ZBTB1 (zinc finger and BTB domain containing 1)

Gene: ZBTB1 (zinc finger and BTB domain containing 1) Homo sapiens

Analyze

Symbol:

ZBTB1

Name:

zinc finger and BTB domain containing 1

RGD ID:

1343689

HGNC Page

HGNC:20259

Description:

Enables K63-linked polyubiquitin modification-dependent protein binding activity; protein heterodimerization activity; and protein homodimerization activity. Involved in several processes, including negative regulation of transcription by RNA polymerase II; nucleobase-containing compound biosynthetic process; and protein homooligomerization. Located in nuclear body and nuclear membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

KIAA0997; zinc finger and BTB domain-containing protein 1; ZNF909

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	14	64,503,716 - 64,533,693 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	64,503,712 - 64,533,690 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	64,971,488 - 65,000,411 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	64,041,174 - 64,070,161 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	64,041,173 - 64,070,161	NCBI
Celera	14	45,029,022 - 45,058,137 (+)	NCBI		Celera
Cytogenetic Map	14	q23.3	NCBI
HuRef	14	45,143,919 - 45,173,044 (+)	NCBI		HuRef
CHM1_1	14	64,910,965 - 64,940,072 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	14	58,711,422 - 58,741,460 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(-)-demecolcine (EXP)

1,2-dichloroethane (ISO)

1,2-dimethylhydrazine (ISO)

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

2-deoxy-D-glucose (EXP)

3,4-dichloroaniline (EXP)

3,4-methylenedioxymethamphetamine (ISO)

3-isobutyl-1-methyl-7H-xanthine (EXP)

4,4'-sulfonyldiphenol (EXP)

aflatoxin B1 (EXP)

amphetamine (ISO)

aristolochic acid A (EXP)

arsenous acid (EXP)

belinostat (EXP)

benzo[a]pyrene (EXP)

benzo[a]pyrene diol epoxide I (EXP)

bisphenol A (ISO)

butanal (EXP)

cadmium dichloride (EXP,ISO)

caffeine (EXP)

clorgyline (EXP)

cobalt dichloride (EXP)

copper atom (EXP)

copper(0) (EXP)

coumarin (EXP)

coumestrol (EXP)

dexamethasone (EXP)

diarsenic trioxide (EXP)

dicrotophos (EXP)

diuron (EXP)

dorsomorphin (EXP)

epoxiconazole (ISO)

fipronil (ISO)

formaldehyde (EXP)

FR900359 (EXP)

geraniol (EXP)

indometacin (EXP)

leflunomide (EXP)

mercury atom (EXP)

mercury(0) (EXP)

methylmercury chloride (EXP)

methylparaben (EXP)

N-methyl-4-phenylpyridinium (ISO)

panobinostat (EXP)

phenylmercury acetate (EXP)

pirinixic acid (ISO)

quercetin (EXP)

SB 431542 (EXP)

silicon dioxide (ISO)

silver atom (ISO)

silver(0) (ISO)

sodium dichromate (EXP)

titanium dioxide (ISO)

trichostatin A (EXP)

valproic acid (EXP)

vanadyl sulfate (EXP)

vorinostat (EXP)

zinc atom (EXP)

zinc(0) (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

B cell differentiation (IEA,ISO)

cell differentiation (IEA)

cellular response to UV (IMP)

chromatin remodeling (IMP)

DNA damage response (IMP)

DNA repair (IEA,IMP)

innate immune response (IEA)

mRNA transcription by RNA polymerase II (IDA)

negative regulation of transcription by RNA polymerase II (IBA,IDA)

positive regulation of natural killer cell differentiation (IEA,ISS)

positive regulation of pro-T cell differentiation (IEA,ISS)

positive regulation of T cell differentiation (IEA,ISS)

positive regulation of T cell mediated immunity (IEA,ISS)

protein homooligomerization (IDA)

regulation of cytokine production (IBA)

regulation of immune system process (IBA)

regulation of transcription by RNA polymerase II (IEA)

T cell differentiation in thymus (IEA,ISO)

thymus development (IEA,ISS)

translesion synthesis (IMP)

Cellular Component

nuclear body (IDA)

nuclear membrane (IDA)

nucleoplasm (IBA,IDA,IEA)

nucleus (IDA,IEA)

Molecular Function

DNA binding (IEA)

DNA-binding transcription factor activity, RNA polymerase II-specific (IEA)

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

K63-linked polyubiquitin modification-dependent protein binding (IDA)

metal ion binding (IEA)

protein binding (IPI)

protein heterodimerization activity (IDA)

protein homodimerization activity (IDA,IEA)

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

References

References - curated

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

Additional References at PubMed

PMID:8889548	PMID:10231032	PMID:12477932	PMID:15146197	PMID:15334068	PMID:15489334	PMID:19762545	PMID:20211142	PMID:20797634	PMID:21706167	PMID:21873635	PMID:22753936
PMID:24657165	PMID:24722188	PMID:24740910	PMID:25416956	PMID:25659891	PMID:26186194	PMID:26673895	PMID:26871637	PMID:26972000	PMID:27107012	PMID:28514442	PMID:29656893
PMID:31180492	PMID:31253590	PMID:31515488	PMID:32268116	PMID:32296183	PMID:32690611	PMID:32891193	PMID:33729478	PMID:33961781	PMID:34244565	PMID:34312970	PMID:34709266
PMID:35140242	PMID:35394175	PMID:35563538	PMID:35944360

Genomics

Comparative Map Data

ZBTB1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	14	64,503,716 - 64,533,693 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	64,503,712 - 64,533,690 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	64,971,488 - 65,000,411 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	64,041,174 - 64,070,161 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	64,041,173 - 64,070,161	NCBI
Celera	14	45,029,022 - 45,058,137 (+)	NCBI		Celera
Cytogenetic Map	14	q23.3	NCBI
HuRef	14	45,143,919 - 45,173,044 (+)	NCBI		HuRef
CHM1_1	14	64,910,965 - 64,940,072 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	14	58,711,422 - 58,741,460 (+)	NCBI		T2T-CHM13v2.0

Zbtb1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	12	76,416,825 - 76,443,729 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	12	76,417,040 - 76,443,724 (+)	Ensembl		GRCm39 Ensembl
GRCm38	12	76,370,051 - 76,396,955 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	12	76,370,266 - 76,396,950 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	12	77,471,253 - 77,489,734 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	12	77,289,106 - 77,307,290 (+)	NCBI		MGSCv36	mm8
Celera	12	77,461,603 - 77,479,773 (+)	NCBI		Celera
Cytogenetic Map	12	C3	NCBI
cM Map	12	33.73	NCBI

Zbtb1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	6	100,832,506 - 100,864,019 (+)	NCBI		GRCr8
mRatBN7.2	6	95,096,838 - 95,125,811 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	6	95,096,387 - 95,118,996 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	6	95,502,842 - 95,506,108 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	6	95,801,356 - 95,804,622 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	6	95,230,169 - 95,233,435 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	6	99,401,775 - 99,425,739 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	6	99,402,360 - 99,424,019 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	6	108,813,081 - 108,936,519 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	6	98,981,038 - 98,984,303 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	6	98,984,493 - 98,987,759 (+)	NCBI
Celera	6	93,534,115 - 93,537,380 (+)	NCBI		Celera
Cytogenetic Map	6	q24	NCBI

Zbtb1
(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_004955466	5,355,344 - 5,376,240 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955466	5,353,355 - 5,376,240 (-)	NCBI	ChiLan1.0	ChiLan1.0

ZBTB1
(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	15	65,615,544 - 65,645,388 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	14	64,832,059 - 64,864,228 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	14	45,085,146 - 45,114,965 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	14	63,337,806 - 63,366,653 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	14	63,354,458 - 63,359,403 (+)	Ensembl	panpan1.1		panPan2

ZBTB1
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	8	38,933,721 - 38,959,306 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	8	38,933,805 - 38,959,306 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	8	38,625,165 - 38,650,702 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	8	39,155,081 - 39,180,556 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	8	39,154,947 - 39,180,556 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	8	38,776,929 - 38,802,424 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	8	38,848,165 - 38,873,674 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	8	39,208,582 - 39,234,081 (+)	NCBI		UU_Cfam_GSD_1.0

Zbtb1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024408640	65,954,381 - 65,979,097 (-)	NCBI		HiC_Itri_2
SpeTri2.0	NW_004936495	8,212,136 - 8,238,876 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZBTB1
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	7	88,576,008 - 88,602,724 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	7	88,575,563 - 88,602,726 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	7	94,956,867 - 94,981,373 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ZBTB1
(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	24	41,712,721 - 41,738,853 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	24	41,712,114 - 41,740,654 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666053	29,889,458 - 29,915,735 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Zbtb1
(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_004624734	36,479,670 - 36,509,655 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ZBTB1
18 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 14q23.1-23.3(chr14:59917051-66750803)x1	copy number loss	See cases [RCV000050892]	Chr14:59917051..66750803 [GRCh38] Chr14:60383769..67217521 [GRCh37] Chr14:59453522..66287274 [NCBI36] Chr14:14q23.1-23.3	pathogenic
GRCh38/hg38 14q22.3-23.3(chr14:57041036-67208231)x1	copy number loss	See cases [RCV000051521]	Chr14:57041036..67208231 [GRCh38] Chr14:57507754..67674948 [GRCh37] Chr14:56577507..66744701 [NCBI36] Chr14:14q22.3-23.3	pathogenic
NM_001123329.1(ZBTB1):c.561G>A (p.Glu187=)	single nucleotide variant	Malignant melanoma [RCV000062776]	Chr14:64522065 [GRCh38] Chr14:64988783 [GRCh37] Chr14:64058536 [NCBI36] Chr14:14q23.3	not provided
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3	copy number gain	See cases [RCV000135543]	Chr14:20151149..106855263 [GRCh38] Chr14:20619308..107263478 [GRCh37] Chr14:19689148..106334523 [NCBI36] Chr14:14q11.2-32.33	pathogenic
GRCh38/hg38 14q23.2-23.3(chr14:62252700-65753416)x1	copy number loss	See cases [RCV000138250]	Chr14:62252700..65753416 [GRCh38] Chr14:62719418..66220134 [GRCh37] Chr14:61789171..65289887 [NCBI36] Chr14:14q23.2-23.3	pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3	copy number gain	See cases [RCV000143373]	Chr14:20043514..106877229 [GRCh38] Chr14:20511673..107285437 [GRCh37] Chr14:19581513..106356482 [NCBI36] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q23.2-23.3(chr14:64016496-65834490)x3	copy number gain	See cases [RCV002285053]	Chr14:64016496..65834490 [GRCh37] Chr14:14q23.2-23.3	uncertain significance
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3	copy number gain	See cases [RCV000446256]	Chr14:19794561..107234280 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3	copy number gain	See cases [RCV000448557]	Chr14:62493932..107285437 [GRCh37] Chr14:14q23.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437)	copy number gain	See cases [RCV000512041]	Chr14:20511673..107285437 [GRCh37] Chr14:14q11.2-32.33	pathogenic
NM_001123329.2(ZBTB1):c.899G>A (p.Gly300Glu)	single nucleotide variant	Inborn genetic diseases [RCV003299297]	Chr14:64522403 [GRCh38] Chr14:64989121 [GRCh37] Chr14:14q23.3	uncertain significance
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3	copy number gain	not provided [RCV000738412]	Chr14:19000422..107289053 [GRCh37] Chr14:14q11.1-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3	copy number gain	not provided [RCV000738413]	Chr14:19280733..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3	copy number gain	not provided [RCV000738414]	Chr14:19327823..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
NM_001123329.2(ZBTB1):c.1272G>C (p.Glu424Asp)	single nucleotide variant	Inborn genetic diseases [RCV003245933]	Chr14:64522776 [GRCh38] Chr14:64989494 [GRCh37] Chr14:14q23.3	uncertain significance
GRCh37/hg19 14q23.1-23.3(chr14:61409856-65742610)x3	copy number gain	not provided [RCV001259780]	Chr14:61409856..65742610 [GRCh37] Chr14:14q23.1-23.3	likely pathogenic
GRCh37/hg19 14q22.2-24.3(chr14:54654001-75828024)x3	copy number gain	14q22.2q24.3 duplication [RCV001506967]	Chr14:54654001..75828024 [GRCh37] Chr14:14q22.2-24.3	likely pathogenic
NC_000014.8:g.(?_64746679)_(66975329_?)del	deletion	Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C [RCV002007295]	Chr14:64746679..66975329 [GRCh37] Chr14:14q23.2-23.3	pathogenic
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2	copy number gain	See cases [RCV002286356]	Chr14:37671058..106985955 [GRCh37] Chr14:14q13.3-32.33	pathogenic
NM_001123329.2(ZBTB1):c.1509G>A (p.Met503Ile)	single nucleotide variant	Inborn genetic diseases [RCV002687102]	Chr14:64523013 [GRCh38] Chr14:64989731 [GRCh37] Chr14:14q23.3	uncertain significance
NM_001123329.2(ZBTB1):c.940G>A (p.Glu314Lys)	single nucleotide variant	Inborn genetic diseases [RCV002759630]	Chr14:64522444 [GRCh38] Chr14:64989162 [GRCh37] Chr14:14q23.3	uncertain significance
NM_001123329.2(ZBTB1):c.626C>T (p.Ser209Leu)	single nucleotide variant	Inborn genetic diseases [RCV002911678]	Chr14:64522130 [GRCh38] Chr14:64988848 [GRCh37] Chr14:14q23.3	uncertain significance
NM_001123329.2(ZBTB1):c.1640A>G (p.Asn547Ser)	single nucleotide variant	Inborn genetic diseases [RCV002737986]	Chr14:64523144 [GRCh38] Chr14:64989862 [GRCh37] Chr14:14q23.3	uncertain significance
NM_001123329.2(ZBTB1):c.1506T>G (p.Asp502Glu)	single nucleotide variant	Inborn genetic diseases [RCV002987618]	Chr14:64523010 [GRCh38] Chr14:64989728 [GRCh37] Chr14:14q23.3	uncertain significance
NM_001123329.2(ZBTB1):c.2010A>G (p.Ile670Met)	single nucleotide variant	Inborn genetic diseases [RCV002984202]	Chr14:64523514 [GRCh38] Chr14:64990232 [GRCh37] Chr14:14q23.3	uncertain significance
NM_001123329.2(ZBTB1):c.739A>T (p.Thr247Ser)	single nucleotide variant	Inborn genetic diseases [RCV002787702]	Chr14:64522243 [GRCh38] Chr14:64988961 [GRCh37] Chr14:14q23.3	uncertain significance
NM_001123329.2(ZBTB1):c.1250A>G (p.Asp417Gly)	single nucleotide variant	Inborn genetic diseases [RCV002981913]	Chr14:64522754 [GRCh38] Chr14:64989472 [GRCh37] Chr14:14q23.3	uncertain significance
NM_001123329.2(ZBTB1):c.1984A>G (p.Thr662Ala)	single nucleotide variant	Inborn genetic diseases [RCV002836433]	Chr14:64523488 [GRCh38] Chr14:64990206 [GRCh37] Chr14:14q23.3	uncertain significance
NM_001123329.2(ZBTB1):c.1505A>G (p.Asp502Gly)	single nucleotide variant	Inborn genetic diseases [RCV002897496]	Chr14:64523009 [GRCh38] Chr14:64989727 [GRCh37] Chr14:14q23.3	uncertain significance
NM_001123329.2(ZBTB1):c.1033A>G (p.Ile345Val)	single nucleotide variant	Inborn genetic diseases [RCV002702393]	Chr14:64522537 [GRCh38] Chr14:64989255 [GRCh37] Chr14:14q23.3	uncertain significance
NM_001123329.2(ZBTB1):c.1001T>C (p.Ile334Thr)	single nucleotide variant	Inborn genetic diseases [RCV003195489]	Chr14:64522505 [GRCh38] Chr14:64989223 [GRCh37] Chr14:14q23.3	uncertain significance
GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3	copy number gain	not provided [RCV003485036]	Chr14:58894502..107227240 [GRCh37] Chr14:14q23.1-32.33	pathogenic
GRCh37/hg19 14q22.3-24.1(chr14:57588965-68334517)x3	copy number gain	not provided [RCV003485034]	Chr14:57588965..68334517 [GRCh37] Chr14:14q22.3-24.1	likely pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1508
Count of miRNA genes:	849
Interacting mature miRNAs:	991
Transcripts:	ENST00000358738, ENST00000394712, ENST00000553583, ENST00000554015, ENST00000555321, ENST00000556818, ENST00000556965
Prediction methods:	Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

A007C14

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	64,990,421 - 64,990,693	UniSTS	GRCh37
Build 36	14	64,060,174 - 64,060,446	RGD	NCBI36
Celera	14	45,048,150 - 45,048,422	RGD
Cytogenetic Map	14	q23.3	UniSTS
HuRef	14	45,163,055 - 45,163,327	UniSTS
GeneMap99-GB4 RH Map	14	153.14	UniSTS
NCBI RH Map	14	647.8	UniSTS

D14S1194

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	64,990,473 - 64,990,640	UniSTS	GRCh37
Build 36	14	64,060,226 - 64,060,393	RGD	NCBI36
Celera	14	45,048,202 - 45,048,369	RGD
Cytogenetic Map	14	q23.3	UniSTS
HuRef	14	45,163,107 - 45,163,274	UniSTS
TNG Radiation Hybrid Map	14	21017.0	UniSTS
Stanford-G3 RH Map	14	2212.0	UniSTS
NCBI RH Map	14	651.1	UniSTS
GeneMap99-G3 RH Map	14	2260.0	UniSTS

AF005211

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	64,986,678 - 64,986,807	UniSTS	GRCh37
Build 36	14	64,056,431 - 64,056,560	RGD	NCBI36
Celera	14	45,044,407 - 45,044,536	RGD
Cytogenetic Map	14	q23.3	UniSTS
HuRef	14	45,159,312 - 45,159,441	UniSTS

D14S1339

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	64,990,338 - 64,990,643	UniSTS	GRCh37
Build 36	14	64,060,091 - 64,060,396	RGD	NCBI36
Celera	14	45,048,067 - 45,048,372	RGD
Cytogenetic Map	14	q23.3	UniSTS
HuRef	14	45,162,972 - 45,163,277	UniSTS

RH94359

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	64,988,775 - 64,988,903	UniSTS	GRCh37
Build 36	14	64,058,528 - 64,058,656	RGD	NCBI36
Celera	14	45,046,504 - 45,046,632	RGD
Cytogenetic Map	14	q23.3	UniSTS
HuRef	14	45,161,409 - 45,161,537	UniSTS
GeneMap99-GB4 RH Map	14	153.14	UniSTS

STS-AA019734

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	64,995,098 - 64,995,326	UniSTS	GRCh37
Build 36	14	64,064,851 - 64,065,079	RGD	NCBI36
Celera	14	45,052,827 - 45,053,055	RGD
Cytogenetic Map	14	q23.3	UniSTS
HuRef	14	45,167,734 - 45,167,962	UniSTS
GeneMap99-GB4 RH Map	14	153.14	UniSTS
NCBI RH Map	14	647.8	UniSTS

Zbtb1

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	64,990,882 - 64,990,937	UniSTS	GRCh37
Celera	14	45,048,611 - 45,048,666	UniSTS
HuRef	14	45,163,517 - 45,163,572	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

2265

1651

1334

290

1271

140

3876

1322

1834

284

1403

1587

163

1179

2340

Low

174

1324

392

333

665

325

480

874

1900

135

448

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001123329	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_014950	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005267410	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011536566	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011536568	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017021095	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431086	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431087	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431088	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431090	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431091	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431092	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431093	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431094	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431095	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431096	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431097	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431098	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431100	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431101	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431102	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431103	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431104	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431105	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431106	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431107	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431108	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431110	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431111	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375581	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375582	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375583	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375584	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375585	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375586	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375587	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375588	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375589	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375590	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375591	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375592	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375593	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375594	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375595	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375596	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375597	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375598	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375599	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375600	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375601	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375602	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375603	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375604	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375605	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375606	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375607	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB023214	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK291743	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL049869	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AW965994	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY598321	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC050719	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM975910	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX248777	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX537646	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471061	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CN362091	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000358738 ⟹ ENSP00000351587

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	64,504,574 - 64,533,690 (+)	Ensembl

RefSeq Acc Id:

ENST00000553583 ⟹ ENSP00000451584

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	64,503,725 - 64,521,970 (+)	Ensembl

RefSeq Acc Id:

ENST00000554015 ⟹ ENSP00000451000

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	64,503,985 - 64,523,898 (+)	Ensembl

RefSeq Acc Id:

ENST00000555321 ⟹ ENSP00000451332

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	64,504,726 - 64,521,606 (+)	Ensembl

RefSeq Acc Id:

ENST00000556818

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	64,503,712 - 64,504,854 (+)	Ensembl

RefSeq Acc Id:

ENST00000556965 ⟹ ENSP00000450689

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	64,503,951 - 64,521,895 (+)	Ensembl

RefSeq Acc Id:

ENST00000683701 ⟹ ENSP00000506911

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	64,504,770 - 64,524,951 (+)	Ensembl

RefSeq Acc Id:

NM_001123329 ⟹ NP_001116801

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,504,770 - 64,524,951 (+)	NCBI
GRCh37	14	64,971,292 - 65,000,408 (+)	RGD
Celera	14	45,029,022 - 45,058,137 (+)	RGD
HuRef	14	45,143,919 - 45,173,044 (+)	RGD
CHM1_1	14	64,910,965 - 64,931,333 (+)	NCBI
T2T-CHM13v2.0	14	58,712,530 - 58,732,717 (+)	NCBI

Sequence:

show sequence

GTTGCAGCACAGTCCCTGGCAGAGCCAGAGCCTCTCCGCGCAGCCCAGCCCGAGCGCCGAGCGC
CGCGCGCCGCCGCCACTGCAGCTCGCGGCCCCTTCGCCTTCGCCCGCCTTTCCCGCGGCTGATT
TGCCTTAAACTCCCTAAAATCTCCGCAGCTCTGGTTCCTGTTGCGGCCGGTCTCTAATTAACAG
AAGATGGCAAAGCCCAGCCACAGCAGCTATGTCCTTCAGCAGCTAAACAACCAAAGAGAATGGG
GTTTTCTCTGTGACTGCTGTATTGCAATTGATGACATTTACTTTCAAGCACACAAGGCAGTTCT
AGCTGCCTGTAGCTCCTATTTTAGAATGTTTTTCATGAACCATCAGCATAGTACTGCACAACTG
AATCTCAGCAACATGAAAATTAGTGCAGAATGTTTTGATCTCATTTTGCAGTTTATGTATTTAG
GAAAAATTATGACAGCTCCCTCCAGTTTTGAGCAGTTTAAAGTGGCAATGAACTACCTACAGCT
ATACAATGTTCCTGACTGTTTAGAAGACATCCAGGATGCAGATTGTTCTAGTTCAAAATGTTCC
TCTTCTGCTTCCAGCAAACAGAACAGCAAAATGATATTTGGGGTAAGAATGTATGAAGATACTG
TGGCTCGAAATGGCAATGAAGCCAACAGGTGGTGTGCAGAGCCAAGTTCAACGGTAAATACACC
ACATAATAGAGAGGCTGATGAAGAGTCTTTACAATTAGGTAATTTTCCTGAGCCACTATTTGAT
GTATGTAAAAAAAGTTCCGTGTCCAAATTATCTACTCCAAAAGAACGTGTGTCAAGACGCTTTG
GGCGGAGTTTTACCTGTGATAGCTGTGGATTTGGCTTTAGCTGTGAAAAATTATTAGATGAGCA
TGTGCTAACCTGTACTAACAGACATTTATACCAAAACACAAGATCTTACCATAGAATAGTAGAT
ATTAGAGATGGAAAAGACAGTAACATCAAAGCTGAATTTGGTGAAAAAGATTCTTCCAAAACAT
TTTCTGCACAGACGGACAAATACAGAGGAGACACAAGCCAGGCTGCTGATGATTCAGCTTCAAC
CACTGGAAGCAGAAAAAGTAGCACAGTGGAGTCTGAAATAGCAAGCGAAGAGAAAAGCAGAGCT
GCTGAGAGGAAAAGGATTATTATTAAGATGGAGCCAGAAGATATTCCTACAGATGAACTGAAAG
ACTTTAACATTATTAAAGTTACTGATAAAGACTGTAATGAATCCACTGACAATGATGAATTAGA
AGATGAACCTGAAGAGCCATTTTATAGATACTATGTTGAAGAAGATGTCAGCATAAAAAAAAGT
GGTAGGAAAACTCTAAAACCTCGAATGTCAGTAAGTGCTGATGAAAGAGGTGGTTTAGAGAATA
TGAGGCCCCCTAACAACAGCAGTCCAGTACAAGAGGATGCTGAAAATGCATCTTGTGAGCTGTG
TGGACTTACAATAACCGAGGAGGACCTGTCATCTCATTACTTAGCCAAACACATTGAAAATATC
TGTGCATGTGGTAAATGTGGACAAATACTTGTAAAGGGTAGGCAGCTTCAGGAACATGCTCAAC
GATGTGGCGAGCCCCAAGATCTGACCATGAATGGGTTAGGAAATACTGAGGAGAAAATGGACTT
GGAAGAGAATCCTGATGAGCAGTCCGAAATAAGAGATATGTTTGTTGAAATGCTGGATGATTTT
AGGGACAATCATTACCAGATAAACAGTATCCAAAAAAAGCAGTTATTTAAACATTCTGCCTGCC
CTTTTCGATGTCCTAATTGTGGCCAGCGTTTTGAAACTGAAAATCTAGTGGTTGAACATATGTC
TAGCTGCTTAGATCAAGATATGTTTAAGAGTGCCATCATGGAAGAAAATGAAAGAGATCACAGA
CGAAAGCATTTTTGTAATCTGTGTGGAAAAGGATTTTATCAGCGGTGTCACTTAAGAGAACACT
ATACTGTTCATACTAAGGAAAAACAGTTTGTTTGTCAAACATGTGGAAAGCAGTTTTTAAGAGA
GCGTCAGTTGCGACTGCACAATGATATGCACAAAGGCATGGCCAGGTATGTCTGTTCCATTTGT
GATCAAGGAAACTTCAGAAAACATGACCATGTACGGCATATGATTTCTCATTTATCTGCTGGTG
AGACTATATGCCAGGTCTGCTTTCAGATATTCCCAAATAATGAACAGTTGGAGCAGCACATGGA
TGTTCATCTGTATACATGTGGAATATGTGGAGCAAAATTTAATTTGAGGAAAGATATGAGATCA
CATTATAATGCCAAGCATTTGAAAAGAACCTGAGTGATTTTCTACTGTACTAATGTTTAGATGA
TAGCAGATAAAACACCAAAGCAAAGGATATGAGCTATTTAGGAATTGATTATATAAGATGATTT
GTTAGAAACAAATTTCAAGGCCCTTTTAACTTTAATATTTTTGTTTAGGATTTTAAGTATCTAC
ATTTAGGTATTAAATGTTTATCATTTTTGTTGTTTCTTAATAGAATTATTTGTTTTTAGTTTTT
CTTAGCTATGATTAAAATTTTTAAATGTAGACTACAAGTGGTTGTTACCCATTCAATGACTATT
AAACTTTAGTTTTTCATCAATAAGGTGATGACTTCACTATTTCTATGTGTTTTTTTTTTTTTAA
GGTTATCCTGTGAAATTTTAAACCCAGAATCATTGGCCATTTCTGTTTAAATTTTAAAAATTCC
TTAAGTAATTATTTGAAACTATCCCGTTTGCTTTTAGTGAGTTAACTACTCTTTATTCCCCCTT
ATTAATGAAATTCATATTCTTAAATTGACAAGCTTATTAGGCAAGTTAGGTGCACTGAATCTAA
CCTTTAAGGTTGACATGGGCTCAAACTTGGCCTAAAAAGATTGATGAACCTGAGGAAATTTTTA
TAAATGAATATTTCCTATAATTGATAAAATATTATCATTTAATTATCACATTTAAAACTTATAT
TAAGTGTAAATTCCAGTGGCTTTACCTCACTTGAAAAATTAGTGGGGATAAGCCATTTTGTTTT
GTGATATTAAATTTAACTATGATAGTTAATTAAAAAGACATATCTTGTATTCATTAAAAATATT
TTAATTTAAAATATTCTGATTTCTAAAGTGTGTTAGCTTATCAATTATTTTTGTTTATAAATAG
ACTTTAATAGCTCTCTAAGAATATGACCTCTAAAGGAAAAGATGATTTTTTACAATACATACTT
CTGGAACTTTGAGATTTGAGAAAGCTTCCATGTATATTGATAAATCTAATAAAATAAAGAGATC
AATTATAAACCTGGTTGTTCTATAAAAGTAGAGTGCACAAAAAAATGTCTTGTGTTTTATACTG
TCTAAGATTTGGAGGAAATGTGGCAAATTGCAGTTTATCGCCATATTTTATTATCATTTTTTTC
TGTAAAAGACTATAAAACTTGAGGATTATAAAATAATCACAGAGTATATCAATGGAAACAGTTT
ATCATTTTTTCAGTTAAAGTAGTAGTATTGTTAGTTGTTGCTGACACAGGGTCTACATAATTAC
ATGTGAATTAAAACATTGGCAAAACTGACCCACCAATAAACACATCTATTGAATAGAA

hide sequence

RefSeq Acc Id:

NM_014950 ⟹ NP_055765

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,504,770 - 64,533,693 (+)	NCBI
GRCh37	14	64,971,292 - 65,000,408 (+)	RGD
Build 36	14	64,041,174 - 64,070,161 (+)	NCBI Archive
Celera	14	45,029,022 - 45,058,137 (+)	RGD
HuRef	14	45,143,919 - 45,173,044 (+)	RGD
CHM1_1	14	64,910,965 - 64,940,072 (+)	NCBI
T2T-CHM13v2.0	14	58,712,530 - 58,741,460 (+)	NCBI

Sequence:

show sequence

GTTGCAGCACAGTCCCTGGCAGAGCCAGAGCCTCTCCGCGCAGCCCAGCCCGAGCGCCGAGCGC
CGCGCGCCGCCGCCACTGCAGCTCGCGGCCCCTTCGCCTTCGCCCGCCTTTCCCGCGGCTGATT
TGCCTTAAACTCCCTAAAATCTCCGCAGCTCTGGTTCCTGTTGCGGCCGGTCTCTAATTAACAG
AAGATGGCAAAGCCCAGCCACAGCAGCTATGTCCTTCAGCAGCTAAACAACCAAAGAGAATGGG
GTTTTCTCTGTGACTGCTGTATTGCAATTGATGACATTTACTTTCAAGCACACAAGGCAGTTCT
AGCTGCCTGTAGCTCCTATTTTAGAATGTTTTTCATGAACCATCAGCATAGTACTGCACAACTG
AATCTCAGCAACATGAAAATTAGTGCAGAATGTTTTGATCTCATTTTGCAGTTTATGTATTTAG
GAAAAATTATGACAGCTCCCTCCAGTTTTGAGCAGTTTAAAGTGGCAATGAACTACCTACAGCT
ATACAATGTTCCTGACTGTTTAGAAGACATCCAGGATGCAGATTGTTCTAGTTCAAAATGTTCC
TCTTCTGCTTCCAGCAAACAGAACAGCAAAATGATATTTGGGGTAAGAATGTATGAAGATACTG
TGGCTCGAAATGGCAATGAAGCCAACAGGTGGTGTGCAGAGCCAAGTTCAACGGTAAATACACC
ACATAATAGAGAGGCTGATGAAGAGTCTTTACAATTAGGTAATTTTCCTGAGCCACTATTTGAT
GTATGTAAAAAAAGTTCCGTGTCCAAATTATCTACTCCAAAAGAACGTGTGTCAAGACGCTTTG
GGCGGAGTTTTACCTGTGATAGCTGTGGATTTGGCTTTAGCTGTGAAAAATTATTAGATGAGCA
TGTGCTAACCTGTACTAACAGACATTTATACCAAAACACAAGATCTTACCATAGAATAGTAGAT
ATTAGAGATGGAAAAGACAGTAACATCAAAGCTGAATTTGGTGAAAAAGATTCTTCCAAAACAT
TTTCTGCACAGACGGACAAATACAGAGGAGACACAAGCCAGGCTGCTGATGATTCAGCTTCAAC
CACTGGAAGCAGAAAAAGTAGCACAGTGGAGTCTGAAATAGCAAGCGAAGAGAAAAGCAGAGCT
GCTGAGAGGAAAAGGATTATTATTAAGATGGAGCCAGAAGATATTCCTACAGATGAACTGAAAG
ACTTTAACATTATTAAAGTTACTGATAAAGACTGTAATGAATCCACTGACAATGATGAATTAGA
AGATGAACCTGAAGAGCCATTTTATAGATACTATGTTGAAGAAGATGTCAGCATAAAAAAAAGT
GGTAGGAAAACTCTAAAACCTCGAATGTCAGTAAGTGCTGATGAAAGAGGTGGTTTAGAGAATA
TGAGGCCCCCTAACAACAGCAGTCCAGTACAAGAGGATGCTGAAAATGCATCTTGTGAGCTGTG
TGGACTTACAATAACCGAGGAGGACCTGTCATCTCATTACTTAGCCAAACACATTGAAAATATC
TGTGCATGTGGTAAATGTGGACAAATACTTGTAAAGGGTAGGCAGCTTCAGGAACATGCTCAAC
GATGTGGCGAGCCCCAAGATCTGACCATGAATGGGTTAGGAAATACTGAGGAGAAAATGGACTT
GGAAGAGAATCCTGATGAGCAGTCCGAAATAAGAGATATGTTTGTTGAAATGCTGGATGATTTT
AGGGACAATCATTACCAGATAAACAGTATCCAAAAAAAGCAGTTATTTAAACATTCTGCCTGCC
CTTTTCGATGTCCTAATTGTGGCCAGCGTTTTGAAACTGAAAATCTAGTGGTTGAACATATGTC
TAGCTGCTTAGATCAAGATATGTTTAAGAGTGCCATCATGGAAGAAAATGAAAGAGATCACAGA
CGAAAGCATTTTTGTAATCTGTGTGGAAAAGGATTTTATCAGCGGTGTCACTTAAGAGAACACT
ATACTGTTCATACTAAGGAAAAACAGTTTGTTTGTCAAACATGTGGAAAGCAGTTTTTAAGAGA
GCGTCAGTTGCGACTGCACAATGATATGCACAAAGGCATGGCCAGTGGTGAAATAGGGCCTTCT
AAACCTGTGGAGAAGTGAGAGATCTGAATTTGGAGAGGACATGGGGAAGAATCAATCTTCAACA
GATAATCTTTAAGTACAGACCCAGGAATATCAGATCTGAAGTGGCACCATCTTTTCTGTCTTCC
TGACAAACTTCCATCAACCCAAAAAGTTCCAGTTGCAAAGATCCAAGAAAACTCAGTAAAGATC
ACTTTGGAATCACTTTGTTGTAACAAAATTGATTCATGGTGACTCTAATATTTGTGTAAATCTG
CTGAAGAAAAGTAACTAGAAAATTCATACAACATCAGTGGTTACAGCTATACTAAAATAAAACT
TTATATGCTAATTATCTTCAAGGGTCTTTCTAAAATAAAAGGGGTTGTTAGGCTACTGCAAATA
TAAAGAGACATAATCACAAATCTATTTATATAGATATAAATAATTCTAAACTTAAAATCACTAG
AATTATAGCTTAAATATTATGAAATGTACTTAGTCAACTTAAAAACTTACACCAAAAATCTGTA
GTTTAGAGTGTAAGAAGTAATGGGTACAGAGAAAAAAAATTTAAGACCAATATTTTAACAGGAT
AATTTGGTTATTACTCACTATAGTAAAACACTTGCCCTTCTTCCTTTTCCACTGTATATGCCAG
TCACAATCTTGATCATTTATATGAATGAAACTCCCTTTTAAACCTGTTAACTTGAAGGAGAACA
GAAATGGTATTACTTCAATAGTGGTAGATTTCCACAAATCAGACACATTATTTTCTTCTGAACT
TGGCAATATAACCTAATAAGGCAGAATAAGTTTCTGTTAAAATACTTATTCTCAATATTTATGT
ATAAACCATGCTTCTCAGCTTTCAAATTTCAAGATAAAATTTAAGTATTCAGTAAAATGATGGT
TAACATGTTTTAAAAAATCTTTAATGGAGAAGTTAAATATTTGGTGAGATTTTAGTCTGGCTAT
AAATGCTTTGTTTGATATATATATGTGCACATATATATATTACTTAACCATATGAATTTTATTT
CCTTATTCTGAATATACTTGTAGTTTTACTTCTTTCTGTTTATGTACCCAATTCCTTATGATTA
TTTTGTTTCTTCTGCAATATCAAGATGTTATTTATTTTGAGAAATGCTTATTTTTATGACTATT
TATTCCAATGTTTTAACAAGAAGCACAGAGATTTATAGTATTCTTAATAGTATGTGCAGAAGTT
ACATCATTTAAAAAACCCTTGCTGTAAAGTAGGATAACTTGAATATTCATTCTAATAATTAGAC
TAAGTGAAAATCTGAGAAAGAGTTAATTGCAATGTGATAGTGGGTAGAAAGGAGAGAAAAACCC
ACTGAAGGGTTCAAATACATGTGAATTCTACTGCTTTAAGAGAAATAAAACAAATAAGCCTAGG
GAAATATTAGAGTCTAAAAAACCCTAGAGTTAATCTCTTTTGGGAACATAAGGAGGTATACAGA
ACTGCAGACCTCTAAACATAAGTAGGAAAAAGAAAAATAAAAGAATATTACCAATAATTAAAGG
TGCCAGATCAAAATAGTAATAAATCAACAAATAATTTTTGATTGACTGGTGGAATTAGATTTAC
TAAATAAAAATGGCTTAAATTTTGACTGTACTAACTATAAATGTAATGAATTATAATAATTATA
AATGGTATAAATGCATTCTACAATGTGATTATTTTCTGTATTTTAGTATATAGTATAAAATGGA
ATTATTGGGTTAAAGTACTTTTATTACATTTCTTAATCCATTGTTTTTACCTAATAAAATTTCC
TCCTCTATATTCCAAAGTTAAA

hide sequence

RefSeq Acc Id:

XM_005267410 ⟹ XP_005267467

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,504,770 - 64,524,951 (+)	NCBI
GRCh37	14	64,971,292 - 65,000,408 (+)	NCBI

Sequence:

show sequence

AGTGCGGTGCGGCAGGCGCGGCTGTGCGGCAGCGGAAGTCCTTTGTTGCAGCACAGTCCCTGGC
AGAGCCAGAGCCTCTCCGCGCAGCCCAGCCCGAGCGCCGAGCGCCGCGCGCCGCCGCCACTGCA
GCTCGCGGCCCCTTCGCCTTCGCCCGCCTTTCCCGCGGCTGATTTGCCTTAAACTCCCTAAAAT
CTCCGCAGCTCTGGTTCCTGTTGCGGCCGTGCCCTCTGGTGGTCAGAAGATGCTGTGCTGTCTC
GTTAGGATGAATGGATTAAAATGTACTTTTCCTCCTCTGCTTCTGGAGAGGGAGAGAGGAATAT
TCCAGAAGCCACTGTGTTCCTTCTGCTTTCTGTGTGGCATGATGCCTTCTTCTGTAGAGTGGGC
GCTTTGCAGAATACGTGTTGAATGAAATCACTGATCTAGGAAAAGTAAAAATTCCTCAAATGAA
TACAGAATACTTGTGCTACTGCTGATGATCAACACTTTATACAGTGCCTGGTATACCAAAGGTC
TCTAATTAACAGAAGATGGCAAAGCCCAGCCACAGCAGCTATGTCCTTCAGCAGCTAAACAACC
AAAGAGAATGGGGTTTTCTCTGTGACTGCTGTATTGCAATTGATGACATTTACTTTCAAGCACA
CAAGGCAGTTCTAGCTGCCTGTAGCTCCTATTTTAGAATGTTTTTCATGAACCATCAGCATAGT
ACTGCACAACTGAATCTCAGCAACATGAAAATTAGTGCAGAATGTTTTGATCTCATTTTGCAGT
TTATGTATTTAGGAAAAATTATGACAGCTCCCTCCAGTTTTGAGCAGTTTAAAGTGGCAATGAA
CTACCTACAGCTATACAATGTTCCTGACTGTTTAGAAGACATCCAGGATGCAGATTGTTCTAGT
TCAAAATGTTCCTCTTCTGCTTCCAGCAAACAGAACAGCAAAATGATATTTGGGGTAAGAATGT
ATGAAGATACTGTGGCTCGAAATGGCAATGAAGCCAACAGGTGGTGTGCAGAGCCAAGTTCAAC
GGTAAATACACCACATAATAGAGAGGCTGATGAAGAGTCTTTACAATTAGGTAATTTTCCTGAG
CCACTATTTGATGTATGTAAAAAAAGTTCCGTGTCCAAATTATCTACTCCAAAAGAACGTGTGT
CAAGACGCTTTGGGCGGAGTTTTACCTGTGATAGCTGTGGATTTGGCTTTAGCTGTGAAAAATT
ATTAGATGAGCATGTGCTAACCTGTACTAACAGACATTTATACCAAAACACAAGATCTTACCAT
AGAATAGTAGATATTAGAGATGGAAAAGACAGTAACATCAAAGCTGAATTTGGTGAAAAAGATT
CTTCCAAAACATTTTCTGCACAGACGGACAAATACAGAGGAGACACAAGCCAGGCTGCTGATGA
TTCAGCTTCAACCACTGGAAGCAGAAAAAGTAGCACAGTGGAGTCTGAAATAGCAAGCGAAGAG
AAAAGCAGAGCTGCTGAGAGGAAAAGGATTATTATTAAGATGGAGCCAGAAGATATTCCTACAG
ATGAACTGAAAGACTTTAACATTATTAAAGTTACTGATAAAGACTGTAATGAATCCACTGACAA
TGATGAATTAGAAGATGAACCTGAAGAGCCATTTTATAGATACTATGTTGAAGAAGATGTCAGC
ATAAAAAAAAGTGGTAGGAAAACTCTAAAACCTCGAATGTCAGTAAGTGCTGATGAAAGAGGTG
GTTTAGAGAATATGAGGCCCCCTAACAACAGCAGTCCAGTACAAGAGGATGCTGAAAATGCATC
TTGTGAGCTGTGTGGACTTACAATAACCGAGGAGGACCTGTCATCTCATTACTTAGCCAAACAC
ATTGAAAATATCTGTGCATGTGGTAAATGTGGACAAATACTTGTAAAGGGTAGGCAGCTTCAGG
AACATGCTCAACGATGTGGCGAGCCCCAAGATCTGACCATGAATGGGTTAGGAAATACTGAGGA
GAAAATGGACTTGGAAGAGAATCCTGATGAGCAGTCCGAAATAAGAGATATGTTTGTTGAAATG
CTGGATGATTTTAGGGACAATCATTACCAGATAAACAGTATCCAAAAAAAGCAGTTATTTAAAC
ATTCTGCCTGCCCTTTTCGATGTCCTAATTGTGGCCAGCGTTTTGAAACTGAAAATCTAGTGGT
TGAACATATGTCTAGCTGCTTAGATCAAGATATGTTTAAGAGTGCCATCATGGAAGAAAATGAA
AGAGATCACAGACGAAAGCATTTTTGTAATCTGTGTGGAAAAGGATTTTATCAGCGGTGTCACT
TAAGAGAACACTATACTGTTCATACTAAGGAAAAACAGTTTGTTTGTCAAACATGTGGAAAGCA
GTTTTTAAGAGAGCGTCAGTTGCGACTGCACAATGATATGCACAAAGGCATGGCCAGGTATGTC
TGTTCCATTTGTGATCAAGGAAACTTCAGAAAACATGACCATGTACGGCATATGATTTCTCATT
TATCTGCTGGTGAGACTATATGCCAGGTCTGCTTTCAGATATTCCCAAATAATGAACAGTTGGA
GCAGCACATGGATGTTCATCTGTATACATGTGGAATATGTGGAGCAAAATTTAATTTGAGGAAA
GATATGAGATCACATTATAATGCCAAGCATTTGAAAAGAACCTGAGTGATTTTCTACTGTACTA
ATGTTTAGATGATAGCAGATAAAACACCAAAGCAAAGGATATGAGCTATTTAGGAATTGATTAT
ATAAGATGATTTGTTAGAAACAAATTTCAAGGCCCTTTTAACTTTAATATTTTTGTTTAGGATT
TTAAGTATCTACATTTAGGTATTAAATGTTTATCATTTTTGTTGTTTCTTAATAGAATTATTTG
TTTTTAGTTTTTCTTAGCTATGATTAAAATTTTTAAATGTAGACTACAAGTGGTTGTTACCCAT
TCAATGACTATTAAACTTTAGTTTTTCATCAATAAGGTGATGACTTCACTATTTCTATGTGTTT
TTTTTTTTTTAAGGTTATCCTGTGAAATTTTAAACCCAGAATCATTGGCCATTTCTGTTTAAAT
TTTAAAAATTCCTTAAGTAATTATTTGAAACTATCCCGTTTGCTTTTAGTGAGTTAACTACTCT
TTATTCCCCCTTATTAATGAAATTCATATTCTTAAATTGACAAGCTTATTAGGCAAGTTAGGTG
CACTGAATCTAACCTTTAAGGTTGACATGGGCTCAAACTTGGCCTAAAAAGATTGATGAACCTG
AGGAAATTTTTATAAATGAATATTTCCTATAATTGATAAAATATTATCATTTAATTATCACATT
TAAAACTTATATTAAGTGTAAATTCCAGTGGCTTTACCTCACTTGAAAAATTAGTGGGGATAAG
CCATTTTGTTTTGTGATATTAAATTTAACTATGATAGTTAATTAAAAAGACATATCTTGTATTC
ATTAAAAATATTTTAATTTAAAATATTCTGATTTCTAAAGTGTGTTAGCTTATCAATTATTTTT
GTTTATAAATAGACTTTAATAGCTCTCTAAGAATATGACCTCTAAAGGAAAAGATGATTTTTTA
CAATACATACTTCTGGAACTTTGAGATTTGAGAAAGCTTCCATGTATATTGATAAATCTAATAA
AATAAAGAGATCAATTATAAACCTGGTTGTTCTATAAAAGTAGAGTGCACAAAAAAATGTCTTG
TGTTTTATACTGTCTAAGATTTGGAGGAAATGTGGCAAATTGCAGTTTATCGCCATATTTTATT
ATCATTTTTTTCTGTAAAAGACTATAAAACTTGAGGATTATAAAATAATCACAGAGTATATCAA
TGGAAACAGTTTATCATTTTTTCAGTTAAAGTAGTAGTATTGTTAGTTGTTGCTGACACAGGGT
CTACATAATTACATGTGAATTAAAACATTGGCAAAACTGACCCACCAATAAACACATCTATTGA
ATAGAA

hide sequence

RefSeq Acc Id:

XM_011536566 ⟹ XP_011534868

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,504,770 - 64,524,951 (+)	NCBI

Sequence:

show sequence

AGCTCGCGGCCCCTTCGCCTTCGCCCGCCTTTCCCGCGGCTGATTTGCCTTAAACTCCCTAAAA
TCTCCGCAGCTCTGGTTCCTGTTGCGGCCGCATGATGCCTTCTTCTGTAGAGTGGGCGCTTTGC
AGAATACGTGTTGAATGAAATCACTGATCTAGGAAAAGTAAAAATTCCTCAAATGAATACAGAA
TACTTGTGCTACTGCTGATGATCAACACTTTATACAGTGCCTGGTATACCAAAGGTCTCTAATT
AACAGAAGATGGCAAAGCCCAGCCACAGCAGCTATGTCCTTCAGCAGCTAAACAACCAAAGAGA
ATGGGGTTTTCTCTGTGACTGCTGTATTGCAATTGATGACATTTACTTTCAAGCACACAAGGCA
GTTCTAGCTGCCTGTAGCTCCTATTTTAGAATGTTTTTCATGAACCATCAGCATAGTACTGCAC
AACTGAATCTCAGCAACATGAAAATTAGTGCAGAATGTTTTGATCTCATTTTGCAGTTTATGTA
TTTAGGAAAAATTATGACAGCTCCCTCCAGTTTTGAGCAGTTTAAAGTGGCAATGAACTACCTA
CAGCTATACAATGTTCCTGACTGTTTAGAAGACATCCAGGATGCAGATTGTTCTAGTTCAAAAT
GTTCCTCTTCTGCTTCCAGCAAACAGAACAGCAAAATGATATTTGGGGTAAGAATGTATGAAGA
TACTGTGGCTCGAAATGGCAATGAAGCCAACAGGTGGTGTGCAGAGCCAAGTTCAACGGTAAAT
ACACCACATAATAGAGAGGCTGATGAAGAGTCTTTACAATTAGGTAATTTTCCTGAGCCACTAT
TTGATGTATGTAAAAAAAGTTCCGTGTCCAAATTATCTACTCCAAAAGAACGTGTGTCAAGACG
CTTTGGGCGGAGTTTTACCTGTGATAGCTGTGGATTTGGCTTTAGCTGTGAAAAATTATTAGAT
GAGCATGTGCTAACCTGTACTAACAGACATTTATACCAAAACACAAGATCTTACCATAGAATAG
TAGATATTAGAGATGGAAAAGACAGTAACATCAAAGCTGAATTTGGTGAAAAAGATTCTTCCAA
AACATTTTCTGCACAGACGGACAAATACAGAGGAGACACAAGCCAGGCTGCTGATGATTCAGCT
TCAACCACTGGAAGCAGAAAAAGTAGCACAGTGGAGTCTGAAATAGCAAGCGAAGAGAAAAGCA
GAGCTGCTGAGAGGAAAAGGATTATTATTAAGATGGAGCCAGAAGATATTCCTACAGATGAACT
GAAAGACTTTAACATTATTAAAGTTACTGATAAAGACTGTAATGAATCCACTGACAATGATGAA
TTAGAAGATGAACCTGAAGAGCCATTTTATAGATACTATGTTGAAGAAGATGTCAGCATAAAAA
AAAGTGGTAGGAAAACTCTAAAACCTCGAATGTCAGTAAGTGCTGATGAAAGAGGTGGTTTAGA
GAATATGAGGCCCCCTAACAACAGCAGTCCAGTACAAGAGGATGCTGAAAATGCATCTTGTGAG
CTGTGTGGACTTACAATAACCGAGGAGGACCTGTCATCTCATTACTTAGCCAAACACATTGAAA
ATATCTGTGCATGTGGTAAATGTGGACAAATACTTGTAAAGGGTAGGCAGCTTCAGGAACATGC
TCAACGATGTGGCGAGCCCCAAGATCTGACCATGAATGGGTTAGGAAATACTGAGGAGAAAATG
GACTTGGAAGAGAATCCTGATGAGCAGTCCGAAATAAGAGATATGTTTGTTGAAATGCTGGATG
ATTTTAGGGACAATCATTACCAGATAAACAGTATCCAAAAAAAGCAGTTATTTAAACATTCTGC
CTGCCCTTTTCGATGTCCTAATTGTGGCCAGCGTTTTGAAACTGAAAATCTAGTGGTTGAACAT
ATGTCTAGCTGCTTAGATCAAGATATGTTTAAGAGTGCCATCATGGAAGAAAATGAAAGAGATC
ACAGACGAAAGCATTTTTGTAATCTGTGTGGAAAAGGATTTTATCAGCGGTGTCACTTAAGAGA
ACACTATACTGTTCATACTAAGGAAAAACAGTTTGTTTGTCAAACATGTGGAAAGCAGTTTTTA
AGAGAGCGTCAGTTGCGACTGCACAATGATATGCACAAAGGCATGGCCAGGTATGTCTGTTCCA
TTTGTGATCAAGGAAACTTCAGAAAACATGACCATGTACGGCATATGATTTCTCATTTATCTGC
TGGTGAGACTATATGCCAGGTCTGCTTTCAGATATTCCCAAATAATGAACAGTTGGAGCAGCAC
ATGGATGTTCATCTGTATACATGTGGAATATGTGGAGCAAAATTTAATTTGAGGAAAGATATGA
GATCACATTATAATGCCAAGCATTTGAAAAGAACCTGAGTGATTTTCTACTGTACTAATGTTTA
GATGATAGCAGATAAAACACCAAAGCAAAGGATATGAGCTATTTAGGAATTGATTATATAAGAT
GATTTGTTAGAAACAAATTTCAAGGCCCTTTTAACTTTAATATTTTTGTTTAGGATTTTAAGTA
TCTACATTTAGGTATTAAATGTTTATCATTTTTGTTGTTTCTTAATAGAATTATTTGTTTTTAG
TTTTTCTTAGCTATGATTAAAATTTTTAAATGTAGACTACAAGTGGTTGTTACCCATTCAATGA
CTATTAAACTTTAGTTTTTCATCAATAAGGTGATGACTTCACTATTTCTATGTGTTTTTTTTTT
TTTAAGGTTATCCTGTGAAATTTTAAACCCAGAATCATTGGCCATTTCTGTTTAAATTTTAAAA
ATTCCTTAAGTAATTATTTGAAACTATCCCGTTTGCTTTTAGTGAGTTAACTACTCTTTATTCC
CCCTTATTAATGAAATTCATATTCTTAAATTGACAAGCTTATTAGGCAAGTTAGGTGCACTGAA
TCTAACCTTTAAGGTTGACATGGGCTCAAACTTGGCCTAAAAAGATTGATGAACCTGAGGAAAT
TTTTATAAATGAATATTTCCTATAATTGATAAAATATTATCATTTAATTATCACATTTAAAACT
TATATTAAGTGTAAATTCCAGTGGCTTTACCTCACTTGAAAAATTAGTGGGGATAAGCCATTTT
GTTTTGTGATATTAAATTTAACTATGATAGTTAATTAAAAAGACATATCTTGTATTCATTAAAA
ATATTTTAATTTAAAATATTCTGATTTCTAAAGTGTGTTAGCTTATCAATTATTTTTGTTTATA
AATAGACTTTAATAGCTCTCTAAGAATATGACCTCTAAAGGAAAAGATGATTTTTTACAATACA
TACTTCTGGAACTTTGAGATTTGAGAAAGCTTCCATGTATATTGATAAATCTAATAAAATAAAG
AGATCAATTATAAACCTGGTTGTTCTATAAAAGTAGAGTGCACAAAAAAATGTCTTGTGTTTTA
TACTGTCTAAGATTTGGAGGAAATGTGGCAAATTGCAGTTTATCGCCATATTTTATTATCATTT
TTTTCTGTAAAAGACTATAAAACTTGAGGATTATAAAATAATCACAGAGTATATCAATGGAAAC
AGTTTATCATTTTTTCAGTTAAAGTAGTAGTATTGTTAGTTGTTGCTGACACAGGGTCTACATA
ATTACATGTGAATTAAAACATTGGCAAAACTGACCCACCAATAAACACATCTATTGAATAGAA

hide sequence

RefSeq Acc Id:

XM_017021095 ⟹ XP_016876584

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,504,770 - 64,524,951 (+)	NCBI

Sequence:

show sequence

TCCCTGGCAGAGCCAGAGCCTCTCCGCGCAGCCCAGCCCGAGCGCCGAGCGCCGCGCGCCGCCG
CCACTGCAGCTCGCGGCCCCTTCGCCTTCGCCCGCCTTTCCCGCGGCTGATTTGCCTTAAACTC
CCTAAAATCTCCGCAGCTCTGGTTCCTGTTGCGGCCGTGCCCTCTGGTGGTCAGAAGATGCTGT
GCTGTCTCGTTAGGATGAATGGATTAAAATGTACTTTTCCTCCTCTGCTTCTGGAGAGGGAGAG
AGGAATATTCCAGAAGCCACTGTGTTCCTTCTGCTTTCTGTGTGGGTCTCTAATTAACAGAAGA
TGGCAAAGCCCAGCCACAGCAGCTATGTCCTTCAGCAGCTAAACAACCAAAGAGAATGGGGTTT
TCTCTGTGACTGCTGTATTGCAATTGATGACATTTACTTTCAAGCACACAAGGCAGTTCTAGCT
GCCTGTAGCTCCTATTTTAGAATGTTTTTCATGAACCATCAGCATAGTACTGCACAACTGAATC
TCAGCAACATGAAAATTAGTGCAGAATGTTTTGATCTCATTTTGCAGTTTATGTATTTAGGAAA
AATTATGACAGCTCCCTCCAGTTTTGAGCAGTTTAAAGTGGCAATGAACTACCTACAGCTATAC
AATGTTCCTGACTGTTTAGAAGACATCCAGGATGCAGATTGTTCTAGTTCAAAATGTTCCTCTT
CTGCTTCCAGCAAACAGAACAGCAAAATGATATTTGGGGTAAGAATGTATGAAGATACTGTGGC
TCGAAATGGCAATGAAGCCAACAGGTGGTGTGCAGAGCCAAGTTCAACGGTAAATACACCACAT
AATAGAGAGGCTGATGAAGAGTCTTTACAATTAGGTAATTTTCCTGAGCCACTATTTGATGTAT
GTAAAAAAAGTTCCGTGTCCAAATTATCTACTCCAAAAGAACGTGTGTCAAGACGCTTTGGGCG
GAGTTTTACCTGTGATAGCTGTGGATTTGGCTTTAGCTGTGAAAAATTATTAGATGAGCATGTG
CTAACCTGTACTAACAGACATTTATACCAAAACACAAGATCTTACCATAGAATAGTAGATATTA
GAGATGGAAAAGACAGTAACATCAAAGCTGAATTTGGTGAAAAAGATTCTTCCAAAACATTTTC
TGCACAGACGGACAAATACAGAGGAGACACAAGCCAGGCTGCTGATGATTCAGCTTCAACCACT
GGAAGCAGAAAAAGTAGCACAGTGGAGTCTGAAATAGCAAGCGAAGAGAAAAGCAGAGCTGCTG
AGAGGAAAAGGATTATTATTAAGATGGAGCCAGAAGATATTCCTACAGATGAACTGAAAGACTT
TAACATTATTAAAGTTACTGATAAAGACTGTAATGAATCCACTGACAATGATGAATTAGAAGAT
GAACCTGAAGAGCCATTTTATAGATACTATGTTGAAGAAGATGTCAGCATAAAAAAAAGTGGTA
GGAAAACTCTAAAACCTCGAATGTCAGTAAGTGCTGATGAAAGAGGTGGTTTAGAGAATATGAG
GCCCCCTAACAACAGCAGTCCAGTACAAGAGGATGCTGAAAATGCATCTTGTGAGCTGTGTGGA
CTTACAATAACCGAGGAGGACCTGTCATCTCATTACTTAGCCAAACACATTGAAAATATCTGTG
CATGTGGTAAATGTGGACAAATACTTGTAAAGGGTAGGCAGCTTCAGGAACATGCTCAACGATG
TGGCGAGCCCCAAGATCTGACCATGAATGGGTTAGGAAATACTGAGGAGAAAATGGACTTGGAA
GAGAATCCTGATGAGCAGTCCGAAATAAGAGATATGTTTGTTGAAATGCTGGATGATTTTAGGG
ACAATCATTACCAGATAAACAGTATCCAAAAAAAGCAGTTATTTAAACATTCTGCCTGCCCTTT
TCGATGTCCTAATTGTGGCCAGCGTTTTGAAACTGAAAATCTAGTGGTTGAACATATGTCTAGC
TGCTTAGATCAAGATATGTTTAAGAGTGCCATCATGGAAGAAAATGAAAGAGATCACAGACGAA
AGCATTTTTGTAATCTGTGTGGAAAAGGATTTTATCAGCGGTGTCACTTAAGAGAACACTATAC
TGTTCATACTAAGGAAAAACAGTTTGTTTGTCAAACATGTGGAAAGCAGTTTTTAAGAGAGCGT
CAGTTGCGACTGCACAATGATATGCACAAAGGCATGGCCAGGTATGTCTGTTCCATTTGTGATC
AAGGAAACTTCAGAAAACATGACCATGTACGGCATATGATTTCTCATTTATCTGCTGGTGAGAC
TATATGCCAGGTCTGCTTTCAGATATTCCCAAATAATGAACAGTTGGAGCAGCACATGGATGTT
CATCTGTATACATGTGGAATATGTGGAGCAAAATTTAATTTGAGGAAAGATATGAGATCACATT
ATAATGCCAAGCATTTGAAAAGAACCTGAGTGATTTTCTACTGTACTAATGTTTAGATGATAGC
AGATAAAACACCAAAGCAAAGGATATGAGCTATTTAGGAATTGATTATATAAGATGATTTGTTA
GAAACAAATTTCAAGGCCCTTTTAACTTTAATATTTTTGTTTAGGATTTTAAGTATCTACATTT
AGGTATTAAATGTTTATCATTTTTGTTGTTTCTTAATAGAATTATTTGTTTTTAGTTTTTCTTA
GCTATGATTAAAATTTTTAAATGTAGACTACAAGTGGTTGTTACCCATTCAATGACTATTAAAC
TTTAGTTTTTCATCAATAAGGTGATGACTTCACTATTTCTATGTGTTTTTTTTTTTTTAAGGTT
ATCCTGTGAAATTTTAAACCCAGAATCATTGGCCATTTCTGTTTAAATTTTAAAAATTCCTTAA
GTAATTATTTGAAACTATCCCGTTTGCTTTTAGTGAGTTAACTACTCTTTATTCCCCCTTATTA
ATGAAATTCATATTCTTAAATTGACAAGCTTATTAGGCAAGTTAGGTGCACTGAATCTAACCTT
TAAGGTTGACATGGGCTCAAACTTGGCCTAAAAAGATTGATGAACCTGAGGAAATTTTTATAAA
TGAATATTTCCTATAATTGATAAAATATTATCATTTAATTATCACATTTAAAACTTATATTAAG
TGTAAATTCCAGTGGCTTTACCTCACTTGAAAAATTAGTGGGGATAAGCCATTTTGTTTTGTGA
TATTAAATTTAACTATGATAGTTAATTAAAAAGACATATCTTGTATTCATTAAAAATATTTTAA
TTTAAAATATTCTGATTTCTAAAGTGTGTTAGCTTATCAATTATTTTTGTTTATAAATAGACTT
TAATAGCTCTCTAAGAATATGACCTCTAAAGGAAAAGATGATTTTTTACAATACATACTTCTGG
AACTTTGAGATTTGAGAAAGCTTCCATGTATATTGATAAATCTAATAAAATAAAGAGATCAATT
ATAAACCTGGTTGTTCTATAAAAGTAGAGTGCACAAAAAAATGTCTTGTGTTTTATACTGTCTA
AGATTTGGAGGAAATGTGGCAAATTGCAGTTTATCGCCATATTTTATTATCATTTTTTTCTGTA
AAAGACTATAAAACTTGAGGATTATAAAATAATCACAGAGTATATCAATGGAAACAGTTTATCA
TTTTTTCAGTTAAAGTAGTAGTATTGTTAGTTGTTGCTGACACAGGGTCTACATAATTACATGT
GAATTAAAACATTGGCAAAACTGACCCACCAATAAACACATCTATTGAATAGAA

hide sequence

RefSeq Acc Id:

XM_047431086 ⟹ XP_047287042

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,887 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431087 ⟹ XP_047287043

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,887 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431088 ⟹ XP_047287044

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,887 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431090 ⟹ XP_047287046

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,887 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431091 ⟹ XP_047287047

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,716 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431092 ⟹ XP_047287048

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,887 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431093 ⟹ XP_047287049

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,716 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431094 ⟹ XP_047287050

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,505,328 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431095 ⟹ XP_047287051

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,716 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431096 ⟹ XP_047287052

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,887 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431097 ⟹ XP_047287053

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,887 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431098 ⟹ XP_047287054

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,716 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431100 ⟹ XP_047287056

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,716 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431101 ⟹ XP_047287057

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,505,328 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431102 ⟹ XP_047287058

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,887 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431103 ⟹ XP_047287059

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,504,770 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431104 ⟹ XP_047287060

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,887 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431105 ⟹ XP_047287061

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,505,328 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431106 ⟹ XP_047287062

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,716 - 64,524,951 (+)	NCBI

RefSeq Acc Id:

XM_047431107 ⟹ XP_047287063

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,887 - 64,533,693 (+)	NCBI

RefSeq Acc Id:

XM_047431108 ⟹ XP_047287064

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,504,770 - 64,533,693 (+)	NCBI

RefSeq Acc Id:

XM_047431110 ⟹ XP_047287066

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,504,770 - 64,533,693 (+)	NCBI

RefSeq Acc Id:

XM_047431111 ⟹ XP_047287067

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,716 - 64,533,693 (+)	NCBI

RefSeq Acc Id:

XM_054375581 ⟹ XP_054231556

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,636 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375582 ⟹ XP_054231557

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,522 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375583 ⟹ XP_054231558

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,712,530 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375584 ⟹ XP_054231559

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,626 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375585 ⟹ XP_054231560

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,712,530 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375586 ⟹ XP_054231561

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,475 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375587 ⟹ XP_054231562

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,454 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375588 ⟹ XP_054231563

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,646 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375589 ⟹ XP_054231564

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,422 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375590 ⟹ XP_054231565

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,713,088 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375591 ⟹ XP_054231566

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,437 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375592 ⟹ XP_054231567

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,648 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375593 ⟹ XP_054231568

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,475 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375594 ⟹ XP_054231569

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,475 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375595 ⟹ XP_054231570

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,454 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375596 ⟹ XP_054231571

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,713,088 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375597 ⟹ XP_054231572

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,712,530 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375598 ⟹ XP_054231573

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,710 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375599 ⟹ XP_054231574

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,712,366 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375600 ⟹ XP_054231575

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,475 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375601 ⟹ XP_054231576

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,713,088 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375602 ⟹ XP_054231577

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,422 - 58,732,717 (+)	NCBI

RefSeq Acc Id:

XM_054375603 ⟹ XP_054231578

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,712,530 - 58,741,460 (+)	NCBI

RefSeq Acc Id:

XM_054375604 ⟹ XP_054231579

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,646 - 58,741,460 (+)	NCBI

RefSeq Acc Id:

XM_054375605 ⟹ XP_054231580

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,712,530 - 58,741,460 (+)	NCBI

RefSeq Acc Id:

XM_054375606 ⟹ XP_054231581

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,712,530 - 58,741,460 (+)	NCBI

RefSeq Acc Id:

XM_054375607 ⟹ XP_054231582

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	58,711,482 - 58,741,460 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001116801	(Get FASTA)	NCBI Sequence Viewer
	NP_055765	(Get FASTA)	NCBI Sequence Viewer
	XP_005267467	(Get FASTA)	NCBI Sequence Viewer
	XP_011534868	(Get FASTA)	NCBI Sequence Viewer
	XP_016876584	(Get FASTA)	NCBI Sequence Viewer
	XP_047287042	(Get FASTA)	NCBI Sequence Viewer
	XP_047287043	(Get FASTA)	NCBI Sequence Viewer
	XP_047287044	(Get FASTA)	NCBI Sequence Viewer
	XP_047287046	(Get FASTA)	NCBI Sequence Viewer
	XP_047287047	(Get FASTA)	NCBI Sequence Viewer
	XP_047287048	(Get FASTA)	NCBI Sequence Viewer
	XP_047287049	(Get FASTA)	NCBI Sequence Viewer
	XP_047287050	(Get FASTA)	NCBI Sequence Viewer
	XP_047287051	(Get FASTA)	NCBI Sequence Viewer
	XP_047287052	(Get FASTA)	NCBI Sequence Viewer
	XP_047287053	(Get FASTA)	NCBI Sequence Viewer
	XP_047287054	(Get FASTA)	NCBI Sequence Viewer
	XP_047287056	(Get FASTA)	NCBI Sequence Viewer
	XP_047287057	(Get FASTA)	NCBI Sequence Viewer
	XP_047287058	(Get FASTA)	NCBI Sequence Viewer
	XP_047287059	(Get FASTA)	NCBI Sequence Viewer
	XP_047287060	(Get FASTA)	NCBI Sequence Viewer
	XP_047287061	(Get FASTA)	NCBI Sequence Viewer
	XP_047287062	(Get FASTA)	NCBI Sequence Viewer
	XP_047287063	(Get FASTA)	NCBI Sequence Viewer
	XP_047287064	(Get FASTA)	NCBI Sequence Viewer
	XP_047287066	(Get FASTA)	NCBI Sequence Viewer
	XP_047287067	(Get FASTA)	NCBI Sequence Viewer
	XP_054231556	(Get FASTA)	NCBI Sequence Viewer
	XP_054231557	(Get FASTA)	NCBI Sequence Viewer
	XP_054231558	(Get FASTA)	NCBI Sequence Viewer
	XP_054231559	(Get FASTA)	NCBI Sequence Viewer
	XP_054231560	(Get FASTA)	NCBI Sequence Viewer
	XP_054231561	(Get FASTA)	NCBI Sequence Viewer
	XP_054231562	(Get FASTA)	NCBI Sequence Viewer
	XP_054231563	(Get FASTA)	NCBI Sequence Viewer
	XP_054231564	(Get FASTA)	NCBI Sequence Viewer
	XP_054231565	(Get FASTA)	NCBI Sequence Viewer
	XP_054231566	(Get FASTA)	NCBI Sequence Viewer
	XP_054231567	(Get FASTA)	NCBI Sequence Viewer
	XP_054231568	(Get FASTA)	NCBI Sequence Viewer
	XP_054231569	(Get FASTA)	NCBI Sequence Viewer
	XP_054231570	(Get FASTA)	NCBI Sequence Viewer
	XP_054231571	(Get FASTA)	NCBI Sequence Viewer
	XP_054231572	(Get FASTA)	NCBI Sequence Viewer
	XP_054231573	(Get FASTA)	NCBI Sequence Viewer
	XP_054231574	(Get FASTA)	NCBI Sequence Viewer
	XP_054231575	(Get FASTA)	NCBI Sequence Viewer
	XP_054231576	(Get FASTA)	NCBI Sequence Viewer
	XP_054231577	(Get FASTA)	NCBI Sequence Viewer
	XP_054231578	(Get FASTA)	NCBI Sequence Viewer
	XP_054231579	(Get FASTA)	NCBI Sequence Viewer
	XP_054231580	(Get FASTA)	NCBI Sequence Viewer
	XP_054231581	(Get FASTA)	NCBI Sequence Viewer
	XP_054231582	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH50719	(Get FASTA)	NCBI Sequence Viewer
	AAT06732	(Get FASTA)	NCBI Sequence Viewer
	BAA76841	(Get FASTA)	NCBI Sequence Viewer
	BAF84432	(Get FASTA)	NCBI Sequence Viewer
	CAD66584	(Get FASTA)	NCBI Sequence Viewer
	EAW80863	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000351587
	ENSP00000351587.3
	ENSP00000450689.1
	ENSP00000451000
	ENSP00000451000.1
	ENSP00000451332.1
	ENSP00000451584.1
	ENSP00000506911
	ENSP00000506911.1
GenBank Protein	Q9Y2K1	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_055765 ⟸ NM_014950
- Peptide Label:	isoform 2
- UniProtKB:	Q5UW39 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAKPSHSSYVLQQLNNQREWGFLCDCCIAIDDIYFQAHKAVLAACSSYFRMFFMNHQHSTAQLN LSNMKISAECFDLILQFMYLGKIMTAPSSFEQFKVAMNYLQLYNVPDCLEDIQDADCSSSKCSS SASSKQNSKMIFGVRMYEDTVARNGNEANRWCAEPSSTVNTPHNREADEESLQLGNFPEPLFDV CKKSSVSKLSTPKERVSRRFGRSFTCDSCGFGFSCEKLLDEHVLTCTNRHLYQNTRSYHRIVDI RDGKDSNIKAEFGEKDSSKTFSAQTDKYRGDTSQAADDSASTTGSRKSSTVESEIASEEKSRAA ERKRIIIKMEPEDIPTDELKDFNIIKVTDKDCNESTDNDELEDEPEEPFYRYYVEEDVSIKKSG RKTLKPRMSVSADERGGLENMRPPNNSSPVQEDAENASCELCGLTITEEDLSSHYLAKHIENIC ACGKCGQILVKGRQLQEHAQRCGEPQDLTMNGLGNTEEKMDLEENPDEQSEIRDMFVEMLDDFR DNHYQINSIQKKQLFKHSACPFRCPNCGQRFETENLVVEHMSSCLDQDMFKSAIMEENERDHRR KHFCNLCGKGFYQRCHLREHYTVHTKEKQFVCQTCGKQFLRERQLRLHNDMHKGMASGEIGPSK PVEK hide sequence

RefSeq Acc Id:	NP_001116801 ⟸ NM_001123329
- Peptide Label:	isoform 1
- UniProtKB:	A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot), Q9Y2K1 (UniProtKB/Swiss-Prot), Q5UW39 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAKPSHSSYVLQQLNNQREWGFLCDCCIAIDDIYFQAHKAVLAACSSYFRMFFMNHQHSTAQLN LSNMKISAECFDLILQFMYLGKIMTAPSSFEQFKVAMNYLQLYNVPDCLEDIQDADCSSSKCSS SASSKQNSKMIFGVRMYEDTVARNGNEANRWCAEPSSTVNTPHNREADEESLQLGNFPEPLFDV CKKSSVSKLSTPKERVSRRFGRSFTCDSCGFGFSCEKLLDEHVLTCTNRHLYQNTRSYHRIVDI RDGKDSNIKAEFGEKDSSKTFSAQTDKYRGDTSQAADDSASTTGSRKSSTVESEIASEEKSRAA ERKRIIIKMEPEDIPTDELKDFNIIKVTDKDCNESTDNDELEDEPEEPFYRYYVEEDVSIKKSG RKTLKPRMSVSADERGGLENMRPPNNSSPVQEDAENASCELCGLTITEEDLSSHYLAKHIENIC ACGKCGQILVKGRQLQEHAQRCGEPQDLTMNGLGNTEEKMDLEENPDEQSEIRDMFVEMLDDFR DNHYQINSIQKKQLFKHSACPFRCPNCGQRFETENLVVEHMSSCLDQDMFKSAIMEENERDHRR KHFCNLCGKGFYQRCHLREHYTVHTKEKQFVCQTCGKQFLRERQLRLHNDMHKGMARYVCSICD QGNFRKHDHVRHMISHLSAGETICQVCFQIFPNNEQLEQHMDVHLYTCGICGAKFNLRKDMRSH YNAKHLKRT hide sequence

RefSeq Acc Id:	XP_005267467 ⟸ XM_005267410
- Peptide Label:	isoform X1
- UniProtKB:	A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot), Q9Y2K1 (UniProtKB/Swiss-Prot), Q5UW39 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAKPSHSSYVLQQLNNQREWGFLCDCCIAIDDIYFQAHKAVLAACSSYFRMFFMNHQHSTAQLN LSNMKISAECFDLILQFMYLGKIMTAPSSFEQFKVAMNYLQLYNVPDCLEDIQDADCSSSKCSS SASSKQNSKMIFGVRMYEDTVARNGNEANRWCAEPSSTVNTPHNREADEESLQLGNFPEPLFDV CKKSSVSKLSTPKERVSRRFGRSFTCDSCGFGFSCEKLLDEHVLTCTNRHLYQNTRSYHRIVDI RDGKDSNIKAEFGEKDSSKTFSAQTDKYRGDTSQAADDSASTTGSRKSSTVESEIASEEKSRAA ERKRIIIKMEPEDIPTDELKDFNIIKVTDKDCNESTDNDELEDEPEEPFYRYYVEEDVSIKKSG RKTLKPRMSVSADERGGLENMRPPNNSSPVQEDAENASCELCGLTITEEDLSSHYLAKHIENIC ACGKCGQILVKGRQLQEHAQRCGEPQDLTMNGLGNTEEKMDLEENPDEQSEIRDMFVEMLDDFR DNHYQINSIQKKQLFKHSACPFRCPNCGQRFETENLVVEHMSSCLDQDMFKSAIMEENERDHRR KHFCNLCGKGFYQRCHLREHYTVHTKEKQFVCQTCGKQFLRERQLRLHNDMHKGMARYVCSICD QGNFRKHDHVRHMISHLSAGETICQVCFQIFPNNEQLEQHMDVHLYTCGICGAKFNLRKDMRSH YNAKHLKRT hide sequence

RefSeq Acc Id:	XP_011534868 ⟸ XM_011536566
- Peptide Label:	isoform X1
- UniProtKB:	A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot), Q9Y2K1 (UniProtKB/Swiss-Prot), Q5UW39 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAKPSHSSYVLQQLNNQREWGFLCDCCIAIDDIYFQAHKAVLAACSSYFRMFFMNHQHSTAQLN LSNMKISAECFDLILQFMYLGKIMTAPSSFEQFKVAMNYLQLYNVPDCLEDIQDADCSSSKCSS SASSKQNSKMIFGVRMYEDTVARNGNEANRWCAEPSSTVNTPHNREADEESLQLGNFPEPLFDV CKKSSVSKLSTPKERVSRRFGRSFTCDSCGFGFSCEKLLDEHVLTCTNRHLYQNTRSYHRIVDI RDGKDSNIKAEFGEKDSSKTFSAQTDKYRGDTSQAADDSASTTGSRKSSTVESEIASEEKSRAA ERKRIIIKMEPEDIPTDELKDFNIIKVTDKDCNESTDNDELEDEPEEPFYRYYVEEDVSIKKSG RKTLKPRMSVSADERGGLENMRPPNNSSPVQEDAENASCELCGLTITEEDLSSHYLAKHIENIC ACGKCGQILVKGRQLQEHAQRCGEPQDLTMNGLGNTEEKMDLEENPDEQSEIRDMFVEMLDDFR DNHYQINSIQKKQLFKHSACPFRCPNCGQRFETENLVVEHMSSCLDQDMFKSAIMEENERDHRR KHFCNLCGKGFYQRCHLREHYTVHTKEKQFVCQTCGKQFLRERQLRLHNDMHKGMARYVCSICD QGNFRKHDHVRHMISHLSAGETICQVCFQIFPNNEQLEQHMDVHLYTCGICGAKFNLRKDMRSH YNAKHLKRT hide sequence

RefSeq Acc Id:	XP_016876584 ⟸ XM_017021095
- Peptide Label:	isoform X1
- UniProtKB:	A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot), Q9Y2K1 (UniProtKB/Swiss-Prot), Q5UW39 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAKPSHSSYVLQQLNNQREWGFLCDCCIAIDDIYFQAHKAVLAACSSYFRMFFMNHQHSTAQLN LSNMKISAECFDLILQFMYLGKIMTAPSSFEQFKVAMNYLQLYNVPDCLEDIQDADCSSSKCSS SASSKQNSKMIFGVRMYEDTVARNGNEANRWCAEPSSTVNTPHNREADEESLQLGNFPEPLFDV CKKSSVSKLSTPKERVSRRFGRSFTCDSCGFGFSCEKLLDEHVLTCTNRHLYQNTRSYHRIVDI RDGKDSNIKAEFGEKDSSKTFSAQTDKYRGDTSQAADDSASTTGSRKSSTVESEIASEEKSRAA ERKRIIIKMEPEDIPTDELKDFNIIKVTDKDCNESTDNDELEDEPEEPFYRYYVEEDVSIKKSG RKTLKPRMSVSADERGGLENMRPPNNSSPVQEDAENASCELCGLTITEEDLSSHYLAKHIENIC ACGKCGQILVKGRQLQEHAQRCGEPQDLTMNGLGNTEEKMDLEENPDEQSEIRDMFVEMLDDFR DNHYQINSIQKKQLFKHSACPFRCPNCGQRFETENLVVEHMSSCLDQDMFKSAIMEENERDHRR KHFCNLCGKGFYQRCHLREHYTVHTKEKQFVCQTCGKQFLRERQLRLHNDMHKGMARYVCSICD QGNFRKHDHVRHMISHLSAGETICQVCFQIFPNNEQLEQHMDVHLYTCGICGAKFNLRKDMRSH YNAKHLKRT hide sequence

RefSeq Acc Id:

ENSP00000451332 ⟸ ENST00000555321

RefSeq Acc Id:

ENSP00000450689 ⟸ ENST00000556965

RefSeq Acc Id:

ENSP00000451584 ⟸ ENST00000553583

RefSeq Acc Id:

ENSP00000451000 ⟸ ENST00000554015

RefSeq Acc Id:

ENSP00000351587 ⟸ ENST00000358738

RefSeq Acc Id:

ENSP00000506911 ⟸ ENST00000683701

RefSeq Acc Id:	XP_047287067 ⟸ XM_047431111
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047287049 ⟸ XM_047431093
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287051 ⟸ XM_047431095
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287054 ⟸ XM_047431098
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287047 ⟸ XM_047431091
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287062 ⟸ XM_047431106
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287056 ⟸ XM_047431100
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287063 ⟸ XM_047431107
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047287048 ⟸ XM_047431092
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287044 ⟸ XM_047431088
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287058 ⟸ XM_047431102
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287042 ⟸ XM_047431086
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287052 ⟸ XM_047431096
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287046 ⟸ XM_047431090
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287060 ⟸ XM_047431104
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287053 ⟸ XM_047431097
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287043 ⟸ XM_047431087
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287064 ⟸ XM_047431108
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047287066 ⟸ XM_047431110
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047287059 ⟸ XM_047431103
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287050 ⟸ XM_047431094
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287061 ⟸ XM_047431105
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287057 ⟸ XM_047431101
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231564 ⟸ XM_054375589
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231577 ⟸ XM_054375602
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231566 ⟸ XM_054375591
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231562 ⟸ XM_054375587
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231570 ⟸ XM_054375595
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231561 ⟸ XM_054375586
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231575 ⟸ XM_054375600
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231568 ⟸ XM_054375593
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231569 ⟸ XM_054375594
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231582 ⟸ XM_054375607
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054231557 ⟸ XM_054375582
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231559 ⟸ XM_054375584
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231556 ⟸ XM_054375581
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231579 ⟸ XM_054375604
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054231563 ⟸ XM_054375588
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231567 ⟸ XM_054375592
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231573 ⟸ XM_054375598
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231574 ⟸ XM_054375599
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231580 ⟸ XM_054375605
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054231578 ⟸ XM_054375603
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054231581 ⟸ XM_054375606
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054231558 ⟸ XM_054375583
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231572 ⟸ XM_054375597
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231560 ⟸ XM_054375585
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231565 ⟸ XM_054375590
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231576 ⟸ XM_054375601
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054231571 ⟸ XM_054375596
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2K1 (UniProtKB/Swiss-Prot), A8K6S8 (UniProtKB/Swiss-Prot), Q86SW8 (UniProtKB/Swiss-Prot)

Protein Domains

BTB C2H2-type

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9Y2K1-F1-model_v2	AlphaFold	Q9Y2K1	1-713	view protein structure

Promoters

RGD ID:

6792043

Promoter ID:

HG_KWN:19578

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:

ENST00000261683, NM_001123329, NM_014950, UC001XHH.2

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	14	64,039,231 - 64,041,177 (-)	MPROMDB

RGD ID:

7227857

Promoter ID:

EPDNEW_H19674

Type:

initiation region

Name:

ZBTB1_4

Description:

zinc finger and BTB domain containing 1

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H19676 EPDNEW_H19678 EPDNEW_H19681

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,097 - 64,503,157	EPDNEW

RGD ID:

7227861

Promoter ID:

EPDNEW_H19676

Type:

initiation region

Name:

ZBTB1_2

Description:

zinc finger and BTB domain containing 1

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H19674 EPDNEW_H19678 EPDNEW_H19681

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,716 - 64,503,776	EPDNEW

RGD ID:

7227865

Promoter ID:

EPDNEW_H19678

Type:

initiation region

Name:

ZBTB1_1

Description:

zinc finger and BTB domain containing 1

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H19674 EPDNEW_H19676 EPDNEW_H19681

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,503,887 - 64,503,947	EPDNEW

RGD ID:

7227873

Promoter ID:

EPDNEW_H19681

Type:

initiation region

Name:

ZBTB1_3

Description:

zinc finger and BTB domain containing 1

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H19674 EPDNEW_H19676 EPDNEW_H19678

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	64,505,346 - 64,505,406	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:20259	AgrOrtholog
COSMIC	ZBTB1	COSMIC
Ensembl Genes	ENSG00000126804	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000358738	ENTREZGENE
	ENST00000358738.3	UniProtKB/Swiss-Prot
	ENST00000553583.1	UniProtKB/TrEMBL
	ENST00000554015	ENTREZGENE
	ENST00000554015.5	UniProtKB/Swiss-Prot
	ENST00000555321.1	UniProtKB/TrEMBL
	ENST00000556965.1	UniProtKB/TrEMBL
	ENST00000683701	ENTREZGENE
	ENST00000683701.1	UniProtKB/Swiss-Prot
Gene3D-CATH	Classic Zinc Finger	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000126804	GTEx
HGNC ID	HGNC:20259	ENTREZGENE
Human Proteome Map	ZBTB1	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:22890	UniProtKB/Swiss-Prot
NCBI Gene	22890	ENTREZGENE
OMIM	616578	OMIM
PANTHER	GM08392P	UniProtKB/Swiss-Prot
	ZINC FINGER AND BTB DOMAIN CONTAINING 1	UniProtKB/TrEMBL
	ZINC FINGER PROTEIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	BTB	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	zf-C2H2	UniProtKB/Swiss-Prot
PharmGKB	PA128395769	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	beta-beta-alpha zinc fingers	UniProtKB/TrEMBL
	SSF54695	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF57667	UniProtKB/Swiss-Prot
UniProt	A8K6S8	ENTREZGENE
	G3V2I8_HUMAN	UniProtKB/TrEMBL
	G3V3N0_HUMAN	UniProtKB/TrEMBL
	G3V447_HUMAN	UniProtKB/TrEMBL
	Q5UW39	ENTREZGENE, UniProtKB/TrEMBL
	Q86SW8	ENTREZGENE
	Q9Y2K1	ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary	A8K6S8	UniProtKB/Swiss-Prot
	Q86SW8	UniProtKB/Swiss-Prot

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

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

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

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

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Imported Disease Annotations - ClinVar