ZNF689 (zinc finger protein 689) - Rat Genome Database

Name: ZNF689
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

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Gene: ZNF689 (zinc finger protein 689) Homo sapiens

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Symbol:

ZNF689

Name:

zinc finger protein 689

RGD ID:

1603925

HGNC Page

HGNC:25173

Description:

Enables histone binding activity. Involved in regulation of transcription by RNA polymerase II. Located in cytoplasm and nucleus.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

DKFZp762C173; FLJ90415; TIPUH1; transcription-involved protein upregulated in HCC 1

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Zfp689 (zinc finger protein 689)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Zfp689 (zinc finger protein 689)	HGNC	EggNOG, HomoloGene, Inparanoid, NCBI, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Znf689 (zinc finger protein 689)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	ZNF689 (zinc finger protein 689)	NCBI	Ortholog
Canis lupus familiaris (dog):	ZNF689 (zinc finger protein 689)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, OMA, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	LOC101960186 (zinc finger protein 689)	NCBI	Ortholog
Sus scrofa (pig):	ZNF689 (zinc finger protein 689)	HGNC	Ensembl, NCBI, OrthoDB
Chlorocebus sabaeus (green monkey):	ZNF689 (zinc finger protein 689)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Znf689 (zinc finger protein 689)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Zfp629 (zinc finger protein 629)	HGNC	OrthoDB
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Zfp689 (zinc finger protein 689)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Zfp689 (zinc finger protein 689)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Saccharomyces cerevisiae (baker's yeast):	ZAP1	Alliance	DIOPT (Hieranoid\|InParanoid\|SonicParanoid)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	30,602,558 - 30,610,775 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	30,602,558 - 30,624,012 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	30,613,879 - 30,622,096 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	30,522,187 - 30,529,183 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	16	29,676,732 - 29,683,727 (+)	NCBI		Celera
Cytogenetic Map	16	p11.2	NCBI
HuRef	16	28,177,463 - 28,185,679 (-)	NCBI		HuRef
CHM1_1	16	31,931,058 - 31,939,273 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	16	30,989,540 - 30,997,757 (-)	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

branched-chain keto acid dehydrogenase kinase deficiency (IAGP)

dilated cardiomyopathy (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

2,3',4,4',5-Pentachlorobiphenyl (ISO)

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

3-isobutyl-1-methyl-7H-xanthine (EXP)

acrylamide (EXP,ISO)

ammonium chloride (ISO)

arsane (EXP)

arsenic atom (EXP)

atrazine (EXP)

bisphenol A (EXP,ISO)

bisphenol F (EXP)

cadmium dichloride (EXP)

CGP 52608 (EXP)

choline (ISO)

copper(II) sulfate (EXP)

cyclosporin A (EXP)

decabromodiphenyl ether (ISO)

dexamethasone (EXP,ISO)

doxorubicin (EXP)

endosulfan (ISO)

epoxiconazole (ISO)

folic acid (ISO)

gentamycin (ISO)

indometacin (EXP)

L-methionine (ISO)

methyl methanesulfonate (EXP)

N-nitrosodiethylamine (ISO)

paracetamol (EXP)

piperonyl butoxide (ISO)

potassium dichromate (ISO)

temozolomide (EXP)

testosterone (ISO)

titanium dioxide (ISO)

triphenyl phosphate (EXP)

urethane (EXP)

valproic acid (EXP,ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

regulation of DNA-templated transcription (IEA)

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

skeletal muscle cell differentiation (IEA,ISO)

Cellular Component

cytoplasm (IDA,IEA)

nucleus (IBA,IDA,IEA)

Molecular Function

DNA binding (IEA)

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

histone binding (IDA)

metal ion binding (IEA)

protein binding (IPI)

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

References

References - curated

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

Additional References at PubMed

PMID:12477932	PMID:14702039	PMID:15146197	PMID:15489334	PMID:16344560	PMID:16568080	PMID:16751776	PMID:20562864	PMID:21549307	PMID:21624362	PMID:21873635	PMID:26186194
PMID:27705803	PMID:28514442	PMID:33468658	PMID:33961781	PMID:34921745	PMID:35271311	PMID:35563538	PMID:35715550	PMID:37372979	PMID:38168642

Genomics

Comparative Map Data

ZNF689
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	30,602,558 - 30,610,775 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	30,602,558 - 30,624,012 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	30,613,879 - 30,622,096 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	30,522,187 - 30,529,183 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	16	29,676,732 - 29,683,727 (+)	NCBI		Celera
Cytogenetic Map	16	p11.2	NCBI
HuRef	16	28,177,463 - 28,185,679 (-)	NCBI		HuRef
CHM1_1	16	31,931,058 - 31,939,273 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	16	30,989,540 - 30,997,757 (-)	NCBI		T2T-CHM13v2.0

Zfp689
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	7	127,041,308 - 127,048,330 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	7	127,041,308 - 127,048,330 (-)	Ensembl		GRCm39 Ensembl
GRCm38	7	127,442,136 - 127,449,158 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	7	127,442,136 - 127,449,158 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	7	134,585,650 - 134,592,672 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	7	127,233,286 - 127,240,269 (-)	NCBI		MGSCv36	mm8
Celera	7	127,288,031 - 127,295,054 (-)	NCBI		Celera
Cytogenetic Map	7	F3	NCBI
cM Map	7	69.53	NCBI

Zfp689
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	191,496,370 - 191,507,277 (-)	NCBI		GRCr8
mRatBN7.2	1	182,065,885 - 182,074,343 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	182,065,826 - 182,076,679 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	190,416,447 - 190,423,828 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	197,602,533 - 197,609,914 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	190,273,052 - 190,280,430 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	198,894,000 - 198,900,364 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	198,894,000 - 199,064,150 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	205,892,549 - 205,898,913 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	186,711,808 - 186,717,877 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	1	186,861,688 - 186,867,758 (-)	NCBI
Celera	1	179,719,685 - 179,725,754 (-)	NCBI		Celera
Cytogenetic Map	1	q37	NCBI

Znf689
(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_004955759	2,457 - 11,900 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955759	5,615 - 11,900 (-)	NCBI	ChiLan1.0	ChiLan1.0

ZNF689
(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	18	33,809,784 - 33,820,185 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	16	38,611,229 - 38,621,633 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	16	24,356,711 - 24,365,116 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	16	30,973,859 - 30,981,882 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	16	30,973,859 - 30,981,882 (-)	Ensembl	panpan1.1		panPan2

ZNF689
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	6	17,552,119 - 17,557,077 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	6	17,540,075 - 17,591,092 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	6	19,125,900 - 19,133,232 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	6	17,683,006 - 17,690,337 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	6	17,671,556 - 17,722,463 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	6	17,483,183 - 17,490,514 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	6	17,398,250 - 17,405,582 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	6	17,713,485 - 17,720,817 (+)	NCBI		UU_Cfam_GSD_1.0

LOC101960186
(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_024409344	124,918,494 - 124,929,518 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936501	13,016,340 - 13,023,690 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936501	13,017,941 - 13,023,640 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZNF689
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	3	17,766,764 - 17,772,871 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	3	17,766,740 - 17,772,875 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	3	18,226,377 - 18,228,897 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ZNF689
(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	5	27,291,363 - 27,299,404 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	5	27,290,555 - 27,298,904 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666068	2,203,167 - 2,211,691 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Znf689
(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_004624782	13,752,341 - 13,758,637 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624782	13,752,341 - 13,758,871 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ZNF689
23 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 16p12.2-11.2(chr16:23047969-30632245)x3	copy number gain	See cases [RCV000052401]	Chr16:23047969..30632245 [GRCh38] Chr16:23059290..30643566 [GRCh37] Chr16:22966791..30551067 [NCBI36] Chr16:16p12.2-11.2	pathogenic
GRCh38/hg38 16p11.2(chr16:29909613-31438697)x3	copy number gain	See cases [RCV000135339]	Chr16:29909613..31438697 [GRCh38] Chr16:29920934..31450018 [GRCh37] Chr16:29828435..31357519 [NCBI36] Chr16:16p11.2	pathogenic
GRCh38/hg38 16p11.2(chr16:29581462-30691912)x1	copy number loss	See cases [RCV000135589]	Chr16:29581462..30691912 [GRCh38] Chr16:29592783..30703233 [GRCh37] Chr16:29500284..30610734 [NCBI36] Chr16:16p11.2	pathogenic
GRCh38/hg38 16p12.1-11.2(chr16:27311746-31193406)x3	copy number gain	See cases [RCV000140341]	Chr16:27311746..31193406 [GRCh38] Chr16:27323067..31204727 [GRCh37] Chr16:27230568..31112228 [NCBI36] Chr16:16p12.1-11.2	pathogenic
GRCh38/hg38 16p12.2-11.2(chr16:23752047-31943755)x3	copy number gain	See cases [RCV000141141]	Chr16:23752047..31943755 [GRCh38] Chr16:23763368..31955076 [GRCh37] Chr16:23670869..31862577 [NCBI36] Chr16:16p12.2-11.2	pathogenic
GRCh37/hg19 16p11.2(chr16:30391304-31122666)x3	copy number gain	Breast ductal adenocarcinoma [RCV000207028]	Chr16:30391304..31122666 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3	copy number gain	Breast ductal adenocarcinoma [RCV000207053]	Chr16:1279324..31926800 [GRCh37] Chr16:16p13.3-11.2	uncertain significance
Single allele	deletion	Branched-chain keto acid dehydrogenase kinase deficiency [RCV000735205]	Chr16:30554158..31536880 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3	copy number gain	See cases [RCV000446684]	Chr16:69193..90274381 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p11.2(chr16:30515442-30792856)x1	copy number loss	See cases [RCV000445894]	Chr16:30515442..30792856 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p11.2(chr16:28826162-29043901)x1	copy number loss	See cases [RCV000448084]	Chr16:28826162..29043901 [GRCh37] Chr16:16p11.2	likely pathogenic
GRCh37/hg19 16p11.2(chr16:30607048-31117069)x1	copy number loss	See cases [RCV000511454]	Chr16:30607048..31117069 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3	copy number gain	See cases [RCV000511622]	Chr16:9273328..89548493 [GRCh37] Chr16:16p13.2-q24.3	uncertain significance
maternal UPD(16p)	complex	Hemimegalencephaly [RCV000494707]	Chr16:1280042..33710558 [GRCh37] Chr16:16p13.3-11.2	pathogenic
NM_138447.3(ZNF689):c.1237C>G (p.Pro413Ala)	single nucleotide variant	not specified [RCV004291036]	Chr16:30604530 [GRCh38] Chr16:30615851 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)	copy number gain	See cases [RCV000511296]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3	copy number gain	See cases [RCV000512138]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3	copy number gain	not provided [RCV000738917]	Chr16:88165..90163275 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3	copy number gain	not provided [RCV000738918]	Chr16:88165..90274695 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3	copy number gain	not provided [RCV000738915]	Chr16:61451..90294632 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
NM_138447.3(ZNF689):c.1468A>G (p.Ile490Val)	single nucleotide variant	not specified [RCV004291453]	Chr16:30604299 [GRCh38] Chr16:30615620 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.110A>T (p.Tyr37Phe)	single nucleotide variant	not specified [RCV004319379]	Chr16:30609932 [GRCh38] Chr16:30621253 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.3-11.2(chr16:5805001-34230001)	copy number gain	Microcephaly [RCV001252948]	Chr16:5805001..34230001 [GRCh37] Chr16:16p13.3-11.2	pathogenic
GRCh37/hg19 16p11.2(chr16:30350747-31905898)x3	copy number gain	not provided [RCV001258619]	Chr16:30350747..31905898 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p11.2(chr16:29808153-30750270)x3	copy number gain	Chromosome 16p11.2 duplication syndrome [RCV001801218]	Chr16:29808153..30750270 [GRCh37] Chr16:16p11.2	pathogenic
GRCh37/hg19 16p11.2(chr16:30460206-30906733)x3	copy number gain	not provided [RCV002475788]	Chr16:30460206..30906733 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.283C>T (p.Pro95Ser)	single nucleotide variant	not specified [RCV004195824]	Chr16:30609561 [GRCh38] Chr16:30620882 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.356T>G (p.Val119Gly)	single nucleotide variant	not specified [RCV004125191]	Chr16:30605411 [GRCh38] Chr16:30616732 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.1139G>A (p.Arg380His)	single nucleotide variant	not specified [RCV004179308]	Chr16:30604628 [GRCh38] Chr16:30615949 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.25C>T (p.Pro9Ser)	single nucleotide variant	not specified [RCV004146989]	Chr16:30610017 [GRCh38] Chr16:30621338 [GRCh37] Chr16:16p11.2	likely benign
NM_138447.3(ZNF689):c.1355C>A (p.Thr452Lys)	single nucleotide variant	not specified [RCV004114131]	Chr16:30604412 [GRCh38] Chr16:30615733 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.1323G>C (p.Trp441Cys)	single nucleotide variant	not specified [RCV004120271]	Chr16:30604444 [GRCh38] Chr16:30615765 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.1259G>A (p.Arg420Gln)	single nucleotide variant	not specified [RCV004233550]	Chr16:30604508 [GRCh38] Chr16:30615829 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.55A>G (p.Ser19Gly)	single nucleotide variant	not specified [RCV004130727]	Chr16:30609987 [GRCh38] Chr16:30621308 [GRCh37] Chr16:16p11.2	likely benign
NM_138447.3(ZNF689):c.967G>C (p.Glu323Gln)	single nucleotide variant	not specified [RCV004148368]	Chr16:30604800 [GRCh38] Chr16:30616121 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.463G>A (p.Gly155Ser)	single nucleotide variant	not specified [RCV004196475]	Chr16:30605304 [GRCh38] Chr16:30616625 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.539C>T (p.Pro180Leu)	single nucleotide variant	not specified [RCV004250383]	Chr16:30605228 [GRCh38] Chr16:30616549 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.99C>A (p.Asp33Glu)	single nucleotide variant	not specified [RCV004347863]	Chr16:30609943 [GRCh38] Chr16:30621264 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.269C>T (p.Pro90Leu)	single nucleotide variant	not specified [RCV004358108]	Chr16:30609575 [GRCh38] Chr16:30620896 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.424C>T (p.Pro142Ser)	single nucleotide variant	not specified [RCV004357723]	Chr16:30605343 [GRCh38] Chr16:30616664 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.766A>G (p.Thr256Ala)	single nucleotide variant	not specified [RCV004358254]	Chr16:30605001 [GRCh38] Chr16:30616322 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.1106G>T (p.Gly369Val)	single nucleotide variant	not specified [RCV004353392]	Chr16:30604661 [GRCh38] Chr16:30615982 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.1264G>A (p.Val422Met)	single nucleotide variant	not specified [RCV004490071]	Chr16:30604503 [GRCh38] Chr16:30615824 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.637C>T (p.Arg213Cys)	single nucleotide variant	not specified [RCV004490073]	Chr16:30605130 [GRCh38] Chr16:30616451 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.373G>A (p.Ala125Thr)	single nucleotide variant	not specified [RCV004490072]	Chr16:30605394 [GRCh38] Chr16:30616715 [GRCh37] Chr16:16p11.2	uncertain significance
NC_000016.9:g.(?_28889993)_(31202759_?)del	deletion	Dilated Cardiomyopathy, Dominant [RCV004582801]	Chr16:28889993..31202759 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.1447A>G (p.Asn483Asp)	single nucleotide variant	not specified [RCV004601733]	Chr16:30604320 [GRCh38] Chr16:30615641 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.1031C>G (p.Pro344Arg)	single nucleotide variant	not specified [RCV004601735]	Chr16:30604736 [GRCh38] Chr16:30616057 [GRCh37] Chr16:16p11.2	uncertain significance
NM_138447.3(ZNF689):c.501C>A (p.His167Gln)	single nucleotide variant	not specified [RCV004601734]	Chr16:30605266 [GRCh38] Chr16:30616587 [GRCh37] Chr16:16p11.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2210
Count of miRNA genes:	936
Interacting mature miRNAs:	1086
Transcripts:	ENST00000287461, ENST00000563304, ENST00000564262, ENST00000565440, ENST00000565710, ENST00000566673
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
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.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
406900593	GWAS549569_H	atrial fibrillation QTL GWAS549569 (human)		2e-14	atrial fibrillation		16	30608424	30608425	Human
407172102	GWAS821078_H	alkaline phosphatase measurement QTL GWAS821078 (human)		1e-10	alkaline phosphatase measurement	blood alkaline phosphatase activity level (CMO:0000576)	16	30606377	30606378	Human

Markers in Region

SHGC-61056

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	30,613,931 - 30,614,061	UniSTS	GRCh37
Build 36	16	30,521,432 - 30,521,562	RGD	NCBI36
Celera	16	29,684,352 - 29,684,482	RGD
Cytogenetic Map	16	p11.2	UniSTS
HuRef	16	28,177,515 - 28,177,645	UniSTS

RH75465

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	30,613,883 - 30,614,114	UniSTS	GRCh37
Build 36	16	30,521,384 - 30,521,615	RGD	NCBI36
Celera	16	29,684,299 - 29,684,530	RGD
Cytogenetic Map	16	p11.2	UniSTS
HuRef	16	28,177,467 - 28,177,698	UniSTS

D16S2667

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	30,613,946 - 30,614,026	UniSTS	GRCh37
Build 36	16	30,521,447 - 30,521,527	RGD	NCBI36
Celera	16	29,684,387 - 29,684,467	RGD
Cytogenetic Map	16	p11.2	UniSTS
HuRef	16	28,177,530 - 28,177,610	UniSTS

Expression

RNA-SEQ Expression

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

Download All Expressed Objects for this Gene

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	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2438	2788	2253	4973	1726	2351	6	624	1950	465	2269	7304	6471	53	3734	1	852	1744	1617	174	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_138447	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_073480	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_073481	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_073482	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_104166	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB065282	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC093249	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC243616	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF086510	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK074896	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK310459	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL834299	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC014000	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CD243730	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471192	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CN406120	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CQ756574	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CQ783987	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA010230	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA485303	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB456506	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY005770	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KT584473	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000287461 ⟹ ENSP00000287461

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	30,602,558 - 30,610,389 (-)	Ensembl

Ensembl Acc Id:

ENST00000563304

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	30,604,540 - 30,610,386 (-)	Ensembl

Ensembl Acc Id:

ENST00000564262

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	30,604,783 - 30,609,485 (-)	Ensembl

Ensembl Acc Id:

ENST00000565440

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	30,604,618 - 30,623,948 (-)	Ensembl

Ensembl Acc Id:

ENST00000565710

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	30,605,047 - 30,609,828 (-)	Ensembl

Ensembl Acc Id:

ENST00000566673

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	30,604,618 - 30,624,012 (-)	Ensembl

RefSeq Acc Id:

NM_138447 ⟹ NP_612456

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	30,602,558 - 30,610,389 (-)	NCBI
GRCh37	16	30,613,879 - 30,622,096 (-)	NCBI
Build 36	16	30,522,187 - 30,529,183 (-)	NCBI Archive
Celera	16	29,676,732 - 29,683,727 (+)	RGD
HuRef	16	28,177,463 - 28,185,679 (-)	NCBI
CHM1_1	16	31,931,058 - 31,938,884 (-)	NCBI
T2T-CHM13v2.0	16	30,989,540 - 30,997,371 (-)	NCBI

Sequence:

show sequence

GCCATTACACTTGAGGGCAAAGAGGTTAGGAAGCCGGCATGGCGCTCCGGTCAATAAAATCGAT
AGCTGGAAGCTGCCTGTGTTCCAGGCAAAGGCGGTGCGGTAGCAGCGCCGCCATTTTCCCCGAA
GGCATCTTCCGGTGCCTTTCACCCAAGTTCGGGCAGGAGTTTCCTGAATAACAGCAAAAGGTTT
CCGTTAGCCCCGCGGGCGACCAATTCCGATTCCCTCCGGGCCTCCCCGGCCACGCTCAGCCCTG
GTCCGGCAGGGGCTCCTCGATCCCAGGGGCCGCCAGCGCCCGAGGGCCGAGGCCTGGACACGGA
AGGCCGTGGCGCCGGCTTCTCGGGTCCCATGGCGCCACCTTCGGCTCCGCTCCCTGCGCAGGGA
CCAGGAAAGGCCAGACCCAGTCGGAAAAGGGGCAGGAGGCCGAGGGCTCTGAAGTTCGTGGACG
TGGCCGTGTACTTCTCCCCGGAGGAGTGGGGCTGCCTGCGGCCCGCGCAGAGGGCCCTGTACCG
GGACGTGATGCGGGAGACCTACGGTCACCTGGGCGCGCTCGGGTGCGCAGGTCCCAAACCAGCC
CTCATCTCCTGGTTGGAACGAAACACCGATGACTGGGAACCGGCTGCTCTAGATCCGCAGGAGT
ACCCGAGAGGGCTAACAGTCCAGAGAAAAAGCAGAACCAGAAAGAAGAATGGGGAGAAGGAAGT
ATTCCCGCCTAAGGAGGCACCCCGAAAGGGGAAGCGAGGCCGGAGGCCCAGCAAACCCCGACTG
ATTCCTAGGCAGACGTCCGGGGGCCCCATCTGCCCTGACTGCGGCTGTACCTTCCCTGATCATC
AGGCCCTGGAGAGCCACAAGTGCGCCCAGAATCTAAAAAAGCCTTACCCTTGCCCAGACTGTGG
GCGCCGCTTTTCCTATCCATCCCTGCTGGTCAGTCACCGGCGGGCACACTCCGGCGAGTGCCCC
TATGTTTGTGACCAGTGTGGCAAACGTTTCTCCCAGCGCAAGAACCTCTCCCAGCACCAGGTCA
TCCATACAGGGGAGAAGCCCTATCACTGCCCTGACTGTGGTCGCTGCTTCCGGAGGAGCCGGTC
CTTGGCCAATCACCGGACCACACACACAGGTGAAAAACCCCACCAGTGCCCTAGCTGTGGACGT
CGCTTCGCCTACCCCTCCCTGCTAGCCATCCACCAGCGTACACACACGGGAGAGAAGCCCTACA
CTTGCCTCGAGTGCAACCGCCGCTTCCGCCAGCGCACGGCCCTCGTCATCCACCAGCGCATCCA
CACGGGCGAGAAGCCCTACCCGTGCCCGGACTGCGAGCGGCGCTTCTCCTCCTCCTCTCGCCTG
GTCAGTCACCGGCGTGTGCACTCTGGGGAGCGTCCCTATGCCTGCGAGCACTGTGAGGCCCGCT
TCTCCCAGCGCAGCACGCTGCTCCAGCACCAGCTCTTGCACACCGGAGAGAAGCCCTACCCCTG
CCCAGACTGTGGGCGTGCCTTCCGGCGGAGCGGCTCCCTGGCCATCCATCGCAGCACGCACACA
GAGGAGAAGCTGCACGCCTGCGACGACTGTGGTCGCCGCTTTGCCTACCCCTCACTGCTGGCCA
GCCACCGGCGCGTGCACTCGGGCGAGCGGCCCTATGCCTGCGACCTTTGCTCCAAGCGTTTTGC
TCAGTGGAGCCACCTGGCCCAGCACCAGCTGCTGCACACGGGGGAGAAGCCTTTCCCCTGCCTC
GAGTGTGGCCGGTGCTTCCGCCAGAGGTGGTCTCTGGCTGTCCACAAGTGTAGCCCCAAGGCCC
CAAACTGTAGCCCTAGATCTGCTATCGGGGGCTCCAGTCAGAGGGGCAACGCCCATTAGAAGGG
GAAGGACTGCCTACGTTCATTTCATTTTATGGAGGGTCCCAGAAAAGGGAAGGAGGAGCCCCAG
GTCATACAGGGCAGAGTCAGAACTAAACCCGGGTCTCCTGCTGCACAGAGCTGAACTTTGTATC
TTGCAATGCGCTGGCTGCCTCCCTGTGCGTGTCTGGAACAGTCCCATTAGGAGAGGTGACGTCA
TTTGCTTAAAGTTTTCCAAGCTACCCTATCCTAAAATAGTTTGTGTGGATATCAGGGCTAAAAG
TTCTCCCCATCTATTTTAGGGGCTGTCTGCTTTTCTAGTCTGTCCACACAGGGATTACCTGTCA
TCTTGCATGCAATCAGGAGAATCTCATAGGGGCAGGACCTTCCCCTACTCTGCCTCTTCCTCCA
TACTAGGTTGGAAAAATCTGGTTTAGCCCACTTTTTGCAACACTCCTGCCAAGTGGTCTTCTAC
CCATTGCTTGAAAATCTCTCTTGACAGGGAGCTCACTACCTCACAAGGCAGGTCATTTCATTGT
GGGATCTATAGAAGGTTAAGTACCACATTCTCCTCTAAACCTTGCCTACGACATGTTTAATACT
TCATCTACATAGCAGCCCTTCAGATAATCACAACCACTTTGCCCCCAAGTTTTCAGGTTAAGTA
GCATGAATTTGGTCATTCCTTAAAGACAGGGTTTCAATTTCCACACATGATCTCTGCAAACAGG
CACTGGGTTTTCAGTGTCCTTTTTGAAGGGTCATATAAAAATAAGGTAACACCACAGTGCCACT
ACACCTTCTGGGGCTGGACTTGTTTCAGCAGCTTTGGTTGCACTGAATTTGGGGGAGCTGCATG
GTACCAGGGGTTTATTGGGTTGCAGATATATAAATGCCCTAAACTTAAAAAAAAAAAAAAAAGC
TATAAAACTAAGTCTTCATCTTGTATTTGGAAAATTGGTTCAAGCTGGGTATGAGACATAAGTG
TAGTCAGCTCTGGGAGAAGGTTGCTCTTAAGGAGAAGCAGGGACCTGTGGTTTAGCAGCAGGAA
GTGCAAATGGGACTGGCTTGTGCTCTACCTGGCAGACCTGGATTGGCTTCAGGCAGCCAGTGCC
TGGAAAAGCCTGGAGAATTGGGCCGTACTTGACCCTGATTCTCATCAGGCACAGATGAATCACA
GGCACCTAAGAATCGGCACAGAACTTCCATGAGGCCTCAGTCAGCATTTTTTCACAAAATGAGC
TGAGGCCATTCAAGGAGGCTAGAAAGAGGGAACTGAATCCAGAGAGGAAGAGTCTATAGTCATC
AAGTTGTATCCATGCCAGCCTCCCTCCACAGAGGTGGCAGCAGCGTGGCTCAATCTGATCCACC
TCCATGGCACCCACTGGGTAGGTGCTTCATAAAGCTTTACCGAGTTAAATGTGAACAAGGCCTA
CCACTTTGCCTTGGGCAGCTGCACCAAATTAGAATTTCCAGATGTGACTCATCTCATATTCCAA
CAGCTGGAGTGGGTCATCCTTTACCCCTGTGGCTCCTTCCTACAGCTCTCCTGATCTCAGCACA
AGCAGGGGAGCAGCTGGGGGAACACAGCTTTATGTAATTACCTCTGTTCAATATTTAGCAAGTT
GCATTGTAACATTGTAACTGTTTGTTTCTCCTTGGATGATGAGCTACCCCCAAGAAGGGGTCAT
ATCAGATTGGGTCTCATTAAAATGTCTGATGAATGAA

hide sequence

RefSeq Acc Id:

NR_073480

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	30,602,558 - 30,610,389 (-)	NCBI
GRCh37	16	30,613,879 - 30,622,096 (-)	NCBI
HuRef	16	28,177,463 - 28,185,679 (-)	NCBI
CHM1_1	16	31,931,058 - 31,938,884 (-)	NCBI
T2T-CHM13v2.0	16	30,989,540 - 30,997,371 (-)	NCBI

Sequence:

show sequence

GCCATTACACTTGAGGGCAAAGAGGTTAGGAAGCCGGCATGGCGCTCCGGTCAATAAAATCGAT
AGCTGGAAGCTGCCTGTGTTCCAGGCAAAGGCGGTGCGGTAGCAGCGCCGCCATTTTCCCCGAA
GGCATCTTCCGGTGCCTTTCACCCAAGTTCGGGCAGGAGTTTCCTGAATAACAGCAAAAGGGTG
CGCAGGTCCCAAACCAGCCCTCATCTCCTGGTTGGAACGAAACACCGATGACTGGGAACCGGCT
GCTCTAGATCCGCAGGAGTACCCGAGAGGGCTAACAGTCCAGAGAAAAAGCAGAACCAGAAAGA
AGAATGGGGAGAAGGAAGTATTCCCGCCTAAGGAGGCACCCCGAAAGGGGAAGCGAGGCCGGAG
GCCCAGCAAACCCCGACTGATTCCTAGGCAGACGTCCGGGGGCCCCATCTGCCCTGACTGCGGC
TGTACCTTCCCTGATCATCAGGCCCTGGAGAGCCACAAGTGCGCCCAGAATCTAAAAAAGCCTT
ACCCTTGCCCAGACTGTGGGCGCCGCTTTTCCTATCCATCCCTGCTGGTCAGTCACCGGCGGGC
ACACTCCGGCGAGTGCCCCTATGTTTGTGACCAGTGTGGCAAACGTTTCTCCCAGCGCAAGAAC
CTCTCCCAGCACCAGGTCATCCATACAGGGGAGAAGCCCTATCACTGCCCTGACTGTGGTCGCT
GCTTCCGGAGGAGCCGGTCCTTGGCCAATCACCGGACCACACACACAGGTGAAAAACCCCACCA
GTGCCCTAGCTGTGGACGTCGCTTCGCCTACCCCTCCCTGCTAGCCATCCACCAGCGTACACAC
ACGGGAGAGAAGCCCTACACTTGCCTCGAGTGCAACCGCCGCTTCCGCCAGCGCACGGCCCTCG
TCATCCACCAGCGCATCCACACGGGCGAGAAGCCCTACCCGTGCCCGGACTGCGAGCGGCGCTT
CTCCTCCTCCTCTCGCCTGGTCAGTCACCGGCGTGTGCACTCTGGGGAGCGTCCCTATGCCTGC
GAGCACTGTGAGGCCCGCTTCTCCCAGCGCAGCACGCTGCTCCAGCACCAGCTCTTGCACACCG
GAGAGAAGCCCTACCCCTGCCCAGACTGTGGGCGTGCCTTCCGGCGGAGCGGCTCCCTGGCCAT
CCATCGCAGCACGCACACAGAGGAGAAGCTGCACGCCTGCGACGACTGTGGTCGCCGCTTTGCC
TACCCCTCACTGCTGGCCAGCCACCGGCGCGTGCACTCGGGCGAGCGGCCCTATGCCTGCGACC
TTTGCTCCAAGCGTTTTGCTCAGTGGAGCCACCTGGCCCAGCACCAGCTGCTGCACACGGGGGA
GAAGCCTTTCCCCTGCCTCGAGTGTGGCCGGTGCTTCCGCCAGAGGTGGTCTCTGGCTGTCCAC
AAGTGTAGCCCCAAGGCCCCAAACTGTAGCCCTAGATCTGCTATCGGGGGCTCCAGTCAGAGGG
GCAACGCCCATTAGAAGGGGAAGGACTGCCTACGTTCATTTCATTTTATGGAGGGTCCCAGAAA
AGGGAAGGAGGAGCCCCAGGTCATACAGGGCAGAGTCAGAACTAAACCCGGGTCTCCTGCTGCA
CAGAGCTGAACTTTGTATCTTGCAATGCGCTGGCTGCCTCCCTGTGCGTGTCTGGAACAGTCCC
ATTAGGAGAGGTGACGTCATTTGCTTAAAGTTTTCCAAGCTACCCTATCCTAAAATAGTTTGTG
TGGATATCAGGGCTAAAAGTTCTCCCCATCTATTTTAGGGGCTGTCTGCTTTTCTAGTCTGTCC
ACACAGGGATTACCTGTCATCTTGCATGCAATCAGGAGAATCTCATAGGGGCAGGACCTTCCCC
TACTCTGCCTCTTCCTCCATACTAGGTTGGAAAAATCTGGTTTAGCCCACTTTTTGCAACACTC
CTGCCAAGTGGTCTTCTACCCATTGCTTGAAAATCTCTCTTGACAGGGAGCTCACTACCTCACA
AGGCAGGTCATTTCATTGTGGGATCTATAGAAGGTTAAGTACCACATTCTCCTCTAAACCTTGC
CTACGACATGTTTAATACTTCATCTACATAGCAGCCCTTCAGATAATCACAACCACTTTGCCCC
CAAGTTTTCAGGTTAAGTAGCATGAATTTGGTCATTCCTTAAAGACAGGGTTTCAATTTCCACA
CATGATCTCTGCAAACAGGCACTGGGTTTTCAGTGTCCTTTTTGAAGGGTCATATAAAAATAAG
GTAACACCACAGTGCCACTACACCTTCTGGGGCTGGACTTGTTTCAGCAGCTTTGGTTGCACTG
AATTTGGGGGAGCTGCATGGTACCAGGGGTTTATTGGGTTGCAGATATATAAATGCCCTAAACT
TAAAAAAAAAAAAAAAAGCTATAAAACTAAGTCTTCATCTTGTATTTGGAAAATTGGTTCAAGC
TGGGTATGAGACATAAGTGTAGTCAGCTCTGGGAGAAGGTTGCTCTTAAGGAGAAGCAGGGACC
TGTGGTTTAGCAGCAGGAAGTGCAAATGGGACTGGCTTGTGCTCTACCTGGCAGACCTGGATTG
GCTTCAGGCAGCCAGTGCCTGGAAAAGCCTGGAGAATTGGGCCGTACTTGACCCTGATTCTCAT
CAGGCACAGATGAATCACAGGCACCTAAGAATCGGCACAGAACTTCCATGAGGCCTCAGTCAGC
ATTTTTTCACAAAATGAGCTGAGGCCATTCAAGGAGGCTAGAAAGAGGGAACTGAATCCAGAGA
GGAAGAGTCTATAGTCATCAAGTTGTATCCATGCCAGCCTCCCTCCACAGAGGTGGCAGCAGCG
TGGCTCAATCTGATCCACCTCCATGGCACCCACTGGGTAGGTGCTTCATAAAGCTTTACCGAGT
TAAATGTGAACAAGGCCTACCACTTTGCCTTGGGCAGCTGCACCAAATTAGAATTTCCAGATGT
GACTCATCTCATATTCCAACAGCTGGAGTGGGTCATCCTTTACCCCTGTGGCTCCTTCCTACAG
CTCTCCTGATCTCAGCACAAGCAGGGGAGCAGCTGGGGGAACACAGCTTTATGTAATTACCTCT
GTTCAATATTTAGCAAGTTGCATTGTAACATTGTAACTGTTTGTTTCTCCTTGGATGATGAGCT
ACCCCCAAGAAGGGGTCATATCAGATTGGGTCTCATTAAAATGTCTGATGAATGAA

hide sequence

RefSeq Acc Id:

NR_073481

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	30,602,558 - 30,610,775 (-)	NCBI
HuRef	16	28,177,463 - 28,185,679 (-)	NCBI
CHM1_1	16	31,931,058 - 31,939,273 (-)	NCBI
T2T-CHM13v2.0	16	30,989,540 - 30,997,757 (-)	NCBI

Sequence:

show sequence

AAAGAAGATAACCATTCTCCAAAGTCAAGGATGCTCTGAGAACACCAGTAAAAGGAACTCAGGA
TAATCTCAGCTCTAACTCGGCCAGAGTGGCTCCATCGCTCAAATCGTTCCCTCCTTCAGTGATT
GGCTGAGCCTGCCAGAGTCGAACAGCGGAAAGCAGCCCCGGGGCCTCTTGCTGCCCCCAGGGTG
CGCAGGTCCCAAACCAGCCCTCATCTCCTGGTTGGAACGAAACACCGATGACTGGGAACCGGCT
GCTCTAGATCCGCAGGAGTACCCGAGAGGGCTAACAGTCCAGAGAAAAAGCAGAACCAGAAAGA
AGAATGGGGAGAAGGAAGTATTCCCGCCTAAGGAGGCACCCCGAAAGGGGAAGCGAGGCCGGAG
GCCCAGCAAACCCCGACTGATTCCTAGGCAGACGTCCGGGGGCCCCATCTGCCCTGACTGCGGC
TGTACCTTCCCTGATCATCAGGCCCTGGAGAGCCACAAGTGCGCCCAGAATCTAAAAAAGCCTT
ACCCTTGCCCAGACTGTGGGCGCCGCTTTTCCTATCCATCCCTGCTGGTCAGTCACCGGCGGGC
ACACTCCGGCGAGTGCCCCTATGTTTGTGACCAGTGTGGCAAACGTTTCTCCCAGCGCAAGAAC
CTCTCCCAGCACCAGGTCATCCATACAGGGGAGAAGCCCTATCACTGCCCTGACTGTGGTCGCT
GCTTCCGGAGGAGCCGGTCCTTGGCCAATCACCGGACCACACACACAGGTGAAAAACCCCACCA
GTGCCCTAGCTGTGGACGTCGCTTCGCCTACCCCTCCCTGCTAGCCATCCACCAGCGTACACAC
ACGGGAGAGAAGCCCTACACTTGCCTCGAGTGCAACCGCCGCTTCCGCCAGCGCACGGCCCTCG
TCATCCACCAGCGCATCCACACGGGCGAGAAGCCCTACCCGTGCCCGGACTGCGAGCGGCGCTT
CTCCTCCTCCTCTCGCCTGGTCAGTCACCGGCGTGTGCACTCTGGGGAGCGTCCCTATGCCTGC
GAGCACTGTGAGGCCCGCTTCTCCCAGCGCAGCACGCTGCTCCAGCACCAGCTCTTGCACACCG
GAGAGAAGCCCTACCCCTGCCCAGACTGTGGGCGTGCCTTCCGGCGGAGCGGCTCCCTGGCCAT
CCATCGCAGCACGCACACAGAGGAGAAGCTGCACGCCTGCGACGACTGTGGTCGCCGCTTTGCC
TACCCCTCACTGCTGGCCAGCCACCGGCGCGTGCACTCGGGCGAGCGGCCCTATGCCTGCGACC
TTTGCTCCAAGCGTTTTGCTCAGTGGAGCCACCTGGCCCAGCACCAGCTGCTGCACACGGGGGA
GAAGCCTTTCCCCTGCCTCGAGTGTGGCCGGTGCTTCCGCCAGAGGTGGTCTCTGGCTGTCCAC
AAGTGTAGCCCCAAGGCCCCAAACTGTAGCCCTAGATCTGCTATCGGGGGCTCCAGTCAGAGGG
GCAACGCCCATTAGAAGGGGAAGGACTGCCTACGTTCATTTCATTTTATGGAGGGTCCCAGAAA
AGGGAAGGAGGAGCCCCAGGTCATACAGGGCAGAGTCAGAACTAAACCCGGGTCTCCTGCTGCA
CAGAGCTGAACTTTGTATCTTGCAATGCGCTGGCTGCCTCCCTGTGCGTGTCTGGAACAGTCCC
ATTAGGAGAGGTGACGTCATTTGCTTAAAGTTTTCCAAGCTACCCTATCCTAAAATAGTTTGTG
TGGATATCAGGGCTAAAAGTTCTCCCCATCTATTTTAGGGGCTGTCTGCTTTTCTAGTCTGTCC
ACACAGGGATTACCTGTCATCTTGCATGCAATCAGGAGAATCTCATAGGGGCAGGACCTTCCCC
TACTCTGCCTCTTCCTCCATACTAGGTTGGAAAAATCTGGTTTAGCCCACTTTTTGCAACACTC
CTGCCAAGTGGTCTTCTACCCATTGCTTGAAAATCTCTCTTGACAGGGAGCTCACTACCTCACA
AGGCAGGTCATTTCATTGTGGGATCTATAGAAGGTTAAGTACCACATTCTCCTCTAAACCTTGC
CTACGACATGTTTAATACTTCATCTACATAGCAGCCCTTCAGATAATCACAACCACTTTGCCCC
CAAGTTTTCAGGTTAAGTAGCATGAATTTGGTCATTCCTTAAAGACAGGGTTTCAATTTCCACA
CATGATCTCTGCAAACAGGCACTGGGTTTTCAGTGTCCTTTTTGAAGGGTCATATAAAAATAAG
GTAACACCACAGTGCCACTACACCTTCTGGGGCTGGACTTGTTTCAGCAGCTTTGGTTGCACTG
AATTTGGGGGAGCTGCATGGTACCAGGGGTTTATTGGGTTGCAGATATATAAATGCCCTAAACT
TAAAAAAAAAAAAAAAAGCTATAAAACTAAGTCTTCATCTTGTATTTGGAAAATTGGTTCAAGC
TGGGTATGAGACATAAGTGTAGTCAGCTCTGGGAGAAGGTTGCTCTTAAGGAGAAGCAGGGACC
TGTGGTTTAGCAGCAGGAAGTGCAAATGGGACTGGCTTGTGCTCTACCTGGCAGACCTGGATTG
GCTTCAGGCAGCCAGTGCCTGGAAAAGCCTGGAGAATTGGGCCGTACTTGACCCTGATTCTCAT
CAGGCACAGATGAATCACAGGCACCTAAGAATCGGCACAGAACTTCCATGAGGCCTCAGTCAGC
ATTTTTTCACAAAATGAGCTGAGGCCATTCAAGGAGGCTAGAAAGAGGGAACTGAATCCAGAGA
GGAAGAGTCTATAGTCATCAAGTTGTATCCATGCCAGCCTCCCTCCACAGAGGTGGCAGCAGCG
TGGCTCAATCTGATCCACCTCCATGGCACCCACTGGGTAGGTGCTTCATAAAGCTTTACCGAGT
TAAATGTGAACAAGGCCTACCACTTTGCCTTGGGCAGCTGCACCAAATTAGAATTTCCAGATGT
GACTCATCTCATATTCCAACAGCTGGAGTGGGTCATCCTTTACCCCTGTGGCTCCTTCCTACAG
CTCTCCTGATCTCAGCACAAGCAGGGGAGCAGCTGGGGGAACACAGCTTTATGTAATTACCTCT
GTTCAATATTTAGCAAGTTGCATTGTAACATTGTAACTGTTTGTTTCTCCTTGGATGATGAGCT
ACCCCCAAGAAGGGGTCATATCAGATTGGGTCTCATTAAAATGTCTGATGAATGAA

hide sequence

RefSeq Acc Id:

NR_073482

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	30,602,558 - 30,610,433 (-)	NCBI
HuRef	16	28,177,463 - 28,185,679 (-)	NCBI
CHM1_1	16	31,931,058 - 31,938,931 (-)	NCBI
T2T-CHM13v2.0	16	30,989,540 - 30,997,415 (-)	NCBI

Sequence:

show sequence

GTATTGGGGAGGGGAAAAAAGACGGCGTGAAGCCCAATCGCAGCGCCATTACACTTGAGGGCAA
AGAGGGTGCGCAGGTCCCAAACCAGCCCTCATCTCCTGGTTGGAACGAAACACCGATGACTGGG
AACCGGCTGCTCTAGATCCGCAGGAGTACCCGAGAGGGCTAACAGTCCAGAGAAAAAGCAGAAC
CAGAAAGAAGAATGGGGAGAAGGAAGTATTCCCGCCTAAGGAGGCACCCCGAAAGGGGAAGCGA
GGCCGGAGGCCCAGCAAACCCCGACTGATTCCTAGGCAGACGTCCGGGGGCCCCATCTGCCCTG
ACTGCGGCTGTACCTTCCCTGATCATCAGGCCCTGGAGAGCCACAAGTGCGCCCAGAATCTAAA
AAAGCCTTACCCTTGCCCAGACTGTGGGCGCCGCTTTTCCTATCCATCCCTGCTGGTCAGTCAC
CGGCGGGCACACTCCGGCGAGTGCCCCTATGTTTGTGACCAGTGTGGCAAACGTTTCTCCCAGC
GCAAGAACCTCTCCCAGCACCAGGTCATCCATACAGGGGAGAAGCCCTATCACTGCCCTGACTG
TGGTCGCTGCTTCCGGAGGAGCCGGTCCTTGGCCAATCACCGGACCACACACACAGGTGAAAAA
CCCCACCAGTGCCCTAGCTGTGGACGTCGCTTCGCCTACCCCTCCCTGCTAGCCATCCACCAGC
GTACACACACGGGAGAGAAGCCCTACACTTGCCTCGAGTGCAACCGCCGCTTCCGCCAGCGCAC
GGCCCTCGTCATCCACCAGCGCATCCACACGGGCGAGAAGCCCTACCCGTGCCCGGACTGCGAG
CGGCGCTTCTCCTCCTCCTCTCGCCTGGTCAGTCACCGGCGTGTGCACTCTGGGGAGCGTCCCT
ATGCCTGCGAGCACTGTGAGGCCCGCTTCTCCCAGCGCAGCACGCTGCTCCAGCACCAGCTCTT
GCACACCGGAGAGAAGCCCTACCCCTGCCCAGACTGTGGGCGTGCCTTCCGGCGGAGCGGCTCC
CTGGCCATCCATCGCAGCACGCACACAGAGGAGAAGCTGCACGCCTGCGACGACTGTGGTCGCC
GCTTTGCCTACCCCTCACTGCTGGCCAGCCACCGGCGCGTGCACTCGGGCGAGCGGCCCTATGC
CTGCGACCTTTGCTCCAAGCGTTTTGCTCAGTGGAGCCACCTGGCCCAGCACCAGCTGCTGCAC
ACGGGGGAGAAGCCTTTCCCCTGCCTCGAGTGTGGCCGGTGCTTCCGCCAGAGGTGGTCTCTGG
CTGTCCACAAGTGTAGCCCCAAGGCCCCAAACTGTAGCCCTAGATCTGCTATCGGGGGCTCCAG
TCAGAGGGGCAACGCCCATTAGAAGGGGAAGGACTGCCTACGTTCATTTCATTTTATGGAGGGT
CCCAGAAAAGGGAAGGAGGAGCCCCAGGTCATACAGGGCAGAGTCAGAACTAAACCCGGGTCTC
CTGCTGCACAGAGCTGAACTTTGTATCTTGCAATGCGCTGGCTGCCTCCCTGTGCGTGTCTGGA
ACAGTCCCATTAGGAGAGGTGACGTCATTTGCTTAAAGTTTTCCAAGCTACCCTATCCTAAAAT
AGTTTGTGTGGATATCAGGGCTAAAAGTTCTCCCCATCTATTTTAGGGGCTGTCTGCTTTTCTA
GTCTGTCCACACAGGGATTACCTGTCATCTTGCATGCAATCAGGAGAATCTCATAGGGGCAGGA
CCTTCCCCTACTCTGCCTCTTCCTCCATACTAGGTTGGAAAAATCTGGTTTAGCCCACTTTTTG
CAACACTCCTGCCAAGTGGTCTTCTACCCATTGCTTGAAAATCTCTCTTGACAGGGAGCTCACT
ACCTCACAAGGCAGGTCATTTCATTGTGGGATCTATAGAAGGTTAAGTACCACATTCTCCTCTA
AACCTTGCCTACGACATGTTTAATACTTCATCTACATAGCAGCCCTTCAGATAATCACAACCAC
TTTGCCCCCAAGTTTTCAGGTTAAGTAGCATGAATTTGGTCATTCCTTAAAGACAGGGTTTCAA
TTTCCACACATGATCTCTGCAAACAGGCACTGGGTTTTCAGTGTCCTTTTTGAAGGGTCATATA
AAAATAAGGTAACACCACAGTGCCACTACACCTTCTGGGGCTGGACTTGTTTCAGCAGCTTTGG
TTGCACTGAATTTGGGGGAGCTGCATGGTACCAGGGGTTTATTGGGTTGCAGATATATAAATGC
CCTAAACTTAAAAAAAAAAAAAAAAGCTATAAAACTAAGTCTTCATCTTGTATTTGGAAAATTG
GTTCAAGCTGGGTATGAGACATAAGTGTAGTCAGCTCTGGGAGAAGGTTGCTCTTAAGGAGAAG
CAGGGACCTGTGGTTTAGCAGCAGGAAGTGCAAATGGGACTGGCTTGTGCTCTACCTGGCAGAC
CTGGATTGGCTTCAGGCAGCCAGTGCCTGGAAAAGCCTGGAGAATTGGGCCGTACTTGACCCTG
ATTCTCATCAGGCACAGATGAATCACAGGCACCTAAGAATCGGCACAGAACTTCCATGAGGCCT
CAGTCAGCATTTTTTCACAAAATGAGCTGAGGCCATTCAAGGAGGCTAGAAAGAGGGAACTGAA
TCCAGAGAGGAAGAGTCTATAGTCATCAAGTTGTATCCATGCCAGCCTCCCTCCACAGAGGTGG
CAGCAGCGTGGCTCAATCTGATCCACCTCCATGGCACCCACTGGGTAGGTGCTTCATAAAGCTT
TACCGAGTTAAATGTGAACAAGGCCTACCACTTTGCCTTGGGCAGCTGCACCAAATTAGAATTT
CCAGATGTGACTCATCTCATATTCCAACAGCTGGAGTGGGTCATCCTTTACCCCTGTGGCTCCT
TCCTACAGCTCTCCTGATCTCAGCACAAGCAGGGGAGCAGCTGGGGGAACACAGCTTTATGTAA
TTACCTCTGTTCAATATTTAGCAAGTTGCATTGTAACATTGTAACTGTTTGTTTCTCCTTGGAT
GATGAGCTACCCCCAAGAAGGGGTCATATCAGATTGGGTCTCATTAAAATGTCTGATGAATGAA
AAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NR_104166

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	30,602,558 - 30,609,828 (-)	NCBI
HuRef	16	28,177,463 - 28,185,679 (-)	NCBI
CHM1_1	16	31,931,058 - 31,938,326 (-)	NCBI
T2T-CHM13v2.0	16	30,989,540 - 30,996,810 (-)	NCBI

Sequence:

show sequence

GGCCCCATCCGCTGCCGCGGGGCGCGAAGGGATGCAGGAGCCGGAGAGGGTGTAGGCAGGGAGG
CCACGGTCCTGGCAGGCGACCAGGGTGCGCAGGTCCCAAACCAGCCCTCATCTCCTGGTTGGAA
CGAAACACCGATGACTGGGAACCGGCTGCTCTAGATCCGCAGGAGTACCCGAGAGGGCTAACAG
TCCAGAGAAAAAGCAGAACCAGAAAGAAGAATGGGGAGAAGGAAGTATTCCCGCCTAAGGAGGC
ACCCCGAAAGGGGAAGCGAGGCCGGAGGCCCAGCAAACCCCGACTGATTCCTAGGCAGACGTCC
GGGGGCCCCATCTGCCCTGACTGCGGCTGTACCTTCCCTGATCATCAGGCCCTGGAGAGCCACA
AGTGCGCCCAGAATCTAAAAAAGCCTTACCCTTGCCCAGACTGTGGGCGCCGCTTTTCCTATCC
ATCCCTGCTGGTCAGTCACCGGCGGGCACACTCCGGCGAGTGCCCCTATGTTTGTGACCAGTGT
GGCAAACGTTTCTCCCAGCGCAAGAACCTCTCCCAGCACCAGGTCATCCATACAGGGGAGAAGC
CCTATCACTGCCCTGACTGTGGTCGCTGCTTCCGGAGGAGCCGGTCCTTGGCCAATCACCGGAC
CACACACACAGGTGAAAAACCCCACCAGTGCCCTAGCTGTGGACGTCGCTTCGCCTACCCCTCC
CTGCTAGCCATCCACCAGCGTACACACACGGGAGAGAAGCCCTACACTTGCCTCGAGTGCAACC
GCCGCTTCCGCCAGCGCACGGCCCTCGTCATCCACCAGCGCATCCACACGGGCGAGAAGCCCTA
CCCGTGCCCGGACTGCGAGCGGCGCTTCTCCTCCTCCTCTCGCCTGGTCAGTCACCGGCGTGTG
CACTCTGGGGAGCGTCCCTATGCCTGCGAGCACTGTGAGGCCCGCTTCTCCCAGCGCAGCACGC
TGCTCCAGCACCAGCTCTTGCACACCGGAGAGAAGCCCTACCCCTGCCCAGACTGTGGGCGTGC
CTTCCGGCGGAGCGGCTCCCTGGCCATCCATCGCAGCACGCACACAGAGGAGAAGCTGCACGCC
TGCGACGACTGTGGTCGCCGCTTTGCCTACCCCTCACTGCTGGCCAGCCACCGGCGCGTGCACT
CGGGCGAGCGGCCCTATGCCTGCGACCTTTGCTCCAAGCGTTTTGCTCAGTGGAGCCACCTGGC
CCAGCACCAGCTGCTGCACACGGGGGAGAAGCCTTTCCCCTGCCTCGAGTGTGGCCGGTGCTTC
CGCCAGAGGTGGTCTCTGGCTGTCCACAAGTGTAGCCCCAAGGCCCCAAACTGTAGCCCTAGAT
CTGCTATCGGGGGCTCCAGTCAGAGGGGCAACGCCCATTAGAAGGGGAAGGACTGCCTACGTTC
ATTTCATTTTATGGAGGGTCCCAGAAAAGGGAAGGAGGAGCCCCAGGTCATACAGGGCAGAGTC
AGAACTAAACCCGGGTCTCCTGCTGCACAGAGCTGAACTTTGTATCTTGCAATGCGCTGGCTGC
CTCCCTGTGCGTGTCTGGAACAGTCCCATTAGGAGAGGTGACGTCATTTGCTTAAAGTTTTCCA
AGCTACCCTATCCTAAAATAGTTTGTGTGGATATCAGGGCTAAAAGTTCTCCCCATCTATTTTA
GGGGCTGTCTGCTTTTCTAGTCTGTCCACACAGGGATTACCTGTCATCTTGCATGCAATCAGGA
GAATCTCATAGGGGCAGGACCTTCCCCTACTCTGCCTCTTCCTCCATACTAGGTTGGAAAAATC
TGGTTTAGCCCACTTTTTGCAACACTCCTGCCAAGTGGTCTTCTACCCATTGCTTGAAAATCTC
TCTTGACAGGGAGCTCACTACCTCACAAGGCAGGTCATTTCATTGTGGGATCTATAGAAGGTTA
AGTACCACATTCTCCTCTAAACCTTGCCTACGACATGTTTAATACTTCATCTACATAGCAGCCC
TTCAGATAATCACAACCACTTTGCCCCCAAGTTTTCAGGTTAAGTAGCATGAATTTGGTCATTC
CTTAAAGACAGGGTTTCAATTTCCACACATGATCTCTGCAAACAGGCACTGGGTTTTCAGTGTC
CTTTTTGAAGGGTCATATAAAAATAAGGTAACACCACAGTGCCACTACACCTTCTGGGGCTGGA
CTTGTTTCAGCAGCTTTGGTTGCACTGAATTTGGGGGAGCTGCATGGTACCAGGGGTTTATTGG
GTTGCAGATATATAAATGCCCTAAACTTAAAAAAAAAAAAAAAAGCTATAAAACTAAGTCTTCA
TCTTGTATTTGGAAAATTGGTTCAAGCTGGGTATGAGACATAAGTGTAGTCAGCTCTGGGAGAA
GGTTGCTCTTAAGGAGAAGCAGGGACCTGTGGTTTAGCAGCAGGAAGTGCAAATGGGACTGGCT
TGTGCTCTACCTGGCAGACCTGGATTGGCTTCAGGCAGCCAGTGCCTGGAAAAGCCTGGAGAAT
TGGGCCGTACTTGACCCTGATTCTCATCAGGCACAGATGAATCACAGGCACCTAAGAATCGGCA
CAGAACTTCCATGAGGCCTCAGTCAGCATTTTTTCACAAAATGAGCTGAGGCCATTCAAGGAGG
CTAGAAAGAGGGAACTGAATCCAGAGAGGAAGAGTCTATAGTCATCAAGTTGTATCCATGCCAG
CCTCCCTCCACAGAGGTGGCAGCAGCGTGGCTCAATCTGATCCACCTCCATGGCACCCACTGGG
TAGGTGCTTCATAAAGCTTTACCGAGTTAAATGTGAACAAGGCCTACCACTTTGCCTTGGGCAG
CTGCACCAAATTAGAATTTCCAGATGTGACTCATCTCATATTCCAACAGCTGGAGTGGGTCATC
CTTTACCCCTGTGGCTCCTTCCTACAGCTCTCCTGATCTCAGCACAAGCAGGGGAGCAGCTGGG
GGAACACAGCTTTATGTAATTACCTCTGTTCAATATTTAGCAAGTTGCATTGTAACATTGTAAC
TGTTTGTTTCTCCTTGGATGATGAGCTACCCCCAAGAAGGGGTCATATCAGATTGGGTCTCATT
AAAATGTCTGATGAATGAA

hide sequence

Protein Sequences


Protein RefSeqs	NP_612456	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH14000	(Get FASTA)	NCBI Sequence Viewer
	BAB83744	(Get FASTA)	NCBI Sequence Viewer
	BAC11275	(Get FASTA)	NCBI Sequence Viewer
	C0HLU2	(Get FASTA)	NCBI Sequence Viewer
	CAF32597	(Get FASTA)	NCBI Sequence Viewer
	CAF86958	(Get FASTA)	NCBI Sequence Viewer
	CAH56363	(Get FASTA)	NCBI Sequence Viewer
	EAW52228	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000287461
	ENSP00000287461.3
GenBank Protein	Q96CS4	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_612456 ⟸ NM_138447

- UniProtKB:

Q96CS4 (UniProtKB/Swiss-Prot), Q658J5 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MAPPSAPLPAQGPGKARPSRKRGRRPRALKFVDVAVYFSPEEWGCLRPAQRALYRDVMRETYGH
LGALGCAGPKPALISWLERNTDDWEPAALDPQEYPRGLTVQRKSRTRKKNGEKEVFPPKEAPRK
GKRGRRPSKPRLIPRQTSGGPICPDCGCTFPDHQALESHKCAQNLKKPYPCPDCGRRFSYPSLL
VSHRRAHSGECPYVCDQCGKRFSQRKNLSQHQVIHTGEKPYHCPDCGRCFRRSRSLANHRTTHT
GEKPHQCPSCGRRFAYPSLLAIHQRTHTGEKPYTCLECNRRFRQRTALVIHQRIHTGEKPYPCP
DCERRFSSSSRLVSHRRVHSGERPYACEHCEARFSQRSTLLQHQLLHTGEKPYPCPDCGRAFRR
SGSLAIHRSTHTEEKLHACDDCGRRFAYPSLLASHRRVHSGERPYACDLCSKRFAQWSHLAQHQ
LLHTGEKPFPCLECGRCFRQRWSLAVHKCSPKAPNCSPRSAIGGSSQRGNAH

hide sequence

Ensembl Acc Id:

ENSP00000287461 ⟸ ENST00000287461

Protein Domains

KRAB

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96CS4-F1-model_v2	AlphaFold	Q96CS4	1-500	view protein structure

Promoters

RGD ID:

6815122

Promoter ID:

HG_MRA:5993

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

AF086510, AL834299

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	16	30,522,611 - 30,523,111 (-)	MPROMDB

RGD ID:

6793641

Promoter ID:

HG_KWN:23552

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:

OTTHUMT00000255552, UC010BZY.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	16	30,528,914 - 30,529,414 (-)	MPROMDB

RGD ID:

7232003

Promoter ID:

EPDNEW_H21747

Type:

initiation region

Name:

ZNF689_1

Description:

zinc finger protein 689

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	30,610,383 - 30,610,443	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:25173	AgrOrtholog
COSMIC	ZNF689	COSMIC
Ensembl Genes	ENSG00000156853	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000287461	ENTREZGENE
	ENST00000287461.8	UniProtKB/Swiss-Prot
Gene3D-CATH	6.10.140.140	UniProtKB/Swiss-Prot
	Classic Zinc Finger	UniProtKB/Swiss-Prot
GTEx	ENSG00000156853	GTEx
HGNC ID	HGNC:25173	ENTREZGENE
Human Proteome Map	ZNF689	Human Proteome Map
InterPro	KRAB	UniProtKB/Swiss-Prot
	KRAB_dom_sf	UniProtKB/Swiss-Prot
	Krueppel_C2H2_ZnF	UniProtKB/Swiss-Prot
	SEHBP	UniProtKB/Swiss-Prot
	Znf_C2H2_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_type	UniProtKB/Swiss-Prot
KEGG Report	hsa:115509	UniProtKB/Swiss-Prot
NCBI Gene	ZNF689	ENTREZGENE
OMIM	618033	OMIM
PANTHER	KRAB DOMAIN C2H2 ZINC FINGER	UniProtKB/Swiss-Prot
	ZINC FINGER PROTEIN 688	UniProtKB/Swiss-Prot
Pfam	KRAB	UniProtKB/Swiss-Prot
	SEHBP	UniProtKB/Swiss-Prot
	zf-C2H2	UniProtKB/Swiss-Prot
PharmGKB	PA142670488	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	C0HLU2	ENTREZGENE
	Q658J5	ENTREZGENE
	Q96CS4	ENTREZGENE
	SEHBP_HUMAN	UniProtKB/Swiss-Prot
	ZN689_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	Q658J5	UniProtKB/Swiss-Prot

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

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

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

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

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Imported Disease Annotations - ClinVar