ZSCAN26 (zinc finger and SCAN domain containing 26)

Gene: ZSCAN26 (zinc finger and SCAN domain containing 26) Homo sapiens

Analyze

Symbol:

ZSCAN26

Name:

zinc finger and SCAN domain containing 26

RGD ID:

1345585

HGNC Page

HGNC:12978

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 transcription by RNA polymerase II. Located in cytosol and nucleoplasm.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

MGC2815; SRE-ZBP; SREZBP; zinc finger and SCAN domain-containing protein 26; zinc finger protein 187; ZNF187

RGD Orthologs

Alliance Genes

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	6	28,267,058 - 28,278,224 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	6	28,234,921 - 28,245,981 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	6	28,342,872 - 28,353,960 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	6	28,342,911 - 28,353,957	NCBI
Celera	6	29,841,233 - 29,852,427 (+)	NCBI		Celera
Cytogenetic Map	6	p22.1	NCBI
HuRef	6	28,042,442 - 28,053,636 (+)	NCBI		HuRef
CHM1_1	6	28,237,154 - 28,248,348 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

genetic disease (IAGP)

megacolon (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

17beta-estradiol (ISO)

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

4,4'-sulfonyldiphenol (ISO)

acrylamide (EXP)

amphetamine (ISO)

antirheumatic drug (EXP)

aristolochic acid A (EXP)

Aroclor 1254 (ISO)

atrazine (EXP)

avobenzone (EXP)

benzo[a]pyrene (EXP)

bisphenol A (ISO)

bisphenol F (ISO)

cadmium atom (EXP)

cadmium dichloride (ISO)

cadmium sulfate (ISO)

carbon nanotube (ISO)

CGP 52608 (EXP)

copper atom (EXP)

copper(0) (EXP)

copper(II) sulfate (EXP)

cyclosporin A (EXP)

dicrotophos (EXP)

dioxygen (ISO)

disulfiram (EXP)

dorsomorphin (EXP)

doxorubicin (EXP)

epoxiconazole (ISO)

ethyl methanesulfonate (EXP)

formaldehyde (EXP)

gentamycin (ISO)

methapyrilene (ISO)

methyl methanesulfonate (EXP)

methylmercury chloride (EXP)

nickel atom (EXP)

ozone (ISO)

quercetin (EXP)

SB 431542 (EXP)

sodium arsenite (EXP,ISO)

sunitinib (EXP)

temozolomide (EXP)

tetraphene (ISO)

urethane (EXP)

valproic acid (EXP)

vinclozolin (ISO)

zinc atom (EXP)

zinc(0) (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

regulation of DNA-templated transcription (IEA,NAS)

regulation of transcription by RNA polymerase II (IBA,IEA)

Cellular Component

cytosol (IDA)

nucleoplasm (IDA)

nucleus (IEA,NAS)

Molecular Function

DNA-binding transcription factor activity (NAS)

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

metal ion binding (IEA)

protein binding (IPI)

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

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Aganglionic megacolon (IAGP)

References

References - curated

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

Additional References at PubMed

PMID:1569959	PMID:12477932	PMID:14702039	PMID:16344560	PMID:19416867	PMID:21873635	PMID:21988832	PMID:25416956	PMID:26186194	PMID:26496610	PMID:28514442	PMID:29180619
PMID:32296183	PMID:32814053	PMID:33961781	PMID:35563538	PMID:36089195	PMID:37689310

Genomics

Comparative Map Data

ZSCAN26
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	6	28,267,058 - 28,278,224 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	6	28,234,921 - 28,245,981 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	6	28,342,872 - 28,353,960 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	6	28,342,911 - 28,353,957	NCBI
Celera	6	29,841,233 - 29,852,427 (+)	NCBI		Celera
Cytogenetic Map	6	p22.1	NCBI
HuRef	6	28,042,442 - 28,053,636 (+)	NCBI		HuRef
CHM1_1	6	28,237,154 - 28,248,348 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI		T2T-CHM13v2.0

Zscan26
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	13	21,626,344 - 21,637,901 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	13	21,626,350 - 21,637,900 (-)	Ensembl		GRCm39 Ensembl
GRCm38	13	21,442,180 - 21,453,727 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	13	21,442,180 - 21,453,730 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	13	21,534,044 - 21,545,596 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	13	21,449,702 - 21,455,407 (-)	NCBI		MGSCv36	mm8
Celera	13	21,708,080 - 21,719,630 (-)	NCBI		Celera
Cytogenetic Map	13	A3.1	NCBI
cM Map	13	7.8	NCBI

Zscan26
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	17	47,843,822 - 47,863,799 (+)	NCBI		GRCr8
mRatBN7.2	17	43,148,063 - 43,168,070 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	17	43,148,079 - 43,168,070 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	17	45,205,514 - 45,225,474 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	17	49,964,628 - 49,984,588 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	17	44,455,001 - 44,474,976 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	17	45,188,221 - 45,207,846 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	17	45,188,248 - 45,207,065 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	17	58,261,028 - 58,283,803 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	17	50,790,889 - 50,811,601 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	17	50,811,382 - 50,811,474 (+)	NCBI
Celera	17	53,299,163 - 53,320,052 (-)	NCBI		Celera
Cytogenetic Map	17	p11	NCBI

Zscan26
(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_004955465	13,626,541 - 13,640,818 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955465	13,626,552 - 13,638,819 (+)	NCBI	ChiLan1.0	ChiLan1.0

ZSCAN26
(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	5	42,882,293 - 42,894,125 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	6	38,883,155 - 38,894,987 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	6	28,069,220 - 28,080,625 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	6	28,741,890 - 28,752,403 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	6	28,741,984 - 28,752,403 (+)	Ensembl	panpan1.1		panPan2

ZSCAN26
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	35	25,406,872 - 25,415,377 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	35	25,398,717 - 25,415,382 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	35	25,264,958 - 25,274,121 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	35	25,704,876 - 25,714,039 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	35	25,697,177 - 25,713,632 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	35	25,369,512 - 25,380,949 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	35	25,422,733 - 25,431,898 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	35	26,892,180 - 26,901,539 (+)	NCBI		UU_Cfam_GSD_1.0

Zscan26
(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_024404946	28,687,869 - 28,699,952 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936772	86,251 - 90,873 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936772	85,439 - 97,363 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZSCAN26
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	7	22,114,868 - 22,132,502 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	7	22,114,768 - 22,135,139 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1

ZSCAN26
(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	17	44,289,206 - 44,299,823 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666044	27,957,009 - 27,967,844 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Zscan26
(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_004624756	24,622,629 - 24,633,916 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624756	24,623,786 - 24,633,882 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ZSCAN26
5 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 6p22.3-21.33(chr6:18120520-30767516)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052180]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052180]\|See cases [RCV000052180]	Chr6:18120520..30767516 [GRCh38] Chr6:18120751..30735293 [GRCh37] Chr6:18228730..30843272 [NCBI36] Chr6:6p22.3-21.33	pathogenic
GRCh38/hg38 6p22.2-22.1(chr6:26280579-28727313)x3	copy number gain	See cases [RCV000133692]	Chr6:26280579..28727313 [GRCh38] Chr6:26280807..28695090 [GRCh37] Chr6:26388786..28803069 [NCBI36] Chr6:6p22.2-22.1	uncertain significance
GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3	copy number gain	See cases [RCV000138956]	Chr6:3224310..30657190 [GRCh38] Chr6:3224544..30624967 [GRCh37] Chr6:3169543..30732946 [NCBI36] Chr6:6p25.2-21.33	pathogenic
GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3	copy number gain	See cases [RCV000143497]	Chr6:156974..46789291 [GRCh38] Chr6:156974..46757028 [GRCh37] Chr6:101974..46864987 [NCBI36] Chr6:6p25.3-12.3	pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3	copy number gain	See cases [RCV000512067]	Chr6:156975..170919482 [GRCh37] Chr6:6p25.3-q27	pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)	copy number gain	See cases [RCV000510595]	Chr6:156975..170919482 [GRCh37] Chr6:6p25.3-q27	pathogenic
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3	copy number gain	not provided [RCV000745400]	Chr6:60107..171054786 [GRCh37] Chr6:6p25.3-q27	pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3	copy number gain	not provided [RCV000745404]	Chr6:165632..170919470 [GRCh37] Chr6:6p25.3-q27	pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3	copy number gain	not provided [RCV000745403]	Chr6:108666..170980171 [GRCh37] Chr6:6p25.3-q27	pathogenic
GRCh37/hg19 6p22.1-21.32(chr6:28130359-32108367)x3	copy number gain	not provided [RCV000745592]	Chr6:28130359..32108367 [GRCh37] Chr6:6p22.1-21.32	uncertain significance
NC_000006.11:g.28005012_31683185del	deletion	Megacolon [RCV001290055]	Chr6:28005012..31683185 [GRCh37] Chr6:6p22.1-21.33	likely pathogenic
NM_001023560.4(ZSCAN26):c.953A>T (p.Lys318Ile)	single nucleotide variant	Inborn genetic diseases [RCV002783600]	Chr6:28276609 [GRCh38] Chr6:28244386 [GRCh37] Chr6:6p22.1	uncertain significance
NM_001023560.4(ZSCAN26):c.212G>A (p.Arg71Gln)	single nucleotide variant	Inborn genetic diseases [RCV002708219]	Chr6:28272131 [GRCh38] Chr6:28239909 [GRCh37] Chr6:6p22.1	uncertain significance
NM_001023560.4(ZSCAN26):c.1393G>A (p.Gly465Ser)	single nucleotide variant	Inborn genetic diseases [RCV002980491]	Chr6:28277049 [GRCh38] Chr6:28244826 [GRCh37] Chr6:6p22.1	uncertain significance
NM_001023560.4(ZSCAN26):c.1124C>A (p.Thr375Asn)	single nucleotide variant	Inborn genetic diseases [RCV003216233]	Chr6:28276780 [GRCh38] Chr6:28244557 [GRCh37] Chr6:6p22.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	482
Count of miRNA genes:	322
Interacting mature miRNAs:	343
Transcripts:	ENST00000316606, ENST00000421553, ENST00000423234
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

D6S2118

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	28,245,618 - 28,245,752	UniSTS	GRCh37
Build 36	6	28,353,597 - 28,353,731	RGD	NCBI36
Celera	6	29,852,064 - 29,852,198	RGD
Cytogenetic Map	6	p21.31	UniSTS
HuRef	6	28,053,273 - 28,053,407	UniSTS
Stanford-G3 RH Map	6	1379.0	UniSTS
NCBI RH Map	6	406.6	UniSTS
GeneMap99-G3 RH Map	6	1511.0	UniSTS

D6S1940

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	28,244,913 - 28,245,243	UniSTS	GRCh37
Build 36	6	28,352,892 - 28,353,222	RGD	NCBI36
Celera	6	29,851,359 - 29,851,689	RGD
Cytogenetic Map	6	p21.31	UniSTS
HuRef	6	28,052,568 - 28,052,898	UniSTS
TNG Radiation Hybrid Map	6	15016.0	UniSTS
GeneMap99-GB4 RH Map	6	119.27	UniSTS
GeneMap99-GB4 RH Map	6	114.63	UniSTS
Whitehead-RH Map	6	165.1	UniSTS
NCBI RH Map	6	490.5	UniSTS
GeneMap99-G3 RH Map	6	1442.0	UniSTS

SHGC-132144

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	28,245,578 - 28,245,768	UniSTS	GRCh37
Build 36	6	28,353,557 - 28,353,747	RGD	NCBI36
Celera	6	29,852,024 - 29,852,214	RGD
Cytogenetic Map	6	p21.31	UniSTS
HuRef	6	28,053,233 - 28,053,423	UniSTS
TNG Radiation Hybrid Map	6	15025.0	UniSTS

RH46597

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	28,245,647 - 28,245,804	UniSTS	GRCh37
Build 36	6	28,353,626 - 28,353,783	RGD	NCBI36
Celera	6	29,852,093 - 29,852,250	RGD
Cytogenetic Map	6	p21.31	UniSTS
HuRef	6	28,053,302 - 28,053,459	UniSTS
GeneMap99-GB4 RH Map	6	115.64	UniSTS
NCBI RH Map	6	490.5	UniSTS

D6S2280

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	28,238,575 - 28,238,693	UniSTS	GRCh37
Build 36	6	28,346,554 - 28,346,672	RGD	NCBI36
Celera	6	29,845,020 - 29,845,138	RGD
Cytogenetic Map	6	p21.31	UniSTS
HuRef	6	28,046,229 - 28,046,347	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

1790

1433

1237

180

1027

2248

975

2541

245

1304

1250

784

1397

Low

645

1525

489

443

893

374

2108

1220

1191

174

152

360

420

1391

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001023560	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001111039	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001287421	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001287422	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_152736	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011514862	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011514864	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011514866	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011514867	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011514869	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017011264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017011265	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024446538	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024446539	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419311	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419312	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419313	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419314	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356342	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356343	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356344	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356345	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356346	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356347	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356348	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356349	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AJ420533	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK095948	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK293524	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK295393	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
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	AK301081	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK315645	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL021997	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL526328	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL832741	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC013951	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC013962	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX537535	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471081	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068272	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA167287	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA341149	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA528922	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA566660	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA884554	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB262147	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
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	KF459630	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	Z11773	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000316606 ⟹ ENSP00000484931

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	28,267,058 - 28,278,201 (+)	Ensembl

RefSeq Acc Id:

ENST00000421553 ⟹ ENSP00000481707

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	28,267,143 - 28,278,204 (+)	Ensembl

RefSeq Acc Id:

ENST00000611552 ⟹ ENSP00000478769

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	28,267,149 - 28,277,159 (+)	Ensembl

RefSeq Acc Id:

ENST00000614088 ⟹ ENSP00000479314

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	28,267,359 - 28,278,221 (+)	Ensembl

RefSeq Acc Id:

ENST00000617168 ⟹ ENSP00000481024

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	28,267,143 - 28,272,703 (+)	Ensembl

RefSeq Acc Id:

ENST00000619937 ⟹ ENSP00000484018

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	28,267,359 - 28,278,224 (+)	Ensembl

RefSeq Acc Id:

ENST00000623276 ⟹ ENSP00000485228

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	28,267,153 - 28,277,530 (+)	Ensembl

RefSeq Acc Id:

NM_001023560 ⟹ NP_001018854

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI
GRCh37	6	28,234,788 - 28,246,001 (+)	NCBI
Build 36	6	28,342,872 - 28,353,960 (+)	NCBI Archive
Celera	6	29,841,233 - 29,852,427 (+)	RGD
HuRef	6	28,042,442 - 28,053,656 (+)	NCBI
CHM1_1	6	28,237,154 - 28,248,368 (+)	NCBI
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

Sequence:

show sequence

AGAGCTGACACTCGGCGATGAGCTAAGACGCTGTTTCAGAGCGTTTGGGTCCTCTGAGGCCCCT
TGACCAGGAGTGTCTCTGAAGATACAGTCCAAAGAAAGTTCTCCAAAACAAGGAGAACAGTCTG
AAGCTGGGGATGGCAACAGCATTGGTGAGTGCCCATTCCCTGGCTCCCCTGAATCTGAAGAAGG
AGGGGCTTCGGGTAGTGAGGGAGGATCACTACTCTACTTGGGAACAGGGATTCAAGCTGCAAGG
AAACAGTAAAGGCCTTGGACAGGAGCCATTGTGCAAACAATTCAGGCAGTTGCGTTATGAAGAG
ACCACAGGACCTCGAGAAGCACTAAGTCGGCTCCGGGAGCTCTGTCAACAGTGGCTACAGCCCG
AGACCCATACCAAGGAGCAGATCCTGGAGCTGCTGGTGCTGGAGCAGTTTCTGATCATCCTGCC
TAAGGAGCTCCAGGCCCGGGTGCAGGAGCATCACCCAGAGAGCAGGGAGGACGTGGTTGTTGTT
CTGGAGGATTTGCAGCTGGATCTTGGAGAAACAGGACAACAGGTGGACCCAGACCAGCCAAAGA
AACAAAAAATACTTGTGGAGGAGATGGCCCCTCTGAAAGGAGTACAGGAACAGCAGGTTCGGCA
TGAGTGTGAAGTTACAAAGCCTGAGAAAGAGAAGGGTGAGGAGACAAGGATTGAGAATGGGAAG
CTTATTGTAGTAACAGACTCTTGTGGAAGAGTAGAGTCATCTGGGAAAATATCTGAACCCATGG
AGGCTCATAATGAGGGCTCTAACTTGGAAAGGCATCAGGCCAAGCCCAAAGAGAAGATTGAGTA
TAAATGCTCAGAACGTGAGCAGAGATTCATCCAGCACTTGGACCTGATTGAACATGCGAGTACA
CACACGGGAAAGAAACTCTGCGAGTCTGATGTGTGTCAGAGTTCCAGTCTTACAGGACATAAGA
AAGTCCTCTCTAGAGAGAAAGGTCATCAGTGTCATGAGTGTGGGAAAGCCTTTCAGAGGAGTTC
ACACCTCGTCAGACATCAGAAAATCCATCTTGGTGAGAAGCCTTATCAGTGCAATGAGTGTGGC
AAAGTCTTTAGCCAGAATGCAGGCCTTTTGGAACATCTCAGAATTCATACTGGAGAGAAACCTT
ATCTATGTATCCATTGTGGAAAAAATTTTAGGCGCAGCTCTCACCTTAATCGACATCAGAGAAT
TCACAGTCAGGAGGAGCCCTGTGAGTGCAAGGAGTGTGGAAAAACCTTTAGTCAGGCCTTACTC
CTCACCCACCATCAGAGAATCCATAGTCACTCCAAAAGCCATCAATGTAACGAGTGTGGAAAAG
CTTTCAGTTTGACCTCAGACCTTATTCGACACCACAGAATTCATACTGGAGAAAAACCTTTCAA
GTGTAACATATGCCAGAAAGCCTTCCGACTAAACTCACACCTTGCTCAGCATGTAAGAATCCAC
AATGAAGAAAAACCCTATCAGTGTAGTGAATGTGGAGAAGCCTTCAGGCAAAGGTCAGGTCTTT
TTCAACATCAGAGATATCACCACAAAGACAAACTGGCTTGATGAGGTGTTCTCTCCTTGTAGAA
CATCAGAGAAGGCACATTGACTAGCAAACAGCACTTTAGGAAAAGTCACCGTAGCCCACTGTGG
CATCAGAAAATTCTTGGGGGCTGAGTTGGAGGCTCCCTGCCTCTATTCTCTCTCCTTTGCTTTC
CTTGAAGTCAGCTTTGGACCACAATAATTTCACTGTAGATGATATGCTAGGATCAAAGTTAAAC
AGCATTCTTCACTGCAGGACATCTCAGAGCATGTAACATAACTGCATGATTATATACTCTAAGC
AATAGAGAGCTTCATGACTGAGTAAGAGTTTTGAAGTCAGCAGTGAATCAAGTGCCCACAGATT
TGCAGGCTTAAGCAGAACAAGGGAAGATTGATATTTTTGGATATGCTATAGCAGCTTTCTCCTA
TGAAATAAAACTGATGATGTTTGGAAGTATACTACTCTCAAAGGTGTCTTTAAAGTACAGGTTA
ATGGTGAACATTTTCCCCCAGTGGCTTCACCTCATTCCTCCCACTGGCCTTACCCCTTCCTTCC
CCAGTGGAAGCATTTTCAAAAGCAAAGATAATTTTCGCTGGTGAACTTCAGAACTTGCCTTCAG
GGTTAGCTTCATGTAATTTTACCATTTCCCATCCCCATTCCCCACCACATTATGTCAAGATTCA
AGTTATAAATTAACGTTTTACTTAGACTTTGAAAGAGATTTCATGAGTAATTTGAATGAACCTT
GCTGAATTAATCTGAATAGCAACTGTCTGACTTGATAACTCCAGTGCCAGTATAGTGGCTGCTG
CATAGACACTATTCAGTAAATGTCTGATGAAAGAAATTGGACTTTTTCCCTTTAATACTGATGA
TGCAATTTTGAAATGTTGCTTGTTCTGGAATACTTCGGAAGTTAAACAATAAAGTCAGCTTGGA
GAGGAGATCATGATCTTTATACTGTGAATAGCAGAATGTCACAGATGAAGAATATTAAAATTAG
GGGCGTCCACTCCAAAACATATCACCAGAGTGACAACTTCAGCCCTCAGCCTCTGCAATCCATA
TATATCCTGGTCTTGGGAGTCCATAGAATACTGTTTCCTTCTAATAAAGGTTTCAAACAAA

hide sequence

RefSeq Acc Id:

NM_001111039 ⟹ NP_001104509

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI
GRCh37	6	28,234,788 - 28,246,001 (+)	NCBI
Celera	6	29,841,233 - 29,852,427 (+)	RGD
HuRef	6	28,042,442 - 28,053,656 (+)	NCBI
CHM1_1	6	28,237,154 - 28,248,368 (+)	NCBI
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

Sequence:

show sequence

AGAGCTGACACTCGGCGATGAGCTAAGACGCTGTTTCAGAGCGTTTGGGTCCTCTGAGGCCCCT
TGACCAGGAGTGTCTCTGAAGATACAGTCCAAAGAAAGTTCTCCAAAACAAGGAGAACAGTCTG
AAGCTGGGGATGGCAACAGCATTGGTGAGTGCCCATTCCCTGGCTCCCCTGAATCTGAAGAAGG
AGGGGCTTCGGGTAGTGAGGGAGGATCACTACTCTACTTGGGAACAGGGATTCAAGCTGCAAGG
AAACAGTAAAGGCCTTGGACAGGAGCCATTGTGCAAACAATTCAGGCAGTTGCGTTATGAAGAG
ACCACAGGACCTCGAGAAGCACTAAGTCGGCTCCGGGAGCTCTGTCAACAGTGGCTACAGCCCG
AGACCCATACCAAGGAGCAGATCCTGGAGCTGCTGGTGCTGGAGCAGTTTCTGATCATCCTGCC
TAAGGAGCTCCAGGCCCGGGTGCAGGAGCATCACCCAGAGAGCAGGGAGGACGTGGTTGTTGTT
CTGGAGGATTTGCAGCTGGATCTTGGAGAAACAGGACAACAGGACCCAGACCAGCCAAAGAAAC
AAAAAATACTTGTGGAGGAGATGGCCCCTCTGAAAGGAGTACAGGAACAGCAGGTTCGGCATGA
GTGTGAAGTTACAAAGCCTGAGAAAGAGAAGGGTGAGGAGACAAGGATTGAGAATGGGAAGCTT
ATTGTAGTAACAGACTCTTGTGGAAGAGTAGAGTCATCTGGGAAAATATCTGAACCCATGGAGG
CTCATAATGAGGGCTCTAACTTGGAAAGGCATCAGGCCAAGCCCAAAGAGAAGATTGAGTATAA
ATGCTCAGAACGTGAGCAGAGATTCATCCAGCACTTGGACCTGATTGAACATGCGAGTACACAC
ACGGGAAAGAAACTCTGCGAGTCTGATGTGTGTCAGAGTTCCAGTCTTACAGGACATAAGAAAG
TCCTCTCTAGAGAGAAAGGTCATCAGTGTCATGAGTGTGGGAAAGCCTTTCAGAGGAGTTCACA
CCTCGTCAGACATCAGAAAATCCATCTTGGTGAGAAGCCTTATCAGTGCAATGAGTGTGGCAAA
GTCTTTAGCCAGAATGCAGGCCTTTTGGAACATCTCAGAATTCATACTGGAGAGAAACCTTATC
TATGTATCCATTGTGGAAAAAATTTTAGGCGCAGCTCTCACCTTAATCGACATCAGAGAATTCA
CAGTCAGGAGGAGCCCTGTGAGTGCAAGGAGTGTGGAAAAACCTTTAGTCAGGCCTTACTCCTC
ACCCACCATCAGAGAATCCATAGTCACTCCAAAAGCCATCAATGTAACGAGTGTGGAAAAGCTT
TCAGTTTGACCTCAGACCTTATTCGACACCACAGAATTCATACTGGAGAAAAACCTTTCAAGTG
TAACATATGCCAGAAAGCCTTCCGACTAAACTCACACCTTGCTCAGCATGTAAGAATCCACAAT
GAAGAAAAACCCTATCAGTGTAGTGAATGTGGAGAAGCCTTCAGGCAAAGGTCAGGTCTTTTTC
AACATCAGAGATATCACCACAAAGACAAACTGGCTTGATGAGGTGTTCTCTCCTTGTAGAACAT
CAGAGAAGGCACATTGACTAGCAAACAGCACTTTAGGAAAAGTCACCGTAGCCCACTGTGGCAT
CAGAAAATTCTTGGGGGCTGAGTTGGAGGCTCCCTGCCTCTATTCTCTCTCCTTTGCTTTCCTT
GAAGTCAGCTTTGGACCACAATAATTTCACTGTAGATGATATGCTAGGATCAAAGTTAAACAGC
ATTCTTCACTGCAGGACATCTCAGAGCATGTAACATAACTGCATGATTATATACTCTAAGCAAT
AGAGAGCTTCATGACTGAGTAAGAGTTTTGAAGTCAGCAGTGAATCAAGTGCCCACAGATTTGC
AGGCTTAAGCAGAACAAGGGAAGATTGATATTTTTGGATATGCTATAGCAGCTTTCTCCTATGA
AATAAAACTGATGATGTTTGGAAGTATACTACTCTCAAAGGTGTCTTTAAAGTACAGGTTAATG
GTGAACATTTTCCCCCAGTGGCTTCACCTCATTCCTCCCACTGGCCTTACCCCTTCCTTCCCCA
GTGGAAGCATTTTCAAAAGCAAAGATAATTTTCGCTGGTGAACTTCAGAACTTGCCTTCAGGGT
TAGCTTCATGTAATTTTACCATTTCCCATCCCCATTCCCCACCACATTATGTCAAGATTCAAGT
TATAAATTAACGTTTTACTTAGACTTTGAAAGAGATTTCATGAGTAATTTGAATGAACCTTGCT
GAATTAATCTGAATAGCAACTGTCTGACTTGATAACTCCAGTGCCAGTATAGTGGCTGCTGCAT
AGACACTATTCAGTAAATGTCTGATGAAAGAAATTGGACTTTTTCCCTTTAATACTGATGATGC
AATTTTGAAATGTTGCTTGTTCTGGAATACTTCGGAAGTTAAACAATAAAGTCAGCTTGGAGAG
GAGATCATGATCTTTATACTGTGAATAGCAGAATGTCACAGATGAAGAATATTAAAATTAGGGG
CGTCCACTCCAAAACATATCACCAGAGTGACAACTTCAGCCCTCAGCCTCTGCAATCCATATAT
ATCCTGGTCTTGGGAGTCCATAGAATACTGTTTCCTTCTAATAAAGGTTTCAAACAAA

hide sequence

RefSeq Acc Id:

NM_001287421 ⟹ NP_001274350

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI
HuRef	6	28,042,442 - 28,053,656 (+)	NCBI
CHM1_1	6	28,237,503 - 28,248,368 (+)	NCBI
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

Sequence:

show sequence

AGAGCTGACACTCGGCGATGAGCTAAGACGCTGTTTCAGAGCGTTTGGGTCCTCTGAGGCCCCT
TGACCAGGTGAGCGGACCCTGGAGCTGGGCCCCGGGCTGGGGCGGAACTGCGGCCTAGGGGCCT
AGGGAGCAGCTGCTTCCCGGCGGGTGCAGAGAATCTTCCCTCGACCGAGGGGGCGGGGTCCGTA
GCGGAGGTGTCGGCCCTGGGGCCTATGAGAGTGATGAAGCTGTGGATCTGGTAAACAGAGTACA
ACCTTCTGCTGCATATTTTTCATCCATTCAGCGCAATTTTAAGTAGATATTAAAGGAGTGTCTC
TGAAGATACAGTCCAAAGAAAGTTCTCCAAAACAAGGAGAACAGTCTGAAGCTGGGGATGGCAA
CAGCATTGGACCCAGACCAGCCAAAGAAACAAAAAATACTTGTGGAGGAGATGGCCCCTCTGAA
AGGAGTACAGGAACAGCAGGTTCGGCATGAGTGTGAAGTTACAAAGCCTGAGAAAGAGAAGGGT
GAGGAGACAAGGATTGAGAATGGGAAGCTTATTGTAGTAACAGACTCTTGTGGAAGAGTAGAGT
CATCTGGGAAAATATCTGAACCCATGGAGGCTCATAATGAGGGCTCTAACTTGGAAAGGCATCA
GGCCAAGCCCAAAGAGAAGATTGAGTATAAATGCTCAGAACGTGAGCAGAGATTCATCCAGCAC
TTGGACCTGATTGAACATGCGAGTACACACACGGGAAAGAAACTCTGCGAGTCTGATGTGTGTC
AGAGTTCCAGTCTTACAGGACATAAGAAAGTCCTCTCTAGAGAGAAAGGTCATCAGTGTCATGA
GTGTGGGAAAGCCTTTCAGAGGAGTTCACACCTCGTCAGACATCAGAAAATCCATCTTGGTGAG
AAGCCTTATCAGTGCAATGAGTGTGGCAAAGTCTTTAGCCAGAATGCAGGCCTTTTGGAACATC
TCAGAATTCATACTGGAGAGAAACCTTATCTATGTATCCATTGTGGAAAAAATTTTAGGCGCAG
CTCTCACCTTAATCGACATCAGAGAATTCACAGTCAGGAGGAGCCCTGTGAGTGCAAGGAGTGT
GGAAAAACCTTTAGTCAGGCCTTACTCCTCACCCACCATCAGAGAATCCATAGTCACTCCAAAA
GCCATCAATGTAACGAGTGTGGAAAAGCTTTCAGTTTGACCTCAGACCTTATTCGACACCACAG
AATTCATACTGGAGAAAAACCTTTCAAGTGTAACATATGCCAGAAAGCCTTCCGACTAAACTCA
CACCTTGCTCAGCATGTAAGAATCCACAATGAAGAAAAACCCTATCAGTGTAGTGAATGTGGAG
AAGCCTTCAGGCAAAGGTCAGGTCTTTTTCAACATCAGAGATATCACCACAAAGACAAACTGGC
TTGATGAGGTGTTCTCTCCTTGTAGAACATCAGAGAAGGCACATTGACTAGCAAACAGCACTTT
AGGAAAAGTCACCGTAGCCCACTGTGGCATCAGAAAATTCTTGGGGGCTGAGTTGGAGGCTCCC
TGCCTCTATTCTCTCTCCTTTGCTTTCCTTGAAGTCAGCTTTGGACCACAATAATTTCACTGTA
GATGATATGCTAGGATCAAAGTTAAACAGCATTCTTCACTGCAGGACATCTCAGAGCATGTAAC
ATAACTGCATGATTATATACTCTAAGCAATAGAGAGCTTCATGACTGAGTAAGAGTTTTGAAGT
CAGCAGTGAATCAAGTGCCCACAGATTTGCAGGCTTAAGCAGAACAAGGGAAGATTGATATTTT
TGGATATGCTATAGCAGCTTTCTCCTATGAAATAAAACTGATGATGTTTGGAAGTATACTACTC
TCAAAGGTGTCTTTAAAGTACAGGTTAATGGTGAACATTTTCCCCCAGTGGCTTCACCTCATTC
CTCCCACTGGCCTTACCCCTTCCTTCCCCAGTGGAAGCATTTTCAAAAGCAAAGATAATTTTCG
CTGGTGAACTTCAGAACTTGCCTTCAGGGTTAGCTTCATGTAATTTTACCATTTCCCATCCCCA
TTCCCCACCACATTATGTCAAGATTCAAGTTATAAATTAACGTTTTACTTAGACTTTGAAAGAG
ATTTCATGAGTAATTTGAATGAACCTTGCTGAATTAATCTGAATAGCAACTGTCTGACTTGATA
ACTCCAGTGCCAGTATAGTGGCTGCTGCATAGACACTATTCAGTAAATGTCTGATGAAAGAAAT
TGGACTTTTTCCCTTTAATACTGATGATGCAATTTTGAAATGTTGCTTGTTCTGGAATACTTCG
GAAGTTAAACAATAAAGTCAGCTTGGAGAGGAGATCATGATCTTTATACTGTGAATAGCAGAAT
GTCACAGATGAAGAATATTAAAATTAGGGGCGTCCACTCCAAAACATATCACCAGAGTGACAAC
TTCAGCCCTCAGCCTCTGCAATCCATATATATCCTGGTCTTGGGAGTCCATAGAATACTGTTTC
CTTCTAATAAAGGTTTCAAACAAA

hide sequence

RefSeq Acc Id:

NM_001287422 ⟹ NP_001274351

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI
HuRef	6	28,042,442 - 28,053,656 (+)	NCBI
CHM1_1	6	28,237,154 - 28,248,368 (+)	NCBI
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

Sequence:

show sequence

AGAGCTGACACTCGGCGATGAGCTAAGACGCTGTTTCAGAGCGTTTGGGTCCTCTGAGGCCCCT
TGACCAGGTGAGGAGACAAGGATTGAGAATGGGAAGCTTATTGTAGTAACAGACTCTTGTGGAA
GAGTAGAGTCATCTGGGAAAATATCTGAACCCATGGAGGCTCATAATGAGGGCTCTAACTTGGA
AAGGCATCAGGCCAAGCCCAAAGAGAAGATTGAGTATAAATGCTCAGAACGTGAGCAGAGATTC
ATCCAGCACTTGGACCTGATTGAACATGCGAGTACACACACGGGAAAGAAACTCTGCGAGTCTG
ATGTGTGTCAGAGTTCCAGTCTTACAGGACATAAGAAAGTCCTCTCTAGAGAGAAAGGTCATCA
GTGTCATGAGTGTGGGAAAGCCTTTCAGAGGAGTTCACACCTCGTCAGACATCAGAAAATCCAT
CTTGGTGAGAAGCCTTATCAGTGCAATGAGTGTGGCAAAGTCTTTAGCCAGAATGCAGGCCTTT
TGGAACATCTCAGAATTCATACTGGAGAGAAACCTTATCTATGTATCCATTGTGGAAAAAATTT
TAGGCGCAGCTCTCACCTTAATCGACATCAGAGAATTCACAGTCAGGAGGAGCCCTGTGAGTGC
AAGGAGTGTGGAAAAACCTTTAGTCAGGCCTTACTCCTCACCCACCATCAGAGAATCCATAGTC
ACTCCAAAAGCCATCAATGTAACGAGTGTGGAAAAGCTTTCAGTTTGACCTCAGACCTTATTCG
ACACCACAGAATTCATACTGGAGAAAAACCTTTCAAGTGTAACATATGCCAGAAAGCCTTCCGA
CTAAACTCACACCTTGCTCAGCATGTAAGAATCCACAATGAAGAAAAACCCTATCAGTGTAGTG
AATGTGGAGAAGCCTTCAGGCAAAGGTCAGGTCTTTTTCAACATCAGAGATATCACCACAAAGA
CAAACTGGCTTGATGAGGTGTTCTCTCCTTGTAGAACATCAGAGAAGGCACATTGACTAGCAAA
CAGCACTTTAGGAAAAGTCACCGTAGCCCACTGTGGCATCAGAAAATTCTTGGGGGCTGAGTTG
GAGGCTCCCTGCCTCTATTCTCTCTCCTTTGCTTTCCTTGAAGTCAGCTTTGGACCACAATAAT
TTCACTGTAGATGATATGCTAGGATCAAAGTTAAACAGCATTCTTCACTGCAGGACATCTCAGA
GCATGTAACATAACTGCATGATTATATACTCTAAGCAATAGAGAGCTTCATGACTGAGTAAGAG
TTTTGAAGTCAGCAGTGAATCAAGTGCCCACAGATTTGCAGGCTTAAGCAGAACAAGGGAAGAT
TGATATTTTTGGATATGCTATAGCAGCTTTCTCCTATGAAATAAAACTGATGATGTTTGGAAGT
ATACTACTCTCAAAGGTGTCTTTAAAGTACAGGTTAATGGTGAACATTTTCCCCCAGTGGCTTC
ACCTCATTCCTCCCACTGGCCTTACCCCTTCCTTCCCCAGTGGAAGCATTTTCAAAAGCAAAGA
TAATTTTCGCTGGTGAACTTCAGAACTTGCCTTCAGGGTTAGCTTCATGTAATTTTACCATTTC
CCATCCCCATTCCCCACCACATTATGTCAAGATTCAAGTTATAAATTAACGTTTTACTTAGACT
TTGAAAGAGATTTCATGAGTAATTTGAATGAACCTTGCTGAATTAATCTGAATAGCAACTGTCT
GACTTGATAACTCCAGTGCCAGTATAGTGGCTGCTGCATAGACACTATTCAGTAAATGTCTGAT
GAAAGAAATTGGACTTTTTCCCTTTAATACTGATGATGCAATTTTGAAATGTTGCTTGTTCTGG
AATACTTCGGAAGTTAAACAATAAAGTCAGCTTGGAGAGGAGATCATGATCTTTATACTGTGAA
TAGCAGAATGTCACAGATGAAGAATATTAAAATTAGGGGCGTCCACTCCAAAACATATCACCAG
AGTGACAACTTCAGCCCTCAGCCTCTGCAATCCATATATATCCTGGTCTTGGGAGTCCATAGAA
TACTGTTTCCTTCTAATAAAGGTTTCAAACAAA

hide sequence

RefSeq Acc Id:

NM_152736 ⟹ NP_689949

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI
GRCh37	6	28,234,788 - 28,246,001 (+)	NCBI
Build 36	6	28,342,872 - 28,353,960 (+)	NCBI Archive
Celera	6	29,841,233 - 29,852,427 (+)	RGD
HuRef	6	28,042,442 - 28,053,656 (+)	NCBI
CHM1_1	6	28,237,154 - 28,248,368 (+)	NCBI
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

Sequence:

show sequence

AGAGCTGACACTCGGCGATGAGCTAAGACGCTGTTTCAGAGCGTTTGGGTCCTCTGAGGCCCCT
TGACCAGGAGTGTCTCTGAAGATACAGTCCAAAGAAAGTTCTCCAAAACAAGGAGAACAGTCTG
AAGCTGGGGATGGCAACAGCATTGGACCCAGACCAGCCAAAGAAACAAAAAATACTTGTGGAGG
AGATGGCCCCTCTGAAAGGAGTACAGGAACAGCAGGTTCGGCATGAGTGTGAAGTTACAAAGCC
TGAGAAAGAGAAGGGTGAGGAGACAAGGATTGAGAATGGGAAGCTTATTGTAGTAACAGACTCT
TGTGGAAGAGTAGAGTCATCTGGGAAAATATCTGAACCCATGGAGGCTCATAATGAGGGCTCTA
ACTTGGAAAGGCATCAGGCCAAGCCCAAAGAGAAGATTGAGTATAAATGCTCAGAACGTGAGCA
GAGATTCATCCAGCACTTGGACCTGATTGAACATGCGAGTACACACACGGGAAAGAAACTCTGC
GAGTCTGATGTGTGTCAGAGTTCCAGTCTTACAGGACATAAGAAAGTCCTCTCTAGAGAGAAAG
GTCATCAGTGTCATGAGTGTGGGAAAGCCTTTCAGAGGAGTTCACACCTCGTCAGACATCAGAA
AATCCATCTTGGTGAGAAGCCTTATCAGTGCAATGAGTGTGGCAAAGTCTTTAGCCAGAATGCA
GGCCTTTTGGAACATCTCAGAATTCATACTGGAGAGAAACCTTATCTATGTATCCATTGTGGAA
AAAATTTTAGGCGCAGCTCTCACCTTAATCGACATCAGAGAATTCACAGTCAGGAGGAGCCCTG
TGAGTGCAAGGAGTGTGGAAAAACCTTTAGTCAGGCCTTACTCCTCACCCACCATCAGAGAATC
CATAGTCACTCCAAAAGCCATCAATGTAACGAGTGTGGAAAAGCTTTCAGTTTGACCTCAGACC
TTATTCGACACCACAGAATTCATACTGGAGAAAAACCTTTCAAGTGTAACATATGCCAGAAAGC
CTTCCGACTAAACTCACACCTTGCTCAGCATGTAAGAATCCACAATGAAGAAAAACCCTATCAG
TGTAGTGAATGTGGAGAAGCCTTCAGGCAAAGGTCAGGTCTTTTTCAACATCAGAGATATCACC
ACAAAGACAAACTGGCTTGATGAGGTGTTCTCTCCTTGTAGAACATCAGAGAAGGCACATTGAC
TAGCAAACAGCACTTTAGGAAAAGTCACCGTAGCCCACTGTGGCATCAGAAAATTCTTGGGGGC
TGAGTTGGAGGCTCCCTGCCTCTATTCTCTCTCCTTTGCTTTCCTTGAAGTCAGCTTTGGACCA
CAATAATTTCACTGTAGATGATATGCTAGGATCAAAGTTAAACAGCATTCTTCACTGCAGGACA
TCTCAGAGCATGTAACATAACTGCATGATTATATACTCTAAGCAATAGAGAGCTTCATGACTGA
GTAAGAGTTTTGAAGTCAGCAGTGAATCAAGTGCCCACAGATTTGCAGGCTTAAGCAGAACAAG
GGAAGATTGATATTTTTGGATATGCTATAGCAGCTTTCTCCTATGAAATAAAACTGATGATGTT
TGGAAGTATACTACTCTCAAAGGTGTCTTTAAAGTACAGGTTAATGGTGAACATTTTCCCCCAG
TGGCTTCACCTCATTCCTCCCACTGGCCTTACCCCTTCCTTCCCCAGTGGAAGCATTTTCAAAA
GCAAAGATAATTTTCGCTGGTGAACTTCAGAACTTGCCTTCAGGGTTAGCTTCATGTAATTTTA
CCATTTCCCATCCCCATTCCCCACCACATTATGTCAAGATTCAAGTTATAAATTAACGTTTTAC
TTAGACTTTGAAAGAGATTTCATGAGTAATTTGAATGAACCTTGCTGAATTAATCTGAATAGCA
ACTGTCTGACTTGATAACTCCAGTGCCAGTATAGTGGCTGCTGCATAGACACTATTCAGTAAAT
GTCTGATGAAAGAAATTGGACTTTTTCCCTTTAATACTGATGATGCAATTTTGAAATGTTGCTT
GTTCTGGAATACTTCGGAAGTTAAACAATAAAGTCAGCTTGGAGAGGAGATCATGATCTTTATA
CTGTGAATAGCAGAATGTCACAGATGAAGAATATTAAAATTAGGGGCGTCCACTCCAAAACATA
TCACCAGAGTGACAACTTCAGCCCTCAGCCTCTGCAATCCATATATATCCTGGTCTTGGGAGTC
CATAGAATACTGTTTCCTTCTAATAAAGGTTTCAAACAAA

hide sequence

RefSeq Acc Id:

XM_011514862 ⟹ XP_011513164

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI

Sequence:

show sequence

TTAGTCTCCTTCTGCGATGCCTAAGCGGCAGCACCATCGAGCCAAGGTCCTCCAGCGTTCCTAG
AGCGGAGAAGAAAGCGCTCCGAAGAGCTAGAGCTGACACTCGGCGATGAGCTAAGACGCTGTTT
CAGAGCGTTTGGGTCCTCTGAGGCCCCTTGACCAGGTGAGCGGACCCTGGAGCTGGGCCCCGGG
CTGGGGCGGAACTGCGGCCTAGGGGCCTAGGGAGCAGCTGCTTCCCGGCGGGTGCAGAGAATCT
TCCCTCGACCGAGGGGGCGGGGTCCGTAGCGGAGGTGTCGGCCCTGGGGCCTATGAGAGTGATG
AAGCTGTGGATCTGGTAAACAGAGTACAACCTTCTGCTGCATATTTTTCATCCATTCAGCGCAA
TTTTAAGTAGATATTAAAGGAGTGTCTCTGAAGATACAGTCCAAAGAAAGTTCTCCAAAACAAG
GAGAACAGTCTGAAGCTGGGGATGGCAACAGCATTGGTGAGTGCCCATTCCCTGGCTCCCCTGA
ATCTGAAGAAGGAGGGGCTTCGGGTAGTGAGGGAGGATCACTACTCTACTTGGGAACAGGGATT
CAAGCTGCAAGGAAACAGTAAAGGCCTTGGACAGGAGCCATTGTGCAAACAATTCAGGCAGTTG
CGTTATGAAGAGACCACAGGACCTCGAGAAGCACTAAGTCGGCTCCGGGAGCTCTGTCAACAGT
GGCTACAGCCCGAGACCCATACCAAGGAGCAGATCCTGGAGCTGCTGGTGCTGGAGCAGTTTCT
GATCATCCTGCCTAAGGAGCTCCAGGCCCGGGTGCAGGAGCATCACCCAGAGAGCAGGGAGGAC
GTGGTTGTTGTTCTGGAGGATTTGCAGCTGGATCTTGGAGAAACAGGACAACAGGTGGACCCAG
ACCAGCCAAAGAAACAAAAAATACTTGTGGAGGAGATGGCCCCTCTGAAAGGAGTACAGGAACA
GCAGGTTCGGCATGAGTGTGAAGTTACAAAGCCTGAGAAAGAGAAGGGTGAGGAGACAAGGATT
GAGAATGGGAAGCTTATTGTAGTAACAGACTCTTGTGGAAGAGTAGAGTCATCTGGGAAAATAT
CTGAACCCATGGAGGCTCATAATGAGGGCTCTAACTTGGAAAGGCATCAGGCCAAGCCCAAAGA
GAAGATTGAGTATAAATGCTCAGAACGTGAGCAGAGATTCATCCAGCACTTGGACCTGATTGAA
CATGCGAGTACACACACGGGAAAGAAACTCTGCGAGTCTGATGTGTGTCAGAGTTCCAGTCTTA
CAGGACATAAGAAAGTCCTCTCTAGAGAGAAAGGTCATCAGTGTCATGAGTGTGGGAAAGCCTT
TCAGAGGAGTTCACACCTCGTCAGACATCAGAAAATCCATCTTGGTGAGAAGCCTTATCAGTGC
AATGAGTGTGGCAAAGTCTTTAGCCAGAATGCAGGCCTTTTGGAACATCTCAGAATTCATACTG
GAGAGAAACCTTATCTATGTATCCATTGTGGAAAAAATTTTAGGCGCAGCTCTCACCTTAATCG
ACATCAGAGAATTCACAGTCAGGAGGAGCCCTGTGAGTGCAAGGAGTGTGGAAAAACCTTTAGT
CAGGCCTTACTCCTCACCCACCATCAGAGAATCCATAGTCACTCCAAAAGCCATCAATGTAACG
AGTGTGGAAAAGCTTTCAGTTTGACCTCAGACCTTATTCGACACCACAGAATTCATACTGGAGA
AAAACCTTTCAAGTGTAACATATGCCAGAAAGCCTTCCGACTAAACTCACACCTTGCTCAGCAT
GTAAGAATCCACAATGAAGAAAAACCCTATCAGTGTAGTGAATGTGGAGAAGCCTTCAGGCAAA
GGTCAGGTCTTTTTCAACATCAGAGATATCACCACAAAGACAAACTGGCTTGATGAGGTGTTCT
CTCCTTGTAGAACATCAGAGAAGGCACATTGACTAGCAAACAGCACTTTAGGAAAAGTCACCGT
AGCCCACTGTGGCATCAGAAAATTCTTGGGGGCTGAGTTGGAGGCTCCCTGCCTCTATTCTCTC
TCCTTTGCTTTCCTTGAAGTCAGCTTTGGACCACAATAATTTCACTGTAGATGATATGCTAGGA
TCAAAGTTAAACAGCATTCTTCACTGCAGGACATCTCAGAGCATGTAACATAACTGCATGATTA
TATACTCTAAGCAATAGAGAGCTTCATGACTGAGTAAGAGTTTTGAAGTCAGCAGTGAATCAAG
TGCCCACAGATTTGCAGGCTTAAGCAGAACAAGGGAAGATTGATATTTTTGGATATGCTATAGC
AGCTTTCTCCTATGAAATAAAACTGATGATGTTTGGAAGTATACTACTCTCAAAGGTGTCTTTA
AAGTACAGGTTAATGGTGAACATTTTCCCCCAGTGGCTTCACCTCATTCCTCCCACTGGCCTTA
CCCCTTCCTTCCCCAGTGGAAGCATTTTCAAAAGCAAAGATAATTTTCGCTGGTGAACTTCAGA
ACTTGCCTTCAGGGTTAGCTTCATGTAATTTTACCATTTCCCATCCCCATTCCCCACCACATTA
TGTCAAGATTCAAGTTATAAATTAACGTTTTACTTAGACTTTGAAAGAGATTTCATGAGTAATT
TGAATGAACCTTGCTGAATTAATCTGAATAGCAACTGTCTGACTTGATAACTCCAGTGCCAGTA
TAGTGGCTGCTGCATAGACACTATTCAGTAAATGTCTGATGAAAGAAATTGGACTTTTTCCCTT
TAATACTGATGATGCAATTTTGAAATGTTGCTTGTTCTGGAATACTTCGGAAGTTAAACAATAA
AGTCAGCTTGGAGAGGAGATCATGATCTTTATACTGTGAATAGCAGAATGTCACAGATGAAGAA
TATTAAAATTAGGGGCGTCCACTCCAAAACATATCACCAGAGTGACAACTTCAGCCCTCAGCCT
CTGCAATCCATATATATCCTGGTCTTGGGAGTCCATAGAATACTGTTTCCTTCTAATAAAGGTT
TCAAACAAATCCCTGCAGATTTA

hide sequence

RefSeq Acc Id:

XM_011514864 ⟹ XP_011513166

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI

Sequence:

show sequence

AAACAGAGTACAACCTTCTGCTGCATATTTTTCATCCATTCAGCGCAATTTTAAGTAGATATTA
AAGGAGTGTCTCTGAAGATACAGTCCAAAGAAAGTTCTCCAAAACAAGGAGAACAGTCTGAAGC
TGGGGATGGCAACAGCATTGGGATTCAAGCTGCAAGGAAACAGTAAAGGCCTTGGACAGGAGCC
ATTGTGCAAACAATTCAGGCAGTTGCGTTATGAAGAGACCACAGGACCTCGAGAAGCACTAAGT
CGGCTCCGGGAGCTCTGTCAACAGTGGCTACAGCCCGAGACCCATACCAAGGAGCAGATCCTGG
AGCTGCTGGTGCTGGAGCAGTTTCTGATCATCCTGCCTAAGGAGCTCCAGGCCCGGGTGCAGGA
GCATCACCCAGAGAGCAGGGAGGACGTGGTTGTTGTTCTGGAGGATTTGCAGCTGGATCTTGGA
GAAACAGGACAACAGGTGGACCCAGACCAGCCAAAGAAACAAAAAATACTTGTGGAGGAGATGG
CCCCTCTGAAAGGAGTACAGGAACAGCAGGTTCGGCATGAGTGTGAAGTTACAAAGCCTGAGAA
AGAGAAGGGTGAGGAGACAAGGATTGAGAATGGGAAGCTTATTGTAGTAACAGACTCTTGTGGA
AGAGTAGAGTCATCTGGGAAAATATCTGAACCCATGGAGGCTCATAATGAGGGCTCTAACTTGG
AAAGGCATCAGGCCAAGCCCAAAGAGAAGATTGAGTATAAATGCTCAGAACGTGAGCAGAGATT
CATCCAGCACTTGGACCTGATTGAACATGCGAGTACACACACGGGAAAGAAACTCTGCGAGTCT
GATGTGTGTCAGAGTTCCAGTCTTACAGGACATAAGAAAGTCCTCTCTAGAGAGAAAGGTCATC
AGTGTCATGAGTGTGGGAAAGCCTTTCAGAGGAGTTCACACCTCGTCAGACATCAGAAAATCCA
TCTTGGTGAGAAGCCTTATCAGTGCAATGAGTGTGGCAAAGTCTTTAGCCAGAATGCAGGCCTT
TTGGAACATCTCAGAATTCATACTGGAGAGAAACCTTATCTATGTATCCATTGTGGAAAAAATT
TTAGGCGCAGCTCTCACCTTAATCGACATCAGAGAATTCACAGTCAGGAGGAGCCCTGTGAGTG
CAAGGAGTGTGGAAAAACCTTTAGTCAGGCCTTACTCCTCACCCACCATCAGAGAATCCATAGT
CACTCCAAAAGCCATCAATGTAACGAGTGTGGAAAAGCTTTCAGTTTGACCTCAGACCTTATTC
GACACCACAGAATTCATACTGGAGAAAAACCTTTCAAGTGTAACATATGCCAGAAAGCCTTCCG
ACTAAACTCACACCTTGCTCAGCATGTAAGAATCCACAATGAAGAAAAACCCTATCAGTGTAGT
GAATGTGGAGAAGCCTTCAGGCAAAGGTCAGGTCTTTTTCAACATCAGAGATATCACCACAAAG
ACAAACTGGCTTGATGAGGTGTTCTCTCCTTGTAGAACATCAGAGAAGGCACATTGACTAGCAA
ACAGCACTTTAGGAAAAGTCACCGTAGCCCACTGTGGCATCAGAAAATTCTTGGGGGCTGAGTT
GGAGGCTCCCTGCCTCTATTCTCTCTCCTTTGCTTTCCTTGAAGTCAGCTTTGGACCACAATAA
TTTCACTGTAGATGATATGCTAGGATCAAAGTTAAACAGCATTCTTCACTGCAGGACATCTCAG
AGCATGTAACATAACTGCATGATTATATACTCTAAGCAATAGAGAGCTTCATGACTGAGTAAGA
GTTTTGAAGTCAGCAGTGAATCAAGTGCCCACAGATTTGCAGGCTTAAGCAGAACAAGGGAAGA
TTGATATTTTTGGATATGCTATAGCAGCTTTCTCCTATGAAATAAAACTGATGATGTTTGGAAG
TATACTACTCTCAAAGGTGTCTTTAAAGTACAGGTTAATGGTGAACATTTTCCCCCAGTGGCTT
CACCTCATTCCTCCCACTGGCCTTACCCCTTCCTTCCCCAGTGGAAGCATTTTCAAAAGCAAAG
ATAATTTTCGCTGGTGAACTTCAGAACTTGCCTTCAGGGTTAGCTTCATGTAATTTTACCATTT
CCCATCCCCATTCCCCACCACATTATGTCAAGATTCAAGTTATAAATTAACGTTTTACTTAGAC
TTTGAAAGAGATTTCATGAGTAATTTGAATGAACCTTGCTGAATTAATCTGAATAGCAACTGTC
TGACTTGATAACTCCAGTGCCAGTATAGTGGCTGCTGCATAGACACTATTCAGTAAATGTCTGA
TGAAAGAAATTGGACTTTTTCCCTTTAATACTGATGATGCAATTTTGAAATGTTGCTTGTTCTG
GAATACTTCGGAAGTTAAACAATAAAGTCAGCTTGGAGAGGAGATCATGATCTTTATACTGTGA
ATAGCAGAATGTCACAGATGAAGAATATTAAAATTAGGGGCGTCCACTCCAAAACATATCACCA
GAGTGACAACTTCAGCCCTCAGCCTCTGCAATCCATATATATCCTGGTCTTGGGAGTCCATAGA
ATACTGTTTCCTTCTAATAAAGGTTTCAAACAAATCCCTGCAGATTTA

hide sequence

RefSeq Acc Id:

XM_017011264 ⟹ XP_016866753

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI

Sequence:

show sequence

GTTAGTCTCCTTCTGCGATGCCTAAGCGGCAGCACCATCGAGCCAAGGTCCTCCAGCGTTCCTA
GAGCGGAGAAGAAAGCGCTCCGAAGAGCTAGAGCTGACACTCGGCGATGAGCTAAGACGCTGTT
TCAGAGCGTTTGGGTCCTCTGAGGCCCCTTGACCAGGTGAGCGGACCCTGGAGCTGGGCCCCGG
GCTGGGGCGGAACTGCGGCCTAGGGGCCTAGGGAGCAGCTGCTTCCCGGCGGGTGCAGAGAATC
TTCCCTCGACCGAGGGGGCGGGGTCCGTAGCGGAGGTGTCGGCCCTGGGGCCTATGAGAGTGAT
GAAGCTGTGGATCTGGTAAACAGAGTACAACCTTCTGCTGCATATTTTTCATCCATTCAGCGCA
ATTTTAAGTAGATATTAAAGGAGTGTCTCTGAAGATACAGTCCAAAGAAAGTTCTCCAAAACAA
GGAGAACAGTCTGAAGCTGGGGATGGCAACAGCATTGGTGAGTGCCCATTCCCTGGCTCCCCTG
AATCTGAAGAAGGAGGGGCTTCGGGTAGTGAGGGAGGATCACTACTCTACTTGGGAACAGGGAT
TCAAGCTGCAAGGAAACAGTAAAGGCCTTGGACAGGAGCCATTGTGCAAACAATTCAGGCAGTT
GCGTTATGAAGAGACCACAGGACCTCGAGAAGCACTAAGTCGGCTCCGGGAGCTCTGTCAACAG
TGGCTACAGCCCGAGACCCATACCAAGGAGCAGATCCTGGAGCTGCTGGTGCTGGAGCAGTTTC
TGATCATCCTGCCTAAGGAGCTCCAGGCCCGGGTGCAGGAGCATCACCCAGAGAGCAGGGAGGA
CGTGGTTGTTGTTCTGGAGGATTTGCAGCTGGATCTTGGAGAAACAGGACAACAGGACCCAGAC
CAGCCAAAGAAACAAAAAATACTTGTGGAGGAGATGGCCCCTCTGAAAGGAGTACAGGAACAGC
AGGTTCGGCATGAGTGTGAAGTTACAAAGCCTGAGAAAGAGAAGGGTGAGGAGACAAGGATTGA
GAATGGGAAGCTTATTGTAGTAACAGACTCTTGTGGAAGAGTAGAGTCATCTGGGAAAATATCT
GAACCCATGGAGGCTCATAATGAGGGCTCTAACTTGGAAAGGCATCAGGCCAAGCCCAAAGAGA
AGATTGAGTATAAATGCTCAGAACGTGAGCAGAGATTCATCCAGCACTTGGACCTGATTGAACA
TGCGAGTACACACACGGGAAAGAAACTCTGCGAGTCTGATGTGTGTCAGAGTTCCAGTCTTACA
GGACATAAGAAAGTCCTCTCTAGAGAGAAAGGTCATCAGTGTCATGAGTGTGGGAAAGCCTTTC
AGAGGAGTTCACACCTCGTCAGACATCAGAAAATCCATCTTGGTGAGAAGCCTTATCAGTGCAA
TGAGTGTGGCAAAGTCTTTAGCCAGAATGCAGGCCTTTTGGAACATCTCAGAATTCATACTGGA
GAGAAACCTTATCTATGTATCCATTGTGGAAAAAATTTTAGGCGCAGCTCTCACCTTAATCGAC
ATCAGAGAATTCACAGTCAGGAGGAGCCCTGTGAGTGCAAGGAGTGTGGAAAAACCTTTAGTCA
GGCCTTACTCCTCACCCACCATCAGAGAATCCATAGTCACTCCAAAAGCCATCAATGTAACGAG
TGTGGAAAAGCTTTCAGTTTGACCTCAGACCTTATTCGACACCACAGAATTCATACTGGAGAAA
AACCTTTCAAGTGTAACATATGCCAGAAAGCCTTCCGACTAAACTCACACCTTGCTCAGCATGT
AAGAATCCACAATGAAGAAAAACCCTATCAGTGTAGTGAATGTGGAGAAGCCTTCAGGCAAAGG
TCAGGTCTTTTTCAACATCAGAGATATCACCACAAAGACAAACTGGCTTGATGAGGTGTTCTCT
CCTTGTAGAACATCAGAGAAGGCACATTGACTAGCAAACAGCACTTTAGGAAAAGTCACCGTAG
CCCACTGTGGCATCAGAAAATTCTTGGGGGCTGAGTTGGAGGCTCCCTGCCTCTATTCTCTCTC
CTTTGCTTTCCTTGAAGTCAGCTTTGGACCACAATAATTTCACTGTAGATGATATGCTAGGATC
AAAGTTAAACAGCATTCTTCACTGCAGGACATCTCAGAGCATGTAACATAACTGCATGATTATA
TACTCTAAGCAATAGAGAGCTTCATGACTGAGTAAGAGTTTTGAAGTCAGCAGTGAATCAAGTG
CCCACAGATTTGCAGGCTTAAGCAGAACAAGGGAAGATTGATATTTTTGGATATGCTATAGCAG
CTTTCTCCTATGAAATAAAACTGATGATGTTTGGAAGTATACTACTCTCAAAGGTGTCTTTAAA
GTACAGGTTAATGGTGAACATTTTCCCCCAGTGGCTTCACCTCATTCCTCCCACTGGCCTTACC
CCTTCCTTCCCCAGTGGAAGCATTTTCAAAAGCAAAGATAATTTTCGCTGGTGAACTTCAGAAC
TTGCCTTCAGGGTTAGCTTCATGTAATTTTACCATTTCCCATCCCCATTCCCCACCACATTATG
TCAAGATTCAAGTTATAAATTAACGTTTTACTTAGACTTTGAAAGAGATTTCATGAGTAATTTG
AATGAACCTTGCTGAATTAATCTGAATAGCAACTGTCTGACTTGATAACTCCAGTGCCAGTATA
GTGGCTGCTGCATAGACACTATTCAGTAAATGTCTGATGAAAGAAATTGGACTTTTTCCCTTTA
ATACTGATGATGCAATTTTGAAATGTTGCTTGTTCTGGAATACTTCGGAAGTTAAACAATAAAG
TCAGCTTGGAGAGGAGATCATGATCTTTATACTGTGAATAGCAGAATGTCACAGATGAAGAATA
TTAAAATTAGGGGCGTCCACTCCAAAACATATCACCAGAGTGACAACTTCAGCCCTCAGCCTCT
GCAATCCATATATATCCTGGTCTTGGGAGTCCATAGAATACTGTTTCCTTCTAATAAAGGTTTC
AAACAAATCCCTGCAGATTTA

hide sequence

RefSeq Acc Id:

XM_024446538 ⟹ XP_024302306

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI

Sequence:

show sequence

AGAGCTGACACTCGGCGATGAGCTAAGACGCTGTTTCAGAGCGTTTGGGTCCTCTGAGGCCCCT
TGACCAGGAGTGTCTCTGAAGATACAGTCCAAAGAAAGTTCTCCAAAACAAGGAGAACAGTCTG
AAGCTGGGGATGGCAACAGCATTGGGATTCAAGCTGCAAGGAAACAGTAAAGGCCTTGGACAGG
AGCCATTGTGCAAACAATTCAGGCAGTTGCGTTATGAAGAGACCACAGGACCTCGAGAAGCACT
AAGTCGGCTCCGGGAGCTCTGTCAACAGTGGCTACAGCCCGAGACCCATACCAAGGAGCAGATC
CTGGAGCTGCTGGTGCTGGAGCAGTTTCTGATCATCCTGCCTAAGGAGCTCCAGGCCCGGGTGC
AGGAGCATCACCCAGAGAGCAGGGAGGACGTGGTTGTTGTTCTGGAGGATTTGCAGCTGGATCT
TGGAGAAACAGGACAACAGGTGGACCCAGACCAGCCAAAGAAACAAAAAATACTTGTGGAGGAG
ATGGCCCCTCTGAAAGGAGTACAGGAACAGCAGGTTCGGCATGAGTGTGAAGTTACAAAGCCTG
AGAAAGAGAAGGGTGAGGAGACAAGGATTGAGAATGGGAAGCTTATTGTAGTAACAGACTCTTG
TGGAAGAGTAGAGTCATCTGGGAAAATATCTGAACCCATGGAGGCTCATAATGAGGGCTCTAAC
TTGGAAAGGCATCAGGCCAAGCCCAAAGAGAAGATTGAGTATAAATGCTCAGAACGTGAGCAGA
GATTCATCCAGCACTTGGACCTGATTGAACATGCGAGTACACACACGGGAAAGAAACTCTGCGA
GTCTGATGTGTGTCAGAGTTCCAGTCTTACAGGACATAAGAAAGTCCTCTCTAGAGAGAAAGGT
CATCAGTGTCATGAGTGTGGGAAAGCCTTTCAGAGGAGTTCACACCTCGTCAGACATCAGAAAA
TCCATCTTGGTGAGAAGCCTTATCAGTGCAATGAGTGTGGCAAAGTCTTTAGCCAGAATGCAGG
CCTTTTGGAACATCTCAGAATTCATACTGGAGAGAAACCTTATCTATGTATCCATTGTGGAAAA
AATTTTAGGCGCAGCTCTCACCTTAATCGACATCAGAGAATTCACAGTCAGGAGGAGCCCTGTG
AGTGCAAGGAGTGTGGAAAAACCTTTAGTCAGGCCTTACTCCTCACCCACCATCAGAGAATCCA
TAGTCACTCCAAAAGCCATCAATGTAACGAGTGTGGAAAAGCTTTCAGTTTGACCTCAGACCTT
ATTCGACACCACAGAATTCATACTGGAGAAAAACCTTTCAAGTGTAACATATGCCAGAAAGCCT
TCCGACTAAACTCACACCTTGCTCAGCATGTAAGAATCCACAATGAAGAAAAACCCTATCAGTG
TAGTGAATGTGGAGAAGCCTTCAGGCAAAGGTCAGGTCTTTTTCAACATCAGAGATATCACCAC
AAAGACAAACTGGCTTGATGAGGTGTTCTCTCCTTGTAGAACATCAGAGAAGGCACATTGACTA
GCAAACAGCACTTTAGGAAAAGTCACCGTAGCCCACTGTGGCATCAGAAAATTCTTGGGGGCTG
AGTTGGAGGCTCCCTGCCTCTATTCTCTCTCCTTTGCTTTCCTTGAAGTCAGCTTTGGACCACA
ATAATTTCACTGTAGATGATATGCTAGGATCAAAGTTAAACAGCATTCTTCACTGCAGGACATC
TCAGAGCATGTAACATAACTGCATGATTATATACTCTAAGCAATAGAGAGCTTCATGACTGAGT
AAGAGTTTTGAAGTCAGCAGTGAATCAAGTGCCCACAGATTTGCAGGCTTAAGCAGAACAAGGG
AAGATTGATATTTTTGGATATGCTATAGCAGCTTTCTCCTATGAAATAAAACTGATGATGTTTG
GAAGTATACTACTCTCAAAGGTGTCTTTAAAGTACAGGTTAATGGTGAACATTTTCCCCCAGTG
GCTTCACCTCATTCCTCCCACTGGCCTTACCCCTTCCTTCCCCAGTGGAAGCATTTTCAAAAGC
AAAGATAATTTTCGCTGGTGAACTTCAGAACTTGCCTTCAGGGTTAGCTTCATGTAATTTTACC
ATTTCCCATCCCCATTCCCCACCACATTATGTCAAGATTCAAGTTATAAATTAACGTTTTACTT
AGACTTTGAAAGAGATTTCATGAGTAATTTGAATGAACCTTGCTGAATTAATCTGAATAGCAAC
TGTCTGACTTGATAACTCCAGTGCCAGTATAGTGGCTGCTGCATAGACACTATTCAGTAAATGT
CTGATGAAAGAAATTGGACTTTTTCCCTTTAATACTGATGATGCAATTTTGAAATGTTGCTTGT
TCTGGAATACTTCGGAAGTTAAACAATAAAGTCAGCTTGGAGAGGAGATCATGATCTTTATACT
GTGAATAGCAGAATGTCACAGATGAAGAATATTAAAATTAGGGGCGTCCACTCCAAAACATATC
ACCAGAGTGACAACTTCAGCCCTCAGCCTCTGCAATCCATATATATCCTGGTCTTGGGAGTCCA
TAGAATACTGTTTCCTTCTAATAAAGGTTTCAAACAAATCCCTGCAGATTTA

hide sequence

RefSeq Acc Id:

XM_047419311 ⟹ XP_047275267

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI

RefSeq Acc Id:

XM_047419312 ⟹ XP_047275268

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI

RefSeq Acc Id:

XM_047419313 ⟹ XP_047275269

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI

RefSeq Acc Id:

XM_047419314 ⟹ XP_047275270

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,278,204 (+)	NCBI

RefSeq Acc Id:

XM_054356342 ⟹ XP_054212317

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

RefSeq Acc Id:

XM_054356343 ⟹ XP_054212318

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

RefSeq Acc Id:

XM_054356344 ⟹ XP_054212319

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

RefSeq Acc Id:

XM_054356345 ⟹ XP_054212320

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

RefSeq Acc Id:

XM_054356346 ⟹ XP_054212321

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

RefSeq Acc Id:

XM_054356347 ⟹ XP_054212322

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

RefSeq Acc Id:

XM_054356348 ⟹ XP_054212323

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

RefSeq Acc Id:

XM_054356349 ⟹ XP_054212324

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	28,138,885 - 28,149,946 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001018854	(Get FASTA)	NCBI Sequence Viewer
	NP_001104509	(Get FASTA)	NCBI Sequence Viewer
	NP_001274350	(Get FASTA)	NCBI Sequence Viewer
	NP_001274351	(Get FASTA)	NCBI Sequence Viewer
	NP_689949	(Get FASTA)	NCBI Sequence Viewer
	XP_011513164	(Get FASTA)	NCBI Sequence Viewer
	XP_011513166	(Get FASTA)	NCBI Sequence Viewer
	XP_016866753	(Get FASTA)	NCBI Sequence Viewer
	XP_024302306	(Get FASTA)	NCBI Sequence Viewer
	XP_047275267	(Get FASTA)	NCBI Sequence Viewer
	XP_047275268	(Get FASTA)	NCBI Sequence Viewer
	XP_047275269	(Get FASTA)	NCBI Sequence Viewer
	XP_047275270	(Get FASTA)	NCBI Sequence Viewer
	XP_054212317	(Get FASTA)	NCBI Sequence Viewer
	XP_054212318	(Get FASTA)	NCBI Sequence Viewer
	XP_054212319	(Get FASTA)	NCBI Sequence Viewer
	XP_054212320	(Get FASTA)	NCBI Sequence Viewer
	XP_054212321	(Get FASTA)	NCBI Sequence Viewer
	XP_054212322	(Get FASTA)	NCBI Sequence Viewer
	XP_054212323	(Get FASTA)	NCBI Sequence Viewer
	XP_054212324	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH13951	(Get FASTA)	NCBI Sequence Viewer
	AAH13962	(Get FASTA)	NCBI Sequence Viewer
	BAG38012	(Get FASTA)	NCBI Sequence Viewer
	BAG53173	(Get FASTA)	NCBI Sequence Viewer
	BAG57006	(Get FASTA)	NCBI Sequence Viewer
	BAG58347	(Get FASTA)	NCBI Sequence Viewer
	BAG59993	(Get FASTA)	NCBI Sequence Viewer
	BAG62685	(Get FASTA)	NCBI Sequence Viewer
	CAA77818	(Get FASTA)	NCBI Sequence Viewer
	CAD97775	(Get FASTA)	NCBI Sequence Viewer
	CAI46119	(Get FASTA)	NCBI Sequence Viewer
	EAX03147	(Get FASTA)	NCBI Sequence Viewer
	EAX03148	(Get FASTA)	NCBI Sequence Viewer
	EAX03149	(Get FASTA)	NCBI Sequence Viewer
	EAX03150	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000478769
	ENSP00000478769.1
	ENSP00000479314
	ENSP00000479314.1
	ENSP00000481024.1
	ENSP00000481707
	ENSP00000481707.1
	ENSP00000484018
	ENSP00000484018.1
	ENSP00000484931
	ENSP00000484931.1
	ENSP00000485228
	ENSP00000485228.1
GenBank Protein	Q16670	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_689949 ⟸ NM_152736
- Peptide Label:	isoform c
- UniProtKB:	A0A087X2F1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATALDPDQPKKQKILVEEMAPLKGVQEQQVRHECEVTKPEKEKGEETRIENGKLIVVTDSCGR VESSGKISEPMEAHNEGSNLERHQAKPKEKIEYKCSEREQRFIQHLDLIEHASTHTGKKLCESD VCQSSSLTGHKKVLSREKGHQCHECGKAFQRSSHLVRHQKIHLGEKPYQCNECGKVFSQNAGLL EHLRIHTGEKPYLCIHCGKNFRRSSHLNRHQRIHSQEEPCECKECGKTFSQALLLTHHQRIHSH SKSHQCNECGKAFSLTSDLIRHHRIHTGEKPFKCNICQKAFRLNSHLAQHVRIHNEEKPYQCSE CGEAFRQRSGLFQHQRYHHKDKLA hide sequence

RefSeq Acc Id:	NP_001018854 ⟸ NM_001023560
- Peptide Label:	isoform a
- UniProtKB:	A0A024RCN4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATALVSAHSLAPLNLKKEGLRVVREDHYSTWEQGFKLQGNSKGLGQEPLCKQFRQLRYEETTG PREALSRLRELCQQWLQPETHTKEQILELLVLEQFLIILPKELQARVQEHHPESREDVVVVLED LQLDLGETGQQVDPDQPKKQKILVEEMAPLKGVQEQQVRHECEVTKPEKEKGEETRIENGKLIV VTDSCGRVESSGKISEPMEAHNEGSNLERHQAKPKEKIEYKCSEREQRFIQHLDLIEHASTHTG KKLCESDVCQSSSLTGHKKVLSREKGHQCHECGKAFQRSSHLVRHQKIHLGEKPYQCNECGKVF SQNAGLLEHLRIHTGEKPYLCIHCGKNFRRSSHLNRHQRIHSQEEPCECKECGKTFSQALLLTH HQRIHSHSKSHQCNECGKAFSLTSDLIRHHRIHTGEKPFKCNICQKAFRLNSHLAQHVRIHNEE KPYQCSECGEAFRQRSGLFQHQRYHHKDKLA hide sequence

RefSeq Acc Id:	NP_001104509 ⟸ NM_001111039
- Peptide Label:	isoform b
- UniProtKB:	Q7Z3Q6 (UniProtKB/Swiss-Prot), Q5JPG4 (UniProtKB/Swiss-Prot), Q96A17 (UniProtKB/Swiss-Prot), Q16670 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MATALVSAHSLAPLNLKKEGLRVVREDHYSTWEQGFKLQGNSKGLGQEPLCKQFRQLRYEETTG PREALSRLRELCQQWLQPETHTKEQILELLVLEQFLIILPKELQARVQEHHPESREDVVVVLED LQLDLGETGQQDPDQPKKQKILVEEMAPLKGVQEQQVRHECEVTKPEKEKGEETRIENGKLIVV TDSCGRVESSGKISEPMEAHNEGSNLERHQAKPKEKIEYKCSEREQRFIQHLDLIEHASTHTGK KLCESDVCQSSSLTGHKKVLSREKGHQCHECGKAFQRSSHLVRHQKIHLGEKPYQCNECGKVFS QNAGLLEHLRIHTGEKPYLCIHCGKNFRRSSHLNRHQRIHSQEEPCECKECGKTFSQALLLTHH QRIHSHSKSHQCNECGKAFSLTSDLIRHHRIHTGEKPFKCNICQKAFRLNSHLAQHVRIHNEEK PYQCSECGEAFRQRSGLFQHQRYHHKDKLA hide sequence

RefSeq Acc Id:	NP_001274351 ⟸ NM_001287422
- Peptide Label:	isoform d
- UniProtKB:	B4DMT1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEAHNEGSNLERHQAKPKEKIEYKCSEREQRFIQHLDLIEHASTHTGKKLCESDVCQSSSLTGH KKVLSREKGHQCHECGKAFQRSSHLVRHQKIHLGEKPYQCNECGKVFSQNAGLLEHLRIHTGEK PYLCIHCGKNFRRSSHLNRHQRIHSQEEPCECKECGKTFSQALLLTHHQRIHSHSKSHQCNECG KAFSLTSDLIRHHRIHTGEKPFKCNICQKAFRLNSHLAQHVRIHNEEKPYQCSECGEAFRQRSG LFQHQRYHHKDKLA hide sequence

RefSeq Acc Id:	NP_001274350 ⟸ NM_001287421
- Peptide Label:	isoform c
- UniProtKB:	A0A087X2F1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATALDPDQPKKQKILVEEMAPLKGVQEQQVRHECEVTKPEKEKGEETRIENGKLIVVTDSCGR VESSGKISEPMEAHNEGSNLERHQAKPKEKIEYKCSEREQRFIQHLDLIEHASTHTGKKLCESD VCQSSSLTGHKKVLSREKGHQCHECGKAFQRSSHLVRHQKIHLGEKPYQCNECGKVFSQNAGLL EHLRIHTGEKPYLCIHCGKNFRRSSHLNRHQRIHSQEEPCECKECGKTFSQALLLTHHQRIHSH SKSHQCNECGKAFSLTSDLIRHHRIHTGEKPFKCNICQKAFRLNSHLAQHVRIHNEEKPYQCSE CGEAFRQRSGLFQHQRYHHKDKLA hide sequence

RefSeq Acc Id:	XP_011513164 ⟸ XM_011514862
- Peptide Label:	isoform X1
- UniProtKB:	A0A024RCN4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATALVSAHSLAPLNLKKEGLRVVREDHYSTWEQGFKLQGNSKGLGQEPLCKQFRQLRYEETTG PREALSRLRELCQQWLQPETHTKEQILELLVLEQFLIILPKELQARVQEHHPESREDVVVVLED LQLDLGETGQQVDPDQPKKQKILVEEMAPLKGVQEQQVRHECEVTKPEKEKGEETRIENGKLIV VTDSCGRVESSGKISEPMEAHNEGSNLERHQAKPKEKIEYKCSEREQRFIQHLDLIEHASTHTG KKLCESDVCQSSSLTGHKKVLSREKGHQCHECGKAFQRSSHLVRHQKIHLGEKPYQCNECGKVF SQNAGLLEHLRIHTGEKPYLCIHCGKNFRRSSHLNRHQRIHSQEEPCECKECGKTFSQALLLTH HQRIHSHSKSHQCNECGKAFSLTSDLIRHHRIHTGEKPFKCNICQKAFRLNSHLAQHVRIHNEE KPYQCSECGEAFRQRSGLFQHQRYHHKDKLA hide sequence

RefSeq Acc Id:

XP_011513166 ⟸ XM_011514864

- Peptide Label:

isoform X3

- Sequence:

show sequence

MATALGFKLQGNSKGLGQEPLCKQFRQLRYEETTGPREALSRLRELCQQWLQPETHTKEQILEL
LVLEQFLIILPKELQARVQEHHPESREDVVVVLEDLQLDLGETGQQVDPDQPKKQKILVEEMAP
LKGVQEQQVRHECEVTKPEKEKGEETRIENGKLIVVTDSCGRVESSGKISEPMEAHNEGSNLER
HQAKPKEKIEYKCSEREQRFIQHLDLIEHASTHTGKKLCESDVCQSSSLTGHKKVLSREKGHQC
HECGKAFQRSSHLVRHQKIHLGEKPYQCNECGKVFSQNAGLLEHLRIHTGEKPYLCIHCGKNFR
RSSHLNRHQRIHSQEEPCECKECGKTFSQALLLTHHQRIHSHSKSHQCNECGKAFSLTSDLIRH
HRIHTGEKPFKCNICQKAFRLNSHLAQHVRIHNEEKPYQCSECGEAFRQRSGLFQHQRYHHKDK
LA

hide sequence

RefSeq Acc Id:	XP_016866753 ⟸ XM_017011264
- Peptide Label:	isoform X2
- UniProtKB:	Q7Z3Q6 (UniProtKB/Swiss-Prot), Q5JPG4 (UniProtKB/Swiss-Prot), Q96A17 (UniProtKB/Swiss-Prot), Q16670 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MATALVSAHSLAPLNLKKEGLRVVREDHYSTWEQGFKLQGNSKGLGQEPLCKQFRQLRYEETTG PREALSRLRELCQQWLQPETHTKEQILELLVLEQFLIILPKELQARVQEHHPESREDVVVVLED LQLDLGETGQQDPDQPKKQKILVEEMAPLKGVQEQQVRHECEVTKPEKEKGEETRIENGKLIVV TDSCGRVESSGKISEPMEAHNEGSNLERHQAKPKEKIEYKCSEREQRFIQHLDLIEHASTHTGK KLCESDVCQSSSLTGHKKVLSREKGHQCHECGKAFQRSSHLVRHQKIHLGEKPYQCNECGKVFS QNAGLLEHLRIHTGEKPYLCIHCGKNFRRSSHLNRHQRIHSQEEPCECKECGKTFSQALLLTHH QRIHSHSKSHQCNECGKAFSLTSDLIRHHRIHTGEKPFKCNICQKAFRLNSHLAQHVRIHNEEK PYQCSECGEAFRQRSGLFQHQRYHHKDKLA hide sequence

RefSeq Acc Id:

XP_024302306 ⟸ XM_024446538

- Peptide Label:

isoform X3

- Sequence:

show sequence

MATALGFKLQGNSKGLGQEPLCKQFRQLRYEETTGPREALSRLRELCQQWLQPETHTKEQILEL
LVLEQFLIILPKELQARVQEHHPESREDVVVVLEDLQLDLGETGQQVDPDQPKKQKILVEEMAP
LKGVQEQQVRHECEVTKPEKEKGEETRIENGKLIVVTDSCGRVESSGKISEPMEAHNEGSNLER
HQAKPKEKIEYKCSEREQRFIQHLDLIEHASTHTGKKLCESDVCQSSSLTGHKKVLSREKGHQC
HECGKAFQRSSHLVRHQKIHLGEKPYQCNECGKVFSQNAGLLEHLRIHTGEKPYLCIHCGKNFR
RSSHLNRHQRIHSQEEPCECKECGKTFSQALLLTHHQRIHSHSKSHQCNECGKAFSLTSDLIRH
HRIHTGEKPFKCNICQKAFRLNSHLAQHVRIHNEEKPYQCSECGEAFRQRSGLFQHQRYHHKDK
LA

hide sequence

RefSeq Acc Id:

ENSP00000485228 ⟸ ENST00000623276

RefSeq Acc Id:

ENSP00000478769 ⟸ ENST00000611552

RefSeq Acc Id:

ENSP00000479314 ⟸ ENST00000614088

RefSeq Acc Id:

ENSP00000481024 ⟸ ENST00000617168

RefSeq Acc Id:

ENSP00000484018 ⟸ ENST00000619937

RefSeq Acc Id:

ENSP00000484931 ⟸ ENST00000316606

RefSeq Acc Id:

ENSP00000481707 ⟸ ENST00000421553

RefSeq Acc Id:	XP_047275270 ⟸ XM_047419314
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047275268 ⟸ XM_047419312
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047275269 ⟸ XM_047419313
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047275267 ⟸ XM_047419311
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054212324 ⟸ XM_054356349
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054212317 ⟸ XM_054356342
- Peptide Label:	isoform X1
- UniProtKB:	A0A024RCN4 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212318 ⟸ XM_054356343
- Peptide Label:	isoform X2
- UniProtKB:	Q7Z3Q6 (UniProtKB/Swiss-Prot), Q5JPG4 (UniProtKB/Swiss-Prot), Q16670 (UniProtKB/Swiss-Prot), Q96A17 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054212320 ⟸ XM_054356345
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054212322 ⟸ XM_054356347
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054212323 ⟸ XM_054356348
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054212319 ⟸ XM_054356344
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054212321 ⟸ XM_054356346
- Peptide Label:	isoform X4

Protein Domains

C2H2-type SCAN box

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q16670-F1-model_v2	AlphaFold	Q16670	1-478	view protein structure

Promoters

RGD ID:

6872312

Promoter ID:

EPDNEW_H9321

Type:

initiation region

Name:

ZSCAN26_1

Description:

zinc finger and SCAN domain containing 26

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H9322

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,267,143 - 28,267,203	EPDNEW

RGD ID:

6872314

Promoter ID:

EPDNEW_H9322

Type:

multiple initiation site

Name:

ZSCAN26_2

Description:

zinc finger and SCAN domain containing 26

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H9321

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	28,277,204 - 28,277,264	EPDNEW

RGD ID:

6805043

Promoter ID:

HG_KWN:52676

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_001023560, NM_001111039, NM_152736, UC003NKW.2

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	6	28,342,709 - 28,343,209 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:12978	AgrOrtholog
COSMIC	ZSCAN26	COSMIC
Ensembl Genes	ENSG00000197062	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000316606	ENTREZGENE
	ENST00000316606.10	UniProtKB/TrEMBL
	ENST00000421553	ENTREZGENE
	ENST00000421553.7	UniProtKB/TrEMBL
	ENST00000611552	ENTREZGENE
	ENST00000611552.2	UniProtKB/TrEMBL
	ENST00000614088	ENTREZGENE
	ENST00000614088.1	UniProtKB/TrEMBL
	ENST00000617168.4	UniProtKB/TrEMBL
	ENST00000619937	ENTREZGENE
	ENST00000619937.4	UniProtKB/TrEMBL
	ENST00000623276	ENTREZGENE
	ENST00000623276.3	UniProtKB/Swiss-Prot
Gene3D-CATH	1.10.4020.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Classic Zinc Finger	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000197062	GTEx
HGNC ID	HGNC:12978	ENTREZGENE
Human Proteome Map	ZSCAN26	Human Proteome Map
InterPro	SCAN_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SCAN_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_C2H2_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_C2H2_type	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:7741	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	7741	ENTREZGENE
OMIM	616474	OMIM
PANTHER	FINGER PUTATIVE TRANSCRIPTION FACTOR FAMILY-RELATED	UniProtKB/TrEMBL
	PROTEIN ZBED8-RELATED	UniProtKB/TrEMBL
	SCAN DOMAIN-CONTAINING PROTEIN 3	UniProtKB/TrEMBL
	SI:DKEY-15H8.11 PROTEIN-RELATED	UniProtKB/TrEMBL
	ZINC FINGER AND SCAN DOMAIN-CONTAINING	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC FINGER AND SCAN DOMAIN-CONTAINING PROTEIN 16	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC FINGER AND SCAN DOMAIN-CONTAINING PROTEIN 30	UniProtKB/TrEMBL
	ZINC FINGER PROTEIN	UniProtKB/TrEMBL
	ZINC FINGER PROTEIN 281-RELATED	UniProtKB/TrEMBL
Pfam	SCAN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	zf-C2H2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA37559	PharmGKB
PROSITE	SCAN_BOX	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	SCAN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZnF_BED	UniProtKB/TrEMBL
	ZnF_C2H2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	Retrovirus capsid dimerization domain-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF57667	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A024RCN4	ENTREZGENE, UniProtKB/TrEMBL
	A0A087WXH0_HUMAN	UniProtKB/TrEMBL
	A0A087X2F1	ENTREZGENE, UniProtKB/TrEMBL
	B3KTR1_HUMAN	UniProtKB/TrEMBL
	B4DMT1	ENTREZGENE, UniProtKB/TrEMBL
	B4DVH3_HUMAN	UniProtKB/TrEMBL
	Q16670	ENTREZGENE
	Q5JPG4	ENTREZGENE
	Q7Z3Q6	ENTREZGENE
	Q96A17	ENTREZGENE
	ZSC26_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	Q5JPG4	UniProtKB/Swiss-Prot
	Q7Z3Q6	UniProtKB/Swiss-Prot
	Q96A17	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2013-01-16	ZSCAN26	zinc finger and SCAN domain containing 26	ZNF187	zinc finger protein 187	Symbol and/or name change	5135510	APPROVED

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

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

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

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

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