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Gene: ZNF730 (zinc finger protein 730) Homo sapiens

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Symbol:

ZNF730

Name:

zinc finger protein 730

RGD ID:

2293897

HGNC Page

HGNC:32470

Description:

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

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

putative zinc finger protein 730

RGD Orthologs

Green Monkey

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	23,075,211 - 23,147,221 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	23,075,210 - 23,147,221 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	23,299,827 - 23,330,023 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	23,083,163 - 23,124,603 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	19	23,131,471 - 23,161,066 (+)	NCBI		Celera
Cytogenetic Map	19	p12	NCBI
HuRef	19	22,840,606 - 22,870,541 (+)	NCBI		HuRef
CHM1_1	19	23,299,418 - 23,329,344 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	23,210,338 - 23,282,034 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZNF730	Human	17beta-estradiol	decreases expression	EXP		6480464	Estradiol results in decreased expression of ZNF730 mRNA	CTD	PMID:21185374
ZNF730	Human	2,3,7,8-tetrachlorodibenzodioxine	affects expression	EXP		6480464	Tetrachlorodibenzodioxin affects the expression of ZNF730 mRNA	CTD	PMID:22574217
ZNF730	Human	2-palmitoylglycerol	increases expression	EXP		6480464	2-palmitoylglycerol results in increased expression of ZNF730 mRNA	CTD	PMID:37199045
ZNF730	Human	arsenite(3-)	decreases expression	EXP		6480464	arsenite results in decreased expression of ZNF730 mRNA	CTD	PMID:23974009
ZNF730	Human	benzo[a]pyrene	increases expression	EXP		6480464	Benzo(a)pyrene results in increased expression of ZNF730 mRNA	CTD	PMID:32234424
ZNF730	Human	nickel sulfate	increases expression	EXP		6480464	nickel sulfate results in increased expression of ZNF730 mRNA	CTD	PMID:22714537
ZNF730	Human	niclosamide	decreases expression	EXP		6480464	Niclosamide results in decreased expression of ZNF730 mRNA	CTD	PMID:36318118
ZNF730	Human	potassium chromate	decreases expression	EXP		6480464	potassium chromate(VI) results in decreased expression of ZNF730 mRNA	CTD	PMID:22714537
ZNF730	Human	sodium arsenite	increases expression	EXP		6480464	sodium arsenite results in increased expression of ZNF730 mRNA	CTD	PMID:22714537
ZNF730	Human	tunicamycin	increases expression	EXP		6480464	Tunicamycin results in increased expression of ZNF730 mRNA	CTD	PMID:29453283

Biological Process

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZNF730	Human	regulation of DNA-templated transcription	involved_in	IEA	InterPro:IPR001909 and InterPro:IPR036051	150520179		InterPro	GO_REF:0000002
ZNF730	Human	regulation of DNA-templated transcription	involved_in	IBA	PANTHER:PTN002810793 more ...	150520179		GO_Central	GO_REF:0000033
ZNF730	Human	regulation of transcription by RNA polymerase II	involved_in	IEA	GO:0000981	150520179		GOC	GO_REF:0000108

Cellular Component

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZNF730	Human	nucleus	located_in	IEA	UniProtKB-KW:KW-0539	150520179		UniProt	GO_REF:0000043
ZNF730	Human	nucleus	located_in	IEA	UniProtKB-SubCell:SL-0191	150520179		UniProt	GO_REF:0000044

Molecular Function

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZNF730	Human	DNA binding	enables	IEA	UniProtKB-KW:KW-0238	150520179		UniProt	GO_REF:0000043
ZNF730	Human	DNA-binding transcription factor activity, RNA polymerase II-specific	enables	IBA	PANTHER:PTN002810793 more ...	150520179		GO_Central	GO_REF:0000033
ZNF730	Human	metal ion binding	enables	IEA	UniProtKB-KW:KW-0479	150520179		UniProt	GO_REF:0000043
ZNF730	Human	RNA polymerase II cis-regulatory region sequence-specific DNA binding	enables	IBA	PANTHER:PTN002810793 more ...	150520179		GO_Central	GO_REF:0000033
ZNF730	Human	zinc ion binding	enables	IEA	UniProtKB-KW:KW-0863	150520179		UniProt	GO_REF:0000043

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

PMID:21873635	PMID:33541421

ZNF730
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	23,075,211 - 23,147,221 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	23,075,210 - 23,147,221 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	23,299,827 - 23,330,023 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	23,083,163 - 23,124,603 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	19	23,131,471 - 23,161,066 (+)	NCBI		Celera
Cytogenetic Map	19	p12	NCBI
HuRef	19	22,840,606 - 22,870,541 (+)	NCBI		HuRef
CHM1_1	19	23,299,418 - 23,329,344 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	23,210,338 - 23,282,034 (+)	NCBI		T2T-CHM13v2.0

LOC103234290
(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	20,820,498 - 20,828,917 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666088	917,976 - 943,611 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Variants in ZNF730
9 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 19p13.11-q13.11(chr19:17176767-34924150)x3	copy number gain	See cases [RCV000050635]	Chr19:17176767..34924150 [GRCh38] Chr19:17287576..35415054 [GRCh37] Chr19:17148576..40106894 [NCBI36] Chr19:19p13.11-q13.11	pathogenic
GRCh38/hg38 19p13.12-q11(chr19:13974677-27839676)x3	copy number gain	See cases [RCV000052912]	Chr19:13974677..27839676 [GRCh38] Chr19:14085489..28330584 [GRCh37] Chr19:13946489..33022424 [NCBI36] Chr19:19p13.12-q11	pathogenic
GRCh38/hg38 19p13.12-12(chr19:15133594-24193591)x3	copy number gain	See cases [RCV000136696]	Chr19:15133594..24193591 [GRCh38] Chr19:15244405..24376393 [GRCh37] Chr19:15105405..24168233 [NCBI36] Chr19:19p13.12-12	pathogenic\|likely pathogenic
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	copy number gain	See cases [RCV000133888]	Chr19:11227942..44626354 [GRCh38] Chr19:11338618..45129651 [GRCh37] Chr19:11199618..49821491 [NCBI36] Chr19:19p13.2-q13.31	pathogenic
GRCh38/hg38 19p12(chr19:22987611-23189484)x1	copy number loss	See cases [RCV000140874]	Chr19:22987611..23189484 [GRCh38] Chr19:23170413..23372286 [GRCh37] Chr19:22962253..23164126 [NCBI36] Chr19:19p12	uncertain significance
GRCh37/hg19 19p12(chr19:22867705-23645194)x4	copy number gain	See cases [RCV000598637]	Chr19:22867705..23645194 [GRCh37] Chr19:19p12	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	copy number gain	See cases [RCV000511289]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic\|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	copy number gain	See cases [RCV000512296]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
chr19:19230868-24115369 complex variant	complex	Breast ductal adenocarcinoma [RCV000207223]	Chr19:19230868..24115369 [GRCh37] Chr19:19p13.11-12	uncertain significance
GRCh37/hg19 19p13.11-11(chr19:16526787-24631604)x3	copy number gain	not provided [RCV000752593]	Chr19:16526787..24631604 [GRCh37] Chr19:19p13.11-11	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 19p12(chr19:23262262-23379015)x1	copy number loss	not provided [RCV001007039]	Chr19:23262262..23379015 [GRCh37] Chr19:19p12	likely benign
GRCh37/hg19 19p12(chr19:23217767-23956831)x3	copy number gain	not provided [RCV002473524]	Chr19:23217767..23956831 [GRCh37] Chr19:19p12	uncertain significance
GRCh37/hg19 19p12-11(chr19:22635439-24505637)x3	copy number gain	not provided [RCV000684090]	Chr19:22635439..24505637 [GRCh37] Chr19:19p12-11	likely benign
GRCh37/hg19 19p12(chr19:22789865-23338320)x3	copy number gain	not provided [RCV000684083]	Chr19:22789865..23338320 [GRCh37] Chr19:19p12	likely benign
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 19p12(chr19:23030170-23316525)x1	copy number loss	not provided [RCV001259367]	Chr19:23030170..23316525 [GRCh37] Chr19:19p12	likely benign
GRCh37/hg19 19p12-11(chr19:22630650-24487350)x3	copy number gain	See cases [RCV001007435]	Chr19:22630650..24487350 [GRCh37] Chr19:19p12-11	uncertain significance
GRCh37/hg19 19p12(chr19:23166550-23307438)x1	copy number loss	not provided [RCV001259368]	Chr19:23166550..23307438 [GRCh37] Chr19:19p12	likely benign
GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)x3	copy number gain	Specific learning disability [RCV001801194]	Chr19:19546923..41313229 [GRCh37] Chr19:19p13.11-q13.2	pathogenic
NM_001277403.2(ZNF730):c.906dup (p.Lys303Ter)	duplication	not provided [RCV003425080]	Chr19:23145949..23145950 [GRCh38] Chr19:23328751..23328752 [GRCh37] Chr19:19p12	likely benign
GRCh37/hg19 19p12-q12(chr19:22521477-28934362)x3	copy number gain	not provided [RCV004819643]	Chr19:22521477..28934362 [GRCh37] Chr19:19p12-q12	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	450
Count of miRNA genes:	264
Interacting mature miRNAs:	278
Transcripts:	ENST00000593635, ENST00000597761, ENST00000599195
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1300034	BP50_H	Blood pressure QTL 50 (human)	2.1	0.00094	Blood pressure	systolic	19	11089463	37089463	Human

RH91862

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	23,329,737 - 23,329,909	UniSTS	GRCh37
Build 36	19	23,121,577 - 23,121,749	RGD	NCBI36
Celera	19	23,161,046 - 23,161,218	RGD
Cytogenetic Map	19	p12	UniSTS
HuRef	19	22,870,264 - 22,870,436	UniSTS
GeneMap99-GB4 RH Map	19	123.42	UniSTS

UniSTS:481985

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	105,879,494 - 105,879,872	UniSTS	GRCh37
GRCh37	5	105,879,410 - 105,879,872	UniSTS	GRCh37
Build 36	5	105,907,309 - 105,907,771	RGD	NCBI36
Celera	5	101,820,188 - 101,820,566	RGD
HuRef	5	101,055,598 - 101,055,976	UniSTS
HuRef	5	101,055,514 - 101,055,976	UniSTS

ERV3

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Stanford-G3 RH Map	9	1514.0	UniSTS
NCBI RH Map	9	474.9	UniSTS

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

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system
1087	2042	2017	1850	4575	1385	1943	4	348	1336	211	1950	5313	5205	41	3573	720	1643	1468	142


RefSeq Transcripts	NM_001277403	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026114	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026115	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047437993	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047437994	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047437995	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047437996	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047437997	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047437998	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047437999	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047438000	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047438001	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047438002	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047438003	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047438004	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047438005	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319431	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319432	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319433	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319434	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319435	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319436	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319437	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319438	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319439	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319440	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319441	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319442	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319443	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319444	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319445	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319446	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319447	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319448	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001753564	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001753565	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001753566	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001753567	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001753568	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001753569	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_007066501	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC074135	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC092329	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC124856	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK131472	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471106	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000593635 ⟹ ENSP00000469853

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	23,075,210 - 23,136,106 (+)	Ensembl

Ensembl Acc Id:

ENST00000597761 ⟹ ENSP00000472959

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	23,117,025 - 23,147,221 (+)	Ensembl

Ensembl Acc Id:

ENST00000599195 ⟹ ENSP00000469805

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	23,134,187 - 23,144,249 (+)	Ensembl

RefSeq Acc Id:

NM_001277403 ⟹ NP_001264332

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,117,025 - 23,147,221 (+)	NCBI
HuRef	19	22,840,606 - 22,870,541 (+)	NCBI
CHM1_1	19	23,299,418 - 23,329,344 (+)	NCBI
T2T-CHM13v2.0	19	23,252,142 - 23,282,034 (+)	NCBI

Sequence:

show sequence

GCCTTTGTTTCTCGCTGCCGCCGAAGCTCCAATTTTCGTCTGTCTGCTTTGTGTCCTCTGCACGTAGAAGCCCAGCCTGTGTGGCCCTGCGACCTGCGGGTATTGGGAGATCCACAGCTAAGACGCCA
GGGCCCCCTGGAAGCCTAGAAATGGGAGCGTTGACATTTAGAGATGTGGCCATAGAATTCTCTCTGGAGGAGTGGCAATGTCTGGACACCGAACAACAGAATTTATATAGAAATGTAATGTTAGATAA
CTACAGAAACCTGGTCTTCCTGGGTATTGCTGTCTCAAAGCCAGACCTGATCACCTGTCTGGAGCAAGAAAAAGAGCCTTGGAATTTGAAGACACATGATATGGTAGCCAAACCCCCAGTTATATGTT
CTCATATTGCCCAAGACCTTTGGCCAGAGCAAGGCATAAAAGATTATTTCCAAGAAGTCATACTGAGACAATATAAAAAATGTAGACATGAGAATTTACTGTTAAGAAAAGGCTGTAAAAATGTGGAT
GAGTTTAAGATGCACAAAAAAGGTTATAATAGACATAACCAGTGTTTGACAACTTCCCATAGCAAAATATTTCAGTGTGACAAATATGTGAAAGTCTTTCATAAATTTTCAAATTCAAACAGACATAA
GATAAGACATACTTCGAAGAAACCTTTCAAATGTAAAGAATGTGGAAAATTATTTTGCATTCTTTCACACTTAGCTCAACATAAAAAAATTCATACTGGAGAGAAATCCTACAAATGTGAAGAATATG
GCAAAGCCTTTAATGAGTCCTCAAACTGTACTACACATAAAAGAATTACTGAGAAAAAACCTTACAAATGTAAAGAATGTGGCAAAGCCTTTAACTGGTTTTCACATTTTACTACACATAAGAGAATT
CATACTGGAGAAAAACCCTACCAATGTGAGAAATGTGGCAAATTTTTTAACCAATCCACAAACCTTACTACACATAAAAGAATTCATACTGGAGAGAAACCCTATAAATGTGAAGAATGTGGCAAAGC
CTTTAACCAGTCCTCAAACCTTACTGAACATAAGAAAATTCATACTAAAGAGCAACCATACAAATGCGAAAAATGTGGCAAAGCTTTTAAGTGGTCCTCAACCCTTACAAAACATAAAAGAATTCATA
ATGGAGAAAAACCCTACAAATGTGAAGAATGTGGCAAAGCTTTTAACCGATCCTCAACCCTTAATAGACATAAGATAACTCATACTGGAGGGAAACCCTACAAATATAAAGAATGTGGTAAAGCTTTT
AACCAATCCTCAACTCTTACTATACATAAGATAATTCATACTGTAGAGAAATTTTACAAATGTGAAGAATGTGGCAAAGCCTTTAGCCGTATCTCACACCTTACTACACATAAGAGAATTCATACTGG
AGAGAAACCCTACAAATGTGAAGAATGTGGCAGAGCTTTCAACCAGTCCTCAACCCTTACTACACATAAAAGAATTCATACTGGAGAGAAACCCTATGAATGTGAAGAATGTGGCAAAGCTTTTAACC
GGTCCTCAACCCTCACTACACATAAGATAATTCATTCTGGGGAAAAAATCTACAAATGTAAAGAATGTGGTAAAGCCTTTAGGCGGTTCTCACACCTTACTAGGCATAAGACAATTCATACATAAAAT
TGTAAAGACTGTGGCAAAGCTTTTAAACAATCTTTATACCTTACTACACATAAGATAATTCATACTGAAGAGAAACCCTACAAATGTGAAGAATGTGGCAAAGCTTTTAACCAGTCCTCAAATCTTAC
TAAACATAAGGTAATTCATACTGGAGAAAAACCTACAAATGTGAAGAATGTGGCAAAGTCTTCAACCAATCTTCACACCTTACTACACATAAGATAATTCATACTGGAGAGAAACCCTACAAGTGTGA
AGAATGTGACAAAGCCTTTAACAAATCCTTAATTCTTAACAGACATGATTCATACCAGAGAGAAACTCTACAAACCTGAAAGTTTTAACAGTGCTTTTGACAACACCTCAAACTTTTCCAGATGTCAA
AGAAATGCTGGTGAGAAATTCTAGAAATATGAAGAATGTGACAAAGCCATTAAATTGTTGTCACATTTAATTGTAGGTAAGGTGATTCATACTGGAGAAAACTTCTACAAGTGTAAACAAAGTGGCAA
AACTTTTAACCAATGCTCACACTTTATTGCACAGGACATTTATACTTGAGAATAAATATACAAGTGTAAAGAAAGTGAAAACCCTATTAATATCTGCTCACATCAACTCAACATCAGAGTTCATACTT
AATAAAATCATTAAAAGTGCAA

hide sequence

RefSeq Acc Id:

XM_017026114 ⟹ XP_016881603

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,122,139 - 23,147,221 (+)	NCBI

Sequence:

show sequence

ACTCCCTAGAAACTTGTTGAATGGCTGTGACCAAGATGCTGATAATGATATAGAAAATAAAATC
CAGGCTGAAATGGTCTCAGATGGACATGAGGAACTTGCTGAGAACTGGAGCAAAGGGAGCGTTGACATTTAGAGATGTGGCCATAGAATTCTCTCTGGAGGAGTGGCAATGTCTGGACACCGAACAAC
AGAATTTATATAGAAATGTAATGTTAGATAACTACAGAAACCTGGTCTTCCTGGGTATTGCTGTCTCAAAGCCAGACCTGATCACCTGTCTGGAGCAAGAAAAAGAGCCTTGGAATTTGAAGACACAT
GATATGGTAGCCAAACCCCCAGTTATATGTTCTCATATTGCCCAAGACCTTTGGCCAGAGCAAGGCATAAAAGATTATTTCCAAGAAGTCATACTGAGACAATATAAAAAATGTAGACATGAGAATTT
ACTGTTAAGAAAAGGCTGTAAAAATGTGGATGAGTTTAAGATGCACAAAAAAGGTTATAATAGACATAACCAGTGTTTGACAACTTCCCATAGCAAAATATTTCAGTGTGACAAATATGTGAAAGTCT
TTCATAAATTTTCAAATTCAAACAGACATAAGATAAGACATACTTCGAAGAAACCTTTCAAATGTAAAGAATGTGGAAAATTATTTTGCATTCTTTCACACTTAGCTCAACATAAAAAAATTCATACT
GGAGAGAAATCCTACAAATGTGAAGAATATGGCAAAGCCTTTAATGAGTCCTCAAACTGTACTACACATAAAAGAATTACTGAGAAAAAACCTTACAAATGTAAAGAATGTGGCAAAGCCTTTAACTG
GTTTTCACATTTTACTACACATAAGAGAATTCATACTGGAGAAAAACCCTACCAATGTGAGAAATGTGGCAAATTTTTTAACCAATCCACAAACCTTACTACACATAAAAGAATTCATACTGGAGAGA
AACCCTATAAATGTGAAGAATGTGGCAAAGCCTTTAACCAGTCCTCAAACCTTACTGAACATAAGAAAATTCATACTAAAGAGCAACCATACAAATGCGAAAAATGTGGCAAAGCTTTTAAGTGGTCC
TCAACCCTTACAAAACATAAAAGAATTCATAATGGAGAAAAACCCTACAAATGTGAAGAATGTGGCAAAGCTTTTAACCGATCCTCAACCCTTAATAGACATAAGATAACTCATACTGGAGGGAAACC
CTACAAATATAAAGAATGTGGTAAAGCTTTTAACCAATCCTCAACTCTTACTATACATAAGATAATTCATACTGTAGAGAAATTTTACAAATGTGAAGAATGTGGCAAAGCCTTTAGCCGTATCTCAC
ACCTTACTACACATAAGAGAATTCATACTGGAGAGAAACCCTACAAATGTGAAGAATGTGGCAGAGCTTTCAACCAGTCCTCAACCCTTACTACACATAAAAGAATTCATACTGGAGAGAAACCCTAT
GAATGTGAAGAATGTGGCAAAGCTTTTAACCGGTCCTCAACCCTCACTACACATAAGATAATTCATTCTGGGGAAAAAATCTACAAATGTAAAGAATGTGGTAAAGCCTTTAGGCGGTTCTCACACCT
TACTAGGCATAAGACAATTCATACATAAAATTGTAAAGACTGTGGCAAAGCTTTTAAACAATCTTTATACCTTACTACACATAAGATAATTCATACTGAAGAGAAACCCTACAAATGTGAAGAATGTG
GCAAAGCTTTTAACCAGTCCTCAAATCTTACTAAACATAAGGTAATTCATACTGGAGAAAAACCTACAAATGTGAAGAATGTGGCAAAGTCTTCAACCAATCTTCACACCTTACTACACATAAGATAA
TTCATACTGGAGAGAAACCCTACAAGTGTGAAGAATGTGACAAAGCCTTTAACAAATCCTTAATTCTTAACAGACATGATTCATACCAGAGAGAAACTCTACAAACCTGAAAGTTTTAACAGTGCTTT
TGACAACACCTCAAACTTTTCCAGATGTCAAAGAAATGCTGGTGAGAAATTCTAGAAATATGAAGAATGTGACAAAGCCATTAAATTGTTGTCACATTTAATTGTAGGTAAGGTGATTCATACTGGAG
AAAACTTCTACAAGTGTAAACAAAGTGGCAAAACTTTTAACCAATGCTCACACTTTATTGCACAGGACATTTATACTTGAGAATAAATATACAAGTGTAAAGAAAGTGAAAACCCTATTAATATCTGC
TCACATCAACTCAACATCAGAGTTCATACTTAATAAAATCATTAAAAGTGCAATTACTGTCCAAAGATTTTTTCAGAAAATATAAGCCTTTAAACTTCAGAAGATGATTTATTTTGAAGACAAACATT
GAAATGTAGAGAGTTATAGTAACTTTACTTGTATCACAATCTTATTCTACTCATTTTGTACTAGAGGCAAACCCTGAAGCCATTGCTCAAATTTTGTTCGACATCAGACAGATAATTTGTATTAATGA
AAAACTCTCCAAATAAAATAGATTTGGAGAAAACATTTTTTTCAAAAACTACAGCTTAGGAAACTTCAGAGAGTTTATACTAAAATATATTTTTGTGGATGCAATAAATAGAAAAAAAAATTTAATCC
AAAATTAAGTTTAGGTAAGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGTACCTTGGGATGCCAAGGCTTGCATTTCTGTAATAATAATTGACATTGATAATTTCTTAATGTATCTGTTGGTCAT
ATGTATGTATTTTCTTGAAAAATATTTATGCCTCTTGCTCATTTGTAACAGTTATTTGTTGTTTGTTGTGTAGTCATTTAAGTTTCTGATGTATTTTTGATATTAACCCCTTGACACATGTATGATTT
ACAAATATTTTGTTCCAATTTTTAGTTGACTTGTTGATTGTGTCAGATTCTGTGCAACAGCATTTTAATTTGTAGTAA

hide sequence

RefSeq Acc Id:

XM_017026115 ⟹ XP_016881604

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,211 - 23,147,221 (+)	NCBI

Sequence:

show sequence

GTGGGTCCTGGAGCTCCATCCAATCAGTGGCACTGGTGTAGGAACCGCCCGATCAGGCGCGCAGTTGGAGAGGAGGGCGTGGCTTCCGGCATTTGGCGGGGTCTTTGTCTCTCGCTCCCGCCAGAGCT
TGGGATCGGTCTTCACTGTTCCGCGTCCTCTACCTGGGAACCACCGACCCCCGCCCGGCGACTTTGTCACAGACTCTGTTGCCCTGTGATCTGCAGGTCCTGGGAGACGCACAGCCAAGATGCCAGGG
CACCCTGGAAGCTGTGAAGTGGGAGCGTTGACATTTAGAGATGTGGCCATAGAATTCTCTCTGGAGGAGTGGCAATGTCTGGACACCGAACAACAGAATTTATATAGAAATGTAATGTTAGATAACTA
CAGAAACCTGGTCTTCCTGGGTATTGCTGTCTCAAAGCCAGACCTGATCACCTGTCTGGAGCAAGAAAAAGAGCCTTGGAATTTGAAGACACATGATATGGTAGCCAAACCCCCAGTTATATGTTCTC
ATATTGCCCAAGACCTTTGGCCAGAGCAAGGCATAAAAGATTATTTCCAAGAAGTCATACTGAGACAATATAAAAAATGTAGACATGAGAATTTACTGTTAAGAAAAGGCTGTAAAAATGTGGATGAG
TTTAAGATGCACAAAAAAGGTTATAATAGACATAACCAGTGTTTGACAACTTCCCATAGCAAAATATTTCAGTGTGACAAATATGTGAAAGTCTTTCATAAATTTTCAAATTCAAACAGACATAAGAT
AAGACATACTTCGAAGAAACCTTTCAAATGTAAAGAATGTGGAAAATTATTTTGCATTCTTTCACACTTAGCTCAACATAAAAAAATTCATACTGGAGAGAAATCCTACAAATGTGAAGAATATGGCA
AAGCCTTTAATGAGTCCTCAAACTGTACTACACATAAAAGAATTACTGAGAAAAAACCTTACAAATGTAAAGAATGTGGCAAAGCCTTTAACTGGTTTTCACATTTTACTACACATAAGAGAATTCAT
ACTGGAGAAAAACCCTACCAATGTGAGAAATGTGGCAAATTTTTTAACCAATCCACAAACCTTACTACACATAAAAGAATTCATACTGGAGAGAAACCCTATAAATGTGAAGAATGTGGCAAAGCCTT
TAACCAGTCCTCAAACCTTACTGAACATAAGAAAATTCATACTAAAGAGCAACCATACAAATGCGAAAAATGTGGCAAAGCTTTTAAGTGGTCCTCAACCCTTACAAAACATAAAAGAATTCATAATG
GAGAAAAACCCTACAAATGTGAAGAATGTGGCAAAGCTTTTAACCGATCCTCAACCCTTAATAGACATAAGATAACTCATACTGGAGGGAAACCCTACAAATATAAAGAATGTGGTAAAGCTTTTAAC
CAATCCTCAACTCTTACTATACATAAGATAATTCATACTGTAGAGAAATTTTACAAATGTGAAGAATGTGGCAAAGCCTTTAGCCGTATCTCACACCTTACTACACATAAGAGAATTCATACTGGAGA
GAAACCCTACAAATGTGAAGAATGTGGCAGAGCTTTCAACCAGTCCTCAACCCTTACTACACATAAAAGAATTCATACTGGAGAGAAACCCTATGAATGTGAAGAATGTGGCAAAGCTTTTAACCGGT
CCTCAACCCTCACTACACATAAGATAATTCATTCTGGGGAAAAAATCTACAAATGTAAAGAATGTGGTAAAGCCTTTAGGCGGTTCTCACACCTTACTAGGCATAAGACAATTCATACATAAAATTGT
AAAGACTGTGGCAAAGCTTTTAAACAATCTTTATACCTTACTACACATAAGATAATTCATACTGAAGAGAAACCCTACAAATGTGAAGAATGTGGCAAAGCTTTTAACCAGTCCTCAAATCTTACTAA
ACATAAGGTAATTCATACTGGAGAAAAACCTACAAATGTGAAGAATGTGGCAAAGTCTTCAACCAATCTTCACACCTTACTACACATAAGATAATTCATACTGGAGAGAAACCCTACAAGTGTGAAGA
ATGTGACAAAGCCTTTAACAAATCCTTAATTCTTAACAGACATGATTCATACCAGAGAGAAACTCTACAAACCTGAAAGTTTTAACAGTGCTTTTGACAACACCTCAAACTTTTCCAGATGTCAAAGA
AATGCTGGTGAGAAATTCTAGAAATATGAAGAATGTGACAAAGCCATTAAATTGTTGTCACATTTAATTGTAGGTAAGGTGATTCATACTGGAGAAAACTTCTACAAGTGTAAACAAAGTGGCAAAAC
TTTTAACCAATGCTCACACTTTATTGCACAGGACATTTATACTTGAGAATAAATATACAAGTGTAAAGAAAGTGAAAACCCTATTAATATCTGCTCACATCAACTCAACATCAGAGTTCATACTTAAT
AAAATCATTAAAAGTGCAATTACTGTCCAAAGATTTTTTCAGAAAATATAAGCCTTTAAACTTCAGAAGATGATTTATTTTGAAGACAAACATTGAAATGTAGAGAGTTATAGTAACTTTACTTGTAT
CACAATCTTATTCTACTCATTTTGTACTAGAGGCAAACCCTGAAGCCATTGCTCAAATTTTGTTCGACATCAGACAGATAATTTGTATTAATGAAAAACTCTCCAAATAAAATAGATTTGGAGAAAAC
ATTTTTTTCAAAAACTACAGCTTAGGAAACTTCAGAGAGTTTATACTAAAATATATTTTTGTGGATGCAATAAATAGAAAAAAAAATTTAATCCAAAATTAAGTTTAGGTAAGGCCAGGCACAGTGGC
TCACACCTGTAATCCCAGTACCTTGGGATGCCAAGGCTTGCATTTCTGTAATAATAATTGACATTGATAATTTCTTAATGTATCTGTTGGTCATATGTATGTATTTTCTTGAAAAATATTTATGCCTC
TTGCTCATTTGTAACAGTTATTTGTTGTTTGTTGTGTAGTCATTTAAGTTTCTGATGTATTTTTGATATTAACCCCTTGACACATGTATGATTTACAAATATTTTGTTCCAATTTTTAGTTGACTTGT
TGATTGTGTCAGATTCTGTGCAACAGCATTTTAATTTGTAGTAA

hide sequence

RefSeq Acc Id:

XM_047437993 ⟹ XP_047293949

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,130,366 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047437994 ⟹ XP_047293950

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,092,678 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047437995 ⟹ XP_047293951

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,211 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047437996 ⟹ XP_047293952

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,211 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047437997 ⟹ XP_047293953

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,211 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047437998 ⟹ XP_047293954

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,211 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047437999 ⟹ XP_047293955

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,211 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047438000 ⟹ XP_047293956

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,347 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047438001 ⟹ XP_047293957

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,120,187 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047438002 ⟹ XP_047293958

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,135,958 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047438003 ⟹ XP_047293959

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,135,981 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047438004 ⟹ XP_047293960

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,102,334 - 23,147,221 (+)	NCBI

RefSeq Acc Id:

XM_047438005 ⟹ XP_047293961

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,125,379 - 23,136,051 (+)	NCBI

RefSeq Acc Id:

XM_054319431 ⟹ XP_054175406

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,257,255 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319432 ⟹ XP_054175407

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,210,338 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319433 ⟹ XP_054175408

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,265,491 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319434 ⟹ XP_054175409

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,210,339 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319435 ⟹ XP_054175410

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,227,881 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319436 ⟹ XP_054175411

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,210,339 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319437 ⟹ XP_054175412

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,210,339 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319438 ⟹ XP_054175413

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,210,339 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319439 ⟹ XP_054175414

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,210,551 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319440 ⟹ XP_054175415

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,210,339 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319441 ⟹ XP_054175416

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,210,339 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319442 ⟹ XP_054175417

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,210,339 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319443 ⟹ XP_054175418

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,210,551 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319444 ⟹ XP_054175419

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,255,304 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319445 ⟹ XP_054175420

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,271,075 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319446 ⟹ XP_054175421

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,271,100 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319447 ⟹ XP_054175422

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,237,524 - 23,282,034 (+)	NCBI

RefSeq Acc Id:

XM_054319448 ⟹ XP_054175423

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	23,260,503 - 23,271,168 (+)	NCBI

RefSeq Acc Id:

XR_001753564

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,211 - 23,107,052 (+)	NCBI

Sequence:

show sequence

ACGCCTCAGCTCATTTGTTAATTAGCAGTAATTGCCCGGGTCAGTGACACCTCCTACTTGAGCC
TCTTTCCCTGTCCATAAAATGCACTAATACTGGGGTGGGTGGGATTGGGAGGTGGGTCCTGGAGCTCCATCCAATCAGTGGCACTGGTGTAGGAACCGCCCGATCAGGCGCGCAGTTGGAGAGGAGGG
CGTGGCTTCCGGCATTTGGCGGGGTCTTTGTCTCTCGCTCCCGCCAGAGCTTGGGATCGGTCTTCACTGTTCCGCGTCCTCTACCTGGGAACCACCGACCCCCGCCCGGCGACTTTGTCACAGACTCT
GTTGCCCTGTGATCTGCAGGTCCTGGGAGACGCACAGCCAAGATGCCAGGGCACCCTGGAAGCTGTGAAGTGTTCAGATGCATAATCTCATCCCTGAACATCCTGCTGGTGCGATTATGACATATGAT
TTTACCCAGCACCAGAGGGATTTGATGCTCCTGCCTGGGCCCAACTCACAGAAGGGATTGTGACATATCACTGGACCCAGCACTGAGGGGACATTGTGTAATATCGTTGGGCCTCACACGTACGTTAT
GTGACTCTCCTGCGTGTGCCCTGTCCATGTGGGCCATTGTGACATATTGCTGGGTCCAACAACTGGTTGATGTAGCTCTACTGCCTAGGTCCTGCCTATGGAGGACTTTGTGATGTATCCCTGAACCC
ATCACACAGATTCTGCCCTCAGAGGACATTGTGACATGTCACTGGGCCTAATACTAAGATGACATCATTCTTTAGTTTTGGCACTGCCCTCAGAAGCCGTGGTGGTGTATTGCTGGGCCCAGAGCCAA
TGTGATGTGAGTCTCCTGCCTGGATCCTGCCTACAAGGTGCATTGTGACATACCTCTGGGCCCTTTGACTATTTTATGTGACTCTCCTCTCTTACCTGGATGTTGCCCAAAAAGAGATTGTGACATAC
TTTGCACCCAGCACTGAGGTGATTTGACTGTCCTCTTCTGCCTGTGCTTTGCCTACAGGAGAGAGAGTGACTTATTACTGAGTTTAGCATACACATGATGTGATTTTCCTCCACTCACAGAAGTCATT
GTGACATATATCTTGGCCCATCACTGAGATTGTGACTGTCTTTTTCCTGGGACCTGTCCACAGTGGAGAGTATGACACTTTTTGGCCAAGCACCTACAAGATACGACTCTCTTCTTACACCTGGGCCA
CTGGGGTGATTTTGACATGTAGTTGGCCCCAGCTCCAAGATTATGTGACTCCACACTTCTTCCTGAGCCCTACCTACAGGTAGCATTGTGTCATATCTGTGAGACCCTCAATTAGGTGAAATGACTCT
TTGTTTGGGCCCTCTTCTCAAGGTACCGTGACATTGCTGGGCCCAGCATCTAGGTGATGTAACTCTACTGTACTGTTTGGTTTCTGCCTAAAAAGGGATTGTGACATACCACTCTATCAAGAACCTAG
GTGAGGTGACTCCTCTCCAGCCTGGGACCTGCATACATTGCTTATTGACACATATCACTGGCTCCAGCACCTAGGTTATGTGAATCCTCTTCTTCCCAGATCCTGCCAAAAGGAAAGATTGTGACATA
TCACTGGAACCAGCACTTAGGCTATTGTGACATATGCCTGAGGCTAACACCCAGATGATATAAGTCTTCATCCTGGACCCTGTCTACAGAAGTCATTGCGATATATGTCTTCACCAATCACTGAGGTC
GAACGCCCAGTGATGTGACTCTCCTTCCTGGTCCATGCCCTCAGGGAAGATTGTGACATACCCCGGCCCAGCACACAGTTAATGTCACTCTTGTGCTTGCTGTCTACCCATGGGTAGGATTGTGACAT
ATATCGTGGCCAAGCACAAAGATGTAATGACTGTCATACCTCGAAGAAAGCAATAGAGTTAATGTTGCTCCTAGGTAGGCTTAGGAAAATGAGGAAGTCGTCTTTCTGTTCAAATCTCACTCTCTGAC
ATATATAAAGCCCTAGTGTGTTACAGAGAATGTCATAACAGGGCTCCTCACACAGGTGAGATCGTGTTCTATACACAGCCCACCAATCTTGAGAATTGTCACCCTCACACATGGACAGAGTCCACTGG
TGAAGTCCTGAATCACACATGAATGCAGTTCACAATTGGAATTGTGACTGTCATCATTGAACATCTAGCCACAATTTGGATGGTGATTCTTTTTTTTTTTTTTTTTTT

hide sequence

RefSeq Acc Id:

XR_001753565

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,211 - 23,107,052 (+)	NCBI

Sequence:

show sequence

CAGCTCATTTGTTAATTAGCAGTAATTGCCCGGGTCAGTGACACCTCCTACTTGAGCCTCTTTCCCTGTCCATAAAATGCACTAATACTGGGGTGGGTGGGATTGGGAGGTGGGTCCTGGAGCTCCAT
CCAATCAGTGGCACTGGTGTAGGAACCGCCCGATCAGGCGCGCAGTTGGAGAGGAGGGCGTGGCTTCCGGCATTTGGCGGGGTCTTTGTCTCTCGCTCCCGCCAGAGCTTGGGATCGGTCTTCACTGT
TCCGCGTCCTCTACCTGGGAACCACCGACCCCCGCCCGGCGACTTTGTCACAGACTCTGTTGCCCTGTGATCTGCAGGTCCTGGGAGACGCACAGCCAAGATGCCAGGGCACCCTGGAAGCTGTGAAG
TGTTCAGATGCATAATCTCATCCCTGAACATCCTGCTGGTGCGATTATGACATATGATTTTACCCAGCACCAGAGGGATTTGATGCTCCTGCCTGGGCCCAACTCACAGAAGGGATTGTGACATATCA
CTGGACCCAGCACTGAGGGGACATTGTGTAATATCGTTGGGCCTCACACGTACGTTATGTGACTCTCCTGCGTGTGCCCTGTCCATGTGGGCCATTGTGACATATTGCTGGGTCCAACAACTGGTTGA
TGTAGCTCTACTGCCTAGGTCCTGCCTATGGAGGACTTTGTGATGTATCCCTGAACCCATCACACAGATTCTGCCCTCAGAGGACATTGTGACATGTCACTGGGCCTAATACTAAGATGACATCATTC
TTTAGTTTTGGCACTGCCCTCAGAAGCCGTGGTGGTGTATTGCTGGGCCCAGAGCCAATGTGATGTGAGTCTCCTGCCTGGATCCTGCCTACAAGGTGCATTGTGACATACCTCTGGGCCCTTTGACT
ATTTTATGTGACTCTCCTCTCTTACCTGGATGTTGCCCAAAAAGAGATTGTGACATACTTTGCACCCAGCACTGAGGTGATTTGACTGTCCTCTTCTGCCTGTGCTTTGCCTACAGGAGAGAGAGTGA
CTTATTACTGAGTTTAGCATACACATGATGTGATTTTCCTCCACTCACAGAAGTCATTGTGACATATATCTTGGCCCATCACTGAGATTGTGACTGTCTTTTTCCTGGGACCTGTCCACAGTGGAGAG
TATGACACTTTTTGGCCAAGCACCTACAAGATACGACTCTCTTCTTACACCTGGGCCACTGGGGTGATTTTGACATGTAGTTGGCCCCAGCTCCAAGATTATGTGACTCCACACTTCTTCCTGAGCCC
TACCTACAGGTTATGTGAATCCTCTTCTTCCCAGATCCTGCCAAAAGGAAAGATTGTGACATATCACTGGAACCAGCACTTAGGCTATTGTGACATATGCCTGAGGCTAACACCCAGATGATATAAGT
CTTCATCCTGGACCCTGTCTACAGAAGTCATTGCGATATATGTCTTCACCAATCACTGAGGTCGAACGCCCAGTGATGTGACTCTCCTTCCTGGTCCATGCCCTCAGGGAAGATTGTGACATACCCCG
GCCCAGCACACAGTTAATGTCACTCTTGTGCTTGCTGTCTACCCATGGGTAGGATTGTGACATATATCGTGGCCAAGCACAAAGATGTAATGACTGTCATACCTCGAAGAAAGCAATAGAGTTAATGT
TGCTCCTAGGTAGGCTTAGGAAAATGAGGAAGTCGTCTTTCTGTTCAAATCTCACTCTCTGACATATATAAAGCCCTAGTGTGTTACAGAGAATGTCATAACAGGGCTCCTCACACAGGTGAGATCGT
GTTCTATACACAGCCCACCAATCTTGAGAATTGTCACCCTCACACATGGACAGAGTCCACTGGTGAAGTCCTGAATCACACATGAATGCAGTTCACAATTGGAATTGTGACTGTCATCATTGAACATC
TAGCCACAATTTGGATGGTGATTCTTTTTTTTTTTTTTTTTTT

hide sequence

RefSeq Acc Id:

XR_001753566

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,211 - 23,107,052 (+)	NCBI

Sequence:

show sequence

CCCCCCGACGCCTCAGCTCATTTGTTAATTAGCAGTAATTGCCCGGGTCAGTGACACCTCCTAC
TTGAGCCTCTTTCCCTGTCCATAAAATGCACTAATACTGGGGTGGGTGGGATTGGGAGGTGGGTCCTGGAGCTCCATCCAATCAGTGGCACTGGTGTAGGAACCGCCCGATCAGGCGCGCAGTTGGAG
AGGAGGGCGTGGCTTCCGGCATTTGGCGGGGTCTTTGTCTCTCGCTCCCGCCAGAGCTTGGGATCGGTCTTCACTGTTCCGCGTCCTCTACCTGGGAACCACCGACCCCCGCCCGGCGACTTTGTCAC
AGACTCTGTTGCCCTGTGATCTGCAGGTCCTGGGAGACGCACAGCCAAGATGCCAGGGCACCCTGGAAGCTGTGAAGTGTTCAGATGCATAATCTCATCCCTGAACATCCTGCTGGTGCGATTATGAC
ATATGATTTTACCCAGCACCAGAGGGATTTGATGCTCCTGCCTGGGCCCAACTCACAGAAGGGATTGTGACATATCACTGGACCCAGCACTGAGGGGACATTGTGTAATATCGTTGGGCCTCACACGT
ACGTTATGTGACTCTCCTGCGTGTGCCCTGTCCATGTGGGCCATTGTGACATATTGCTGGGTCCAACAACTGGTTGATGTAGCTCTACTGCCTAGGTCCTGCCTATGGAGGACTTTGTGATGTATCCC
TGAACCCATCACACAGATTCTGCCCTCAGAGGACATTGTGACATGTCACTGGGCCTAATACTAAGATGACATCATTCTTTAGTTTTGGCACTGCCCTCAGAAGCCGTGGTGGTGTATTGCTGGGCCCA
GAGCCAATGTGATGTGAGTCTCCTGCCTGGATCCTGCCTACAAGGTGCATTGTGACATACCTCTGGGCCCTTTGACTATTTTATGTGACTCTCCTCTCTTACCTGGATGTTGCCCAAAAAGAGATTGT
GACATACTTTGCACCCAGCACTGAGGTGATTTGACTGTCCTCTTCTGCCTGTGCTTTGCCTACAGGAGAGAGAGTGACTTATTACTGAGTTTAGCATACACATGATGTGATTTTCCTCCACTCACAGA
AGTCATTGTGACATATATCTTGGCCCATCACTGAGATTGTGACTGTCTTTTTCCTGGGACCTGTCCACAGTGGAGAGTATGACACTTTTTGGCCAAGCACCTACAAGATACGACTCTCTTCTTACACC
TGGGCCACTGGGGTGATTTTGACATGTAGTTGGCCCCAGCTCCAAGATTATGTGACTCCACACTTCTTCCTGAGCCCTACCTACAGGTAGCATTGTGTCATATCTGTGAGACCCTCAATTAGGTGAAA
TGACTCTTTGTTTGGGCCCTCTTCTCAAGGTACCGTGACATTGCTGGGCCCAGCATCTAGGTGATGTAACTCTACTGTACTGTTTGGTTTCTGCCTAAAAAGGGATTGTGACATACCACTCTATCAAG
AACCTAGGTGAGGTGACTCCTCTCCAGCCTGGGACCTGCATACATTGCTTATTGACACATATCACTGGCTCCAGCACCTAGGTTATGTGAATCCTCTTCTTCCCAGATCCTGCCAAAAGGAAAGATTG
TGACATATCACTGGAACCAGCACTTAGGAGAAGGCTGTAACATATTCCTGGTTGAGTATTCAGGTGATGTGACACTCCTGTTTGGTCCCTGCCTTCAGAAAAGATTGTGATGTACTCCTGGCCAAAAA
CCCAGGTGATGTGACTCTTATCTCTCCCTATTCACAGATTGATGACATATCAGATCCATTTAGAGTGGAAAAAATATGTTGGCCATTTAAAAATAGTCATTGGAAGGCCTATGCACCTAAGAGAACCT
CATGTATCTTCTGCTACTGAAGTCTAATATTACTAAATTCAAAAAGGCTTTAATGCATTATGACAAAGCATATGAAGAAAGCCTTAAGGTGAAGAAAGCCTTAATAGTCTACTGACTGTGGACAGTAA
AACCCTTTATTATCTAGAACCCAGAGATTGAGTCTGCCTGCCATGTACACTGAAGCAAGACATCAAGACTTTGAAAGCTGGGTTGATAATCTCACAACTTAGAAGGGCCCCTCCAGACTCTTTAATTG
TAAACCCATAGGAGATCTTAAAGCTAACCAGAAAGATTTCTCCTAAAAAGCAGATGGATATCTTTATGTAGATAGCTTTTTTAATAAGATCAAAAATCAAGACACATTTGCTATCATGATACTCTTAG
TTAAGTTTGTTTATGGCTCTACAAACAATAGAAATTTAAAAAGCATCTTTTGTGTGCACTCATTGGGTATACTTATATGTAGAGAATTTTGCAGCCAACGTGTGAAAAAACATAACATCTTTTATAGG
TAAAAAATGAAAGGCAGGCCAGGCACGGTGGCTAATGCCTGTAATCCCAACACTTTGGGAGGCTGAGGTGGGCAGATCATGAGGTCAG

hide sequence

RefSeq Acc Id:

XR_001753567

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,092,678 - 23,107,052 (+)	NCBI

Sequence:

show sequence

GGATTGGGAGGTGGGTCCTGGAGCTCCATCCAATCAGTGGCACTGGTGTAGGAACCGCCCGATCAGGCGCGCAGTTGGAGAGGAGGGCGTGGCTTCCGGCATTTGGCGGGGTCTTTGTCTCTCGCTCC
CGCCAGAGCTTGGGATCGGTCTTCACTGTTCCGCGTCCTCTACCTGGGAACCACCGACCCCCGCCCGGCGACTTTGTCACAGACTCTGTTGCCCTGTGATCTGCAGGTCCTGGGAGACGCACAGCCAA
GATGCCAGGGCACCCTGGAAGCTGTGAAGTGTTCAGATGCATAATCTCATCCCTGAACATCCTGCTGGTGCGATTATGACATATGATTTTACCCAGCACCAGAGGGATTTGATGCTCCTGCCTGGGCC
CAACTCACAGAAGGGATTGTGACATATCACTGGACCCAGCACTGAGGGGACATTGTGTAATATCGTTGGGCCTCACACGTACGTTATGTGACTCTCCTGCGTGTGCCCTGTCCATGTGGGCCATTGTG
ACATATTGCTGGGTCCAACAACTGGTTGATGTAGCTCTACTGCCTAGGTCCTGCCTATGGAGGACTTTGTGATGTATCCCTGAACCCATCACACAGATTCTGCCCTCAGAGGACATTGTGACATGTCA
CTGGGCCTAATACTAAGATGACATCATTCTTTAGTTTTGGCACTGCCCTCAGAAGCCGTGGTGGTGTATTGCTGGGCCCAGAGCCAATGTGATGTGAGTCTCCTGCCTGGATCCTGCCTACAAGGTTA
TGTGAATCCTCTTCTTCCCAGATCCTGCCAAAAGGAAAGATTGTGACATATCACTGGAACCAGCACTTAGGCTATTGTGACATATGCCTGAGGCTAACACCCAGATGATATAAGTCTTCATCCTGGAC
CCTGTCTACAGAAGTCATTGCGATATATGTCTTCACCAATCACTGAGGTCGAACGCCCAGTGATGTGACTCTCCTTCCTGGTCCATGCCCTCAGGGAAGATTGTGACATACCCCGGCCCAGCACACAG
TTAATGTCACTCTTGTGCTTGCTGTCTACCCATGGGTAGGATTGTGACATATATCGTGGCCAAGCACAAAGATGTAATGACTGTCATACCTCGAAGAAAGCAATAGAGTTAATGTTGCTCCTAGGTAG
GCTTAGGAAAATGAGGAAGTCGTCTTTCTGTTCAAATCTCACTCTCTGACATATATAAAGCCCTAGTGTGTTACAGAGAATGTCATAACAGGGCTCCTCACACAGGTGAGATCGTGTTCTATACACAG
CCCACCAATCTTGAGAATTGTCACCCTCACACATGGACAGAGTCCACTGGTGAAGTCCTGAATCACACATGAATGCAGTTCACAATTGGAATTGTGACTGTCATCATTGAACATCTAGCCACAATTTG
GATGGTGATTCTTTTTTTTTTTTTTTTTTT

hide sequence

RefSeq Acc Id:

XR_001753568

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,211 - 23,107,052 (+)	NCBI

Sequence:

show sequence

GATTGGGAGGTGGGTCCTGGAGCTCCATCCAATCAGTGGCACTGGTGTAGGAACCGCCCGATCA
GGCGCGCAGTTGGAGAGGAGGGCGTGGCTTCCGGCATTTGGCGGGGTCTTTGTCTCTCGCTCCCGCCAGAGCTTGGGATCGGTCTTCACTGTTCCGCGTCCTCTACCTGGGAACCACCGACCCCCGCC
CGGCGACTTTGTCACAGACTCTGTTGCCCTGTGATCTGCAGGTCCTGGGAGACGCACAGCCAAGATGCCAGGGCACCCTGGAAGCTGTGAAGTGTTCAGATGCATAATCTCATCCCTGAACATCCTGC
TGGTGCGATTATGACATATGATTTTACCCAGCACCAGAGGGATTTGATGCTCCTGCCTGGGCCCAACTCACAGAAGGGATTGTGACATATCACTGGACCCAGCACTGAGGGGACATTGTGTAATATCG
TTGGGCCTCACACGTACGTTATGTGACTCTCCTGCGTGTGCCCTGTCCATGTGGGCCATTGTGACATATTGCTGGGTCCAACAACTGGTTGATGTAGCTCTACTGCCTAGGTCCTGCCTATGGAGGAC
TTTGTGATGTATCCCTGAACCCATCACACAGATTCTGCCCTCAGAGGACATTGTGACATGTCACTGGGCCTAATACTAAGATGACATCATTCTTTAGTTTTGGCACTGCCCTCAGAAGCCGTGGTGGT
GTATTGCTGGGCCCAGAGCCAATGTGATGTTATGTGAATCCTCTTCTTCCCAGATCCTGCCAAAAGGAAAGATTGTGACATATCACTGGAACCAGCACTTAGGCTATTGTGACATATGCCTGAGGCTA
ACACCCAGATGATATAAGTCTTCATCCTGGACCCTGTCTACAGAAGTCATTGCGATATATGTCTTCACCAATCACTGAGGTCGAACGCCCAGTGATGTGACTCTCCTTCCTGGTCCATGCCCTCAGGG
AAGATTGTGACATACCCCGGCCCAGCACACAGTTAATGTCACTCTTGTGCTTGCTGTCTACCCATGGGTAGGATTGTGACATATATCGTGGCCAAGCACAAAGATGTAATGACTGTCATACCTCGAAG
AAAGCAATAGAGTTAATGTTGCTCCTAGGTAGGCTTAGGAAAATGAGGAAGTCGTCTTTCTGTTCAAATCTCACTCTCTGACATATATAAAGCCCTAGTGTGTTACAGAGAATGTCATAACAGGGCTC
CTCACACAGGTGAGATCGTGTTCTATACACAGCCCACCAATCTTGAGAATTGTCACCCTCACACATGGACAGAGTCCACTGGTGAAGTCCTGAATCACACATGAATGCAGTTCACAATTGGAATTGTG
ACTGTCATCATTGAACATCTAGCCACAATTTGGATGGTGATTCTTTTTTTTTTTTTTTTTTT

hide sequence

RefSeq Acc Id:

XR_007066501

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	23,075,211 - 23,107,052 (+)	NCBI


Protein RefSeqs	NP_001264332	(Get FASTA)	NCBI Sequence Viewer
	XP_016881603	(Get FASTA)	NCBI Sequence Viewer
	XP_016881604	(Get FASTA)	NCBI Sequence Viewer
	XP_047293949	(Get FASTA)	NCBI Sequence Viewer
	XP_047293950	(Get FASTA)	NCBI Sequence Viewer
	XP_047293951	(Get FASTA)	NCBI Sequence Viewer
	XP_047293952	(Get FASTA)	NCBI Sequence Viewer
	XP_047293953	(Get FASTA)	NCBI Sequence Viewer
	XP_047293954	(Get FASTA)	NCBI Sequence Viewer
	XP_047293955	(Get FASTA)	NCBI Sequence Viewer
	XP_047293956	(Get FASTA)	NCBI Sequence Viewer
	XP_047293957	(Get FASTA)	NCBI Sequence Viewer
	XP_047293958	(Get FASTA)	NCBI Sequence Viewer
	XP_047293959	(Get FASTA)	NCBI Sequence Viewer
	XP_047293960	(Get FASTA)	NCBI Sequence Viewer
	XP_047293961	(Get FASTA)	NCBI Sequence Viewer
	XP_054175406	(Get FASTA)	NCBI Sequence Viewer
	XP_054175407	(Get FASTA)	NCBI Sequence Viewer
	XP_054175408	(Get FASTA)	NCBI Sequence Viewer
	XP_054175409	(Get FASTA)	NCBI Sequence Viewer
	XP_054175410	(Get FASTA)	NCBI Sequence Viewer
	XP_054175411	(Get FASTA)	NCBI Sequence Viewer
	XP_054175412	(Get FASTA)	NCBI Sequence Viewer
	XP_054175413	(Get FASTA)	NCBI Sequence Viewer
	XP_054175414	(Get FASTA)	NCBI Sequence Viewer
	XP_054175415	(Get FASTA)	NCBI Sequence Viewer
	XP_054175416	(Get FASTA)	NCBI Sequence Viewer
	XP_054175417	(Get FASTA)	NCBI Sequence Viewer
	XP_054175418	(Get FASTA)	NCBI Sequence Viewer
	XP_054175419	(Get FASTA)	NCBI Sequence Viewer
	XP_054175420	(Get FASTA)	NCBI Sequence Viewer
	XP_054175421	(Get FASTA)	NCBI Sequence Viewer
	XP_054175422	(Get FASTA)	NCBI Sequence Viewer
	XP_054175423	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	BAD18617	(Get FASTA)	NCBI Sequence Viewer
	EAW84934	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000472959
	ENSP00000472959.1
GenBank Protein	Q6ZMV8	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_001264332 ⟸ NM_001277403

- UniProtKB:

Q6ZMV8 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MGALTFRDVAIEFSLEEWQCLDTEQQNLYRNVMLDNYRNLVFLGIAVSKPDLITCLEQEKEPWNLKTHDMVAKPPVICSHIAQDLWPEQGIKDYFQEVILRQYKKCRHENLLLRKGCKNVDEFKMHKK
GYNRHNQCLTTSHSKIFQCDKYVKVFHKFSNSNRHKIRHTSKKPFKCKECGKLFCILSHLAQHKKIHTGEKSYKCEEYGKAFNESSNCTTHKRITEKKPYKCKECGKAFNWFSHFTTHKRIHTGEKPY
QCEKCGKFFNQSTNLTTHKRIHTGEKPYKCEECGKAFNQSSNLTEHKKIHTKEQPYKCEKCGKAFKWSSTLTKHKRIHNGEKPYKCEECGKAFNRSSTLNRHKITHTGGKPYKYKECGKAFNQSSTLT
IHKIIHTVEKFYKCEECGKAFSRISHLTTHKRIHTGEKPYKCEECGRAFNQSSTLTTHKRIHTGEKPYECEECGKAFNRSSTLTTHKIIHSGEKIYKCKECGKAFRRFSHLTRHKTIHT

hide sequence

RefSeq Acc Id:

XP_016881604 ⟸ XM_017026115

- Peptide Label:

isoform X2

- Sequence:

show sequence

MPGHPGSCEVGALTFRDVAIEFSLEEWQCLDTEQQNLYRNVMLDNYRNLVFLGIAVSKPDLITCLEQEKEPWNLKTHDMVAKPPVICSHIAQDLWPEQGIKDYFQEVILRQYKKCRHENLLLRKGCKN
VDEFKMHKKGYNRHNQCLTTSHSKIFQCDKYVKVFHKFSNSNRHKIRHTSKKPFKCKECGKLFCILSHLAQHKKIHTGEKSYKCEEYGKAFNESSNCTTHKRITEKKPYKCKECGKAFNWFSHFTTHK
RIHTGEKPYQCEKCGKFFNQSTNLTTHKRIHTGEKPYKCEECGKAFNQSSNLTEHKKIHTKEQPYKCEKCGKAFKWSSTLTKHKRIHNGEKPYKCEECGKAFNRSSTLNRHKITHTGGKPYKYKECGK
AFNQSSTLTIHKIIHTVEKFYKCEECGKAFSRISHLTTHKRIHTGEKPYKCEECGRAFNQSSTLTTHKRIHTGEKPYECEECGKAFNRSSTLTTHKIIHSGEKIYKCKECGKAFRRFSHLTRHKTIHT

hide sequence

RefSeq Acc Id:

XP_016881603 ⟸ XM_017026114

- Peptide Label:

isoform X1

- Sequence:

show sequence

MDMRNLLRTGAKGALTFRDVAIEFSLEEWQCLDTEQQNLYRNVMLDNYRNLVFLGIAVSKPDLITCLEQEKEPWNLKTHDMVAKPPVICSHIAQDLWPEQGIKDYFQEVILRQYKKCRHENLLLRKGC
KNVDEFKMHKKGYNRHNQCLTTSHSKIFQCDKYVKVFHKFSNSNRHKIRHTSKKPFKCKECGKLFCILSHLAQHKKIHTGEKSYKCEEYGKAFNESSNCTTHKRITEKKPYKCKECGKAFNWFSHFTT
HKRIHTGEKPYQCEKCGKFFNQSTNLTTHKRIHTGEKPYKCEECGKAFNQSSNLTEHKKIHTKEQPYKCEKCGKAFKWSSTLTKHKRIHNGEKPYKCEECGKAFNRSSTLNRHKITHTGGKPYKYKEC
GKAFNQSSTLTIHKIIHTVEKFYKCEECGKAFSRISHLTTHKRIHTGEKPYKCEECGRAFNQSSTLTTHKRIHTGEKPYECEECGKAFNRSSTLTTHKIIHSGEKIYKCKECGKAFRRFSHLTRHKTI
HT

hide sequence

Ensembl Acc Id:

ENSP00000472959 ⟸ ENST00000597761

Ensembl Acc Id:

ENSP00000469805 ⟸ ENST00000599195

Protein Domains

KRAB

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q6ZMV8-F1-model_v2	AlphaFold	Q6ZMV8	1-503	view protein structure

RGD ID:

6795119

Promoter ID:

HG_KWN:29457

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid, NB4

Transcripts:

ENST00000327867, UC002NRB.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	23,091,521 - 23,092,021 (+)	MPROMDB

Database	Acc Id	Source(s)
COSMIC	ZNF730	COSMIC
Ensembl Genes	ENSG00000183850	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000597761	ENTREZGENE
	ENST00000597761.7	UniProtKB/Swiss-Prot
Gene3D-CATH	6.10.140.140	UniProtKB/Swiss-Prot
	Classic Zinc Finger	UniProtKB/Swiss-Prot
GTEx	ENSG00000183850	GTEx
HGNC ID	HGNC:32470	ENTREZGENE
Human Proteome Map	ZNF730	Human Proteome Map
InterPro	KRAB	UniProtKB/Swiss-Prot
	KRAB_dom_sf	UniProtKB/Swiss-Prot
	Znf_C2H2-type	UniProtKB/Swiss-Prot
	Znf_C2H2_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_type	UniProtKB/Swiss-Prot
KEGG Report	hsa:100129543	UniProtKB/Swiss-Prot
NCBI Gene	100129543	ENTREZGENE
PANTHER	C2H2-TYPE DOMAIN-CONTAINING PROTEIN	UniProtKB/Swiss-Prot
	ZNF44 PROTEIN	UniProtKB/Swiss-Prot
Pfam	KRAB	UniProtKB/Swiss-Prot
	zf-C2H2	UniProtKB/Swiss-Prot
	zf-H2C2_2	UniProtKB/Swiss-Prot
PharmGKB	PA162410249	PharmGKB
PROSITE	KRAB	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot
SMART	KRAB	UniProtKB/Swiss-Prot
	ZnF_C2H2	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF109640	UniProtKB/Swiss-Prot
	SSF57667	UniProtKB/Swiss-Prot
UniProt	M0QYG2_HUMAN	UniProtKB/TrEMBL
	M0QYI4_HUMAN	UniProtKB/TrEMBL
	Q6ZMV8	ENTREZGENE
	Q75LP1	ENTREZGENE, UniProtKB/TrEMBL
	ZN730_HUMAN	UniProtKB/Swiss-Prot

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


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


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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