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Gene: ZNF660-ZNF197 (ZNF660-ZNF197 readthrough) Homo sapiens

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Symbol:

ZNF660-ZNF197

Name:

ZNF660-ZNF197 readthrough

RGD ID:

38626576

Description:

This gene represents naturally-occurring readthrough transcription between the adjacent zinc finger protein 660 (ZNF660) and zinc finger protein 197 (ZNF197) genes. Readthrough transcripts may encode proteins similar to the proteins encoded by ZNF197. [provided by RefSeq, May 2017]

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

pVHL-associated KRAB domain-containing protein; zinc finger protein 197; zinc finger protein with KRAB and SCAN domains 9

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	3	44,584,964 - 44,648,471 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh37	3	44,626,456 - 44,689,963 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Cytogenetic Map	3	p21.31	NCBI
T2T-CHM13v2.0	3	44,600,686 - 44,664,179 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

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)

Cellular Component

nucleus (IBA,IEA)

Molecular Function

DNA binding (IEA)

nucleic acid binding (IEA)

zinc ion binding (IEA)

References

Additional References at PubMed

PMID:8353497	PMID:9380504	PMID:12682018	PMID:14702039	PMID:16344560	PMID:16641997	PMID:19274049	PMID:21873635

Genomics

Variants

Variants in ZNF660-ZNF197
85 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_006991.5(ZNF197):c.296G>A (p.Arg99Gln)	single nucleotide variant	not specified [RCV004299099]	Chr3:44629450 [GRCh38] Chr3:44670942 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2580C>G (p.Asn860Lys)	single nucleotide variant	not specified [RCV004329640]	Chr3:44643710 [GRCh38] Chr3:44685202 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1129A>G (p.Lys377Glu)	single nucleotide variant	not specified [RCV004321026]	Chr3:44642259 [GRCh38] Chr3:44683751 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.182G>A (p.Ser61Asn)	single nucleotide variant	not specified [RCV004312320]	Chr3:44629336 [GRCh38] Chr3:44670828 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2758C>G (p.His920Asp)	single nucleotide variant	not specified [RCV004310752]	Chr3:44643888 [GRCh38] Chr3:44685380 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.780C>G (p.Asn260Lys)	single nucleotide variant	not specified [RCV004304662]	Chr3:44594973 [GRCh38] Chr3:44636465 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2128G>A (p.Glu710Lys)	single nucleotide variant	not specified [RCV004296510]	Chr3:44643258 [GRCh38] Chr3:44684750 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.869G>T (p.Ser290Ile)	single nucleotide variant	not specified [RCV004159795]	Chr3:44641999 [GRCh38] Chr3:44683491 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.721C>T (p.Arg241Cys)	single nucleotide variant	not provided [RCV000144230]	Chr3:44594914 [GRCh38] Chr3:44636406 [GRCh37] Chr3:3p21.31	uncertain significance\|not provided
NM_006991.5(ZNF197):c.2482A>C (p.Ser828Arg)	single nucleotide variant	not specified [RCV004299305]	Chr3:44643612 [GRCh38] Chr3:44685104 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.722G>A (p.Arg241His)	single nucleotide variant	not specified [RCV004200189]	Chr3:44594915 [GRCh38] Chr3:44636407 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1505G>C (p.Arg502Thr)	single nucleotide variant	not specified [RCV004124627]	Chr3:44642635 [GRCh38] Chr3:44684127 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.184C>T (p.Arg62Trp)	single nucleotide variant	not specified [RCV004239929]	Chr3:44629338 [GRCh38] Chr3:44670830 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2882A>G (p.Asn961Ser)	single nucleotide variant	not specified [RCV004224679]	Chr3:44644012 [GRCh38] Chr3:44685504 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2305A>G (p.Arg769Gly)	single nucleotide variant	not specified [RCV004135086]	Chr3:44643435 [GRCh38] Chr3:44684927 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2257C>T (p.Arg753Trp)	single nucleotide variant	not specified [RCV004183371]	Chr3:44643387 [GRCh38] Chr3:44684879 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.649C>G (p.Pro217Ala)	single nucleotide variant	not specified [RCV004087050]	Chr3:44594842 [GRCh38] Chr3:44636334 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1565A>C (p.Lys522Thr)	single nucleotide variant	not specified [RCV004142931]	Chr3:44642695 [GRCh38] Chr3:44684187 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.494T>C (p.Ile165Thr)	single nucleotide variant	not specified [RCV004201324]	Chr3:44594687 [GRCh38] Chr3:44636179 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1499A>C (p.His500Pro)	single nucleotide variant	not specified [RCV004220340]	Chr3:44642629 [GRCh38] Chr3:44684121 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.658G>A (p.Glu220Lys)	single nucleotide variant	not specified [RCV004204715]	Chr3:44632488 [GRCh38] Chr3:44673980 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2207G>C (p.Cys736Ser)	single nucleotide variant	not specified [RCV004074879]	Chr3:44643337 [GRCh38] Chr3:44684829 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.662A>C (p.Asp221Ala)	single nucleotide variant	not specified [RCV004108766]	Chr3:44594855 [GRCh38] Chr3:44636347 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.62A>G (p.Asp21Gly)	single nucleotide variant	not specified [RCV004243706]	Chr3:44629216 [GRCh38] Chr3:44670708 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1229G>A (p.Arg410His)	single nucleotide variant	not specified [RCV004202325]	Chr3:44642359 [GRCh38] Chr3:44683851 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.902G>T (p.Cys301Phe)	single nucleotide variant	not specified [RCV004219781]	Chr3:44642032 [GRCh38] Chr3:44683524 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.538C>T (p.His180Tyr)	single nucleotide variant	not specified [RCV004119955]	Chr3:44594731 [GRCh38] Chr3:44636223 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.434G>A (p.Arg145Gln)	single nucleotide variant	not specified [RCV004210191]	Chr3:44594627 [GRCh38] Chr3:44636119 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1730G>A (p.Arg577Gln)	single nucleotide variant	not specified [RCV004192447]	Chr3:44642860 [GRCh38] Chr3:44684352 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.718G>A (p.Ala240Thr)	single nucleotide variant	not specified [RCV004114434]	Chr3:44632548 [GRCh38] Chr3:44674040 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2545A>G (p.Ser849Gly)	single nucleotide variant	not specified [RCV004087544]	Chr3:44643675 [GRCh38] Chr3:44685167 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.328G>C (p.Glu110Gln)	single nucleotide variant	not specified [RCV004222358]	Chr3:44594521 [GRCh38] Chr3:44636013 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1702T>C (p.Cys568Arg)	single nucleotide variant	not specified [RCV004302537]	Chr3:44642832 [GRCh38] Chr3:44684324 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1423C>T (p.Arg475Cys)	single nucleotide variant	not specified [RCV004249971]	Chr3:44642553 [GRCh38] Chr3:44684045 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1964G>A (p.Cys655Tyr)	single nucleotide variant	not specified [RCV004249326]	Chr3:44643094 [GRCh38] Chr3:44684586 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.673T>C (p.Cys225Arg)	single nucleotide variant	not specified [RCV004266212]	Chr3:44632503 [GRCh38] Chr3:44673995 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.640G>A (p.Gly214Arg)	single nucleotide variant	not specified [RCV004265069]	Chr3:44594833 [GRCh38] Chr3:44636325 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.152A>G (p.His51Arg)	single nucleotide variant	not specified [RCV004277786]	Chr3:44629306 [GRCh38] Chr3:44670798 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2540C>T (p.Ala847Val)	single nucleotide variant	not specified [RCV004258010]	Chr3:44643670 [GRCh38] Chr3:44685162 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2480T>G (p.Phe827Cys)	single nucleotide variant	not specified [RCV004327899]	Chr3:44643610 [GRCh38] Chr3:44685102 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2623G>A (p.Glu875Lys)	single nucleotide variant	not specified [RCV004361907]	Chr3:44643753 [GRCh38] Chr3:44685245 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.367C>T (p.Arg123Trp)	single nucleotide variant	not specified [RCV004348202]	Chr3:44594560 [GRCh38] Chr3:44636052 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.3050A>G (p.Gln1017Arg)	single nucleotide variant	not specified [RCV004347897]	Chr3:44644180 [GRCh38] Chr3:44685672 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1137T>G (p.Phe379Leu)	single nucleotide variant	not specified [RCV004355049]	Chr3:44642267 [GRCh38] Chr3:44683759 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.127G>C (p.Val43Leu)	single nucleotide variant	not specified [RCV004365216]	Chr3:44594320 [GRCh38] Chr3:44635812 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1598C>T (p.Ser533Phe)	single nucleotide variant	not specified [RCV004491630]	Chr3:44642728 [GRCh38] Chr3:44684220 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.22C>T (p.His8Tyr)	single nucleotide variant	not specified [RCV004491637]	Chr3:44629176 [GRCh38] Chr3:44670668 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2804G>A (p.Cys935Tyr)	single nucleotide variant	not specified [RCV004491638]	Chr3:44643934 [GRCh38] Chr3:44685426 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2936T>G (p.Ile979Ser)	single nucleotide variant	not specified [RCV004491640]	Chr3:44644066 [GRCh38] Chr3:44685558 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.3016A>C (p.Lys1006Gln)	single nucleotide variant	not specified [RCV004491641]	Chr3:44644146 [GRCh38] Chr3:44685638 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.340G>A (p.Val114Met)	single nucleotide variant	not specified [RCV004491643]	Chr3:44629494 [GRCh38] Chr3:44670986 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.664G>A (p.Glu222Lys)	single nucleotide variant	not specified [RCV004489865]	Chr3:44594857 [GRCh38] Chr3:44636349 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.681C>A (p.Phe227Leu)	single nucleotide variant	not specified [RCV004489866]	Chr3:44594874 [GRCh38] Chr3:44636366 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.870T>G (p.Ile290Met)	single nucleotide variant	not specified [RCV004489867]	Chr3:44595063 [GRCh38] Chr3:44636555 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2230A>G (p.Ser744Gly)	single nucleotide variant	not specified [RCV004491633]	Chr3:44643360 [GRCh38] Chr3:44684852 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2240C>T (p.Ser747Leu)	single nucleotide variant	not specified [RCV004491634]	Chr3:44643370 [GRCh38] Chr3:44684862 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.758T>C (p.Val253Ala)	single nucleotide variant	not specified [RCV004491645]	Chr3:44632588 [GRCh38] Chr3:44674080 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1637C>T (p.Thr546Ile)	single nucleotide variant	not specified [RCV004491631]	Chr3:44642767 [GRCh38] Chr3:44684259 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2151G>A (p.Met717Ile)	single nucleotide variant	not specified [RCV004491632]	Chr3:44643281 [GRCh38] Chr3:44684773 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.676T>G (p.Phe226Val)	single nucleotide variant	not specified [RCV004491644]	Chr3:44632506 [GRCh38] Chr3:44673998 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.226C>T (p.Arg76Cys)	single nucleotide variant	not specified [RCV004491635]	Chr3:44629380 [GRCh38] Chr3:44670872 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.227G>T (p.Arg76Leu)	single nucleotide variant	not specified [RCV004491636]	Chr3:44629381 [GRCh38] Chr3:44670873 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.209G>A (p.Arg70Gln)	single nucleotide variant	not specified [RCV004489861]	Chr3:44594402 [GRCh38] Chr3:44635894 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.583T>C (p.Cys195Arg)	single nucleotide variant	not specified [RCV004489864]	Chr3:44594776 [GRCh38] Chr3:44636268 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.280C>G (p.Leu94Val)	single nucleotide variant	not specified [RCV004491639]	Chr3:44629434 [GRCh38] Chr3:44670926 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.3039C>A (p.Phe1013Leu)	single nucleotide variant	not specified [RCV004491642]	Chr3:44644169 [GRCh38] Chr3:44685661 [GRCh37] Chr3:3p21.31	likely benign
NM_173658.4(ZNF660):c.537A>C (p.Gln179His)	single nucleotide variant	not specified [RCV004489863]	Chr3:44594730 [GRCh38] Chr3:44636222 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.99G>T (p.Gln33His)	single nucleotide variant	not specified [RCV004489868]	Chr3:44594292 [GRCh38] Chr3:44635784 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.853A>G (p.Lys285Glu)	single nucleotide variant	not specified [RCV004688097]	Chr3:44641983 [GRCh38] Chr3:44683475 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.787G>A (p.Glu263Lys)	single nucleotide variant	not specified [RCV004688102]	Chr3:44641917 [GRCh38] Chr3:44683409 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.478C>T (p.His160Tyr)	single nucleotide variant	not specified [RCV004688099]	Chr3:44631149 [GRCh38] Chr3:44672641 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1007C>T (p.Pro336Leu)	single nucleotide variant	not specified [RCV004688104]	Chr3:44642137 [GRCh38] Chr3:44683629 [GRCh37] Chr3:3p21.31	likely benign
NM_006991.5(ZNF197):c.4A>T (p.Thr2Ser)	single nucleotide variant	not specified [RCV004688107]	Chr3:44629158 [GRCh38] Chr3:44670650 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2924T>C (p.Val975Ala)	single nucleotide variant	not specified [RCV004688108]	Chr3:44644054 [GRCh38] Chr3:44685546 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.469A>G (p.Thr157Ala)	single nucleotide variant	not specified [RCV004614695]	Chr3:44594662 [GRCh38] Chr3:44636154 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1001G>A (p.Arg334Lys)	single nucleotide variant	not specified [RCV004688098]	Chr3:44642131 [GRCh38] Chr3:44683623 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2063G>A (p.Gly688Asp)	single nucleotide variant	not specified [RCV004688103]	Chr3:44643193 [GRCh38] Chr3:44684685 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1421G>A (p.Arg474Lys)	single nucleotide variant	not specified [RCV004688105]	Chr3:44642551 [GRCh38] Chr3:44684043 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2438C>T (p.Thr813Met)	single nucleotide variant	not specified [RCV004688100]	Chr3:44643568 [GRCh38] Chr3:44685060 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.1207T>C (p.Cys403Arg)	single nucleotide variant	not specified [RCV004688109]	Chr3:44642337 [GRCh38] Chr3:44683829 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.986A>C (p.Glu329Ala)	single nucleotide variant	not specified [RCV004601624]	Chr3:44595179 [GRCh38] Chr3:44636671 [GRCh37] Chr3:3p21.31	uncertain significance
NM_173658.4(ZNF660):c.493A>G (p.Ile165Val)	single nucleotide variant	not specified [RCV004601623]	Chr3:44594686 [GRCh38] Chr3:44636178 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.523G>T (p.Ala175Ser)	single nucleotide variant	not specified [RCV004688101]	Chr3:44631194 [GRCh38] Chr3:44672686 [GRCh37] Chr3:3p21.31	uncertain significance
NM_006991.5(ZNF197):c.2585T>C (p.Ile862Thr)	single nucleotide variant	not specified [RCV004688106]	Chr3:44643715 [GRCh38] Chr3:44685207 [GRCh37] Chr3:3p21.31	uncertain significance

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
1298487	BFD1_H	Body fluid distribution QTL 1 (human)	3.94		Body fluid distribution	impedance ratio	3	36380712	62380712	Human
597389388	GWAS1485462_H	macrophage inflammatory protein 1b measurement QTL GWAS1485462 (human)		7e-10	macrophage inflammatory protein 1b measurement		3	44599303	44599304	Human
1298489	RA4_H	Rheumatoid arthritis QTL 4 (human)		0.0283	Joint/bone inflammation	rheumatoid arthritis	3	36380712	62380712	Human
1643509	BW293_H	Body Weight QTL 293 (human)	1.42		Body weight	BMI	3	36380712	62380712	Human
2316061	GLUCO194_H	Glucose level QTL 194 (human)		0.02	Glucose level		3	23380774	49380774	Human
2289308	BW392_H	Body weight QTL 392 (human)	1.42		Body weight	BMI	3	36380712	62380712	Human

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.

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001351732	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001351733	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001351734	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001351735	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_147691	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_147692	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC099669	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068275	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB092136	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

NM_001351732 ⟹ NP_001338661

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,584,964 - 44,648,471 (+)	NCBI
T2T-CHM13v2.0	3	44,600,686 - 44,664,179 (+)	NCBI

Sequence:

show sequence

AGTTCCTTCTGCGCTTTGTTCAAGATGTGGGTCTGGCGCTTTCGTGACTCAAGACCCTCTTAGG
AACTTCTTCACTGAACTCAAGGAGGAGATCAGGCAAGATCTGTGCTGTGCAGATCCTTTGGATT
GAGGCTGCTGTGCACAGGAATATGGATGATACTCTCCAAGCTGTAAGGAAGAAGTCAAGGATTA
AGGAGACCTGGACTGGAGAGGAGCCTTTTTCAAAAAACAACAATGACAAGAGAAAATGTAGCCC
ACAATGCTCTGAGACAAGAGGGCCTTGTGAAGGGGAAGGATGATACCTGGAAATGGGGAACCAG
CTTCCAAGGAAGTAGCTCCTCTGTTTGGGAGACCTCCCACCTACACTTTAGACAATTACGTTAC
CATGAGACATCTGGACCCCAGGAAGCCCTGAGCCGGCTCAGGGAACTCTGTCGCCGGTGGCTGA
GACCAGAAGCACGCACCAAGGCACAGATCCTGGAGCTGCTGGTGCTGGAGCAGTTTCTGAGCAT
CCTGCCTGGGGAGATTCGGACCTGGGTACAGCTCCATCACCCTGGAAGTGGCGAGGAGGCTGTG
GCCCTGGTAGAGGAGCTGCAGAAAGACCTTGATGGACCAGCAATACAAGTTCCAGTCCTTGTCA
AGGATCAGGACACTCTCCAGAAGGTGGTGAGTGCCCCAGGAACAACACTTCCTCCTGTACTTCC
TGGCAGCCACATAGCAGCTGAAATTTGCCCGCATCCTCCTACTGACCTAGTGGCATTCAACCTC
CAGGATCCTCAGCATGATTCTCCTGCCCCTGAAGCTTCTGCCCTTTCCCAGGAAGAGAACCCAA
GAAATCAATTAATGGCACTTATGCTCCTAACAGCCCAGCCCCAGGAGTTGGTGATGTTCGAGGA
GGTGTCAGTATGCTTCACTTCAGAGGAATGGGCATGTCTGGGCCCAATCCAGAGGGCCTTGTAC
TGGGATGTGATGCTGGAGAATTATGGAAATGTGACCTCCCTAGAATGGGAGACCATGACCGAGA
ATGAGGAGGTGACATCAAAGCCAAGTAGTTCTCAAAGAGCAGACTCTCATAAAGGAACATCAAA
AAGACTTCAAGGAAGTGTTCCCCAGGTCCTTGATTTTGAAGAAGAGTGTGAATGGCAAGTTTTG
GCAAGTCAGTGGGGAAATGAAACAGATGAAAGGGCAGATACAGTGAAGAAAGTTTCCCTTTGTG
AACGAGACAAGAAGAAAAGGACTCCACCAGAGAAACAAGGCCAAAAGTGGAAGGAATTAGGAGA
CAGCTTGACTTTCGGTTCAGCTATTTCTGAAAGTTTAATAGGTACTGAAGGAAAGAAGTTTTAT
AAATGTGATATGTGTTGTAAACATTTTAATAAAATCTCCCATCTTATAAACCATCGGAGAATCC
ACACTGGTGAGAAACCTCATAAATGTAAGGAATGTGGAAAAGGCTTTATTCAGCGTTCGAGCCT
TCTAATGCATTTACGGAACCATTCAGGGGAGAAACCTTATAAATGTAATGAATGTGGGAAAGCA
TTTTCTCAAAGTGCTTACCTTCTAAACCATCAGAGGATCCACACTGGGGAGAAACCTTATAAGT
GTAAGGAGTGTGGAAAGGGCTTCTATAGGCACTCAGGCCTAATTATACATCTAAGGCGCCATTC
AGGGGAGAGACCTTATAAGTGTAATGAATGTGGGAAAGTCTTCTCTCAGAATGCTTACCTCATT
GACCATCAGAGGCTCCACAAAGGGGAAGAACCTTATAAATGTAATAAGTGTCAGAAAGCTTTCA
TTCTGAAGAAGAGCCTCATTCTGCACCAGAGAATCCACTCTGGGGAAAAACCCTATAAATGTGA
TGAATGTGGAAAGACCTTTGCTCAGACCACTTATCTTATTGACCATCAGCGACTCCACAGTGCA
GAGAACCCTTACAAGTGTAAAGAATGTGGAAAAGTTTTCATTCGAAGCAAAAGCCTCCTCTTAC
ATCAGAGAGTCCACACAGAAAAGAAAACCTTTGGTTGTAAAAAGTGTGGGAAGATTTTCAGTTC
TAAGTCAAACTTCATTGACCATAAGAGGATGCACAGCAGAGAGAAACCTTACAAATGCACTGAA
TGTGGGAAAGCCTTTACTCAAAGTGCTTACCTTTTTGACCACCAGAGACTCCACAATGGGGAGA
AGCCCTATGAATGTAATGAATGTGGGAAAGTTTTTATTCTGAAGAAGAGCCTCATTTTACATCA
AAGGTTCCACACTGGAGAGAATCTCTATGAATGTAAAGATTGTGGTAAGGTCTTCGGTTCAAAC
AGAAACCTCATTGACCATGAGAGACTCCACAATGGGGAGAAGCCATATGAATGTCGAGAGTGTG
GGAAAACCTTTATTATGAGCAAAAGTTTTATGGTCCATCAGAAACTCCATACACAAGAGAAAGC
CTACAAATGTGAGGATTGTGGGAAGGCTTTCAGTTACAATTCAAGCCTGCTTGTACATCGGAGA
ATCCACACCGGAGAAAAACCCTTTGAATGCAGTGAGTGTGGAAGAGCTTTCAGTTCAAACAGAA
ACCTCATTGAGCATAAGAGAATCCACAGTGGTGAGAAACCCTATGAGTGTGATGAGTGTGGCAA
ATGCTTCATTCTGAAGAAAAGCCTCATTGGACATCAGAGAATTCACACGAGGGAAAAATCTTAT
AAATGCAATGACTGTGGGAAGGTCTTCAGTTACCGCTCAAACCTTATAGCCCATCAGAGGATCC
ATACTGGTGAGAAGCCCTATGCGTGTAGTGAGTGTGGAAAAGGTTTTACGTACAACAGAAACCT
GATTGAACATCAAAGAATTCACAGTGGAGAAAAAACCTACGAATGTCATGTATGTAGGAAAGTC
CTTACCTCTAGTAGAAATCTTATGGTACATCAAAGAATCCATACTGGAGAGAAACCTTATAAAT
GTAATGAGTGTGGAAAAGACTTTAGTCAGAATAAAAACCTTGTTGTACATCAGAGAATGCACAC
TGGGGAAAAACCTTATGAGTGTGACAAGTGTAGGAAATCCTTTACTTCTAAGAGGAATTTAGTT
GGCCACCAGAGAATTCACACAGGGGAGAAACCCTATGGGTGTAATGATTGTAGTAAAGTTTTTA
GGCAAAGAAAAAACCTTACTGTACATCAGAAAATCCACACAGATGAAAAACCTTGTGAATGTGA
TGTGTCTGAAAAAGAATTCTCTCAGACTTCCAACCTTCATCTTCAACAGAAAATCCATACCATT
GAGGAATTCTCTTGGCTACAAAACACCAATGAGTCCAAGATTGAGATTCAGAAAATCTAGTGTC
ATATGTAAAATGGAATAGAATCCCTGCCTACTTAAGTAACTGTTGGACAAATGATATATATTTC
TTCTAAGGAAAAAGTTTATTATTTACTCTTTACTAGACAAATGAGTAGCATATAGAAGAAAGTT
AATAGGCCGGGCTTGGTGGCTCATGCCTGTAATCCCAGCACTTTGAGAGGCCGAAGCGAGTGGA
TCACCTGAGGTCAGGATTTTGAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAA
TACAAAAATTATCCGGGCATGGGGGCACACACCGGTAATCCCAGCTACTCAGGAGGCTGAGACA
GGAGAGTCGCTTGAACCTGGGAGGGCGGAGGTTGCAGTGAGCCAGGATCGCGCCATTGCACTCC
AGCCTGGGCAACAAGAGCGAAACTCTTGTCTGAAAAAATAAAGTTCATCCCAACTTTCAAGTCT
ACAAAAACATAATCCAAATCTAATAACATAGTTGTAAATGAGAGCAACAATAAAAAGTAGACAT
GGGCTGGGTGCAGTGGCTCACTCCTGTAGTCCCAGGACTTTGGGAGGCCGAGGTGGGAAGATCC
CTTGAGCCCAGGAGTTCGAGACAAGCCTGGGTAACACGGGGAGACCCGTCTTTAGTAAATAAAA
ATAAATTTATTAATAAAACTAAAAATTTAATAATAAAAAGTGGACATTGTTTTTTAAAATGTGT
ATAGTATGCATTTTAAAGATAGTGTCACTGCTGTGGAAAACCTGAACAGACAGTATGATCCAGA
ATGTCAGGTGTGGAGTTGGGCGGACAAGAGTCTGCTGATGAGGACAACCTAAAAGAGCACTGGA
TTTGGAATCAGAAGACCTACCTTTGATTCCTGGCTTTCCCTTAATGGCCATGTGATGTTATTAA
GTCAGCCTCTAAAGCTTTAGTTTCCTGTCAGTCAAATGTTGACATGATACCTACCTCACAGGGT
TGTTGTGAGGGTTAAGTGAAAGGATCTTTGTGAAAGTACTTTTTGAAATCATTCAGTTGTCAAT
AAAGTTGGATAAAAGAGGTTATGGTAAAAGTTTAGAACATGGGATCATGTAAGTTTGTGTATTA
AGTCAATATTAGAATGAGGGGGATTCCAGGAACCTAAAAGATACTCATTTTCATAAGAGGAAGT
ATGGTGAATAGCTAACTGGAATTTAGTGTTCTAAGAATAATTTTGTTAAATTTACCTTTAAAAA
TATCTGAGGGAGTTACTAGATTATATATCTAGTTTATGTATATGGAAAAAAATGTTATGGCCAG
CCATTAACAGTGATGCCAAGGAAAACAATTTATTTCCCAGCTTTTGAATTTGAAACTTAACAGA
TGGAGAGTGTCAAAATGGAAGGGCAGTGGTACCCTGCTTTCCCTATTCAGAGGGAAAAAAATCC
TTGACCCGCAGTTGAGCTGATGATCCCTGCCACAGTCATTGTGAATTCTAATCAATATTTCATC
ATTGCTGTCAAATGATAGCCTGTTACTAATGAAACAACATTCTGTCCCAGCACTAAATTTACTG
GGACATAAATTTTTCACATGGAGCCAAGCTCTTCACTGATTAAGCCAGTGCAGAATCCACTTGT
GGGCAGTCAGTGCCCATTACCCCCTGTGAACCATTCTGTGCCCTTGAGTACATTTGTGGGTTTA
ACTCAGTCTATATTCTTAAGTTGGTAATTTTTATGTTGTAATTCTCAAAGTTCTGTTTCTGTAG
CTGGACTATGAATAATACCTGAATATGAAGATTGTGTTTTTTAATAATGTCAAAGTGGTGTGTT
GATTATCATAAATGTTATTAATTCAACCCCACAGTTTCTTGGGGGCTGGTTCCTCATTAGAGTG
AAAGGTAGCCAAGAGTGAAAACTGGAAGGGGCCTAAGGCTTAAAGTCTTAAGACCTGGATGTGG
TTCAGGTTTTGCCATCTGCCTCAGAAAAAATCTCTTCAGTTCTTGGAGCCTTGAATTCCTCATC
TGTTAAACAGGAGGAAGAATATCTACCTCACAAAGTTCTTATGAGATAATGAATATAAAAATGT
TTCATCCAGGTTGTTGAATCATCCCAGCTTATATAATAATTACAAAGGACATATGTACTTTAAC
AATGGAGAATGCTGTGATTTACCTCTTCACCGAGTAACAAAATGTCACATTGCTTAGATTGAGA
CAGCCCACATAATGTGCCACCTTCTGTGATGTAATAAGCTGAAAAATGTTCAACCTGAATTTAA
TCAAGCTTCTTGGACCTCATTGCCAGGTTACAGGAAATACAGGAGGCAGAGGAACAAATAAAAG
ACACCACGAGAAACAGACACATCCAGAACGTGGAATATTGCATAAGAAAGCTGCCCTGGATTCT
TCAAAATATTATTATGATGAAAAAGAGAGGGGAGTGAAAATTGTTCAAGCTGTCTTGAGTCTGC
TGTGAGTTTATTATACCATTCTCTGCTTTTGTGTATGTATGAAAATTTCGATATGAAAGGTATA
AAACATGGATGAGGAGGCTTGTTTTTAAAAGATAATACTAGAGAGCCGTTAGGTACTAAGAACC
AGAAATAGACTCACATAAATGGCCAATTGATTTTTGACAGGGGCAAAAGCAATTCAATGGAGGA
GGGATCGCCTTTTCAGCAAATACTGTTGGAGTAATTGGATATCCATAGGCAGTAAACCAACAAC
TTCAGGACCTAGGACTGAGCTAAGAAGGCTCAGATGACTCAAAAGCATGCTCCTTAGAAGGAAA
AAAAATGTTAAATTGGACTTCATCAAAATTAAGATAATTTACCCTGTAAGAGACCTTTTTACAA
AGATGATATTACAGGTTGGGAAAAAATATTTGCAAATCATATCCAACAAGGGATTTGTATGTAA
ACTACATAAAGAACTTTCCAAATTTAACAGTAATAAGTAAATACAATTAGAAAATAAGCAAAAG
ACAGACATTTCACTGAAGTATAGATAGCAAATAAGCAAATGAAAAGATGTTCAACATCATTAGG
CATGAGGGAAATGCAGAGTAAAATCGTGAGATATCACCTATCAGAATAGCTTAACTTTTTTTTT
TTAATGGTGGTAACTGCTGGCAAGGATGAAGAGAAACAGGATCTCATACATTGCTGGGAATGTA
AAATGGTACAGCCACTCTGGAATATAATTTGGCAGTTTCTTGTAAAACCACACATGTATATGTC
ATGCTTCAGGAATTGCACTTCTGAGCATTTATCCCAGAGAAATGAAAACTTGCGTTCACACAAA
AACCTGTATACGAATGTTCATAGCAGCTTTATTTGTAATGGTCGAAACCTGTAGGCAACCCATA
TATCCTTCCTTAGGTGGTTAAAACAAATTGTGGTTTATGTATTACCATGGAATACTTGTTACTC
TGCAATAAAATTGACTTATTGATATCCATAACAACTCAAATAAATTTCAAGGGAATTAATGCTG
AGTGAAAATAATCACAAAAGGCCATATTCTGTATGAAAATATTCATATAACATTCTCAAAATGA
TAAAACTATAGAGATGAAAAATGGATTAATGGTTGCCAAAGGTTAGGGATGGTGGGAGGAAAAA
TGGGGAGAGGGTTGGATGGAACTATTAAAAGGTAGCACCAGAAAGGTCTTTGTGGTGATGGAAC
ACTTGTGTATCTTGATTGCAGTGGTGGTTACACAAATCTATAGGTGCTATACCTATACACACAT
ACTGTACCAATGTTGATTTCCTTTTTCATTTTATGTAAGATGTAACCATGAGGGGAAAGTGGGT
GAAGGGTGCTATCTTTGCAACTTCCTGTGATTCTATCATTTCAAAATAAAAAGTAAAAACCAAC
AATGGCAACGAAAACCCAAAACTAAAGAGCTGTAACCAACTAAAGTGTGTGAAACTGATTTGAA
AAAAAGTTATAAAATACATGTTTTAGGACAGTTGGGAAATTTGAATATGACTGGTTATTAGATG
GTATTAGGGAATTTTTGTTGATTTTCTTACCTGTGACGGTGGTGGTAGTTTGAAGAATATTCTT
AATCTTAAGGGATGCATGTTGAAGTATTTGGAATGAAGTGTTCTGATGTTTACAACTTTCAAAA
AAATGATTTTAAATATGTATTGAGAGATCAGGCAAACATAGCAAAATGTTCATTGTTGAGTCCA
CATGGAAAATACGGGTATTCAATGTGCCATACTTTCAACTCTTCTGTACTCTGATATTTTCAAA
ATAAAACATTTGAGGGGAAATTA

hide sequence

RefSeq Acc Id:

NM_001351733 ⟹ NP_001338662

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,584,964 - 44,648,471 (+)	NCBI
T2T-CHM13v2.0	3	44,600,686 - 44,664,179 (+)	NCBI

Sequence:

show sequence

AGTTCCTTCTGCGCTTTGTTCAAGATGTGGGTCTGGCGCTTTCGTGACTCAAGACCCTCTTAGG
AACTTCTTCACTGAACTCAAGGAGGAGATCAGGCAAGATCTGTGCTGTGCAGATCCTTTGGATT
GAGGCTGCTGTGCACAGGAATATGGGTCTTGTAGATGATACTCTCCAAGCTGTAAGGAAGAAGT
CAAGGATTAAGGAGACCTGGACTGGAGAGGAGCCTTTTTCAAAAAACAACAATGACAAGAGAAA
ATGTAGCCCACAATGCTCTGAGACAAGAGGGCCTTGTGAAGGGGAAGGATGATACCTGGAAATG
GGGAACCAGCTTCCAAGGAAGTAGCTCCTCTGTTTGGGAGACCTCCCACCTACACTTTAGACAA
TTACGTTACCATGAGACATCTGGACCCCAGGAAGCCCTGAGCCGGCTCAGGGAACTCTGTCGCC
GGTGGCTGAGACCAGAAGCACGCACCAAGGCACAGATCCTGGAGCTGCTGGTGCTGGAGCAGTT
TCTGAGCATCCTGCCTGGGGAGATTCGGACCTGGGTACAGCTCCATCACCCTGGAAGTGGCGAG
GAGGCTGTGGCCCTGGTAGAGGAGCTGCAGAAAGACCTTGATGGACCAGCAATACAAGTTCCAG
TCCTTGTCAAGGATCAGGACACTCTCCAGAAGGTGGTGAGTGCCCCAGGAACAACACTTCCTCC
TGTACTTCCTGGCAGCCACATAGCAGCTGAAATTTGCCCGCATCCTCCTACTGACCTAGTGGCA
TTCAACCTCCAGGATCCTCAGCATGATTCTCCTGCCCCTGAAGCTTCTGCCCTTTCCCAGGAAG
AGAACCCAAGAAATCAATTAATGGCACTTATGCTCCTAACAGCCCAGCCCCAGGAGTTGGTGAT
GTTCGAGGAGGTGTCAGTATGCTTCACTTCAGAGGAATGGGCATGTCTGGGCCCAATCCAGAGG
GCCTTGTACTGGGATGTGATGCTGGAGAATTATGGAAATGTGACCTCCCTAGAATGGGAGACCA
TGACCGAGAATGAGGAGGTGACATCAAAGCCAAGTAGTTCTCAAAGAGCAGACTCTCATAAAGG
AACATCAAAAAGACTTCAAGGAAGTGTTCCCCAGGTCCTTGATTTTGAAGAAGAGTGTGAATGG
CAAGTTTTGGCAAGTCAGTGGGGAAATGAAACAGATGAAAGGGCAGATACAGTGAAGAAAGTTT
CCCTTTGTGAACGAGACAAGAAGAAAAGGACTCCACCAGAGAAACAAGGCCAAAAGTGGAAGGA
ATTAGGAGACAGCTTGACTTTCGGTTCAGCTATTTCTGAAAGTTTAATAGGTACTGAAGGAAAG
AAGTTTTATAAATGTGATATGTGTTGTAAACATTTTAATAAAATCTCCCATCTTATAAACCATC
GGAGAATCCACACTGGTGAGAAACCTCATAAATGTAAGGAATGTGGAAAAGGCTTTATTCAGCG
TTCGAGCCTTCTAATGCATTTACGGAACCATTCAGGGGAGAAACCTTATAAATGTAATGAATGT
GGGAAAGCATTTTCTCAAAGTGCTTACCTTCTAAACCATCAGAGGATCCACACTGGGGAGAAAC
CTTATAAGTGTAAGGAGTGTGGAAAGGGCTTCTATAGGCACTCAGGCCTAATTATACATCTAAG
GCGCCATTCAGGGGAGAGACCTTATAAGTGTAATGAATGTGGGAAAGTCTTCTCTCAGAATGCT
TACCTCATTGACCATCAGAGGCTCCACAAAGGGGAAGAACCTTATAAATGTAATAAGTGTCAGA
AAGCTTTCATTCTGAAGAAGAGCCTCATTCTGCACCAGAGAATCCACTCTGGGGAAAAACCCTA
TAAATGTGATGAATGTGGAAAGACCTTTGCTCAGACCACTTATCTTATTGACCATCAGCGACTC
CACAGTGCAGAGAACCCTTACAAGTGTAAAGAATGTGGAAAAGTTTTCATTCGAAGCAAAAGCC
TCCTCTTACATCAGAGAGTCCACACAGAAAAGAAAACCTTTGGTTGTAAAAAGTGTGGGAAGAT
TTTCAGTTCTAAGTCAAACTTCATTGACCATAAGAGGATGCACAGCAGAGAGAAACCTTACAAA
TGCACTGAATGTGGGAAAGCCTTTACTCAAAGTGCTTACCTTTTTGACCACCAGAGACTCCACA
ATGGGGAGAAGCCCTATGAATGTAATGAATGTGGGAAAGTTTTTATTCTGAAGAAGAGCCTCAT
TTTACATCAAAGGTTCCACACTGGAGAGAATCTCTATGAATGTAAAGATTGTGGTAAGGTCTTC
GGTTCAAACAGAAACCTCATTGACCATGAGAGACTCCACAATGGGGAGAAGCCATATGAATGTC
GAGAGTGTGGGAAAACCTTTATTATGAGCAAAAGTTTTATGGTCCATCAGAAACTCCATACACA
AGAGAAAGCCTACAAATGTGAGGATTGTGGGAAGGCTTTCAGTTACAATTCAAGCCTGCTTGTA
CATCGGAGAATCCACACCGGAGAAAAACCCTTTGAATGCAGTGAGTGTGGAAGAGCTTTCAGTT
CAAACAGAAACCTCATTGAGCATAAGAGAATCCACAGTGGTGAGAAACCCTATGAGTGTGATGA
GTGTGGCAAATGCTTCATTCTGAAGAAAAGCCTCATTGGACATCAGAGAATTCACACGAGGGAA
AAATCTTATAAATGCAATGACTGTGGGAAGGTCTTCAGTTACCGCTCAAACCTTATAGCCCATC
AGAGGATCCATACTGGTGAGAAGCCCTATGCGTGTAGTGAGTGTGGAAAAGGTTTTACGTACAA
CAGAAACCTGATTGAACATCAAAGAATTCACAGTGGAGAAAAAACCTACGAATGTCATGTATGT
AGGAAAGTCCTTACCTCTAGTAGAAATCTTATGGTACATCAAAGAATCCATACTGGAGAGAAAC
CTTATAAATGTAATGAGTGTGGAAAAGACTTTAGTCAGAATAAAAACCTTGTTGTACATCAGAG
AATGCACACTGGGGAAAAACCTTATGAGTGTGACAAGTGTAGGAAATCCTTTACTTCTAAGAGG
AATTTAGTTGGCCACCAGAGAATTCACACAGGGGAGAAACCCTATGGGTGTAATGATTGTAGTA
AAGTTTTTAGGCAAAGAAAAAACCTTACTGTACATCAGAAAATCCACACAGATGAAAAACCTTG
TGAATGTGATGTGTCTGAAAAAGAATTCTCTCAGACTTCCAACCTTCATCTTCAACAGAAAATC
CATACCATTGAGGAATTCTCTTGGCTACAAAACACCAATGAGTCCAAGATTGAGATTCAGAAAA
TCTAGTGTCATATGTAAAATGGAATAGAATCCCTGCCTACTTAAGTAACTGTTGGACAAATGAT
ATATATTTCTTCTAAGGAAAAAGTTTATTATTTACTCTTTACTAGACAAATGAGTAGCATATAG
AAGAAAGTTAATAGGCCGGGCTTGGTGGCTCATGCCTGTAATCCCAGCACTTTGAGAGGCCGAA
GCGAGTGGATCACCTGAGGTCAGGATTTTGAGACCAGCCTGACCAACATGGTGAAACCCCATCT
CTACTAAAATACAAAAATTATCCGGGCATGGGGGCACACACCGGTAATCCCAGCTACTCAGGAG
GCTGAGACAGGAGAGTCGCTTGAACCTGGGAGGGCGGAGGTTGCAGTGAGCCAGGATCGCGCCA
TTGCACTCCAGCCTGGGCAACAAGAGCGAAACTCTTGTCTGAAAAAATAAAGTTCATCCCAACT
TTCAAGTCTACAAAAACATAATCCAAATCTAATAACATAGTTGTAAATGAGAGCAACAATAAAA
AGTAGACATGGGCTGGGTGCAGTGGCTCACTCCTGTAGTCCCAGGACTTTGGGAGGCCGAGGTG
GGAAGATCCCTTGAGCCCAGGAGTTCGAGACAAGCCTGGGTAACACGGGGAGACCCGTCTTTAG
TAAATAAAAATAAATTTATTAATAAAACTAAAAATTTAATAATAAAAAGTGGACATTGTTTTTT
AAAATGTGTATAGTATGCATTTTAAAGATAGTGTCACTGCTGTGGAAAACCTGAACAGACAGTA
TGATCCAGAATGTCAGGTGTGGAGTTGGGCGGACAAGAGTCTGCTGATGAGGACAACCTAAAAG
AGCACTGGATTTGGAATCAGAAGACCTACCTTTGATTCCTGGCTTTCCCTTAATGGCCATGTGA
TGTTATTAAGTCAGCCTCTAAAGCTTTAGTTTCCTGTCAGTCAAATGTTGACATGATACCTACC
TCACAGGGTTGTTGTGAGGGTTAAGTGAAAGGATCTTTGTGAAAGTACTTTTTGAAATCATTCA
GTTGTCAATAAAGTTGGATAAAAGAGGTTATGGTAAAAGTTTAGAACATGGGATCATGTAAGTT
TGTGTATTAAGTCAATATTAGAATGAGGGGGATTCCAGGAACCTAAAAGATACTCATTTTCATA
AGAGGAAGTATGGTGAATAGCTAACTGGAATTTAGTGTTCTAAGAATAATTTTGTTAAATTTAC
CTTTAAAAATATCTGAGGGAGTTACTAGATTATATATCTAGTTTATGTATATGGAAAAAAATGT
TATGGCCAGCCATTAACAGTGATGCCAAGGAAAACAATTTATTTCCCAGCTTTTGAATTTGAAA
CTTAACAGATGGAGAGTGTCAAAATGGAAGGGCAGTGGTACCCTGCTTTCCCTATTCAGAGGGA
AAAAAATCCTTGACCCGCAGTTGAGCTGATGATCCCTGCCACAGTCATTGTGAATTCTAATCAA
TATTTCATCATTGCTGTCAAATGATAGCCTGTTACTAATGAAACAACATTCTGTCCCAGCACTA
AATTTACTGGGACATAAATTTTTCACATGGAGCCAAGCTCTTCACTGATTAAGCCAGTGCAGAA
TCCACTTGTGGGCAGTCAGTGCCCATTACCCCCTGTGAACCATTCTGTGCCCTTGAGTACATTT
GTGGGTTTAACTCAGTCTATATTCTTAAGTTGGTAATTTTTATGTTGTAATTCTCAAAGTTCTG
TTTCTGTAGCTGGACTATGAATAATACCTGAATATGAAGATTGTGTTTTTTAATAATGTCAAAG
TGGTGTGTTGATTATCATAAATGTTATTAATTCAACCCCACAGTTTCTTGGGGGCTGGTTCCTC
ATTAGAGTGAAAGGTAGCCAAGAGTGAAAACTGGAAGGGGCCTAAGGCTTAAAGTCTTAAGACC
TGGATGTGGTTCAGGTTTTGCCATCTGCCTCAGAAAAAATCTCTTCAGTTCTTGGAGCCTTGAA
TTCCTCATCTGTTAAACAGGAGGAAGAATATCTACCTCACAAAGTTCTTATGAGATAATGAATA
TAAAAATGTTTCATCCAGGTTGTTGAATCATCCCAGCTTATATAATAATTACAAAGGACATATG
TACTTTAACAATGGAGAATGCTGTGATTTACCTCTTCACCGAGTAACAAAATGTCACATTGCTT
AGATTGAGACAGCCCACATAATGTGCCACCTTCTGTGATGTAATAAGCTGAAAAATGTTCAACC
TGAATTTAATCAAGCTTCTTGGACCTCATTGCCAGGTTACAGGAAATACAGGAGGCAGAGGAAC
AAATAAAAGACACCACGAGAAACAGACACATCCAGAACGTGGAATATTGCATAAGAAAGCTGCC
CTGGATTCTTCAAAATATTATTATGATGAAAAAGAGAGGGGAGTGAAAATTGTTCAAGCTGTCT
TGAGTCTGCTGTGAGTTTATTATACCATTCTCTGCTTTTGTGTATGTATGAAAATTTCGATATG
AAAGGTATAAAACATGGATGAGGAGGCTTGTTTTTAAAAGATAATACTAGAGAGCCGTTAGGTA
CTAAGAACCAGAAATAGACTCACATAAATGGCCAATTGATTTTTGACAGGGGCAAAAGCAATTC
AATGGAGGAGGGATCGCCTTTTCAGCAAATACTGTTGGAGTAATTGGATATCCATAGGCAGTAA
ACCAACAACTTCAGGACCTAGGACTGAGCTAAGAAGGCTCAGATGACTCAAAAGCATGCTCCTT
AGAAGGAAAAAAAATGTTAAATTGGACTTCATCAAAATTAAGATAATTTACCCTGTAAGAGACC
TTTTTACAAAGATGATATTACAGGTTGGGAAAAAATATTTGCAAATCATATCCAACAAGGGATT
TGTATGTAAACTACATAAAGAACTTTCCAAATTTAACAGTAATAAGTAAATACAATTAGAAAAT
AAGCAAAAGACAGACATTTCACTGAAGTATAGATAGCAAATAAGCAAATGAAAAGATGTTCAAC
ATCATTAGGCATGAGGGAAATGCAGAGTAAAATCGTGAGATATCACCTATCAGAATAGCTTAAC
TTTTTTTTTTTAATGGTGGTAACTGCTGGCAAGGATGAAGAGAAACAGGATCTCATACATTGCT
GGGAATGTAAAATGGTACAGCCACTCTGGAATATAATTTGGCAGTTTCTTGTAAAACCACACAT
GTATATGTCATGCTTCAGGAATTGCACTTCTGAGCATTTATCCCAGAGAAATGAAAACTTGCGT
TCACACAAAAACCTGTATACGAATGTTCATAGCAGCTTTATTTGTAATGGTCGAAACCTGTAGG
CAACCCATATATCCTTCCTTAGGTGGTTAAAACAAATTGTGGTTTATGTATTACCATGGAATAC
TTGTTACTCTGCAATAAAATTGACTTATTGATATCCATAACAACTCAAATAAATTTCAAGGGAA
TTAATGCTGAGTGAAAATAATCACAAAAGGCCATATTCTGTATGAAAATATTCATATAACATTC
TCAAAATGATAAAACTATAGAGATGAAAAATGGATTAATGGTTGCCAAAGGTTAGGGATGGTGG
GAGGAAAAATGGGGAGAGGGTTGGATGGAACTATTAAAAGGTAGCACCAGAAAGGTCTTTGTGG
TGATGGAACACTTGTGTATCTTGATTGCAGTGGTGGTTACACAAATCTATAGGTGCTATACCTA
TACACACATACTGTACCAATGTTGATTTCCTTTTTCATTTTATGTAAGATGTAACCATGAGGGG
AAAGTGGGTGAAGGGTGCTATCTTTGCAACTTCCTGTGATTCTATCATTTCAAAATAAAAAGTA
AAAACCAACAATGGCAACGAAAACCCAAAACTAAAGAGCTGTAACCAACTAAAGTGTGTGAAAC
TGATTTGAAAAAAAGTTATAAAATACATGTTTTAGGACAGTTGGGAAATTTGAATATGACTGGT
TATTAGATGGTATTAGGGAATTTTTGTTGATTTTCTTACCTGTGACGGTGGTGGTAGTTTGAAG
AATATTCTTAATCTTAAGGGATGCATGTTGAAGTATTTGGAATGAAGTGTTCTGATGTTTACAA
CTTTCAAAAAAATGATTTTAAATATGTATTGAGAGATCAGGCAAACATAGCAAAATGTTCATTG
TTGAGTCCACATGGAAAATACGGGTATTCAATGTGCCATACTTTCAACTCTTCTGTACTCTGAT
ATTTTCAAAATAAAACATTTGAGGGGAAATTA

hide sequence

RefSeq Acc Id:

NM_001351734 ⟹ NP_001338663

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,584,964 - 44,648,471 (+)	NCBI
T2T-CHM13v2.0	3	44,600,686 - 44,664,179 (+)	NCBI

Sequence:

show sequence

AGTTCCTTCTGCGCTTTGTTCAAGATGTGGGTCTGGCGCTTTCGTGACTCAAGACCCTCTTAGG
AACTTCTTCACTGAACTCAAGGAGGAGATCAGGCAAGATCTGTGCTGTGCAGATCCTTTGGATT
GAGGCTGCTGTGCACAGGAATATGGATGATACTCTCCAAGCTGTAAGGAAGAAGTCAAGGATTA
AGGAGACCTGGACTGGAGAGGAGCCTTTTTCAAAAAACAACAATGACAAGAGAAAATGTAGCCC
ACAATGCTCTGAGACAAGAGGGCCTTGTGAAGGGGAAGGATGATACCTGGAAATGGGGAACCAG
CTTCCAAGGAAGTAGCTCCTCTGTTTGGGAGACCTCCCACCTACACTTTAGACAATTACGTTAC
CATGAGACATCTGGACCCCAGGAAGCCCTGAGCCGGCTCAGGGAACTCTGTCGCCGGTGGCTGA
GACCAGAAGCACGCACCAAGGCACAGATCCTGGAGCTGCTGGTGCTGGAGCAGTTTCTGAGCAT
CCTGCCTGGGGAGATTCGGACCTGGGTACAGCTCCATCACCCTGGAAGTGGCGAGGAGGCTGTG
GCCCTGGTAGAGGAGCTGCAGAAAGACCTTGATGGACCAGCAATACAAGTTCCAGTCCTTGTCA
AGGATCAGGACACTCTCCAGAAGGTGGTGAGTGCCCCAGGAACAACACTTCCTCCTGTACTTCC
TGGCAGCCACATAGCAGCTGAAATTTGCCCGCATCCTCCTACTGACCTAGTGGCATTCAACCTC
CAGGATCCTCAGCATGATTCTCCTGCCCCTGAAGCTTCTGCCCTTTCCCAGGAAGAGAACCCAA
GAAATCAATTAATGGCACTTATGCTCCTAACAGCCCAGCCCCAGGAGTTGGTGATGTTCGAGGA
GGTGTCAGTATGCTTCACTTCAGAGGAATGGGCATGTCTGGGCCCAATCCAGAGGGCCTTGTAC
TGGGATGTGATGCTGGAGAATTATGGAAATGTGACCTCCCTAGGTTACAGGAAATACAGGAGGC
AGAGGAACAAATAAAAGACACCACGAGAAACAGACACATCCAGAACGTGGAATATTGCATAAGA
AAGCTGCCCTGGATTCTTCAAAATATTATTATGATGAAAAAGAGAGGGGAGTGAAAATTGTTCA
AGCTGTCTTGAGTCTGCTGTGAGTTTATTATACCATTCTCTGCTTTTGTGTATGTATGAAAATT
TCGATATGAAAGGTATAAAACATGGATGAGGAGGCTTGTTTTTAAAAGATAATACTAGAGAGCC
GTTAGGTACTAAGAACCAGAAATAGACTCACATAAATGGCCAATTGATTTTTGACAGGGGCAAA
AGCAATTCAATGGAGGAGGGATCGCCTTTTCAGCAAATACTGTTGGAGTAATTGGATATCCATA
GGCAGTAAACCAACAACTTCAGGACCTAGGACTGAGCTAAGAAGGCTCAGATGACTCAAAAGCA
TGCTCCTTAGAAGGAAAAAAAATGTTAAATTGGACTTCATCAAAATTAAGATAATTTACCCTGT
AAGAGACCTTTTTACAAAGATGATATTACAGGTTGGGAAAAAATATTTGCAAATCATATCCAAC
AAGGGATTTGTATGTAAACTACATAAAGAACTTTCCAAATTTAACAGTAATAAGTAAATACAAT
TAGAAAATAAGCAAAAGACAGACATTTCACTGAAGTATAGATAGCAAATAAGCAAATGAAAAGA
TGTTCAACATCATTAGGCATGAGGGAAATGCAGAGTAAAATCGTGAGATATCACCTATCAGAAT
AGCTTAACTTTTTTTTTTTAATGGTGGTAACTGCTGGCAAGGATGAAGAGAAACAGGATCTCAT
ACATTGCTGGGAATGTAAAATGGTACAGCCACTCTGGAATATAATTTGGCAGTTTCTTGTAAAA
CCACACATGTATATGTCATGCTTCAGGAATTGCACTTCTGAGCATTTATCCCAGAGAAATGAAA
ACTTGCGTTCACACAAAAACCTGTATACGAATGTTCATAGCAGCTTTATTTGTAATGGTCGAAA
CCTGTAGGCAACCCATATATCCTTCCTTAGGTGGTTAAAACAAATTGTGGTTTATGTATTACCA
TGGAATACTTGTTACTCTGCAATAAAATTGACTTATTGATATCCATAACAACTCAAATAAATTT
CAAGGGAATTAATGCTGAGTGAAAATAATCACAAAAGGCCATATTCTGTATGAAAATATTCATA
TAACATTCTCAAAATGATAAAACTATAGAGATGAAAAATGGATTAATGGTTGCCAAAGGTTAGG
GATGGTGGGAGGAAAAATGGGGAGAGGGTTGGATGGAACTATTAAAAGGTAGCACCAGAAAGGT
CTTTGTGGTGATGGAACACTTGTGTATCTTGATTGCAGTGGTGGTTACACAAATCTATAGGTGC
TATACCTATACACACATACTGTACCAATGTTGATTTCCTTTTTCATTTTATGTAAGATGTAACC
ATGAGGGGAAAGTGGGTGAAGGGTGCTATCTTTGCAACTTCCTGTGATTCTATCATTTCAAAAT
AAAAAGTAAAAACCAACAATGGCAACGAAAACCCAAAACTAAAGAGCTGTAACCAACTAAAGTG
TGTGAAACTGATTTGAAAAAAAGTTATAAAATACATGTTTTAGGACAGTTGGGAAATTTGAATA
TGACTGGTTATTAGATGGTATTAGGGAATTTTTGTTGATTTTCTTACCTGTGACGGTGGTGGTA
GTTTGAAGAATATTCTTAATCTTAAGGGATGCATGTTGAAGTATTTGGAATGAAGTGTTCTGAT
GTTTACAACTTTCAAAAAAATGATTTTAAATATGTATTGAGAGATCAGGCAAACATAGCAAAAT
GTTCATTGTTGAGTCCACATGGAAAATACGGGTATTCAATGTGCCATACTTTCAACTCTTCTGT
ACTCTGATATTTTCAAAATAAAACATTTGAGGGGAAATTA

hide sequence

RefSeq Acc Id:

NM_001351735 ⟹ NP_001338664

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,584,964 - 44,648,471 (+)	NCBI
T2T-CHM13v2.0	3	44,600,686 - 44,664,179 (+)	NCBI

Sequence:

show sequence

AGTTCCTTCTGCGCTTTGTTCAAGATGTGGGTCTGGCGCTTTCGTGACTCAAGACCCTCTTAGG
AACTTCTTCACTGAACTCAAGGAGGAGATCAGGCAAGATCTGTGCTGTGCAGATCCTTTGGATT
GAGGCTGCTGTGCACAGGAATATGGGTCTTGTAGATGATACTCTCCAAGCTGTAAGGAAGAAGT
CAAGGATTAAGGAGACCTGGACTGGAGAGGAGCCTTTTTCAAAAAACAACAATGACAAGAGAAA
ATGTAGCCCACAATGCTCTGAGACAAGAGGGCCTTGTGAAGGGGAAGGATGATACCTGGAAATG
GGGAACCAGCTTCCAAGGAAGTAGCTCCTCTGTTTGGGAGACCTCCCACCTACACTTTAGACAA
TTACGTTACCATGAGACATCTGGACCCCAGGAAGCCCTGAGCCGGCTCAGGGAACTCTGTCGCC
GGTGGCTGAGACCAGAAGCACGCACCAAGGCACAGATCCTGGAGCTGCTGGTGCTGGAGCAGTT
TCTGAGCATCCTGCCTGGGGAGATTCGGACCTGGGTACAGCTCCATCACCCTGGAAGTGGCGAG
GAGGCTGTGGCCCTGGTAGAGGAGCTGCAGAAAGACCTTGATGGACCAGCAATACAAGTTCCAG
TCCTTGTCAAGGATCAGGACACTCTCCAGAAGGTGGTGAGTGCCCCAGGAACAACACTTCCTCC
TGTACTTCCTGGCAGCCACATAGCAGCTGAAATTTGCCCGCATCCTCCTACTGACCTAGTGGCA
TTCAACCTCCAGGATCCTCAGCATGATTCTCCTGCCCCTGAAGCTTCTGCCCTTTCCCAGGAAG
AGAACCCAAGAAATCAATTAATGGCACTTATGCTCCTAACAGCCCAGCCCCAGGAGTTGGTGAT
GTTCGAGGAGGTGTCAGTATGCTTCACTTCAGAGGAATGGGCATGTCTGGGCCCAATCCAGAGG
GCCTTGTACTGGGATGTGATGCTGGAGAATTATGGAAATGTGACCTCCCTAGGTTACAGGAAAT
ACAGGAGGCAGAGGAACAAATAAAAGACACCACGAGAAACAGACACATCCAGAACGTGGAATAT
TGCATAAGAAAGCTGCCCTGGATTCTTCAAAATATTATTATGATGAAAAAGAGAGGGGAGTGAA
AATTGTTCAAGCTGTCTTGAGTCTGCTGTGAGTTTATTATACCATTCTCTGCTTTTGTGTATGT
ATGAAAATTTCGATATGAAAGGTATAAAACATGGATGAGGAGGCTTGTTTTTAAAAGATAATAC
TAGAGAGCCGTTAGGTACTAAGAACCAGAAATAGACTCACATAAATGGCCAATTGATTTTTGAC
AGGGGCAAAAGCAATTCAATGGAGGAGGGATCGCCTTTTCAGCAAATACTGTTGGAGTAATTGG
ATATCCATAGGCAGTAAACCAACAACTTCAGGACCTAGGACTGAGCTAAGAAGGCTCAGATGAC
TCAAAAGCATGCTCCTTAGAAGGAAAAAAAATGTTAAATTGGACTTCATCAAAATTAAGATAAT
TTACCCTGTAAGAGACCTTTTTACAAAGATGATATTACAGGTTGGGAAAAAATATTTGCAAATC
ATATCCAACAAGGGATTTGTATGTAAACTACATAAAGAACTTTCCAAATTTAACAGTAATAAGT
AAATACAATTAGAAAATAAGCAAAAGACAGACATTTCACTGAAGTATAGATAGCAAATAAGCAA
ATGAAAAGATGTTCAACATCATTAGGCATGAGGGAAATGCAGAGTAAAATCGTGAGATATCACC
TATCAGAATAGCTTAACTTTTTTTTTTTAATGGTGGTAACTGCTGGCAAGGATGAAGAGAAACA
GGATCTCATACATTGCTGGGAATGTAAAATGGTACAGCCACTCTGGAATATAATTTGGCAGTTT
CTTGTAAAACCACACATGTATATGTCATGCTTCAGGAATTGCACTTCTGAGCATTTATCCCAGA
GAAATGAAAACTTGCGTTCACACAAAAACCTGTATACGAATGTTCATAGCAGCTTTATTTGTAA
TGGTCGAAACCTGTAGGCAACCCATATATCCTTCCTTAGGTGGTTAAAACAAATTGTGGTTTAT
GTATTACCATGGAATACTTGTTACTCTGCAATAAAATTGACTTATTGATATCCATAACAACTCA
AATAAATTTCAAGGGAATTAATGCTGAGTGAAAATAATCACAAAAGGCCATATTCTGTATGAAA
ATATTCATATAACATTCTCAAAATGATAAAACTATAGAGATGAAAAATGGATTAATGGTTGCCA
AAGGTTAGGGATGGTGGGAGGAAAAATGGGGAGAGGGTTGGATGGAACTATTAAAAGGTAGCAC
CAGAAAGGTCTTTGTGGTGATGGAACACTTGTGTATCTTGATTGCAGTGGTGGTTACACAAATC
TATAGGTGCTATACCTATACACACATACTGTACCAATGTTGATTTCCTTTTTCATTTTATGTAA
GATGTAACCATGAGGGGAAAGTGGGTGAAGGGTGCTATCTTTGCAACTTCCTGTGATTCTATCA
TTTCAAAATAAAAAGTAAAAACCAACAATGGCAACGAAAACCCAAAACTAAAGAGCTGTAACCA
ACTAAAGTGTGTGAAACTGATTTGAAAAAAAGTTATAAAATACATGTTTTAGGACAGTTGGGAA
ATTTGAATATGACTGGTTATTAGATGGTATTAGGGAATTTTTGTTGATTTTCTTACCTGTGACG
GTGGTGGTAGTTTGAAGAATATTCTTAATCTTAAGGGATGCATGTTGAAGTATTTGGAATGAAG
TGTTCTGATGTTTACAACTTTCAAAAAAATGATTTTAAATATGTATTGAGAGATCAGGCAAACA
TAGCAAAATGTTCATTGTTGAGTCCACATGGAAAATACGGGTATTCAATGTGCCATACTTTCAA
CTCTTCTGTACTCTGATATTTTCAAAATAAAACATTTGAGGGGAAATTA

hide sequence

RefSeq Acc Id:

NR_147691

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,584,964 - 44,648,471 (+)	NCBI
T2T-CHM13v2.0	3	44,600,686 - 44,664,179 (+)	NCBI

Sequence:

show sequence

AGTTCCTTCTGCGCTTTGTTCAAGATGTGGGTCTGGCGCTTTCGTGACTCAAGACCCTCTTAGG
AACTTCTTCACTGAACTCAAGGAGGAGATCAGGCAAGATCTGTGCTGTGCAGATCCTTTGGATT
GAGGCTGCTGTGCACAGGAATATGGATGATACTCTCCAAGCTGTAAGGAAGAAGTCAAGGATTA
AGGAGACCTGGACTGGAGAGGAGCCTTTTTCAAAAAACAACAATGACAAGAGAAAATGTAGCCC
ACAATGCTCTGAGACAAGAGGGCCTTGTGAAGGGGAAGGATGATACCTGGAAATGGGGAACCAG
CTTCCAAGGAAGTAGCTCCTCTGTTTGGGAGACCTCCCACCTACACTTTAGACAATTACGTTAC
CATGAGACATCTGGACCCCAGGAAGCCCTGAGCCGGCTCAGGGAACTCTGTCGCCGGTGGCTGA
GACCAGAAGCACGCACCAAGGCACAGATCCTGGAGCTGCTGGTGCTGGAGCAGTTTCTGAGCAT
CCTGCCTGGGGAGATTCGGACCTGGGTACAGCTCCATCACCCTGGAAGTGGCGAGGAGGCTGTG
GCCCTGGTAGAGGAGCTGCAGAAAGACCTTGATGGACCAGCAATACAAGTCTGGCTTCTGTTCC
CACCGTTGTGTACAGTCTCCTCTGGGAGAGGTCACCAGTGCCATGAGTGGGGCTCGAGGGCAGC
TCCATTGTTCTCAATGCAAAGCTTTACTGCTGTTTTGATGCTCCATACTTGAGGTTCCAGTCCT
TGTCAAGGATCAGGACACTCTCCAGAAGGTGGTGAGTGCCCCAGGAACAACACTTCCTCCTGTA
CTTCCTGGCAGCCACATAGCAGCTGAAATTTGCCCGCATCCTCCTACTGACCTAGTGGCATTCA
ACCTCCAGGATCCTCAGCATGATTCTCCTGCCCCTGAAGCTTCTGCCCTTTCCCAGGAAGAGAA
CCCAAGAAATCAATTAATGGCACTTATGCTCCTAACAGCCCAGCCCCAGGAGTTGGTGATGTTC
GAGGAGGTGTCAGTATGCTTCACTTCAGAGGAATGGGCATGTCTGGGCCCAATCCAGAGGGCCT
TGTACTGGGATGTGATGCTGGAGAATTATGGAAATGTGACCTCCCTAGGTTACAGGAAATACAG
GAGGCAGAGGAACAAATAAAAGACACCACGAGAAACAGACACATCCAGAACGTGGAATATTGCA
TAAGAAAGCTGCCCTGGATTCTTCAAAATATTATTATGATGAAAAAGAGAGGGGAGTGAAAATT
GTTCAAGCTGTCTTGAGTCTGCTGTGAGTTTATTATACCATTCTCTGCTTTTGTGTATGTATGA
AAATTTCGATATGAAAGGTATAAAACATGGATGAGGAGGCTTGTTTTTAAAAGATAATACTAGA
GAGCCGTTAGGTACTAAGAACCAGAAATAGACTCACATAAATGGCCAATTGATTTTTGACAGGG
GCAAAAGCAATTCAATGGAGGAGGGATCGCCTTTTCAGCAAATACTGTTGGAGTAATTGGATAT
CCATAGGCAGTAAACCAACAACTTCAGGACCTAGGACTGAGCTAAGAAGGCTCAGATGACTCAA
AAGCATGCTCCTTAGAAGGAAAAAAAATGTTAAATTGGACTTCATCAAAATTAAGATAATTTAC
CCTGTAAGAGACCTTTTTACAAAGATGATATTACAGGTTGGGAAAAAATATTTGCAAATCATAT
CCAACAAGGGATTTGTATGTAAACTACATAAAGAACTTTCCAAATTTAACAGTAATAAGTAAAT
ACAATTAGAAAATAAGCAAAAGACAGACATTTCACTGAAGTATAGATAGCAAATAAGCAAATGA
AAAGATGTTCAACATCATTAGGCATGAGGGAAATGCAGAGTAAAATCGTGAGATATCACCTATC
AGAATAGCTTAACTTTTTTTTTTTAATGGTGGTAACTGCTGGCAAGGATGAAGAGAAACAGGAT
CTCATACATTGCTGGGAATGTAAAATGGTACAGCCACTCTGGAATATAATTTGGCAGTTTCTTG
TAAAACCACACATGTATATGTCATGCTTCAGGAATTGCACTTCTGAGCATTTATCCCAGAGAAA
TGAAAACTTGCGTTCACACAAAAACCTGTATACGAATGTTCATAGCAGCTTTATTTGTAATGGT
CGAAACCTGTAGGCAACCCATATATCCTTCCTTAGGTGGTTAAAACAAATTGTGGTTTATGTAT
TACCATGGAATACTTGTTACTCTGCAATAAAATTGACTTATTGATATCCATAACAACTCAAATA
AATTTCAAGGGAATTAATGCTGAGTGAAAATAATCACAAAAGGCCATATTCTGTATGAAAATAT
TCATATAACATTCTCAAAATGATAAAACTATAGAGATGAAAAATGGATTAATGGTTGCCAAAGG
TTAGGGATGGTGGGAGGAAAAATGGGGAGAGGGTTGGATGGAACTATTAAAAGGTAGCACCAGA
AAGGTCTTTGTGGTGATGGAACACTTGTGTATCTTGATTGCAGTGGTGGTTACACAAATCTATA
GGTGCTATACCTATACACACATACTGTACCAATGTTGATTTCCTTTTTCATTTTATGTAAGATG
TAACCATGAGGGGAAAGTGGGTGAAGGGTGCTATCTTTGCAACTTCCTGTGATTCTATCATTTC
AAAATAAAAAGTAAAAACCAACAATGGCAACGAAAACCCAAAACTAAAGAGCTGTAACCAACTA
AAGTGTGTGAAACTGATTTGAAAAAAAGTTATAAAATACATGTTTTAGGACAGTTGGGAAATTT
GAATATGACTGGTTATTAGATGGTATTAGGGAATTTTTGTTGATTTTCTTACCTGTGACGGTGG
TGGTAGTTTGAAGAATATTCTTAATCTTAAGGGATGCATGTTGAAGTATTTGGAATGAAGTGTT
CTGATGTTTACAACTTTCAAAAAAATGATTTTAAATATGTATTGAGAGATCAGGCAAACATAGC
AAAATGTTCATTGTTGAGTCCACATGGAAAATACGGGTATTCAATGTGCCATACTTTCAACTCT
TCTGTACTCTGATATTTTCAAAATAAAACATTTGAGGGGAAATTA

hide sequence

RefSeq Acc Id:

NR_147692

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,584,964 - 44,648,471 (+)	NCBI
T2T-CHM13v2.0	3	44,600,686 - 44,664,179 (+)	NCBI

Sequence:

show sequence

AGTTCCTTCTGCGCTTTGTTCAAGATGTGGGTCTGGCGCTTTCGTGACTCAAGACCCTCTTAGG
AACTTCTTCACTGAACTCAAGGAGGAGATCAGGCAAGATCTGTGCTGTGCAGATCCTTTGGATT
GAGGCTGCTGTGCACAGGAATATGGATGATACTCTCCAAGCTGTAAGGAAGAAGTCAAGGATTA
AGGAGACCTGGACTGGAGAGGAGCCTTTTTCAAAAAACAACAATGACAAGAGAAAATGTAGCCC
ACAATGCTCTGAGACAAGAGGGCCTTGTGAAGGGGAAGGATGATACCTGGAAATGGGGAACCAG
CTTCCAAGGAAGTAGCTCCTCTGTTTGGGAGACCTCCCACCTACACTTTAGACAATTACGTTAC
CATGAGACATCTGGACCCCAGGAAGCCCTGAGCCGGCTCAGGGAACTCTGTCGCCGGTGGCTGA
GACCAGAAGCACGCACCAAGGCACAGATCCTGGAGCTGCTGGTGCTGGAGCAGTTTCTGAGCAT
CCTGCCTGGGGAGATTCGGACCTGGGTACAGCTCCATCACCCTGGAAGTGGCGAGGAGGCTGTG
GCCCTGGTAGAGGAGCTGCAGAAAGACCTTGATGGACCAGCAATACAAGTCTGGCTTCTGTTCC
CACCGTTGTGTACAGTCTCCTCTGGGAGAGGTCACCAGTGCCATGAGTGGGGCTCGAGGGCAGC
TCCATTGTTCTCAATGCAAAGCTTTACTGCTGTTTTGATGCTCCATACTTGAGGTTCCAGTCCT
TGTCAAGGATCAGGACACTCTCCAGAAGGTGGTGAGTGCCCCAGGAACAACACTTCCTCCTGTA
CTTCCTGGCAGCCACATAGCAGCTGAAATTTGCCCGCATCCTCCTACTGACCTAGTGGCATTCA
ACCTCCAGGATCCTCAGCATGATTCTCCTGCCCCTGAAGCTTCTGCCCTTTCCCAGGAAGAGAA
CCCAAGAAATCAATTAATGGCACTTATGCTCCTAACAGCCCAGCCCCAGGAGTTGGTGATGTTC
GAGGAGGTGTCAGTATGCTTCACTTCAGAGGAATGGGCATGTCTGGGCCCAATCCAGAGGGCCT
TGTACTGGGATGTGATGCTGGAGAATTATGGAAATGTGACCTCCCTAGAATGGGAGACCATGAC
CGAGAATGAGGAGGTGACATCAAAGCCAAGTAGTTCTCAAAGAGCAGACTCTCATAAAGGAACA
TCAAAAAGACTTCAAGGAAGTGTTCCCCAGGTCCTTGATTTTGAAGAAGAGTGTGAATGGCAAG
TTTTGGCAAGTCAGTGGGGAAATGAAACAGATGAAAGGGCAGATACAGTGAAGAAAGTTTCCCT
TTGTGAACGAGACAAGAAGAAAAGGACTCCACCAGAGAAACAAGGCCAAAAGTGGAAGGAATTA
GGAGACAGCTTGACTTTCGGTTCAGCTATTTCTGAAAGTTTAATAGGTACTGAAGGAAAGAAGT
TTTATAAATGTGATATGTGTTGTAAACATTTTAATAAAATCTCCCATCTTATAAACCATCGGAG
AATCCACACTGGTGAGAAACCTCATAAATGTAAGGAATGTGGAAAAGGCTTTATTCAGCGTTCG
AGCCTTCTAATGCATTTACGGAACCATTCAGGGGAGAAACCTTATAAATGTAATGAATGTGGGA
AAGCATTTTCTCAAAGTGCTTACCTTCTAAACCATCAGAGGATCCACACTGGGGAGAAACCTTA
TAAGTGTAAGGAGTGTGGAAAGGGCTTCTATAGGCACTCAGGCCTAATTATACATCTAAGGCGC
CATTCAGGGGAGAGACCTTATAAGTGTAATGAATGTGGGAAAGTCTTCTCTCAGAATGCTTACC
TCATTGACCATCAGAGGCTCCACAAAGGGGAAGAACCTTATAAATGTAATAAGTGTCAGAAAGC
TTTCATTCTGAAGAAGAGCCTCATTCTGCACCAGAGAATCCACTCTGGGGAAAAACCCTATAAA
TGTGATGAATGTGGAAAGACCTTTGCTCAGACCACTTATCTTATTGACCATCAGCGACTCCACA
GTGCAGAGAACCCTTACAAGTGTAAAGAATGTGGAAAAGTTTTCATTCGAAGCAAAAGCCTCCT
CTTACATCAGAGAGTCCACACAGAAAAGAAAACCTTTGGTTGTAAAAAGTGTGGGAAGATTTTC
AGTTCTAAGTCAAACTTCATTGACCATAAGAGGATGCACAGCAGAGAGAAACCTTACAAATGCA
CTGAATGTGGGAAAGCCTTTACTCAAAGTGCTTACCTTTTTGACCACCAGAGACTCCACAATGG
GGAGAAGCCCTATGAATGTAATGAATGTGGGAAAGTTTTTATTCTGAAGAAGAGCCTCATTTTA
CATCAAAGGTTCCACACTGGAGAGAATCTCTATGAATGTAAAGATTGTGGTAAGGTCTTCGGTT
CAAACAGAAACCTCATTGACCATGAGAGACTCCACAATGGGGAGAAGCCATATGAATGTCGAGA
GTGTGGGAAAACCTTTATTATGAGCAAAAGTTTTATGGTCCATCAGAAACTCCATACACAAGAG
AAAGCCTACAAATGTGAGGATTGTGGGAAGGCTTTCAGTTACAATTCAAGCCTGCTTGTACATC
GGAGAATCCACACCGGAGAAAAACCCTTTGAATGCAGTGAGTGTGGAAGAGCTTTCAGTTCAAA
CAGAAACCTCATTGAGCATAAGAGAATCCACAGTGGTGAGAAACCCTATGAGTGTGATGAGTGT
GGCAAATGCTTCATTCTGAAGAAAAGCCTCATTGGACATCAGAGAATTCACACGAGGGAAAAAT
CTTATAAATGCAATGACTGTGGGAAGGTCTTCAGTTACCGCTCAAACCTTATAGCCCATCAGAG
GATCCATACTGGTGAGAAGCCCTATGCGTGTAGTGAGTGTGGAAAAGGTTTTACGTACAACAGA
AACCTGATTGAACATCAAAGAATTCACAGTGGAGAAAAAACCTACGAATGTCATGTATGTAGGA
AAGTCCTTACCTCTAGTAGAAATCTTATGGTACATCAAAGAATCCATACTGGAGAGAAACCTTA
TAAATGTAATGAGTGTGGAAAAGACTTTAGTCAGAATAAAAACCTTGTTGTACATCAGAGAATG
CACACTGGGGAAAAACCTTATGAGTGTGACAAGTGTAGGAAATCCTTTACTTCTAAGAGGAATT
TAGTTGGCCACCAGAGAATTCACACAGGGGAGAAACCCTATGGGTGTAATGATTGTAGTAAAGT
TTTTAGGCAAAGAAAAAACCTTACTGTACATCAGAAAATCCACACAGATGAAAAACCTTGTGAA
TGTGATGTGTCTGAAAAAGAATTCTCTCAGACTTCCAACCTTCATCTTCAACAGAAAATCCATA
CCATTGAGGAATTCTCTTGGCTACAAAACACCAATGAGTCCAAGATTGAGATTCAGAAAATCTA
GTGTCATATGTAAAATGGAATAGAATCCCTGCCTACTTAAGTAACTGTTGGACAAATGATATAT
ATTTCTTCTAAGGAAAAAGTTTATTATTTACTCTTTACTAGACAAATGAGTAGCATATAGAAGA
AAGTTAATAGGCCGGGCTTGGTGGCTCATGCCTGTAATCCCAGCACTTTGAGAGGCCGAAGCGA
GTGGATCACCTGAGGTCAGGATTTTGAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTAC
TAAAATACAAAAATTATCCGGGCATGGGGGCACACACCGGTAATCCCAGCTACTCAGGAGGCTG
AGACAGGAGAGTCGCTTGAACCTGGGAGGGCGGAGGTTGCAGTGAGCCAGGATCGCGCCATTGC
ACTCCAGCCTGGGCAACAAGAGCGAAACTCTTGTCTGAAAAAATAAAGTTCATCCCAACTTTCA
AGTCTACAAAAACATAATCCAAATCTAATAACATAGTTGTAAATGAGAGCAACAATAAAAAGTA
GACATGGGCTGGGTGCAGTGGCTCACTCCTGTAGTCCCAGGACTTTGGGAGGCCGAGGTGGGAA
GATCCCTTGAGCCCAGGAGTTCGAGACAAGCCTGGGTAACACGGGGAGACCCGTCTTTAGTAAA
TAAAAATAAATTTATTAATAAAACTAAAAATTTAATAATAAAAAGTGGACATTGTTTTTTAAAA
TGTGTATAGTATGCATTTTAAAGATAGTGTCACTGCTGTGGAAAACCTGAACAGACAGTATGAT
CCAGAATGTCAGGTGTGGAGTTGGGCGGACAAGAGTCTGCTGATGAGGACAACCTAAAAGAGCA
CTGGATTTGGAATCAGAAGACCTACCTTTGATTCCTGGCTTTCCCTTAATGGCCATGTGATGTT
ATTAAGTCAGCCTCTAAAGCTTTAGTTTCCTGTCAGTCAAATGTTGACATGATACCTACCTCAC
AGGGTTGTTGTGAGGGTTAAGTGAAAGGATCTTTGTGAAAGTACTTTTTGAAATCATTCAGTTG
TCAATAAAGTTGGATAAAAGAGGTTATGGTAAAAGTTTAGAACATGGGATCATGTAAGTTTGTG
TATTAAGTCAATATTAGAATGAGGGGGATTCCAGGAACCTAAAAGATACTCATTTTCATAAGAG
GAAGTATGGTGAATAGCTAACTGGAATTTAGTGTTCTAAGAATAATTTTGTTAAATTTACCTTT
AAAAATATCTGAGGGAGTTACTAGATTATATATCTAGTTTATGTATATGGAAAAAAATGTTATG
GCCAGCCATTAACAGTGATGCCAAGGAAAACAATTTATTTCCCAGCTTTTGAATTTGAAACTTA
ACAGATGGAGAGTGTCAAAATGGAAGGGCAGTGGTACCCTGCTTTCCCTATTCAGAGGGAAAAA
AATCCTTGACCCGCAGTTGAGCTGATGATCCCTGCCACAGTCATTGTGAATTCTAATCAATATT
TCATCATTGCTGTCAAATGATAGCCTGTTACTAATGAAACAACATTCTGTCCCAGCACTAAATT
TACTGGGACATAAATTTTTCACATGGAGCCAAGCTCTTCACTGATTAAGCCAGTGCAGAATCCA
CTTGTGGGCAGTCAGTGCCCATTACCCCCTGTGAACCATTCTGTGCCCTTGAGTACATTTGTGG
GTTTAACTCAGTCTATATTCTTAAGTTGGTAATTTTTATGTTGTAATTCTCAAAGTTCTGTTTC
TGTAGCTGGACTATGAATAATACCTGAATATGAAGATTGTGTTTTTTAATAATGTCAAAGTGGT
GTGTTGATTATCATAAATGTTATTAATTCAACCCCACAGTTTCTTGGGGGCTGGTTCCTCATTA
GAGTGAAAGGTAGCCAAGAGTGAAAACTGGAAGGGGCCTAAGGCTTAAAGTCTTAAGACCTGGA
TGTGGTTCAGGTTTTGCCATCTGCCTCAGAAAAAATCTCTTCAGTTCTTGGAGCCTTGAATTCC
TCATCTGTTAAACAGGAGGAAGAATATCTACCTCACAAAGTTCTTATGAGATAATGAATATAAA
AATGTTTCATCCAGGTTGTTGAATCATCCCAGCTTATATAATAATTACAAAGGACATATGTACT
TTAACAATGGAGAATGCTGTGATTTACCTCTTCACCGAGTAACAAAATGTCACATTGCTTAGAT
TGAGACAGCCCACATAATGTGCCACCTTCTGTGATGTAATAAGCTGAAAAATGTTCAACCTGAA
TTTAATCAAGCTTCTTGGACCTCATTGCCAGGTTACAGGAAATACAGGAGGCAGAGGAACAAAT
AAAAGACACCACGAGAAACAGACACATCCAGAACGTGGAATATTGCATAAGAAAGCTGCCCTGG
ATTCTTCAAAATATTATTATGATGAAAAAGAGAGGGGAGTGAAAATTGTTCAAGCTGTCTTGAG
TCTGCTGTGAGTTTATTATACCATTCTCTGCTTTTGTGTATGTATGAAAATTTCGATATGAAAG
GTATAAAACATGGATGAGGAGGCTTGTTTTTAAAAGATAATACTAGAGAGCCGTTAGGTACTAA
GAACCAGAAATAGACTCACATAAATGGCCAATTGATTTTTGACAGGGGCAAAAGCAATTCAATG
GAGGAGGGATCGCCTTTTCAGCAAATACTGTTGGAGTAATTGGATATCCATAGGCAGTAAACCA
ACAACTTCAGGACCTAGGACTGAGCTAAGAAGGCTCAGATGACTCAAAAGCATGCTCCTTAGAA
GGAAAAAAAATGTTAAATTGGACTTCATCAAAATTAAGATAATTTACCCTGTAAGAGACCTTTT
TACAAAGATGATATTACAGGTTGGGAAAAAATATTTGCAAATCATATCCAACAAGGGATTTGTA
TGTAAACTACATAAAGAACTTTCCAAATTTAACAGTAATAAGTAAATACAATTAGAAAATAAGC
AAAAGACAGACATTTCACTGAAGTATAGATAGCAAATAAGCAAATGAAAAGATGTTCAACATCA
TTAGGCATGAGGGAAATGCAGAGTAAAATCGTGAGATATCACCTATCAGAATAGCTTAACTTTT
TTTTTTTAATGGTGGTAACTGCTGGCAAGGATGAAGAGAAACAGGATCTCATACATTGCTGGGA
ATGTAAAATGGTACAGCCACTCTGGAATATAATTTGGCAGTTTCTTGTAAAACCACACATGTAT
ATGTCATGCTTCAGGAATTGCACTTCTGAGCATTTATCCCAGAGAAATGAAAACTTGCGTTCAC
ACAAAAACCTGTATACGAATGTTCATAGCAGCTTTATTTGTAATGGTCGAAACCTGTAGGCAAC
CCATATATCCTTCCTTAGGTGGTTAAAACAAATTGTGGTTTATGTATTACCATGGAATACTTGT
TACTCTGCAATAAAATTGACTTATTGATATCCATAACAACTCAAATAAATTTCAAGGGAATTAA
TGCTGAGTGAAAATAATCACAAAAGGCCATATTCTGTATGAAAATATTCATATAACATTCTCAA
AATGATAAAACTATAGAGATGAAAAATGGATTAATGGTTGCCAAAGGTTAGGGATGGTGGGAGG
AAAAATGGGGAGAGGGTTGGATGGAACTATTAAAAGGTAGCACCAGAAAGGTCTTTGTGGTGAT
GGAACACTTGTGTATCTTGATTGCAGTGGTGGTTACACAAATCTATAGGTGCTATACCTATACA
CACATACTGTACCAATGTTGATTTCCTTTTTCATTTTATGTAAGATGTAACCATGAGGGGAAAG
TGGGTGAAGGGTGCTATCTTTGCAACTTCCTGTGATTCTATCATTTCAAAATAAAAAGTAAAAA
CCAACAATGGCAACGAAAACCCAAAACTAAAGAGCTGTAACCAACTAAAGTGTGTGAAACTGAT
TTGAAAAAAAGTTATAAAATACATGTTTTAGGACAGTTGGGAAATTTGAATATGACTGGTTATT
AGATGGTATTAGGGAATTTTTGTTGATTTTCTTACCTGTGACGGTGGTGGTAGTTTGAAGAATA
TTCTTAATCTTAAGGGATGCATGTTGAAGTATTTGGAATGAAGTGTTCTGATGTTTACAACTTT
CAAAAAAATGATTTTAAATATGTATTGAGAGATCAGGCAAACATAGCAAAATGTTCATTGTTGA
GTCCACATGGAAAATACGGGTATTCAATGTGCCATACTTTCAACTCTTCTGTACTCTGATATTT
TCAAAATAAAACATTTGAGGGGAAATTA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001338661	(Get FASTA)	NCBI Sequence Viewer
	NP_001338662	(Get FASTA)	NCBI Sequence Viewer
	NP_001338663	(Get FASTA)	NCBI Sequence Viewer
	NP_001338664	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	O14709	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001338662 ⟸ NM_001351733
- Peptide Label:	isoform 1
- UniProtKB:	O14709 (UniProtKB/Swiss-Prot), B2RAH8 (UniProtKB/Swiss-Prot), Q86VG0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTRENVAHNALRQEGLVKGKDDTWKWGTSFQGSSSSVWETSHLHFRQLRYHETSGPQEALSRLR ELCRRWLRPEARTKAQILELLVLEQFLSILPGEIRTWVQLHHPGSGEEAVALVEELQKDLDGPA IQVPVLVKDQDTLQKVVSAPGTTLPPVLPGSHIAAEICPHPPTDLVAFNLQDPQHDSPAPEASA LSQEENPRNQLMALMLLTAQPQELVMFEEVSVCFTSEEWACLGPIQRALYWDVMLENYGNVTSL EWETMTENEEVTSKPSSSQRADSHKGTSKRLQGSVPQVLDFEEECEWQVLASQWGNETDERADT VKKVSLCERDKKKRTPPEKQGQKWKELGDSLTFGSAISESLIGTEGKKFYKCDMCCKHFNKISH LINHRRIHTGEKPHKCKECGKGFIQRSSLLMHLRNHSGEKPYKCNECGKAFSQSAYLLNHQRIH TGEKPYKCKECGKGFYRHSGLIIHLRRHSGERPYKCNECGKVFSQNAYLIDHQRLHKGEEPYKC NKCQKAFILKKSLILHQRIHSGEKPYKCDECGKTFAQTTYLIDHQRLHSAENPYKCKECGKVFI RSKSLLLHQRVHTEKKTFGCKKCGKIFSSKSNFIDHKRMHSREKPYKCTECGKAFTQSAYLFDH QRLHNGEKPYECNECGKVFILKKSLILHQRFHTGENLYECKDCGKVFGSNRNLIDHERLHNGEK PYECRECGKTFIMSKSFMVHQKLHTQEKAYKCEDCGKAFSYNSSLLVHRRIHTGEKPFECSECG RAFSSNRNLIEHKRIHSGEKPYECDECGKCFILKKSLIGHQRIHTREKSYKCNDCGKVFSYRSN LIAHQRIHTGEKPYACSECGKGFTYNRNLIEHQRIHSGEKTYECHVCRKVLTSSRNLMVHQRIH TGEKPYKCNECGKDFSQNKNLVVHQRMHTGEKPYECDKCRKSFTSKRNLVGHQRIHTGEKPYGC NDCSKVFRQRKNLTVHQKIHTDEKPCECDVSEKEFSQTSNLHLQQKIHTIEEFSWLQNTNESKI EIQKI hide sequence

RefSeq Acc Id:

NP_001338664 ⟸ NM_001351735

- Peptide Label:

isoform 2

- Sequence:

show sequence

MTRENVAHNALRQEGLVKGKDDTWKWGTSFQGSSSSVWETSHLHFRQLRYHETSGPQEALSRLR
ELCRRWLRPEARTKAQILELLVLEQFLSILPGEIRTWVQLHHPGSGEEAVALVEELQKDLDGPA
IQVPVLVKDQDTLQKVVSAPGTTLPPVLPGSHIAAEICPHPPTDLVAFNLQDPQHDSPAPEASA
LSQEENPRNQLMALMLLTAQPQELVMFEEVSVCFTSEEWACLGPIQRALYWDVMLENYGNVTSL
GYRKYRRQRNK

hide sequence

RefSeq Acc Id:	NP_001338661 ⟸ NM_001351732
- Peptide Label:	isoform 1
- UniProtKB:	O14709 (UniProtKB/Swiss-Prot), B2RAH8 (UniProtKB/Swiss-Prot), Q86VG0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTRENVAHNALRQEGLVKGKDDTWKWGTSFQGSSSSVWETSHLHFRQLRYHETSGPQEALSRLR ELCRRWLRPEARTKAQILELLVLEQFLSILPGEIRTWVQLHHPGSGEEAVALVEELQKDLDGPA IQVPVLVKDQDTLQKVVSAPGTTLPPVLPGSHIAAEICPHPPTDLVAFNLQDPQHDSPAPEASA LSQEENPRNQLMALMLLTAQPQELVMFEEVSVCFTSEEWACLGPIQRALYWDVMLENYGNVTSL EWETMTENEEVTSKPSSSQRADSHKGTSKRLQGSVPQVLDFEEECEWQVLASQWGNETDERADT VKKVSLCERDKKKRTPPEKQGQKWKELGDSLTFGSAISESLIGTEGKKFYKCDMCCKHFNKISH LINHRRIHTGEKPHKCKECGKGFIQRSSLLMHLRNHSGEKPYKCNECGKAFSQSAYLLNHQRIH TGEKPYKCKECGKGFYRHSGLIIHLRRHSGERPYKCNECGKVFSQNAYLIDHQRLHKGEEPYKC NKCQKAFILKKSLILHQRIHSGEKPYKCDECGKTFAQTTYLIDHQRLHSAENPYKCKECGKVFI RSKSLLLHQRVHTEKKTFGCKKCGKIFSSKSNFIDHKRMHSREKPYKCTECGKAFTQSAYLFDH QRLHNGEKPYECNECGKVFILKKSLILHQRFHTGENLYECKDCGKVFGSNRNLIDHERLHNGEK PYECRECGKTFIMSKSFMVHQKLHTQEKAYKCEDCGKAFSYNSSLLVHRRIHTGEKPFECSECG RAFSSNRNLIEHKRIHSGEKPYECDECGKCFILKKSLIGHQRIHTREKSYKCNDCGKVFSYRSN LIAHQRIHTGEKPYACSECGKGFTYNRNLIEHQRIHSGEKTYECHVCRKVLTSSRNLMVHQRIH TGEKPYKCNECGKDFSQNKNLVVHQRMHTGEKPYECDKCRKSFTSKRNLVGHQRIHTGEKPYGC NDCSKVFRQRKNLTVHQKIHTDEKPCECDVSEKEFSQTSNLHLQQKIHTIEEFSWLQNTNESKI EIQKI hide sequence

RefSeq Acc Id:

NP_001338663 ⟸ NM_001351734

- Peptide Label:

isoform 2

- Sequence:

show sequence

MTRENVAHNALRQEGLVKGKDDTWKWGTSFQGSSSSVWETSHLHFRQLRYHETSGPQEALSRLR
ELCRRWLRPEARTKAQILELLVLEQFLSILPGEIRTWVQLHHPGSGEEAVALVEELQKDLDGPA
IQVPVLVKDQDTLQKVVSAPGTTLPPVLPGSHIAAEICPHPPTDLVAFNLQDPQHDSPAPEASA
LSQEENPRNQLMALMLLTAQPQELVMFEEVSVCFTSEEWACLGPIQRALYWDVMLENYGNVTSL
GYRKYRRQRNK

hide sequence

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-O14709-F1-model_v2	AlphaFold	O14709	1-1029	view protein structure

Additional Information

External Database Links

Database	Acc Id	Source(s)
COSMIC	ZNF660-ZNF197	COSMIC
GTEx	ZNF660-ZNF197	GTEx
Human Proteome Map	ZNF660-ZNF197	Human Proteome Map
NCBI Gene	ZNF660-ZNF197	ENTREZGENE
UniProt	B2RAH8	ENTREZGENE
	O14709	ENTREZGENE
	Q86VG0	ENTREZGENE

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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