ZNF574 (zinc finger protein 574) - Rat Genome Database

Name: ZNF574
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: ZNF574 (zinc finger protein 574) Homo sapiens

Analyze

Symbol:

ZNF574

Name:

zinc finger protein 574

RGD ID:

1322875

HGNC Page

HGNC:26166

Description:

Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FLJ22059; FP972

RGD Orthologs

Alliance Orthologs

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):	Zfp574 (zinc finger protein 574)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Zfp574 (zinc finger protein 574)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, Panther, PhylomeDB
Chinchilla lanigera (long-tailed chinchilla):	Znf574 (zinc finger protein 574)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	ZNF574 (zinc finger protein 574)	NCBI	Ortholog
Canis lupus familiaris (dog):	ZNF574 (zinc finger protein 574)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Znf574 (zinc finger protein 574)	NCBI	Ortholog
Sus scrofa (pig):	ZNF574 (zinc finger protein 574)	HGNC	Ensembl, NCBI, OrthoDB
Chlorocebus sabaeus (green monkey):	ZNF574 (zinc finger protein 574)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Znf574 (zinc finger protein 574)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Klhdc2 (kelch domain containing 2)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Zfp574 (zinc finger protein 574)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Zfp574 (zinc finger protein 574)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	znf574 (zinc finger protein 574)	Alliance	DIOPT (ZFIN)
Danio rerio (zebrafish):	znf526 (zinc finger protein 526)	Alliance	DIOPT (Hieranoid\|InParanoid\|OrthoInspector\|PANTHER\|SonicParanoid)
Caenorhabditis elegans (roundworm):	Y48G8AL.10	Alliance	DIOPT (Ensembl Compara\|InParanoid\|PANTHER)
Drosophila melanogaster (fruit fly):	mld	Alliance	DIOPT (Ensembl Compara\|PANTHER)
Xenopus tropicalis (tropical clawed frog):	znf574	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	znf574.S	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	znf574.L	Alliance	DIOPT (Xenbase)

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	42,068,477 - 42,081,552 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	42,068,477 - 42,081,552 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	42,572,629 - 42,585,704 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	47,272,130 - 47,277,559 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	47,266,357 - 47,277,541	NCBI
Celera	19	39,379,908 - 39,385,337 (+)	NCBI		Celera
Cytogenetic Map	19	q13.2	NCBI
HuRef	19	39,012,215 - 39,016,635 (+)	NCBI		HuRef
CHM1_1	19	42,581,940 - 42,587,369 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	44,887,841 - 44,900,921 (+)	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

Carpenter Syndrome 2 (IAGP)

congenital hypoplastic anemia (IAGP)

COVID-19 (HEP)

craniosynostosis (IAGP)

Diamond-Blackfan anemia (IAGP)

maple syrup urine disease (IAGP)

schizophrenia (IAGP)

syndromic intellectual disability (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(-)-epigallocatechin 3-gallate (EXP)

(1->4)-beta-D-glucan (ISO)

1,2-dimethylhydrazine (ISO)

2,4-dinitrotoluene (ISO)

2,6-dinitrotoluene (ISO)

2-palmitoylglycerol (EXP)

4-hydroxyphenyl retinamide (ISO)

antirheumatic drug (EXP)

aristolochic acid A (EXP)

arsane (EXP)

arsenic atom (EXP)

bisphenol A (ISO)

C60 fullerene (ISO)

cadmium dichloride (ISO)

CGP 52608 (EXP)

chlorpyrifos (ISO)

choline (ISO)

cyclosporin A (EXP)

diuron (EXP)

doxorubicin (EXP)

erythromycin estolate (ISO)

fenthion (ISO)

folic acid (ISO)

FR900359 (EXP)

irinotecan (EXP)

L-methionine (ISO)

perfluorohexanesulfonic acid (ISO)

perfluorooctane-1-sulfonic acid (ISO)

pirinixic acid (ISO)

potassium chloride (EXP)

potassium chromate (EXP)

resveratrol (EXP)

rotenone (ISO)

trovafloxacin (ISO)

valproic acid (EXP)

vinclozolin (ISO)

zinc atom (EXP)

zinc(0) (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

positive regulation of transcription by RNA polymerase II (IEA)

regulation of transcription by RNA polymerase II (IBA)

Cellular Component

nucleus (IBA,IEA)

Molecular Function

DNA binding (IEA)

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

metal ion binding (IEA)

protein binding (IPI)

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

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Congenital hypoplastic anemia (IAGP)

Schizophrenia (IAGP)

References

References - curated

#	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.	Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.	Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
4.	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.

Additional References at PubMed

PMID:8125298	PMID:14702039	PMID:15489334	PMID:16344560	PMID:16964243	PMID:21244100	PMID:21832049	PMID:21873635	PMID:22898364	PMID:24778252	PMID:25693804	PMID:25921289
PMID:26186194	PMID:26471122	PMID:26496610	PMID:27114453	PMID:27503909	PMID:28514442	PMID:29180619	PMID:29507755	PMID:29509190	PMID:30033366	PMID:31091453	PMID:31527615
PMID:31753913	PMID:32296183	PMID:32694731	PMID:32807901	PMID:33961781	PMID:34373451	PMID:34921745	PMID:35509820	PMID:35563538	PMID:35944360	PMID:36197766	PMID:36244648
PMID:36537216	PMID:36724073	PMID:37827155

Genomics

Comparative Map Data

ZNF574
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	42,068,477 - 42,081,552 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	42,068,477 - 42,081,552 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	42,572,629 - 42,585,704 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	47,272,130 - 47,277,559 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	47,266,357 - 47,277,541	NCBI
Celera	19	39,379,908 - 39,385,337 (+)	NCBI		Celera
Cytogenetic Map	19	q13.2	NCBI
HuRef	19	39,012,215 - 39,016,635 (+)	NCBI		HuRef
CHM1_1	19	42,581,940 - 42,587,369 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	44,887,841 - 44,900,921 (+)	NCBI		T2T-CHM13v2.0

Zfp574
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	7	24,775,099 - 24,782,917 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	7	24,771,992 - 24,782,917 (+)	Ensembl		GRCm39 Ensembl
GRCm38	7	25,075,674 - 25,083,492 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	7	25,072,567 - 25,083,492 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	7	25,862,224 - 25,868,511 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	7	24,786,044 - 24,791,240 (+)	NCBI		MGSCv36	mm8
Celera	7	19,693,100 - 19,699,435 (+)	NCBI		Celera
Cytogenetic Map	7	A3	NCBI
cM Map	7	13.73	NCBI

Zfp574
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	89,798,412 - 89,805,490 (+)	NCBI		GRCr8
mRatBN7.2	1	80,667,984 - 80,678,257 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	80,664,259 - 80,679,427 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	86,064,885 - 86,070,148 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	94,615,747 - 94,621,010 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	87,820,653 - 87,825,916 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	81,952,067 - 81,957,330 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	81,952,067 - 81,957,329 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	83,212,053 - 83,217,315 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	80,390,353 - 80,395,599 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	1	80,468,463 - 80,473,709 (+)	NCBI
Celera	1	75,117,588 - 75,122,851 (+)	NCBI		Celera
Cytogenetic Map	1	q21	NCBI

Znf574
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955555	798,779 - 804,608 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955555	798,779 - 804,608 (-)	NCBI	ChiLan1.0	ChiLan1.0

ZNF574
(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	48,178,971 - 48,185,537 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	19	50,047,579 - 50,054,145 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	19	38,962,843 - 38,968,286 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	19	47,547,089 - 47,560,710 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	19	47,547,382 - 47,560,710 (+)	Ensembl	panpan1.1		panPan2

ZNF574
(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	112,261,547 - 112,266,706 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
Dog10K_Boxer_Tasha	1	111,691,922 - 111,702,991 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	1	112,879,173 - 112,890,242 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	1	112,879,173 - 112,890,337 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	1	112,432,589 - 112,443,659 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	1	112,069,070 - 112,080,121 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	1	112,995,319 - 113,006,393 (-)	NCBI		UU_Cfam_GSD_1.0

Znf574
(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	16,053,845 - 16,060,034 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936706	401,447 - 404,140 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936706	401,188 - 406,481 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZNF574
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1	6	49,834,647 - 49,844,563 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	6	45,836,135 - 45,839,206 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ZNF574
(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	36,273,756 - 36,284,968 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	6	36,282,007 - 36,284,697 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666073	14,516,217 - 14,527,388 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Znf574
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624907	643,752 - 649,465 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624907	643,752 - 649,486 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ZNF574
46 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 19q13.2-13.31(chr19:41930894-43141456)x1	copy number loss	See cases [RCV000053975]	Chr19:41930894..43141456 [GRCh38] Chr19:42514712..43645608 [GRCh37] Chr19:47126886..48337448 [NCBI36] Chr19:19q13.2-13.31	pathogenic
GRCh38/hg38 19q13.12-13.2(chr19:37319377-42738688)x3	copy number gain	See cases [RCV000050636]	Chr19:37319377..42738688 [GRCh38] Chr19:37810279..43242840 [GRCh37] Chr19:42502119..47934680 [NCBI36] Chr19:19q13.12-13.2	pathogenic
NM_022752.5(ZNF574):c.955C>T (p.Leu319Phe)	single nucleotide variant	Malignant melanoma [RCV000072174]	Chr19:42079561 [GRCh38] Chr19:42583713 [GRCh37] Chr19:47275553 [NCBI36] Chr19:19q13.2	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
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 19q13.2(chr19:42380680-42738966)x3	copy number gain	See cases [RCV000448991]	Chr19:42380680..42738966 [GRCh37] Chr19:19q13.2	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
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
Single allele	duplication	Schizophrenia [RCV000754211]	Chr19:41608672..44315856 [GRCh38] Chr19:19q13.2-13.31	likely pathogenic
GRCh37/hg19 19q13.2(chr19:42553198-42580706)x1	copy number loss	not provided [RCV000752693]	Chr19:42553198..42580706 [GRCh37] Chr19:19q13.2	benign
GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	copy number gain	not provided [RCV000845733]	Chr19:28271106..49213832 [GRCh37] Chr19:19q11-13.33	pathogenic
GRCh38/hg38 19q13.2(chr19:41987984-42252574)x1	copy number loss	Syndromic intellectual disability [RCV001374690]	Chr19:41987984..42252574 [GRCh38] Chr19:19q13.2	pathogenic
NC_000019.10:g.41952441_42266625del	deletion	Syndromic craniosynostosis [RCV001374686]	Chr19:41952441..42266625 [GRCh38] Chr19:19q13.2	pathogenic
NC_000019.10:g.41983952_42247520del	deletion	Syndromic intellectual disability [RCV001374687]	Chr19:41983952..42247520 [GRCh38] Chr19:19q13.2	pathogenic
NC_000019.10:g.42032860_42297536del	deletion	Syndromic craniosynostosis [RCV001374689]	Chr19:42032860..42297536 [GRCh38] Chr19:19q13.2	pathogenic
NM_022752.6(ZNF574):c.1955G>A (p.Arg652Gln)	single nucleotide variant	not specified [RCV004083865]	Chr19:42080561 [GRCh38] Chr19:42584713 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2117G>A (p.Arg706Gln)	single nucleotide variant	not specified [RCV004126721]	Chr19:42080723 [GRCh38] Chr19:42584875 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2621C>T (p.Ala874Val)	single nucleotide variant	not specified [RCV004088868]	Chr19:42081227 [GRCh38] Chr19:42585379 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1163C>T (p.Pro388Leu)	single nucleotide variant	not specified [RCV004086118]	Chr19:42079769 [GRCh38] Chr19:42583921 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1400G>A (p.Arg467His)	single nucleotide variant	not specified [RCV004077164]	Chr19:42080006 [GRCh38] Chr19:42584158 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.934T>C (p.Ser312Pro)	single nucleotide variant	not specified [RCV004173378]	Chr19:42079540 [GRCh38] Chr19:42583692 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1546A>G (p.Thr516Ala)	single nucleotide variant	not specified [RCV004238713]	Chr19:42080152 [GRCh38] Chr19:42584304 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1760G>A (p.Arg587His)	single nucleotide variant	not specified [RCV004201823]	Chr19:42080366 [GRCh38] Chr19:42584518 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.595G>A (p.Ala199Thr)	single nucleotide variant	not specified [RCV004069678]	Chr19:42079201 [GRCh38] Chr19:42583353 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1399C>T (p.Arg467Cys)	single nucleotide variant	not specified [RCV004214168]	Chr19:42080005 [GRCh38] Chr19:42584157 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.724C>T (p.Pro242Ser)	single nucleotide variant	not specified [RCV004117035]	Chr19:42079330 [GRCh38] Chr19:42583482 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1562G>A (p.Arg521Gln)	single nucleotide variant	not specified [RCV004118994]	Chr19:42080168 [GRCh38] Chr19:42584320 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.718C>T (p.Pro240Ser)	single nucleotide variant	not specified [RCV004108792]	Chr19:42079324 [GRCh38] Chr19:42583476 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1655G>C (p.Arg552Pro)	single nucleotide variant	not specified [RCV004218295]	Chr19:42080261 [GRCh38] Chr19:42584413 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.929T>G (p.Phe310Cys)	single nucleotide variant	not specified [RCV004133505]	Chr19:42079535 [GRCh38] Chr19:42583687 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1481G>A (p.Arg494His)	single nucleotide variant	not specified [RCV004138146]	Chr19:42080087 [GRCh38] Chr19:42584239 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1949G>A (p.Arg650Gln)	single nucleotide variant	not specified [RCV004205876]	Chr19:42080555 [GRCh38] Chr19:42584707 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1298G>A (p.Gly433Asp)	single nucleotide variant	not specified [RCV004192448]	Chr19:42079904 [GRCh38] Chr19:42584056 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2561A>G (p.Gln854Arg)	single nucleotide variant	not specified [RCV004180132]	Chr19:42081167 [GRCh38] Chr19:42585319 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.304A>C (p.Met102Leu)	single nucleotide variant	not specified [RCV004091909]	Chr19:42078910 [GRCh38] Chr19:42583062 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2203C>T (p.Arg735Cys)	single nucleotide variant	not specified [RCV004088682]	Chr19:42080809 [GRCh38] Chr19:42584961 [GRCh37] Chr19:19q13.2	uncertain significance
NC_000019.9:g.(?_39904727)_(42931301_?)dup	duplication	Diamond-Blackfan anemia [RCV003122291]\|MEGF8-related Carpenter syndrome [RCV003105286]\|Maple syrup urine disease [RCV003105287]\|TWIST1-related craniosynostosis [RCV003105285]	Chr19:39904727..42931301 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2473C>T (p.Pro825Ser)	single nucleotide variant	not specified [RCV004284994]	Chr19:42081079 [GRCh38] Chr19:42585231 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2527A>G (p.Thr843Ala)	single nucleotide variant	not specified [RCV004274767]	Chr19:42081133 [GRCh38] Chr19:42585285 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2189C>T (p.Ala730Val)	single nucleotide variant	not specified [RCV004260751]	Chr19:42080795 [GRCh38] Chr19:42584947 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2122C>T (p.Pro708Ser)	single nucleotide variant	not specified [RCV004316154]	Chr19:42080728 [GRCh38] Chr19:42584880 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1502G>C (p.Gly501Ala)	single nucleotide variant	not specified [RCV004263095]	Chr19:42080108 [GRCh38] Chr19:42584260 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1816C>T (p.Pro606Ser)	single nucleotide variant	not specified [RCV004273920]	Chr19:42080422 [GRCh38] Chr19:42584574 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.299A>G (p.Lys100Arg)	single nucleotide variant	not specified [RCV004257579]	Chr19:42078905 [GRCh38] Chr19:42583057 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1457G>A (p.Arg486His)	single nucleotide variant	not specified [RCV004253112]	Chr19:42080063 [GRCh38] Chr19:42584215 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2107C>T (p.Pro703Ser)	single nucleotide variant	not specified [RCV004321768]	Chr19:42080713 [GRCh38] Chr19:42584865 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1909C>T (p.Arg637Cys)	single nucleotide variant	not specified [RCV004292176]	Chr19:42080515 [GRCh38] Chr19:42584667 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1910G>A (p.Arg637His)	single nucleotide variant	not specified [RCV004315747]	Chr19:42080516 [GRCh38] Chr19:42584668 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.536T>C (p.Val179Ala)	single nucleotide variant	not specified [RCV004330867]	Chr19:42079142 [GRCh38] Chr19:42583294 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.143G>A (p.Gly48Asp)	single nucleotide variant	not specified [RCV004328591]	Chr19:42078749 [GRCh38] Chr19:42582901 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1793G>A (p.Arg598His)	single nucleotide variant	not specified [RCV004322865]	Chr19:42080399 [GRCh38] Chr19:42584551 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2150C>T (p.Ser717Phe)	single nucleotide variant	not specified [RCV004290303]	Chr19:42080756 [GRCh38] Chr19:42584908 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.434G>A (p.Arg145Gln)	single nucleotide variant	not specified [RCV004324064]	Chr19:42079040 [GRCh38] Chr19:42583192 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.592G>T (p.Ala198Ser)	single nucleotide variant	not specified [RCV004305988]	Chr19:42079198 [GRCh38] Chr19:42583350 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.593C>T (p.Ala198Val)	single nucleotide variant	not specified [RCV004305989]	Chr19:42079199 [GRCh38] Chr19:42583351 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.872G>A (p.Arg291His)	single nucleotide variant	not specified [RCV004345942]	Chr19:42079478 [GRCh38] Chr19:42583630 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.154C>G (p.Pro52Ala)	single nucleotide variant	not specified [RCV004364938]	Chr19:42078760 [GRCh38] Chr19:42582912 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1268C>T (p.Thr423Ile)	single nucleotide variant	not specified [RCV004494723]	Chr19:42079874 [GRCh38] Chr19:42584026 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1289C>G (p.Pro430Arg)	single nucleotide variant	not specified [RCV004494724]	Chr19:42079895 [GRCh38] Chr19:42584047 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1414A>G (p.Ser472Gly)	single nucleotide variant	not specified [RCV004494726]	Chr19:42080020 [GRCh38] Chr19:42584172 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2558G>A (p.Arg853Gln)	single nucleotide variant	not specified [RCV004494739]	Chr19:42081164 [GRCh38] Chr19:42585316 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.433C>T (p.Arg145Trp)	single nucleotide variant	not specified [RCV004494740]	Chr19:42079039 [GRCh38] Chr19:42583191 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.556G>A (p.Ala186Thr)	single nucleotide variant	not specified [RCV004494742]	Chr19:42079162 [GRCh38] Chr19:42583314 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.578C>T (p.Ala193Val)	single nucleotide variant	not specified [RCV004494743]	Chr19:42079184 [GRCh38] Chr19:42583336 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2069C>T (p.Ala690Val)	single nucleotide variant	not specified [RCV004494735]	Chr19:42080675 [GRCh38] Chr19:42584827 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.166G>A (p.Val56Met)	single nucleotide variant	not specified [RCV004494729]	Chr19:42078772 [GRCh38] Chr19:42582924 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2111C>T (p.Ala704Val)	single nucleotide variant	not specified [RCV004494736]	Chr19:42080717 [GRCh38] Chr19:42584869 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.523G>A (p.Ala175Thr)	single nucleotide variant	not specified [RCV004494741]	Chr19:42079129 [GRCh38] Chr19:42583281 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.850A>G (p.Ile284Val)	single nucleotide variant	not specified [RCV004494745]	Chr19:42079456 [GRCh38] Chr19:42583608 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1343C>T (p.Pro448Leu)	single nucleotide variant	not specified [RCV004494725]	Chr19:42079949 [GRCh38] Chr19:42584101 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1456C>T (p.Arg486Cys)	single nucleotide variant	not specified [RCV004494727]	Chr19:42080062 [GRCh38] Chr19:42584214 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1654C>T (p.Arg552Trp)	single nucleotide variant	not specified [RCV004494728]	Chr19:42080260 [GRCh38] Chr19:42584412 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1855C>T (p.Arg619Cys)	single nucleotide variant	not specified [RCV004494730]	Chr19:42080461 [GRCh38] Chr19:42584613 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.1906C>T (p.His636Tyr)	single nucleotide variant	not specified [RCV004494731]	Chr19:42080512 [GRCh38] Chr19:42584664 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.203A>G (p.Gln68Arg)	single nucleotide variant	not specified [RCV004494733]	Chr19:42078809 [GRCh38] Chr19:42582961 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2042G>A (p.Arg681Gln)	single nucleotide variant	not specified [RCV004494734]	Chr19:42080648 [GRCh38] Chr19:42584800 [GRCh37] Chr19:19q13.2	uncertain significance
NM_022752.6(ZNF574):c.2164G>A (p.Gly722Arg)	single nucleotide variant	not specified [RCV004494737]	Chr19:42080770 [GRCh38] Chr19:42584922 [GRCh37] Chr19:19q13.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1119
Count of miRNA genes:	513
Interacting mature miRNAs:	553
Transcripts:	ENST00000222339, ENST00000359044, ENST00000597391, ENST00000600245
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

SHGC-32127

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	42,585,548 - 42,585,687	UniSTS	GRCh37
Build 36	19	47,277,388 - 47,277,527	RGD	NCBI36
Celera	19	39,385,166 - 39,385,305	RGD
Cytogenetic Map	19	q13.2	UniSTS
HuRef	19	39,016,464 - 39,016,603	UniSTS
TNG Radiation Hybrid Map	19	15846.0	UniSTS
Stanford-G3 RH Map	19	2093.0	UniSTS
GeneMap99-GB4 RH Map	19	242.5	UniSTS
Whitehead-RH Map	19	320.1	UniSTS
NCBI RH Map	19	445.7	UniSTS
GeneMap99-G3 RH Map	19	2104.0	UniSTS

RH11929

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	42,585,480 - 42,585,653	UniSTS	GRCh37
Build 36	19	47,277,320 - 47,277,493	RGD	NCBI36
Celera	19	39,385,098 - 39,385,271	RGD
Cytogenetic Map	19	q13.2	UniSTS
HuRef	19	39,016,396 - 39,016,569	UniSTS
GeneMap99-GB4 RH Map	19	242.6	UniSTS
NCBI RH Map	19	455.9	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

1126

571

366

754

2493

589

1120

155

1162

596

318

1478

Low

1313

2404

1360

575

1183

426

1864

1606

2613

264

298

1017

153

886

1310

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001330519	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_022752	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005259159	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011527228	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011527229	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011527230	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321780	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321781	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321782	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321783	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC022515	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF447880	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK025712	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK027895	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK074788	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK131369	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK131418	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK225342	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL137516	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC001184	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC071962	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471126	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA404303	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KT584177	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000222339 ⟹ ENSP00000222339

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	42,068,477 - 42,081,410 (+)	Ensembl

RefSeq Acc Id:

ENST00000359044 ⟹ ENSP00000351939

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	42,076,166 - 42,081,552 (+)	Ensembl

RefSeq Acc Id:

ENST00000597391 ⟹ ENSP00000471611

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	42,074,671 - 42,078,982 (+)	Ensembl

RefSeq Acc Id:

ENST00000600245 ⟹ ENSP00000469029

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	42,070,366 - 42,081,549 (+)	Ensembl

RefSeq Acc Id:

NM_001330519 ⟹ NP_001317448

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	42,068,477 - 42,081,552 (+)	NCBI
T2T-CHM13v2.0	19	44,887,841 - 44,900,921 (+)	NCBI

Sequence:

show sequence

AGCTGAGGAGGGAGGGACTGAGGAGCCGGGCACCCAGAGTGGATCTGGGGGAAAGAGGTGGAAA
AGTGACAGAGGGAAGACAGCCTCCAAGCTCAGAGGCAGAGAGAGGGAGGAGGACAGGTGAGCGG
AGGCACAGAATAGAAAGAGAAATGGAAAGAGACCTGCCGAGGGAGACTTGGAAAGAGGGAAGCC
AGGGTGGAGGAGTTCTGACAGAGAGAGGGATCTAAACAGAGACATGCCGAGAGCAACCTGGGCT
AACAGCAAAGAGAGAAGTTGGGCAGAGTCAGAGAGGGGCCCAAGAGACACAGGAAATGGGGGCT
CAAAAGCGGAAAGACATATCCAGGAGATAGAGACTGGACGGGGTGGGGACAGGGCCAAGGCCCA
CCGCAGGCAGAGGATGAGGCTCAGAGGAACAGAAAGAGCCAGTCTGGGACCAGGACGGAGGCTT
GGAGACAGCAGGGGCACGGACATGCCAGGGGCCCGGGCCCAGGGCCTTGCTGCCGCCATGACTG
AGGAATCAGAGGAGACAGTCCTGTACATTGAGCACCGCTATGTCTGCTCTGAGTGCAACCAGCT
GTATGGATCACTGGAAGAGGTGCTTATGCACCAAAACTCCCACGTGCCCCAGCAGCACTTTGAG
CTGGTGGGCGTGGCTGATCCCGGAGTCACTGTGGCCACAGACACAGCTTCAGGCACGGGCCTCT
ATCAGACCCTTGTGCAGGAGAGCCAGTACCAGTGCCTGGAGTGTGGTCAACTGCTGATGTCACC
CAGCCAGCTCCTGGAGCACCAGGAGCTGCACCTGAAGATGATGGCACCCCAGGAGGCAGTGCCA
GCTGAGCCATCACCTAAGGCACCACCCCTGAGCTCCAGCACCATCCACTACGAGTGTGTGGATT
GCAAGGCTCTCTTTGCCAGCCAGGAGCTCTGGCTGAACCACCGGCAGACGCACCTCCGGGCCAC
ACCCACCAAGGCTCCTGCCCCTGTTGTCCTGGGGTCCCCAGTTGTTCTAGGGCCTCCTGTGGGC
CAGGCCCGAGTGGCTGTGGAGCACTCATACCGAAAGGCAGAAGAGGGTGGGGAAGGGGCGACTG
TCCCATCTGCCGCTGCCACCACCACTGAGGTAGTGACTGAGGTGGAGCTGCTCCTCTACAAGTG
CTCTGAGTGCTCCCAGCTCTTCCAGCTGCCGGCGGATTTCCTGGAGCACCAGGCCACTCACTTC
CCTGCTCCTGTACCCGAGTCTCAGGAGCCTGCCTTACAGCAGGAGGTGCAGGCCTCGTCACCTG
CAGAGGTGCCTGTGTCTCAGCCTGACCCCTTGCCAGCTTCTGACCACAGTTACGAGCTGCGCAA
TGGTGAAGCCATTGGGCGGGATCGCCGGGGGCGCAGGGCCCGGAGGAACAACAGTGGAGAAGCA
GGCGGGGCAGCCACACAGGAGCTCTTCTGCTCAGCCTGTGACCAGCTCTTTCTCTCACCCCACC
AGCTACAGCAGCACCTGCGGAGTCACCGGGAGGGCGTCTTTAAGTGCCCCCTGTGCAGTCGTGT
CTTCCCTAGCCCTTCCAGTCTGGACCAGCACCTTGGAGACCATAGCAGCGAGTCACACTTCCTG
TGTGTAGACTGTGGCCTGGCCTTCGGCACAGAGGCCCTCCTCCTGGCCCACCGGCGAGCCCACA
CCCCGAATCCTCTGCATTCATGTCCATGTGGGAAGACCTTTGTCAACCTTACCAAGTTCCTTTA
TCACCGGCGTACTCATGGGGTAGGGGGTGTCCCTCTGCCCACAACACCAGTCCCACCAGAGGAA
CCTGTCATTGGTTTCCCTGAGCCAGCCCCAGCAGAGACTGGAGAGCCAGAGGCCCCTGAGCCCC
CTGTGTCTGAGGAGACCTCAGCAGGGCCCGCTGCCCCAGGCACCTACCGCTGCCTCCTGTGCAG
CCGTGAATTTGGAAAGGCCTTGCAGCTGACCCGGCACCAACGTTTTGTGCATCGGCTGGAGCGG
CGCCATAAATGCAGCATTTGTGGCAAGATGTTCAAGAAGAAGTCTCACGTGCGTAACCACCTGC
GCACACACACAGGGGAGCGGCCCTTCCCCTGCCCTGACTGCTCCAAGCCCTTCAACTCACCTGC
CAACCTGGCCCGCCACCGGCTCACACACACAGGAGAGCGGCCCTACCGGTGTGGGGACTGTGGC
AAGGCTTTCACGCAAAGCTCCACACTGAGGCAGCACCGCTTGGTGCATGCCCAGCACTTCCCCT
ACCGCTGCCAGGAATGTGGGGTGCGTTTTCACCGTCCTTACCGCCTGCTCATGCACCGCTACCA
TCACACAGGTGAATACCCCTACAAGTGTCGCGAGTGCCCCCGCTCCTTCTTGCTGCGTCGGCTG
CTGGAGGTGCACCAGCTCGTGGTCCATGCCGGGCGCCAGCCCCACCGCTGCCCATCCTGTGGGG
CTGCCTTCCCCTCCTCACTGCGGCTCCGGGAGCACCGCTGTGCAGCCGCTGCTGCCCAGGCCCC
ACGGCGCTTTGAGTGTGGCACCTGTGGCAAGAAAGTGGGCTCAGCTGCTCGACTGCAGGCACAC
GAGGCGGCCCATGCAGCTGCTGGGCCTGGAGAGGTCCTGGCTAAGGAGCCCCCTGCCCCTCGAG
CCCCACGGGCCACTCGTGCACCAGTTGCCTCTCCAGCAGCCCTTGGAAGCACTGCTACAGCATC
CCCTGCGGCCCCTGCCCGCCGCCGGGGTCTAGAGTGCAGCGAGTGCAAGAAGCTGTTCAGCACA
GAGACGTCACTGCAGGTGCACCGGCGCATCCACACAGGTGAGCGGCCATACCCATGTCCAGACT
GTGGCAAAGCGTTCCGTCAGAGTACCCACCTGAAAGACCACCGGCGCCTGCACACAGGTGAGCG
GCCCTTTGCCTGTGAAGTGTGTGGCAAGGCCTTTGCCATCTCCATGCGCCTGGCAGAACATCGC
CGCATCCACACAGGCGAACGACCCTACTCCTGCCCTGACTGTGGCAAGAGCTACCGCTCCTTCT
CCAACCTCTGGAAGCACCGCAAGACCCATCAGCAGCAGCATCAGGCAGCTGTGCGGCAGCAGCT
GGCAGAGGCGGAGGCTGCCGTTGGCCTGGCCGTCATGGAGACTGCTGTGGAGGCGCTACCCCTG
GTGGAAGCCATTGAGATCTACCCTCTGGCCGAGGCTGAGGGGGTCCAGATCAGTGGCTGACTCT
GCCCGACTTCCTCTTTGGCACCTCCATTCCCTGTTGCTGAAGGCCCTCCAGCATCCCCTTAAGC
ATCTGTACATACTGTGTCCCTTCCTCTTCCCATCCCCACCACCTTGTAAGTTCTAAATTGGATT
TATTCTCTCGTGAGGGGGGTGCTCTGGGGTCCTTGACACACATAAAGGTGCCCCCCCACCTTCC
ACCTCTTAGCACTGGTGACCCCAAAAATGAAACCATCAATAAAGACTGAGTTGCCAGCA

hide sequence

RefSeq Acc Id:

NM_022752 ⟹ NP_073589

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	42,076,166 - 42,081,552 (+)	NCBI
GRCh37	19	42,579,057 - 42,585,719 (+)	NCBI
Build 36	19	47,272,130 - 47,277,559 (+)	NCBI Archive
Celera	19	39,379,908 - 39,385,337 (+)	RGD
HuRef	19	39,012,215 - 39,016,635 (+)	RGD
CHM1_1	19	42,581,940 - 42,587,369 (+)	NCBI
T2T-CHM13v2.0	19	44,895,535 - 44,900,921 (+)	NCBI

Sequence:

show sequence

GAGAGCGAGGCTACGGAGCAGGCGAGAGGCGACGGCGAGAGCTAGAGCGGGCGCAGCGTTAGGG
TGGCCGTGCAAGGGGAGCCGTGGCCCGGGCCCGGGGCGTGCGAGACGGCGGAAGCAGCCCAGGG
CCTTGCTGCCGCCATGACTGAGGAATCAGAGGAGACAGTCCTGTACATTGAGCACCGCTATGTC
TGCTCTGAGTGCAACCAGCTGTATGGATCACTGGAAGAGGTGCTTATGCACCAAAACTCCCACG
TGCCCCAGCAGCACTTTGAGCTGGTGGGCGTGGCTGATCCCGGAGTCACTGTGGCCACAGACAC
AGCTTCAGGCACGGGCCTCTATCAGACCCTTGTGCAGGAGAGCCAGTACCAGTGCCTGGAGTGT
GGTCAACTGCTGATGTCACCCAGCCAGCTCCTGGAGCACCAGGAGCTGCACCTGAAGATGATGG
CACCCCAGGAGGCAGTGCCAGCTGAGCCATCACCTAAGGCACCACCCCTGAGCTCCAGCACCAT
CCACTACGAGTGTGTGGATTGCAAGGCTCTCTTTGCCAGCCAGGAGCTCTGGCTGAACCACCGG
CAGACGCACCTCCGGGCCACACCCACCAAGGCTCCTGCCCCTGTTGTCCTGGGGTCCCCAGTTG
TTCTAGGGCCTCCTGTGGGCCAGGCCCGAGTGGCTGTGGAGCACTCATACCGAAAGGCAGAAGA
GGGTGGGGAAGGGGCGACTGTCCCATCTGCCGCTGCCACCACCACTGAGGTAGTGACTGAGGTG
GAGCTGCTCCTCTACAAGTGCTCTGAGTGCTCCCAGCTCTTCCAGCTGCCGGCGGATTTCCTGG
AGCACCAGGCCACTCACTTCCCTGCTCCTGTACCCGAGTCTCAGGAGCCTGCCTTACAGCAGGA
GGTGCAGGCCTCGTCACCTGCAGAGGTGCCTGTGTCTCAGCCTGACCCCTTGCCAGCTTCTGAC
CACAGTTACGAGCTGCGCAATGGTGAAGCCATTGGGCGGGATCGCCGGGGGCGCAGGGCCCGGA
GGAACAACAGTGGAGAAGCAGGCGGGGCAGCCACACAGGAGCTCTTCTGCTCAGCCTGTGACCA
GCTCTTTCTCTCACCCCACCAGCTACAGCAGCACCTGCGGAGTCACCGGGAGGGCGTCTTTAAG
TGCCCCCTGTGCAGTCGTGTCTTCCCTAGCCCTTCCAGTCTGGACCAGCACCTTGGAGACCATA
GCAGCGAGTCACACTTCCTGTGTGTAGACTGTGGCCTGGCCTTCGGCACAGAGGCCCTCCTCCT
GGCCCACCGGCGAGCCCACACCCCGAATCCTCTGCATTCATGTCCATGTGGGAAGACCTTTGTC
AACCTTACCAAGTTCCTTTATCACCGGCGTACTCATGGGGTAGGGGGTGTCCCTCTGCCCACAA
CACCAGTCCCACCAGAGGAACCTGTCATTGGTTTCCCTGAGCCAGCCCCAGCAGAGACTGGAGA
GCCAGAGGCCCCTGAGCCCCCTGTGTCTGAGGAGACCTCAGCAGGGCCCGCTGCCCCAGGCACC
TACCGCTGCCTCCTGTGCAGCCGTGAATTTGGAAAGGCCTTGCAGCTGACCCGGCACCAACGTT
TTGTGCATCGGCTGGAGCGGCGCCATAAATGCAGCATTTGTGGCAAGATGTTCAAGAAGAAGTC
TCACGTGCGTAACCACCTGCGCACACACACAGGGGAGCGGCCCTTCCCCTGCCCTGACTGCTCC
AAGCCCTTCAACTCACCTGCCAACCTGGCCCGCCACCGGCTCACACACACAGGAGAGCGGCCCT
ACCGGTGTGGGGACTGTGGCAAGGCTTTCACGCAAAGCTCCACACTGAGGCAGCACCGCTTGGT
GCATGCCCAGCACTTCCCCTACCGCTGCCAGGAATGTGGGGTGCGTTTTCACCGTCCTTACCGC
CTGCTCATGCACCGCTACCATCACACAGGTGAATACCCCTACAAGTGTCGCGAGTGCCCCCGCT
CCTTCTTGCTGCGTCGGCTGCTGGAGGTGCACCAGCTCGTGGTCCATGCCGGGCGCCAGCCCCA
CCGCTGCCCATCCTGTGGGGCTGCCTTCCCCTCCTCACTGCGGCTCCGGGAGCACCGCTGTGCA
GCCGCTGCTGCCCAGGCCCCACGGCGCTTTGAGTGTGGCACCTGTGGCAAGAAAGTGGGCTCAG
CTGCTCGACTGCAGGCACACGAGGCGGCCCATGCAGCTGCTGGGCCTGGAGAGGTCCTGGCTAA
GGAGCCCCCTGCCCCTCGAGCCCCACGGGCCACTCGTGCACCAGTTGCCTCTCCAGCAGCCCTT
GGAAGCACTGCTACAGCATCCCCTGCGGCCCCTGCCCGCCGCCGGGGTCTAGAGTGCAGCGAGT
GCAAGAAGCTGTTCAGCACAGAGACGTCACTGCAGGTGCACCGGCGCATCCACACAGGTGAGCG
GCCATACCCATGTCCAGACTGTGGCAAAGCGTTCCGTCAGAGTACCCACCTGAAAGACCACCGG
CGCCTGCACACAGGTGAGCGGCCCTTTGCCTGTGAAGTGTGTGGCAAGGCCTTTGCCATCTCCA
TGCGCCTGGCAGAACATCGCCGCATCCACACAGGCGAACGACCCTACTCCTGCCCTGACTGTGG
CAAGAGCTACCGCTCCTTCTCCAACCTCTGGAAGCACCGCAAGACCCATCAGCAGCAGCATCAG
GCAGCTGTGCGGCAGCAGCTGGCAGAGGCGGAGGCTGCCGTTGGCCTGGCCGTCATGGAGACTG
CTGTGGAGGCGCTACCCCTGGTGGAAGCCATTGAGATCTACCCTCTGGCCGAGGCTGAGGGGGT
CCAGATCAGTGGCTGACTCTGCCCGACTTCCTCTTTGGCACCTCCATTCCCTGTTGCTGAAGGC
CCTCCAGCATCCCCTTAAGCATCTGTACATACTGTGTCCCTTCCTCTTCCCATCCCCACCACCT
TGTAAGTTCTAAATTGGATTTATTCTCTCGTGAGGGGGGTGCTCTGGGGTCCTTGACACACATA
AAGGTGCCCCCCCACCTTCCACCTCTTAGCACTGGTGACCCCAAAAATGAAACCATCAATAAAG
ACTGAGTTGCCAGCA

hide sequence

RefSeq Acc Id:

XM_005259159 ⟹ XP_005259216

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	42,076,629 - 42,081,552 (+)	NCBI
GRCh37	19	42,579,057 - 42,585,719 (+)	NCBI

Sequence:

show sequence

GTTGATACAGAGCCCAGGGCCTTGCTGCCGCCATGACTGAGGAATCAGAGGAGACAGTCCTGTA
CATTGAGCACCGCTATGTCTGCTCTGAGTGCAACCAGCTGTATGGATCACTGGAAGAGGTGCTT
ATGCACCAAAACTCCCACGTGCCCCAGCAGCACTTTGAGCTGGTGGGCGTGGCTGATCCCGGAG
TCACTGTGGCCACAGACACAGCTTCAGGCACGGGCCTCTATCAGACCCTTGTGCAGGAGAGCCA
GTACCAGTGCCTGGAGTGTGGTCAACTGCTGATGTCACCCAGCCAGCTCCTGGAGCACCAGGAG
CTGCACCTGAAGATGATGGCACCCCAGGAGGCAGTGCCAGCTGAGCCATCACCTAAGGCACCAC
CCCTGAGCTCCAGCACCATCCACTACGAGTGTGTGGATTGCAAGGCTCTCTTTGCCAGCCAGGA
GCTCTGGCTGAACCACCGGCAGACGCACCTCCGGGCCACACCCACCAAGGCTCCTGCCCCTGTT
GTCCTGGGGTCCCCAGTTGTTCTAGGGCCTCCTGTGGGCCAGGCCCGAGTGGCTGTGGAGCACT
CATACCGAAAGGCAGAAGAGGGTGGGGAAGGGGCGACTGTCCCATCTGCCGCTGCCACCACCAC
TGAGGTAGTGACTGAGGTGGAGCTGCTCCTCTACAAGTGCTCTGAGTGCTCCCAGCTCTTCCAG
CTGCCGGCGGATTTCCTGGAGCACCAGGCCACTCACTTCCCTGCTCCTGTACCCGAGTCTCAGG
AGCCTGCCTTACAGCAGGAGGTGCAGGCCTCGTCACCTGCAGAGGTGCCTGTGTCTCAGCCTGA
CCCCTTGCCAGCTTCTGACCACAGTTACGAGCTGCGCAATGGTGAAGCCATTGGGCGGGATCGC
CGGGGGCGCAGGGCCCGGAGGAACAACAGTGGAGAAGCAGGCGGGGCAGCCACACAGGAGCTCT
TCTGCTCAGCCTGTGACCAGCTCTTTCTCTCACCCCACCAGCTACAGCAGCACCTGCGGAGTCA
CCGGGAGGGCGTCTTTAAGTGCCCCCTGTGCAGTCGTGTCTTCCCTAGCCCTTCCAGTCTGGAC
CAGCACCTTGGAGACCATAGCAGCGAGTCACACTTCCTGTGTGTAGACTGTGGCCTGGCCTTCG
GCACAGAGGCCCTCCTCCTGGCCCACCGGCGAGCCCACACCCCGAATCCTCTGCATTCATGTCC
ATGTGGGAAGACCTTTGTCAACCTTACCAAGTTCCTTTATCACCGGCGTACTCATGGGGTAGGG
GGTGTCCCTCTGCCCACAACACCAGTCCCACCAGAGGAACCTGTCATTGGTTTCCCTGAGCCAG
CCCCAGCAGAGACTGGAGAGCCAGAGGCCCCTGAGCCCCCTGTGTCTGAGGAGACCTCAGCAGG
GCCCGCTGCCCCAGGCACCTACCGCTGCCTCCTGTGCAGCCGTGAATTTGGAAAGGCCTTGCAG
CTGACCCGGCACCAACGTTTTGTGCATCGGCTGGAGCGGCGCCATAAATGCAGCATTTGTGGCA
AGATGTTCAAGAAGAAGTCTCACGTGCGTAACCACCTGCGCACACACACAGGGGAGCGGCCCTT
CCCCTGCCCTGACTGCTCCAAGCCCTTCAACTCACCTGCCAACCTGGCCCGCCACCGGCTCACA
CACACAGGAGAGCGGCCCTACCGGTGTGGGGACTGTGGCAAGGCTTTCACGCAAAGCTCCACAC
TGAGGCAGCACCGCTTGGTGCATGCCCAGCACTTCCCCTACCGCTGCCAGGAATGTGGGGTGCG
TTTTCACCGTCCTTACCGCCTGCTCATGCACCGCTACCATCACACAGGTGAATACCCCTACAAG
TGTCGCGAGTGCCCCCGCTCCTTCTTGCTGCGTCGGCTGCTGGAGGTGCACCAGCTCGTGGTCC
ATGCCGGGCGCCAGCCCCACCGCTGCCCATCCTGTGGGGCTGCCTTCCCCTCCTCACTGCGGCT
CCGGGAGCACCGCTGTGCAGCCGCTGCTGCCCAGGCCCCACGGCGCTTTGAGTGTGGCACCTGT
GGCAAGAAAGTGGGCTCAGCTGCTCGACTGCAGGCACACGAGGCGGCCCATGCAGCTGCTGGGC
CTGGAGAGGTCCTGGCTAAGGAGCCCCCTGCCCCTCGAGCCCCACGGGCCACTCGTGCACCAGT
TGCCTCTCCAGCAGCCCTTGGAAGCACTGCTACAGCATCCCCTGCGGCCCCTGCCCGCCGCCGG
GGTCTAGAGTGCAGCGAGTGCAAGAAGCTGTTCAGCACAGAGACGTCACTGCAGGTGCACCGGC
GCATCCACACAGGTGAGCGGCCATACCCATGTCCAGACTGTGGCAAAGCGTTCCGTCAGAGTAC
CCACCTGAAAGACCACCGGCGCCTGCACACAGGTGAGCGGCCCTTTGCCTGTGAAGTGTGTGGC
AAGGCCTTTGCCATCTCCATGCGCCTGGCAGAACATCGCCGCATCCACACAGGCGAACGACCCT
ACTCCTGCCCTGACTGTGGCAAGAGCTACCGCTCCTTCTCCAACCTCTGGAAGCACCGCAAGAC
CCATCAGCAGCAGCATCAGGCAGCTGTGCGGCAGCAGCTGGCAGAGGCGGAGGCTGCCGTTGGC
CTGGCCGTCATGGAGACTGCTGTGGAGGCGCTACCCCTGGTGGAAGCCATTGAGATCTACCCTC
TGGCCGAGGCTGAGGGGGTCCAGATCAGTGGCTGACTCTGCCCGACTTCCTCTTTGGCACCTCC
ATTCCCTGTTGCTGAAGGCCCTCCAGCATCCCCTTAAGCATCTGTACATACTGTGTCCCTTCCT
CTTCCCATCCCCACCACCTTGTAAGTTCTAAATTGGATTTATTCTCTCGTGAGGGGGGTGCTCT
GGGGTCCTTGACACACATAAAGGTGCCCCCCCACCTTCCACCTCTTAGCACTGGTGACCCCAAA
AATGAAACCATCAATAAAGACTGAGTTGCCAGCAGTGTGTAGA

hide sequence

RefSeq Acc Id:

XM_011527228 ⟹ XP_011525530

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	42,074,857 - 42,081,552 (+)	NCBI

Sequence:

show sequence

AATGTTTTGTATTTTTAGTAAAGATGGTAGTTTCACCAGGTTGGCCAGGTGGGTCTCGAATGCC
TGACTTCAAGTGAACCCGCCTCAGCGTCCCAAAATGTTGGGATTGCAGGCGTGAGCCACCACGC
CCAGCCTGGAAACGTTTCTAACAGTACTGGGGCAACTCCCTCCCAAGGCCCTGAGGGGCGCAGG
AACGAGCCCAGGGCCTTGCTGCCGCCATGACTGAGGAATCAGAGGAGACAGTCCTGTACATTGA
GCACCGCTATGTCTGCTCTGAGTGCAACCAGCTGTATGGATCACTGGAAGAGGTGCTTATGCAC
CAAAACTCCCACGTGCCCCAGCAGCACTTTGAGCTGGTGGGCGTGGCTGATCCCGGAGTCACTG
TGGCCACAGACACAGCTTCAGGCACGGGCCTCTATCAGACCCTTGTGCAGGAGAGCCAGTACCA
GTGCCTGGAGTGTGGTCAACTGCTGATGTCACCCAGCCAGCTCCTGGAGCACCAGGAGCTGCAC
CTGAAGATGATGGCACCCCAGGAGGCAGTGCCAGCTGAGCCATCACCTAAGGCACCACCCCTGA
GCTCCAGCACCATCCACTACGAGTGTGTGGATTGCAAGGCTCTCTTTGCCAGCCAGGAGCTCTG
GCTGAACCACCGGCAGACGCACCTCCGGGCCACACCCACCAAGGCTCCTGCCCCTGTTGTCCTG
GGGTCCCCAGTTGTTCTAGGGCCTCCTGTGGGCCAGGCCCGAGTGGCTGTGGAGCACTCATACC
GAAAGGCAGAAGAGGGTGGGGAAGGGGCGACTGTCCCATCTGCCGCTGCCACCACCACTGAGGT
AGTGACTGAGGTGGAGCTGCTCCTCTACAAGTGCTCTGAGTGCTCCCAGCTCTTCCAGCTGCCG
GCGGATTTCCTGGAGCACCAGGCCACTCACTTCCCTGCTCCTGTACCCGAGTCTCAGGAGCCTG
CCTTACAGCAGGAGGTGCAGGCCTCGTCACCTGCAGAGGTGCCTGTGTCTCAGCCTGACCCCTT
GCCAGCTTCTGACCACAGTTACGAGCTGCGCAATGGTGAAGCCATTGGGCGGGATCGCCGGGGG
CGCAGGGCCCGGAGGAACAACAGTGGAGAAGCAGGCGGGGCAGCCACACAGGAGCTCTTCTGCT
CAGCCTGTGACCAGCTCTTTCTCTCACCCCACCAGCTACAGCAGCACCTGCGGAGTCACCGGGA
GGGCGTCTTTAAGTGCCCCCTGTGCAGTCGTGTCTTCCCTAGCCCTTCCAGTCTGGACCAGCAC
CTTGGAGACCATAGCAGCGAGTCACACTTCCTGTGTGTAGACTGTGGCCTGGCCTTCGGCACAG
AGGCCCTCCTCCTGGCCCACCGGCGAGCCCACACCCCGAATCCTCTGCATTCATGTCCATGTGG
GAAGACCTTTGTCAACCTTACCAAGTTCCTTTATCACCGGCGTACTCATGGGGTAGGGGGTGTC
CCTCTGCCCACAACACCAGTCCCACCAGAGGAACCTGTCATTGGTTTCCCTGAGCCAGCCCCAG
CAGAGACTGGAGAGCCAGAGGCCCCTGAGCCCCCTGTGTCTGAGGAGACCTCAGCAGGGCCCGC
TGCCCCAGGCACCTACCGCTGCCTCCTGTGCAGCCGTGAATTTGGAAAGGCCTTGCAGCTGACC
CGGCACCAACGTTTTGTGCATCGGCTGGAGCGGCGCCATAAATGCAGCATTTGTGGCAAGATGT
TCAAGAAGAAGTCTCACGTGCGTAACCACCTGCGCACACACACAGGGGAGCGGCCCTTCCCCTG
CCCTGACTGCTCCAAGCCCTTCAACTCACCTGCCAACCTGGCCCGCCACCGGCTCACACACACA
GGAGAGCGGCCCTACCGGTGTGGGGACTGTGGCAAGGCTTTCACGCAAAGCTCCACACTGAGGC
AGCACCGCTTGGTGCATGCCCAGCACTTCCCCTACCGCTGCCAGGAATGTGGGGTGCGTTTTCA
CCGTCCTTACCGCCTGCTCATGCACCGCTACCATCACACAGGTGAATACCCCTACAAGTGTCGC
GAGTGCCCCCGCTCCTTCTTGCTGCGTCGGCTGCTGGAGGTGCACCAGCTCGTGGTCCATGCCG
GGCGCCAGCCCCACCGCTGCCCATCCTGTGGGGCTGCCTTCCCCTCCTCACTGCGGCTCCGGGA
GCACCGCTGTGCAGCCGCTGCTGCCCAGGCCCCACGGCGCTTTGAGTGTGGCACCTGTGGCAAG
AAAGTGGGCTCAGCTGCTCGACTGCAGGCACACGAGGCGGCCCATGCAGCTGCTGGGCCTGGAG
AGGTCCTGGCTAAGGAGCCCCCTGCCCCTCGAGCCCCACGGGCCACTCGTGCACCAGTTGCCTC
TCCAGCAGCCCTTGGAAGCACTGCTACAGCATCCCCTGCGGCCCCTGCCCGCCGCCGGGGTCTA
GAGTGCAGCGAGTGCAAGAAGCTGTTCAGCACAGAGACGTCACTGCAGGTGCACCGGCGCATCC
ACACAGGTGAGCGGCCATACCCATGTCCAGACTGTGGCAAAGCGTTCCGTCAGAGTACCCACCT
GAAAGACCACCGGCGCCTGCACACAGGTGAGCGGCCCTTTGCCTGTGAAGTGTGTGGCAAGGCC
TTTGCCATCTCCATGCGCCTGGCAGAACATCGCCGCATCCACACAGGCGAACGACCCTACTCCT
GCCCTGACTGTGGCAAGAGCTACCGCTCCTTCTCCAACCTCTGGAAGCACCGCAAGACCCATCA
GCAGCAGCATCAGGCAGCTGTGCGGCAGCAGCTGGCAGAGGCGGAGGCTGCCGTTGGCCTGGCC
GTCATGGAGACTGCTGTGGAGGCGCTACCCCTGGTGGAAGCCATTGAGATCTACCCTCTGGCCG
AGGCTGAGGGGGTCCAGATCAGTGGCTGACTCTGCCCGACTTCCTCTTTGGCACCTCCATTCCC
TGTTGCTGAAGGCCCTCCAGCATCCCCTTAAGCATCTGTACATACTGTGTCCCTTCCTCTTCCC
ATCCCCACCACCTTGTAAGTTCTAAATTGGATTTATTCTCTCGTGAGGGGGGTGCTCTGGGGTC
CTTGACACACATAAAGGTGCCCCCCCACCTTCCACCTCTTAGCACTGGTGACCCCAAAAATGAA
ACCATCAATAAAGACTGAGTTGCCAGCAGTGTGTAGA

hide sequence

RefSeq Acc Id:

XM_011527229 ⟹ XP_011525531

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	42,076,546 - 42,081,552 (+)	NCBI

Sequence:

show sequence

CCTGGGCGGGAAGGGGAGGCCTCAGAGCTGTCCCAAGAGGGCTCCGCGGCTCCCCAGGGTTTGG
GCCCAGGGCCTTGCTGCCGCCATGACTGAGGAATCAGAGGAGACAGTCCTGTACATTGAGCACC
GCTATGTCTGCTCTGAGTGCAACCAGCTGTATGGATCACTGGAAGAGGTGCTTATGCACCAAAA
CTCCCACGTGCCCCAGCAGCACTTTGAGCTGGTGGGCGTGGCTGATCCCGGAGTCACTGTGGCC
ACAGACACAGCTTCAGGCACGGGCCTCTATCAGACCCTTGTGCAGGAGAGCCAGTACCAGTGCC
TGGAGTGTGGTCAACTGCTGATGTCACCCAGCCAGCTCCTGGAGCACCAGGAGCTGCACCTGAA
GATGATGGCACCCCAGGAGGCAGTGCCAGCTGAGCCATCACCTAAGGCACCACCCCTGAGCTCC
AGCACCATCCACTACGAGTGTGTGGATTGCAAGGCTCTCTTTGCCAGCCAGGAGCTCTGGCTGA
ACCACCGGCAGACGCACCTCCGGGCCACACCCACCAAGGCTCCTGCCCCTGTTGTCCTGGGGTC
CCCAGTTGTTCTAGGGCCTCCTGTGGGCCAGGCCCGAGTGGCTGTGGAGCACTCATACCGAAAG
GCAGAAGAGGGTGGGGAAGGGGCGACTGTCCCATCTGCCGCTGCCACCACCACTGAGGTAGTGA
CTGAGGTGGAGCTGCTCCTCTACAAGTGCTCTGAGTGCTCCCAGCTCTTCCAGCTGCCGGCGGA
TTTCCTGGAGCACCAGGCCACTCACTTCCCTGCTCCTGTACCCGAGTCTCAGGAGCCTGCCTTA
CAGCAGGAGGTGCAGGCCTCGTCACCTGCAGAGGTGCCTGTGTCTCAGCCTGACCCCTTGCCAG
CTTCTGACCACAGTTACGAGCTGCGCAATGGTGAAGCCATTGGGCGGGATCGCCGGGGGCGCAG
GGCCCGGAGGAACAACAGTGGAGAAGCAGGCGGGGCAGCCACACAGGAGCTCTTCTGCTCAGCC
TGTGACCAGCTCTTTCTCTCACCCCACCAGCTACAGCAGCACCTGCGGAGTCACCGGGAGGGCG
TCTTTAAGTGCCCCCTGTGCAGTCGTGTCTTCCCTAGCCCTTCCAGTCTGGACCAGCACCTTGG
AGACCATAGCAGCGAGTCACACTTCCTGTGTGTAGACTGTGGCCTGGCCTTCGGCACAGAGGCC
CTCCTCCTGGCCCACCGGCGAGCCCACACCCCGAATCCTCTGCATTCATGTCCATGTGGGAAGA
CCTTTGTCAACCTTACCAAGTTCCTTTATCACCGGCGTACTCATGGGGTAGGGGGTGTCCCTCT
GCCCACAACACCAGTCCCACCAGAGGAACCTGTCATTGGTTTCCCTGAGCCAGCCCCAGCAGAG
ACTGGAGAGCCAGAGGCCCCTGAGCCCCCTGTGTCTGAGGAGACCTCAGCAGGGCCCGCTGCCC
CAGGCACCTACCGCTGCCTCCTGTGCAGCCGTGAATTTGGAAAGGCCTTGCAGCTGACCCGGCA
CCAACGTTTTGTGCATCGGCTGGAGCGGCGCCATAAATGCAGCATTTGTGGCAAGATGTTCAAG
AAGAAGTCTCACGTGCGTAACCACCTGCGCACACACACAGGGGAGCGGCCCTTCCCCTGCCCTG
ACTGCTCCAAGCCCTTCAACTCACCTGCCAACCTGGCCCGCCACCGGCTCACACACACAGGAGA
GCGGCCCTACCGGTGTGGGGACTGTGGCAAGGCTTTCACGCAAAGCTCCACACTGAGGCAGCAC
CGCTTGGTGCATGCCCAGCACTTCCCCTACCGCTGCCAGGAATGTGGGGTGCGTTTTCACCGTC
CTTACCGCCTGCTCATGCACCGCTACCATCACACAGGTGAATACCCCTACAAGTGTCGCGAGTG
CCCCCGCTCCTTCTTGCTGCGTCGGCTGCTGGAGGTGCACCAGCTCGTGGTCCATGCCGGGCGC
CAGCCCCACCGCTGCCCATCCTGTGGGGCTGCCTTCCCCTCCTCACTGCGGCTCCGGGAGCACC
GCTGTGCAGCCGCTGCTGCCCAGGCCCCACGGCGCTTTGAGTGTGGCACCTGTGGCAAGAAAGT
GGGCTCAGCTGCTCGACTGCAGGCACACGAGGCGGCCCATGCAGCTGCTGGGCCTGGAGAGGTC
CTGGCTAAGGAGCCCCCTGCCCCTCGAGCCCCACGGGCCACTCGTGCACCAGTTGCCTCTCCAG
CAGCCCTTGGAAGCACTGCTACAGCATCCCCTGCGGCCCCTGCCCGCCGCCGGGGTCTAGAGTG
CAGCGAGTGCAAGAAGCTGTTCAGCACAGAGACGTCACTGCAGGTGCACCGGCGCATCCACACA
GGTGAGCGGCCATACCCATGTCCAGACTGTGGCAAAGCGTTCCGTCAGAGTACCCACCTGAAAG
ACCACCGGCGCCTGCACACAGGTGAGCGGCCCTTTGCCTGTGAAGTGTGTGGCAAGGCCTTTGC
CATCTCCATGCGCCTGGCAGAACATCGCCGCATCCACACAGGCGAACGACCCTACTCCTGCCCT
GACTGTGGCAAGAGCTACCGCTCCTTCTCCAACCTCTGGAAGCACCGCAAGACCCATCAGCAGC
AGCATCAGGCAGCTGTGCGGCAGCAGCTGGCAGAGGCGGAGGCTGCCGTTGGCCTGGCCGTCAT
GGAGACTGCTGTGGAGGCGCTACCCCTGGTGGAAGCCATTGAGATCTACCCTCTGGCCGAGGCT
GAGGGGGTCCAGATCAGTGGCTGACTCTGCCCGACTTCCTCTTTGGCACCTCCATTCCCTGTTG
CTGAAGGCCCTCCAGCATCCCCTTAAGCATCTGTACATACTGTGTCCCTTCCTCTTCCCATCCC
CACCACCTTGTAAGTTCTAAATTGGATTTATTCTCTCGTGAGGGGGGTGCTCTGGGGTCCTTGA
CACACATAAAGGTGCCCCCCCACCTTCCACCTCTTAGCACTGGTGACCCCAAAAATGAAACCAT
CAATAAAGACTGAGTTGCCAGCAGTGTGTAGA

hide sequence

RefSeq Acc Id:

XM_011527230 ⟹ XP_011525532

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	42,076,484 - 42,081,552 (+)	NCBI

Sequence:

show sequence

GTCGCGTGCGGGGCTGACCCAGGGCCTTGCTGCCGCCATGACTGAGGAATCAGAGGAGACAGTC
CTGTACATTGAGCACCGCTATGTCTGCTCTGAGTGCAACCAGCTGTATGGATCACTGGAAGAGG
TGCTTATGCACCAAAACTCCCACGTGCCCCAGCAGCACTTTGAGCTGGTGGGCGTGGCTGATCC
CGGAGTCACTGTGGCCACAGACACAGCTTCAGGCACGGGCCTCTATCAGACCCTTGTGCAGGAG
AGCCAGTACCAGTGCCTGGAGTGTGGTCAACTGCTGATGTCACCCAGCCAGCTCCTGGAGCACC
AGGAGCTGCACCTGAAGATGATGGCACCCCAGGAGGCAGTGCCAGCTGAGCCATCACCTAAGGC
ACCACCCCTGAGCTCCAGCACCATCCACTACGAGTGTGTGGATTGCAAGGCTCTCTTTGCCAGC
CAGGAGCTCTGGCTGAACCACCGGCAGACGCACCTCCGGGCCACACCCACCAAGGCTCCTGCCC
CTGTTGTCCTGGGGTCCCCAGTTGTTCTAGGGCCTCCTGTGGGCCAGGCCCGAGTGGCTGTGGA
GCACTCATACCGAAAGGCAGAAGAGGGTGGGGAAGGGGCGACTGTCCCATCTGCCGCTGCCACC
ACCACTGAGGTAGTGACTGAGGTGGAGCTGCTCCTCTACAAGTGCTCTGAGTGCTCCCAGCTCT
TCCAGCTGCCGGCGGATTTCCTGGAGCACCAGGCCACTCACTTCCCTGCTCCTGTACCCGAGTC
TCAGGAGCCTGCCTTACAGCAGGAGGTGCAGGCCTCGTCACCTGCAGAGGTGCCTGTGTCTCAG
CCTGACCCCTTGCCAGCTTCTGACCACAGTTACGAGCTGCGCAATGGTGAAGCCATTGGGCGGG
ATCGCCGGGGGCGCAGGGCCCGGAGGAACAACAGTGGAGAAGCAGGCGGGGCAGCCACACAGGA
GCTCTTCTGCTCAGCCTGTGACCAGCTCTTTCTCTCACCCCACCAGCTACAGCAGCACCTGCGG
AGTCACCGGGAGGGCGTCTTTAAGTGCCCCCTGTGCAGTCGTGTCTTCCCTAGCCCTTCCAGTC
TGGACCAGCACCTTGGAGACCATAGCAGCGAGTCACACTTCCTGTGTGTAGACTGTGGCCTGGC
CTTCGGCACAGAGGCCCTCCTCCTGGCCCACCGGCGAGCCCACACCCCGAATCCTCTGCATTCA
TGTCCATGTGGGAAGACCTTTGTCAACCTTACCAAGTTCCTTTATCACCGGCGTACTCATGGGG
TAGGGGGTGTCCCTCTGCCCACAACACCAGTCCCACCAGAGGAACCTGTCATTGGTTTCCCTGA
GCCAGCCCCAGCAGAGACTGGAGAGCCAGAGGCCCCTGAGCCCCCTGTGTCTGAGGAGACCTCA
GCAGGGCCCGCTGCCCCAGGCACCTACCGCTGCCTCCTGTGCAGCCGTGAATTTGGAAAGGCCT
TGCAGCTGACCCGGCACCAACGTTTTGTGCATCGGCTGGAGCGGCGCCATAAATGCAGCATTTG
TGGCAAGATGTTCAAGAAGAAGTCTCACGTGCGTAACCACCTGCGCACACACACAGGGGAGCGG
CCCTTCCCCTGCCCTGACTGCTCCAAGCCCTTCAACTCACCTGCCAACCTGGCCCGCCACCGGC
TCACACACACAGGAGAGCGGCCCTACCGGTGTGGGGACTGTGGCAAGGCTTTCACGCAAAGCTC
CACACTGAGGCAGCACCGCTTGGTGCATGCCCAGCACTTCCCCTACCGCTGCCAGGAATGTGGG
GTGCGTTTTCACCGTCCTTACCGCCTGCTCATGCACCGCTACCATCACACAGGTGAATACCCCT
ACAAGTGTCGCGAGTGCCCCCGCTCCTTCTTGCTGCGTCGGCTGCTGGAGGTGCACCAGCTCGT
GGTCCATGCCGGGCGCCAGCCCCACCGCTGCCCATCCTGTGGGGCTGCCTTCCCCTCCTCACTG
CGGCTCCGGGAGCACCGCTGTGCAGCCGCTGCTGCCCAGGCCCCACGGCGCTTTGAGTGTGGCA
CCTGTGGCAAGAAAGTGGGCTCAGCTGCTCGACTGCAGGCACACGAGGCGGCCCATGCAGCTGC
TGGGCCTGGAGAGGTCCTGGCTAAGGAGCCCCCTGCCCCTCGAGCCCCACGGGCCACTCGTGCA
CCAGTTGCCTCTCCAGCAGCCCTTGGAAGCACTGCTACAGCATCCCCTGCGGCCCCTGCCCGCC
GCCGGGGTCTAGAGTGCAGCGAGTGCAAGAAGCTGTTCAGCACAGAGACGTCACTGCAGGTGCA
CCGGCGCATCCACACAGGTGAGCGGCCATACCCATGTCCAGACTGTGGCAAAGCGTTCCGTCAG
AGTACCCACCTGAAAGACCACCGGCGCCTGCACACAGGTGAGCGGCCCTTTGCCTGTGAAGTGT
GTGGCAAGGCCTTTGCCATCTCCATGCGCCTGGCAGAACATCGCCGCATCCACACAGGCGAACG
ACCCTACTCCTGCCCTGACTGTGGCAAGAGCTACCGCTCCTTCTCCAACCTCTGGAAGCACCGC
AAGACCCATCAGCAGCAGCATCAGGCAGCTGTGCGGCAGCAGCTGGCAGAGGCGGAGGCTGCCG
TTGGCCTGGCCGTCATGGAGACTGCTGTGGAGGCGCTACCCCTGGTGGAAGCCATTGAGATCTA
CCCTCTGGCCGAGGCTGAGGGGGTCCAGATCAGTGGCTGACTCTGCCCGACTTCCTCTTTGGCA
CCTCCATTCCCTGTTGCTGAAGGCCCTCCAGCATCCCCTTAAGCATCTGTACATACTGTGTCCC
TTCCTCTTCCCATCCCCACCACCTTGTAAGTTCTAAATTGGATTTATTCTCTCGTGAGGGGGGT
GCTCTGGGGTCCTTGACACACATAAAGGTGCCCCCCCACCTTCCACCTCTTAGCACTGGTGACC
CCAAAAATGAAACCATCAATAAAGACTGAGTTGCCAGCAGTGTGTAGA

hide sequence

RefSeq Acc Id:

XM_054321780 ⟹ XP_054177755

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	44,895,998 - 44,900,921 (+)	NCBI

RefSeq Acc Id:

XM_054321781 ⟹ XP_054177756

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	44,894,226 - 44,900,921 (+)	NCBI

RefSeq Acc Id:

XM_054321782 ⟹ XP_054177757

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	44,895,915 - 44,900,921 (+)	NCBI

RefSeq Acc Id:

XM_054321783 ⟹ XP_054177758

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	44,895,853 - 44,900,921 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001317448	(Get FASTA)	NCBI Sequence Viewer
	NP_073589	(Get FASTA)	NCBI Sequence Viewer
	XP_005259216	(Get FASTA)	NCBI Sequence Viewer
	XP_011525530	(Get FASTA)	NCBI Sequence Viewer
	XP_011525531	(Get FASTA)	NCBI Sequence Viewer
	XP_011525532	(Get FASTA)	NCBI Sequence Viewer
	XP_054177755	(Get FASTA)	NCBI Sequence Viewer
	XP_054177756	(Get FASTA)	NCBI Sequence Viewer
	XP_054177757	(Get FASTA)	NCBI Sequence Viewer
	XP_054177758	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH01184	(Get FASTA)	NCBI Sequence Viewer
	AAH71962	(Get FASTA)	NCBI Sequence Viewer
	AAQ04655	(Get FASTA)	NCBI Sequence Viewer
	BAB15225	(Get FASTA)	NCBI Sequence Viewer
	BAC11210	(Get FASTA)	NCBI Sequence Viewer
	BAD18520	(Get FASTA)	NCBI Sequence Viewer
	BAD18565	(Get FASTA)	NCBI Sequence Viewer
	CAB70782	(Get FASTA)	NCBI Sequence Viewer
	EAW57093	(Get FASTA)	NCBI Sequence Viewer
	EAW57094	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000222339
	ENSP00000222339.6
	ENSP00000351939
	ENSP00000351939.3
	ENSP00000469029
	ENSP00000469029.1
	ENSP00000471611.1
GenBank Protein	Q6ZN55	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_073589 ⟸ NM_022752
- Peptide Label:	isoform 1
- UniProtKB:	Q8NCE3 (UniProtKB/Swiss-Prot), Q7L5Z5 (UniProtKB/Swiss-Prot), Q6ZN10 (UniProtKB/Swiss-Prot), Q6IPE0 (UniProtKB/Swiss-Prot), Q9H6N0 (UniProtKB/Swiss-Prot), Q6ZN55 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTEESEETVLYIEHRYVCSECNQLYGSLEEVLMHQNSHVPQQHFELVGVADPGVTVATDTASGT GLYQTLVQESQYQCLECGQLLMSPSQLLEHQELHLKMMAPQEAVPAEPSPKAPPLSSSTIHYEC VDCKALFASQELWLNHRQTHLRATPTKAPAPVVLGSPVVLGPPVGQARVAVEHSYRKAEEGGEG ATVPSAAATTTEVVTEVELLLYKCSECSQLFQLPADFLEHQATHFPAPVPESQEPALQQEVQAS SPAEVPVSQPDPLPASDHSYELRNGEAIGRDRRGRRARRNNSGEAGGAATQELFCSACDQLFLS PHQLQQHLRSHREGVFKCPLCSRVFPSPSSLDQHLGDHSSESHFLCVDCGLAFGTEALLLAHRR AHTPNPLHSCPCGKTFVNLTKFLYHRRTHGVGGVPLPTTPVPPEEPVIGFPEPAPAETGEPEAP EPPVSEETSAGPAAPGTYRCLLCSREFGKALQLTRHQRFVHRLERRHKCSICGKMFKKKSHVRN HLRTHTGERPFPCPDCSKPFNSPANLARHRLTHTGERPYRCGDCGKAFTQSSTLRQHRLVHAQH FPYRCQECGVRFHRPYRLLMHRYHHTGEYPYKCRECPRSFLLRRLLEVHQLVVHAGRQPHRCPS CGAAFPSSLRLREHRCAAAAAQAPRRFECGTCGKKVGSAARLQAHEAAHAAAGPGEVLAKEPPA PRAPRATRAPVASPAALGSTATASPAAPARRRGLECSECKKLFSTETSLQVHRRIHTGERPYPC PDCGKAFRQSTHLKDHRRLHTGERPFACEVCGKAFAISMRLAEHRRIHTGERPYSCPDCGKSYR SFSNLWKHRKTHQQQHQAAVRQQLAEAEAAVGLAVMETAVEALPLVEAIEIYPLAEAEGVQISG hide sequence

RefSeq Acc Id:	XP_005259216 ⟸ XM_005259159
- Peptide Label:	isoform X1
- UniProtKB:	Q8NCE3 (UniProtKB/Swiss-Prot), Q7L5Z5 (UniProtKB/Swiss-Prot), Q6ZN10 (UniProtKB/Swiss-Prot), Q6IPE0 (UniProtKB/Swiss-Prot), Q9H6N0 (UniProtKB/Swiss-Prot), Q6ZN55 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTEESEETVLYIEHRYVCSECNQLYGSLEEVLMHQNSHVPQQHFELVGVADPGVTVATDTASGT GLYQTLVQESQYQCLECGQLLMSPSQLLEHQELHLKMMAPQEAVPAEPSPKAPPLSSSTIHYEC VDCKALFASQELWLNHRQTHLRATPTKAPAPVVLGSPVVLGPPVGQARVAVEHSYRKAEEGGEG ATVPSAAATTTEVVTEVELLLYKCSECSQLFQLPADFLEHQATHFPAPVPESQEPALQQEVQAS SPAEVPVSQPDPLPASDHSYELRNGEAIGRDRRGRRARRNNSGEAGGAATQELFCSACDQLFLS PHQLQQHLRSHREGVFKCPLCSRVFPSPSSLDQHLGDHSSESHFLCVDCGLAFGTEALLLAHRR AHTPNPLHSCPCGKTFVNLTKFLYHRRTHGVGGVPLPTTPVPPEEPVIGFPEPAPAETGEPEAP EPPVSEETSAGPAAPGTYRCLLCSREFGKALQLTRHQRFVHRLERRHKCSICGKMFKKKSHVRN HLRTHTGERPFPCPDCSKPFNSPANLARHRLTHTGERPYRCGDCGKAFTQSSTLRQHRLVHAQH FPYRCQECGVRFHRPYRLLMHRYHHTGEYPYKCRECPRSFLLRRLLEVHQLVVHAGRQPHRCPS CGAAFPSSLRLREHRCAAAAAQAPRRFECGTCGKKVGSAARLQAHEAAHAAAGPGEVLAKEPPA PRAPRATRAPVASPAALGSTATASPAAPARRRGLECSECKKLFSTETSLQVHRRIHTGERPYPC PDCGKAFRQSTHLKDHRRLHTGERPFACEVCGKAFAISMRLAEHRRIHTGERPYSCPDCGKSYR SFSNLWKHRKTHQQQHQAAVRQQLAEAEAAVGLAVMETAVEALPLVEAIEIYPLAEAEGVQISG hide sequence

RefSeq Acc Id:	XP_011525530 ⟸ XM_011527228
- Peptide Label:	isoform X1
- UniProtKB:	Q8NCE3 (UniProtKB/Swiss-Prot), Q7L5Z5 (UniProtKB/Swiss-Prot), Q6ZN10 (UniProtKB/Swiss-Prot), Q6IPE0 (UniProtKB/Swiss-Prot), Q9H6N0 (UniProtKB/Swiss-Prot), Q6ZN55 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTEESEETVLYIEHRYVCSECNQLYGSLEEVLMHQNSHVPQQHFELVGVADPGVTVATDTASGT GLYQTLVQESQYQCLECGQLLMSPSQLLEHQELHLKMMAPQEAVPAEPSPKAPPLSSSTIHYEC VDCKALFASQELWLNHRQTHLRATPTKAPAPVVLGSPVVLGPPVGQARVAVEHSYRKAEEGGEG ATVPSAAATTTEVVTEVELLLYKCSECSQLFQLPADFLEHQATHFPAPVPESQEPALQQEVQAS SPAEVPVSQPDPLPASDHSYELRNGEAIGRDRRGRRARRNNSGEAGGAATQELFCSACDQLFLS PHQLQQHLRSHREGVFKCPLCSRVFPSPSSLDQHLGDHSSESHFLCVDCGLAFGTEALLLAHRR AHTPNPLHSCPCGKTFVNLTKFLYHRRTHGVGGVPLPTTPVPPEEPVIGFPEPAPAETGEPEAP EPPVSEETSAGPAAPGTYRCLLCSREFGKALQLTRHQRFVHRLERRHKCSICGKMFKKKSHVRN HLRTHTGERPFPCPDCSKPFNSPANLARHRLTHTGERPYRCGDCGKAFTQSSTLRQHRLVHAQH FPYRCQECGVRFHRPYRLLMHRYHHTGEYPYKCRECPRSFLLRRLLEVHQLVVHAGRQPHRCPS CGAAFPSSLRLREHRCAAAAAQAPRRFECGTCGKKVGSAARLQAHEAAHAAAGPGEVLAKEPPA PRAPRATRAPVASPAALGSTATASPAAPARRRGLECSECKKLFSTETSLQVHRRIHTGERPYPC PDCGKAFRQSTHLKDHRRLHTGERPFACEVCGKAFAISMRLAEHRRIHTGERPYSCPDCGKSYR SFSNLWKHRKTHQQQHQAAVRQQLAEAEAAVGLAVMETAVEALPLVEAIEIYPLAEAEGVQISG hide sequence

RefSeq Acc Id:	XP_011525532 ⟸ XM_011527230
- Peptide Label:	isoform X1
- UniProtKB:	Q8NCE3 (UniProtKB/Swiss-Prot), Q7L5Z5 (UniProtKB/Swiss-Prot), Q6ZN10 (UniProtKB/Swiss-Prot), Q6IPE0 (UniProtKB/Swiss-Prot), Q9H6N0 (UniProtKB/Swiss-Prot), Q6ZN55 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTEESEETVLYIEHRYVCSECNQLYGSLEEVLMHQNSHVPQQHFELVGVADPGVTVATDTASGT GLYQTLVQESQYQCLECGQLLMSPSQLLEHQELHLKMMAPQEAVPAEPSPKAPPLSSSTIHYEC VDCKALFASQELWLNHRQTHLRATPTKAPAPVVLGSPVVLGPPVGQARVAVEHSYRKAEEGGEG ATVPSAAATTTEVVTEVELLLYKCSECSQLFQLPADFLEHQATHFPAPVPESQEPALQQEVQAS SPAEVPVSQPDPLPASDHSYELRNGEAIGRDRRGRRARRNNSGEAGGAATQELFCSACDQLFLS PHQLQQHLRSHREGVFKCPLCSRVFPSPSSLDQHLGDHSSESHFLCVDCGLAFGTEALLLAHRR AHTPNPLHSCPCGKTFVNLTKFLYHRRTHGVGGVPLPTTPVPPEEPVIGFPEPAPAETGEPEAP EPPVSEETSAGPAAPGTYRCLLCSREFGKALQLTRHQRFVHRLERRHKCSICGKMFKKKSHVRN HLRTHTGERPFPCPDCSKPFNSPANLARHRLTHTGERPYRCGDCGKAFTQSSTLRQHRLVHAQH FPYRCQECGVRFHRPYRLLMHRYHHTGEYPYKCRECPRSFLLRRLLEVHQLVVHAGRQPHRCPS CGAAFPSSLRLREHRCAAAAAQAPRRFECGTCGKKVGSAARLQAHEAAHAAAGPGEVLAKEPPA PRAPRATRAPVASPAALGSTATASPAAPARRRGLECSECKKLFSTETSLQVHRRIHTGERPYPC PDCGKAFRQSTHLKDHRRLHTGERPFACEVCGKAFAISMRLAEHRRIHTGERPYSCPDCGKSYR SFSNLWKHRKTHQQQHQAAVRQQLAEAEAAVGLAVMETAVEALPLVEAIEIYPLAEAEGVQISG hide sequence

RefSeq Acc Id:	XP_011525531 ⟸ XM_011527229
- Peptide Label:	isoform X1
- UniProtKB:	Q8NCE3 (UniProtKB/Swiss-Prot), Q7L5Z5 (UniProtKB/Swiss-Prot), Q6ZN10 (UniProtKB/Swiss-Prot), Q6IPE0 (UniProtKB/Swiss-Prot), Q9H6N0 (UniProtKB/Swiss-Prot), Q6ZN55 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTEESEETVLYIEHRYVCSECNQLYGSLEEVLMHQNSHVPQQHFELVGVADPGVTVATDTASGT GLYQTLVQESQYQCLECGQLLMSPSQLLEHQELHLKMMAPQEAVPAEPSPKAPPLSSSTIHYEC VDCKALFASQELWLNHRQTHLRATPTKAPAPVVLGSPVVLGPPVGQARVAVEHSYRKAEEGGEG ATVPSAAATTTEVVTEVELLLYKCSECSQLFQLPADFLEHQATHFPAPVPESQEPALQQEVQAS SPAEVPVSQPDPLPASDHSYELRNGEAIGRDRRGRRARRNNSGEAGGAATQELFCSACDQLFLS PHQLQQHLRSHREGVFKCPLCSRVFPSPSSLDQHLGDHSSESHFLCVDCGLAFGTEALLLAHRR AHTPNPLHSCPCGKTFVNLTKFLYHRRTHGVGGVPLPTTPVPPEEPVIGFPEPAPAETGEPEAP EPPVSEETSAGPAAPGTYRCLLCSREFGKALQLTRHQRFVHRLERRHKCSICGKMFKKKSHVRN HLRTHTGERPFPCPDCSKPFNSPANLARHRLTHTGERPYRCGDCGKAFTQSSTLRQHRLVHAQH FPYRCQECGVRFHRPYRLLMHRYHHTGEYPYKCRECPRSFLLRRLLEVHQLVVHAGRQPHRCPS CGAAFPSSLRLREHRCAAAAAQAPRRFECGTCGKKVGSAARLQAHEAAHAAAGPGEVLAKEPPA PRAPRATRAPVASPAALGSTATASPAAPARRRGLECSECKKLFSTETSLQVHRRIHTGERPYPC PDCGKAFRQSTHLKDHRRLHTGERPFACEVCGKAFAISMRLAEHRRIHTGERPYSCPDCGKSYR SFSNLWKHRKTHQQQHQAAVRQQLAEAEAAVGLAVMETAVEALPLVEAIEIYPLAEAEGVQISG hide sequence

RefSeq Acc Id:	NP_001317448 ⟸ NM_001330519
- Peptide Label:	isoform 2
- UniProtKB:	A0A0C4DFM2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPRATWANSKERSWAESERGPRDTGNGGSKAERHIQEIETGRGGDRAKAHRRQRMRLRGTERAS LGPGRRLGDSRGTDMPGARAQGLAAAMTEESEETVLYIEHRYVCSECNQLYGSLEEVLMHQNSH VPQQHFELVGVADPGVTVATDTASGTGLYQTLVQESQYQCLECGQLLMSPSQLLEHQELHLKMM APQEAVPAEPSPKAPPLSSSTIHYECVDCKALFASQELWLNHRQTHLRATPTKAPAPVVLGSPV VLGPPVGQARVAVEHSYRKAEEGGEGATVPSAAATTTEVVTEVELLLYKCSECSQLFQLPADFL EHQATHFPAPVPESQEPALQQEVQASSPAEVPVSQPDPLPASDHSYELRNGEAIGRDRRGRRAR RNNSGEAGGAATQELFCSACDQLFLSPHQLQQHLRSHREGVFKCPLCSRVFPSPSSLDQHLGDH SSESHFLCVDCGLAFGTEALLLAHRRAHTPNPLHSCPCGKTFVNLTKFLYHRRTHGVGGVPLPT TPVPPEEPVIGFPEPAPAETGEPEAPEPPVSEETSAGPAAPGTYRCLLCSREFGKALQLTRHQR FVHRLERRHKCSICGKMFKKKSHVRNHLRTHTGERPFPCPDCSKPFNSPANLARHRLTHTGERP YRCGDCGKAFTQSSTLRQHRLVHAQHFPYRCQECGVRFHRPYRLLMHRYHHTGEYPYKCRECPR SFLLRRLLEVHQLVVHAGRQPHRCPSCGAAFPSSLRLREHRCAAAAAQAPRRFECGTCGKKVGS AARLQAHEAAHAAAGPGEVLAKEPPAPRAPRATRAPVASPAALGSTATASPAAPARRRGLECSE CKKLFSTETSLQVHRRIHTGERPYPCPDCGKAFRQSTHLKDHRRLHTGERPFACEVCGKAFAIS MRLAEHRRIHTGERPYSCPDCGKSYRSFSNLWKHRKTHQQQHQAAVRQQLAEAEAAVGLAVMET AVEALPLVEAIEIYPLAEAEGVQISG hide sequence

RefSeq Acc Id:

ENSP00000351939 ⟸ ENST00000359044

RefSeq Acc Id:

ENSP00000471611 ⟸ ENST00000597391

RefSeq Acc Id:

ENSP00000469029 ⟸ ENST00000600245

RefSeq Acc Id:

ENSP00000222339 ⟸ ENST00000222339

RefSeq Acc Id:	XP_054177756 ⟸ XM_054321781
- Peptide Label:	isoform X1
- UniProtKB:	Q8NCE3 (UniProtKB/Swiss-Prot), Q7L5Z5 (UniProtKB/Swiss-Prot), Q6ZN55 (UniProtKB/Swiss-Prot), Q6ZN10 (UniProtKB/Swiss-Prot), Q6IPE0 (UniProtKB/Swiss-Prot), Q9H6N0 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054177758 ⟸ XM_054321783
- Peptide Label:	isoform X1
- UniProtKB:	Q8NCE3 (UniProtKB/Swiss-Prot), Q7L5Z5 (UniProtKB/Swiss-Prot), Q6ZN55 (UniProtKB/Swiss-Prot), Q6ZN10 (UniProtKB/Swiss-Prot), Q6IPE0 (UniProtKB/Swiss-Prot), Q9H6N0 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054177757 ⟸ XM_054321782
- Peptide Label:	isoform X1
- UniProtKB:	Q8NCE3 (UniProtKB/Swiss-Prot), Q7L5Z5 (UniProtKB/Swiss-Prot), Q6ZN55 (UniProtKB/Swiss-Prot), Q6ZN10 (UniProtKB/Swiss-Prot), Q6IPE0 (UniProtKB/Swiss-Prot), Q9H6N0 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054177755 ⟸ XM_054321780
- Peptide Label:	isoform X1
- UniProtKB:	Q8NCE3 (UniProtKB/Swiss-Prot), Q7L5Z5 (UniProtKB/Swiss-Prot), Q6ZN55 (UniProtKB/Swiss-Prot), Q6ZN10 (UniProtKB/Swiss-Prot), Q6IPE0 (UniProtKB/Swiss-Prot), Q9H6N0 (UniProtKB/Swiss-Prot)

Protein Domains

C2H2-type

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q6ZN55-F1-model_v2	AlphaFold	Q6ZN55	1-896	view protein structure

Promoters

RGD ID:

7240145

Promoter ID:

EPDNEW_H25818

Type:

initiation region

Name:

ZNF574_1

Description:

zinc finger protein 574

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	42,076,185 - 42,076,245	EPDNEW

RGD ID:

6796368

Promoter ID:

HG_KWN:30067

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_022752

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	47,271,661 - 47,272,302 (+)	MPROMDB

RGD ID:

6796371

Promoter ID:

HG_KWN:30068

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell_12Hour

Transcripts:

UC010EIC.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	47,276,896 - 47,277,396 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:26166	AgrOrtholog
COSMIC	ZNF574	COSMIC
Ensembl Genes	ENSG00000105732	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000222339	ENTREZGENE
	ENST00000222339.7	UniProtKB/TrEMBL
	ENST00000359044	ENTREZGENE
	ENST00000359044.5	UniProtKB/Swiss-Prot
	ENST00000597391.1	UniProtKB/TrEMBL
	ENST00000600245	ENTREZGENE
	ENST00000600245.1	UniProtKB/Swiss-Prot
Gene3D-CATH	Classic Zinc Finger	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000105732	GTEx
HGNC ID	HGNC:26166	ENTREZGENE
Human Proteome Map	ZNF574	Human Proteome Map
InterPro	Znf_C2H2_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_C2H2_type	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:64763	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	64763	ENTREZGENE
PANTHER	CHROMATIN-LINKED ADAPTOR FOR MSL PROTEINS, ISOFORM B-RELATED	UniProtKB/Swiss-Prot
	IP01257P-RELATED	UniProtKB/TrEMBL
	KRAB AND ZINC FINGER DOMAIN-CONTAINING	UniProtKB/TrEMBL
	LOW QUALITY PROTEIN: ZINC FINGER PROTEIN 595-LIKE-RELATED	UniProtKB/TrEMBL
	ZINC FINGER PROTEIN	UniProtKB/Swiss-Prot
	ZINC FINGER PROTEIN	UniProtKB/TrEMBL
Pfam	zf-C2H2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	zf-C2H2_6	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	zf-met	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134916492	PharmGKB
PROSITE	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	ZnF_C2H2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF57667	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A0C4DFM2	ENTREZGENE, UniProtKB/TrEMBL
	M0R133_HUMAN	UniProtKB/TrEMBL
	Q6IPE0	ENTREZGENE
	Q6ZN10	ENTREZGENE
	Q6ZN55	ENTREZGENE
	Q71MF7_HUMAN	UniProtKB/TrEMBL
	Q7L5Z5	ENTREZGENE
	Q8NCE3	ENTREZGENE
	Q9H6N0	ENTREZGENE
	ZN574_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	Q6IPE0	UniProtKB/Swiss-Prot
	Q6ZN10	UniProtKB/Swiss-Prot
	Q7L5Z5	UniProtKB/Swiss-Prot
	Q8NCE3	UniProtKB/Swiss-Prot
	Q9H6N0	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)

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar

Send us a Message

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar