAGAAGCTGAGGCCGCTTTGTCCGAGAGCTCGGAGCAAGAAATGGAGGTGGAGCCCGCCCGGA
AAGGGGAAGAGGAGCAAAAGGAGCAAGAGGAGCAAGAGGAGGAGGGCGCAGGGCCAGCTGAGGT
CAAGGAGGAGGGTTCCCAGCTGGAGAACGGAGAGGCCCCCGAGGAGAACGAGAATGAGGAGTCA
GCGGGCACAGACTCGGGGCAGGAGCTCGGCTCCGAGGCCCGGGGCCTGCGCTCAGGCACCTACG
GCGACCGCACGGAGTCCAAGGCCTACGGCTCCGTCATCCACAAGTGCGAGGACTGTGGGAAGGA
GTTCACGCACACGGGGAACTTCAAGCGGCACATCCGCATCCACACGGGGGAGAAGCCCTTCTCG
TGCCGGGAGTGCAGCAAGGCCTTTTCCGACCCGGCCGCGTGCAAGGCCCATGAGAAGACGCACA
GCCCTCTGAAGCCCTACGGCTGCGAGGAGTGCGGGAAGAGCTACCGCCTCATCAGCCTGCTGAA
CCTGCACAAGAAGCGGCACTCGGGCGAGGCGCGCTACCGCTGCGAGGACTGCGGCAAGCTCTTC
ACCACCTCGGGCAACCTCAAGCGCCACCAGCTGGTGCACAGCGGCGAGAAGCCCTACCAGTGCG
ACTACTGCGGCCGCTCCTTCTCCGACCCCACTTCCAAGATGCGCCACCTGGAGACCCACGACAC
GGACAAGGAGCACAAGTGCCCACACTGCGACAAGAAGTTCAACCAGGTAGGGAACCTGAAGGCC
CACCTGAAGATCCACATCGCTGACGGGCCCCTCAAGTGCCGAGAGTGTGGGAAGCAGTTCACCA
CCTCAGGGAACCTGAAGCGGCACCTTCGGATCCACAGCGGGGAGAAGCCCTACGTGTGCATCCA
CTGCCAGCGACAGTTTGCAGACCCCGGCGCTCTGCAGCGGCACGTCCGCATTCACACAGGTGAG
AAGCCATGCCAGTGTGTGATGTGCGGTAAGGCCTTCACCCAGGCCAGCTCCCTCATCGCCCACG
TGCGCCAGCACACCGGGGAGAAGCCCTACGTCTGCGAGCGCTGCGGCAAGAGATTCGTCCAGTC
CAGCCAGTTGGCCAATCATATTCGCCACCACGACAACATCCGCCCACACAAGTGCAGCGTGTGC
AGCAAGGCCTTCGTGAACGTGGGGGACCTGTCCAAGCACATCATCATTCACACTGGAGAGAAGC
CTTACCTGTGTGATAAGTGTGGGCGTGGCTTCAACCGGGTAGACAACCTGCGCTCCCACGTGAA
GACCGTGCACCAGGGCAAGGCAGGCATCAAGATCCTGGAGCCCGAGGAGGGCAGTGAGGTCAGC
GTGGTCACTGTGGATGACATGGTCACGCTGGCTACCGAGGCACTGGCAGCGACAGCCGTCACTC
AGCTCACAGTGGTGCCGGTGGGAGCTGCAGTGACAGCCGATGAGACGGAAGTCCTGAAGGCCGA
GATCAGCAAAGCTGTGAAGCAAGTGCAGGAAGAAGACCCCAACACTCACATCCTCTACGCCTGT
GACTCCTGTGGGGACAAGTTTCTGGATGCCAACAGCCTGGCTCAGCATGTGCGAATCCACACAG
CCCAGGCACTGGTCATGTTCCAGACAGACGCGGACTTCTATCAGCAGTATGGGCCAGGTGGCAC
GTGGCCTGCCGGGCAGGTGCTGCAGGCTGGGGAGCTGGTCTTCCGCCCTCGCGACGGGGCTGAG
GGCCAGCCCGCACTGGCAGAGACCTCCCCTACAGCTCCTGAATGTCCCCCGCCTGCCGAGTGAG
CTGGCGGCCCTTCTGACTGTTTATTTAAGGATGGATGGCACCCTGGAACCGGGAAGGGTGGCCT
GTTCCCTAGAGAGAATAAATTGGATTATTTTCTAA

hide sequence

RefSeq Acc Id:

NM_003443 ⟹ NP_003434

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	15,941,869 - 15,976,101 (-)	NCBI
GRCh37	1	16,268,364 - 16,302,627 (-)	ENTREZGENE
GRCh37	1	16,268,364 - 16,302,627 (-)	NCBI
Build 36	1	16,140,951 - 16,175,101 (-)	NCBI Archive
HuRef	1	14,787,372 - 14,821,661 (-)	ENTREZGENE
CHM1_1	1	16,066,899 - 16,101,159 (-)	NCBI
T2T-CHM13v2.0	1	15,383,149 - 15,417,408 (-)	NCBI

Sequence:

show sequence

GAGGTCGGTTCCGCCCGACTCTAACATGGCGGCGCCCTTTGTCTGCTCTGGAGTGCCGTCCCCG
GCCTTCTCGCGGCCGTGATGCACCTCCCTCTGCGGTGGGGTCCGGGACATGGCAGGTAATGAGC
CGGACGAGGGGAGCCAAGCTGGAGTTTACACAGGCAAACTGTCAGAAAAGAGTAGCCTGGGCTG
TCTGGAAATCTGAGCCATGGACTTTCCCCAGCACAGCCAGCATGTCTTGGAACAGCTGAACCAG
CAGCGGCAGCTGGGGCTTCTCTGTGACTGCACCTTTGTGGTGGACGGTGTTCACTTTAAGGCTC
ATAAAGCAGTGCTGGCGGCCTGCAGCGAGTACTTCAAGATGCTCTTCGTGGACCAGAAGGACGT
GGTGCACCTGGACATCAGTAACGCGGCAGGCCTGGGGCAGGTGCTGGAGTTTATGTACACGGCC
AAGCTGAGCCTGAGCCCTGAGAACGTGGATGATGTGCTGGCCGTGGCCACTTTCCTCCAAATGC
AGGACATCATCACGGCCTGCCATGCCCTCAAGTCACTTGCTGAGCCGGCTACCAGCCCTGGGGG
AAATGCGGAGGCCTTGGCCACAGAAGGAGGGGACAAGAGAGCCAAAGAGGAGAAGGTGGCCACC
AGCACGCTGAGCAGGCTGGAGCAGGCAGGACGCAGCACACCCATAGGCCCCAGCAGGGACCTCA
AGGAGGAGCGCGGCGGTCAGGCCCAGAGTGCGGCCAGCGGTGCAGAGCAGACAGAGAAAGCCGA
TGCGCCCCGGGAGCCGCCGCCTGTGGAGCTCAAGCCAGACCCCACGAGTGGCATGGCTGCTGCA
GAAGCTGAGGCCGCTTTGTCCGAGAGCTCGGAGCAAGAAATGGAGGTGGAGCCCGCCCGGAAAG
GGGAAGAGGAGCAAAAGGAGCAAGAGGAGCAAGAGGAGGAGGGCGCAGGGCCAGCTGAGGTCAA
GGAGGAGGGTTCCCAGCTGGAGAACGGAGAGGCCCCCGAGGAGAACGAGAATGAGGAGTCAGCG
GGCACAGACTCGGGGCAGGAGCTCGGCTCCGAGGCCCGGGGCCTGCGCTCAGGCACCTACGGCG
ACCGCACGGAGTCCAAGGCCTACGGCTCCGTCATCCACAAGTGCGAGGACTGTGGGAAGGAGTT
CACGCACACGGGGAACTTCAAGCGGCACATCCGCATCCACACGGGGGAGAAGCCCTTCTCGTGC
CGGGAGTGCAGCAAGGCCTTTTCCGACCCGGCCGCGTGCAAGGCCCATGAGAAGACGCACAGCC
CTCTGAAGCCCTACGGCTGCGAGGAGTGCGGGAAGAGCTACCGCCTCATCAGCCTGCTGAACCT
GCACAAGAAGCGGCACTCGGGCGAGGCGCGCTACCGCTGCGAGGACTGCGGCAAGCTCTTCACC
ACCTCGGGCAACCTCAAGCGCCACCAGCTGGTGCACAGCGGCGAGAAGCCCTACCAGTGCGACT
ACTGCGGCCGCTCCTTCTCCGACCCCACTTCCAAGATGCGCCACCTGGAGACCCACGACACGGA
CAAGGAGCACAAGTGCCCACACTGCGACAAGAAGTTCAACCAGGTAGGGAACCTGAAGGCCCAC
CTGAAGATCCACATCGCTGACGGGCCCCTCAAGTGCCGAGAGTGTGGGAAGCAGTTCACCACCT
CAGGGAACCTGAAGCGGCACCTTCGGATCCACAGCGGGGAGAAGCCCTACGTGTGCATCCACTG
CCAGCGACAGTTTGCAGACCCCGGCGCTCTGCAGCGGCACGTCCGCATTCACACAGGTGAGAAG
CCATGCCAGTGTGTGATGTGCGGTAAGGCCTTCACCCAGGCCAGCTCCCTCATCGCCCACGTGC
GCCAGCACACCGGGGAGAAGCCCTACGTCTGCGAGCGCTGCGGCAAGAGATTCGTCCAGTCCAG
CCAGTTGGCCAATCATATTCGCCACCACGACAACATCCGCCCACACAAGTGCAGCGTGTGCAGC
AAGGCCTTCGTGAACGTGGGGGACCTGTCCAAGCACATCATCATTCACACTGGAGAGAAGCCTT
ACCTGTGTGATAAGTGTGGGCGTGGCTTCAACCGGGTAGACAACCTGCGCTCCCACGTGAAGAC
CGTGCACCAGGGCAAGGCAGGCATCAAGATCCTGGAGCCCGAGGAGGGCAGTGAGGTCAGCGTG
GTCACTGTGGATGACATGGTCACGCTGGCTACCGAGGCACTGGCAGCGACAGCCGTCACTCAGC
TCACAGTGGTGCCGGTGGGAGCTGCAGTGACAGCCGATGAGACGGAAGTCCTGAAGGCCGAGAT
CAGCAAAGCTGTGAAGCAAGTGCAGGAAGAAGACCCCAACACTCACATCCTCTACGCCTGTGAC
TCCTGTGGGGACAAGTTTCTGGATGCCAACAGCCTGGCTCAGCATGTGCGAATCCACACAGCCC
AGGCACTGGTCATGTTCCAGACAGACGCGGACTTCTATCAGCAGTATGGGCCAGGTGGCACGTG
GCCTGCCGGGCAGGTGCTGCAGGCTGGGGAGCTGGTCTTCCGCCCTCGCGACGGGGCTGAGGGC
CAGCCCGCACTGGCAGAGACCTCCCCTACAGCTCCTGAATGTCCCCCGCCTGCCGAGTGAGCTG
GCGGCCCTTCTGACTGTTTATTTAAGGATGGATGGCACCCTGGAACCGGGAAGGGTGGCCTGTT
CCCTAGAGAGAATAAATTGGATTATTTTCTAA

hide sequence

RefSeq Acc Id:

XM_005245986 ⟹ XP_005246043

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	15,941,869 - 15,976,101 (-)	NCBI

Sequence:

show sequence

ATGCGCCGGAAGTTGCAGCCGGGAAGCCTGCGAGGTCGGTTCCGCCCGACTCTAACATGGCGGC
GCCCTTTGTCTGCTCTGGAGTGCCGTCCCCGGCCTTCTCGCGGCCGTGATGCACCTCCCTCTGC
GGTGGGGTCCGGGACATGGCAGGTAATGAGCCGGACGAGGGGAGCCAAGCTGGAGTTTACACAG
GCAAACTGTCAGAAAAGAGTAGCCTGGGCTGTCTGGAAATCTGAGCCATGGACTTTCCCCAGCA
CAGCCAGCATGTCTTGGAACAGCTGAACCAGCAGCGGCAGCTGGGGCTTCTCTGTGACTGCACC
TTTGTGGTGGACGGTGTTCACTTTAAGGCTCATAAAGCAGTGCTGGCGGCCTGCAGCGAGTACT
TCAAGATGCTCTTCGTGGACCAGAAGGACGTGGTGCACCTGGACATCAGTAACGCGGCAGGAGG
GGACAAGAGAGCCAAAGAGGAGAAGGTGGCCACCAGCACGCTGAGCAGGCTGGAGCAGGCAGGA
CGCAGCACACCCATAGGCCCCAGCAGGGACCTCAAGGAGGAGCGCGGCGGTCAGGCCCAGAGTG
CGGCCAGCGGTGCAGAGCAGACAGAGAAAGCCGATGCGCCCCGGGAGCCGCCGCCTGTGGAGCT
CAAGCCAGACCCCACGAGTGGCATGGCTGCTGCAGAAGCTGAGGCCGCTTTGTCCGAGAGCTCG
GAGCAAGAAATGGAGGTGGAGCCCGCCCGGAAAGGGGAAGAGGAGCAAAAGGAGCAAGAGGAGC
AAGAGGAGGAGGGCGCAGGGCCAGCTGAGGTCAAGGAGGAGGGTTCCCAGCTGGAGAACGGAGA
GGCCCCCGAGGAGAACGAGAATGAGGAGTCAGCGGGCACAGACTCGGGGCAGGAGCTCGGCTCC
GAGGCCCGGGGCCTGCGCTCAGGCACCTACGGCGACCGCACGGAGTCCAAGGCCTACGGCTCCG
TCATCCACAAGTGCGAGGACTGTGGGAAGGAGTTCACGCACACGGGGAACTTCAAGCGGCACAT
CCGCATCCACACGGGGGAGAAGCCCTTCTCGTGCCGGGAGTGCAGCAAGGCCTTTTCCGACCCG
GCCGCGTGCAAGGCCCATGAGAAGACGCACAGCCCTCTGAAGCCCTACGGCTGCGAGGAGTGCG
GGAAGAGCTACCGCCTCATCAGCCTGCTGAACCTGCACAAGAAGCGGCACTCGGGCGAGGCGCG
CTACCGCTGCGAGGACTGCGGCAAGCTCTTCACCACCTCGGGCAACCTCAAGCGCCACCAGCTG
GTGCACAGCGGCGAGAAGCCCTACCAGTGCGACTACTGCGGCCGCTCCTTCTCCGACCCCACTT
CCAAGATGCGCCACCTGGAGACCCACGACACGGACAAGGAGCACAAGTGCCCACACTGCGACAA
GAAGTTCAACCAGGTAGGGAACCTGAAGGCCCACCTGAAGATCCACATCGCTGACGGGCCCCTC
AAGTGCCGAGAGTGTGGGAAGCAGTTCACCACCTCAGGGAACCTGAAGCGGCACCTTCGGATCC
ACAGCGGGGAGAAGCCCTACGTGTGCATCCACTGCCAGCGACAGTTTGCAGACCCCGGCGCTCT
GCAGCGGCACGTCCGCATTCACACAGGTGAGAAGCCATGCCAGTGTGTGATGTGCGGTAAGGCC
TTCACCCAGGCCAGCTCCCTCATCGCCCACGTGCGCCAGCACACCGGGGAGAAGCCCTACGTCT
GCGAGCGCTGCGGCAAGAGATTCGTCCAGTCCAGCCAGTTGGCCAATCATATTCGCCACCACGA
CAACATCCGCCCACACAAGTGCAGCGTGTGCAGCAAGGCCTTCGTGAACGTGGGGGACCTGTCC
AAGCACATCATCATTCACACTGGAGAGAAGCCTTACCTGTGTGATAAGTGTGGGCGTGGCTTCA
ACCGGGTAGACAACCTGCGCTCCCACGTGAAGACCGTGCACCAGGGCAAGGCAGGCATCAAGAT
CCTGGAGCCCGAGGAGGGCAGTGAGGTCAGCGTGGTCACTGTGGATGACATGGTCACGCTGGCT
ACCGAGGCACTGGCAGCGACAGCCGTCACTCAGCTCACAGGCCCTGCGACTCTGCCCGCAGTGG
TGCCGGTGGGAGCTGCAGTGACAGCCGATGAGACGGAAGTCCTGAAGGCCGAGATCAGCAAAGC
TGTGAAGCAAGTGCAGGAAGAAGACCCCAACACTCACATCCTCTACGCCTGTGACTCCTGTGGG
GACAAGTTTCTGGATGCCAACAGCCTGGCTCAGCATGTGCGAATCCACACAGCCCAGGCACTGG
TCATGTTCCAGACAGACGCGGACTTCTATCAGCAGTATGGGCCAGGTGGCACGTGGCCTGCCGG
GCAGGTGCTGCAGGCTGGGGAGCTGGTCTTCCGCCCTCGCGACGGGGCTGAGGGCCAGCCCGCA
CTGGCAGAGACCTCCCCTACAGCTCCTGAATGTCCCCCGCCTGCCGAGTGAGCTGGCGGCCCTT
CTGACTGTTTATTTAAGGATGGATGGCACCCTGGAACCGGGAAGGGTGGCCTGTTCCCTAGAGA
GAATAAATTGGATTATTTTCTAATGCTGCCTATAGGTCCCTGTGGGGTGGGTGGGGAGCTGGCA
GCTACAACTGATGCCACAGAAAGGCTGTACCACCCAGGAACCAGCCTTCCTGGGAAGGTCAGCC
CGTCCCTCTTGCTGAATGCGACTAGAATCAGAGCCAGGCTGGCTGCTTTGCCCCAAGTTGAGGA
GTGGGCAGTACACTCAGGCTGGAGAGACCTCGGCACCACGTGCCCCATGCCCTCATCCCATCTT
GTTTGGAGGCTTCTCACCTGTTCATCTTTAGGGCCTGGCCTCCCCTCGCCCCACAGCTATGACC
CTGCTCCCCCTCGGCCCAGGTTGGGGAGAGGTTGGGAAGTTGGGGAAGGGACCAGCAGGGGCGG
CCACCAACTGCTTACCAGGGTACAGGCAACCCAGAGCGAGCCTGGCTCACAGGCCACTGCTGCC
AGGCCTGGCTCAGGGGTCCTTCCAGCCAGAGTGGCAAGGTAGGCCAAGGAGAGTGCCAGGCCCA
GGCCACTGCCCTGGCTCTGATGGGCCTAAGGGAGCAGATGGAAGCCACACTTGCTTCAGGGTTA
CCTGGCCCGAGGACTAAGGCCAAGCCGGTGCCATCATCTTTTGGGAAGGTTCAAAAGATGGCAT
CTCTGCCACCAGGCTGGGGGCCCAGAGGGACAGGAAGGAGCAGCCAGGGGCTTTGATGGGGAGG
TAGGGAGCTGGTGGAACAGCTTTCTCACTCCTGTCAGCAAGGAGTCAGGAGGTACCATCTCGTC
CCCCCACAGTGGCCCCGGCATCTATGGCCCACCGTTCAGAGGGGGATGCTATCTTCTCACACCA
GGACAGGCCCATTTGTAGGAGCCCATTGGTATTCCAAGTGAGACCACCAACTTTATAGTCCCCA
TGTCCCTGTCCCAACTCCACAGCTTCTAGAGAATCCAGCTGCAGGGGAAGCCTGTCCCCAACTC
CCATTCTCCTGTCTGGAGGCAGAGACGGGATCAAATGAGCCCCCAGGGGCCCCAGGAGGCCACT
GCCTCTGCAGGAGTCAGCCTGCTTCACACTGGGAGAAGGGAAGAGGGGGCAAGAGAGAGACAAG
AAACCAAAGCTTGCTAAAATGTTTCTGAGATGGCATGGGGTGTGGTTATATTCTGTATCAAAAT
TGGAAGTGCCTTCCTTCCACATTACCTAAGAACCAGTTAGGACTCTGAAGACACCACAAGAGTG
AGAAATGGTTAAGTTCAGTGTCCGTGACAAAAATCTCCTTTGTACAAGATAAAATTATCCTTGG
GGAGGAGGACTGACTGACTAGGAGGCAGAAGGGAAACAGTTCCCATGTACAGACTTGGCATGGG
GATCAAAAGCGGGATGAGGGCTGACTGTTCCCATAAGCCAAGGACCCATGGTTCGTCCTCCCAC
CCAAGTGACAATCACACTCACACTTGGTGTGTTTTATATTTTTTAATAAAGTTTGTAATCCAAT
GGACACACAAAACAAAACTGCGCTGAGAAAAACAGTTTCATAAATTAATAAGTGTTAGGAAGTT
GGGGGAAGAGATCAAGGTAATAGGAAGAGGGGTTAGCCAGTCTTTTTGTACAGGTGCCGTGTGA
CACTTCCACATCGCGGGAGCAGGACCCGTGCTGTACCGAAGCGCACTTATACAAATGAGTGGGC
AATACAAAGTCTGAATATGAAAATAAGATTTCCTCTGAAAACACATTTTTGGCACAGATTAAAA
AAAACGTATGTCGGGGGATTTGATTTTTTAAGTCAGTATTATATATATTTATATATATTATATA
TTTATATATACACACATCCCAAGTTCTGCATATCCCACCAAGAGAAAACCTTTCTGTTTGCTCT
TCAACTGTAAACTGTACATCCCGGTGAATCAAAGACGGTGGCAGCAGGAGAATTAAGGTGACGC
ATCCAAATGAGCAAGGGAGATGGGGGTGGACAAAAAAAA

hide sequence

RefSeq Acc Id:

XM_011542085 ⟹ XP_011540387

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	15,941,869 - 15,976,101 (-)	NCBI

Sequence:

show sequence

GGAAGTTGCAGCCGGGAAGCCTGCGAGGTCGGTTCCGCCCGACTCTAACATGGCGGCGCCCTTT
GTCTGCTCTGGAGTGCCGTCCCCGGCCTTCTCGCGGCCGTGATGCACCTCCCTCTGCGGTGGGG
TCCGGGACATGGCAGGTAATGAGCCGGACGAGGGGAGCCAAGCTGGAGTTTACACAGGCAAACT
GTCAGAAAAGAGTAGCCTGGGCTGTCTGGAAATCTGAGGCCTGGGGCAGGTGCTGGAGTTTATG
TACACGGCCAAGCTGAGCCTGAGCCCTGAGAACGTGGATGATGTGCTGGCCGTGGCCACTTTCC
TCCAAATGCAGGACATCATCACGGCCTGCCATGCCCTCAAGTCACTTGCTGAGCCGGCTACCAG
CCCTGGGGGAAATGCGGAGGCCTTGGCCACAGAAGGAGGGGACAAGAGAGCCAAAGAGGAGAAG
GTGGCCACCAGCACGCTGAGCAGGCTGGAGCAGGCAGGACGCAGCACACCCATAGGCCCCAGCA
GGGACCTCAAGGAGGAGCGCGGCGGTCAGGCCCAGAGTGCGGCCAGCGGTGCAGAGCAGACAGA
GAAAGCCGATGCGCCCCGGGAGCCGCCGCCTGTGGAGCTCAAGCCAGACCCCACGAGTGGCATG
GCTGCTGCAGAAGCTGAGGCCGCTTTGTCCGAGAGCTCGGAGCAAGAAATGGAGGTGGAGCCCG
CCCGGAAAGGGGAAGAGGAGCAAAAGGAGCAAGAGGAGCAAGAGGAGGAGGGCGCAGGGCCAGC
TGAGGTCAAGGAGGAGGGTTCCCAGCTGGAGAACGGAGAGGCCCCCGAGGAGAACGAGAATGAG
GAGTCAGCGGGCACAGACTCGGGGCAGGAGCTCGGCTCCGAGGCCCGGGGCCTGCGCTCAGGCA
CCTACGGCGACCGCACGGAGTCCAAGGCCTACGGCTCCGTCATCCACAAGTGCGAGGACTGTGG
GAAGGAGTTCACGCACACGGGGAACTTCAAGCGGCACATCCGCATCCACACGGGGGAGAAGCCC
TTCTCGTGCCGGGAGTGCAGCAAGGCCTTTTCCGACCCGGCCGCGTGCAAGGCCCATGAGAAGA
CGCACAGCCCTCTGAAGCCCTACGGCTGCGAGGAGTGCGGGAAGAGCTACCGCCTCATCAGCCT
GCTGAACCTGCACAAGAAGCGGCACTCGGGCGAGGCGCGCTACCGCTGCGAGGACTGCGGCAAG
CTCTTCACCACCTCGGGCAACCTCAAGCGCCACCAGCTGGTGCACAGCGGCGAGAAGCCCTACC
AGTGCGACTACTGCGGCCGCTCCTTCTCCGACCCCACTTCCAAGATGCGCCACCTGGAGACCCA
CGACACGGACAAGGAGCACAAGTGCCCACACTGCGACAAGAAGTTCAACCAGGTAGGGAACCTG
AAGGCCCACCTGAAGATCCACATCGCTGACGGGCCCCTCAAGTGCCGAGAGTGTGGGAAGCAGT
TCACCACCTCAGGGAACCTGAAGCGGCACCTTCGGATCCACAGCGGGGAGAAGCCCTACGTGTG
CATCCACTGCCAGCGACAGTTTGCAGACCCCGGCGCTCTGCAGCGGCACGTCCGCATTCACACA
GGTGAGAAGCCATGCCAGTGTGTGATGTGCGGTAAGGCCTTCACCCAGGCCAGCTCCCTCATCG
CCCACGTGCGCCAGCACACCGGGGAGAAGCCCTACGTCTGCGAGCGCTGCGGCAAGAGATTCGT
CCAGTCCAGCCAGTTGGCCAATCATATTCGCCACCACGACAACATCCGCCCACACAAGTGCAGC
GTGTGCAGCAAGGCCTTCGTGAACGTGGGGGACCTGTCCAAGCACATCATCATTCACACTGGAG
AGAAGCCTTACCTGTGTGATAAGTGTGGGCGTGGCTTCAACCGGGTAGACAACCTGCGCTCCCA
CGTGAAGACCGTGCACCAGGGCAAGGCAGGCATCAAGATCCTGGAGCCCGAGGAGGGCAGTGAG
GTCAGCGTGGTCACTGTGGATGACATGGTCACGCTGGCTACCGAGGCACTGGCAGCGACAGCCG
TCACTCAGCTCACAGGCCCTGCGACTCTGCCCGCAGTGGTGCCGGTGGGAGCTGCAGTGACAGC
CGATGAGACGGAAGTCCTGAAGGCCGAGATCAGCAAAGCTGTGAAGCAAGTGCAGGAAGAAGAC
CCCAACACTCACATCCTCTACGCCTGTGACTCCTGTGGGGACAAGTTTCTGGATGCCAACAGCC
TGGCTCAGCATGTGCGAATCCACACAGCCCAGGCACTGGTCATGTTCCAGACAGACGCGGACTT
CTATCAGCAGTATGGGCCAGGTGGCACGTGGCCTGCCGGGCAGGTGCTGCAGGCTGGGGAGCTG
GTCTTCCGCCCTCGCGACGGGGCTGAGGGCCAGCCCGCACTGGCAGAGACCTCCCCTACAGCTC
CTGAATGTCCCCCGCCTGCCGAGTGAGCTGGCGGCCCTTCTGACTGTTTATTTAAGGATGGATG
GCACCCTGGAACCGGGAAGGGTGGCCTGTTCCCTAGAGAGAATAAATTGGATTATTTTCTAATG
CTGCCTATAGGTCCCTGTGGGGTGGGTGGGGAGCTGGCAGCTACAACTGATGCCACAGAAAGGC
TGTACCACCCAGGAACCAGCCTTCCTGGGAAGGTCAGCCCGTCCCTCTTGCTGAATGCGACTAG
AATCAGAGCCAGGCTGGCTGCTTTGCCCCAAGTTGAGGAGTGGGCAGTACACTCAGGCTGGAGA
GACCTCGGCACCACGTGCCCCATGCCCTCATCCCATCTTGTTTGGAGGCTTCTCACCTGTTCAT
CTTTAGGGCCTGGCCTCCCCTCGCCCCACAGCTATGACCCTGCTCCCCCTCGGCCCAGGTTGGG
GAGAGGTTGGGAAGTTGGGGAAGGGACCAGCAGGGGCGGCCACCAACTGCTTACCAGGGTACAG
GCAACCCAGAGCGAGCCTGGCTCACAGGCCACTGCTGCCAGGCCTGGCTCAGGGGTCCTTCCAG
CCAGAGTGGCAAGGTAGGCCAAGGAGAGTGCCAGGCCCAGGCCACTGCCCTGGCTCTGATGGGC
CTAAGGGAGCAGATGGAAGCCACACTTGCTTCAGGGTTACCTGGCCCGAGGACTAAGGCCAAGC
CGGTGCCATCATCTTTTGGGAAGGTTCAAAAGATGGCATCTCTGCCACCAGGCTGGGGGCCCAG
AGGGACAGGAAGGAGCAGCCAGGGGCTTTGATGGGGAGGTAGGGAGCTGGTGGAACAGCTTTCT
CACTCCTGTCAGCAAGGAGTCAGGAGGTACCATCTCGTCCCCCCACAGTGGCCCCGGCATCTAT
GGCCCACCGTTCAGAGGGGGATGCTATCTTCTCACACCAGGACAGGCCCATTTGTAGGAGCCCA
TTGGTATTCCAAGTGAGACCACCAACTTTATAGTCCCCATGTCCCTGTCCCAACTCCACAGCTT
CTAGAGAATCCAGCTGCAGGGGAAGCCTGTCCCCAACTCCCATTCTCCTGTCTGGAGGCAGAGA
CGGGATCAAATGAGCCCCCAGGGGCCCCAGGAGGCCACTGCCTCTGCAGGAGTCAGCCTGCTTC
ACACTGGGAGAAGGGAAGAGGGGGCAAGAGAGAGACAAGAAACCAAAGCTTGCTAAAATGTTTC
TGAGATGGCATGGGGTGTGGTTATATTCTGTATCAAAATTGGAAGTGCCTTCCTTCCACATTAC
CTAAGAACCAGTTAGGACTCTGAAGACACCACAAGAGTGAGAAATGGTTAAGTTCAGTGTCCGT
GACAAAAATCTCCTTTGTACAAGATAAAATTATCCTTGGGGAGGAGGACTGACTGACTAGGAGG
CAGAAGGGAAACAGTTCCCATGTACAGACTTGGCATGGGGATCAAAAGCGGGATGAGGGCTGAC
TGTTCCCATAAGCCAAGGACCCATGGTTCGTCCTCCCACCCAAGTGACAATCACACTCACACTT
GGTGTGTTTTATATTTTTTAATAAAGTTTGTAATCCAATGGACACACAAAACAAAACTGCGCTG
AGAAAAACAGTTTCATAAATTAATAAGTGTTAGGAAGTTGGGGGAAGAGATCAAGGTAATAGGA
AGAGGGGTTAGCCAGTCTTTTTGTACAGGTGCCGTGTGACACTTCCACATCGCGGGAGCAGGAC
CCGTGCTGTACCGAAGCGCACTTATACAAATGAGTGGGCAATACAAAGTCTGAATATGAAAATA
AGATTTCCTCTGAAAACACATTTTTGGCACAGATTAAAAAAAACGTATGTCGGGGGATTTGATT
TTTTAAGTCAGTATTATATATATTTATATATATTATATATTTATATATACACACATCCCAAGTT
CTGCATATCCCACCAAGAGAAAACCTTTCTGTTTGCTCTTCAACTGTAAACTGTACATCCCGGT
GAATCAAAGACGGTGGCAGCAGGAGAATTAAGGTGACGCATCCAAATGAGCAAGGGAGATGGGG
GTGGACAAAAAAAA

hide sequence

RefSeq Acc Id:

XM_011542087 ⟹ XP_011540389

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	15,941,869 - 15,976,101 (-)	NCBI

Sequence:

show sequence

CGGAAGTTGCAGCCGGGAAGCCTGCGAGGTCGGTTCCGCCCGACTCTAACATGGCGGCGCCCTT
TGTCTGCTCTGGAGTGCCGTCCCCGGCCTTCTCGCGGCCGTGATGCACCTCCCTCTGCGGTGGG
GTCCGGGACATGGCAGGTAATGAGCCGGACGAGGGGAGCCAAGCTGGAGTTTACACAGGCAAAC
TGTCAGAAAAGAGTAGCCTGGGCTGTCTGGAAATCTGAGGCCTGGGGCAGGTGCTGGAGTTTAT
GTACACGGCCAAGCTGAGCCTGAGCCCTGAGAACGTGGATGATGTGCTGGCCGTGGCCACTTTC
CTCCAAATGCAGGACATCATCACGGCCTGCCATGCCCTCAAGTCACTTGCTGAGCCGGCTACCA
GCCCTGGGGGAAATGCGGAGGCCTTGGCCACAGAAGGTCTGCCCTGTTCCATCTCCAGGAGGGG
ACAAGAGAGCCAAAGAGGAGAAGGTGGCCACCAGCACGCTGAGCAGGCTGGAGCAGGCAGGACG
CAGCACACCCATAGGCCCCAGCAGGGACCTCAAGGAGGAGCGCGGCGGTCAGGCCCAGAGTGCG
GCCAGCGGTGCAGAGCAGACAGAGAAAGCCGATGCGCCCCGGGAGCCGCCGCCTGTGGAGCTCA
AGCCAGACCCCACGAGTGGCATGGCTGCTGCAGAAGCTGAGGCCGCTTTGTCCGAGAGCTCGGA
GCAAGAAATGGAGGTGGAGCCCGCCCGGAAAGGGGAAGAGGAGCAAAAGGAGCAAGAGGAGCAA
GAGGAGGAGGGCGCAGGGCCAGCTGAGGTCAAGGAGGAGGGTTCCCAGCTGGAGAACGGAGAGG
CCCCCGAGGAGAACGAGAATGAGGAGTCAGCGGGCACAGACTCGGGGCAGGAGCTCGGCTCCGA
GGCCCGGGGCCTGCGCTCAGGCACCTACGGCGACCGCACGGAGTCCAAGGCCTACGGCTCCGTC
ATCCACAAGTGCGAGGACTGTGGGAAGGAGTTCACGCACACGGGGAACTTCAAGCGGCACATCC
GCATCCACACGGGGGAGAAGCCCTTCTCGTGCCGGGAGTGCAGCAAGGCCTTTTCCGACCCGGC
CGCGTGCAAGGCCCATGAGAAGACGCACAGCCCTCTGAAGCCCTACGGCTGCGAGGAGTGCGGG
AAGAGCTACCGCCTCATCAGCCTGCTGAACCTGCACAAGAAGCGGCACTCGGGCGAGGCGCGCT
ACCGCTGCGAGGACTGCGGCAAGCTCTTCACCACCTCGGGCAACCTCAAGCGCCACCAGCTGGT
GCACAGCGGCGAGAAGCCCTACCAGTGCGACTACTGCGGCCGCTCCTTCTCCGACCCCACTTCC
AAGATGCGCCACCTGGAGACCCACGACACGGACAAGGAGCACAAGTGCCCACACTGCGACAAGA
AGTTCAACCAGGTAGGGAACCTGAAGGCCCACCTGAAGATCCACATCGCTGACGGGCCCCTCAA
GTGCCGAGAGTGTGGGAAGCAGTTCACCACCTCAGGGAACCTGAAGCGGCACCTTCGGATCCAC
AGCGGGGAGAAGCCCTACGTGTGCATCCACTGCCAGCGACAGTTTGCAGACCCCGGCGCTCTGC
AGCGGCACGTCCGCATTCACACAGGTGAGAAGCCATGCCAGTGTGTGATGTGCGGTAAGGCCTT
CACCCAGGCCAGCTCCCTCATCGCCCACGTGCGCCAGCACACCGGGGAGAAGCCCTACGTCTGC
GAGCGCTGCGGCAAGAGATTCGTCCAGTCCAGCCAGTTGGCCAATCATATTCGCCACCACGACA
ACATCCGCCCACACAAGTGCAGCGTGTGCAGCAAGGCCTTCGTGAACGTGGGGGACCTGTCCAA
GCACATCATCATTCACACTGGAGAGAAGCCTTACCTGTGTGATAAGTGTGGGCGTGGCTTCAAC
CGGGTAGACAACCTGCGCTCCCACGTGAAGACCGTGCACCAGGGCAAGGCAGGCATCAAGATCC
TGGAGCCCGAGGAGGGCAGTGAGGTCAGCGTGGTCACTGTGGATGACATGGTCACGCTGGCTAC
CGAGGCACTGGCAGCGACAGCCGTCACTCAGCTCACAGGCCCTGCGACTCTGCCCGCAGTGGTG
CCGGTGGGAGCTGCAGTGACAGCCGATGAGACGGAAGTCCTGAAGGCCGAGATCAGCAAAGCTG
TGAAGCAAGTGCAGGAAGAAGACCCCAACACTCACATCCTCTACGCCTGTGACTCCTGTGGGGA
CAAGTTTCTGGATGCCAACAGCCTGGCTCAGCATGTGCGAATCCACACAGCCCAGGCACTGGTC
ATGTTCCAGACAGACGCGGACTTCTATCAGCAGTATGGGCCAGGTGGCACGTGGCCTGCCGGGC
AGGTGCTGCAGGCTGGGGAGCTGGTCTTCCGCCCTCGCGACGGGGCTGAGGGCCAGCCCGCACT
GGCAGAGACCTCCCCTACAGCTCCTGAATGTCCCCCGCCTGCCGAGTGAGCTGGCGGCCCTTCT
GACTGTTTATTTAAGGATGGATGGCACCCTGGAACCGGGAAGGGTGGCCTGTTCCCTAGAGAGA
ATAAATTGGATTATTTTCTAATGCTGCCTATAGGTCCCTGTGGGGTGGGTGGGGAGCTGGCAGC
TACAACTGATGCCACAGAAAGGCTGTACCACCCAGGAACCAGCCTTCCTGGGAAGGTCAGCCCG
TCCCTCTTGCTGAATGCGACTAGAATCAGAGCCAGGCTGGCTGCTTTGCCCCAAGTTGAGGAGT
GGGCAGTACACTCAGGCTGGAGAGACCTCGGCACCACGTGCCCCATGCCCTCATCCCATCTTGT
TTGGAGGCTTCTCACCTGTTCATCTTTAGGGCCTGGCCTCCCCTCGCCCCACAGCTATGACCCT
GCTCCCCCTCGGCCCAGGTTGGGGAGAGGTTGGGAAGTTGGGGAAGGGACCAGCAGGGGCGGCC
ACCAACTGCTTACCAGGGTACAGGCAACCCAGAGCGAGCCTGGCTCACAGGCCACTGCTGCCAG
GCCTGGCTCAGGGGTCCTTCCAGCCAGAGTGGCAAGGTAGGCCAAGGAGAGTGCCAGGCCCAGG
CCACTGCCCTGGCTCTGATGGGCCTAAGGGAGCAGATGGAAGCCACACTTGCTTCAGGGTTACC
TGGCCCGAGGACTAAGGCCAAGCCGGTGCCATCATCTTTTGGGAAGGTTCAAAAGATGGCATCT
CTGCCACCAGGCTGGGGGCCCAGAGGGACAGGAAGGAGCAGCCAGGGGCTTTGATGGGGAGGTA
GGGAGCTGGTGGAACAGCTTTCTCACTCCTGTCAGCAAGGAGTCAGGAGGTACCATCTCGTCCC
CCCACAGTGGCCCCGGCATCTATGGCCCACCGTTCAGAGGGGGATGCTATCTTCTCACACCAGG
ACAGGCCCATTTGTAGGAGCCCATTGGTATTCCAAGTGAGACCACCAACTTTATAGTCCCCATG
TCCCTGTCCCAACTCCACAGCTTCTAGAGAATCCAGCTGCAGGGGAAGCCTGTCCCCAACTCCC
ATTCTCCTGTCTGGAGGCAGAGACGGGATCAAATGAGCCCCCAGGGGCCCCAGGAGGCCACTGC
CTCTGCAGGAGTCAGCCTGCTTCACACTGGGAGAAGGGAAGAGGGGGCAAGAGAGAGACAAGAA
ACCAAAGCTTGCTAAAATGTTTCTGAGATGGCATGGGGTGTGGTTATATTCTGTATCAAAATTG
GAAGTGCCTTCCTTCCACATTACCTAAGAACCAGTTAGGACTCTGAAGACACCACAAGAGTGAG
AAATGGTTAAGTTCAGTGTCCGTGACAAAAATCTCCTTTGTACAAGATAAAATTATCCTTGGGG
AGGAGGACTGACTGACTAGGAGGCAGAAGGGAAACAGTTCCCATGTACAGACTTGGCATGGGGA
TCAAAAGCGGGATGAGGGCTGACTGTTCCCATAAGCCAAGGACCCATGGTTCGTCCTCCCACCC
AAGTGACAATCACACTCACACTTGGTGTGTTTTATATTTTTTAATAAAGTTTGTAATCCAATGG
ACACACAAAACAAAACTGCGCTGAGAAAAACAGTTTCATAAATTAATAAGTGTTAGGAAGTTGG
GGGAAGAGATCAAGGTAATAGGAAGAGGGGTTAGCCAGTCTTTTTGTACAGGTGCCGTGTGACA
CTTCCACATCGCGGGAGCAGGACCCGTGCTGTACCGAAGCGCACTTATACAAATGAGTGGGCAA
TACAAAGTCTGAATATGAAAATAAGATTTCCTCTGAAAACACATTTTTGGCACAGATTAAAAAA
AACGTATGTCGGGGGATTTGATTTTTTAAGTCAGTATTATATATATTTATATATATTATATATT
TATATATACACACATCCCAAGTTCTGCATATCCCACCAAGAGAAAACCTTTCTGTTTGCTCTTC
AACTGTAAACTGTACATCCCGGTGAATCAAAGACGGTGGCAGCAGGAGAATTAAGGTGACGCAT
CCAAATGAGCAAGGGAGATGGGGGTGGACAAAAAAAA

hide sequence

RefSeq Acc Id:

XM_047429978 ⟹ XP_047285934

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	15,941,869 - 15,948,378 (-)	NCBI

RefSeq Acc Id:

XM_054338630 ⟹ XP_054194605

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	15,383,149 - 15,417,408 (-)	NCBI

RefSeq Acc Id:

XM_054338631 ⟹ XP_054194606

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	15,383,149 - 15,417,408 (-)	NCBI

RefSeq Acc Id:

XM_054338632 ⟹ XP_054194607

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	15,383,149 - 15,389,658 (-)	NCBI

RefSeq Acc Id:

XM_054338633 ⟹ XP_054194608

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	15,383,149 - 15,417,408 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001229813	(Get FASTA)	NCBI Sequence Viewer
	NP_001274532	(Get FASTA)	NCBI Sequence Viewer
	NP_001274533	(Get FASTA)	NCBI Sequence Viewer
	NP_001311066	(Get FASTA)	NCBI Sequence Viewer
	NP_001311067	(Get FASTA)	NCBI Sequence Viewer
	NP_003434	(Get FASTA)	NCBI Sequence Viewer
	XP_005246043	(Get FASTA)	NCBI Sequence Viewer
	XP_011540387	(Get FASTA)	NCBI Sequence Viewer
	XP_011540389	(Get FASTA)	NCBI Sequence Viewer
	XP_047285934	(Get FASTA)	NCBI Sequence Viewer
	XP_054194605	(Get FASTA)	NCBI Sequence Viewer
	XP_054194606	(Get FASTA)	NCBI Sequence Viewer
	XP_054194607	(Get FASTA)	NCBI Sequence Viewer
	XP_054194608	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA61327	(Get FASTA)	NCBI Sequence Viewer
	AAC50256	(Get FASTA)	NCBI Sequence Viewer
	AAI26164	(Get FASTA)	NCBI Sequence Viewer
	AAI43966	(Get FASTA)	NCBI Sequence Viewer
	BAD97338	(Get FASTA)	NCBI Sequence Viewer
	BAG37639	(Get FASTA)	NCBI Sequence Viewer
	BAG57917	(Get FASTA)	NCBI Sequence Viewer
	BAG61689	(Get FASTA)	NCBI Sequence Viewer
	BAG63326	(Get FASTA)	NCBI Sequence Viewer
	BAG63857	(Get FASTA)	NCBI Sequence Viewer
	BAG64771	(Get FASTA)	NCBI Sequence Viewer
	CAA70889	(Get FASTA)	NCBI Sequence Viewer
	EAW51757	(Get FASTA)	NCBI Sequence Viewer
	EAW51758	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000364885
	ENSP00000364885.2
	ENSP00000364895
	ENSP00000364895.4
	ENSP00000400827.1
	ENSP00000408483.1
	ENSP00000438529
	ENSP00000438529.1
GenBank Protein	Q13105	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001229813 ⟸ NM_001242884
- Peptide Label:	isoform 1
- UniProtKB:	B2RCP2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MMCWPWPLSSKCRTSSRPAMPSSHLLSRLPALGEMRRPWPQKVCPVPSPGGDKRAKEEKVATST LSRLEQAGRSTPIGPSRDLKEERGGQAQSAASGAEQTEKADAPREPPPVELKPDPTSGMAAAEA EAALSESSEQEMEVEPARKGEEEQKEQEEQEEEGAGPAEVKEEGSQLENGEAPEENENEESAGT DSGQELGSEARGLRSGTYGDRTESKAYGSVIHKCEDCGKEFTHTGNFKRHIRIHTGEKPFSCRE CSKAFSDPAACKAHEKTHSPLKPYGCEECGKSYRLISLLNLHKKRHSGEARYRCEDCGKLFTTS GNLKRHQLVHSGEKPYQCDYCGRSFSDPTSKMRHLETHDTDKEHKCPHCDKKFNQVGNLKAHLK IHIADGPLKCRECGKQFTTSGNLKRHLRIHSGEKPYVCIHCQRQFADPGALQRHVRIHTGEKPC QCVMCGKAFTQASSLIAHVRQHTGEKPYVCERCGKRFVQSSQLANHIRHHDNIRPHKCSVCSKA FVNVGDLSKHIIIHTGEKPYLCDKCGRGFNRVDNLRSHVKTVHQGKAGIKILEPEEGSEVSVVT VDDMVTLATEALAATAVTQLTVVPVGAAVTADETEVLKAEISKAVKQVQEEDPNTHILYACDSC GDKFLDANSLAQHVRIHTAQALVMFQTDADFYQQYGPGGTWPAGQVLQAGELVFRPRDGAEGQP ALAETSPTAPECPPPAE hide sequence

RefSeq Acc Id:	NP_003434 ⟸ NM_003443
- Peptide Label:	isoform 2
- UniProtKB:	Q5JYB2 (UniProtKB/Swiss-Prot), Q15932 (UniProtKB/Swiss-Prot), F5H411 (UniProtKB/Swiss-Prot), B7ZLQ9 (UniProtKB/Swiss-Prot), B4DXB4 (UniProtKB/Swiss-Prot), A0AV07 (UniProtKB/Swiss-Prot), Q9NUC9 (UniProtKB/Swiss-Prot), Q13105 (UniProtKB/Swiss-Prot), B2RCP2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MDFPQHSQHVLEQLNQQRQLGLLCDCTFVVDGVHFKAHKAVLAACSEYFKMLFVDQKDVVHLDI SNAAGLGQVLEFMYTAKLSLSPENVDDVLAVATFLQMQDIITACHALKSLAEPATSPGGNAEAL ATEGGDKRAKEEKVATSTLSRLEQAGRSTPIGPSRDLKEERGGQAQSAASGAEQTEKADAPREP PPVELKPDPTSGMAAAEAEAALSESSEQEMEVEPARKGEEEQKEQEEQEEEGAGPAEVKEEGSQ LENGEAPEENENEESAGTDSGQELGSEARGLRSGTYGDRTESKAYGSVIHKCEDCGKEFTHTGN FKRHIRIHTGEKPFSCRECSKAFSDPAACKAHEKTHSPLKPYGCEECGKSYRLISLLNLHKKRH SGEARYRCEDCGKLFTTSGNLKRHQLVHSGEKPYQCDYCGRSFSDPTSKMRHLETHDTDKEHKC PHCDKKFNQVGNLKAHLKIHIADGPLKCRECGKQFTTSGNLKRHLRIHSGEKPYVCIHCQRQFA DPGALQRHVRIHTGEKPCQCVMCGKAFTQASSLIAHVRQHTGEKPYVCERCGKRFVQSSQLANH IRHHDNIRPHKCSVCSKAFVNVGDLSKHIIIHTGEKPYLCDKCGRGFNRVDNLRSHVKTVHQGK AGIKILEPEEGSEVSVVTVDDMVTLATEALAATAVTQLTVVPVGAAVTADETEVLKAEISKAVK QVQEEDPNTHILYACDSCGDKFLDANSLAQHVRIHTAQALVMFQTDADFYQQYGPGGTWPAGQV LQAGELVFRPRDGAEGQPALAETSPTAPECPPPAE hide sequence

RefSeq Acc Id:	XP_005246043 ⟸ XM_005245986
- Peptide Label:	isoform X1
- UniProtKB:	B4E1F9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MDFPQHSQHVLEQLNQQRQLGLLCDCTFVVDGVHFKAHKAVLAACSEYFKMLFVDQKDVVHLDI SNAAGGDKRAKEEKVATSTLSRLEQAGRSTPIGPSRDLKEERGGQAQSAASGAEQTEKADAPRE PPPVELKPDPTSGMAAAEAEAALSESSEQEMEVEPARKGEEEQKEQEEQEEEGAGPAEVKEEGS QLENGEAPEENENEESAGTDSGQELGSEARGLRSGTYGDRTESKAYGSVIHKCEDCGKEFTHTG NFKRHIRIHTGEKPFSCRECSKAFSDPAACKAHEKTHSPLKPYGCEECGKSYRLISLLNLHKKR HSGEARYRCEDCGKLFTTSGNLKRHQLVHSGEKPYQCDYCGRSFSDPTSKMRHLETHDTDKEHK CPHCDKKFNQVGNLKAHLKIHIADGPLKCRECGKQFTTSGNLKRHLRIHSGEKPYVCIHCQRQF ADPGALQRHVRIHTGEKPCQCVMCGKAFTQASSLIAHVRQHTGEKPYVCERCGKRFVQSSQLAN HIRHHDNIRPHKCSVCSKAFVNVGDLSKHIIIHTGEKPYLCDKCGRGFNRVDNLRSHVKTVHQG KAGIKILEPEEGSEVSVVTVDDMVTLATEALAATAVTQLTGPATLPAVVPVGAAVTADETEVLK AEISKAVKQVQEEDPNTHILYACDSCGDKFLDANSLAQHVRIHTAQALVMFQTDADFYQQYGPG GTWPAGQVLQAGELVFRPRDGAEGQPALAETSPTAPECPPPAE hide sequence

RefSeq Acc Id:	NP_001274533 ⟸ NM_001287604
- Peptide Label:	isoform 4
- UniProtKB:	B2RCP2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MYTAKLSLSPENVDDVLAVATFLQMQDIITACHALKSLAEPATSPGGNAEALATEGGDKRAKEE KVATSTLSRLEQAGRSTPIGPSRDLKEERGGQAQSAASGAEQTEKADAPREPPPVELKPDPTSG MAAAEAEAALSESSEQEMEVEPARKGEEEQKEQEEQEEEGAGPAEVKEEGSQLENGEAPEENEN EESAGTDSGQELGSEARGLRSGTYGDRTESKAYGSVIHKCEDCGKEFTHTGNFKRHIRIHTGEK PFSCRECSKAFSDPAACKAHEKTHSPLKPYGCEECGKSYRLISLLNLHKKRHSGEARYRCEDCG KLFTTSGNLKRHQLVHSGEKPYQCDYCGRSFSDPTSKMRHLETHDTDKEHKCPHCDKKFNQVGN LKAHLKIHIADGPLKCRECGKQFTTSGNLKRHLRIHSGEKPYVCIHCQRQFADPGALQRHVRIH TGEKPCQCVMCGKAFTQASSLIAHVRQHTGEKPYVCERCGKRFVQSSQLANHIRHHDNIRPHKC SVCSKAFVNVGDLSKHIIIHTGEKPYLCDKCGRGFNRVDNLRSHVKTVHQGKAGIKILEPEEGS EVSVVTVDDMVTLATEALAATAVTQLTVVPVGAAVTADETEVLKAEISKAVKQVQEEDPNTHIL YACDSCGDKFLDANSLAQHVRIHTAQALVMFQTDADFYQQYGPGGTWPAGQVLQAGELVFRPRD GAEGQPALAETSPTAPECPPPAE hide sequence

RefSeq Acc Id:	NP_001274532 ⟸ NM_001287603
- Peptide Label:	isoform 3
- UniProtKB:	B2RCP2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MDFPQHSQHVLEQLNQQRQLGLLCDCTFVVDGVHFKAHKAVLAACSEYFKMLFVDQKDVVHLDI SNAAGLGQVLEFMYTAKLSLSPENVDDVLAVATFLQMQDIITACHALKSLAEPATSPGGNAEAL ATEGGDKRAKEEKVATSTLSRLEQAGRSTPIGPSRDLKEERGGQAQSAASGAEQTEKADAPREP PPVELKPDPTSGMAAAEAEAALSESSEQEMEVEPARKGEEEQKEQEEQEEEGAGPAEVKEEGSQ LENGEAPEENENEESAGTDSGQELGSEARGLRSGTYGDRTESKAYGSVIHKCEDCGKEFTHTGN FKRHIRIHTGEKPFSCRECSKAFSDPAACKAHEKTHSPLKPYGCEECGKSYRLISLLNLHKKRH SGEARYRCEDCGKLFTTSGNLKRHQLVHSGEKPYQCDYCGRSFSDPTSKMRHLETHDTDKEHKC PHCDKKFNQVGNLKAHLKIHIADGPLKCRECGKQFTTSGNLKRHLRIHSGEKPYVCIHCQRQFA DPGALQRHVRIHTGEKPCQCVMCGKAFTQASSLIAHVRQHTGEKPYVCERCGKRFVQSSQLANH IRHHDNIRPHKCSVCSKAFVNVGDLSKHIIIHTGEKPYLCDKCGRGFNRVDNLRSHVKTVHQGK AGIKILEPEEGSEVSVVTVDDMVTLATEALAATAVTQLTGPATLPAVVPVGAAVTADETEVLKA EISKAVKQVQEEDPNTHILYACDSCGDKFLDANSLAQHVRIHTAQALVMFQTDADFYQQYGPGG TWPAGQVLQAGELVFRPRDGAEGQPALAETSPTAPECPPPAE hide sequence

RefSeq Acc Id:	XP_011540387 ⟸ XM_011542085
- Peptide Label:	isoform X2
- UniProtKB:	B2RCP2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MYTAKLSLSPENVDDVLAVATFLQMQDIITACHALKSLAEPATSPGGNAEALATEGGDKRAKEE KVATSTLSRLEQAGRSTPIGPSRDLKEERGGQAQSAASGAEQTEKADAPREPPPVELKPDPTSG MAAAEAEAALSESSEQEMEVEPARKGEEEQKEQEEQEEEGAGPAEVKEEGSQLENGEAPEENEN EESAGTDSGQELGSEARGLRSGTYGDRTESKAYGSVIHKCEDCGKEFTHTGNFKRHIRIHTGEK PFSCRECSKAFSDPAACKAHEKTHSPLKPYGCEECGKSYRLISLLNLHKKRHSGEARYRCEDCG KLFTTSGNLKRHQLVHSGEKPYQCDYCGRSFSDPTSKMRHLETHDTDKEHKCPHCDKKFNQVGN LKAHLKIHIADGPLKCRECGKQFTTSGNLKRHLRIHSGEKPYVCIHCQRQFADPGALQRHVRIH TGEKPCQCVMCGKAFTQASSLIAHVRQHTGEKPYVCERCGKRFVQSSQLANHIRHHDNIRPHKC SVCSKAFVNVGDLSKHIIIHTGEKPYLCDKCGRGFNRVDNLRSHVKTVHQGKAGIKILEPEEGS EVSVVTVDDMVTLATEALAATAVTQLTGPATLPAVVPVGAAVTADETEVLKAEISKAVKQVQEE DPNTHILYACDSCGDKFLDANSLAQHVRIHTAQALVMFQTDADFYQQYGPGGTWPAGQVLQAGE LVFRPRDGAEGQPALAETSPTAPECPPPAE hide sequence

RefSeq Acc Id:	XP_011540389 ⟸ XM_011542087
- Peptide Label:	isoform X3
- UniProtKB:	B2RCP2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MMCWPWPLSSKCRTSSRPAMPSSHLLSRLPALGEMRRPWPQKVCPVPSPGGDKRAKEEKVATST LSRLEQAGRSTPIGPSRDLKEERGGQAQSAASGAEQTEKADAPREPPPVELKPDPTSGMAAAEA EAALSESSEQEMEVEPARKGEEEQKEQEEQEEEGAGPAEVKEEGSQLENGEAPEENENEESAGT DSGQELGSEARGLRSGTYGDRTESKAYGSVIHKCEDCGKEFTHTGNFKRHIRIHTGEKPFSCRE CSKAFSDPAACKAHEKTHSPLKPYGCEECGKSYRLISLLNLHKKRHSGEARYRCEDCGKLFTTS GNLKRHQLVHSGEKPYQCDYCGRSFSDPTSKMRHLETHDTDKEHKCPHCDKKFNQVGNLKAHLK IHIADGPLKCRECGKQFTTSGNLKRHLRIHSGEKPYVCIHCQRQFADPGALQRHVRIHTGEKPC QCVMCGKAFTQASSLIAHVRQHTGEKPYVCERCGKRFVQSSQLANHIRHHDNIRPHKCSVCSKA FVNVGDLSKHIIIHTGEKPYLCDKCGRGFNRVDNLRSHVKTVHQGKAGIKILEPEEGSEVSVVT VDDMVTLATEALAATAVTQLTGPATLPAVVPVGAAVTADETEVLKAEISKAVKQVQEEDPNTHI LYACDSCGDKFLDANSLAQHVRIHTAQALVMFQTDADFYQQYGPGGTWPAGQVLQAGELVFRPR DGAEGQPALAETSPTAPECPPPAE hide sequence

RefSeq Acc Id:	NP_001311066 ⟸ NM_001324137
- Peptide Label:	isoform 4
- UniProtKB:	B2RCP2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MYTAKLSLSPENVDDVLAVATFLQMQDIITACHALKSLAEPATSPGGNAEALATEGGDKRAKEE KVATSTLSRLEQAGRSTPIGPSRDLKEERGGQAQSAASGAEQTEKADAPREPPPVELKPDPTSG MAAAEAEAALSESSEQEMEVEPARKGEEEQKEQEEQEEEGAGPAEVKEEGSQLENGEAPEENEN EESAGTDSGQELGSEARGLRSGTYGDRTESKAYGSVIHKCEDCGKEFTHTGNFKRHIRIHTGEK PFSCRECSKAFSDPAACKAHEKTHSPLKPYGCEECGKSYRLISLLNLHKKRHSGEARYRCEDCG KLFTTSGNLKRHQLVHSGEKPYQCDYCGRSFSDPTSKMRHLETHDTDKEHKCPHCDKKFNQVGN LKAHLKIHIADGPLKCRECGKQFTTSGNLKRHLRIHSGEKPYVCIHCQRQFADPGALQRHVRIH TGEKPCQCVMCGKAFTQASSLIAHVRQHTGEKPYVCERCGKRFVQSSQLANHIRHHDNIRPHKC SVCSKAFVNVGDLSKHIIIHTGEKPYLCDKCGRGFNRVDNLRSHVKTVHQGKAGIKILEPEEGS EVSVVTVDDMVTLATEALAATAVTQLTVVPVGAAVTADETEVLKAEISKAVKQVQEEDPNTHIL YACDSCGDKFLDANSLAQHVRIHTAQALVMFQTDADFYQQYGPGGTWPAGQVLQAGELVFRPRD GAEGQPALAETSPTAPECPPPAE hide sequence

RefSeq Acc Id:	NP_001311067 ⟸ NM_001324138
- Peptide Label:	isoform 5
- UniProtKB:	B4E1F9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MDFPQHSQHVLEQLNQQRQLGLLCDCTFVVDGVHFKAHKAVLAACSEYFKMLFVDQKDVVHLDI SNAAGGDKRAKEEKVATSTLSRLEQAGRSTPIGPSRDLKEERGGQAQSAASGAEQTEKADAPRE PPPVELKPDPTSGMAAAEAEAALSESSEQEMEVEPARKGEEEQKEQEEQEEEGAGPAEVKEEGS QLENGEAPEENENEESAGTDSGQELGSEARGLRSGTYGDRTESKAYGSVIHKCEDCGKEFTHTG NFKRHIRIHTGEKPFSCRECSKAFSDPAACKAHEKTHSPLKPYGCEECGKSYRLISLLNLHKKR HSGEARYRCEDCGKLFTTSGNLKRHQLVHSGEKPYQCDYCGRSFSDPTSKMRHLETHDTDKEHK CPHCDKKFNQVGNLKAHLKIHIADGPLKCRECGKQFTTSGNLKRHLRIHSGEKPYVCIHCQRQF ADPGALQRHVRIHTGEKPCQCVMCGKAFTQASSLIAHVRQHTGEKPYVCERCGKRFVQSSQLAN HIRHHDNIRPHKCSVCSKAFVNVGDLSKHIIIHTGEKPYLCDKCGRGFNRVDNLRSHVKTVHQG KAGIKILEPEEGSEVSVVTVDDMVTLATEALAATAVTQLTVVPVGAAVTADETEVLKAEISKAV KQVQEEDPNTHILYACDSCGDKFLDANSLAQHVRIHTAQALVMFQTDADFYQQYGPGGTWPAGQ VLQAGELVFRPRDGAEGQPALAETSPTAPECPPPAE hide sequence

RefSeq Acc Id:

ENSP00000364885 ⟸ ENST00000375733

RefSeq Acc Id:

ENSP00000364895 ⟸ ENST00000375743

RefSeq Acc Id:

ENSP00000400827 ⟸ ENST00000440560

RefSeq Acc Id:

ENSP00000408483 ⟸ ENST00000444358

RefSeq Acc Id:

ENSP00000438529 ⟸ ENST00000537142

RefSeq Acc Id:	XP_047285934 ⟸ XM_047429978
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054194606 ⟸ XM_054338631
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054194608 ⟸ XM_054338633
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054194605 ⟸ XM_054338630
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054194607 ⟸ XM_054338632
- Peptide Label:	isoform X2

Protein Domains

BTB C2H2-type

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q13105-F1-model_v2	AlphaFold	Q13105	1-803	view protein structure

Promoters

RGD ID:

6854232

Promoter ID:

EPDNEW_H281

Type:

initiation region

Name:

ZBTB17_1

Description:

zinc finger and BTB domain containing 17

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	1	15,976,079 - 15,976,139	EPDNEW

RGD ID:

6787250

Promoter ID:

HG_KWN:906

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

OTTHUMT00000026004, OTTHUMT00000026005, OTTHUMT00000026006, OTTHUMT00000026007, OTTHUMT00000026008, OTTHUMT00000026009, OTTHUMT00000026010, OTTHUMT00000026011

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	16,141,431 - 16,144,057 (-)	MPROMDB

RGD ID:

6787251

Promoter ID:

HG_KWN:907

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, K562, Lymphoblastoid

Transcripts:

OTTHUMT00000026003

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	16,144,841 - 16,145,457 (-)	MPROMDB

RGD ID:

6787248

Promoter ID:

HG_KWN:908

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, K562, Lymphoblastoid

Transcripts:

OTTHUMT00000026001, OTTHUMT00000026002

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	16,146,091 - 16,147,272 (-)	MPROMDB

RGD ID:

6787249

Promoter ID:

HG_KWN:909

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, HeLa_S3, K562, NB4

Transcripts:

OTTHUMT00000025999

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	16,151,724 - 16,152,224 (-)	MPROMDB

RGD ID:

6785176

Promoter ID:

HG_KWN:911

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000375729, ENST00000375733, NM_003443, OTTHUMT00000026000, UC009VOM.1, UC009VON.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	16,174,949 - 16,175,449 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:12936	AgrOrtholog
COSMIC	ZBTB17	COSMIC
Ensembl Genes	ENSG00000116809	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000375733	ENTREZGENE
	ENST00000375733.6	UniProtKB/Swiss-Prot
	ENST00000375743	ENTREZGENE
	ENST00000375743.9	UniProtKB/Swiss-Prot
	ENST00000440560.5	UniProtKB/TrEMBL
	ENST00000444358.1	UniProtKB/TrEMBL
	ENST00000537142	ENTREZGENE
	ENST00000537142.5	UniProtKB/Swiss-Prot
Gene3D-CATH	Classic Zinc Finger	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000116809	GTEx
HGNC ID	HGNC:12936	ENTREZGENE
Human Proteome Map	ZBTB17	Human Proteome Map
InterPro	BTB/POZ_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SKP1/BTB/POZ_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_C2H2_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_C2H2_type	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:7709	UniProtKB/Swiss-Prot
NCBI Gene	7709	ENTREZGENE
OMIM	604084	OMIM
PANTHER	KRUEPPEL-LIKE FACTOR 15	UniProtKB/TrEMBL
	KRUEPPEL-LIKE TRANSCRIPTION FACTOR	UniProtKB/TrEMBL
	ZINC FINGER PROTEIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC FINGER PROTEIN 60-LIKE	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	BTB	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	zf-C2H2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	zf-C2H2_4	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA37522	PharmGKB
PROSITE	BTB	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	BTB	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZnF_C2H2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF54695	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF57667	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0AV07	ENTREZGENE
	B2RCP2	ENTREZGENE, UniProtKB/TrEMBL
	B4DXB4	ENTREZGENE
	B4E1F9	ENTREZGENE, UniProtKB/TrEMBL
	B7ZLQ9	ENTREZGENE
	F5H411	ENTREZGENE
	H0Y6X2_HUMAN	UniProtKB/TrEMBL
	H7C1K8_HUMAN	UniProtKB/TrEMBL
	Q13105	ENTREZGENE
	Q15932	ENTREZGENE
	Q53EM1_HUMAN	UniProtKB/TrEMBL
	Q5JYB2	ENTREZGENE
	Q9NUC9	ENTREZGENE
	ZBT17_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	A0AV07	UniProtKB/Swiss-Prot
	B4DXB4	UniProtKB/Swiss-Prot
	B7ZLQ9	UniProtKB/Swiss-Prot
	F5H411	UniProtKB/Swiss-Prot
	Q15932	UniProtKB/Swiss-Prot
	Q5JYB2	UniProtKB/Swiss-Prot
	Q9NUC9	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-03-31	ZBTB17	zinc finger and BTB domain containing 17	ZNF60	zinc finger protein 60	Data merged from RGD:1349599	737654	PROVISIONAL

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

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

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

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

Imported Disease Annotations - ClinVar

Imported Annotations - KEGG (archival)

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Imported Disease Annotations - ClinVar

Imported Annotations - KEGG (archival)