MZF1 (myeloid zinc finger 1) - Rat Genome Database

Name: MZF1
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: MZF1 (myeloid zinc finger 1) Homo sapiens

Analyze

Symbol:

MZF1

Name:

myeloid zinc finger 1

RGD ID:

1318132

HGNC Page

HGNC:13108

Description:

Enables DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and protein homodimerization activity. Involved in negative regulation of transcription by RNA polymerase II and positive regulation of transcription by RNA polymerase II. Located in nucleoplasm.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

MZF-1; MZF1B; Zfp98; zinc finger and SCAN domain-containing protein 6; zinc finger protein 42 (myeloid-specific retinoic acid-responsive); ZNF42; ZSCAN6

RGD Orthologs

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Mzf1 (myeloid zinc finger 1)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Mzf1 (myeloid zinc finger 1)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther
Chinchilla lanigera (long-tailed chinchilla):	Mzf1 (myeloid zinc finger 1)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	MZF1 (myeloid zinc finger 1)	NCBI	Ortholog
Canis lupus familiaris (dog):	MZF1 (myeloid zinc finger 1)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Mzf1 (myeloid zinc finger 1)	NCBI	Ortholog
Sus scrofa (pig):	MZF1 (myeloid zinc finger 1)	HGNC	Ensembl, NCBI, OrthoDB
Chlorocebus sabaeus (green monkey):	MZF1 (myeloid zinc finger 1)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Msantd2 (Myb/SANT DNA binding domain containing 2)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Mzf1 (myeloid zinc finger 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Mzf1 (myeloid zinc finger 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)

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	58,561,932 - 58,573,573 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	58,561,931 - 58,573,575 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	59,073,299 - 59,084,940 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	63,765,096 - 63,776,754 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	63,765,096 - 63,776,754	NCBI
Celera	19	56,116,463 - 56,127,681 (-)	NCBI		Celera
Cytogenetic Map	19	q13.43	NCBI
HuRef	19	55,383,492 - 55,395,145 (-)	NCBI		HuRef
CHM1_1	19	59,067,113 - 59,078,772 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	19	61,659,609 - 61,672,553 (-)	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

17beta-estradiol (EXP)

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

2-methylcholine (EXP)

4,4'-diaminodiphenylmethane (ISO)

4,4'-sulfonyldiphenol (ISO)

6-propyl-2-thiouracil (ISO)

amitrole (ISO)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP,ISO)

bisphenol A (ISO)

butan-1-ol (EXP)

butanal (EXP)

calcitriol (EXP)

choline (ISO)

cyclosporin A (EXP)

deoxynivalenol (EXP)

dorsomorphin (EXP)

elemental selenium (EXP)

ethanol (EXP)

finasteride (ISO)

flutamide (ISO)

folic acid (ISO)

furan (ISO)

gallic acid (EXP)

gentamycin (ISO)

isobutanol (EXP)

L-methionine (ISO)

mercury atom (ISO)

mercury(0) (ISO)

methimazole (ISO)

phorbol 13-acetate 12-myristate (EXP)

rotenone (EXP)

SB 431542 (EXP)

selenium atom (EXP)

sulfadimethoxine (ISO)

sulindac (ISO)

thimerosal (ISO)

triptonide (ISO)

trovafloxacin (ISO)

urethane (EXP)

valproic acid (EXP)

zinc atom (EXP)

zinc(0) (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

negative regulation of transcription by RNA polymerase II (IDA)

positive regulation of transcription by RNA polymerase II (IDA)

regulation of DNA-templated transcription (IBA,IDA,TAS)

Cellular Component

nucleoplasm (IDA)

nucleus (IEA)

Molecular Function

DNA binding (IEA)

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

DNA-binding transcription factor activity (NAS)

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

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

metal ion binding (IEA)

protein binding (IPI)

protein homodimerization activity (IPI)

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

transcription cis-regulatory region binding (IDA)

References

References - curated

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

Additional References at PubMed

PMID:1719120	PMID:1860835	PMID:7579328	PMID:10777584	PMID:10974541	PMID:12477932	PMID:15453830	PMID:15528990	PMID:15541732	PMID:15670815	PMID:16297876	PMID:16950398
PMID:17081983	PMID:17851584	PMID:18029348	PMID:18472161	PMID:19196427	PMID:19274049	PMID:20145042	PMID:21873635	PMID:22094256	PMID:22242952	PMID:22464443	PMID:22559731
PMID:22846578	PMID:23241556	PMID:23509792	PMID:24793789	PMID:25065746	PMID:25284586	PMID:25425970	PMID:25814554	PMID:25877752	PMID:25884514	PMID:25899830	PMID:25903835
PMID:26010542	PMID:26186194	PMID:26760575	PMID:27259238	PMID:27764784	PMID:27922669	PMID:28478957	PMID:28514442	PMID:28634046	PMID:28703907	PMID:28986522	PMID:29048625
PMID:29842885	PMID:30021884	PMID:30301827	PMID:31366500	PMID:32449233	PMID:32929338	PMID:33961781	PMID:34602532	PMID:34773072	PMID:38058065

Genomics

Comparative Map Data

MZF1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	58,561,932 - 58,573,573 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	58,561,931 - 58,573,575 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	59,073,299 - 59,084,940 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	63,765,096 - 63,776,754 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	63,765,096 - 63,776,754	NCBI
Celera	19	56,116,463 - 56,127,681 (-)	NCBI		Celera
Cytogenetic Map	19	q13.43	NCBI
HuRef	19	55,383,492 - 55,395,145 (-)	NCBI		HuRef
CHM1_1	19	59,067,113 - 59,078,772 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	19	61,659,609 - 61,672,553 (-)	NCBI		T2T-CHM13v2.0

Mzf1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	7	12,777,074 - 12,792,244 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	7	12,776,230 - 12,788,691 (-)	Ensembl		GRCm39 Ensembl
GRCm38	7	13,042,303 - 13,054,764 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	7	13,042,303 - 13,054,764 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	7	13,627,652 - 13,640,113 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	7	11,943,329 - 11,954,844 (-)	NCBI		MGSCv36	mm8
Celera	7	10,669,491 - 10,681,939 (-)	NCBI		Celera
Cytogenetic Map	7	A1	NCBI
cM Map	7	7.73	NCBI

Mzf1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	82,742,709 - 82,755,069 (-)	NCBI		GRCr8
mRatBN7.2	1	73,670,522 - 73,682,885 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	73,670,541 - 73,681,635 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	79,050,939 - 79,062,048 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	87,615,280 - 87,626,389 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	80,806,021 - 80,817,130 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	65,520,827 - 65,533,233 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	65,522,118 - 65,533,212 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	66,332,120 - 66,344,464 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	72,870,145 - 72,881,239 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	1	72,949,477 - 72,960,898 (+)	NCBI
Celera	1	60,158,171 - 60,169,264 (+)	NCBI		Celera
Cytogenetic Map	1	q21	NCBI

Mzf1
(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_004955584	1,167,428 - 1,174,434 (-)	NCBI	ChiLan1.0	ChiLan1.0

MZF1
(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	64,847,739 - 64,857,878 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	19	66,630,591 - 66,640,838 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	19	55,575,212 - 55,585,473 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	19	64,388,496 - 64,399,874 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	19	64,388,496 - 64,398,938 (-)	Ensembl	panpan1.1		panPan2

MZF1
(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	99,387,780 - 99,398,806 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	1	99,383,711 - 99,397,388 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	1	99,786,019 - 99,795,978 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	1	100,000,874 - 100,010,833 (+)	NCBI		ROS_Cfam_1.0
UMICH_Zoey_3.1	1	99,646,239 - 99,656,198 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	1	99,358,856 - 99,369,028 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	1	100,113,708 - 100,123,667 (+)	NCBI		UU_Cfam_GSD_1.0

Mzf1
(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_024405118	217,963,994 - 217,975,466 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004937062	142,383 - 153,480 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004937062	142,600 - 155,836 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

MZF1
(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	63,111,068 - 63,123,082 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	6	63,112,996 - 63,124,025 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1

MZF1
(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	50,837,680 - 50,849,283 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666045	4,167,836 - 4,179,580 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Variants

Variants in MZF1
39 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 19q13.43(chr19:56363208-58581203)x3	copy number gain	See cases [RCV000052927]	Chr19:56363208..58581203 [GRCh38] Chr19:56874577..59092570 [GRCh37] Chr19:61566389..63784382 [NCBI36] Chr19:19q13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	copy number gain	See cases [RCV000052915]	Chr19:47929575..58572206 [GRCh38] Chr19:48432832..59083573 [GRCh37] Chr19:53124644..63775385 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.43(chr19:58548841-58581203)x3	copy number gain	See cases [RCV000133726]	Chr19:58548841..58581203 [GRCh38] Chr19:59060208..59092570 [GRCh37] Chr19:63752020..63784382 [NCBI36] Chr19:19q13.43	benign
GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3	copy number gain	See cases [RCV000134174]	Chr19:52612432..58581203 [GRCh38] Chr19:53115685..59092570 [GRCh37] Chr19:57807497..63784382 [NCBI36] Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3	copy number gain	See cases [RCV000134139]	Chr19:52955056..58581203 [GRCh38] Chr19:53458309..59092570 [GRCh37] Chr19:58150121..63784382 [NCBI36] Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.43(chr19:58407283-58581129)x1	copy number loss	See cases [RCV000135198]	Chr19:58407283..58581129 [GRCh38] Chr19:58918650..59092496 [GRCh37] Chr19:63610462..63784308 [NCBI36] Chr19:19q13.43	likely benign
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	copy number gain	See cases [RCV000135843]	Chr19:50152520..58581203 [GRCh38] Chr19:50655777..59092570 [GRCh37] Chr19:55347589..63784382 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	copy number gain	See cases [RCV000445925]	Chr19:50489390..59095359 [GRCh37] Chr19:19q13.33-13.43	pathogenic
NM_198055.2(MZF1):c.2051C>A (p.Pro684His)	single nucleotide variant	Inborn genetic diseases [RCV003257851]	Chr19:58562226 [GRCh38] Chr19:59073593 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1907A>T (p.Gln636Leu)	single nucleotide variant	Inborn genetic diseases [RCV003240203]	Chr19:58562370 [GRCh38] Chr19:59073737 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1708G>T (p.Ala570Ser)	single nucleotide variant	Inborn genetic diseases [RCV003253900]	Chr19:58562569 [GRCh38] Chr19:59073936 [GRCh37] Chr19:19q13.43	uncertain significance
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 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 19q13.33-13.43(chr19:50740074-59097160)x3	copy number gain	not provided [RCV000740208]	Chr19:50740074..59097160 [GRCh37] Chr19:19q13.33-13.43	pathogenic
NM_198055.2(MZF1):c.789A>G (p.Leu263=)	single nucleotide variant	not provided [RCV000968400]	Chr19:58563488 [GRCh38] Chr19:59074855 [GRCh37] Chr19:19q13.43	benign
NM_198055.2(MZF1):c.471A>C (p.Glu157Asp)	single nucleotide variant	Inborn genetic diseases [RCV003245292]	Chr19:58570453 [GRCh38] Chr19:59081820 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1427C>T (p.Pro476Leu)	single nucleotide variant	Inborn genetic diseases [RCV003275754]	Chr19:58562850 [GRCh38] Chr19:59074217 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.875T>G (p.Ile292Ser)	single nucleotide variant	not provided [RCV000891254]	Chr19:58563402 [GRCh38] Chr19:59074769 [GRCh37] Chr19:19q13.43	benign
NM_198055.2(MZF1):c.1064G>A (p.Gly355Asp)	single nucleotide variant	Inborn genetic diseases [RCV003264783]	Chr19:58563213 [GRCh38] Chr19:59074580 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1730C>A (p.Ala577Asp)	single nucleotide variant	Inborn genetic diseases [RCV002684253]	Chr19:58562547 [GRCh38] Chr19:59073914 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1007G>A (p.Arg336His)	single nucleotide variant	Inborn genetic diseases [RCV002993003]	Chr19:58563270 [GRCh38] Chr19:59074637 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1037C>T (p.Pro346Leu)	single nucleotide variant	Inborn genetic diseases [RCV002753309]	Chr19:58563240 [GRCh38] Chr19:59074607 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1243G>A (p.Gly415Ser)	single nucleotide variant	Inborn genetic diseases [RCV002865887]	Chr19:58563034 [GRCh38] Chr19:59074401 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1540G>C (p.Gly514Arg)	single nucleotide variant	Inborn genetic diseases [RCV002993152]	Chr19:58562737 [GRCh38] Chr19:59074104 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1511A>T (p.Gln504Leu)	single nucleotide variant	Inborn genetic diseases [RCV002660715]	Chr19:58562766 [GRCh38] Chr19:59074133 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.914T>C (p.Leu305Pro)	single nucleotide variant	Inborn genetic diseases [RCV002845509]	Chr19:58563363 [GRCh38] Chr19:59074730 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1504G>A (p.Glu502Lys)	single nucleotide variant	Inborn genetic diseases [RCV002844330]	Chr19:58562773 [GRCh38] Chr19:59074140 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1932G>T (p.Gln644His)	single nucleotide variant	Inborn genetic diseases [RCV002910805]	Chr19:58562345 [GRCh38] Chr19:59073712 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1028G>T (p.Arg343Leu)	single nucleotide variant	Inborn genetic diseases [RCV002870001]	Chr19:58563249 [GRCh38] Chr19:59074616 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.803C>A (p.Ala268Glu)	single nucleotide variant	Inborn genetic diseases [RCV002661657]	Chr19:58563474 [GRCh38] Chr19:59074841 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.2188G>C (p.Val730Leu)	single nucleotide variant	Inborn genetic diseases [RCV002744417]	Chr19:58562089 [GRCh38] Chr19:59073456 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.790G>C (p.Gly264Arg)	single nucleotide variant	Inborn genetic diseases [RCV002916681]	Chr19:58563487 [GRCh38] Chr19:59074854 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.942A>C (p.Glu314Asp)	single nucleotide variant	Inborn genetic diseases [RCV002984025]	Chr19:58563335 [GRCh38] Chr19:59074702 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.290C>T (p.Pro97Leu)	single nucleotide variant	Inborn genetic diseases [RCV002767834]	Chr19:58571100 [GRCh38] Chr19:59082467 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.338A>G (p.Glu113Gly)	single nucleotide variant	Inborn genetic diseases [RCV002742679]	Chr19:58571052 [GRCh38] Chr19:59082419 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1243G>C (p.Gly415Arg)	single nucleotide variant	Inborn genetic diseases [RCV002940628]	Chr19:58563034 [GRCh38] Chr19:59074401 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1303A>G (p.Thr435Ala)	single nucleotide variant	Inborn genetic diseases [RCV002703307]	Chr19:58562974 [GRCh38] Chr19:59074341 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.920T>C (p.Leu307Pro)	single nucleotide variant	Inborn genetic diseases [RCV002965690]	Chr19:58563357 [GRCh38] Chr19:59074724 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1678C>T (p.Arg560Trp)	single nucleotide variant	Inborn genetic diseases [RCV002879025]	Chr19:58562599 [GRCh38] Chr19:59073966 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1344C>G (p.Ser448Arg)	single nucleotide variant	Inborn genetic diseases [RCV003212230]	Chr19:58562933 [GRCh38] Chr19:59074300 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.2149C>G (p.Arg717Gly)	single nucleotide variant	Inborn genetic diseases [RCV003178797]	Chr19:58562128 [GRCh38] Chr19:59073495 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.812G>T (p.Gly271Val)	single nucleotide variant	Inborn genetic diseases [RCV003360428]	Chr19:58563465 [GRCh38] Chr19:59074832 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1333T>A (p.Cys445Ser)	single nucleotide variant	Inborn genetic diseases [RCV003346050]	Chr19:58562944 [GRCh38] Chr19:59074311 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1614G>T (p.Glu538Asp)	single nucleotide variant	Inborn genetic diseases [RCV003354786]	Chr19:58562663 [GRCh38] Chr19:59074030 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.323G>C (p.Arg108Pro)	single nucleotide variant	Inborn genetic diseases [RCV003366665]	Chr19:58571067 [GRCh38] Chr19:59082434 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1455T>G (p.Phe485Leu)	single nucleotide variant	Inborn genetic diseases [RCV003349230]	Chr19:58562822 [GRCh38] Chr19:59074189 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1976G>A (p.Gly659Asp)	single nucleotide variant	Inborn genetic diseases [RCV003354264]	Chr19:58562301 [GRCh38] Chr19:59073668 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1615C>T (p.Arg539Trp)	single nucleotide variant	Inborn genetic diseases [RCV003354787]	Chr19:58562662 [GRCh38] Chr19:59074029 [GRCh37] Chr19:19q13.43	uncertain significance
NM_198055.2(MZF1):c.1584G>A (p.Leu528=)	single nucleotide variant	not provided [RCV003407146]	Chr19:58562693 [GRCh38] Chr19:59074060 [GRCh37] Chr19:19q13.43	likely benign

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2648
Count of miRNA genes:	914
Interacting mature miRNAs:	1104
Transcripts:	ENST00000215057, ENST00000594108, ENST00000594234, ENST00000595245, ENST00000596039, ENST00000599369, ENST00000600004, ENST00000600048
Prediction methods:	Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

Markers in Region

RH79819

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	59,074,550 - 59,074,667	UniSTS	GRCh37
Build 36	19	63,766,362 - 63,766,479	RGD	NCBI36
Celera	19	56,117,729 - 56,117,846	RGD
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
HuRef	19	55,384,758 - 55,384,875	UniSTS

SHGC-149330

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	59,083,401 - 59,083,713	UniSTS	GRCh37
Build 36	19	63,775,213 - 63,775,525	RGD	NCBI36
Celera	19	56,126,140 - 56,126,452	RGD
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
HuRef	19	55,393,604 - 55,393,916	UniSTS
TNG Radiation Hybrid Map	19	23446.0	UniSTS

RH71384

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	59,073,324 - 59,073,488	UniSTS	GRCh37
Build 36	19	63,765,136 - 63,765,300	RGD	NCBI36
Celera	19	56,116,503 - 56,116,667	RGD
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
HuRef	19	55,383,532 - 55,383,696	UniSTS
GeneMap99-GB4 RH Map	19	291.0	UniSTS

STS-U46465

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	59,076,000 - 59,076,195	UniSTS	GRCh37
Build 36	19	63,767,812 - 63,768,007	RGD	NCBI36
Celera	19	56,119,179 - 56,119,374	RGD
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
HuRef	19	55,386,208 - 55,386,403	UniSTS
GeneMap99-GB4 RH Map	19	290.65	UniSTS
NCBI RH Map	19	600.5	UniSTS

RH36557

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	59,073,364 - 59,073,488	UniSTS	GRCh37
Build 36	19	63,765,176 - 63,765,300	RGD	NCBI36
Celera	19	56,116,543 - 56,116,667	RGD
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
HuRef	19	55,383,572 - 55,383,696	UniSTS
GeneMap99-GB4 RH Map	19	293.71	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

2320

2065

1513

428

1077

271

3726

1457

3431

198

1339

1432

164

1184

2422

Low

119

925

213

196

872

194

630

739

303

221

121

181

366

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001267033	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_003422	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_198055	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005259204	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011527264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027206	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451689	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439312	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439313	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321948	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321949	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321950	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321951	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321952	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB209481	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC016629	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC016630	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF055077	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF055078	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF147345	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF161886	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK308893	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK310381	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC007777	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC053316	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ446552	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU620994	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471135	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M58297	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000215057 ⟹ ENSP00000215057

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,561,932 - 58,573,335 (-)	Ensembl

RefSeq Acc Id:

ENST00000594108 ⟹ ENSP00000472123

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,569,205 - 58,572,775 (-)	Ensembl

RefSeq Acc Id:

ENST00000594234 ⟹ ENSP00000469378

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,561,932 - 58,573,298 (-)	Ensembl

RefSeq Acc Id:

ENST00000595245

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,568,167 - 58,571,545 (-)	Ensembl

RefSeq Acc Id:

ENST00000596039 ⟹ ENSP00000472454

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,571,200 - 58,573,311 (-)	Ensembl

RefSeq Acc Id:

ENST00000599369 ⟹ ENSP00000469493

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,561,933 - 58,573,575 (-)	Ensembl

RefSeq Acc Id:

ENST00000600004

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,561,931 - 58,564,613 (-)	Ensembl

RefSeq Acc Id:

ENST00000600048

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,569,334 - 58,572,737 (-)	Ensembl

RefSeq Acc Id:

NM_001267033 ⟹ NP_001253962

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,561,932 - 58,573,335 (-)	NCBI
GRCh37	19	59,073,284 - 59,085,757 (-)	NCBI
HuRef	19	55,383,492 - 55,395,145 (-)	NCBI
CHM1_1	19	59,067,113 - 59,078,772 (-)	NCBI
T2T-CHM13v2.0	19	61,659,609 - 61,671,013 (-)	NCBI

Sequence:

show sequence

AGGCGGTGCTGCCGTCTGTTGTACCTGAGAGGCTTGCGCATGCCGACGCACGGATTCGAGGCGG
GGAGCATGGGAAGAAGCGGCCAGGAGTATGACCTGATCATTGCGACCACCGCTAGGGGAAGGGA
GGAGAGGGTGTAGAAACGGGGACGAGGGTGGGGGAAGGGCAAGGAGGCGCTCGAGCTGGTGCGC
GGAGCATCCTGGGAGACGTAGTCCAGCGGGAGGGGGAAGTCGAAGACTGCGCGTGCTCAGGAGC
GCGGAGCGGCCCGCTGAGCGCAGAGGGGCAGACACTGGCCTCAGATACCTGACCTGGTACCCTC
TATGAGGCCTGCGGTGCTGGGCTCCCCAGACCGAGCACCCCCAGAAGATGAGGGGCCTGTCATG
GTGAAGCTAGAGGACTCTGAGGAGGAGGGTGAGGCTGCCTTATGGGACCCAGGCCCTGAAGCTG
CACGCCTGCGTTTCCGGTGCTTCCGCTATGAGGAGGCCACAGGGCCCCAAGAGGCCCTGGCCCA
GCTCCGAGAGCTGTGTCGCCAGTGGCTGCGTCCAGAGGTACGCTCCAAGGAGCAGATGCTGGAG
CTGTTGGTGCTGGAGCAGTTCCTGGGCGCACTGCCCCCTGAGATCCAGGCCCGTGTGCAGGGGC
AGCGGCCAGGCAGCCCCGAGGAGGCTGCTGCCCTAGTAGATGGGCTGCGCCGGGAGCCGGGCGG
ACCCCGGAGATGGGTCACAGTCCAGGTGCAGGGCCAGGAGGTCCTATCAGAGAAGATGGAGCCC
TCCAGTTTCCAGCCCCTACCTGAAACTGAGCCTCCAACTCCAGAGCCTGGGCCCAAGACACCTC
CTAGGACTATGCAGGAATCACCACTGGGCCTGCAGGTGAAAGAGGAGTCAGAGGTTACAGAGGA
CTCAGATTTCCTGGAGTCTGGGCCTCTAGCTGCCACCCAGGAGTCTGTACCCACCCTCCTGCCT
GAGGAGGCCCAGAGATGTGGGACCGTGCTGGACCAGATCTTTCCCCACAGCAAGACTGGGCCTG
AGGGTCCCTCATGGAGGGAGCACCCCAGGGCCCTGTGGCATGAGGAAGCTGGGGGCATCTTCTC
CCCAGGGGCCGGAGCCGGGGCCGCCCCAGCACTGGGGGCGGGGTGGTTAGGGGCGGCCGTTGCG
ATGTATGTGGCAAGGTGTTCAGCCAACGCAGCAACCTGCTGAGGCACCAGAAGATCCACACGGG
TGAGCGACCATTCGTGTGCAGCGAGTGCGGCCGCAGCTTCAGCCGCAGCTCGCACCTGCTGCGC
CACCAGCTTACGCACACCGAGGAGCGGCCGTTCGTGTGCGGCGACTGTGGCCAGGGCTTCGTGC
GCAGCGCGCGCCTGGAAGAGCATCGGAGAGTGCACACGGGCGAACAGCCTTTCCGTTGCGCTGA
GTGCGGCCAGAGCTTCCGGCAGCGCTCCAATCTGCTGCAGCACCAGCGCATCCACGGCGATCCC
CCGGGCCCTGGCGCTAAGCCCCCGGCCCCTCCTGGTGCGCCCGAGCCTCCCGGCCCCTTTCCGT
GCAGCGAGTGCCGCGAGAGCTTCGCGCGGCGCGCCGTGCTGCTGGAGCACCAGGCGGTACACAC
GGGCGACAAGTCCTTTGGCTGCGTCGAGTGCGGCGAGCGCTTCGGCCGCCGCTCAGTGCTGCTG
CAGCACCGGCGCGTGCACAGTGGCGAGCGGCCCTTCGCCTGTGCCGAGTGCGGCCAGAGCTTCC
GGCAGCGCTCCAACCTGACGCAGCACCGGCGCATCCACACCGGGGAGCGGCCCTTCGCCTGCGC
CGAGTGTGGCAAGGCCTTCCGCCAGCGGCCTACGCTCACGCAGCATCTCCGCGTACACACGGGC
GAGAAACCCTTTGCCTGCCCCGAGTGTGGCCAGCGCTTCAGCCAGCGCCTCAAGCTCACGCGTC
ATCAGAGGACACACACCGGCGAAAAGCCCTACCACTGCGGTGAGTGCGGCCTGGGCTTCACGCA
GGTCTCGCGGCTCACCGAGCACCAGCGCATCCACACGGGCGAACGGCCCTTCGCCTGCCCCGAG
TGCGGCCAGAGCTTTCGGCAGCACGCCAACCTCACCCAGCACCGGCGCATCCACACGGGTGAAC
GGCCCTACGCATGCCCTGAGTGTGGCAAGGCCTTCCGCCAGCGGCCCACGCTCACGCAGCATCT
GCGCACCCACCGACGAGAGAAGCCCTTCGCCTGCCAGGACTGTGGCCGCCGCTTCCACCAGAGC
ACCAAGCTCATTCAGCACCAGCGCGTCCACAGCGCCGAGTAGCTCCAGCCGGGACGCACTGTGT
CCGCCATGGTCAGAACACCTACCTCCCCTGGTTATTGTGAGGCTGGCGATTACATAAGTATAAG
CAGGTCCGCCCAGGGCTTGGCTACTGTAGGTGTCCAATAAACAGTAGATGGAAA

hide sequence

RefSeq Acc Id:

NM_003422 ⟹ NP_003413

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,561,932 - 58,573,573 (-)	NCBI
GRCh37	19	59,073,284 - 59,085,757 (-)	NCBI
Build 36	19	63,765,096 - 63,776,754 (-)	NCBI Archive
HuRef	19	55,383,492 - 55,395,145 (-)	ENTREZGENE
CHM1_1	19	59,067,113 - 59,078,772 (-)	NCBI
T2T-CHM13v2.0	19	61,659,609 - 61,671,251 (-)	NCBI

Sequence:

show sequence

GCACGTACACACGAAGGGCCTGCTGACTACATCTGCCGGAAAGCATCGGGCCAAGCCTTTCTCC
ATTTTGCGGTCTAGGAAGTAGCAGAGGCCCCTTCCTGTAGGGAGTTGCCATGGAGACGCGGTGG
GGCACCGACGGAGTTCTAATGACGGCCGTGATTGGTGCAGGATCCTGCTAATCTCAGGAAGGCC
CGTAGAGAAGGGCAGACACTGGCCTCAGATACCTGACCTGGTACCCTCTATGAGGCCTGCGGTG
CTGGGCTCCCCAGACCGAGCACCCCCAGAAGATGAGGGGCCTGTCATGGTGAAGCTAGAGGACT
CTGAGGAGGAGGGTGAGGCTGCCTTATGGGACCCAGGCCCTGAAGCTGCACGCCTGCGTTTCCG
GTGCTTCCGCTATGAGGAGGCCACAGGGCCCCAAGAGGCCCTGGCCCAGCTCCGAGAGCTGTGT
CGCCAGTGGCTGCGTCCAGAGGTACGCTCCAAGGAGCAGATGCTGGAGCTGTTGGTGCTGGAGC
AGTTCCTGGGCGCACTGCCCCCTGAGATCCAGGCCCGTGTGCAGGGGCAGCGGCCAGGCAGCCC
CGAGGAGGCTGCTGCCCTAGTAGATGGGCTGCGCCGGGAGCCGGGCGGACCCCGGAGATGGGTC
ACAGTCCAGGTGCAGGGCCAGGAGGTCCTATCAGAGAAGATGGAGCCCTCCAGTTTCCAGCCCC
TACCTGAAACTGAGCCTCCAACTCCAGAGCCTGGGCCCAAGACACCTCCTAGGACTATGCAGGA
ATCACCACTGGGCCTGCAGGTGAAAGAGGAGTCAGAGGTTACAGAGGACTCAGATTTCCTGGAG
TCTGGGCCTCTAGCTGCCACCCAGGAGTCTGTACCCACCCTCCTGCCTGAGGAGGCCCAGAGAT
GTGGGACCGTGCTGGACCAGATCTTTCCCCACAGCAAGACTGGGCCTGAGGGTCCCTCATGGAG
GGAGCACCCCAGGGCCCTGTGGCATGAGGAAGCTGGGGGCATCTTCTCCCCAGGGTTCGCGCTG
CAGCTAGGCAGCATCTCCGCAGGTCCAGGTAGTGTAAGCCCTCACCTCCACGTCCCCTGGGACC
TCGGCATGGCTGGCCTTTCTGGCCAGATCCAATCACCCTCCCGCGAAGGTGGCTTTGCGCATGC
GCTTCTGCTCCCCAGCGATCTGAGGAGTGAACAGGACCCCACGGACGAGGATCCCTGCCGGGGT
GTGGGCCCTGCTCTGATCACCACCCGCTGGCGCTCCCCCAGGGGCCGGAGCCGGGGCCGCCCCA
GCACTGGGGGCGGGGTGGTTAGGGGCGGCCGTTGCGATGTATGTGGCAAGGTGTTCAGCCAACG
CAGCAACCTGCTGAGGCACCAGAAGATCCACACGGGTGAGCGACCATTCGTGTGCAGCGAGTGC
GGCCGCAGCTTCAGCCGCAGCTCGCACCTGCTGCGCCACCAGCTTACGCACACCGAGGAGCGGC
CGTTCGTGTGCGGCGACTGTGGCCAGGGCTTCGTGCGCAGCGCGCGCCTGGAAGAGCATCGGAG
AGTGCACACGGGCGAACAGCCTTTCCGTTGCGCTGAGTGCGGCCAGAGCTTCCGGCAGCGCTCC
AATCTGCTGCAGCACCAGCGCATCCACGGCGATCCCCCGGGCCCTGGCGCTAAGCCCCCGGCCC
CTCCTGGTGCGCCCGAGCCTCCCGGCCCCTTTCCGTGCAGCGAGTGCCGCGAGAGCTTCGCGCG
GCGCGCCGTGCTGCTGGAGCACCAGGCGGTACACACGGGCGACAAGTCCTTTGGCTGCGTCGAG
TGCGGCGAGCGCTTCGGCCGCCGCTCAGTGCTGCTGCAGCACCGGCGCGTGCACAGTGGCGAGC
GGCCCTTCGCCTGTGCCGAGTGCGGCCAGAGCTTCCGGCAGCGCTCCAACCTGACGCAGCACCG
GCGCATCCACACCGGGGAGCGGCCCTTCGCCTGCGCCGAGTGTGGCAAGGCCTTCCGCCAGCGG
CCTACGCTCACGCAGCATCTCCGCGTACACACGGGCGAGAAACCCTTTGCCTGCCCCGAGTGTG
GCCAGCGCTTCAGCCAGCGCCTCAAGCTCACGCGTCATCAGAGGACACACACCGGCGAAAAGCC
CTACCACTGCGGTGAGTGCGGCCTGGGCTTCACGCAGGTCTCGCGGCTCACCGAGCACCAGCGC
ATCCACACGGGCGAACGGCCCTTCGCCTGCCCCGAGTGCGGCCAGAGCTTTCGGCAGCACGCCA
ACCTCACCCAGCACCGGCGCATCCACACGGGTGAACGGCCCTACGCATGCCCTGAGTGTGGCAA
GGCCTTCCGCCAGCGGCCCACGCTCACGCAGCATCTGCGCACCCACCGACGAGAGAAGCCCTTC
GCCTGCCAGGACTGTGGCCGCCGCTTCCACCAGAGCACCAAGCTCATTCAGCACCAGCGCGTCC
ACAGCGCCGAGTAGCTCCAGCCGGGACGCACTGTGTCCGCCATGGTCAGAACACCTACCTCCCC
TGGTTATTGTGAGGCTGGCGATTACATAAGTATAAGCAGGTCCGCCCAGGGCTTGGCTACTGTA
GGTGTCCAATAAACAGTAGATGGAAA

hide sequence

RefSeq Acc Id:

NM_198055 ⟹ NP_932172

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,561,932 - 58,573,335 (-)	NCBI
GRCh37	19	59,073,284 - 59,085,757 (-)	NCBI
Build 36	19	63,765,096 - 63,776,754 (-)	NCBI Archive
HuRef	19	55,383,492 - 55,395,145 (-)	ENTREZGENE
CHM1_1	19	59,067,113 - 59,078,772 (-)	NCBI
T2T-CHM13v2.0	19	61,659,609 - 61,671,013 (-)	NCBI

Sequence:

show sequence

AGGCGGTGCTGCCGTCTGTTGTACCTGAGAGGCTTGCGCATGCCGACGCACGGATTCGAGGCGG
GGAGCATGGGAAGAAGCGGCCAGGAGTATGACCTGATCATTGCGACCACCGCTAGGGGAAGGGA
GGAGAGGGTGTAGAAACGGGGACGAGGGTGGGGGAAGGGCAAGGAGGCGCTCGAGCTGGTGCGC
GGAGCATCCTGGGAGACGTAGTCCAGCGGGAGGGGGAAGTCGAAGACTGCGCGTGCTCAGGAGC
GCGGAGCGGCCCGCTGAGCGCAGAGGGGCAGACACTGGCCTCAGATACCTGACCTGGTACCCTC
TATGAGGCCTGCGGTGCTGGGCTCCCCAGACCGAGCACCCCCAGAAGATGAGGGGCCTGTCATG
GTGAAGCTAGAGGACTCTGAGGAGGAGGGTGAGGCTGCCTTATGGGACCCAGGCCCTGAAGCTG
CACGCCTGCGTTTCCGGTGCTTCCGCTATGAGGAGGCCACAGGGCCCCAAGAGGCCCTGGCCCA
GCTCCGAGAGCTGTGTCGCCAGTGGCTGCGTCCAGAGGTACGCTCCAAGGAGCAGATGCTGGAG
CTGTTGGTGCTGGAGCAGTTCCTGGGCGCACTGCCCCCTGAGATCCAGGCCCGTGTGCAGGGGC
AGCGGCCAGGCAGCCCCGAGGAGGCTGCTGCCCTAGTAGATGGGCTGCGCCGGGAGCCGGGCGG
ACCCCGGAGATGGGTCACAGTCCAGGTGCAGGGCCAGGAGGTCCTATCAGAGAAGATGGAGCCC
TCCAGTTTCCAGCCCCTACCTGAAACTGAGCCTCCAACTCCAGAGCCTGGGCCCAAGACACCTC
CTAGGACTATGCAGGAATCACCACTGGGCCTGCAGGTGAAAGAGGAGTCAGAGGTTACAGAGGA
CTCAGATTTCCTGGAGTCTGGGCCTCTAGCTGCCACCCAGGAGTCTGTACCCACCCTCCTGCCT
GAGGAGGCCCAGAGATGTGGGACCGTGCTGGACCAGATCTTTCCCCACAGCAAGACTGGGCCTG
AGGGTCCCTCATGGAGGGAGCACCCCAGGGCCCTGTGGCATGAGGAAGCTGGGGGCATCTTCTC
CCCAGGGTTCGCGCTGCAGCTAGGCAGCATCTCCGCAGGTCCAGGTAGTGTAAGCCCTCACCTC
CACGTCCCCTGGGACCTCGGCATGGCTGGCCTTTCTGGCCAGATCCAATCACCCTCCCGCGAAG
GTGGCTTTGCGCATGCGCTTCTGCTCCCCAGCGATCTGAGGAGTGAACAGGACCCCACGGACGA
GGATCCCTGCCGGGGTGTGGGCCCTGCTCTGATCACCACCCGCTGGCGCTCCCCCAGGGGCCGG
AGCCGGGGCCGCCCCAGCACTGGGGGCGGGGTGGTTAGGGGCGGCCGTTGCGATGTATGTGGCA
AGGTGTTCAGCCAACGCAGCAACCTGCTGAGGCACCAGAAGATCCACACGGGTGAGCGACCATT
CGTGTGCAGCGAGTGCGGCCGCAGCTTCAGCCGCAGCTCGCACCTGCTGCGCCACCAGCTTACG
CACACCGAGGAGCGGCCGTTCGTGTGCGGCGACTGTGGCCAGGGCTTCGTGCGCAGCGCGCGCC
TGGAAGAGCATCGGAGAGTGCACACGGGCGAACAGCCTTTCCGTTGCGCTGAGTGCGGCCAGAG
CTTCCGGCAGCGCTCCAATCTGCTGCAGCACCAGCGCATCCACGGCGATCCCCCGGGCCCTGGC
GCTAAGCCCCCGGCCCCTCCTGGTGCGCCCGAGCCTCCCGGCCCCTTTCCGTGCAGCGAGTGCC
GCGAGAGCTTCGCGCGGCGCGCCGTGCTGCTGGAGCACCAGGCGGTACACACGGGCGACAAGTC
CTTTGGCTGCGTCGAGTGCGGCGAGCGCTTCGGCCGCCGCTCAGTGCTGCTGCAGCACCGGCGC
GTGCACAGTGGCGAGCGGCCCTTCGCCTGTGCCGAGTGCGGCCAGAGCTTCCGGCAGCGCTCCA
ACCTGACGCAGCACCGGCGCATCCACACCGGGGAGCGGCCCTTCGCCTGCGCCGAGTGTGGCAA
GGCCTTCCGCCAGCGGCCTACGCTCACGCAGCATCTCCGCGTACACACGGGCGAGAAACCCTTT
GCCTGCCCCGAGTGTGGCCAGCGCTTCAGCCAGCGCCTCAAGCTCACGCGTCATCAGAGGACAC
ACACCGGCGAAAAGCCCTACCACTGCGGTGAGTGCGGCCTGGGCTTCACGCAGGTCTCGCGGCT
CACCGAGCACCAGCGCATCCACACGGGCGAACGGCCCTTCGCCTGCCCCGAGTGCGGCCAGAGC
TTTCGGCAGCACGCCAACCTCACCCAGCACCGGCGCATCCACACGGGTGAACGGCCCTACGCAT
GCCCTGAGTGTGGCAAGGCCTTCCGCCAGCGGCCCACGCTCACGCAGCATCTGCGCACCCACCG
ACGAGAGAAGCCCTTCGCCTGCCAGGACTGTGGCCGCCGCTTCCACCAGAGCACCAAGCTCATT
CAGCACCAGCGCGTCCACAGCGCCGAGTAGCTCCAGCCGGGACGCACTGTGTCCGCCATGGTCA
GAACACCTACCTCCCCTGGTTATTGTGAGGCTGGCGATTACATAAGTATAAGCAGGTCCGCCCA
GGGCTTGGCTACTGTAGGTGTCCAATAAACAGTAGATGGAAA

hide sequence

RefSeq Acc Id:

XM_005259204 ⟹ XP_005259261

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,561,932 - 58,573,335 (-)	NCBI

Sequence:

show sequence

GATCGGCATCTCTCTGCCCCAGTACCCTTCCCCACCTCTTCATCCCACATGCCCCATTGCATTT
TCAACGCCCGCCGCGTCTCCGGGTTACCCAGGCGATGTCGAGTCGTGTCCCCAGGTTACCATGG
AGACGTTCAGGGCCCGCCCCTCGCCCATGATCACAGAGGAACGTCATCGCGCCGCGCGCGCACG
TACACACGAAGGGCCTGCTGACTACATCTGCCGGAAAGCATCGGGCCAAGCCTTTCTCCATTTT
GCGGTCTAGGAAGTAGCAGAGGCCCCTTCCTGTAGGGAGTTGCCATGGAGACGCGGTGGGGCAC
CGACGGAGTTCTAATGACGGCCGTGATTGGTGCAGGATCCTGCTAATCTCAGGAAGGCCCGTAG
AGAAGTGAGGAAAACGTGGTGGGGGGCATGCGCGATCTGGTAGGCGGTGCTGCCGTCTGTTGTA
CCTGAGAGGCTTGCGCATGCCGACGCACGGATTCGAGGCGGGGAGCATGGGAAGAAGCGGCCAG
GAGTATGACCTGATCATTGCGACCACCGCTAGGGGAAGGGAGGAGAGGGTGTAGAAACGGGGAC
GAGGGTGGGGGAAGGGCAAGGAGGCGCTCGAGCTGGTGCGCGGAGCATCCTGGGAGACGTAGTC
CAGCGGGAGGGGGAAGTCGAAGACTGCGCGTGCTCAGGAGCGCGGAGCGGCCCGCTGAGCGCAG
AGGGTTTCAGGTTGACTTGGCACCTTGAAGAGTGGAGGCTTGGCCCCCAGGATGAGGCGGCCCT
CGAAATCGATGCCACCCACGGGGGAATGATTCTGCGGTGCCATCCCCTTCATAAACGCAGATTC
CTTCCTAAAGCCGCAGCTGCAGAAGGAACAGCGCGAGGAGGGAGGGGCAGACACTGGCCTCAGA
TACCTGACCTGGTACCCTCTATGAGGCCTGCGGTGCTGGGCTCCCCAGACCGAGCACCCCCAGA
AGATGAGGGGCCTGTCATGGTGAAGCTAGAGGACTCTGAGGAGGAGGGTGAGGCTGCCTTATGG
GACCCAGGCCCTGAAGCTGCACGCCTGCGTTTCCGGTGCTTCCGCTATGAGGAGGCCACAGGGC
CCCAAGAGGCCCTGGCCCAGCTCCGAGAGCTGTGTCGCCAGTGGCTGCGTCCAGAGGTACGCTC
CAAGGAGCAGATGCTGGAGCTGTTGGTGCTGGAGCAGTTCCTGGGCGCACTGCCCCCTGAGATC
CAGGCCCGTGTGCAGGGGCAGCGGCCAGGCAGCCCCGAGGAGGCTGCTGCCCTAGTAGATGGGC
TGCGCCGGGAGCCGGGCGGACCCCGGAGATGGGTCACAGTCCAGGTGCAGGGCCAGGAGGTCCT
ATCAGAGAAGATGGAGCCCTCCAGTTTCCAGCCCCTACCTGAAACTGAGCCTCCAACTCCAGAG
CCTGGGCCCAAGACACCTCCTAGGACTATGCAGGAATCACCACTGGGCCTGCAGGTGAAAGAGG
AGTCAGAGGTTACAGAGGACTCAGATTTCCTGGAGTCTGGGCCTCTAGCTGCCACCCAGGAGTC
TGTACCCACCCTCCTGCCTGAGGAGGCCCAGAGATGTGGGACCGTGCTGGACCAGATCTTTCCC
CACAGCAAGACTGGGCCTGAGGGTCCCTCATGGAGGGAGCACCCCAGGGCCCTGTGGCATGAGG
AAGCTGGGGGCATCTTCTCCCCAGGGTTCGCGCTGCAGCTAGGCAGCATCTCCGCAGGTCCAGG
TAGTGTAAGCCCTCACCTCCACGTCCCCTGGGACCTCGGCATGGCTGGCCTTTCTGGCCAGATC
CAATCACCCTCCCGCGAAGGTGGCTTTGCGCATGCGCTTCTGCTCCCCAGCGATCTGAGGAGTG
AACAGGACCCCACGGACGAGGATCCCTGCCGGGGTGTGGGCCCTGCTCTGATCACCACCCGCTG
GCGCTCCCCCAGGGGCCGGAGCCGGGGCCGCCCCAGCACTGGGGGCGGGGTGGTTAGGGGCGGC
CGTTGCGATGTATGTGGCAAGGTGTTCAGCCAACGCAGCAACCTGCTGAGGCACCAGAAGATCC
ACACGGGTGAGCGACCATTCGTGTGCAGCGAGTGCGGCCGCAGCTTCAGCCGCAGCTCGCACCT
GCTGCGCCACCAGCTTACGCACACCGAGGAGCGGCCGTTCGTGTGCGGCGACTGTGGCCAGGGC
TTCGTGCGCAGCGCGCGCCTGGAAGAGCATCGGAGAGTGCACACGGGCGAACAGCCTTTCCGTT
GCGCTGAGTGCGGCCAGAGCTTCCGGCAGCGCTCCAATCTGCTGCAGCACCAGCGCATCCACGG
CGATCCCCCGGGCCCTGGCGCTAAGCCCCCGGCCCCTCCTGGTGCGCCCGAGCCTCCCGGCCCC
TTTCCGTGCAGCGAGTGCCGCGAGAGCTTCGCGCGGCGCGCCGTGCTGCTGGAGCACCAGGCGG
TACACACGGGCGACAAGTCCTTTGGCTGCGTCGAGTGCGGCGAGCGCTTCGGCCGCCGCTCAGT
GCTGCTGCAGCACCGGCGCGTGCACAGTGGCGAGCGGCCCTTCGCCTGTGCCGAGTGCGGCCAG
AGCTTCCGGCAGCGCTCCAACCTGACGCAGCACCGGCGCATCCACACCGGGGAGCGGCCCTTCG
CCTGCGCCGAGTGTGGCAAGGCCTTCCGCCAGCGGCCTACGCTCACGCAGCATCTCCGCGTACA
CACGGGCGAGAAACCCTTTGCCTGCCCCGAGTGTGGCCAGCGCTTCAGCCAGCGCCTCAAGCTC
ACGCGTCATCAGAGGACACACACCGGCGAAAAGCCCTACCACTGCGGTGAGTGCGGCCTGGGCT
TCACGCAGGTCTCGCGGCTCACCGAGCACCAGCGCATCCACACGGGCGAACGGCCCTTCGCCTG
CCCCGAGTGCGGCCAGAGCTTTCGGCAGCACGCCAACCTCACCCAGCACCGGCGCATCCACACG
GGTGAACGGCCCTACGCATGCCCTGAGTGTGGCAAGGCCTTCCGCCAGCGGCCCACGCTCACGC
AGCATCTGCGCACCCACCGACGAGAGAAGCCCTTCGCCTGCCAGGACTGTGGCCGCCGCTTCCA
CCAGAGCACCAAGCTCATTCAGCACCAGCGCGTCCACAGCGCCGAGTAGCTCCAGCCGGGACGC
ACTGTGTCCGCCATGGTCAGAACACCTACCTCCCCTGGTTATTGTGAGGCTGGCGATTACATAA
GTATAAGCAGGTCCGCCCAGGGCTTGGCTACTGTAGGTGTCCAATAAACAGTAGATGGAAACTG
GGTCTCCA

hide sequence

RefSeq Acc Id:

XM_011527264 ⟹ XP_011525566

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,561,932 - 58,573,573 (-)	NCBI

Sequence:

show sequence

TCGTGCCACTGCACTCCAGTCTGGCAACAGCGAGACTCCGTCAAAAAAAAAAAAAAAAAAAAGA
AAGAAAGAAAAAGAAAAACACTGAAATAAAAGCACAAAGTTGGATACAAAACTGCTTAGTGAGC
TACAAAGCGATACACTGGACAGAAAGCATTTGCAACCTATCAACCTGTACAGGGTAGCATATAA
CTGGACAGCATCTGGACTCCTAAGTTTTCCTAACAGTTTTACCTCGGATTCTCCCTGTCTCTCT
TCGTGCTGTCATCTTTCTCTAGGTCTTCGAAAACTGTCAATCCATCTTACTGTATCTCTAATTT
CTGTCCCTTTTCTCCCTTCTTGTTTCTGTCCCTCTCCCTTCTTGTCTACCTCTTGAGTCTGGAT
ATCTGCATTTCTTGTCTCTGTGAACCCATTCTGCGTTTCCTTCTTTGTGTCTCTTTCATCTGCA
TCCCTTTCTGATCTGCCTCTCTCTTGCTAACTGTTCTGACACCTGTTTGCCCGGCCCTGACCCT
CTGATCCACTCAGCCCTCTTATAACTTGGACCCGTGTCTCTATGTTTGTTCACTTATTTTCACT
GTCTCTCCTCGCGTCGAGTCTCCGGTCCTCCCAGTCTGTGAGTCTGTCTCTCTGTCTCTCTCTC
TCTTCCTCCCGCCGGTCCTTCGTCTCTCTTTGCCCTTGAGTCTCTGGTCTCTCTCCGTCTCTCC
TCGCTGTTTCTATCGATCGGCATCTCTCTGCCCCAGTACCCTTCCCCACCTCTTCATCCCACAT
GCCCCATTGCATTTTCAACGCCCGCCGCGTCTCCGGGTTACCCAGGCGATGTCGAGTCGTGTCC
CCAGGTTACCATGGAGACGTTCAGGGCCCGCCCCTCGCCCATGATCACAGAGGAACGTCATCGC
GCCGCGCGCGCACGTACACACGAAGGGCCTGCTGACTACATCTGCCGGAAAGCATCGGGCCAAG
CCTTTCTCCATTTTGCGGTCTAGGAAGTAGCAGAGGCCCCTTCCTGTAGGGAGTTGCCATGGAG
ACGCGGTGGGGCACCGACGGAGTTCTAATGACGGCCGTGATTGGTGCAGGATCCTGCTAATCTC
AGGAAGGCCCGTAGAGAAGTGAGGAAAACGTGGTGGGGGGCATGCGCGATCTGGTAGGCGGTGC
TGCCGTCTGTTGTACCTGAGAGGCTTGCGCATGCCGACGCACGGATTCGAGGCGGGGAGCATGG
GAAGAAGCGGCCAGGAGGGCAGACACTGGCCTCAGATACCTGACCTGGTACCCTCTATGAGGCC
TGCGGTGCTGGGCTCCCCAGACCGAGCACCCCCAGAAGATGAGGGGCCTGTCATGGTGAAGCTA
GAGGACTCTGAGGAGGAGGGTGAGGCTGCCTTATGGGACCCAGGCCCTGAAGCTGCACGCCTGC
GTTTCCGGTGCTTCCGCTATGAGGAGGCCACAGGGCCCCAAGAGGCCCTGGCCCAGCTCCGAGA
GCTGTGTCGCCAGTGGCTGCGTCCAGAGGTACGCTCCAAGGAGCAGATGCTGGAGCTGTTGGTG
CTGGAGCAGTTCCTGGGCGCACTGCCCCCTGAGATCCAGGCCCGTGTGCAGGGGCAGCGGCCAG
GCAGCCCCGAGGAGGCTGCTGCCCTAGTAGATGGGCTGCGCCGGGAGCCGGGCGGACCCCGGAG
ATGGGTCACAGTCCAGGTGCAGGGCCAGGAGGTCCTATCAGAGAAGATGGAGCCCTCCAGTTTC
CAGCCCCTACCTGAAACTGAGCCTCCAACTCCAGAGCCTGGGCCCAAGACACCTCCTAGGACTA
TGCAGGAATCACCACTGGGCCTGCAGGTGAAAGAGGAGTCAGAGGTTACAGAGGACTCAGATTT
CCTGGAGTCTGGGCCTCTAGCTGCCACCCAGGAGTCTGTACCCACCCTCCTGCCTGAGGAGGCC
CAGAGATGTGGGACCGTGCTGGACCAGATCTTTCCCCACAGCAAGACTGGGCCTGAGGGTCCCT
CATGGAGGGAGCACCCCAGGGCCCTGTGGCATGAGGAAGCTGGGGGCATCTTCTCCCCAGGGTT
CGCGCTGCAGCTAGGCAGCATCTCCGCAGGTCCAGGTAGTGTAAGCCCTCACCTCCACGTCCCC
TGGGACCTCGGCATGGCTGGCCTTTCTGGCCAGATCCAATCACCCTCCCGCGAAGGTGGCTTTG
CGCATGCGCTTCTGCTCCCCAGCGATCTGAGGAGTGAACAGGACCCCACGGACGAGGATCCCTG
CCGGGGTGTGGGCCCTGCTCTGATCACCACCCGCTGGCGCTCCCCCAGGGGCCGGAGCCGGGGC
CGCCCCAGCACTGGGGGCGGGGTGGTTAGGGGCGGCCGTTGCGATGTATGTGGCAAGGTGTTCA
GCCAACGCAGCAACCTGCTGAGGCACCAGAAGATCCACACGGGTGAGCGACCATTCGTGTGCAG
CGAGTGCGGCCGCAGCTTCAGCCGCAGCTCGCACCTGCTGCGCCACCAGCTTACGCACACCGAG
GAGCGGCCGTTCGTGTGCGGCGACTGTGGCCAGGGCTTCGTGCGCAGCGCGCGCCTGGAAGAGC
ATCGGAGAGTGCACACGGGCGAACAGCCTTTCCGTTGCGCTGAGTGCGGCCAGAGCTTCCGGCA
GCGCTCCAATCTGCTGCAGCACCAGCGCATCCACGGCGATCCCCCGGGCCCTGGCGCTAAGCCC
CCGGCCCCTCCTGGTGCGCCCGAGCCTCCCGGCCCCTTTCCGTGCAGCGAGTGCCGCGAGAGCT
TCGCGCGGCGCGCCGTGCTGCTGGAGCACCAGGCGGTACACACGGGCGACAAGTCCTTTGGCTG
CGTCGAGTGCGGCGAGCGCTTCGGCCGCCGCTCAGTGCTGCTGCAGCACCGGCGCGTGCACAGT
GGCGAGCGGCCCTTCGCCTGTGCCGAGTGCGGCCAGAGCTTCCGGCAGCGCTCCAACCTGACGC
AGCACCGGCGCATCCACACCGGGGAGCGGCCCTTCGCCTGCGCCGAGTGTGGCAAGGCCTTCCG
CCAGCGGCCTACGCTCACGCAGCATCTCCGCGTACACACGGGCGAGAAACCCTTTGCCTGCCCC
GAGTGTGGCCAGCGCTTCAGCCAGCGCCTCAAGCTCACGCGTCATCAGAGGACACACACCGGCG
AAAAGCCCTACCACTGCGGTGAGTGCGGCCTGGGCTTCACGCAGGTCTCGCGGCTCACCGAGCA
CCAGCGCATCCACACGGGCGAACGGCCCTTCGCCTGCCCCGAGTGCGGCCAGAGCTTTCGGCAG
CACGCCAACCTCACCCAGCACCGGCGCATCCACACGGGTGAACGGCCCTACGCATGCCCTGAGT
GTGGCAAGGCCTTCCGCCAGCGGCCCACGCTCACGCAGCATCTGCGCACCCACCGACGAGAGAA
GCCCTTCGCCTGCCAGGACTGTGGCCGCCGCTTCCACCAGAGCACCAAGCTCATTCAGCACCAG
CGCGTCCACAGCGCCGAGTAGCTCCAGCCGGGACGCACTGTGTCCGCCATGGTCAGAACACCTA
CCTCCCCTGGTTATTGTGAGGCTGGCGATTACATAAGTATAAGCAGGTCCGCCCAGGGCTTGGC
TACTGTAGGTGTCCAATAAACAGTAGATGGAAACTGGGTCTCCA

hide sequence

RefSeq Acc Id:

XM_017027206 ⟹ XP_016882695

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,561,932 - 58,570,368 (-)	NCBI

Sequence:

show sequence

GATCGGCATCTCTCTGCCCCAGTACCCTTCCCCACCTCTTCATCCCACATGCCCCATTGCATTT
TCAACGCCCGCCGCGTCTCCGGGTTACCCAGGCGATGTCGAGTCGTGTCCCCAGGTTACCATGG
AGACGTTCAGGGCCCGCCCCTCGCCCATGATCACAGAGGAACGTCATCGCGCCGCGCGCGCACG
TACACACGAAGGGCCTGCTGACTACATCTGCCGGAAAGCATCGGGCCAAGCCTTTCTCCATTTT
GCGGTCTAGGAAGTAGCAGAGGCCCCTTCCTGTAGGGAGTTGCCATGGAGACGCGGTGGGGCAC
CGACGGAGTTCTAATGACGGCCGTGATTGGTGCAGGATCCTGCTAATCTCAGGAAGGCCCGTAG
AGAAGTGAGGAAAACGTGGTGGGGGGCATGCGCGATCTGGTAGGCGGTGCTGCCGTCTGTTGTA
CCTGAGAGGCTTGCGCATGCCGACGCACGGATTCGAGGCGGGGAGCATGGGAAGAAGCGGCCAG
GAGTATGACCTGATCATTGCGACCACCGCTAGGGGAAGGGAGGAGAGGGTGTAGAAACGGGGAC
GAGGGTGGGGGAAGGGCAAGGAGGCGCTCGAGCTGGTGCGCGGAGCATCCTGGGAGACGTAGTC
CAGCGGGAGGGGGAAGTCGAAGACTGCGCGTGCTCAGGAGCGCGGAGCGGCCCGCTGAGCGCAG
AGGGGCAGACACTGGCCTCAGATACCTGACCTGGTACCCTCTATGAGGCCTGCGGTGCTGGGCT
CCCCAGACCGAGCACCCCCAGAAGATGAGGGGCCTGTCATGGTGAAGCTAGAGGACTCTGAGGA
GGAGGGTGAGGCTGCCTTATGGGACCCAGGCCCTGAAGCTGCACGCCTGCGTTTCCGGTGCTTC
CGCTATGAGGAGGCCACAGGGCCCCAAGAGGCCCTGGCCCAGCTCCGAGAGCTGTGTCGCCAGT
GGCTGCGTCCAGAGGTACGCTCCAAGGAGCAGATGCTGGAGCTGTTGGTGCTGGAGCAGTTCCT
GGGCGCACTGCCCCCTGAGATCCAGGCCCGTGTGCAGGGGCAGCGGCCAGGCAGCCCCGAGGAG
GCTGCTGCCCTAGTAGATGGGCTGCGCCGGGAGCCGGGCGGACCCCGGAGATGGGTCACAGTCC
AGGTGCAGGGCCAGGAGGTCCTATCAGAGAAGATGGAGCCCTCCAGTTTCCAGCCCCTACCTGA
AACTGAGCCTCCAACTCCAGAGCCTGGGCCCAAGACACCTCCTAGGACTATGCAGGAATCACCA
CTGGGCCTGCAGGTGAAAGAGGAGTCAGAGGTTACAGAGGACTCAGATTTCCTGGAGTCTGGGC
CTCTAGCTGCCACCCAGGAGTCTGTACCCACCCTCCTGCCTGAGGAGGCCCAGTGACCACTGTG
ATTTCAGAGATGTGGGACCGTGCTGGACCAGATCTTTCCCCACAGCAAGACTGGGCCTGAGGGT
CCCTCATGGAGGGAGCACCCCAGGGCCCTGTGGCATGAGGAAGCTGGGGGCATCTTCTCCCCAG
GGTTCGCGCTGCAGCTAGGCAGCATCTCCGCAGGTCCAGGTAGTGTAAGCCCTCACCTCCACGT
CCCCTGGGACCTCGGCATGGCTGGCCTTTCTGGCCAGATCCAATCACCCTCCCGCGAAGGTGGC
TTTGCGCATGCGCTTCTGCTCCCCAGCGATCTGAGGAGTGAACAGGACCCCACGGACGAGGATC
CCTGCCGGGGTGTGGGCCCTGCTCTGATCACCACCCGCTGGCGCTCCCCCAGGGGCCGGAGCCG
GGGCCGCCCCAGCACTGGGGGCGGGGTGGTTAGGGGCGGCCGTTGCGATGTATGTGGCAAGGTG
TTCAGCCAACGCAGCAACCTGCTGAGGCACCAGAAGATCCACACGGGTGAGCGACCATTCGTGT
GCAGCGAGTGCGGCCGCAGCTTCAGCCGCAGCTCGCACCTGCTGCGCCACCAGCTTACGCACAC
CGAGGAGCGGCCGTTCGTGTGCGGCGACTGTGGCCAGGGCTTCGTGCGCAGCGCGCGCCTGGAA
GAGCATCGGAGAGTGCACACGGGCGAACAGCCTTTCCGTTGCGCTGAGTGCGGCCAGAGCTTCC
GGCAGCGCTCCAATCTGCTGCAGCACCAGCGCATCCACGGCGATCCCCCGGGCCCTGGCGCTAA
GCCCCCGGCCCCTCCTGGTGCGCCCGAGCCTCCCGGCCCCTTTCCGTGCAGCGAGTGCCGCGAG
AGCTTCGCGCGGCGCGCCGTGCTGCTGGAGCACCAGGCGGTACACACGGGCGACAAGTCCTTTG
GCTGCGTCGAGTGCGGCGAGCGCTTCGGCCGCCGCTCAGTGCTGCTGCAGCACCGGCGCGTGCA
CAGTGGCGAGCGGCCCTTCGCCTGTGCCGAGTGCGGCCAGAGCTTCCGGCAGCGCTCCAACCTG
ACGCAGCACCGGCGCATCCACACCGGGGAGCGGCCCTTCGCCTGCGCCGAGTGTGGCAAGGCCT
TCCGCCAGCGGCCTACGCTCACGCAGCATCTCCGCGTACACACGGGCGAGAAACCCTTTGCCTG
CCCCGAGTGTGGCCAGCGCTTCAGCCAGCGCCTCAAGCTCACGCGTCATCAGAGGACACACACC
GGCGAAAAGCCCTACCACTGCGGTGAGTGCGGCCTGGGCTTCACGCAGGTCTCGCGGCTCACCG
AGCACCAGCGCATCCACACGGGCGAACGGCCCTTCGCCTGCCCCGAGTGCGGCCAGAGCTTTCG
GCAGCACGCCAACCTCACCCAGCACCGGCGCATCCACACGGGTGAACGGCCCTACGCATGCCCT
GAGTGTGGCAAGGCCTTCCGCCAGCGGCCCACGCTCACGCAGCATCTGCGCACCCACCGACGAG
AGAAGCCCTTCGCCTGCCAGGACTGTGGCCGCCGCTTCCACCAGAGCACCAAGCTCATTCAGCA
CCAGCGCGTCCACAGCGCCGAGTAGCTCCAGCCGGGACGCACTGTGTCCGCCATGGTCAGAACA
CCTACCTCCCCTGGTTATTGTGAGGCTGGCGATTACATAAGTATAAGCAGGTCCGCCCAGGGCT
TGGCTACTGTAGGTGTCCAATAAACAGTAGATGGAAACTGGGTCTCCA

hide sequence

RefSeq Acc Id:

XM_047439312 ⟹ XP_047295268

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,561,932 - 58,573,573 (-)	NCBI

RefSeq Acc Id:

XM_047439313 ⟹ XP_047295269

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,561,932 - 58,573,335 (-)	NCBI

RefSeq Acc Id:

XM_054321948 ⟹ XP_054177923

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	61,659,609 - 61,672,553 (-)	NCBI

RefSeq Acc Id:

XM_054321949 ⟹ XP_054177924

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	61,659,609 - 61,671,013 (-)	NCBI

RefSeq Acc Id:

XM_054321950 ⟹ XP_054177925

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	61,659,609 - 61,671,251 (-)	NCBI

RefSeq Acc Id:

XM_054321951 ⟹ XP_054177926

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	61,659,609 - 61,672,553 (-)	NCBI

RefSeq Acc Id:

XM_054321952 ⟹ XP_054177927

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	61,659,609 - 61,668,046 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001253962	(Get FASTA)	NCBI Sequence Viewer
	NP_003413	(Get FASTA)	NCBI Sequence Viewer
	NP_932172	(Get FASTA)	NCBI Sequence Viewer
	XP_005259261	(Get FASTA)	NCBI Sequence Viewer
	XP_011525566	(Get FASTA)	NCBI Sequence Viewer
	XP_016882695	(Get FASTA)	NCBI Sequence Viewer
	XP_047295268	(Get FASTA)	NCBI Sequence Viewer
	XP_047295269	(Get FASTA)	NCBI Sequence Viewer
	XP_054177923	(Get FASTA)	NCBI Sequence Viewer
	XP_054177924	(Get FASTA)	NCBI Sequence Viewer
	XP_054177925	(Get FASTA)	NCBI Sequence Viewer
	XP_054177926	(Get FASTA)	NCBI Sequence Viewer
	XP_054177927	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA59898	(Get FASTA)	NCBI Sequence Viewer
	AAD55809	(Get FASTA)	NCBI Sequence Viewer
	AAD55810	(Get FASTA)	NCBI Sequence Viewer
	AAF80465	(Get FASTA)	NCBI Sequence Viewer
	AAF80466	(Get FASTA)	NCBI Sequence Viewer
	AAH07777	(Get FASTA)	NCBI Sequence Viewer
	AAH53316	(Get FASTA)	NCBI Sequence Viewer
	BAD92718	(Get FASTA)	NCBI Sequence Viewer
	EAW72614	(Get FASTA)	NCBI Sequence Viewer
	EAW72615	(Get FASTA)	NCBI Sequence Viewer
	EAW72616	(Get FASTA)	NCBI Sequence Viewer
	EAW72617	(Get FASTA)	NCBI Sequence Viewer
	EAW72618	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000215057
	ENSP00000215057.1
	ENSP00000469378
	ENSP00000469378.1
	ENSP00000469493
	ENSP00000469493.1
	ENSP00000472123.1
	ENSP00000472454.1
GenBank Protein	P28698	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_003413 ⟸ NM_003422
- Peptide Label:	isoform 1
- UniProtKB:	Q9NRY0 (UniProtKB/Swiss-Prot), Q96I71 (UniProtKB/Swiss-Prot), Q7Z729 (UniProtKB/Swiss-Prot), M0QXU0 (UniProtKB/Swiss-Prot), Q9UBW2 (UniProtKB/Swiss-Prot), P28698 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MRPAVLGSPDRAPPEDEGPVMVKLEDSEEEGEAALWDPGPEAARLRFRCFRYEEATGPQEALAQ LRELCRQWLRPEVRSKEQMLELLVLEQFLGALPPEIQARVQGQRPGSPEEAAALVDGLRREPGG PRRWVTVQVQGQEVLSEKMEPSSFQPLPETEPPTPEPGPKTPPRTMQESPLGLQVKEESEVTED SDFLESGPLAATQESVPTLLPEEAQRCGTVLDQIFPHSKTGPEGPSWREHPRALWHEEAGGIFS PGFALQLGSISAGPGSVSPHLHVPWDLGMAGLSGQIQSPSREGGFAHALLLPSDLRSEQDPTDE DPCRGVGPALITTRWRSPRGRSRGRPSTGGGVVRGGRCDVCGKVFSQRSNLLRHQKIHTGERPF VCSECGRSFSRSSHLLRHQLTHTEERPFVCGDCGQGFVRSARLEEHRRVHTGEQPFRCAECGQS FRQRSNLLQHQRIHGDPPGPGAKPPAPPGAPEPPGPFPCSECRESFARRAVLLEHQAVHTGDKS FGCVECGERFGRRSVLLQHRRVHSGERPFACAECGQSFRQRSNLTQHRRIHTGERPFACAECGK AFRQRPTLTQHLRVHTGEKPFACPECGQRFSQRLKLTRHQRTHTGEKPYHCGECGLGFTQVSRL TEHQRIHTGERPFACPECGQSFRQHANLTQHRRIHTGERPYACPECGKAFRQRPTLTQHLRTHR REKPFACQDCGRRFHQSTKLIQHQRVHSAE hide sequence

RefSeq Acc Id:	NP_932172 ⟸ NM_198055
- Peptide Label:	isoform 1
- UniProtKB:	Q9NRY0 (UniProtKB/Swiss-Prot), Q96I71 (UniProtKB/Swiss-Prot), Q7Z729 (UniProtKB/Swiss-Prot), M0QXU0 (UniProtKB/Swiss-Prot), Q9UBW2 (UniProtKB/Swiss-Prot), P28698 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MRPAVLGSPDRAPPEDEGPVMVKLEDSEEEGEAALWDPGPEAARLRFRCFRYEEATGPQEALAQ LRELCRQWLRPEVRSKEQMLELLVLEQFLGALPPEIQARVQGQRPGSPEEAAALVDGLRREPGG PRRWVTVQVQGQEVLSEKMEPSSFQPLPETEPPTPEPGPKTPPRTMQESPLGLQVKEESEVTED SDFLESGPLAATQESVPTLLPEEAQRCGTVLDQIFPHSKTGPEGPSWREHPRALWHEEAGGIFS PGFALQLGSISAGPGSVSPHLHVPWDLGMAGLSGQIQSPSREGGFAHALLLPSDLRSEQDPTDE DPCRGVGPALITTRWRSPRGRSRGRPSTGGGVVRGGRCDVCGKVFSQRSNLLRHQKIHTGERPF VCSECGRSFSRSSHLLRHQLTHTEERPFVCGDCGQGFVRSARLEEHRRVHTGEQPFRCAECGQS FRQRSNLLQHQRIHGDPPGPGAKPPAPPGAPEPPGPFPCSECRESFARRAVLLEHQAVHTGDKS FGCVECGERFGRRSVLLQHRRVHSGERPFACAECGQSFRQRSNLTQHRRIHTGERPFACAECGK AFRQRPTLTQHLRVHTGEKPFACPECGQRFSQRLKLTRHQRTHTGEKPYHCGECGLGFTQVSRL TEHQRIHTGERPFACPECGQSFRQHANLTQHRRIHTGERPYACPECGKAFRQRPTLTQHLRTHR REKPFACQDCGRRFHQSTKLIQHQRVHSAE hide sequence

RefSeq Acc Id:	NP_001253962 ⟸ NM_001267033
- Peptide Label:	isoform 2
- UniProtKB:	M0R1U5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRPAVLGSPDRAPPEDEGPVMVKLEDSEEEGEAALWDPGPEAARLRFRCFRYEEATGPQEALAQ LRELCRQWLRPEVRSKEQMLELLVLEQFLGALPPEIQARVQGQRPGSPEEAAALVDGLRREPGG PRRWVTVQVQGQEVLSEKMEPSSFQPLPETEPPTPEPGPKTPPRTMQESPLGLQVKEESEVTED SDFLESGPLAATQESVPTLLPEEAQRCGTVLDQIFPHSKTGPEGPSWREHPRALWHEEAGGIFS PGAGAGAAPALGAGWLGAAVAMYVARCSANAATC hide sequence

RefSeq Acc Id:

XP_005259261 ⟸ XM_005259204

- Peptide Label:

isoform X1

- Sequence:

show sequence

MILRCHPLHKRRFLPKAAAAEGTARGGRGRHWPQIPDLVPSMRPAVLGSPDRAPPEDEGPVMVK
LEDSEEEGEAALWDPGPEAARLRFRCFRYEEATGPQEALAQLRELCRQWLRPEVRSKEQMLELL
VLEQFLGALPPEIQARVQGQRPGSPEEAAALVDGLRREPGGPRRWVTVQVQGQEVLSEKMEPSS
FQPLPETEPPTPEPGPKTPPRTMQESPLGLQVKEESEVTEDSDFLESGPLAATQESVPTLLPEE
AQRCGTVLDQIFPHSKTGPEGPSWREHPRALWHEEAGGIFSPGFALQLGSISAGPGSVSPHLHV
PWDLGMAGLSGQIQSPSREGGFAHALLLPSDLRSEQDPTDEDPCRGVGPALITTRWRSPRGRSR
GRPSTGGGVVRGGRCDVCGKVFSQRSNLLRHQKIHTGERPFVCSECGRSFSRSSHLLRHQLTHT
EERPFVCGDCGQGFVRSARLEEHRRVHTGEQPFRCAECGQSFRQRSNLLQHQRIHGDPPGPGAK
PPAPPGAPEPPGPFPCSECRESFARRAVLLEHQAVHTGDKSFGCVECGERFGRRSVLLQHRRVH
SGERPFACAECGQSFRQRSNLTQHRRIHTGERPFACAECGKAFRQRPTLTQHLRVHTGEKPFAC
PECGQRFSQRLKLTRHQRTHTGEKPYHCGECGLGFTQVSRLTEHQRIHTGERPFACPECGQSFR
QHANLTQHRRIHTGERPYACPECGKAFRQRPTLTQHLRTHRREKPFACQDCGRRFHQSTKLIQH
QRVHSAE

hide sequence

RefSeq Acc Id:

XP_011525566 ⟸ XM_011527264

- Peptide Label:

isoform X2

- Sequence:

show sequence

MPTHGFEAGSMGRSGQEGRHWPQIPDLVPSMRPAVLGSPDRAPPEDEGPVMVKLEDSEEEGEAA
LWDPGPEAARLRFRCFRYEEATGPQEALAQLRELCRQWLRPEVRSKEQMLELLVLEQFLGALPP
EIQARVQGQRPGSPEEAAALVDGLRREPGGPRRWVTVQVQGQEVLSEKMEPSSFQPLPETEPPT
PEPGPKTPPRTMQESPLGLQVKEESEVTEDSDFLESGPLAATQESVPTLLPEEAQRCGTVLDQI
FPHSKTGPEGPSWREHPRALWHEEAGGIFSPGFALQLGSISAGPGSVSPHLHVPWDLGMAGLSG
QIQSPSREGGFAHALLLPSDLRSEQDPTDEDPCRGVGPALITTRWRSPRGRSRGRPSTGGGVVR
GGRCDVCGKVFSQRSNLLRHQKIHTGERPFVCSECGRSFSRSSHLLRHQLTHTEERPFVCGDCG
QGFVRSARLEEHRRVHTGEQPFRCAECGQSFRQRSNLLQHQRIHGDPPGPGAKPPAPPGAPEPP
GPFPCSECRESFARRAVLLEHQAVHTGDKSFGCVECGERFGRRSVLLQHRRVHSGERPFACAEC
GQSFRQRSNLTQHRRIHTGERPFACAECGKAFRQRPTLTQHLRVHTGEKPFACPECGQRFSQRL
KLTRHQRTHTGEKPYHCGECGLGFTQVSRLTEHQRIHTGERPFACPECGQSFRQHANLTQHRRI
HTGERPYACPECGKAFRQRPTLTQHLRTHRREKPFACQDCGRRFHQSTKLIQHQRVHSAE

hide sequence

RefSeq Acc Id:

XP_016882695 ⟸ XM_017027206

- Peptide Label:

isoform X3

- Sequence:

show sequence

MAGLSGQIQSPSREGGFAHALLLPSDLRSEQDPTDEDPCRGVGPALITTRWRSPRGRSRGRPST
GGGVVRGGRCDVCGKVFSQRSNLLRHQKIHTGERPFVCSECGRSFSRSSHLLRHQLTHTEERPF
VCGDCGQGFVRSARLEEHRRVHTGEQPFRCAECGQSFRQRSNLLQHQRIHGDPPGPGAKPPAPP
GAPEPPGPFPCSECRESFARRAVLLEHQAVHTGDKSFGCVECGERFGRRSVLLQHRRVHSGERP
FACAECGQSFRQRSNLTQHRRIHTGERPFACAECGKAFRQRPTLTQHLRVHTGEKPFACPECGQ
RFSQRLKLTRHQRTHTGEKPYHCGECGLGFTQVSRLTEHQRIHTGERPFACPECGQSFRQHANL
TQHRRIHTGERPYACPECGKAFRQRPTLTQHLRTHRREKPFACQDCGRRFHQSTKLIQHQRVHS
AE

hide sequence

RefSeq Acc Id:

ENSP00000472454 ⟸ ENST00000596039

RefSeq Acc Id:

ENSP00000215057 ⟸ ENST00000215057

RefSeq Acc Id:

ENSP00000469493 ⟸ ENST00000599369

RefSeq Acc Id:

ENSP00000469378 ⟸ ENST00000594234

RefSeq Acc Id:

ENSP00000472123 ⟸ ENST00000594108

RefSeq Acc Id:	XP_047295268 ⟸ XM_047439312
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047295269 ⟸ XM_047439313
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054177926 ⟸ XM_054321951
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054177923 ⟸ XM_054321948
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054177925 ⟸ XM_054321950
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054177924 ⟸ XM_054321949
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054177927 ⟸ XM_054321952
- Peptide Label:	isoform X3

Protein Domains

SCAN box

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P28698-F1-model_v2	AlphaFold	P28698	1-734	view protein structure

Promoters

RGD ID:

13206027

Promoter ID:

EPDNEW_H26594

Type:

initiation region

Name:

MZF1_3

Description:

myeloid zinc finger 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26595 EPDNEW_H26596 EPDNEW_H26597

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,572,761 - 58,572,821	EPDNEW

RGD ID:

13206029

Promoter ID:

EPDNEW_H26595

Type:

initiation region

Name:

MZF1_4

Description:

myeloid zinc finger 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26594 EPDNEW_H26596 EPDNEW_H26597

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,573,085 - 58,573,145	EPDNEW

RGD ID:

13206031

Promoter ID:

EPDNEW_H26596

Type:

initiation region

Name:

MZF1_2

Description:

myeloid zinc finger 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26594 EPDNEW_H26595 EPDNEW_H26597

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,573,315 - 58,573,375	EPDNEW

RGD ID:

13206033

Promoter ID:

EPDNEW_H26597

Type:

initiation region

Name:

MZF1_1

Description:

myeloid zinc finger 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26594 EPDNEW_H26595 EPDNEW_H26596

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,573,511 - 58,573,571	EPDNEW

RGD ID:

6811683

Promoter ID:

HG_ACW:42870

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562, Lymphoblastoid

Transcripts:

MZF1.GAPR07-UNSPLICED

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	63,766,231 - 63,766,731 (-)	MPROMDB

RGD ID:

6795829

Promoter ID:

HG_KWN:31255

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_003422, NM_198055, UC010EUU.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	63,775,946 - 63,776,797 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:13108	AgrOrtholog
COSMIC	MZF1	COSMIC
Ensembl Genes	ENSG00000099326	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000215057	ENTREZGENE
	ENST00000215057.7	UniProtKB/Swiss-Prot
	ENST00000594108.1	UniProtKB/TrEMBL
	ENST00000594234	ENTREZGENE
	ENST00000594234.5	UniProtKB/Swiss-Prot
	ENST00000596039.1	UniProtKB/TrEMBL
	ENST00000599369	ENTREZGENE
	ENST00000599369.5	UniProtKB/Swiss-Prot
Gene3D-CATH	1.10.4020.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Classic Zinc Finger	UniProtKB/Swiss-Prot
GTEx	ENSG00000099326	GTEx
HGNC ID	HGNC:13108	ENTREZGENE
Human Proteome Map	MZF1	Human Proteome Map
InterPro	SCAN_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SCAN_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_C2H2_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_type	UniProtKB/Swiss-Prot
KEGG Report	hsa:7593	UniProtKB/Swiss-Prot
NCBI Gene	7593	ENTREZGENE
OMIM	194550	OMIM
PANTHER	PROTEIN ZBED8-RELATED	UniProtKB/TrEMBL
	REDUCED EXPRESSION 2-RELATED	UniProtKB/Swiss-Prot
	SCAN BOX DOMAIN-CONTAINING PROTEIN	UniProtKB/TrEMBL
	ZINC FINGER PROTEIN 200	UniProtKB/Swiss-Prot
Pfam	SCAN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	zf-C2H2	UniProtKB/Swiss-Prot
PharmGKB	PA37683	PharmGKB
PROSITE	SCAN_BOX	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot
SMART	SCAN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZnF_C2H2	UniProtKB/Swiss-Prot
Superfamily-SCOP	Retrovirus capsid dimerization domain-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF57667	UniProtKB/Swiss-Prot
UniProt	M0QXU0	ENTREZGENE
	M0R1U5	ENTREZGENE, UniProtKB/TrEMBL
	M0R2C0_HUMAN	UniProtKB/TrEMBL
	MZF1_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
	Q7Z729	ENTREZGENE
	Q96I71	ENTREZGENE
	Q9NRY0	ENTREZGENE
	Q9UBW2	ENTREZGENE
UniProt Secondary	M0QXU0	UniProtKB/Swiss-Prot
	Q7Z729	UniProtKB/Swiss-Prot
	Q96I71	UniProtKB/Swiss-Prot
	Q9NRY0	UniProtKB/Swiss-Prot
	Q9UBW2	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