ZBTB32 (zinc finger and BTB domain containing 32) - Rat Genome Database

ZBTB32 (zinc finger and BTB domain containing 32) - Rat Genome Database

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Gene: ZBTB32 (zinc finger and BTB domain containing 32) Homo sapiens

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Symbol:

ZBTB32

Name:

zinc finger and BTB domain containing 32

RGD ID:

1604369

HGNC Page

Description:

Enables DNA-binding transcription repressor activity, RNA polymerase II-specific; identical protein binding activity; and sequence-specific double-stranded DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nucleus.

Type:

protein-coding

RefSeq Status:

Previously known as:

FANCC-interacting protein; fanconi anemia zinc finger protein; FAXF; FAZF; mynn; myoneurin; repressor of GATA; Rog; testis zinc finger protein; TZFP; zinc finger and BTB domain-containing protein 32; zinc finger protein 538; ZNF538

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	35,704,558 - 35,717,038 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	35,704,558 - 35,717,038 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	36,195,460 - 36,207,940 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	40,895,670 - 40,899,780 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	19	32,917,304 - 32,921,414 (+)	NCBI		Celera
Cytogenetic Map	19	q13.12	NCBI
HuRef	19	32,708,667 - 32,712,777 (+)	NCBI		HuRef
CHM1_1	19	36,205,270 - 36,209,380 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	38,249,885 - 38,262,352 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZBTB32	Human	COVID-19		HEP		28912744	mRNA:increased expression:peripheral blood mononuclear cell (human)	RGD

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZBTB32	Human	Brugada syndrome 5		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Brugada syndrome 5	ClinVar	PMID:28492532
ZBTB32	Human	dystonia		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Dystonic disorder	ClinVar	PMID:32581362
ZBTB32	Human	hereditary spastic paraplegia 75		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Hereditary spastic paraplegia 75	ClinVar	PMID:28492532

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZBTB32	Human	2,3,7,8-tetrachlorodibenzodioxine	affects expression	ISO	Zbtb32 (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin affects the expression of ZBTB32 mRNA	CTD	PMID:34747641
ZBTB32	Human	2,4-dibromophenyl 2,4,5-tribromophenyl ether	affects expression	ISO	Zbtb32 (Mus musculus)	6480464	2 more ...	CTD	PMID:38648751
ZBTB32	Human	4,4'-sulfonyldiphenol	decreases expression	ISO	Zbtb32 (Mus musculus)	6480464	bisphenol S results in decreased expression of ZBTB32 mRNA	CTD	PMID:30951980
ZBTB32	Human	4,4'-sulfonyldiphenol	affects methylation	ISO	Zbtb32 (Mus musculus)	6480464	bisphenol S affects the methylation of ZBTB32 gene	CTD	PMID:31683443
ZBTB32	Human	8-Br-cAMP	decreases expression	EXP		6480464	8-Bromo Cyclic Adenosine Monophosphate results in decreased expression of ZBTB32 mRNA	CTD	PMID:22079614
ZBTB32	Human	acetamide	increases expression	ISO	Zbtb32 (Rattus norvegicus)	6480464	acetamide results in increased expression of ZBTB32 mRNA	CTD	PMID:31881176
ZBTB32	Human	aflatoxin B1	decreases methylation	EXP		6480464	Aflatoxin B1 results in decreased methylation of ZBTB32 intron	CTD	PMID:30157460
ZBTB32	Human	amphetamine	decreases expression	ISO	Zbtb32 (Rattus norvegicus)	6480464	Amphetamine results in decreased expression of ZBTB32 mRNA	CTD	PMID:30779732
ZBTB32	Human	arsenite(3-)	affects expression	EXP		6480464	arsenite affects the expression of ZBTB32 mRNA	CTD	PMID:22959463
ZBTB32	Human	benzo[a]pyrene	decreases methylation	EXP		6480464	Benzo(a)pyrene results in decreased methylation of ZBTB32 5' UTR	CTD	PMID:27901495
ZBTB32	Human	benzo[a]pyrene	affects methylation	EXP		6480464	Benzo(a)pyrene affects the methylation of ZBTB32 intron and Benzo(a)pyrene affects the methylation of ZBTB32 promoter	CTD	PMID:27901495 and PMID:30157460
ZBTB32	Human	benzo[e]pyrene	decreases methylation	EXP		6480464	benzo(e)pyrene results in decreased methylation of ZBTB32 intron	CTD	PMID:30157460
ZBTB32	Human	bis(2-ethylhexyl) phthalate	increases expression	ISO	Zbtb32 (Mus musculus)	6480464	Diethylhexyl Phthalate results in increased expression of ZBTB32 mRNA	CTD	PMID:34319233
ZBTB32	Human	bisphenol A	increases expression	ISO	Zbtb32 (Mus musculus)	6480464	bisphenol A results in increased expression of ZBTB32 mRNA	CTD	PMID:21932408
ZBTB32	Human	bisphenol A	decreases expression	EXP		6480464	bisphenol A results in decreased expression of ZBTB32 mRNA	CTD	PMID:31715268
ZBTB32	Human	bisphenol A	decreases expression	ISO	Zbtb32 (Rattus norvegicus)	6480464	bisphenol A results in decreased expression of ZBTB32 mRNA	CTD	PMID:25181051
ZBTB32	Human	bisphenol F	decreases expression	ISO	Zbtb32 (Mus musculus)	6480464	bisphenol F results in decreased expression of ZBTB32 mRNA	CTD	PMID:30951980
ZBTB32	Human	cadmium dichloride	decreases methylation	ISO	Zbtb32 (Rattus norvegicus)	6480464	Cadmium Chloride results in decreased methylation of ZBTB32 promoter	CTD	PMID:22457795
ZBTB32	Human	cisplatin	multiple interactions	EXP		6480464	[Cisplatin co-treated with jinfukang] results in increased expression of ZBTB32 mRNA	CTD	PMID:27392435
ZBTB32	Human	DDE	decreases expression	EXP		6480464	Dichlorodiphenyl Dichloroethylene results in decreased expression of ZBTB32 mRNA	CTD	PMID:38568856
ZBTB32	Human	epoxiconazole	decreases expression	ISO	Zbtb32 (Mus musculus)	6480464	epoxiconazole results in decreased expression of ZBTB32 mRNA	CTD	PMID:35436446
ZBTB32	Human	ethanol	multiple interactions	ISO	Zbtb32 (Mus musculus)	6480464	[Carbon Tetrachloride co-treated with Ethanol] results in decreased expression of ZBTB32 mRNA	CTD	PMID:30517762
ZBTB32	Human	ethyl methanesulfonate	decreases expression	EXP		6480464	Ethyl Methanesulfonate results in decreased expression of ZBTB32 mRNA	CTD	PMID:23649840
ZBTB32	Human	fonofos	increases methylation	EXP		6480464	Fonofos results in increased methylation of ZBTB32 promoter	CTD	PMID:22847954
ZBTB32	Human	lead diacetate	increases expression	ISO	Zbtb32 (Mus musculus)	6480464	lead acetate results in increased expression of ZBTB32 mRNA	CTD	PMID:20542052
ZBTB32	Human	lipopolysaccharide	multiple interactions	EXP		6480464	S-(1 and 2-dichlorovinyl)cysteine inhibits the reaction [Lipopolysaccharides results in increased expression of ZBTB32 mRNA]	CTD	PMID:35811015
ZBTB32	Human	lipopolysaccharide	increases expression	EXP		6480464	Lipopolysaccharides results in increased expression of ZBTB32 mRNA	CTD	PMID:35811015
ZBTB32	Human	methapyrilene	decreases methylation	EXP		6480464	Methapyrilene results in decreased methylation of ZBTB32 intron	CTD	PMID:30157460
ZBTB32	Human	methyl methanesulfonate	decreases expression	EXP		6480464	Methyl Methanesulfonate results in decreased expression of ZBTB32 mRNA	CTD	PMID:23649840
ZBTB32	Human	parathion	increases methylation	EXP		6480464	Parathion results in increased methylation of ZBTB32 promoter	CTD	PMID:22847954
ZBTB32	Human	poly(I:C)	multiple interactions	EXP		6480464	[TL8-506 co-treated with Poly I-C] results in increased expression of ZBTB32 mRNA	CTD	PMID:35688559
ZBTB32	Human	S-(1,2-dichlorovinyl)-L-cysteine	multiple interactions	EXP		6480464	S-(1 and 2-dichlorovinyl)cysteine inhibits the reaction [Lipopolysaccharides results in increased expression of ZBTB32 mRNA]	CTD	PMID:35811015
ZBTB32	Human	silicon dioxide	decreases expression	ISO	Zbtb32 (Mus musculus)	6480464	Silicon Dioxide results in decreased expression of ZBTB32 mRNA	CTD	PMID:29203145
ZBTB32	Human	silicon dioxide	increases expression	ISO	Zbtb32 (Mus musculus)	6480464	Silicon Dioxide results in increased expression of ZBTB32 mRNA	CTD	PMID:29341224
ZBTB32	Human	sodium arsenite	decreases expression	ISO	Zbtb32 (Mus musculus)	6480464	sodium arsenite results in decreased expression of ZBTB32 mRNA	CTD	PMID:37682722
ZBTB32	Human	succimer	multiple interactions	ISO	Zbtb32 (Mus musculus)	6480464	[Succimer binds to Magnetite Nanoparticles] which results in increased expression of ZBTB32 mRNA and [Succimer co-treated with Magnetite Nanoparticles] results in increased expression of ZBTB32 mRNA	CTD	PMID:21641980 and PMID:26378955
ZBTB32	Human	terbufos	increases methylation	EXP		6480464	terbufos results in increased methylation of ZBTB32 promoter	CTD	PMID:22847954
ZBTB32	Human	tetrachloromethane	multiple interactions	ISO	Zbtb32 (Mus musculus)	6480464	[Carbon Tetrachloride co-treated with Ethanol] results in decreased expression of ZBTB32 mRNA	CTD	PMID:30517762
ZBTB32	Human	titanium dioxide	increases expression	ISO	Zbtb32 (Mus musculus)	6480464	titanium dioxide results in increased expression of ZBTB32 mRNA	CTD	PMID:23557971
ZBTB32	Human	titanium dioxide	decreases expression	ISO	Zbtb32 (Mus musculus)	6480464	titanium dioxide results in decreased expression of ZBTB32 mRNA	CTD	PMID:29264374
ZBTB32	Human	toluene	increases expression	EXP		6480464	Toluene results in increased expression of ZBTB32 mRNA	CTD	PMID:26717081
ZBTB32	Human	toluene	decreases methylation	EXP		6480464	Toluene results in decreased methylation of ZBTB32 gene	CTD	PMID:26717081
ZBTB32	Human	trimellitic anhydride	increases expression	ISO	Zbtb32 (Mus musculus)	6480464	trimellitic anhydride results in increased expression of ZBTB32 mRNA	CTD	PMID:19042947
ZBTB32	Human	triphenyl phosphate	affects expression	EXP		6480464	triphenyl phosphate affects the expression of ZBTB32 mRNA	CTD	PMID:37042841
ZBTB32	Human	triptonide	increases expression	ISO	Zbtb32 (Mus musculus)	6480464	triptonide results in increased expression of ZBTB32 mRNA	CTD	PMID:33045310
ZBTB32	Human	troglitazone	increases expression	ISO	Zbtb32 (Mus musculus)	6480464	troglitazone results in increased expression of ZBTB32 mRNA	CTD	PMID:28973697
ZBTB32	Human	zinc atom	increases expression	EXP		6480464	Zinc deficiency results in increased expression of ZBTB32 mRNA	CTD	PMID:22171008
ZBTB32	Human	zinc(0)	increases expression	EXP		6480464	Zinc deficiency results in increased expression of ZBTB32 mRNA	CTD	PMID:22171008

Biological Process

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZBTB32	Human	hemopoiesis	acts_upstream_of_or_within	ISO	MGI:3527274	9068941	PMID:15542853	MGI	PMID:15542853
ZBTB32	Human	negative regulation of transcription by RNA polymerase II	involved_in	IDA		150520179	PMID:10572087	GO_Central	PMID:10572087
ZBTB32	Human	negative regulation of transcription by RNA polymerase II	involved_in	IBA	MGI:107187 more ...	150520179		GO_Central	GO_REF:0000033
ZBTB32	Human	regulation of cytokine production	acts_upstream_of_or_within	ISO	MGI:3527274	9068941	PMID:15542853	MGI	PMID:15542853
ZBTB32	Human	regulation of cytokine production	involved_in	IBA	MGI:107187 more ...	150520179		GO_Central	GO_REF:0000033
ZBTB32	Human	regulation of immune system process	involved_in	IBA	MGI:107187 more ...	150520179		GO_Central	GO_REF:0000033
ZBTB32	Human	T cell proliferation	acts_upstream_of_or_within	ISO	MGI:3527274	9068941	PMID:15542853	MGI	PMID:15542853

Cellular Component

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZBTB32	Human	chromatin	located_in	ISA	tfclass:2.3.2	150520179		NTNU_SB	GO_REF:0000113
ZBTB32	Human	nuclear chromosome	located_in	ISO	Zbtb32 (Mus musculus)	9068941	PMID:11555636	MGI	PMID:11555636
ZBTB32	Human	nucleoplasm	is_active_in	IBA	PANTHER:PTN002393396 more ...	150520179		GO_Central	GO_REF:0000033
ZBTB32	Human	nucleus	located_in	IEA	UniProtKB-SubCell:SL-0191	150520179		UniProt	GO_REF:0000044
ZBTB32	Human	nucleus	located_in	IDA		150520179	PMID:10572087	GO_Central	PMID:10572087
ZBTB32	Human	nucleus	located_in	IEA	UniProtKB-KW:KW-0539	150520179		UniProt	GO_REF:0000043

Molecular Function

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZBTB32	Human	DNA binding	enables	IEA	UniProtKB-KW:KW-0238	150520179		UniProt	GO_REF:0000043
ZBTB32	Human	DNA binding	enables	ISS	UniProtKB:Q9JKD9	150520179		UniProt	GO_REF:0000024
ZBTB32	Human	DNA-binding transcription factor activity, RNA polymerase II-specific	enables	ISA	tfclass:2.3.2	150520179		NTNU_SB	GO_REF:0000113
ZBTB32	Human	DNA-binding transcription repressor activity, RNA polymerase II-specific	enables	IDA		150520179	PMID:10572087	GO_Central	PMID:10572087
ZBTB32	Human	DNA-binding transcription repressor activity, RNA polymerase II-specific	enables	IBA	MGI:107187 more ...	150520179		GO_Central	GO_REF:0000033
ZBTB32	Human	identical protein binding	enables	IPI	UniProtKB:A0A0C4DGF1	150520179	PMID:32296183	IntAct	PMID:32296183
ZBTB32	Human	metal ion binding	enables	IEA	UniProtKB-KW:KW-0479	150520179		UniProt	GO_REF:0000043
ZBTB32	Human	protein binding	enables	IPI	UniProtKB:O14787-2 more ...	150520179	PMID:32296183	IntAct	PMID:32296183
ZBTB32	Human	protein binding	enables	IPI	UniProtKB:P09022	150520179	PMID:23088713	IntAct	PMID:23088713
ZBTB32	Human	protein binding	enables	IPI	UniProtKB:Q9BQY4	150520179	PMID:16189514 more ...	IntAct	PMID:16189514 more ...
ZBTB32	Human	protein binding	enables	IPI	UniProtKB:P78337	150520179	PMID:24722188	IntAct	PMID:24722188
ZBTB32	Human	protein binding	enables	IPI	UniProtKB:Q13554-3 more ...	150520179	PMID:26871637	IntAct	PMID:26871637
ZBTB32	Human	protein binding	enables	IPI	UniProtKB:Q93062-3	150520179	PMID:30886144	IntAct	PMID:30886144
ZBTB32	Human	protein binding	enables	IPI	UniProtKB:O75553 more ...	150520179	PMID:25416956	IntAct	PMID:25416956
ZBTB32	Human	RNA polymerase II cis-regulatory region sequence-specific DNA binding	enables	IBA	MGI:107187 more ...	150520179		GO_Central	GO_REF:0000033
ZBTB32	Human	sequence-specific double-stranded DNA binding	enables	IDA		150520179	PMID:28473536	ARUK-UCL	PMID:28473536
ZBTB32	Human	transcription corepressor activity	enables	ISO	Zbtb32 (Mus musculus)	9068941	PMID:10755619	MGI	PMID:10755619
ZBTB32	Human	zinc ion binding	enables	ISS	UniProtKB:Q9JKD9	150520179		UniProt	GO_REF:0000024
ZBTB32	Human	zinc ion binding	enables	IEA	UniProtKB-KW:KW-0863	150520179		UniProt	GO_REF:0000043

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZBTB32	Human	Dystonia		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Dystonia	ClinVar	PMID:32581362

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
3.	Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients.	Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.

PMID:10544010	PMID:10572087	PMID:11964310	PMID:11986317	PMID:12477932	PMID:12821938	PMID:14499622	PMID:15489334	PMID:16189514	PMID:16713569	PMID:17171645	PMID:18082604
PMID:19447967	PMID:20147518	PMID:20211142	PMID:20493880	PMID:21516116	PMID:21873635	PMID:22851713	PMID:23082233	PMID:23088713	PMID:24722188	PMID:25011449	PMID:25416956
PMID:26871637	PMID:27107014	PMID:27357154	PMID:28473536	PMID:28786561	PMID:30404837	PMID:32296183

ZBTB32
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	35,704,558 - 35,717,038 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	35,704,558 - 35,717,038 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	36,195,460 - 36,207,940 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	40,895,670 - 40,899,780 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	19	32,917,304 - 32,921,414 (+)	NCBI		Celera
Cytogenetic Map	19	q13.12	NCBI
HuRef	19	32,708,667 - 32,712,777 (+)	NCBI		HuRef
CHM1_1	19	36,205,270 - 36,209,380 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	38,249,885 - 38,262,352 (+)	NCBI		T2T-CHM13v2.0

Zbtb32
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	7	30,289,105 - 30,302,244 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	7	30,289,106 - 30,298,334 (-)	Ensembl		GRCm39 Ensembl
GRCm38	7	30,589,680 - 30,602,819 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	7	30,589,681 - 30,598,909 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	7	31,374,700 - 31,377,961 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	7	30,298,441 - 30,300,663 (-)	NCBI		MGSCv36	mm8
Celera	7	25,181,236 - 25,184,497 (-)	NCBI		Celera
Cytogenetic Map	7	B1	NCBI
cM Map	7	18.72	NCBI

Zbtb32
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	94,969,374 - 94,978,553 (-)	NCBI		GRCr8
mRatBN7.2	1	85,841,931 - 85,851,116 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	85,841,931 - 85,844,236 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	91,258,641 - 91,260,946 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	99,724,806 - 99,727,111 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	93,016,922 - 93,019,227 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	89,043,121 - 89,052,863 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	89,043,086 - 89,045,586 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	90,197,757 - 90,206,863 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	85,635,284 - 85,637,589 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	1	80,213,494 - 80,215,799 (-)	NCBI		Celera
Cytogenetic Map	1	q21	NCBI

Zbtb32
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0	NW_004955468	2,834,832 - 2,844,258 (-)	NCBI	ChiLan1.0	ChiLan1.0

ZBTB32
(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	20	41,697,806 - 41,711,710 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	19	43,683,118 - 43,696,649 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	19	32,633,923 - 32,647,675 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	19	41,368,960 - 41,381,634 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	19	41,369,043 - 41,381,634 (+)	Ensembl	panpan1.1		panPan2

ZBTB32
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	1	116,914,597 - 116,923,923 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	1	116,914,606 - 116,917,107 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	1	116,319,793 - 116,329,112 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	1	117,517,510 - 117,526,830 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	1	117,517,799 - 117,519,921 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	1	117,080,876 - 117,090,191 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	1	116,704,507 - 116,713,823 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	1	117,759,881 - 117,769,220 (-)	NCBI		UU_Cfam_GSD_1.0

Zbtb32
(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_024409349	11,030,378 - 11,039,795 (+)	NCBI		HiC_Itri_2
SpeTri2.0	NW_004936570	606,087 - 615,473 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZBTB32
(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	45,142,262 - 45,145,898 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	6	45,140,573 - 45,145,903 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	6	40,597,147 - 40,601,346 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ZBTB32
(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	6	30,609,096 - 30,625,664 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	6	30,623,252 - 30,625,386 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666073	8,403,862 - 8,417,251 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Zbtb32
(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_004624794	10,012,622 - 10,022,493 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

.

Variants in ZBTB32
50 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_014383.1(ZBTB32):c.102C>T (p.Thr34=)	single nucleotide variant	Malignant melanoma [RCV000072090]	Chr19:35714728 [GRCh38] Chr19:36205630 [GRCh37] Chr19:40897470 [NCBI36] Chr19:19q13.12	not provided
NM_014383.1(ZBTB32):c.107G>A (p.Gly36Glu)	single nucleotide variant	Malignant melanoma [RCV000072091]	Chr19:35714733 [GRCh38] Chr19:36205635 [GRCh37] Chr19:40897475 [NCBI36] Chr19:19q13.12	not provided
NM_014383.1(ZBTB32):c.1312C>T (p.Pro438Ser)	single nucleotide variant	Malignant melanoma [RCV000072092]	Chr19:35716600 [GRCh38] Chr19:36207502 [GRCh37] Chr19:40899342 [NCBI36] Chr19:19q13.12	not provided
NM_014383.1(ZBTB32):c.1313C>T (p.Pro438Leu)	single nucleotide variant	Malignant melanoma [RCV000072093]	Chr19:35716601 [GRCh38] Chr19:36207503 [GRCh37] Chr19:40899343 [NCBI36] Chr19:19q13.12	not provided
NM_014383.1(ZBTB32):c.187G>A (p.Gly63Arg)	single nucleotide variant	Malignant melanoma [RCV000063513]	Chr19:35714813 [GRCh38] Chr19:36205715 [GRCh37] Chr19:40897555 [NCBI36] Chr19:19q13.12	not provided
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	copy number gain	See cases [RCV000133888]	Chr19:11227942..44626354 [GRCh38] Chr19:11338618..45129651 [GRCh37] Chr19:11199618..49821491 [NCBI36] Chr19:19p13.2-q13.31	pathogenic
GRCh38/hg38 19q12-13.13(chr19:29661858-38114723)x1	copy number loss	See cases [RCV000135879]	Chr19:29661858..38114723 [GRCh38] Chr19:30152765..38605363 [GRCh37] Chr19:34844605..43297203 [NCBI36] Chr19:19q12-13.13	pathogenic
GRCh38/hg38 19q12-13.13(chr19:29671324-37902990)x1	copy number loss	See cases [RCV000136794]	Chr19:29671324..37902990 [GRCh38] Chr19:30162231..38393630 [GRCh37] Chr19:34854071..43085470 [NCBI36] Chr19:19q12-13.13	pathogenic
GRCh37/hg19 19q13.12(chr19:36166726-36207146)x3	copy number gain	See cases [RCV000448162]	Chr19:36166726..36207146 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19q13.12(chr19:36147111-37249653)x1	copy number loss	See cases [RCV000511504]	Chr19:36147111..37249653 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	copy number gain	See cases [RCV000511289]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic\|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	copy number gain	See cases [RCV000512296]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
NM_014383.3(ZBTB32):c.1079C>G (p.Pro360Arg)	single nucleotide variant	not specified [RCV004320097]	Chr19:35716187 [GRCh38] Chr19:36207089 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.1079C>T (p.Pro360Leu)	single nucleotide variant	not specified [RCV004319374]	Chr19:35716187 [GRCh38] Chr19:36207089 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3	copy number gain	not provided [RCV000752444]	Chr19:260912..59097160 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3	copy number gain	not provided [RCV000752439]	Chr19:68029..59110290 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19q13.11-13.12(chr19:35111811-37744992)	copy number loss	Generalized epilepsy with febrile seizures plus, type 1 [RCV000767768]	Chr19:35111811..37744992 [GRCh37] Chr19:19q13.11-13.12	pathogenic
GRCh37/hg19 19q13.11-13.12(chr19:35043556-36316644)	copy number loss	not provided [RCV000767769]	Chr19:35043556..36316644 [GRCh37] Chr19:19q13.11-13.12	pathogenic
GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	copy number gain	not provided [RCV000845733]	Chr19:28271106..49213832 [GRCh37] Chr19:19q11-13.33	pathogenic
NM_014383.3(ZBTB32):c.718C>A (p.Gln240Lys)	single nucleotide variant	not specified [RCV004315244]	Chr19:35715344 [GRCh38] Chr19:36206246 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.601G>A (p.Gly201Ser)	single nucleotide variant	not specified [RCV004292673]	Chr19:35715227 [GRCh38] Chr19:36206129 [GRCh37] Chr19:19q13.12	uncertain significance
NC_000019.9:g.(?_33167170)_(36643309_?)dup	duplication	Hereditary spastic paraplegia 75 [RCV003107659]	Chr19:33167170..36643309 [GRCh37] Chr19:19q13.11-13.12	uncertain significance
Single allele	deletion	Dystonic disorder [RCV001003865]	Chr19:35553425..36264299 [GRCh37] Chr19:19q13.12	pathogenic
GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)x3	copy number gain	Specific learning disability [RCV001801194]	Chr19:19546923..41313229 [GRCh37] Chr19:19p13.11-q13.2	pathogenic
GRCh37/hg19 19q13.12(chr19:36019064-36516110)x3	copy number gain	not provided [RCV001833065]	Chr19:36019064..36516110 [GRCh37] Chr19:19q13.12	uncertain significance
NC_000019.9:g.(?_35521725)_(36643309_?)del	deletion	Brugada syndrome 5 [RCV001910265]	Chr19:35521725..36643309 [GRCh37] Chr19:19q13.12	uncertain significance
NC_000019.9:g.(?_35521725)_(36229458_?)del	deletion	not provided [RCV001975081]	Chr19:35521725..36229458 [GRCh37] Chr19:19q13.12	pathogenic
NM_014383.3(ZBTB32):c.1109C>G (p.Ser370Cys)	single nucleotide variant	not specified [RCV004111635]	Chr19:35716217 [GRCh38] Chr19:36207119 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.1082A>C (p.His361Pro)	single nucleotide variant	not specified [RCV004219854]	Chr19:35716190 [GRCh38] Chr19:36207092 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.287C>T (p.Ala96Val)	single nucleotide variant	not specified [RCV004194928]	Chr19:35714913 [GRCh38] Chr19:36205815 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.418A>G (p.Arg140Gly)	single nucleotide variant	not specified [RCV004151434]	Chr19:35715044 [GRCh38] Chr19:36205946 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.577G>A (p.Glu193Lys)	single nucleotide variant	not specified [RCV004100253]	Chr19:35715203 [GRCh38] Chr19:36206105 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.1300G>C (p.Gly434Arg)	single nucleotide variant	not specified [RCV004222231]	Chr19:35716588 [GRCh38] Chr19:36207490 [GRCh37] Chr19:19q13.12	likely benign
NM_014383.3(ZBTB32):c.1280C>G (p.Pro427Arg)	single nucleotide variant	not specified [RCV004221779]	Chr19:35716568 [GRCh38] Chr19:36207470 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.1121C>A (p.Ala374Glu)	single nucleotide variant	not specified [RCV004223902]	Chr19:35716229 [GRCh38] Chr19:36207131 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.554A>G (p.Gln185Arg)	single nucleotide variant	not specified [RCV004147321]	Chr19:35715180 [GRCh38] Chr19:36206082 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.806C>T (p.Pro269Leu)	single nucleotide variant	not specified [RCV004163998]	Chr19:35715432 [GRCh38] Chr19:36206334 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.400C>A (p.Pro134Thr)	single nucleotide variant	not specified [RCV004183695]	Chr19:35715026 [GRCh38] Chr19:36205928 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.338G>A (p.Arg113Gln)	single nucleotide variant	not specified [RCV004169604]	Chr19:35714964 [GRCh38] Chr19:36205866 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.178T>C (p.Trp60Arg)	single nucleotide variant	not specified [RCV004140289]	Chr19:35714804 [GRCh38] Chr19:36205706 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.1304C>T (p.Ala435Val)	single nucleotide variant	not specified [RCV004207451]	Chr19:35716592 [GRCh38] Chr19:36207494 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.872G>A (p.Arg291Gln)	single nucleotide variant	not specified [RCV004170005]	Chr19:35715498 [GRCh38] Chr19:36206400 [GRCh37] Chr19:19q13.12	likely benign
NM_014383.3(ZBTB32):c.1219C>T (p.Pro407Ser)	single nucleotide variant	not specified [RCV004280116]	Chr19:35716507 [GRCh38] Chr19:36207409 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.631G>T (p.Val211Leu)	single nucleotide variant	not specified [RCV004249809]	Chr19:35715257 [GRCh38] Chr19:36206159 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.459G>T (p.Gln153His)	single nucleotide variant	not specified [RCV004325195]	Chr19:35715085 [GRCh38] Chr19:36205987 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.1048C>T (p.His350Tyr)	single nucleotide variant	not specified [RCV004349653]	Chr19:35716156 [GRCh38] Chr19:36207058 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.1459A>C (p.Thr487Pro)	single nucleotide variant	not specified [RCV004335884]	Chr19:35716747 [GRCh38] Chr19:36207649 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.202C>T (p.Pro68Ser)	single nucleotide variant	not specified [RCV004348291]	Chr19:35714828 [GRCh38] Chr19:36205730 [GRCh37] Chr19:19q13.12	uncertain significance
Single allele	deletion	not provided [RCV003448708]	Chr19:35225414..37357598 [GRCh37] Chr19:19q13.11-13.12	pathogenic
GRCh37/hg19 19q11-13.2(chr19:28271146-41508851)x3	copy number gain	not specified [RCV003986115]	Chr19:28271146..41508851 [GRCh37] Chr19:19q11-13.2	pathogenic
NM_014383.3(ZBTB32):c.1097C>A (p.Pro366His)	single nucleotide variant	not specified [RCV004480924]	Chr19:35716205 [GRCh38] Chr19:36207107 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.121C>G (p.Pro41Ala)	single nucleotide variant	not specified [RCV004480925]	Chr19:35714747 [GRCh38] Chr19:36205649 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.326G>A (p.Cys109Tyr)	single nucleotide variant	not specified [RCV004480927]	Chr19:35714952 [GRCh38] Chr19:36205854 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.970G>C (p.Gly324Arg)	single nucleotide variant	not specified [RCV004480934]	Chr19:35715953 [GRCh38] Chr19:36206855 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19q13.11-13.12(chr19:35223021-36895699)x1	copy number loss	not provided [RCV004577477]	Chr19:35223021..36895699 [GRCh37] Chr19:19q13.11-13.12	pathogenic
NM_014383.3(ZBTB32):c.1027G>A (p.Ala343Thr)	single nucleotide variant	not specified [RCV004480923]	Chr19:35716135 [GRCh38] Chr19:36207037 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.257A>C (p.Gln86Pro)	single nucleotide variant	not specified [RCV004480926]	Chr19:35714883 [GRCh38] Chr19:36205785 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.337C>G (p.Arg113Gly)	single nucleotide variant	not specified [RCV004480928]	Chr19:35714963 [GRCh38] Chr19:36205865 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.431A>T (p.Asp144Val)	single nucleotide variant	not specified [RCV004480930]	Chr19:35715057 [GRCh38] Chr19:36205959 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.492G>A (p.Met164Ile)	single nucleotide variant	not specified [RCV004480931]	Chr19:35715118 [GRCh38] Chr19:36206020 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.769G>A (p.Gly257Arg)	single nucleotide variant	not specified [RCV004480933]	Chr19:35715395 [GRCh38] Chr19:36206297 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.497A>G (p.His166Arg)	single nucleotide variant	not specified [RCV004688907]	Chr19:35715123 [GRCh38] Chr19:36206025 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.1384C>T (p.Arg462Cys)	single nucleotide variant	not specified [RCV004688905]	Chr19:35716672 [GRCh38] Chr19:36207574 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.35A>G (p.Tyr12Cys)	single nucleotide variant	not specified [RCV004884823]	Chr19:35714661 [GRCh38] Chr19:36205563 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19q11-13.13(chr19:28271107-38637350)x1	copy number loss	not provided [RCV004819395]	Chr19:28271107..38637350 [GRCh37] Chr19:19q11-13.13	pathogenic
NM_014383.3(ZBTB32):c.760T>C (p.Trp254Arg)	single nucleotide variant	not specified [RCV004884822]	Chr19:35715386 [GRCh38] Chr19:36206288 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.542C>T (p.Thr181Met)	single nucleotide variant	not specified [RCV004884821]	Chr19:35715168 [GRCh38] Chr19:36206070 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.799C>A (p.Leu267Met)	single nucleotide variant	not specified [RCV004884824]	Chr19:35715425 [GRCh38] Chr19:36206327 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.913C>T (p.Leu305Phe)	single nucleotide variant	not specified [RCV004884820]	Chr19:35715788 [GRCh38] Chr19:36206690 [GRCh37] Chr19:19q13.12	uncertain significance
NM_014383.3(ZBTB32):c.832C>G (p.His278Asp)	single nucleotide variant	not specified [RCV004893015]	Chr19:35715458 [GRCh38] Chr19:36206360 [GRCh37] Chr19:19q13.12	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	1909
Count of miRNA genes:	747
Interacting mature miRNAs:	823
Transcripts:	ENST00000262630, ENST00000392197, ENST00000426659, ENST00000442282, ENST00000451726, ENST00000481182
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.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1300034	BP50_H	Blood pressure QTL 50 (human)	2.1	0.00094	Blood pressure	systolic	19	11089463	37089463	Human
1559110	SCL22_H	Serum cholesterol level QTL 22 (human)	3.59	0.000241	Lipid level	LDL cholesterol	19	31907594	57907594	Human
597194140	GWAS1290214_H	cortical thickness QTL GWAS1290214 (human)		4e-08	cortical thickness		19	35708118	35708119	Human
597194684	GWAS1290758_H	cortical thickness QTL GWAS1290758 (human)		3e-08	cortical thickness		19	35708118	35708119	Human
597139490	GWAS1235564_H	neuroimaging measurement QTL GWAS1235564 (human)		3e-22	neuroimaging measurement		19	35713929	35713930	Human
1331657	COPD9_H	Chronic obstructive pulmonary disease QTL 9 (human)	1.94		Chronic airflow obstruction	post-bronchodilator FEV1	19	31021760	57021760	Human
597179205	GWAS1275279_H	IGF-like family receptor 1 measurement QTL GWAS1275279 (human)		6e-08	IGF-like family receptor 1 measurement		19	35715301	35715302	Human
406982508	GWAS631484_H	white matter microstructure measurement QTL GWAS631484 (human)		1e-10	white matter microstructure measurement		19	35713929	35713930	Human

TZFP_3812

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	36,207,391 - 36,207,930	UniSTS	GRCh37
Build 36	19	40,899,231 - 40,899,770	RGD	NCBI36
Celera	19	32,920,865 - 32,921,404	RGD
HuRef	19	32,712,228 - 32,712,767	UniSTS

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

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system
1200	2380	2713	2168	4842	1682	2240	2	593	1900	432	2231	6993	6309	17	3630	812	1696	1540	170


RefSeq Transcripts	NM_001316902	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001316903	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_014383	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011526718	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026588	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026590	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026591	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026592	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451451	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320531	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320532	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320533	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320534	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320535	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320536	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320537	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001753659	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_935793	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC002314	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AD000671	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF130255	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF165097	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC017700	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX095236	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY027719	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY039545	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU178599	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU178600	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000262630 ⟹ ENSP00000262630

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	35,712,928 - 35,717,038 (+)	Ensembl

Ensembl Acc Id:

ENST00000392197 ⟹ ENSP00000376035

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	35,704,558 - 35,717,038 (+)	Ensembl

Ensembl Acc Id:

ENST00000426659 ⟹ ENSP00000466524

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	35,704,571 - 35,716,497 (+)	Ensembl

Ensembl Acc Id:

ENST00000442282

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	35,704,559 - 35,713,542 (+)	Ensembl

Ensembl Acc Id:

ENST00000451726

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	35,704,579 - 35,714,339 (+)	Ensembl

Ensembl Acc Id:

ENST00000481182 ⟹ ENSP00000433657

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	35,713,433 - 35,717,038 (+)	Ensembl

RefSeq Acc Id:

NM_001316902 ⟹ NP_001303831

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	35,704,558 - 35,717,038 (+)	NCBI
CHM1_1	19	36,196,815 - 36,209,380 (+)	NCBI
T2T-CHM13v2.0	19	38,249,885 - 38,262,352 (+)	NCBI

Sequence:

show sequence

ACTCGGCCTTAAGCCGTCCTGGGTGTATGTGAGGCTGAAAGGGAAGGAGGAACAGGGTCTGGGCCGCTGTGTGCTCTGCCGTCATCTCTAAGAAACAACCATACCACTGAATGCTACTGTGTACTTAC
AAACCACACTCATATTCGTCACGTCATTTCATCTTCACCCCCACCTCCAAATGAGCACCCCCACCACTGGAGCCTGGCAGGAGGTCTGGCGGGAACAGAGGATCCCACTGTCCCTAAATGCCCCCAAA
GGGCTCTGGAGCCAGAACCAGTTGGCCTCCTCCAGCCCTACCCCAGGTTCCCTCCCCCAGGGCCCCGCACAGCTCAGCCCTGGGGAGATGGAAGAGTCTGATCAGGGGCACACAGGCGCACTTGCAAC
CTGTGCGGGTCATGAGGACAAGGCAGGCTGCCCACCTCGCCCGCACCCTCCCCCGGCCCCTCCTGCTCGGTCTCGGCCCTATGCGTGCTCTGTCTGTGGAAAGAGGTTTTCACTCAAGCATCAGATGG
AGACGCACTACCGAGTCCACACAGGAGAGAAGCCCTTCTCCTGTAGCCTTTGTCCTCAGCGCTCCCGGGACTTCTCGGCCATGACCAAGCACCTGCGGACACACGGGGCCGCTCCGTACCGCTGCTCC
CTGTGCGGGGCCGGCTGTCCCAGCCTGGCCTCCATGCAGGCGCACATGCGCGGTCACTCGCCCAGCCAACTCCCGCCCGGATGGACCATCCGCTCCACCTTCCTCTACTCCTCCTCGAGGCCGTCTCG
GCCCTCGACCTCTCCCTGTTGTCCTTCTTCCTCCACCACCTGACGGGGTGTCGGTAGCGTCTTAGCCAAGAGTCCAATTAAAGAACGAAAAGCGGGCCGGCTCGGCTTCTGACCTGGCACCGCTGCTA
CGGCGGCCTAGCAAATTCCGCCCCAGAAGCGCCCCAGGAAGGGCGCCGAGTGCCCTCTCCTGGACGATCGCGGGTCGCAGAAGCCCAGGCCAGCGAGCCCTACAGAGTGAGGACACTGAAGTGTGCAG
GAGCGAAGGTTAACAGTAGGGGAGATTGTCGATCTCATCACCATAATAAAGAGTTTCCTGTGCCCTCCCTTCA

hide sequence

RefSeq Acc Id:

NM_001316903 ⟹ NP_001303832

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	35,704,558 - 35,717,038 (+)	NCBI
CHM1_1	19	36,196,815 - 36,209,380 (+)	NCBI
T2T-CHM13v2.0	19	38,249,885 - 38,262,352 (+)	NCBI

Sequence:

show sequence

ACTCGGCCTTAAGCCGTCCTGGGTGTATGTGAGGCTGAAAGGGAAGGAGGAACAGGGTCTGGGCCGCTGTGTGCTCTGCCGTCATCTCTAAGAAACAACCATACCACTGAATGCTACTGTGTACTTAC
AAACCACACTCATATTCGTCACGTCATTTCATCTTCACCCCCACCTCCAAATGAGCACCCCCACCACTGGAGCCTGGCAGGAGGTCTGGCGGGAACAGAGGTTCCCTCCCCCAGGGCCCCGCACAGCT
CAGCCCTGGGGAGATGGAAGAGTCTGATCAGGGGCACACAGGCGCACTTGCAACCTGTGCGGGTCATGAGGACAAGGCAGGCTGCCCACCTCGCCCGCACCCTCCCCCGGCCCCTCCTGCTCGGTCTC
GGCCCTATGCGTGCTCTGTCTGTGGAAAGAGGTTTTCACTCAAGCATCAGATGGAGACGCACTACCGAGTCCACACAGGAGAGAAGCCCTTCTCCTGTAGCCTTTGTCCTCAGCGCTCCCGGGACTTC
TCGGCCATGACCAAGCACCTGCGGACACACGGGGCCGCTCCGTACCGCTGCTCCCTGTGCGGGGCCGGCTGTCCCAGCCTGGCCTCCATGCAGGCGCACATGCGCGGTCACTCGCCCAGCCAACTCCC
GCCCGGATGGACCATCCGCTCCACCTTCCTCTACTCCTCCTCGAGGCCGTCTCGGCCCTCGACCTCTCCCTGTTGTCCTTCTTCCTCCACCACCTGACGGGGTGTCGGTAGCGTCTTAGCCAAGAGTC
CAATTAAAGAACGAAAAGCGGGCCGGCTCGGCTTCTGACCTGGCACCGCTGCTACGGCGGCCTAGCAAATTCCGCCCCAGAAGCGCCCCAGGAAGGGCGCCGAGTGCCCTCTCCTGGACGATCGCGGG
TCGCAGAAGCCCAGGCCAGCGAGCCCTACAGAGTGAGGACACTGAAGTGTGCAGGAGCGAAGGTTAACAGTAGGGGAGATTGTCGATCTCATCACCATAATAAAGAGTTTCCTGTGCCCTCCCTTCA

hide sequence

RefSeq Acc Id:

NM_014383 ⟹ NP_055198

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	35,704,558 - 35,717,038 (+)	NCBI
GRCh37	19	36,195,389 - 36,207,940 (+)	NCBI
Build 36	19	40,895,670 - 40,899,780 (+)	NCBI Archive
HuRef	19	32,708,667 - 32,712,777 (+)	ENTREZGENE
CHM1_1	19	36,196,815 - 36,209,380 (+)	NCBI
T2T-CHM13v2.0	19	38,249,885 - 38,262,352 (+)	NCBI

Sequence:

show sequence

ACTCGGCCTTAAGCCGTCCTGGGTGTATGTGAGGCTGAAAGGGAAGGAGGAACAGGGTCTGGGCCGCTGTGTGCTCTGCCGTCATCTCTAAGAAACAACCATACCACTGAATGCTACTGTGTACTTAC
AAACCACACTCATATTCGTCACGTCATTTCATCTTCACCCCCACCTCCAAATGAGGCTTGAAATGAGATGAGATGTTCCTCCCTCCCCTTTCAACCATGGACCTCACACTGTGGACTTCCTCTTAGAG
CCTCTGAGTTAGGTACCCAAGCCAAGGCACAATGTCCCTGCCCCCCATAAGACTGCCCAGCCCCTATGGCTCTGATCGGCTGGTACAGCTAGCAGCCAGGCTCCGGCCAGCACTCTGTGATACTCTGA
TCACCGTAGGGAGCCAGGAGTTCCCCGCCCACAGCCTGGTGCTAGCAGGTGTCAGCCAGCAGCTGGGCCGCAGGGGCCAGTGGGCTCTGGGAGAAGGCATCAGCCCTTCTACCTTTGCCCAGCTCCTG
AACTTTGTGTATGGGGAGAGTGTAGAGCTGCAGCCTGGAGAGCTAAGGCCCCTTCAGGAGGCGGCCAGGGCCTTGGGAGTGCAGTCCCTGGAAGAGGCATGCTGGAGGGCTCGAGGGGACAGGGCTAA
AAAGCCAGATCCAGGCCTGAAGAAACATCAGGAGGAGCCAGAGAAACCCTCAAGGAATCCTGAGAGAGAACTGGGGGACCCTGGAGAGAAGCAGAAACCAGAACAGGTTTCTAGAACTGGTGGGAGAG
AACAGGAGATGTTGCACAAGCACTCGCCACCAAGAGGCAGACCCGAGATGGCAGGAGCAACGCAGGAGGCTCAGCAGGAACAGACCAGGTCAAAGGAGAAACGCCTCCAAGCCCCTGTTGGCCAAAGG
GGAGCAGATGGGAAGCATGGAGTGCTCACGTGGTTGAGGGAAAATCCAGGGGGCTCTGAGGAAAGTCTGCGCAAGCTCCCTGGCCCCCTTCCCCCAGCAGGCTCCCTGCAAACCAGCGTCACCCCTAG
GCCCTCGTGGGCTGAGGCCCCTTGGTTGGTGGGGGGCCAGCCTGCCCTGTGGAGCATCCTGCTGATGCCGCCCAGATATGGCATTCCCTTCTACCATAGCACCCCCACCACTGGAGCCTGGCAGGAGG
TCTGGCGGGAACAGAGGATCCCACTGTCCCTAAATGCCCCCAAAGGGCTCTGGAGCCAGAACCAGTTGGCCTCCTCCAGCCCTACCCCAGGTTCCCTCCCCCAGGGCCCCGCACAGCTCAGCCCTGGG
GAGATGGAAGAGTCTGATCAGGGGCACACAGGCGCACTTGCAACCTGTGCGGGTCATGAGGACAAGGCAGGCTGCCCACCTCGCCCGCACCCTCCCCCGGCCCCTCCTGCTCGGTCTCGGCCCTATGC
GTGCTCTGTCTGTGGAAAGAGGTTTTCACTCAAGCATCAGATGGAGACGCACTACCGAGTCCACACAGGAGAGAAGCCCTTCTCCTGTAGCCTTTGTCCTCAGCGCTCCCGGGACTTCTCGGCCATGA
CCAAGCACCTGCGGACACACGGGGCCGCTCCGTACCGCTGCTCCCTGTGCGGGGCCGGCTGTCCCAGCCTGGCCTCCATGCAGGCGCACATGCGCGGTCACTCGCCCAGCCAACTCCCGCCCGGATGG
ACCATCCGCTCCACCTTCCTCTACTCCTCCTCGAGGCCGTCTCGGCCCTCGACCTCTCCCTGTTGTCCTTCTTCCTCCACCACCTGACGGGGTGTCGGTAGCGTCTTAGCCAAGAGTCCAATTAAAGA
ACGAAAAGCGGGCCGGCTCGGCTTCTGACCTGGCACCGCTGCTACGGCGGCCTAGCAAATTCCGCCCCAGAAGCGCCCCAGGAAGGGCGCCGAGTGCCCTCTCCTGGACGATCGCGGGTCGCAGAAGC
CCAGGCCAGCGAGCCCTACAGAGTGAGGACACTGAAGTGTGCAGGAGCGAAGGTTAACAGTAGGGGAGATTGTCGATCTCATCACCATAATAAAGAGTTTCCTGTGCCCTCCCTTCA

hide sequence

RefSeq Acc Id:

XM_017026591 ⟹ XP_016882080

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	35,704,558 - 35,717,038 (+)	NCBI

Sequence:

show sequence

CGCCTCAGGATCCAGGGGTGACCACGTGCGGGAGCGTTGCGTCCCTGGCCTCGCTCCATTCCCCACTTTTAACGGTCACTCGGCCTTAAGCCGTCCTGGGTGTATGTGAGGCTGAAAGGGAAGGAGGA
ACAGGGTCTGGGCCGCTGTGTGCTCTGCCGTCATCTCTAAGAAACAACCATACCACTGAATGCTACTGTGTACTTACAAACCACACTCATATTCGTCACGTCATTTCATCTTCACCCCCACCTCCAAA
TGAGCACCCCCACCACTGGAGCCTGGCAGGAGGTCTGGCGGGAACAGAGGATCCCACTGTCCCTAAATGCCCCCAAAGGGCTCTGGAGCCAGAACCAGTTGGCCTCCTCCAGCCCTACCCCAGGTAAG
CCCCTCGCTGTCCTGCATACACCTGTAACATGGTGTCTTCTCTGGGCTGGGGCTCGAGGAGTCCAGCCTGAGCAGGGCCCCTACCTCCCACTGTTCCTTCCAGGTTCCCTCCCCCAGGGCCCCGCACA
GCTCAGCCCTGGGGAGATGGAAGAGTCTGATCAGGGGCACACAGGCGCACTTGCAACCTGTGCGGGTCATGAGGACAAGGCAGGCTGCCCACCTCGCCCGCACCCTCCCCCGGCCCCTCCTGCTCGGT
CTCGGCCCTATGCGTGCTCTGTCTGTGGAAAGAGGTTTTCACTCAAGCATCAGATGGAGACGCACTACCGAGTCCACACAGGAGAGAAGCCCTTCTCCTGTAGCCTTTGTCCTCAGCGCTCCCGGGAC
TTCTCGGCCATGACCAAGCACCTGCGGACACACGGGGCCGCTCCGTACCGCTGCTCCCTGTGCGGGGCCGGCTGTCCCAGCCTGGCCTCCATGCAGGCGCACATGCGCGGTCACTCGCCCAGCCAACT
CCCGCCCGGATGGACCATCCGCTCCACCTTCCTCTACTCCTCCTCGAGGCCGTCTCGGCCCTCGACCTCTCCCTGTTGTCCTTCTTCCTCCACCACCTGACGGGGTGTCGGTAGCGTCTTAGCCAAGA
GTCCAATTAAAGAACGAAAAGCGGGCCGGCTCGGCTTCTGACCTGGCACCGCTGCTACGGCGGCCTAGCAAATTCCGCCCCAGAAGCGCCCCAGGAAGGGCGCCGAGTGCCCTCTCCTGGACGATCGC
GGGTCGCAGAAGCCCAGGCCAGCGAGCCCTACAGAGTGAGGACACTGAAGTGTGCAGGAGCGAAGGTTAACAGTAGGGGAGATTGTCGATCTCATCACCATAATAAAGAGTTTCCTGTGCCCTCCCTT
CAGGACTAGAAA

hide sequence

RefSeq Acc Id:

XM_054320531 ⟹ XP_054176506

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	38,249,885 - 38,262,352 (+)	NCBI

RefSeq Acc Id:

XM_054320532 ⟹ XP_054176507

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	38,249,885 - 38,262,352 (+)	NCBI

RefSeq Acc Id:

XM_054320533 ⟹ XP_054176508

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	38,249,885 - 38,261,362 (+)	NCBI

RefSeq Acc Id:

XM_054320534 ⟹ XP_054176509

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	38,249,885 - 38,261,337 (+)	NCBI

RefSeq Acc Id:

XM_054320535 ⟹ XP_054176510

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	38,249,885 - 38,262,352 (+)	NCBI

RefSeq Acc Id:

XM_054320536 ⟹ XP_054176511

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	38,249,885 - 38,262,352 (+)	NCBI

RefSeq Acc Id:

XM_054320537 ⟹ XP_054176512

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	38,260,734 - 38,262,352 (+)	NCBI


Protein RefSeqs	NP_001303831	(Get FASTA)	NCBI Sequence Viewer
	NP_001303832	(Get FASTA)	NCBI Sequence Viewer
	NP_055198	(Get FASTA)	NCBI Sequence Viewer
	XP_016882080	(Get FASTA)	NCBI Sequence Viewer
	XP_054176506	(Get FASTA)	NCBI Sequence Viewer
	XP_054176507	(Get FASTA)	NCBI Sequence Viewer
	XP_054176508	(Get FASTA)	NCBI Sequence Viewer
	XP_054176509	(Get FASTA)	NCBI Sequence Viewer
	XP_054176510	(Get FASTA)	NCBI Sequence Viewer
	XP_054176511	(Get FASTA)	NCBI Sequence Viewer
	XP_054176512	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAD27708	(Get FASTA)	NCBI Sequence Viewer
	AAD48448	(Get FASTA)	NCBI Sequence Viewer
	AAH17700	(Get FASTA)	NCBI Sequence Viewer
	ALQ34057	(Get FASTA)	NCBI Sequence Viewer
	ALQ34058	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000262630.3
	ENSP00000376035
	ENSP00000376035.1
GenBank Protein	Q9Y2Y4	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_055198 ⟸ NM_014383
- Peptide Label:	isoform 1
- UniProtKB:	Q8WVP2 (UniProtKB/Swiss-Prot), Q9Y2Y4 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSLPPIRLPSPYGSDRLVQLAARLRPALCDTLITVGSQEFPAHSLVLAGVSQQLGRRGQWALGEGISPSTFAQLLNFVYGESVELQPGELRPLQEAARALGVQSLEEACWRARGDRAKKPDPGLKKHQ EEPEKPSRNPERELGDPGEKQKPEQVSRTGGREQEMLHKHSPPRGRPEMAGATQEAQQEQTRSKEKRLQAPVGQRGADGKHGVLTWLRENPGGSEESLRKLPGPLPPAGSLQTSVTPRPSWAEAPWLV GGQPALWSILLMPPRYGIPFYHSTPTTGAWQEVWREQRIPLSLNAPKGLWSQNQLASSSPTPGSLPQGPAQLSPGEMEESDQGHTGALATCAGHEDKAGCPPRPHPPPAPPARSRPYACSVCGKRFSL KHQMETHYRVHTGEKPFSCSLCPQRSRDFSAMTKHLRTHGAAPYRCSLCGAGCPSLASMQAHMRGHSPSQLPPGWTIRSTFLYSSSRPSRPSTSPCCPSSSTT hide sequence

RefSeq Acc Id:	NP_001303831 ⟸ NM_001316902
- Peptide Label:	isoform 2
- UniProtKB:	Q9Y2Y4 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSTPTTGAWQEVWREQRIPLSLNAPKGLWSQNQLASSSPTPGSLPQGPAQLSPGEMEESDQGHTGALATCAGHEDKAGCPPRPHPPPAPPARSRPYACSVCGKRFSLKHQMETHYRVHTGEKPFSCSL CPQRSRDFSAMTKHLRTHGAAPYRCSLCGAGCPSLASMQAHMRGHSPSQLPPGWTIRSTFLYSSSRPSRPSTSPCCPSSSTT hide sequence

RefSeq Acc Id:	NP_001303832 ⟸ NM_001316903
- Peptide Label:	isoform 3
- UniProtKB:	Q9Y2Y4 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MEESDQGHTGALATCAGHEDKAGCPPRPHPPPAPPARSRPYACSVCGKRFSLKHQMETHYRVHTGEKPFSCSLCPQRSRDFSAMTKHLRTHGAAPYRCSLCGAGCPSLASMQAHMRGHSPSQLPPGWT IRSTFLYSSSRPSRPSTSPCCPSSSTT hide sequence

RefSeq Acc Id:

XP_016882080 ⟸ XM_017026591

- Peptide Label:

isoform X1

- Sequence:

show sequence

MSTPTTGAWQEVWREQRIPLSLNAPKGLWSQNQLASSSPTPGKPLAVLHTPVTWCLLWAGARGV
QPEQGPYLPLFLPGSLPQGPAQLSPGEMEESDQGHTGALATCAGHEDKAGCPPRPHPPPAPPARSRPYACSVCGKRFSLKHQMETHYRVHTGEKPFSCSLCPQRSRDFSAMTKHLRTHGAAPYRCSLC
GAGCPSLASMQAHMRGHSPSQLPPGWTIRSTFLYSSSRPSRPSTSPCCPSSSTT

hide sequence

Ensembl Acc Id:

ENSP00000466524 ⟸ ENST00000426659

Protein Domains

BTB C2H2-type

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9Y2Y4-F1-model_v2	AlphaFold	Q9Y2Y4	1-487	view protein structure

RGD ID:

Promoter ID:

Type:

multiple initiation site

Name:

ZBTB32_1

Description:

zinc finger and BTB domain containing 32

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	19	35,713,426 - 35,713,486	EPDNEW

RGD ID:

Promoter ID:

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, K562, Lymphoblastoid

Transcripts:

ENST00000354109, NM_014383, OTTHUMT00000109492

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	40,895,631 - 40,896,182 (+)	MPROMDB

RGD ID:

Promoter ID:

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_2Hour, K562, Lymphoblastoid

Transcripts:

ENST00000392197

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	40,896,711 - 40,898,182 (+)	MPROMDB

Database	Acc Id	Source(s)
COSMIC	ZBTB32	COSMIC
Ensembl Genes	ENSG00000011590	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000262630.7	UniProtKB/Swiss-Prot
	ENST00000392197	ENTREZGENE
	ENST00000392197.7	UniProtKB/Swiss-Prot
Gene3D-CATH	Classic Zinc Finger	UniProtKB/Swiss-Prot
	Potassium Channel Kv1.1, Chain A	UniProtKB/Swiss-Prot
GTEx	ENSG00000011590	GTEx
HGNC ID	HGNC:16763	ENTREZGENE
Human Proteome Map	ZBTB32	Human Proteome Map
InterPro	BTB/POZ_dom	UniProtKB/Swiss-Prot
	SKP1/BTB/POZ_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_type	UniProtKB/Swiss-Prot
KEGG Report	hsa:27033	UniProtKB/Swiss-Prot
NCBI Gene	27033	ENTREZGENE
OMIM	605859	OMIM
PANTHER	ZINC FINGER AND BTB DOMAIN-CONTAINING	UniProtKB/Swiss-Prot
	ZINC FINGER AND BTB DOMAIN-CONTAINING PROTEIN 32	UniProtKB/Swiss-Prot
Pfam	BTB	UniProtKB/Swiss-Prot
	zf-C2H2	UniProtKB/Swiss-Prot
	zf-met	UniProtKB/Swiss-Prot
PharmGKB	PA142670541	PharmGKB
PROSITE	BTB	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot
SMART	BTB	UniProtKB/Swiss-Prot
	ZnF_C2H2	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF54695	UniProtKB/Swiss-Prot
	SSF57667	UniProtKB/Swiss-Prot
UniProt	A0A0C4DGF1	ENTREZGENE, UniProtKB/TrEMBL
	A0A0S2Z564_HUMAN	UniProtKB/TrEMBL
	A0A0S2Z5S3	ENTREZGENE, UniProtKB/TrEMBL
	K7EMJ1_HUMAN	UniProtKB/TrEMBL
	Q8WVP2	ENTREZGENE
	Q9Y2Y4	ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary	Q8WVP2	UniProtKB/Swiss-Prot