ZNF346 (zinc finger protein 346) - Rat Genome Database

Name: ZNF346
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: ZNF346 (zinc finger protein 346) Homo sapiens

Analyze

Symbol:

ZNF346

Name:

zinc finger protein 346

RGD ID:

1317625

HGNC Page

HGNC:16403

Description:

Enables double-stranded RNA binding activity; enzyme binding activity; and miRNA binding activity. Predicted to act upstream of or within positive regulation of apoptotic process. Located in nucleolus and nucleoplasm.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

DKFZp547M223; double-stranded RNA-binding zinc finger protein JAZ; JAZ; just another zinc finger protein; Zfp346

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):	Zfp346 (zinc finger protein 346)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Zfp346 (zinc finger protein 346)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Znf346 (zinc finger protein 346)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	ZNF346 (zinc finger protein 346)	NCBI	Ortholog
Canis lupus familiaris (dog):	ZNF346 (zinc finger protein 346)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Znf346 (zinc finger protein 346)	NCBI	Ortholog
Sus scrofa (pig):	ZNF346 (zinc finger protein 346)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	ZNF346 (zinc finger protein 346)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Znf346 (zinc finger protein 346)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Wasf1 (WASP family member 1)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Zfp346 (zinc finger protein 346)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Zfp346 (zinc finger protein 346)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	znf346 (zinc finger protein 346)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Drosophila melanogaster (fruit fly):	CG1231	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoFinder)
Drosophila melanogaster (fruit fly):	dbf	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PhylomeDB)
Xenopus laevis (African clawed frog):	znf346.S	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	znf346	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|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	5	177,022,696 - 177,081,189 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	5	177,022,696 - 177,081,189 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	5	176,449,697 - 176,508,190 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	5	176,382,303 - 176,426,364 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	5	176,382,302 - 176,426,349	NCBI
Celera	5	172,007,563 - 172,051,635 (-)	NCBI		Celera
Cytogenetic Map	5	q35.2	NCBI
HuRef	5	171,371,845 - 171,415,482 (+)	NCBI		HuRef
CHM1_1	5	175,882,099 - 175,926,642 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	5	177,565,869 - 177,624,397 (+)	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

Chromosome 5, Trisomy 5q (IAGP)

Ehlers-Danlos syndrome dermatosparaxis type (IAGP)

Ehlers-Danlos syndrome spondylodysplastic type 2 (IAGP)

Marfanoid Mental Retardation Syndrome, Autosomal (IAGP)

Sotos syndrome (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(-)-alpha-phellandrene (EXP)

17beta-estradiol (ISO)

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

3,3',5,5'-tetrabromobisphenol A (ISO)

3,4-methylenedioxymethamphetamine (ISO)

aflatoxin B1 (ISO)

alpha-phellandrene (EXP)

antirheumatic drug (EXP)

aristolochic acid A (EXP)

arsane (EXP)

arsenic atom (EXP)

atrazine (EXP)

benzo[a]pyrene (ISO)

benzo[b]fluoranthene (ISO)

bisphenol A (EXP,ISO)

cadmium dichloride (ISO)

cannabidiol (EXP)

carbon nanotube (ISO)

chloroprene (ISO)

choline (ISO)

chrysene (ISO)

dibutyl phthalate (ISO)

diclofenac (ISO)

dorsomorphin (EXP)

enzyme inhibitor (EXP)

folic acid (ISO)

fulvestrant (EXP)

gentamycin (ISO)

inulin (ISO)

isoprenaline (ISO)

ivermectin (EXP)

L-methionine (ISO)

maneb (ISO)

ozone (ISO)

paracetamol (ISO)

paraquat (ISO)

perfluorooctane-1-sulfonic acid (ISO)

SB 431542 (EXP)

Soman (ISO)

T-2 toxin (EXP)

tetraphene (ISO)

titanium dioxide (ISO)

triptonide (ISO)

trovafloxacin (ISO)

valproic acid (EXP,ISO)

vinclozolin (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

positive regulation of apoptotic process (ISO)

Cellular Component

cytoplasm (IEA)

nucleolus (IDA,IEA)

nucleoplasm (IDA)

nucleus (IDA,IEA)

Molecular Function

double-stranded RNA binding (IBA,IDA)

enzyme binding (IPI)

metal ion binding (IEA)

miRNA binding (IDA)

nucleic acid binding (IEA)

protein binding (IPI)

RNA binding (HDA,IEA)

zinc ion binding (IEA)

References

References - curated

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

Additional References at PubMed

PMID:10488071	PMID:11076863	PMID:11230166	PMID:11256614	PMID:12477932	PMID:14702039	PMID:15254228	PMID:15489334	PMID:15489336	PMID:16344560	PMID:16381901	PMID:18029348
PMID:19828471	PMID:20020773	PMID:21145461	PMID:21715977	PMID:21873635	PMID:21903422	PMID:21913182	PMID:21988832	PMID:22681889	PMID:23382074	PMID:24457600	PMID:24521053
PMID:24778252	PMID:25331946	PMID:25416956	PMID:25544563	PMID:25875936	PMID:26186194	PMID:26496610	PMID:28208259	PMID:28431233	PMID:28514442	PMID:28712289	PMID:29229926
PMID:29395067	PMID:29845934	PMID:30196744	PMID:31091453	PMID:31527615	PMID:32203420	PMID:32296183	PMID:32433965	PMID:32707033	PMID:32814053	PMID:33060197	PMID:33301849
PMID:33658012	PMID:33961781	PMID:34079125	PMID:34578187	PMID:34650049	PMID:35013218	PMID:35271311	PMID:35944360	PMID:36232890	PMID:36273042	PMID:36373674	PMID:36537216
PMID:36834567	PMID:36949045

Genomics

Comparative Map Data

ZNF346
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	5	177,022,696 - 177,081,189 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	5	177,022,696 - 177,081,189 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	5	176,449,697 - 176,508,190 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	5	176,382,303 - 176,426,364 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	5	176,382,302 - 176,426,349	NCBI
Celera	5	172,007,563 - 172,051,635 (-)	NCBI		Celera
Cytogenetic Map	5	q35.2	NCBI
HuRef	5	171,371,845 - 171,415,482 (+)	NCBI		HuRef
CHM1_1	5	175,882,099 - 175,926,642 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	5	177,565,869 - 177,624,397 (+)	NCBI		T2T-CHM13v2.0

Zfp346
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	13	55,253,079 - 55,282,884 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	13	55,253,124 - 55,282,638 (+)	Ensembl		GRCm39 Ensembl
GRCm38	13	55,105,271 - 55,135,071 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	13	55,105,311 - 55,134,825 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	13	55,206,670 - 55,236,432 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	13	55,114,933 - 55,144,438 (+)	NCBI		MGSCv36	mm8
Celera	13	56,166,301 - 56,196,016 (+)	NCBI		Celera
Cytogenetic Map	13	B1	NCBI
cM Map	13	29.8	NCBI

Zfp346
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	17	9,498,933 - 9,528,824 (-)	NCBI		GRCr8
mRatBN7.2	17	9,493,787 - 9,523,681 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	17	9,493,803 - 9,523,635 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	17	9,510,640 - 9,541,007 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	17	11,039,927 - 11,069,987 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	17	9,507,045 - 9,537,410 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	17	10,021,596 - 10,061,803 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	17	10,021,420 - 10,061,772 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	17	12,130,909 - 12,168,917 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	17	15,544,785 - 15,575,512 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	17	15,547,045 - 15,575,515 (-)	NCBI
Celera	17	9,571,731 - 9,601,487 (-)	NCBI		Celera
Cytogenetic Map	17	p14	NCBI

Znf346
(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_004955408	29,312,274 - 29,349,316 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955408	29,312,273 - 29,346,983 (+)	NCBI	ChiLan1.0	ChiLan1.0

ZNF346
(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	4	172,104,227 - 172,165,684 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	5	170,243,769 - 170,307,038 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	5	172,321,875 - 172,386,462 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	5	179,390,239 - 179,449,071 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	5	179,390,239 - 179,449,071 (+)	Ensembl	panpan1.1		panPan2

ZNF346
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	4	36,269,126 - 36,303,647 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	4	36,271,853 - 36,303,594 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	4	36,235,147 - 36,269,673 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	4	36,633,379 - 36,667,914 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	4	36,633,413 - 36,667,875 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	4	36,460,298 - 36,494,813 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	4	36,647,499 - 36,682,090 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	4	37,155,749 - 37,190,501 (-)	NCBI		UU_Cfam_GSD_1.0

Znf346
(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_024407213	122,286,077 - 122,338,890 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936597	1,310,999 - 1,366,227 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936597	1,311,007 - 1,363,731 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZNF346
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	2	80,871,595 - 80,895,585 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	2	80,871,576 - 80,895,592 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	82,445,038 - 82,469,063 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ZNF346
(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	23	79,010,203 - 79,072,063 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	23	79,027,548 - 79,070,705 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666075	10,173,143 - 10,236,987 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Znf346
(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_004624733	12,995,358 - 13,068,150 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624733	12,997,728 - 13,057,640 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ZNF346
23 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 5q35.2-35.3(chr5:176132340-177586960)x1	copy number loss	See cases [RCV000050645]	Chr5:176132340..177586960 [GRCh38] Chr5:175559343..177013961 [GRCh37] Chr5:175491949..176946567 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q32-35.3(chr5:149714592-181272151)x3	copy number gain	See cases [RCV000051863]	Chr5:149714592..181272151 [GRCh38] Chr5:149094155..180699152 [GRCh37] Chr5:149074348..180631758 [NCBI36] Chr5:5q32-35.3	pathogenic
GRCh38/hg38 5q33.3-35.3(chr5:160029980-181269805)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051865]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051865]\|See cases [RCV000051865]	Chr5:160029980..181269805 [GRCh38] Chr5:159456987..180696806 [GRCh37] Chr5:159389565..180629412 [NCBI36] Chr5:5q33.3-35.3	pathogenic
GRCh38/hg38 5q34-35.3(chr5:168689326-181269946)x3	copy number gain	See cases [RCV000051866]	Chr5:168689326..181269946 [GRCh38] Chr5:168116331..180696947 [GRCh37] Chr5:168048909..180629553 [NCBI36] Chr5:5q34-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:175851047-178365049)x3	copy number gain	See cases [RCV000051867]	Chr5:175851047..178365049 [GRCh38] Chr5:175278050..177792050 [GRCh37] Chr5:175210656..177724656 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:175889986-180793986)x3	copy number gain	See cases [RCV000051868]	Chr5:175889986..180793986 [GRCh38] Chr5:175316989..180220986 [GRCh37] Chr5:175249595..180153592 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:175007241-179089812)x1	copy number loss	See cases [RCV000052151]	Chr5:175007241..179089812 [GRCh38] Chr5:174434244..178516813 [GRCh37] Chr5:174366850..178449419 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176043476-177995759)x1	copy number loss	See cases [RCV000053127]	Chr5:176043476..177995759 [GRCh38] Chr5:175470479..177422760 [GRCh37] Chr5:175403085..177355366 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176115257-177646633)x1	copy number loss	See cases [RCV000053128]	Chr5:176115257..177646633 [GRCh38] Chr5:175542260..177073634 [GRCh37] Chr5:175474866..177006240 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176152073-177986213)x1	copy number loss	See cases [RCV000053129]	Chr5:176152073..177986213 [GRCh38] Chr5:175579076..177413214 [GRCh37] Chr5:175511682..177345820 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176152073-177646633)x1	copy number loss	See cases [RCV000053131]	Chr5:176152073..177646633 [GRCh38] Chr5:175579076..177073634 [GRCh37] Chr5:175511682..177006240 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176149599-177716401)x3	copy number gain	See cases [RCV000053481]	Chr5:176149599..177716401 [GRCh38] Chr5:175576602..177143402 [GRCh37] Chr5:175509208..177076008 [NCBI36] Chr5:5q35.2-35.3	pathogenic\|uncertain significance
GRCh38/hg38 5q35.2-35.3(chr5:176043476-177452489)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053860]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053860]\|See cases [RCV000053860]	Chr5:176043476..177452489 [GRCh38] Chr5:175470479..176879490 [GRCh37] Chr5:175403085..176812096 [NCBI36] Chr5:5q35.2-35.3	pathogenic\|uncertain significance
GRCh38/hg38 5q33.3-35.3(chr5:156825512-181269805)x3	copy number gain	See cases [RCV000133847]	Chr5:156825512..181269805 [GRCh38] Chr5:156252523..180696806 [GRCh37] Chr5:156185101..180629412 [NCBI36] Chr5:5q33.3-35.3	pathogenic
GRCh38/hg38 5q34-35.3(chr5:164386701-181269805)x3	copy number gain	See cases [RCV000135546]	Chr5:164386701..181269805 [GRCh38] Chr5:163813707..180696806 [GRCh37] Chr5:163746285..180629412 [NCBI36] Chr5:5q34-35.3	pathogenic
GRCh38/hg38 5q35.1-35.3(chr5:169334755-181285301)x3	copy number gain	See cases [RCV000141249]	Chr5:169334755..181285301 [GRCh38] Chr5:168761759..180712302 [GRCh37] Chr5:168694337..180644908 [NCBI36] Chr5:5q35.1-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:175536771-181292788)x1	copy number loss	See cases [RCV000141987]	Chr5:175536771..181292788 [GRCh38] Chr5:174963774..180719789 [GRCh37] Chr5:174896380..180652395 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:175989092-178009412)x1	copy number loss	See cases [RCV000142365]	Chr5:175989092..178009412 [GRCh38] Chr5:175416095..177436413 [GRCh37] Chr5:175348701..177369019 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176132340-177995759)x1	copy number loss	See cases [RCV000142510]	Chr5:176132340..177995759 [GRCh38] Chr5:175559343..177422760 [GRCh37] Chr5:175491949..177355366 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176291838-178662699)x1	copy number loss	See cases [RCV000142047]	Chr5:176291838..178662699 [GRCh38] Chr5:175718841..178089700 [GRCh37] Chr5:175651447..178022306 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176700128-181269805)x1	copy number loss	See cases [RCV000142648]	Chr5:176700128..181269805 [GRCh38] Chr5:176127129..180696806 [GRCh37] Chr5:176059735..180629412 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176517339-177709289)x1	copy number loss	See cases [RCV000142538]	Chr5:176517339..177709289 [GRCh38] Chr5:175944340..177136290 [GRCh37] Chr5:175876946..177068896 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176143674-178009412)x1	copy number loss	See cases [RCV000143463]	Chr5:176143674..178009412 [GRCh38] Chr5:175570677..177436413 [GRCh37] Chr5:175503283..177369019 [NCBI36] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:174397487-180686444)x1	copy number loss	See cases [RCV000167565]	Chr5:174397487..180686444 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:174990352-180690937)	copy number gain	not provided [RCV000767711]	Chr5:174990352..180690937 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3	copy number gain	not provided [RCV000487658]	Chr5:94844077..178830410 [GRCh37] Chr5:5q15-35.3	likely benign
GRCh37/hg19 5q35.2-35.3(chr5:176274007-180719789)x1	copy number loss	See cases [RCV000447018]	Chr5:176274007..180719789 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175722788-177423091)x3	copy number gain	See cases [RCV000445774]	Chr5:175722788..177423091 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:174427052-180719789)x1	copy number loss	See cases [RCV000448611]	Chr5:174427052..180719789 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175601473-180100378)x1	copy number loss	See cases [RCV000448793]	Chr5:175601473..180100378 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3	copy number gain	See cases [RCV000448245]	Chr5:106716357..180687338 [GRCh37] Chr5:5q21.3-35.3	pathogenic
GRCh37/hg19 5q35.1-35.3(chr5:171396359-180719789)x3	copy number gain	See cases [RCV000448458]	Chr5:171396359..180719789 [GRCh37] Chr5:5q35.1-35.3	pathogenic
GRCh37/hg19 5q35.1-35.3(chr5:172031248-180719789)x3	copy number gain	See cases [RCV000512068]	Chr5:172031248..180719789 [GRCh37] Chr5:5q35.1-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175438045-177392885)x1	copy number loss	See cases [RCV000511974]	Chr5:175438045..177392885 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1	copy number loss	See cases [RCV000511978]	Chr5:17628741..176575720 [GRCh37] Chr5:5p15.1-q35.2	pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3	copy number gain	See cases [RCV000512039]	Chr5:113577..180719789 [GRCh37] Chr5:5p15.33-q35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175570677-177439550)x3	copy number gain	See cases [RCV000511393]	Chr5:175570677..177439550 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)	copy number gain	See cases [RCV000510723]	Chr5:113577..180719789 [GRCh37] Chr5:5p15.33-q35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175570677-180719789)x1	copy number loss	See cases [RCV000510785]	Chr5:175570677..180719789 [GRCh37] Chr5:5q35.2-35.3	pathogenic
NM_012279.4(ZNF346):c.691A>G (p.Thr231Ala)	single nucleotide variant	not specified [RCV004330050]	Chr5:177050924 [GRCh38] Chr5:176477925 [GRCh37] Chr5:5q35.2	uncertain significance
GRCh37/hg19 5q35.2-35.3(chr5:175570678-177437340)x1	copy number loss	See cases [RCV000512405]	Chr5:175570678..177437340 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175570677-177436413)x1	copy number loss	not provided [RCV000682615]	Chr5:175570677..177436413 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:176044976-177023859)x1	copy number loss	not provided [RCV000682618]	Chr5:176044976..177023859 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175438045-177481250)x1	copy number loss	not provided [RCV000682614]	Chr5:175438045..177481250 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3	copy number gain	not provided [RCV000744323]	Chr5:25328..180693344 [GRCh37] Chr5:5p15.33-q35.3	pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3	copy number gain	not provided [RCV000744317]	Chr5:13648..180905029 [GRCh37] Chr5:5p15.33-q35.3	pathogenic
GRCh37/hg19 5q33.2-35.3(chr5:155344802-180693344)x3	copy number gain	not provided [RCV000745284]	Chr5:155344802..180693344 [GRCh37] Chr5:5q33.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:174832617-180693344)x3	copy number gain	not provided [RCV000745336]	Chr5:174832617..180693344 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175346223-177423236)x1	copy number loss	not provided [RCV000745338]	Chr5:175346223..177423236 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175433876-177441189)x1	copy number loss	not provided [RCV000745339]	Chr5:175433876..177441189 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2(chr5:176445698-176535031)x3	copy number gain	not provided [RCV000745346]	Chr5:176445698..176535031 [GRCh37] Chr5:5q35.2	benign
GRCh37/hg19 5q35.2-35.3(chr5:176305543-177422876)	copy number gain	not provided [RCV000767712]	Chr5:176305543..177422876 [GRCh37] Chr5:5q35.2-35.3	pathogenic
Single allele	duplication	not provided [RCV000768450]	Chr5:175843728..180703728 [GRCh37] Chr5:5q35.2-35.3	likely pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175570677-177439550)x3	copy number gain	not provided [RCV000846148]	Chr5:175570677..177439550 [GRCh37] Chr5:5q35.2-35.3	pathogenic
Single allele	deletion	Marfanoid habitus and intellectual disability [RCV000851176]	Chr5:175875407..177036017 [GRCh37] Chr5:5q35.2-35.3	likely pathogenic
NC_000005.9:g.(?_176289625)_(177151363_?)del	deletion	Sotos syndrome [RCV003232856]\|not provided [RCV003113198]	Chr5:176289625..177151363 [GRCh37] Chr5:5q35.2-35.3	pathogenic\|no classifications from unflagged records
GRCh37/hg19 5q35.2-35.3(chr5:175346695-177469711)x1	copy number loss	Sotos syndrome [RCV003232270]	Chr5:175346695..177469711 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q32-35.3(chr5:149010383-180719789)	copy number gain	Hunter-McAlpine craniosynostosis [RCV002280612]	Chr5:149010383..180719789 [GRCh37] Chr5:5q32-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175570677-177114151)x3	copy number gain	not provided [RCV001258712]	Chr5:175570677..177114151 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175394616-177436413)x3	copy number gain	not provided [RCV001258713]	Chr5:175394616..177436413 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.1-35.3(chr5:170805664-180719789)x3	copy number gain	5q35 microduplication syndrome [RCV001263227]	Chr5:170805664..180719789 [GRCh37] Chr5:5q35.1-35.3	pathogenic
NC_000005.9:g.(?_176047812)_(177422934_?)del	deletion	Ehlers-Danlos syndrome progeroid type [RCV001931790]	Chr5:176047812..177422934 [GRCh37] Chr5:5q35.2-35.3	uncertain significance
NC_000005.9:g.(?_176047812)_(177422934_?)dup	duplication	Ehlers-Danlos syndrome progeroid type [RCV001883344]\|not provided [RCV001879660]	Chr5:176047812..177422934 [GRCh37] Chr5:5q35.2-35.3	uncertain significance
NC_000005.9:g.(?_175158654)_(179263593_?)dup	duplication	Ehlers-Danlos syndrome, dermatosparaxis type [RCV003116717]\|Sotos syndrome [RCV003232857]\|not provided [RCV003154288]	Chr5:175158654..179263593 [GRCh37] Chr5:5q35.2-35.3	uncertain significance\|no classifications from unflagged records
Single allele	duplication	5q35 microduplication syndrome [RCV002286375]	Chr5:176449583..177376826 [GRCh38] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.1-35.3(chr5:170350336-180719789)x3	copy number gain	See cases [RCV002292398]	Chr5:170350336..180719789 [GRCh37] Chr5:5q35.1-35.3	pathogenic
GRCh37/hg19 5q35.2(chr5:176448623-176520008)x1	copy number loss	not provided [RCV002474955]	Chr5:176448623..176520008 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.124C>T (p.Arg42Cys)	single nucleotide variant	not specified [RCV004091005]	Chr5:177022862 [GRCh38] Chr5:176449863 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.263A>G (p.Lys88Arg)	single nucleotide variant	not specified [RCV004234942]	Chr5:177041213 [GRCh38] Chr5:176468214 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.65G>C (p.Ser22Thr)	single nucleotide variant	not specified [RCV004161530]	Chr5:177022803 [GRCh38] Chr5:176449804 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.82G>A (p.Gly28Ser)	single nucleotide variant	not specified [RCV004245381]	Chr5:177022820 [GRCh38] Chr5:176449821 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.20C>G (p.Ala7Gly)	single nucleotide variant	not specified [RCV004173034]	Chr5:177022758 [GRCh38] Chr5:176449759 [GRCh37] Chr5:5q35.2	likely benign
NM_012279.4(ZNF346):c.64A>C (p.Ser22Arg)	single nucleotide variant	not specified [RCV004161529]	Chr5:177022802 [GRCh38] Chr5:176449803 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.98G>A (p.Gly33Glu)	single nucleotide variant	not specified [RCV004108155]	Chr5:177022836 [GRCh38] Chr5:176449837 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.170A>G (p.Glu57Gly)	single nucleotide variant	not specified [RCV004318003]	Chr5:177022908 [GRCh38] Chr5:176449909 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.442G>A (p.Val148Met)	single nucleotide variant	not specified [RCV004259179]	Chr5:177044458 [GRCh38] Chr5:176471459 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.189C>G (p.Ile63Met)	single nucleotide variant	not specified [RCV004314215]	Chr5:177041139 [GRCh38] Chr5:176468140 [GRCh37] Chr5:5q35.2	uncertain significance
GRCh38/hg38 5q35.2-35.3(chr5:176447531-177312407)x1	copy number loss	Sotos syndrome [RCV003327703]	Chr5:176447531..177312407 [GRCh38] Chr5:5q35.2-35.3	pathogenic
NM_012279.4(ZNF346):c.643A>G (p.Lys215Glu)	single nucleotide variant	not specified [RCV004358977]	Chr5:177050876 [GRCh38] Chr5:176477877 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.589C>T (p.Pro197Ser)	single nucleotide variant	not specified [RCV004356164]	Chr5:177050822 [GRCh38] Chr5:176477823 [GRCh37] Chr5:5q35.2	uncertain significance
GRCh37/hg19 5q35.1-35.2(chr5:171836503-176517734)x1	copy number loss	not provided [RCV003485492]	Chr5:171836503..176517734 [GRCh37] Chr5:5q35.1-35.2	pathogenic
GRCh37/hg19 5q35.2(chr5:176483840-176588195)x1	copy number loss	not provided [RCV003485497]	Chr5:176483840..176588195 [GRCh37] Chr5:5q35.2	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:175332333-177469711)x1	copy number loss	not provided [RCV003485494]	Chr5:175332333..177469711 [GRCh37] Chr5:5q35.2-35.3	pathogenic
Single allele	deletion	not provided [RCV003448669]	Chr5:175559209..177430432 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2-35.3(chr5:176385815-178410738)x1	copy number loss	not specified [RCV003986570]	Chr5:176385815..178410738 [GRCh37] Chr5:5q35.2-35.3	pathogenic
GRCh37/hg19 5q35.2(chr5:175822822-176520008)x1	copy number loss	not specified [RCV003986588]	Chr5:175822822..176520008 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.868A>G (p.Thr290Ala)	single nucleotide variant	not specified [RCV004486644]	Chr5:177064582 [GRCh38] Chr5:176491583 [GRCh37] Chr5:5q35.2	uncertain significance
NM_012279.4(ZNF346):c.481A>G (p.Asn161Asp)	single nucleotide variant	not specified [RCV004486643]	Chr5:177044497 [GRCh38] Chr5:176471498 [GRCh37] Chr5:5q35.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	6716
Count of miRNA genes:	1058
Interacting mature miRNAs:	1294
Transcripts:	ENST00000261948, ENST00000358149, ENST00000503039, ENST00000503425, ENST00000504600, ENST00000506693, ENST00000508155, ENST00000510933, ENST00000511834, ENST00000512315, ENST00000513587
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

Markers in Region

D5S2196E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	176,486,351 - 176,486,462	UniSTS	GRCh37
Build 36	5	176,418,957 - 176,419,068	RGD	NCBI36
Celera	5	172,014,865 - 172,014,976	RGD
Cytogenetic Map	5	q35.2	UniSTS
HuRef	5	171,408,072 - 171,408,183	UniSTS

D5S2703

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	176,488,890 - 176,489,109	UniSTS	GRCh37
Build 36	5	176,421,496 - 176,421,715	RGD	NCBI36
Celera	5	172,012,212 - 172,012,431	RGD
Cytogenetic Map	5	q35.2	UniSTS
HuRef	5	171,410,614 - 171,410,833	UniSTS

RH47837

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	176,507,938 - 176,508,126	UniSTS	GRCh37
Build 36	5	176,440,544 - 176,440,732	RGD	NCBI36
Celera	5	171,993,195 - 171,993,383	RGD
Cytogenetic Map	5	q35.2	UniSTS
HuRef	5	171,429,662 - 171,429,850	UniSTS
GeneMap99-GB4 RH Map	5	636.91	UniSTS
NCBI RH Map	5	973.0	UniSTS

D5S2863

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	176,492,824 - 176,492,981	UniSTS	GRCh37
Build 36	5	176,425,430 - 176,425,587	RGD	NCBI36
Celera	5	172,008,340 - 172,008,498	RGD
Cytogenetic Map	5	q35.2	UniSTS
HuRef	5	171,414,548 - 171,414,705	UniSTS

ZNF346__4826

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	176,493,067 - 176,493,743	UniSTS	GRCh37
Build 36	5	176,425,673 - 176,426,349	RGD	NCBI36
Celera	5	172,007,578 - 172,008,254	RGD
HuRef	5	171,414,791 - 171,415,467	UniSTS

SGC32143

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	176,492,807 - 176,492,954	UniSTS	GRCh37
Build 36	5	176,425,413 - 176,425,560	RGD	NCBI36
Celera	5	172,008,367 - 172,008,515	RGD
Cytogenetic Map	5	q35.2	UniSTS
HuRef	5	171,414,531 - 171,414,678	UniSTS
GeneMap99-GB4 RH Map	5	636.91	UniSTS
Whitehead-RH Map	5	540.8	UniSTS
NCBI RH Map	5	973.0	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

197

842

734

430

101

970

1030

816

183

Low

2242

2926

884

599

1216

439

3927

2091

2764

330

430

797

164

1180

2605

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001308213	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001308214	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001308215	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001308216	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001308218	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001308219	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001308221	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001308223	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001363713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_012279	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_131773	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_131774	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005265860	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005265864	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011534493	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011534494	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011534495	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011534496	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011534497	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017009295	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017009296	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017009297	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017009298	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017009299	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017009300	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017009301	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017009302	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017009303	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
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RefSeq Acc Id:

ENST00000358149 ⟹ ENSP00000350869

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	5	177,022,696 - 177,067,985 (+)	Ensembl

RefSeq Acc Id:

ENST00000503039 ⟹ ENSP00000424495

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	5	177,022,735 - 177,081,189 (+)	Ensembl

RefSeq Acc Id:

ENST00000503425 ⟹ ENSP00000421212

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	5	177,022,704 - 177,064,966 (+)	Ensembl

RefSeq Acc Id:

ENST00000504600

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	5	177,044,327 - 177,050,892 (+)	Ensembl

RefSeq Acc Id:

ENST00000506693 ⟹ ENSP00000423515

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	5	177,022,696 - 177,065,241 (+)	Ensembl

RefSeq Acc Id:

ENST00000508155 ⟹ ENSP00000421388

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	5	177,022,716 - 177,065,458 (+)	Ensembl

RefSeq Acc Id:

ENST00000510933

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	5	177,022,904 - 177,042,249 (+)	Ensembl

RefSeq Acc Id:

ENST00000511834 ⟹ ENSP00000425725

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	5	177,022,732 - 177,065,965 (+)	Ensembl

RefSeq Acc Id:

ENST00000512315 ⟹ ENSP00000421089

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	5	177,022,696 - 177,080,554 (+)	Ensembl

RefSeq Acc Id:

ENST00000513587 ⟹ ENSP00000423690

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	5	177,022,735 - 177,065,018 (+)	Ensembl

RefSeq Acc Id:

NM_001308213 ⟹ NP_001295142

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,081,189 (+)	NCBI
CHM1_1	5	175,882,083 - 175,941,073 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,624,397 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGCGCAGTTTTTCCCACATTCGAGGACTGTCATCCCTATA
CTCGTCCTGTCGGAGACCTACAGTCTTTGCCATCCCGTGGAGCACATGATCCAGAAGAACCAAT
GTCTCTTCACCAACACCCAGTGTAAGGTTTGCTGCGCCTTGCTTATTTCTGAGTCCCAGAAGCT
GGCACATTACCAGAGCAAAAAACATGCCAACAAAGTGAAGAGATACCTAGCAATCCATGGAATG
GAGACATTAAAGGGGGAAACGAAGAAGCTAGACTCAGATCAGAAGAGCAGCAGAAGCAAAGACA
AGAACCAGTGCTGCCCCATCTGTAACATGACCTTTTCCTCCCCTGTCGTGGCCCAGTCGCACTA
CCTGGGGAAGACCCACGCAAAGAACTTAAAGCTGAAGCAGCAGTCCACTAAGGTGGAAGCCTTG
CACCAGAATAGAGAGATGATAGACCCAGACAAGTTCTGCAGCCTCTGCCATGCAACTTTCAACG
ACCCTGTCATGGCTCAACAACATTATGTGGGCAAGAAACACAGAAAACAGGAGACCAAGCTCAA
ACTAATGGCACGCTATGGGCGGCTGGCGGACCCTGCTGTCACTGACTTTCCAGCTGGAAAGGGC
TACCCCTGCAAAACATGTAAGATAGTGCTGAACTCCATAGAACAGTACCAAGCTCATGTCAGCG
GCTTCAAACACAAGAACCAGTCACCAAAAACAGTGGCATCATCCCTGGGCCAGATTCCAATGCA
AAGGCAACCCATTCAGAAAGACTCAACCACCTTGGAAGACTAGAGCTAGGGGTGGCCGTGTCAC
AGTCTGGCCAAGGAAATGAAATTGGGAGTTGCTGTGTGGAAACTCAACTCTCTGGAACTTCTTC
CTTCCTCCTGCCTCTGCACAAATGTGACGGCAGCAGCTGAAGCCAACATCTTGCGACCATGAGA
GAAAAACCTGGAGAACGGACGAGTCCTCAACCCTGACTTCAGACCAACCTACACCCACCTCTGG
ACGTGGGGCTAAGTGAGAGATGGATACACTGTTTCATTTAGGCCCTGCTCACTTAGGTTTCTGT
TATTCACACCCCAACGAAACCCTCCATGGTCCAGGGCACCGGGCAAAGTACAGAAGGGCACGAG
TTTACTTCCCGCTTCCCTGGAGACCACCAACCCTCTCACCCTTCCAGCCCAGCCTCTGCCACTT
CCCAGCTGTCGGTCCTCCTCCAAACAGACGTGCATGCCAACACCCGGTGGGTGTGAGGCTTGTA
GGCCCAAGTCTAGAGAGGCTGAGTCTGGCAAAGCCTGAAAGCCCCTGTCCTAGCAAGCCAGGCC
ACAGGTCTAGAGTATCCGAGACCAGTGAATAAGGGGACGGGGGGTGCTACTGAGGCTGTGAGAA
GCCCCAGGACCAGCCCAGGGTAGTTAGAACTGAGTGAGGTTAGCCGGGACTAACCTCACTCAGA
TCCCTCCTCCCCAGTTCCCCTCCATCCACTTTGGTTTGGAAGCCTCCCCAGAGCTCTCCCAGGC
TGTCATCAGCTCTAAACTCTCTGCCTCCACAAAAATGCCCTGGGCAACCTGTAACTCACAGCCC
TGCTGTCTTCAGAGTATAAACTGGAGACAGATGTACCCAGAATTGAGGACGGGTGGGAAATGAG
GAGAAATGAAGGCTGAGGAGGGGTCATTCTCACAGTCCCTCCCTTTCGGTCACAGGAGGGTGTT
GCCCATGCTTTTGGGTGGGTCCCAGGCCCATAGCTGCAAATATTCATATTGGCTACTCTTCAGT
GAGCAAGGGGTATATGCCAGGCACTGGCATTGTGCTTGACATACATCATCATACTGAGTCCTCA
CGGAAGATGTATTATTCCCATTTCACAGAAGATGAAACTGAGGCTTGAGGTTAAGTGATTTGTC
CGTGACCACAAAGAGTTTTCGGGACTCAAACCCAGATCTGTCACTGGGCAAGGTGGCTCACACC
TATAATCCCAGCCCTTTGGGAGACTGAGGCCAGCAGATCTCCTGTGGCCAGGAGTTCAAGCCTG
GCCAACAATGGCAAAACCCCGTCTCTACCAAAAATACAAAAATTAGCTGGGCGTGGTGGCACAC
ACCCGTAATCCCAGCTACTCAGGTGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGTGG
TTGCAGTGAGCCTAGATCGTGCCACTGCATTCCAGCCTGAGCGACAGAGTAAGACTCTGTCTCC
AAAAAAAACCCAGATCTGTCCGACTCTGACACCCAACCTTTAATCACTCACTTTCTGTCAATGT
CACCTCCGTTTTGACCAGCCAAGCTAGACCTCCCTGGAGCCTGTGGAGAAGCCAAGGTAGAAAA
GGGTTGGAAAAGAATGATAAAATAGGCCAGGTGCGGTGGCTCAAGCCTGTACTCCCAGCACTTT
TGGAGGCCGAGACAGGCAGATTGCTTGAGCCCAGGAGTTCAAGACCAGCCTGGGCAACATAATG
AGACCCTGTTTCAACTTAAAAAAAAGAAATGGTAATGAACAATTGTCAATTCTGAGCAGCTGGG
TATGGTATGACCCTGTGTACTTTTTCTGTATTTTAAAATGTTCTCAAAATAAAACTTGTTT

hide sequence

RefSeq Acc Id:

NM_001308214 ⟹ NP_001295143

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI
CHM1_1	5	175,882,083 - 175,927,867 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGTGGAGCACATGATCCAGAAGAACCAATGTCTCTTCACC
AACACCCAGTGTAAGGTTTGCTGCGCCTTGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACC
AGAGCAGCAGAAGCAAAGACAAGAACCAGTGCTGCCCCATCTGTAACATGACCTTTTCCTCCCC
TGTCGTGGCCCAGTCGCACTACCTGGGGAAGACCCACGCAAAGAACTTAAAGCTGAAGCAGCAG
TCCACTAAGGTGGAAGCCTTGCACCAGAATAGAGAGATGATAGACCCAGACAAGTTCTGCAGCC
TCTGCCATGCAACTTTCAACGACCCTGTCATGGCTCAACAACATTATGTGGGCAAGAAACACAG
AAAACAGGAGACCAAGCTCAAACTAATGGCACGCTATGGGCGGCTGGCGGACCCTGCTGTCACT
GACTTTCCAGCTGGAAAGGGCTACCCCTGCAAAACATGTAAGATAGTGCTGAACTCCATAGAAC
AGTACCAAGCTCATGTCAGCGGCTTCAAACACAAGAACCAGTCACCAAAAACAGTGGCATCATC
CCTGGGCCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGACTCAACCACCTTGGAAGACTAG
AGGTGATTCTGCCCAGCATCCCATATTGGGCCAGCCATGAGCCAGCTTCCCGTGACTGCTCAGC
CCTTGGCTCCCTCTTGCTCGTTGTTCTCACCAGGAAAGTACACGGGCCTGAGGCAGGATTGGGC
CACAGACAGCCTCTCATTGGTCCGGGCTAATTCACTCCTGCTGCTCCCCTTTGGCAGGGGTCCT
GTAGGTCATGACAGGGGAGGCAAGGGTATTGAGAGACTCGGGGTCTCGCGGGGTGGTAGTTTGG
AGGGTGGCTTTCCCCATTTCCCAACCCCTCTGGGCCTTAGGTGCTGAGGCCCCTGCCACCTGTC
TTTCCTCTAAAGGTCAGTTTTGGGCCAGTTCTTGCAACTAAAGAGCAGAGATCTCTCTGGGCCC
TAGACATTTCCAGCAAAACCTGGAACTTTCATGCCAAACCTGGGGCAGGGCAGGAAACAGAGGA
AATGGCTGCAACATGGGAGCTTGGAGCTAATACGACACTCTGCCTTCCCCCAGAAGGTGCAGGC
TTTCCTGAGTCTTAGACCAGATATGGCCAGTTGCGCAGGTTTCTGCCAACTGTGAAGTATCCTC
CTGGAGCAGTGACACAATCTTGGCGGAGCATTGCTACCCCCGCTGCCCCCTCCACAGTTCCTGA
ATGGTGCTAAGGATCTGCAGCAGTTGGCAACGAGCTGGGGCTGGGGGCGGCCTCCATGTCCACT
GAGATCATAGGACACTCCAATGGGGATGGGACCTTTCCCCTCCTCCATCAGAGGTGCTCTGACC
CTAGGTTACACGGGAAAGTGCCCCACATGCAAGTCTCCCTGAGGGTTCTGCCCCTAAAGGCAGA
CTGCCTCATGCCCGCTAGCTGTGAGGTTCATTGCTACCCTCGGCCCTACTAGCCCTCTCTTCCC
CCTTGTGCAGCGGACCACTTGCCCAGTTTGCTGTGGTGCTAGCCTTCCCCATCATCCACCGGGT
GATTTCTGGGTCCCAGGGAAAGAAAGAGAGAGCTGATGCAGGTTTCTACAGTGAGGAACAGGCG
TTTCCCAGGCCCCACACCCAGATTTCTCTATCTTTGCTGTGTTTTATGGCCTGGGACTGAGTCC
ACACGGATAGATTTTTCCTTGTAACCTTGAGACGAGAATTCCAAGGAGTGTCACCATCAGAGGC
TTCTCTTCATTGTGTCAAAGAAGCCCCTAGCTGCTCTCGTGGCCTCCTTCCCCCACTCCCTATC
CCTTCACCTGTGAAATGCCTTTGCTTTGCATATTGTGTGTGGATGTGTGTGTGTGTGTGTGTGT
GTTTGTGTGTATGTGTGTGCTTCTGTGTGTGCCTAATGCTCTGTCTCTTGGTCACTGAAGCATC
CAAATAAAGAATTTCCCTCATGGGCCAGACTACAACTTAACAGACCTAGGGTTTTGAGCCATAT
TGCCATTGGATCTAGTATGTCTGTCTTGACCCCTCACCCCCACCCCATTCAGACCTCAGTAGTC
CCCAGTAGTCACTTTAGGAGTTGGGACAGAGTCGAGCACCCTGTGAAAGTCTCCCTTGAGTTCA
GGTGCCCTGAACTCAGTACAGCCTCATCTTCTCATCCACCACCTTCTCCTGCTTCTCCTGTCAC
ATAGGGCCTCATGAAGGTCTTTAAAGGGTTTAAGCTGGGGATCTGCTTTATGTTTGAGAGAACT
GTTCTGGCTGTTATGTAAAGGAGTGCAGGGAGGGGCAGGAAAGGAGACAAGGAGGCCAGTATGG
ACACTGTGTCCAGTATGGCTTTCCAGGCTAATCACTTAGGGCAGAGACCCAGCCTTATTCATCT
CTACTTCCTGATGTCCATAGTGGTGTGTCATGAATTTTTATTGAATGAACAAATGAGGTGTATG
AGGAGAGATGGTTTTCTCCTGCTCAGCTCTTACACAGTGATAGGTTTGTTCCATGGGACTTATC
ATAGGCCTGGTGATTCTTGAAAGAGCATTTTTCATGACTCAAAAATGAGCTGAGAAGGAGTGTT
ATGGCCAGGTGCGGCGTCATGCACCTATAGTCCCAGCTGCTCAGGAGGCTAAGGCAGAAAGACC
ATTCAAGCCCAGGAGTTCCAGCCTGAAGTATGCTGTGATCATGCCTGTGAATAACCACTGCACT
CCAGCCAGGGCAACATAACAAGACTCTATCTAAAAAAAAAAAAAAATTATAAAAATAAATTTGA
AGGCTGGGCGCCGTGGCTCACGCCTGTAATCCAAGCACTTTGAGAGGCCAAGGCAGGTGGATAA
CCTGAGGTCAGAAGTTCGAGACCAGCCTGGCCAACATGATGGCAAAACCCCGTCCCTATAAAAA
ATACGAAAATCAGCTGCGCCTGGTGGCACACATCTGTAGTCCCAGCTACTTGGGAGGCTGAGGC
AAGAGAATTGCTTGAACCCGGGAGGCGGAGGGTCGCATTGAGCCAAGATCGTGCCACTGCACTC
CAGCCTAGGTGACAGAGTGAGACTCCTGTCTCAAAATAAATAAATAATAAATTTTAAAAGAAGG
TAGCCAGGTGTGGTGGTGCATTCCTGTAGTCCTGGCTACCTGGAAGGGTGAGGCAGGAGGATCG
CTTTAACCATGAGTTCAAGGCAGCAGTGAGCTATGATTATGCCACTGTACTCCAGCCTGGACAA
CAGAGCAAGACCCTGTCTCTAAAAATAATAATTTTTAAAATTTAAAAAAAGAAAGGAATGTTAT
GGCCTCAAGAGCTCTTTGTCCATCCTTTACTGTAGACAGCCAGATTTGAGGAAGGGGCCCAGGC
AGCCTCAGCTCCCATTCAGTGCCACTCAGCCCCTGCTCCTGGTCAGCTGTGAAAGGCTCTACAC
AGCCCCAAGGGAGGTTCTCAGCTTCCCATGATCAGACTGCCTCAGCAATTCCCCAGAGTCCTTC
TAAGCCACCTAGTATGTCAGATTCAGCCCCATCTACCAAGCAAGGAAATGAAGGGCAGGGGGTG
AGTGGGCTATCATACCGTGAGCCTCCGGCCTGCAAGACCACTTTGTAGTCCCTACCAGCTGTGT
GGCCAGCCCTGTTGGTAAAGGGACCTAGAGATGAACACTTTCTTGCCCTTAGGGGTTCACACAC
AGTCAAAGATCATGATGACAATGATAAGAATGCCCAGGATGCAGGAGCTGACTCAGCCAAGGGC
ATGAAAAAGCTGGAGAGGTTGGAAAGCTAGCATTTCATCTGCATAACAACCTTTGAGCTAAGAG
TTAATATTCCATATAGAGAAGGAGGCCAGGCAGGGTGGCTCACATCTGTAATCCCAGCACTTTG
GGAGGCCAAGGCGGGTGTATCACTTGCGGCCGGGAGTTTAAGACCATCCTGGCCAACGTGGTGA
AATCCCATCTCTACAAAAAATAAAAAATAAAATAAATAAAAACCATGGAGAGAAGGAA

hide sequence

RefSeq Acc Id:

NM_001308215 ⟹ NP_001295144

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI
CHM1_1	5	175,882,083 - 175,927,867 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGTGGAGCACATGATCCAGAAGAACCAATGTCTCTTCACC
AACACCCAGTGTAAGGTTTGCTGCGCCTTGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACC
AGAGCAAAAAACATGCCAACAAAGTGAAGAGATACCTAGCAATCCATGGAATGGAGACATTAAA
GGGGGAAACGAAGAAGCTAGACTCAGATCAGAAGAGCAGCAGAAGCAAAGACAAGAACCAGTGC
TGCCCCATCTGTAACATGACCTTTTCCTCCCCTGTCGTGGCCCAGTCGCACTACCTGGGGAAGA
CCCACGCAAAGAACTTAAAGCTGAAGCAGCAGTCCACTAAGGTGGAAGCTGGAAAGGGCTACCC
CTGCAAAACATGTAAGATAGTGCTGAACTCCATAGAACAGTACCAAGCTCATGTCAGCGGCTTC
AAACACAAGAACCAGTCACCAAAAACAGTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGC
AACCCATTCAGAAAGACTCAACCACCTTGGAAGACTAGAGGTGATTCTGCCCAGCATCCCATAT
TGGGCCAGCCATGAGCCAGCTTCCCGTGACTGCTCAGCCCTTGGCTCCCTCTTGCTCGTTGTTC
TCACCAGGAAAGTACACGGGCCTGAGGCAGGATTGGGCCACAGACAGCCTCTCATTGGTCCGGG
CTAATTCACTCCTGCTGCTCCCCTTTGGCAGGGGTCCTGTAGGTCATGACAGGGGAGGCAAGGG
TATTGAGAGACTCGGGGTCTCGCGGGGTGGTAGTTTGGAGGGTGGCTTTCCCCATTTCCCAACC
CCTCTGGGCCTTAGGTGCTGAGGCCCCTGCCACCTGTCTTTCCTCTAAAGGTCAGTTTTGGGCC
AGTTCTTGCAACTAAAGAGCAGAGATCTCTCTGGGCCCTAGACATTTCCAGCAAAACCTGGAAC
TTTCATGCCAAACCTGGGGCAGGGCAGGAAACAGAGGAAATGGCTGCAACATGGGAGCTTGGAG
CTAATACGACACTCTGCCTTCCCCCAGAAGGTGCAGGCTTTCCTGAGTCTTAGACCAGATATGG
CCAGTTGCGCAGGTTTCTGCCAACTGTGAAGTATCCTCCTGGAGCAGTGACACAATCTTGGCGG
AGCATTGCTACCCCCGCTGCCCCCTCCACAGTTCCTGAATGGTGCTAAGGATCTGCAGCAGTTG
GCAACGAGCTGGGGCTGGGGGCGGCCTCCATGTCCACTGAGATCATAGGACACTCCAATGGGGA
TGGGACCTTTCCCCTCCTCCATCAGAGGTGCTCTGACCCTAGGTTACACGGGAAAGTGCCCCAC
ATGCAAGTCTCCCTGAGGGTTCTGCCCCTAAAGGCAGACTGCCTCATGCCCGCTAGCTGTGAGG
TTCATTGCTACCCTCGGCCCTACTAGCCCTCTCTTCCCCCTTGTGCAGCGGACCACTTGCCCAG
TTTGCTGTGGTGCTAGCCTTCCCCATCATCCACCGGGTGATTTCTGGGTCCCAGGGAAAGAAAG
AGAGAGCTGATGCAGGTTTCTACAGTGAGGAACAGGCGTTTCCCAGGCCCCACACCCAGATTTC
TCTATCTTTGCTGTGTTTTATGGCCTGGGACTGAGTCCACACGGATAGATTTTTCCTTGTAACC
TTGAGACGAGAATTCCAAGGAGTGTCACCATCAGAGGCTTCTCTTCATTGTGTCAAAGAAGCCC
CTAGCTGCTCTCGTGGCCTCCTTCCCCCACTCCCTATCCCTTCACCTGTGAAATGCCTTTGCTT
TGCATATTGTGTGTGGATGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTATGTGTGTGCTTCTGT
GTGTGCCTAATGCTCTGTCTCTTGGTCACTGAAGCATCCAAATAAAGAATTTCCCTCATGGGCC
AGACTACAACTTAACAGACCTAGGGTTTTGAGCCATATTGCCATTGGATCTAGTATGTCTGTCT
TGACCCCTCACCCCCACCCCATTCAGACCTCAGTAGTCCCCAGTAGTCACTTTAGGAGTTGGGA
CAGAGTCGAGCACCCTGTGAAAGTCTCCCTTGAGTTCAGGTGCCCTGAACTCAGTACAGCCTCA
TCTTCTCATCCACCACCTTCTCCTGCTTCTCCTGTCACATAGGGCCTCATGAAGGTCTTTAAAG
GGTTTAAGCTGGGGATCTGCTTTATGTTTGAGAGAACTGTTCTGGCTGTTATGTAAAGGAGTGC
AGGGAGGGGCAGGAAAGGAGACAAGGAGGCCAGTATGGACACTGTGTCCAGTATGGCTTTCCAG
GCTAATCACTTAGGGCAGAGACCCAGCCTTATTCATCTCTACTTCCTGATGTCCATAGTGGTGT
GTCATGAATTTTTATTGAATGAACAAATGAGGTGTATGAGGAGAGATGGTTTTCTCCTGCTCAG
CTCTTACACAGTGATAGGTTTGTTCCATGGGACTTATCATAGGCCTGGTGATTCTTGAAAGAGC
ATTTTTCATGACTCAAAAATGAGCTGAGAAGGAGTGTTATGGCCAGGTGCGGCGTCATGCACCT
ATAGTCCCAGCTGCTCAGGAGGCTAAGGCAGAAAGACCATTCAAGCCCAGGAGTTCCAGCCTGA
AGTATGCTGTGATCATGCCTGTGAATAACCACTGCACTCCAGCCAGGGCAACATAACAAGACTC
TATCTAAAAAAAAAAAAAAATTATAAAAATAAATTTGAAGGCTGGGCGCCGTGGCTCACGCCTG
TAATCCAAGCACTTTGAGAGGCCAAGGCAGGTGGATAACCTGAGGTCAGAAGTTCGAGACCAGC
CTGGCCAACATGATGGCAAAACCCCGTCCCTATAAAAAATACGAAAATCAGCTGCGCCTGGTGG
CACACATCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAAGAGAATTGCTTGAACCCGGGAGGC
GGAGGGTCGCATTGAGCCAAGATCGTGCCACTGCACTCCAGCCTAGGTGACAGAGTGAGACTCC
TGTCTCAAAATAAATAAATAATAAATTTTAAAAGAAGGTAGCCAGGTGTGGTGGTGCATTCCTG
TAGTCCTGGCTACCTGGAAGGGTGAGGCAGGAGGATCGCTTTAACCATGAGTTCAAGGCAGCAG
TGAGCTATGATTATGCCACTGTACTCCAGCCTGGACAACAGAGCAAGACCCTGTCTCTAAAAAT
AATAATTTTTAAAATTTAAAAAAAGAAAGGAATGTTATGGCCTCAAGAGCTCTTTGTCCATCCT
TTACTGTAGACAGCCAGATTTGAGGAAGGGGCCCAGGCAGCCTCAGCTCCCATTCAGTGCCACT
CAGCCCCTGCTCCTGGTCAGCTGTGAAAGGCTCTACACAGCCCCAAGGGAGGTTCTCAGCTTCC
CATGATCAGACTGCCTCAGCAATTCCCCAGAGTCCTTCTAAGCCACCTAGTATGTCAGATTCAG
CCCCATCTACCAAGCAAGGAAATGAAGGGCAGGGGGTGAGTGGGCTATCATACCGTGAGCCTCC
GGCCTGCAAGACCACTTTGTAGTCCCTACCAGCTGTGTGGCCAGCCCTGTTGGTAAAGGGACCT
AGAGATGAACACTTTCTTGCCCTTAGGGGTTCACACACAGTCAAAGATCATGATGACAATGATA
AGAATGCCCAGGATGCAGGAGCTGACTCAGCCAAGGGCATGAAAAAGCTGGAGAGGTTGGAAAG
CTAGCATTTCATCTGCATAACAACCTTTGAGCTAAGAGTTAATATTCCATATAGAGAAGGAGGC
CAGGCAGGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGTATCACTTG
CGGCCGGGAGTTTAAGACCATCCTGGCCAACGTGGTGAAATCCCATCTCTACAAAAAATAAAAA
ATAAAATAAATAAAAACCATGGAGAGAAGGAA

hide sequence

RefSeq Acc Id:

NM_001308216 ⟹ NP_001295145

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI
CHM1_1	5	175,882,083 - 175,927,867 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGTGGAGCACATGATCCAGAAGAACCAATGTCTCTTCACC
AACACCCAGTGTAAGGTTTGCTGCGCCTTGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACC
AGAGCAAAAAACATGCCAACAAAGTGAAGAGATACCTAGCAATCCATGGAATGGAGACATTAAA
GGGGGAAACGAAGAAGCTAGACTCAGATCAGGTCACCAAAAACAGTGGCATCATCCCTGGGCCA
GATTCCAATGCAAAGGCAACCCATTCAGAAAGACTCAACCACCTTGGAAGACTAGAGGTGATTC
TGCCCAGCATCCCATATTGGGCCAGCCATGAGCCAGCTTCCCGTGACTGCTCAGCCCTTGGCTC
CCTCTTGCTCGTTGTTCTCACCAGGAAAGTACACGGGCCTGAGGCAGGATTGGGCCACAGACAG
CCTCTCATTGGTCCGGGCTAATTCACTCCTGCTGCTCCCCTTTGGCAGGGGTCCTGTAGGTCAT
GACAGGGGAGGCAAGGGTATTGAGAGACTCGGGGTCTCGCGGGGTGGTAGTTTGGAGGGTGGCT
TTCCCCATTTCCCAACCCCTCTGGGCCTTAGGTGCTGAGGCCCCTGCCACCTGTCTTTCCTCTA
AAGGTCAGTTTTGGGCCAGTTCTTGCAACTAAAGAGCAGAGATCTCTCTGGGCCCTAGACATTT
CCAGCAAAACCTGGAACTTTCATGCCAAACCTGGGGCAGGGCAGGAAACAGAGGAAATGGCTGC
AACATGGGAGCTTGGAGCTAATACGACACTCTGCCTTCCCCCAGAAGGTGCAGGCTTTCCTGAG
TCTTAGACCAGATATGGCCAGTTGCGCAGGTTTCTGCCAACTGTGAAGTATCCTCCTGGAGCAG
TGACACAATCTTGGCGGAGCATTGCTACCCCCGCTGCCCCCTCCACAGTTCCTGAATGGTGCTA
AGGATCTGCAGCAGTTGGCAACGAGCTGGGGCTGGGGGCGGCCTCCATGTCCACTGAGATCATA
GGACACTCCAATGGGGATGGGACCTTTCCCCTCCTCCATCAGAGGTGCTCTGACCCTAGGTTAC
ACGGGAAAGTGCCCCACATGCAAGTCTCCCTGAGGGTTCTGCCCCTAAAGGCAGACTGCCTCAT
GCCCGCTAGCTGTGAGGTTCATTGCTACCCTCGGCCCTACTAGCCCTCTCTTCCCCCTTGTGCA
GCGGACCACTTGCCCAGTTTGCTGTGGTGCTAGCCTTCCCCATCATCCACCGGGTGATTTCTGG
GTCCCAGGGAAAGAAAGAGAGAGCTGATGCAGGTTTCTACAGTGAGGAACAGGCGTTTCCCAGG
CCCCACACCCAGATTTCTCTATCTTTGCTGTGTTTTATGGCCTGGGACTGAGTCCACACGGATA
GATTTTTCCTTGTAACCTTGAGACGAGAATTCCAAGGAGTGTCACCATCAGAGGCTTCTCTTCA
TTGTGTCAAAGAAGCCCCTAGCTGCTCTCGTGGCCTCCTTCCCCCACTCCCTATCCCTTCACCT
GTGAAATGCCTTTGCTTTGCATATTGTGTGTGGATGTGTGTGTGTGTGTGTGTGTGTTTGTGTG
TATGTGTGTGCTTCTGTGTGTGCCTAATGCTCTGTCTCTTGGTCACTGAAGCATCCAAATAAAG
AATTTCCCTCATGGGCCAGACTACAACTTAACAGACCTAGGGTTTTGAGCCATATTGCCATTGG
ATCTAGTATGTCTGTCTTGACCCCTCACCCCCACCCCATTCAGACCTCAGTAGTCCCCAGTAGT
CACTTTAGGAGTTGGGACAGAGTCGAGCACCCTGTGAAAGTCTCCCTTGAGTTCAGGTGCCCTG
AACTCAGTACAGCCTCATCTTCTCATCCACCACCTTCTCCTGCTTCTCCTGTCACATAGGGCCT
CATGAAGGTCTTTAAAGGGTTTAAGCTGGGGATCTGCTTTATGTTTGAGAGAACTGTTCTGGCT
GTTATGTAAAGGAGTGCAGGGAGGGGCAGGAAAGGAGACAAGGAGGCCAGTATGGACACTGTGT
CCAGTATGGCTTTCCAGGCTAATCACTTAGGGCAGAGACCCAGCCTTATTCATCTCTACTTCCT
GATGTCCATAGTGGTGTGTCATGAATTTTTATTGAATGAACAAATGAGGTGTATGAGGAGAGAT
GGTTTTCTCCTGCTCAGCTCTTACACAGTGATAGGTTTGTTCCATGGGACTTATCATAGGCCTG
GTGATTCTTGAAAGAGCATTTTTCATGACTCAAAAATGAGCTGAGAAGGAGTGTTATGGCCAGG
TGCGGCGTCATGCACCTATAGTCCCAGCTGCTCAGGAGGCTAAGGCAGAAAGACCATTCAAGCC
CAGGAGTTCCAGCCTGAAGTATGCTGTGATCATGCCTGTGAATAACCACTGCACTCCAGCCAGG
GCAACATAACAAGACTCTATCTAAAAAAAAAAAAAAATTATAAAAATAAATTTGAAGGCTGGGC
GCCGTGGCTCACGCCTGTAATCCAAGCACTTTGAGAGGCCAAGGCAGGTGGATAACCTGAGGTC
AGAAGTTCGAGACCAGCCTGGCCAACATGATGGCAAAACCCCGTCCCTATAAAAAATACGAAAA
TCAGCTGCGCCTGGTGGCACACATCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAAGAGAATT
GCTTGAACCCGGGAGGCGGAGGGTCGCATTGAGCCAAGATCGTGCCACTGCACTCCAGCCTAGG
TGACAGAGTGAGACTCCTGTCTCAAAATAAATAAATAATAAATTTTAAAAGAAGGTAGCCAGGT
GTGGTGGTGCATTCCTGTAGTCCTGGCTACCTGGAAGGGTGAGGCAGGAGGATCGCTTTAACCA
TGAGTTCAAGGCAGCAGTGAGCTATGATTATGCCACTGTACTCCAGCCTGGACAACAGAGCAAG
ACCCTGTCTCTAAAAATAATAATTTTTAAAATTTAAAAAAAGAAAGGAATGTTATGGCCTCAAG
AGCTCTTTGTCCATCCTTTACTGTAGACAGCCAGATTTGAGGAAGGGGCCCAGGCAGCCTCAGC
TCCCATTCAGTGCCACTCAGCCCCTGCTCCTGGTCAGCTGTGAAAGGCTCTACACAGCCCCAAG
GGAGGTTCTCAGCTTCCCATGATCAGACTGCCTCAGCAATTCCCCAGAGTCCTTCTAAGCCACC
TAGTATGTCAGATTCAGCCCCATCTACCAAGCAAGGAAATGAAGGGCAGGGGGTGAGTGGGCTA
TCATACCGTGAGCCTCCGGCCTGCAAGACCACTTTGTAGTCCCTACCAGCTGTGTGGCCAGCCC
TGTTGGTAAAGGGACCTAGAGATGAACACTTTCTTGCCCTTAGGGGTTCACACACAGTCAAAGA
TCATGATGACAATGATAAGAATGCCCAGGATGCAGGAGCTGACTCAGCCAAGGGCATGAAAAAG
CTGGAGAGGTTGGAAAGCTAGCATTTCATCTGCATAACAACCTTTGAGCTAAGAGTTAATATTC
CATATAGAGAAGGAGGCCAGGCAGGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCCAA
GGCGGGTGTATCACTTGCGGCCGGGAGTTTAAGACCATCCTGGCCAACGTGGTGAAATCCCATC
TCTACAAAAAATAAAAAATAAAATAAATAAAAACCATGGAGAGAAGGAA

hide sequence

RefSeq Acc Id:

NM_001308218 ⟹ NP_001295147

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI
CHM1_1	5	175,882,083 - 175,927,867 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGCTCTGTCAAAACGCCTTACAAATCCTTTCCTTGTGGCC
TCCACCTTAGCCTTGCACCAGAATAGAGAGATGATAGACCCAGACAAGTTCTGCAGCCTCTGCC
ATGCAACTTTCAACGACCCTGTCATGGCTCAACAACATTATGTGGGCAAGAAACACAGAAAACA
GGAGACCAAGCTCAAACTAATGGCACGCTATGGGCGGCTGGCGGACCCTGCTGTCACTGACTTT
CCAGCTGGAAAGGGCTACCCCTGCAAAACATGTAAGATAGTGCTGAACTCCATAGAACAGTACC
AAGCTCATGTCAGCGGCTTCAAACACAAGAACCAGTCACCAAAAACAGTGGCATCATCCCTGGG
CCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGACTCAACCACCTTGGAAGACTAGAGGTGA
TTCTGCCCAGCATCCCATATTGGGCCAGCCATGAGCCAGCTTCCCGTGACTGCTCAGCCCTTGG
CTCCCTCTTGCTCGTTGTTCTCACCAGGAAAGTACACGGGCCTGAGGCAGGATTGGGCCACAGA
CAGCCTCTCATTGGTCCGGGCTAATTCACTCCTGCTGCTCCCCTTTGGCAGGGGTCCTGTAGGT
CATGACAGGGGAGGCAAGGGTATTGAGAGACTCGGGGTCTCGCGGGGTGGTAGTTTGGAGGGTG
GCTTTCCCCATTTCCCAACCCCTCTGGGCCTTAGGTGCTGAGGCCCCTGCCACCTGTCTTTCCT
CTAAAGGTCAGTTTTGGGCCAGTTCTTGCAACTAAAGAGCAGAGATCTCTCTGGGCCCTAGACA
TTTCCAGCAAAACCTGGAACTTTCATGCCAAACCTGGGGCAGGGCAGGAAACAGAGGAAATGGC
TGCAACATGGGAGCTTGGAGCTAATACGACACTCTGCCTTCCCCCAGAAGGTGCAGGCTTTCCT
GAGTCTTAGACCAGATATGGCCAGTTGCGCAGGTTTCTGCCAACTGTGAAGTATCCTCCTGGAG
CAGTGACACAATCTTGGCGGAGCATTGCTACCCCCGCTGCCCCCTCCACAGTTCCTGAATGGTG
CTAAGGATCTGCAGCAGTTGGCAACGAGCTGGGGCTGGGGGCGGCCTCCATGTCCACTGAGATC
ATAGGACACTCCAATGGGGATGGGACCTTTCCCCTCCTCCATCAGAGGTGCTCTGACCCTAGGT
TACACGGGAAAGTGCCCCACATGCAAGTCTCCCTGAGGGTTCTGCCCCTAAAGGCAGACTGCCT
CATGCCCGCTAGCTGTGAGGTTCATTGCTACCCTCGGCCCTACTAGCCCTCTCTTCCCCCTTGT
GCAGCGGACCACTTGCCCAGTTTGCTGTGGTGCTAGCCTTCCCCATCATCCACCGGGTGATTTC
TGGGTCCCAGGGAAAGAAAGAGAGAGCTGATGCAGGTTTCTACAGTGAGGAACAGGCGTTTCCC
AGGCCCCACACCCAGATTTCTCTATCTTTGCTGTGTTTTATGGCCTGGGACTGAGTCCACACGG
ATAGATTTTTCCTTGTAACCTTGAGACGAGAATTCCAAGGAGTGTCACCATCAGAGGCTTCTCT
TCATTGTGTCAAAGAAGCCCCTAGCTGCTCTCGTGGCCTCCTTCCCCCACTCCCTATCCCTTCA
CCTGTGAAATGCCTTTGCTTTGCATATTGTGTGTGGATGTGTGTGTGTGTGTGTGTGTGTTTGT
GTGTATGTGTGTGCTTCTGTGTGTGCCTAATGCTCTGTCTCTTGGTCACTGAAGCATCCAAATA
AAGAATTTCCCTCATGGGCCAGACTACAACTTAACAGACCTAGGGTTTTGAGCCATATTGCCAT
TGGATCTAGTATGTCTGTCTTGACCCCTCACCCCCACCCCATTCAGACCTCAGTAGTCCCCAGT
AGTCACTTTAGGAGTTGGGACAGAGTCGAGCACCCTGTGAAAGTCTCCCTTGAGTTCAGGTGCC
CTGAACTCAGTACAGCCTCATCTTCTCATCCACCACCTTCTCCTGCTTCTCCTGTCACATAGGG
CCTCATGAAGGTCTTTAAAGGGTTTAAGCTGGGGATCTGCTTTATGTTTGAGAGAACTGTTCTG
GCTGTTATGTAAAGGAGTGCAGGGAGGGGCAGGAAAGGAGACAAGGAGGCCAGTATGGACACTG
TGTCCAGTATGGCTTTCCAGGCTAATCACTTAGGGCAGAGACCCAGCCTTATTCATCTCTACTT
CCTGATGTCCATAGTGGTGTGTCATGAATTTTTATTGAATGAACAAATGAGGTGTATGAGGAGA
GATGGTTTTCTCCTGCTCAGCTCTTACACAGTGATAGGTTTGTTCCATGGGACTTATCATAGGC
CTGGTGATTCTTGAAAGAGCATTTTTCATGACTCAAAAATGAGCTGAGAAGGAGTGTTATGGCC
AGGTGCGGCGTCATGCACCTATAGTCCCAGCTGCTCAGGAGGCTAAGGCAGAAAGACCATTCAA
GCCCAGGAGTTCCAGCCTGAAGTATGCTGTGATCATGCCTGTGAATAACCACTGCACTCCAGCC
AGGGCAACATAACAAGACTCTATCTAAAAAAAAAAAAAAATTATAAAAATAAATTTGAAGGCTG
GGCGCCGTGGCTCACGCCTGTAATCCAAGCACTTTGAGAGGCCAAGGCAGGTGGATAACCTGAG
GTCAGAAGTTCGAGACCAGCCTGGCCAACATGATGGCAAAACCCCGTCCCTATAAAAAATACGA
AAATCAGCTGCGCCTGGTGGCACACATCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAAGAGA
ATTGCTTGAACCCGGGAGGCGGAGGGTCGCATTGAGCCAAGATCGTGCCACTGCACTCCAGCCT
AGGTGACAGAGTGAGACTCCTGTCTCAAAATAAATAAATAATAAATTTTAAAAGAAGGTAGCCA
GGTGTGGTGGTGCATTCCTGTAGTCCTGGCTACCTGGAAGGGTGAGGCAGGAGGATCGCTTTAA
CCATGAGTTCAAGGCAGCAGTGAGCTATGATTATGCCACTGTACTCCAGCCTGGACAACAGAGC
AAGACCCTGTCTCTAAAAATAATAATTTTTAAAATTTAAAAAAAGAAAGGAATGTTATGGCCTC
AAGAGCTCTTTGTCCATCCTTTACTGTAGACAGCCAGATTTGAGGAAGGGGCCCAGGCAGCCTC
AGCTCCCATTCAGTGCCACTCAGCCCCTGCTCCTGGTCAGCTGTGAAAGGCTCTACACAGCCCC
AAGGGAGGTTCTCAGCTTCCCATGATCAGACTGCCTCAGCAATTCCCCAGAGTCCTTCTAAGCC
ACCTAGTATGTCAGATTCAGCCCCATCTACCAAGCAAGGAAATGAAGGGCAGGGGGTGAGTGGG
CTATCATACCGTGAGCCTCCGGCCTGCAAGACCACTTTGTAGTCCCTACCAGCTGTGTGGCCAG
CCCTGTTGGTAAAGGGACCTAGAGATGAACACTTTCTTGCCCTTAGGGGTTCACACACAGTCAA
AGATCATGATGACAATGATAAGAATGCCCAGGATGCAGGAGCTGACTCAGCCAAGGGCATGAAA
AAGCTGGAGAGGTTGGAAAGCTAGCATTTCATCTGCATAACAACCTTTGAGCTAAGAGTTAATA
TTCCATATAGAGAAGGAGGCCAGGCAGGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGC
CAAGGCGGGTGTATCACTTGCGGCCGGGAGTTTAAGACCATCCTGGCCAACGTGGTGAAATCCC
ATCTCTACAAAAAATAAAAAATAAAATAAATAAAAACCATGGAGAGAAGGAA

hide sequence

RefSeq Acc Id:

NM_001308219 ⟹ NP_001295148

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,081,189 (+)	NCBI
CHM1_1	5	175,882,083 - 175,941,073 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,624,397 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGTGGAGCACATGATCCAGAAGAACCAATGTCTCTTCACC
AACACCCAGTGTAAGGTTTGCTGCGCCTTGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACC
AGAGCAAAAAACATGCCAACAAAGTGAAGAGATACCTAGCAATCCATGGAATGGAGACATTAAA
GGGGGAAACGAAGAAGCTAGACTCAGATCAGGTCACCAAAAACAGTGGCATCATCCCTGGGCCA
GATTCCAATGCAAAGGCAACCCATTCAGAAAGACTCAACCACCTTGGAAGACTAGAGCTAGGGG
TGGCCGTGTCACAGTCTGGCCAAGGAAATGAAATTGGGAGTTGCTGTGTGGAAACTCAACTCTC
TGGAACTTCTTCCTTCCTCCTGCCTCTGCACAAATGTGACGGCAGCAGCTGAAGCCAACATCTT
GCGACCATGAGAGAAAAACCTGGAGAACGGACGAGTCCTCAACCCTGACTTCAGACCAACCTAC
ACCCACCTCTGGACGTGGGGCTAAGTGAGAGATGGATACACTGTTTCATTTAGGCCCTGCTCAC
TTAGGTTTCTGTTATTCACACCCCAACGAAACCCTCCATGGTCCAGGGCACCGGGCAAAGTACA
GAAGGGCACGAGTTTACTTCCCGCTTCCCTGGAGACCACCAACCCTCTCACCCTTCCAGCCCAG
CCTCTGCCACTTCCCAGCTGTCGGTCCTCCTCCAAACAGACGTGCATGCCAACACCCGGTGGGT
GTGAGGCTTGTAGGCCCAAGTCTAGAGAGGCTGAGTCTGGCAAAGCCTGAAAGCCCCTGTCCTA
GCAAGCCAGGCCACAGGTCTAGAGTATCCGAGACCAGTGAATAAGGGGACGGGGGGTGCTACTG
AGGCTGTGAGAAGCCCCAGGACCAGCCCAGGGTAGTTAGAACTGAGTGAGGTTAGCCGGGACTA
ACCTCACTCAGATCCCTCCTCCCCAGTTCCCCTCCATCCACTTTGGTTTGGAAGCCTCCCCAGA
GCTCTCCCAGGCTGTCATCAGCTCTAAACTCTCTGCCTCCACAAAAATGCCCTGGGCAACCTGT
AACTCACAGCCCTGCTGTCTTCAGAGTATAAACTGGAGACAGATGTACCCAGAATTGAGGACGG
GTGGGAAATGAGGAGAAATGAAGGCTGAGGAGGGGTCATTCTCACAGTCCCTCCCTTTCGGTCA
CAGGAGGGTGTTGCCCATGCTTTTGGGTGGGTCCCAGGCCCATAGCTGCAAATATTCATATTGG
CTACTCTTCAGTGAGCAAGGGGTATATGCCAGGCACTGGCATTGTGCTTGACATACATCATCAT
ACTGAGTCCTCACGGAAGATGTATTATTCCCATTTCACAGAAGATGAAACTGAGGCTTGAGGTT
AAGTGATTTGTCCGTGACCACAAAGAGTTTTCGGGACTCAAACCCAGATCTGTCACTGGGCAAG
GTGGCTCACACCTATAATCCCAGCCCTTTGGGAGACTGAGGCCAGCAGATCTCCTGTGGCCAGG
AGTTCAAGCCTGGCCAACAATGGCAAAACCCCGTCTCTACCAAAAATACAAAAATTAGCTGGGC
GTGGTGGCACACACCCGTAATCCCAGCTACTCAGGTGGCTGAGGCAGGAGAATCACTTGAACCC
AGGAGGTGGTGGTTGCAGTGAGCCTAGATCGTGCCACTGCATTCCAGCCTGAGCGACAGAGTAA
GACTCTGTCTCCAAAAAAAACCCAGATCTGTCCGACTCTGACACCCAACCTTTAATCACTCACT
TTCTGTCAATGTCACCTCCGTTTTGACCAGCCAAGCTAGACCTCCCTGGAGCCTGTGGAGAAGC
CAAGGTAGAAAAGGGTTGGAAAAGAATGATAAAATAGGCCAGGTGCGGTGGCTCAAGCCTGTAC
TCCCAGCACTTTTGGAGGCCGAGACAGGCAGATTGCTTGAGCCCAGGAGTTCAAGACCAGCCTG
GGCAACATAATGAGACCCTGTTTCAACTTAAAAAAAAGAAATGGTAATGAACAATTGTCAATTC
TGAGCAGCTGGGTATGGTATGACCCTGTGTACTTTTTCTGTATTTTAAAATGTTCTCAAAATAA
AACTTGTTT

hide sequence

RefSeq Acc Id:

NM_001308221 ⟹ NP_001295150

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI
CHM1_1	5	175,882,083 - 175,927,867 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGCTGGAAAGGGCTACCCCTGCAAAACATGTAAGATAGTG
CTGAACTCCATAGAACAGTACCAAGCTCATGTCAGCGGCTTCAAACACAAGAACCAGTCACCAA
AAACAGTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGACTCAAC
CACCTTGGAAGACTAGAGGTGATTCTGCCCAGCATCCCATATTGGGCCAGCCATGAGCCAGCTT
CCCGTGACTGCTCAGCCCTTGGCTCCCTCTTGCTCGTTGTTCTCACCAGGAAAGTACACGGGCC
TGAGGCAGGATTGGGCCACAGACAGCCTCTCATTGGTCCGGGCTAATTCACTCCTGCTGCTCCC
CTTTGGCAGGGGTCCTGTAGGTCATGACAGGGGAGGCAAGGGTATTGAGAGACTCGGGGTCTCG
CGGGGTGGTAGTTTGGAGGGTGGCTTTCCCCATTTCCCAACCCCTCTGGGCCTTAGGTGCTGAG
GCCCCTGCCACCTGTCTTTCCTCTAAAGGTCAGTTTTGGGCCAGTTCTTGCAACTAAAGAGCAG
AGATCTCTCTGGGCCCTAGACATTTCCAGCAAAACCTGGAACTTTCATGCCAAACCTGGGGCAG
GGCAGGAAACAGAGGAAATGGCTGCAACATGGGAGCTTGGAGCTAATACGACACTCTGCCTTCC
CCCAGAAGGTGCAGGCTTTCCTGAGTCTTAGACCAGATATGGCCAGTTGCGCAGGTTTCTGCCA
ACTGTGAAGTATCCTCCTGGAGCAGTGACACAATCTTGGCGGAGCATTGCTACCCCCGCTGCCC
CCTCCACAGTTCCTGAATGGTGCTAAGGATCTGCAGCAGTTGGCAACGAGCTGGGGCTGGGGGC
GGCCTCCATGTCCACTGAGATCATAGGACACTCCAATGGGGATGGGACCTTTCCCCTCCTCCAT
CAGAGGTGCTCTGACCCTAGGTTACACGGGAAAGTGCCCCACATGCAAGTCTCCCTGAGGGTTC
TGCCCCTAAAGGCAGACTGCCTCATGCCCGCTAGCTGTGAGGTTCATTGCTACCCTCGGCCCTA
CTAGCCCTCTCTTCCCCCTTGTGCAGCGGACCACTTGCCCAGTTTGCTGTGGTGCTAGCCTTCC
CCATCATCCACCGGGTGATTTCTGGGTCCCAGGGAAAGAAAGAGAGAGCTGATGCAGGTTTCTA
CAGTGAGGAACAGGCGTTTCCCAGGCCCCACACCCAGATTTCTCTATCTTTGCTGTGTTTTATG
GCCTGGGACTGAGTCCACACGGATAGATTTTTCCTTGTAACCTTGAGACGAGAATTCCAAGGAG
TGTCACCATCAGAGGCTTCTCTTCATTGTGTCAAAGAAGCCCCTAGCTGCTCTCGTGGCCTCCT
TCCCCCACTCCCTATCCCTTCACCTGTGAAATGCCTTTGCTTTGCATATTGTGTGTGGATGTGT
GTGTGTGTGTGTGTGTGTTTGTGTGTATGTGTGTGCTTCTGTGTGTGCCTAATGCTCTGTCTCT
TGGTCACTGAAGCATCCAAATAAAGAATTTCCCTCATGGGCCAGACTACAACTTAACAGACCTA
GGGTTTTGAGCCATATTGCCATTGGATCTAGTATGTCTGTCTTGACCCCTCACCCCCACCCCAT
TCAGACCTCAGTAGTCCCCAGTAGTCACTTTAGGAGTTGGGACAGAGTCGAGCACCCTGTGAAA
GTCTCCCTTGAGTTCAGGTGCCCTGAACTCAGTACAGCCTCATCTTCTCATCCACCACCTTCTC
CTGCTTCTCCTGTCACATAGGGCCTCATGAAGGTCTTTAAAGGGTTTAAGCTGGGGATCTGCTT
TATGTTTGAGAGAACTGTTCTGGCTGTTATGTAAAGGAGTGCAGGGAGGGGCAGGAAAGGAGAC
AAGGAGGCCAGTATGGACACTGTGTCCAGTATGGCTTTCCAGGCTAATCACTTAGGGCAGAGAC
CCAGCCTTATTCATCTCTACTTCCTGATGTCCATAGTGGTGTGTCATGAATTTTTATTGAATGA
ACAAATGAGGTGTATGAGGAGAGATGGTTTTCTCCTGCTCAGCTCTTACACAGTGATAGGTTTG
TTCCATGGGACTTATCATAGGCCTGGTGATTCTTGAAAGAGCATTTTTCATGACTCAAAAATGA
GCTGAGAAGGAGTGTTATGGCCAGGTGCGGCGTCATGCACCTATAGTCCCAGCTGCTCAGGAGG
CTAAGGCAGAAAGACCATTCAAGCCCAGGAGTTCCAGCCTGAAGTATGCTGTGATCATGCCTGT
GAATAACCACTGCACTCCAGCCAGGGCAACATAACAAGACTCTATCTAAAAAAAAAAAAAAATT
ATAAAAATAAATTTGAAGGCTGGGCGCCGTGGCTCACGCCTGTAATCCAAGCACTTTGAGAGGC
CAAGGCAGGTGGATAACCTGAGGTCAGAAGTTCGAGACCAGCCTGGCCAACATGATGGCAAAAC
CCCGTCCCTATAAAAAATACGAAAATCAGCTGCGCCTGGTGGCACACATCTGTAGTCCCAGCTA
CTTGGGAGGCTGAGGCAAGAGAATTGCTTGAACCCGGGAGGCGGAGGGTCGCATTGAGCCAAGA
TCGTGCCACTGCACTCCAGCCTAGGTGACAGAGTGAGACTCCTGTCTCAAAATAAATAAATAAT
AAATTTTAAAAGAAGGTAGCCAGGTGTGGTGGTGCATTCCTGTAGTCCTGGCTACCTGGAAGGG
TGAGGCAGGAGGATCGCTTTAACCATGAGTTCAAGGCAGCAGTGAGCTATGATTATGCCACTGT
ACTCCAGCCTGGACAACAGAGCAAGACCCTGTCTCTAAAAATAATAATTTTTAAAATTTAAAAA
AAGAAAGGAATGTTATGGCCTCAAGAGCTCTTTGTCCATCCTTTACTGTAGACAGCCAGATTTG
AGGAAGGGGCCCAGGCAGCCTCAGCTCCCATTCAGTGCCACTCAGCCCCTGCTCCTGGTCAGCT
GTGAAAGGCTCTACACAGCCCCAAGGGAGGTTCTCAGCTTCCCATGATCAGACTGCCTCAGCAA
TTCCCCAGAGTCCTTCTAAGCCACCTAGTATGTCAGATTCAGCCCCATCTACCAAGCAAGGAAA
TGAAGGGCAGGGGGTGAGTGGGCTATCATACCGTGAGCCTCCGGCCTGCAAGACCACTTTGTAG
TCCCTACCAGCTGTGTGGCCAGCCCTGTTGGTAAAGGGACCTAGAGATGAACACTTTCTTGCCC
TTAGGGGTTCACACACAGTCAAAGATCATGATGACAATGATAAGAATGCCCAGGATGCAGGAGC
TGACTCAGCCAAGGGCATGAAAAAGCTGGAGAGGTTGGAAAGCTAGCATTTCATCTGCATAACA
ACCTTTGAGCTAAGAGTTAATATTCCATATAGAGAAGGAGGCCAGGCAGGGTGGCTCACATCTG
TAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGTATCACTTGCGGCCGGGAGTTTAAGACCATC
CTGGCCAACGTGGTGAAATCCCATCTCTACAAAAAATAAAAAATAAAATAAATAAAAACCATGG
AGAGAAGGAA

hide sequence

RefSeq Acc Id:

NM_001308223 ⟹ NP_001295152

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,081,189 (+)	NCBI
CHM1_1	5	175,882,083 - 175,941,073 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,624,397 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGCTGGAAAGGGCTACCCCTGCAAAACATGTAAGATAGTG
CTGAACTCCATAGAACAGTACCAAGCTCATGTCAGCGGCTTCAAACACAAGAACCAGTCACCAA
AAACAGTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGACTCAAC
CACCTTGGAAGACTAGAGCTAGGGGTGGCCGTGTCACAGTCTGGCCAAGGAAATGAAATTGGGA
GTTGCTGTGTGGAAACTCAACTCTCTGGAACTTCTTCCTTCCTCCTGCCTCTGCACAAATGTGA
CGGCAGCAGCTGAAGCCAACATCTTGCGACCATGAGAGAAAAACCTGGAGAACGGACGAGTCCT
CAACCCTGACTTCAGACCAACCTACACCCACCTCTGGACGTGGGGCTAAGTGAGAGATGGATAC
ACTGTTTCATTTAGGCCCTGCTCACTTAGGTTTCTGTTATTCACACCCCAACGAAACCCTCCAT
GGTCCAGGGCACCGGGCAAAGTACAGAAGGGCACGAGTTTACTTCCCGCTTCCCTGGAGACCAC
CAACCCTCTCACCCTTCCAGCCCAGCCTCTGCCACTTCCCAGCTGTCGGTCCTCCTCCAAACAG
ACGTGCATGCCAACACCCGGTGGGTGTGAGGCTTGTAGGCCCAAGTCTAGAGAGGCTGAGTCTG
GCAAAGCCTGAAAGCCCCTGTCCTAGCAAGCCAGGCCACAGGTCTAGAGTATCCGAGACCAGTG
AATAAGGGGACGGGGGGTGCTACTGAGGCTGTGAGAAGCCCCAGGACCAGCCCAGGGTAGTTAG
AACTGAGTGAGGTTAGCCGGGACTAACCTCACTCAGATCCCTCCTCCCCAGTTCCCCTCCATCC
ACTTTGGTTTGGAAGCCTCCCCAGAGCTCTCCCAGGCTGTCATCAGCTCTAAACTCTCTGCCTC
CACAAAAATGCCCTGGGCAACCTGTAACTCACAGCCCTGCTGTCTTCAGAGTATAAACTGGAGA
CAGATGTACCCAGAATTGAGGACGGGTGGGAAATGAGGAGAAATGAAGGCTGAGGAGGGGTCAT
TCTCACAGTCCCTCCCTTTCGGTCACAGGAGGGTGTTGCCCATGCTTTTGGGTGGGTCCCAGGC
CCATAGCTGCAAATATTCATATTGGCTACTCTTCAGTGAGCAAGGGGTATATGCCAGGCACTGG
CATTGTGCTTGACATACATCATCATACTGAGTCCTCACGGAAGATGTATTATTCCCATTTCACA
GAAGATGAAACTGAGGCTTGAGGTTAAGTGATTTGTCCGTGACCACAAAGAGTTTTCGGGACTC
AAACCCAGATCTGTCACTGGGCAAGGTGGCTCACACCTATAATCCCAGCCCTTTGGGAGACTGA
GGCCAGCAGATCTCCTGTGGCCAGGAGTTCAAGCCTGGCCAACAATGGCAAAACCCCGTCTCTA
CCAAAAATACAAAAATTAGCTGGGCGTGGTGGCACACACCCGTAATCCCAGCTACTCAGGTGGC
TGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGTGGTTGCAGTGAGCCTAGATCGTGCCACTG
CATTCCAGCCTGAGCGACAGAGTAAGACTCTGTCTCCAAAAAAAACCCAGATCTGTCCGACTCT
GACACCCAACCTTTAATCACTCACTTTCTGTCAATGTCACCTCCGTTTTGACCAGCCAAGCTAG
ACCTCCCTGGAGCCTGTGGAGAAGCCAAGGTAGAAAAGGGTTGGAAAAGAATGATAAAATAGGC
CAGGTGCGGTGGCTCAAGCCTGTACTCCCAGCACTTTTGGAGGCCGAGACAGGCAGATTGCTTG
AGCCCAGGAGTTCAAGACCAGCCTGGGCAACATAATGAGACCCTGTTTCAACTTAAAAAAAAGA
AATGGTAATGAACAATTGTCAATTCTGAGCAGCTGGGTATGGTATGACCCTGTGTACTTTTTCT
GTATTTTAAAATGTTCTCAAAATAAAACTTGTTT

hide sequence

RefSeq Acc Id:

NM_001363713 ⟹ NP_001350642

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,081,189 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,624,397 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGTGGAGCACATGATCCAGAAGAACCAATGTCTCTTCACC
AACACCCAGTGTAAGGTTTGCTGCGCCTTGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACC
AGAGCAAAAAACATGCCAACAAAGTGAAGAGATACCTAGCAATCCATGGAATGGAGACATTAAA
GGGGGAAACGAAGAAGCTAGACTCAGATCAGAAGAGCAGCAGAAGCAAAGACAAGAACCAGTGC
TGCCCCATCTGTAACATGACCTTTTCCTCCCCTGTCGTGGCCCAGTCGCACTACCTGGGGAAGA
CCCACGCAAAGAACTTAAAGCTGAAGCAGCAGTCCACTAAGGTGGAAGCTCTGTCAAAACGCCT
TACAAATCCTTTCCTTGTGGCCTCCACCTTAGCCTTGCACCAGAATAGAGAGATGATAGACCCA
GACAAGTTCTGCAGCCTCTGCCATGCAACTTTCAACGACCCTGTCATGGCTCAACAACATTATG
TGGGCAAGAAACACAGAAAACAGGAGACCAAGCTCAAACTAATGGCACGCTATGGGCGGCTGGC
GGACCCTGCTGTCACTGACTTTCCAGCTGGAAAGGGCTACCCCTGCAAAACATGTAAGATAGTG
CTGAACTCCATAGAACAGTACCAAGCTCATGTCAGCGGCTTCAAACACAAGAACCAGTCACCAA
AAACAGTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGACTCAAC
CACCTTGGAAGACTAGAGCTAGGGGTGGCCGTGTCACAGTCTGGCCAAGGAAATGAAATTGGGA
GTTGCTGTGTGGAAACTCAACTCTCTGGAACTTCTTCCTTCCTCCTGCCTCTGCACAAATGTGA
CGGCAGCAGCTGAAGCCAACATCTTGCGACCATGAGAGAAAAACCTGGAGAACGGACGAGTCCT
CAACCCTGACTTCAGACCAACCTACACCCACCTCTGGACGTGGGGCTAAGTGAGAGATGGATAC
ACTGTTTCATTTAGGCCCTGCTCACTTAGGTTTCTGTTATTCACACCCCAACGAAACCCTCCAT
GGTCCAGGGCACCGGGCAAAGTACAGAAGGGCACGAGTTTACTTCCCGCTTCCCTGGAGACCAC
CAACCCTCTCACCCTTCCAGCCCAGCCTCTGCCACTTCCCAGCTGTCGGTCCTCCTCCAAACAG
ACGTGCATGCCAACACCCGGTGGGTGTGAGGCTTGTAGGCCCAAGTCTAGAGAGGCTGAGTCTG
GCAAAGCCTGAAAGCCCCTGTCCTAGCAAGCCAGGCCACAGGTCTAGAGTATCCGAGACCAGTG
AATAAGGGGACGGGGGGTGCTACTGAGGCTGTGAGAAGCCCCAGGACCAGCCCAGGGTAGTTAG
AACTGAGTGAGGTTAGCCGGGACTAACCTCACTCAGATCCCTCCTCCCCAGTTCCCCTCCATCC
ACTTTGGTTTGGAAGCCTCCCCAGAGCTCTCCCAGGCTGTCATCAGCTCTAAACTCTCTGCCTC
CACAAAAATGCCCTGGGCAACCTGTAACTCACAGCCCTGCTGTCTTCAGAGTATAAACTGGAGA
CAGATGTACCCAGAATTGAGGACGGGTGGGAAATGAGGAGAAATGAAGGCTGAGGAGGGGTCAT
TCTCACAGTCCCTCCCTTTCGGTCACAGGAGGGTGTTGCCCATGCTTTTGGGTGGGTCCCAGGC
CCATAGCTGCAAATATTCATATTGGCTACTCTTCAGTGAGCAAGGGGTATATGCCAGGCACTGG
CATTGTGCTTGACATACATCATCATACTGAGTCCTCACGGAAGATGTATTATTCCCATTTCACA
GAAGATGAAACTGAGGCTTGAGGTTAAGTGATTTGTCCGTGACCACAAAGAGTTTTCGGGACTC
AAACCCAGATCTGTCACTGGGCAAGGTGGCTCACACCTATAATCCCAGCCCTTTGGGAGACTGA
GGCCAGCAGATCTCCTGTGGCCAGGAGTTCAAGCCTGGCCAACAATGGCAAAACCCCGTCTCTA
CCAAAAATACAAAAATTAGCTGGGCGTGGTGGCACACACCCGTAATCCCAGCTACTCAGGTGGC
TGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGTGGTTGCAGTGAGCCTAGATCGTGCCACTG
CATTCCAGCCTGAGCGACAGAGTAAGACTCTGTCTCCAAAAAAAACCCAGATCTGTCCGACTCT
GACACCCAACCTTTAATCACTCACTTTCTGTCAATGTCACCTCCGTTTTGACCAGCCAAGCTAG
ACCTCCCTGGAGCCTGTGGAGAAGCCAAGGTAGAAAAGGGTTGGAAAAGAATGATAAAATAGGC
CAGGTGCGGTGGCTCAAGCCTGTACTCCCAGCACTTTTGGAGGCCGAGACAGGCAGATTGCTTG
AGCCCAGGAGTTCAAGACCAGCCTGGGCAACATAATGAGACCCTGTTTCAACTTAAAAAAAAGA
AATGGTAATGAACAATTGTCAATTCTGAGCAGCTGGGTATGGTATGACCCTGTGTACTTTTTCT
GTATTTTAAAATGTTCTCAAAATAAAACTTGTTT

hide sequence

RefSeq Acc Id:

NM_012279 ⟹ NP_036411

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI
GRCh37	5	176,449,681 - 176,508,189 (+)	NCBI
Build 36	5	176,382,303 - 176,426,364 (+)	NCBI Archive
Celera	5	172,007,563 - 172,051,635 (-)	RGD
HuRef	5	171,371,845 - 171,415,482 (+)	ENTREZGENE
CHM1_1	5	175,882,083 - 175,927,867 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGTGGAGCACATGATCCAGAAGAACCAATGTCTCTTCACC
AACACCCAGTGTAAGGTTTGCTGCGCCTTGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACC
AGAGCAAAAAACATGCCAACAAAGTGAAGAGATACCTAGCAATCCATGGAATGGAGACATTAAA
GGGGGAAACGAAGAAGCTAGACTCAGATCAGAAGAGCAGCAGAAGCAAAGACAAGAACCAGTGC
TGCCCCATCTGTAACATGACCTTTTCCTCCCCTGTCGTGGCCCAGTCGCACTACCTGGGGAAGA
CCCACGCAAAGAACTTAAAGCTGAAGCAGCAGTCCACTAAGGTGGAAGCCTTGCACCAGAATAG
AGAGATGATAGACCCAGACAAGTTCTGCAGCCTCTGCCATGCAACTTTCAACGACCCTGTCATG
GCTCAACAACATTATGTGGGCAAGAAACACAGAAAACAGGAGACCAAGCTCAAACTAATGGCAC
GCTATGGGCGGCTGGCGGACCCTGCTGTCACTGACTTTCCAGCTGGAAAGGGCTACCCCTGCAA
AACATGTAAGATAGTGCTGAACTCCATAGAACAGTACCAAGCTCATGTCAGCGGCTTCAAACAC
AAGAACCAGTCACCAAAAACAGTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGCAACCCA
TTCAGAAAGACTCAACCACCTTGGAAGACTAGAGGTGATTCTGCCCAGCATCCCATATTGGGCC
AGCCATGAGCCAGCTTCCCGTGACTGCTCAGCCCTTGGCTCCCTCTTGCTCGTTGTTCTCACCA
GGAAAGTACACGGGCCTGAGGCAGGATTGGGCCACAGACAGCCTCTCATTGGTCCGGGCTAATT
CACTCCTGCTGCTCCCCTTTGGCAGGGGTCCTGTAGGTCATGACAGGGGAGGCAAGGGTATTGA
GAGACTCGGGGTCTCGCGGGGTGGTAGTTTGGAGGGTGGCTTTCCCCATTTCCCAACCCCTCTG
GGCCTTAGGTGCTGAGGCCCCTGCCACCTGTCTTTCCTCTAAAGGTCAGTTTTGGGCCAGTTCT
TGCAACTAAAGAGCAGAGATCTCTCTGGGCCCTAGACATTTCCAGCAAAACCTGGAACTTTCAT
GCCAAACCTGGGGCAGGGCAGGAAACAGAGGAAATGGCTGCAACATGGGAGCTTGGAGCTAATA
CGACACTCTGCCTTCCCCCAGAAGGTGCAGGCTTTCCTGAGTCTTAGACCAGATATGGCCAGTT
GCGCAGGTTTCTGCCAACTGTGAAGTATCCTCCTGGAGCAGTGACACAATCTTGGCGGAGCATT
GCTACCCCCGCTGCCCCCTCCACAGTTCCTGAATGGTGCTAAGGATCTGCAGCAGTTGGCAACG
AGCTGGGGCTGGGGGCGGCCTCCATGTCCACTGAGATCATAGGACACTCCAATGGGGATGGGAC
CTTTCCCCTCCTCCATCAGAGGTGCTCTGACCCTAGGTTACACGGGAAAGTGCCCCACATGCAA
GTCTCCCTGAGGGTTCTGCCCCTAAAGGCAGACTGCCTCATGCCCGCTAGCTGTGAGGTTCATT
GCTACCCTCGGCCCTACTAGCCCTCTCTTCCCCCTTGTGCAGCGGACCACTTGCCCAGTTTGCT
GTGGTGCTAGCCTTCCCCATCATCCACCGGGTGATTTCTGGGTCCCAGGGAAAGAAAGAGAGAG
CTGATGCAGGTTTCTACAGTGAGGAACAGGCGTTTCCCAGGCCCCACACCCAGATTTCTCTATC
TTTGCTGTGTTTTATGGCCTGGGACTGAGTCCACACGGATAGATTTTTCCTTGTAACCTTGAGA
CGAGAATTCCAAGGAGTGTCACCATCAGAGGCTTCTCTTCATTGTGTCAAAGAAGCCCCTAGCT
GCTCTCGTGGCCTCCTTCCCCCACTCCCTATCCCTTCACCTGTGAAATGCCTTTGCTTTGCATA
TTGTGTGTGGATGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTATGTGTGTGCTTCTGTGTGTGC
CTAATGCTCTGTCTCTTGGTCACTGAAGCATCCAAATAAAGAATTTCCCTCATGGGCCAGACTA
CAACTTAACAGACCTAGGGTTTTGAGCCATATTGCCATTGGATCTAGTATGTCTGTCTTGACCC
CTCACCCCCACCCCATTCAGACCTCAGTAGTCCCCAGTAGTCACTTTAGGAGTTGGGACAGAGT
CGAGCACCCTGTGAAAGTCTCCCTTGAGTTCAGGTGCCCTGAACTCAGTACAGCCTCATCTTCT
CATCCACCACCTTCTCCTGCTTCTCCTGTCACATAGGGCCTCATGAAGGTCTTTAAAGGGTTTA
AGCTGGGGATCTGCTTTATGTTTGAGAGAACTGTTCTGGCTGTTATGTAAAGGAGTGCAGGGAG
GGGCAGGAAAGGAGACAAGGAGGCCAGTATGGACACTGTGTCCAGTATGGCTTTCCAGGCTAAT
CACTTAGGGCAGAGACCCAGCCTTATTCATCTCTACTTCCTGATGTCCATAGTGGTGTGTCATG
AATTTTTATTGAATGAACAAATGAGGTGTATGAGGAGAGATGGTTTTCTCCTGCTCAGCTCTTA
CACAGTGATAGGTTTGTTCCATGGGACTTATCATAGGCCTGGTGATTCTTGAAAGAGCATTTTT
CATGACTCAAAAATGAGCTGAGAAGGAGTGTTATGGCCAGGTGCGGCGTCATGCACCTATAGTC
CCAGCTGCTCAGGAGGCTAAGGCAGAAAGACCATTCAAGCCCAGGAGTTCCAGCCTGAAGTATG
CTGTGATCATGCCTGTGAATAACCACTGCACTCCAGCCAGGGCAACATAACAAGACTCTATCTA
AAAAAAAAAAAAAATTATAAAAATAAATTTGAAGGCTGGGCGCCGTGGCTCACGCCTGTAATCC
AAGCACTTTGAGAGGCCAAGGCAGGTGGATAACCTGAGGTCAGAAGTTCGAGACCAGCCTGGCC
AACATGATGGCAAAACCCCGTCCCTATAAAAAATACGAAAATCAGCTGCGCCTGGTGGCACACA
TCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAAGAGAATTGCTTGAACCCGGGAGGCGGAGGG
TCGCATTGAGCCAAGATCGTGCCACTGCACTCCAGCCTAGGTGACAGAGTGAGACTCCTGTCTC
AAAATAAATAAATAATAAATTTTAAAAGAAGGTAGCCAGGTGTGGTGGTGCATTCCTGTAGTCC
TGGCTACCTGGAAGGGTGAGGCAGGAGGATCGCTTTAACCATGAGTTCAAGGCAGCAGTGAGCT
ATGATTATGCCACTGTACTCCAGCCTGGACAACAGAGCAAGACCCTGTCTCTAAAAATAATAAT
TTTTAAAATTTAAAAAAAGAAAGGAATGTTATGGCCTCAAGAGCTCTTTGTCCATCCTTTACTG
TAGACAGCCAGATTTGAGGAAGGGGCCCAGGCAGCCTCAGCTCCCATTCAGTGCCACTCAGCCC
CTGCTCCTGGTCAGCTGTGAAAGGCTCTACACAGCCCCAAGGGAGGTTCTCAGCTTCCCATGAT
CAGACTGCCTCAGCAATTCCCCAGAGTCCTTCTAAGCCACCTAGTATGTCAGATTCAGCCCCAT
CTACCAAGCAAGGAAATGAAGGGCAGGGGGTGAGTGGGCTATCATACCGTGAGCCTCCGGCCTG
CAAGACCACTTTGTAGTCCCTACCAGCTGTGTGGCCAGCCCTGTTGGTAAAGGGACCTAGAGAT
GAACACTTTCTTGCCCTTAGGGGTTCACACACAGTCAAAGATCATGATGACAATGATAAGAATG
CCCAGGATGCAGGAGCTGACTCAGCCAAGGGCATGAAAAAGCTGGAGAGGTTGGAAAGCTAGCA
TTTCATCTGCATAACAACCTTTGAGCTAAGAGTTAATATTCCATATAGAGAAGGAGGCCAGGCA
GGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGTATCACTTGCGGCCG
GGAGTTTAAGACCATCCTGGCCAACGTGGTGAAATCCCATCTCTACAAAAAATAAAAAATAAAA
TAAATAAAAACCATGGAGAGAAGGAA

hide sequence

RefSeq Acc Id:

NR_131773

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI
CHM1_1	5	175,882,083 - 175,927,867 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGTGGAGCACATGATCCAGAAGAACCAATGTCTCTTCACC
AACACCCAGTGTAAGGTTTGCTGCGCCTTGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACC
AGAGCAAAAAACATGCCAACAAAGTGAAGAGATACCTAGCAATCCATGGAATGGAGACATTAAA
GGGGGAAACGAAGAAGCTAGACTCAGATCAGCCTTGCACCAGAATAGAGAGATGATAGACCCAG
ACAAGTTCTGCAGCCTCTGCCATGCAACTTTCAACGACCCTGTCATGGCTCAACAACATTATGT
GGGCAAGAAACACAGAAAACAGGAGACCAAGCTCAAACTAATGGCACGCTATGGGCGGCTGGCG
GACCCTGCTGTCACTGACTTTCCAGCTGGAAAGGGCTACCCCTGCAAAACATGTAAGATAGTGC
TGAACTCCATAGAACAGTACCAAGCTCATGTCAGCGGCTTCAAACACAAGAACCAGTCACCAAA
AACAGTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGACTCAACC
ACCTTGGAAGACTAGAGGTGATTCTGCCCAGCATCCCATATTGGGCCAGCCATGAGCCAGCTTC
CCGTGACTGCTCAGCCCTTGGCTCCCTCTTGCTCGTTGTTCTCACCAGGAAAGTACACGGGCCT
GAGGCAGGATTGGGCCACAGACAGCCTCTCATTGGTCCGGGCTAATTCACTCCTGCTGCTCCCC
TTTGGCAGGGGTCCTGTAGGTCATGACAGGGGAGGCAAGGGTATTGAGAGACTCGGGGTCTCGC
GGGGTGGTAGTTTGGAGGGTGGCTTTCCCCATTTCCCAACCCCTCTGGGCCTTAGGTGCTGAGG
CCCCTGCCACCTGTCTTTCCTCTAAAGGTCAGTTTTGGGCCAGTTCTTGCAACTAAAGAGCAGA
GATCTCTCTGGGCCCTAGACATTTCCAGCAAAACCTGGAACTTTCATGCCAAACCTGGGGCAGG
GCAGGAAACAGAGGAAATGGCTGCAACATGGGAGCTTGGAGCTAATACGACACTCTGCCTTCCC
CCAGAAGGTGCAGGCTTTCCTGAGTCTTAGACCAGATATGGCCAGTTGCGCAGGTTTCTGCCAA
CTGTGAAGTATCCTCCTGGAGCAGTGACACAATCTTGGCGGAGCATTGCTACCCCCGCTGCCCC
CTCCACAGTTCCTGAATGGTGCTAAGGATCTGCAGCAGTTGGCAACGAGCTGGGGCTGGGGGCG
GCCTCCATGTCCACTGAGATCATAGGACACTCCAATGGGGATGGGACCTTTCCCCTCCTCCATC
AGAGGTGCTCTGACCCTAGGTTACACGGGAAAGTGCCCCACATGCAAGTCTCCCTGAGGGTTCT
GCCCCTAAAGGCAGACTGCCTCATGCCCGCTAGCTGTGAGGTTCATTGCTACCCTCGGCCCTAC
TAGCCCTCTCTTCCCCCTTGTGCAGCGGACCACTTGCCCAGTTTGCTGTGGTGCTAGCCTTCCC
CATCATCCACCGGGTGATTTCTGGGTCCCAGGGAAAGAAAGAGAGAGCTGATGCAGGTTTCTAC
AGTGAGGAACAGGCGTTTCCCAGGCCCCACACCCAGATTTCTCTATCTTTGCTGTGTTTTATGG
CCTGGGACTGAGTCCACACGGATAGATTTTTCCTTGTAACCTTGAGACGAGAATTCCAAGGAGT
GTCACCATCAGAGGCTTCTCTTCATTGTGTCAAAGAAGCCCCTAGCTGCTCTCGTGGCCTCCTT
CCCCCACTCCCTATCCCTTCACCTGTGAAATGCCTTTGCTTTGCATATTGTGTGTGGATGTGTG
TGTGTGTGTGTGTGTGTTTGTGTGTATGTGTGTGCTTCTGTGTGTGCCTAATGCTCTGTCTCTT
GGTCACTGAAGCATCCAAATAAAGAATTTCCCTCATGGGCCAGACTACAACTTAACAGACCTAG
GGTTTTGAGCCATATTGCCATTGGATCTAGTATGTCTGTCTTGACCCCTCACCCCCACCCCATT
CAGACCTCAGTAGTCCCCAGTAGTCACTTTAGGAGTTGGGACAGAGTCGAGCACCCTGTGAAAG
TCTCCCTTGAGTTCAGGTGCCCTGAACTCAGTACAGCCTCATCTTCTCATCCACCACCTTCTCC
TGCTTCTCCTGTCACATAGGGCCTCATGAAGGTCTTTAAAGGGTTTAAGCTGGGGATCTGCTTT
ATGTTTGAGAGAACTGTTCTGGCTGTTATGTAAAGGAGTGCAGGGAGGGGCAGGAAAGGAGACA
AGGAGGCCAGTATGGACACTGTGTCCAGTATGGCTTTCCAGGCTAATCACTTAGGGCAGAGACC
CAGCCTTATTCATCTCTACTTCCTGATGTCCATAGTGGTGTGTCATGAATTTTTATTGAATGAA
CAAATGAGGTGTATGAGGAGAGATGGTTTTCTCCTGCTCAGCTCTTACACAGTGATAGGTTTGT
TCCATGGGACTTATCATAGGCCTGGTGATTCTTGAAAGAGCATTTTTCATGACTCAAAAATGAG
CTGAGAAGGAGTGTTATGGCCAGGTGCGGCGTCATGCACCTATAGTCCCAGCTGCTCAGGAGGC
TAAGGCAGAAAGACCATTCAAGCCCAGGAGTTCCAGCCTGAAGTATGCTGTGATCATGCCTGTG
AATAACCACTGCACTCCAGCCAGGGCAACATAACAAGACTCTATCTAAAAAAAAAAAAAAATTA
TAAAAATAAATTTGAAGGCTGGGCGCCGTGGCTCACGCCTGTAATCCAAGCACTTTGAGAGGCC
AAGGCAGGTGGATAACCTGAGGTCAGAAGTTCGAGACCAGCCTGGCCAACATGATGGCAAAACC
CCGTCCCTATAAAAAATACGAAAATCAGCTGCGCCTGGTGGCACACATCTGTAGTCCCAGCTAC
TTGGGAGGCTGAGGCAAGAGAATTGCTTGAACCCGGGAGGCGGAGGGTCGCATTGAGCCAAGAT
CGTGCCACTGCACTCCAGCCTAGGTGACAGAGTGAGACTCCTGTCTCAAAATAAATAAATAATA
AATTTTAAAAGAAGGTAGCCAGGTGTGGTGGTGCATTCCTGTAGTCCTGGCTACCTGGAAGGGT
GAGGCAGGAGGATCGCTTTAACCATGAGTTCAAGGCAGCAGTGAGCTATGATTATGCCACTGTA
CTCCAGCCTGGACAACAGAGCAAGACCCTGTCTCTAAAAATAATAATTTTTAAAATTTAAAAAA
AGAAAGGAATGTTATGGCCTCAAGAGCTCTTTGTCCATCCTTTACTGTAGACAGCCAGATTTGA
GGAAGGGGCCCAGGCAGCCTCAGCTCCCATTCAGTGCCACTCAGCCCCTGCTCCTGGTCAGCTG
TGAAAGGCTCTACACAGCCCCAAGGGAGGTTCTCAGCTTCCCATGATCAGACTGCCTCAGCAAT
TCCCCAGAGTCCTTCTAAGCCACCTAGTATGTCAGATTCAGCCCCATCTACCAAGCAAGGAAAT
GAAGGGCAGGGGGTGAGTGGGCTATCATACCGTGAGCCTCCGGCCTGCAAGACCACTTTGTAGT
CCCTACCAGCTGTGTGGCCAGCCCTGTTGGTAAAGGGACCTAGAGATGAACACTTTCTTGCCCT
TAGGGGTTCACACACAGTCAAAGATCATGATGACAATGATAAGAATGCCCAGGATGCAGGAGCT
GACTCAGCCAAGGGCATGAAAAAGCTGGAGAGGTTGGAAAGCTAGCATTTCATCTGCATAACAA
CCTTTGAGCTAAGAGTTAATATTCCATATAGAGAAGGAGGCCAGGCAGGGTGGCTCACATCTGT
AATCCCAGCACTTTGGGAGGCCAAGGCGGGTGTATCACTTGCGGCCGGGAGTTTAAGACCATCC
TGGCCAACGTGGTGAAATCCCATCTCTACAAAAAATAAAAAATAAAATAAATAAAAACCATGGA
GAGAAGGAA

hide sequence

RefSeq Acc Id:

NR_131774

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI
CHM1_1	5	175,882,083 - 175,927,867 (+)	NCBI
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

Sequence:

show sequence

AGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCCGCGCCGGCC
ACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGCTGGAGGGCC
AGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGG
TGCCCAGCCGGTGGGTAGAGAGGAAGTGGAGCACATGATCCAGAAGAACCAATGTCTCTTCACC
AACACCCAGTGTAAGGTTTGCTGCGCCTTGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACC
AGAGCAAAAAACATGCCAACAAAGTGAAGAGATACCTAGCAATCCATGGAATGGAGACATTAAA
GGGGGAAACGAAGAAGCTAGACTCAGATCAGCTGGAAAGGGCTACCCCTGCAAAACATGTAAGA
TAGTGCTGAACTCCATAGAACAGTACCAAGCTCATGTCAGCGGCTTCAAACACAAGAACCAGTC
ACCAAAAACAGTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGAC
TCAACCACCTTGGAAGACTAGAGGTGATTCTGCCCAGCATCCCATATTGGGCCAGCCATGAGCC
AGCTTCCCGTGACTGCTCAGCCCTTGGCTCCCTCTTGCTCGTTGTTCTCACCAGGAAAGTACAC
GGGCCTGAGGCAGGATTGGGCCACAGACAGCCTCTCATTGGTCCGGGCTAATTCACTCCTGCTG
CTCCCCTTTGGCAGGGGTCCTGTAGGTCATGACAGGGGAGGCAAGGGTATTGAGAGACTCGGGG
TCTCGCGGGGTGGTAGTTTGGAGGGTGGCTTTCCCCATTTCCCAACCCCTCTGGGCCTTAGGTG
CTGAGGCCCCTGCCACCTGTCTTTCCTCTAAAGGTCAGTTTTGGGCCAGTTCTTGCAACTAAAG
AGCAGAGATCTCTCTGGGCCCTAGACATTTCCAGCAAAACCTGGAACTTTCATGCCAAACCTGG
GGCAGGGCAGGAAACAGAGGAAATGGCTGCAACATGGGAGCTTGGAGCTAATACGACACTCTGC
CTTCCCCCAGAAGGTGCAGGCTTTCCTGAGTCTTAGACCAGATATGGCCAGTTGCGCAGGTTTC
TGCCAACTGTGAAGTATCCTCCTGGAGCAGTGACACAATCTTGGCGGAGCATTGCTACCCCCGC
TGCCCCCTCCACAGTTCCTGAATGGTGCTAAGGATCTGCAGCAGTTGGCAACGAGCTGGGGCTG
GGGGCGGCCTCCATGTCCACTGAGATCATAGGACACTCCAATGGGGATGGGACCTTTCCCCTCC
TCCATCAGAGGTGCTCTGACCCTAGGTTACACGGGAAAGTGCCCCACATGCAAGTCTCCCTGAG
GGTTCTGCCCCTAAAGGCAGACTGCCTCATGCCCGCTAGCTGTGAGGTTCATTGCTACCCTCGG
CCCTACTAGCCCTCTCTTCCCCCTTGTGCAGCGGACCACTTGCCCAGTTTGCTGTGGTGCTAGC
CTTCCCCATCATCCACCGGGTGATTTCTGGGTCCCAGGGAAAGAAAGAGAGAGCTGATGCAGGT
TTCTACAGTGAGGAACAGGCGTTTCCCAGGCCCCACACCCAGATTTCTCTATCTTTGCTGTGTT
TTATGGCCTGGGACTGAGTCCACACGGATAGATTTTTCCTTGTAACCTTGAGACGAGAATTCCA
AGGAGTGTCACCATCAGAGGCTTCTCTTCATTGTGTCAAAGAAGCCCCTAGCTGCTCTCGTGGC
CTCCTTCCCCCACTCCCTATCCCTTCACCTGTGAAATGCCTTTGCTTTGCATATTGTGTGTGGA
TGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTATGTGTGTGCTTCTGTGTGTGCCTAATGCTCTG
TCTCTTGGTCACTGAAGCATCCAAATAAAGAATTTCCCTCATGGGCCAGACTACAACTTAACAG
ACCTAGGGTTTTGAGCCATATTGCCATTGGATCTAGTATGTCTGTCTTGACCCCTCACCCCCAC
CCCATTCAGACCTCAGTAGTCCCCAGTAGTCACTTTAGGAGTTGGGACAGAGTCGAGCACCCTG
TGAAAGTCTCCCTTGAGTTCAGGTGCCCTGAACTCAGTACAGCCTCATCTTCTCATCCACCACC
TTCTCCTGCTTCTCCTGTCACATAGGGCCTCATGAAGGTCTTTAAAGGGTTTAAGCTGGGGATC
TGCTTTATGTTTGAGAGAACTGTTCTGGCTGTTATGTAAAGGAGTGCAGGGAGGGGCAGGAAAG
GAGACAAGGAGGCCAGTATGGACACTGTGTCCAGTATGGCTTTCCAGGCTAATCACTTAGGGCA
GAGACCCAGCCTTATTCATCTCTACTTCCTGATGTCCATAGTGGTGTGTCATGAATTTTTATTG
AATGAACAAATGAGGTGTATGAGGAGAGATGGTTTTCTCCTGCTCAGCTCTTACACAGTGATAG
GTTTGTTCCATGGGACTTATCATAGGCCTGGTGATTCTTGAAAGAGCATTTTTCATGACTCAAA
AATGAGCTGAGAAGGAGTGTTATGGCCAGGTGCGGCGTCATGCACCTATAGTCCCAGCTGCTCA
GGAGGCTAAGGCAGAAAGACCATTCAAGCCCAGGAGTTCCAGCCTGAAGTATGCTGTGATCATG
CCTGTGAATAACCACTGCACTCCAGCCAGGGCAACATAACAAGACTCTATCTAAAAAAAAAAAA
AAATTATAAAAATAAATTTGAAGGCTGGGCGCCGTGGCTCACGCCTGTAATCCAAGCACTTTGA
GAGGCCAAGGCAGGTGGATAACCTGAGGTCAGAAGTTCGAGACCAGCCTGGCCAACATGATGGC
AAAACCCCGTCCCTATAAAAAATACGAAAATCAGCTGCGCCTGGTGGCACACATCTGTAGTCCC
AGCTACTTGGGAGGCTGAGGCAAGAGAATTGCTTGAACCCGGGAGGCGGAGGGTCGCATTGAGC
CAAGATCGTGCCACTGCACTCCAGCCTAGGTGACAGAGTGAGACTCCTGTCTCAAAATAAATAA
ATAATAAATTTTAAAAGAAGGTAGCCAGGTGTGGTGGTGCATTCCTGTAGTCCTGGCTACCTGG
AAGGGTGAGGCAGGAGGATCGCTTTAACCATGAGTTCAAGGCAGCAGTGAGCTATGATTATGCC
ACTGTACTCCAGCCTGGACAACAGAGCAAGACCCTGTCTCTAAAAATAATAATTTTTAAAATTT
AAAAAAAGAAAGGAATGTTATGGCCTCAAGAGCTCTTTGTCCATCCTTTACTGTAGACAGCCAG
ATTTGAGGAAGGGGCCCAGGCAGCCTCAGCTCCCATTCAGTGCCACTCAGCCCCTGCTCCTGGT
CAGCTGTGAAAGGCTCTACACAGCCCCAAGGGAGGTTCTCAGCTTCCCATGATCAGACTGCCTC
AGCAATTCCCCAGAGTCCTTCTAAGCCACCTAGTATGTCAGATTCAGCCCCATCTACCAAGCAA
GGAAATGAAGGGCAGGGGGTGAGTGGGCTATCATACCGTGAGCCTCCGGCCTGCAAGACCACTT
TGTAGTCCCTACCAGCTGTGTGGCCAGCCCTGTTGGTAAAGGGACCTAGAGATGAACACTTTCT
TGCCCTTAGGGGTTCACACACAGTCAAAGATCATGATGACAATGATAAGAATGCCCAGGATGCA
GGAGCTGACTCAGCCAAGGGCATGAAAAAGCTGGAGAGGTTGGAAAGCTAGCATTTCATCTGCA
TAACAACCTTTGAGCTAAGAGTTAATATTCCATATAGAGAAGGAGGCCAGGCAGGGTGGCTCAC
ATCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGTATCACTTGCGGCCGGGAGTTTAAGA
CCATCCTGGCCAACGTGGTGAAATCCCATCTCTACAAAAAATAAAAAATAAAATAAATAAAAAC
CATGGAGAGAAGGAA

hide sequence

RefSeq Acc Id:

XM_005265864 ⟹ XP_005265921

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI
GRCh37	5	176,449,681 - 176,508,189 (+)	NCBI

Sequence:

show sequence

GAAGATGGAGTATCCCGCGCCGGCCACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTAC
AGCAGCTCGGAGTTGCTGGAGGGCCAGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGC
GCCGCCTGTGGGAAGCCGTGTCCGGTGCCCAGCCGGTGGGTAGAGAGGAAGCGCAGTTTTTCCC
ACATTCGAGGACTGTCATCCCTATACTCGTCCTGTCGGAGACCTACAGTCTTTGCCATCCCGTG
GAGCACATGATCCAGAAGAACCAATGTCTCTTCACCAACACCCAGTGTAAGGTTTGCTGCGCCT
TGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACCAGAGCAAAAAACATGCCAACAAAGTGAA
GAGATACCTAGCAATCCATGGAATGGAGACATTAAAGGGGGAAACGAAGAAGCTAGACTCAGAT
CAGAAGAGCAGCAGAAGCAAAGACAAGAACCAGTGCTGCCCCATCTGTAACATGACCTTTTCCT
CCCCTGTCGTGGCCCAGTCGCACTACCTGGGGAAGACCCACGCAAAGAACTTAAAGCTGAAGCA
GCAGTCCACTAAGGTGGAAGCTGGAAAGGGCTACCCCTGCAAAACATGTAAGATAGTGCTGAAC
TCCATAGAACAGTACCAAGCTCATGTCAGCGGCTTCAAACACAAGAACCAGTCACCAAAAACAG
TGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGACTCAACCACCTT
GGAAGACTAGAGGTGATTCTGCCCAGCATCCCATATTGGGCCAGCCATGAGCCAGCTTCCCGTG
ACTGCTCAGCCCTTGGCTCCCTCTTGCTCGTTGTTCTCACCAGGAAAGTACACGGGCCTGAGGC
AGGATTGGGCCACAGACAGCCTCTCATTGGTCCGGGCTAATTCACTCCTGCTGCTCCCCTTTGG
CAGGGGTCCTGTAGGTCATGACAGGGGAGGCAAGGGTATTGAGAGACTCGGGGTCTCGCGGGGT
GGTAGTTTGGAGGGTGGCTTTCCCCATTTCCCAACCCCTCTGGGCCTTAGGTGCTGAGGCCCCT
GCCACCTGTCTTTCCTCTAAAGGTCAGTTTTGGGCCAGTTCTTGCAACTAAAGAGCAGAGATCT
CTCTGGGCCCTAGACATTTCCAGCAAAACCTGGAACTTTCATGCCAAACCTGGGGCAGGGCAGG
AAACAGAGGAAATGGCTGCAACATGGGAGCTTGGAGCTAATACGACACTCTGCCTTCCCCCAGA
AGGTGCAGGCTTTCCTGAGTCTTAGACCAGATATGGCCAGTTGCGCAGGTTTCTGCCAACTGTG
AAGTATCCTCCTGGAGCAGTGACACAATCTTGGCGGAGCATTGCTACCCCCGCTGCCCCCTCCA
CAGTTCCTGAATGGTGCTAAGGATCTGCAGCAGTTGGCAACGAGCTGGGGCTGGGGGCGGCCTC
CATGTCCACTGAGATCATAGGACACTCCAATGGGGATGGGACCTTTCCCCTCCTCCATCAGAGG
TGCTCTGACCCTAGGTTACACGGGAAAGTGCCCCACATGCAAGTCTCCCTGAGGGTTCTGCCCC
TAAAGGCAGACTGCCTCATGCCCGCTAGCTGTGAGGTTCATTGCTACCCTCGGCCCTACTAGCC
CTCTCTTCCCCCTTGTGCAGCGGACCACTTGCCCAGTTTGCTGTGGTGCTAGCCTTCCCCATCA
TCCACCGGGTGATTTCTGGGTCCCAGGGAAAGAAAGAGAGAGCTGATGCAGGTTTCTACAGTGA
GGAACAGGCGTTTCCCAGGCCCCACACCCAGATTTCTCTATCTTTGCTGTGTTTTATGGCCTGG
GACTGAGTCCACACGGATAGATTTTTCCTTGTAACCTTGAGACGAGAATTCCAAGGAGTGTCAC
CATCAGAGGCTTCTCTTCATTGTGTCAAAGAAGCCCCTAGCTGCTCTCGTGGCCTCCTTCCCCC
ACTCCCTATCCCTTCACCTGTGAAATGCCTTTGCTTTGCATATTGTGTGTGGATGTGTGTGTGT
GTGTGTGTGTGTTTGTGTGTATGTGTGTGCTTCTGTGTGTGCCTAATGCTCTGTCTCTTGGTCA
CTGAAGCATCCAAATAAAGAATTTCCCTCATGGGCCAGACTACAACTTAACAGACCTAGGGTTT
TGAGCCATATTGCCATTGGATCTAGTATGTCTGTCTTGACCCCTCACCCCCACCCCATTCAGAC
CTCAGTAGTCCCCAGTAGTCACTTTAGGAGTTGGGACAGAGTCGAGCACCCTGTGAAAGTCTCC
CTTGAGTTCAGGTGCCCTGAACTCAGTACAGCCTCATCTTCTCATCCACCACCTTCTCCTGCTT
CTCCTGTCACATAGGGCCTCATGAAGGTCTTTAAAGGGTTTAAGCTGGGGATCTGCTTTATGTT
TGAGAGAACTGTTCTGGCTGTTATGTAAAGGAGTGCAGGGAGGGGCAGGAAAGGAGACAAGGAG
GCCAGTATGGACACTGTGTCCAGTATGGCTTTCCAGGCTAATCACTTAGGGCAGAGACCCAGCC
TTATTCATCTCTACTTCCTGATGTCCATAGTGGTGTGTCATGAATTTTTATTGAATGAACAAAT
GAGGTGTATGAGGAGAGATGGTTTTCTCCTGCTCAGCTCTTACACAGTGATAGGTTTGTTCCAT
GGGACTTATCATAGGCCTGGTGATTCTTGAAAGAGCATTTTTCATGACTCAAAAATGAGCTGAG
AAGGAGTGTTATGGCCAGGTGCGGCGTCATGCACCTATAGTCCCAGCTGCTCAGGAGGCTAAGG
CAGAAAGACCATTCAAGCCCAGGAGTTCCAGCCTGAAGTATGCTGTGATCATGCCTGTGAATAA
CCACTGCACTCCAGCCAGGGCAACATAACAAGACTCTATC

hide sequence

RefSeq Acc Id:

XM_011534494 ⟹ XP_011532796

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,081,189 (+)	NCBI

Sequence:

show sequence

GAAGATGGAGTATCCCGCGCCGGCCACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTAC
AGCAGCTCGGAGTTGCTGGAGGGCCAGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGC
GCCGCCTGTGGGAAGCCGTGTCCGGTGCCCAGCCGGTGGGTAGAGAGGAAGCGCAGTTTTTCCC
ACATTCGAGGACTGTCATCCCTATACTCGTCCTGTCGGAGACCTACAGTCTTTGCCATCCCGTG
GAGCACATGATCCAGAAGAACCAATGTCTCTTCACCAACACCCAGTGTAAGGTTTGCTGCGCCT
TGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACCAGAGCAAAAAACATGCCAACAAAGTGAA
GAGATACCTAGCAATCCATGGAATGGAGACATTAAAGGGGGAAACGAAGAAGCTAGACTCAGAT
CAGAAGAGCAGCAGAAGCAAAGACAAGAACCAGTGCTGCCCCATCTGTAACATGACCTTTTCCT
CCCCTGTCGTGGCCCAGTCGCACTACCTGGGGAAGACCCACGCAAAGAACTTAAAGCTGAAGCA
GCAGTCCACTAAGGTGGAAGCTCTGTCAAAACGCCTTACAAATCCTTTCCTTGTGGCCTCCACC
TTAGCCTTGCACCAGAATAGAGAGATGATAGACCCAGACAAGTTCTGCAGCCTCTGCCATGCAA
CTTTCAACGACCCTGTCATGGCTCAACAACATTATGTGGGCAAGAAACACAGAAAACAGGAGAC
CAAGCTCAAACTAATGGCACGCTATGGGCGGCTGGCGGACCCTGCTGTCACTGACTTTCCAGGT
CACCAAAAACAGTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGA
CTCAACCACCTTGGAAGACTAGAGCTAGGGGTGGCCGTGTCACAGTCTGGCCAAGGAAATGAAA
TTGGGAGTTGCTGTGTGGAAACTCAACTCTCTGGAACTTCTTCCTTCCTCCTGCCTCTGCACAA
ATGTGACGGCAGCAGCTGAAGCCAACATCTTGCGACCATGAGAGAAAAACCTGGAGAACGGACG
AGTCCTCAACCCTGACTTCAGACCAACCTACACCCACCTCTGGACGTGGGGCTAAGTGAGAGAT
GGATACACTGTTTCATTTAGGCCCTGCTCACTTAGGTTTCTGTTATTCACACCCCAACGAAACC
CTCCATGGTCCAGGGCACCGGGCAAAGTACAGAAGGGCACGAGTTTACTTCCCGCTTCCCTGGA
GACCACCAACCCTCTCACCCTTCCAGCCCAGCCTCTGCCACTTCCCAGCTGTCGGTCCTCCTCC
AAACAGACGTGCATGCCAACACCCGGTGGGTGTGAGGCTTGTAGGCCCAAGTCTAGAGAGGCTG
AGTCTGGCAAAGCCTGAAAGCCCCTGTCCTAGCAAGCCAGGCCACAGGTCTAGAGTATCCGAGA
CCAGTGAATAAGGGGACGGGGGGTGCTACTGAGGCTGTGAGAAGCCCCAGGACCAGCCCAGGGT
AGTTAGAACTGAGTGAGGTTAGCCGGGACTAACCTCACTCAGATCCCTCCTCCCCAGTTCCCCT
CCATCCACTTTGGTTTGGAAGCCTCCCCAGAGCTCTCCCAGGCTGTCATCAGCTCTAAACTCTC
TGCCTCCACAAAAATGCCCTGGGCAACCTGTAACTCACAGCCCTGCTGTCTTCAGAGTATAAAC
TGGAGACAGATGTACCCAGAATTGAGGACGGGTGGGAAATGAGGAGAAATGAAGGCTGAGGAGG
GGTCATTCTCACAGTCCCTCCCTTTCGGTCACAGGAGGGTGTTGCCCATGCTTTTGGGTGGGTC
CCAGGCCCATAGCTGCAAATATTCATATTGGCTACTCTTCAGTGAGCAAGGGGTATATGCCAGG
CACTGGCATTGTGCTTGACATACATCATCATACTGAGTCCTCACGGAAGATGTATTATTCCCAT
TTCACAGAAGATGAAACTGAGGCTTGAGGTTAAGTGATTTGTCCGTGACCACAAAGAGTTTTCG
GGACTCAAACCCAGATCTGTCACTGGGCAAGGTGGCTCACACCTATAATCCCAGCCCTTTGGGA
GACTGAGGCCAGCAGATCTCCTGTGGCCAGGAGTTCAAGCCTGGCCAACAATGGCAAAACCCCG
TCTCTACCAAAAATACAAAAATTAGCTGGGCGTGGTGGCACACACCCGTAATCCCAGCTACTCA
GGTGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGTGGTTGCAGTGAGCCTAGATCGTG
CCACTGCATTCCAGCCTGAGCGACAGAGTAAGACTCTGTCTCCAAAAAAAACCCAGATCTGTCC
GACTCTGACACCCAACCTTTAATCACTCACTTTCTGTCAATGTCACCTCCGTTTTGACCAGCCA
AGCTAGACCTCCCTGGAGCCTGTGGAGAAGCCAAGGTAGAAAAGGGTTGGAAAAGAATGATAAA
ATAGGCCAGGTGCGGTGGCTCAAGCCTGTACTCCCAGCACTTTTGGAGGCCGAGACAGGCAGAT
TGCTTGAGCCCAGGAGTTCAAGACCAGCCTGGGCAACATAATGAGACCCTGTTTCAACTTAAAA
AAAAGAAATGGTAATGAACAATTGTCAATTCTGAGCAGCTGGGTATGGTATGACCCTGTGTACT
TTTTCTGTATTTTAAAATGTTCTCAAAATAAAACTTGTT

hide sequence

RefSeq Acc Id:

XM_011534495 ⟹ XP_011532797

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,065,983 (+)	NCBI

Sequence:

show sequence

GAAGATGGAGTATCCCGCGCCGGCCACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTAC
AGCAGCTCGGAGTTGCTGGAGGGCCAGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGC
GCCGCCTGTGGGAAGCCGTGTCCGGTGCCCAGCCGGTGGGTAGAGAGGAAGCGCAGTTTTTCCC
ACATTCGAGGACTGTCATCCCTATACTCGTCCTGTCGGAGACCTACAGTCTTTGCCATCCCGTG
GAGCACATGATCCAGAAGAACCAATGTCTCTTCACCAACACCCAGTGTAAGGTTTGCTGCGCCT
TGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACCAGAGCAAAAAACATGCCAACAAAGTGAA
GAGATACCTAGCAATCCATGGAATGGAGACATTAAAGGGGGAAACGAAGAAGCTAGACTCAGAT
CAGAAGAGCAGCAGAAGCAAAGACAAGAACCAGTGCTGCCCCATCTGTAACATGACCTTTTCCT
CCCCTGTCGTGGCCCAGTCGCACTACCTGGGGAAGACCCACGCAAAGAACTTAAAGCTGAAGCA
GCAGTCCACTAAGGTGGAAGCTCTGTCAAAACGCCTTACAAATCCTTTCCTTGTGGCCTCCACC
TTAGCCTTGCACCAGAATAGAGAGATGATAGACCCAGACAAGTTCTGCAGCCTCTGCCATGCAA
CTTTCAACGACCCTGTCATGGCTCAACAACATTATGTGGGCAAGAAACACAGAAAACAGGAGAC
CAAGCTCAAACTAATGGCACGCTATGGGCGGCTGGCGGACCCTGCTGTCACTGACTTTCCAGGT
CACCAAAAACAGTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGA
CTCAACCACCTTGGAAGACTAGAGAAGGTGCAGGCTTTCCTGAGTCTTAGACCAGATATGGCCA
GTTGCGCAGGTTTCTGCCAACTGTGAAGTATCCTCCTGGAGCAGTGACACAATCTTGGCGGAGC
ATTGCTACCCCCGCTGCCCCCTCCACAGTTCCTGAATGGTGCTAAGGATCTGCAGCAGTTGGCA
ACGAGCTGGGGCTGGGGGCGGCCTCCATGTCCACTGAGATCATAGGACACTCCAATGGGGATGG
GACCTTTCCCCTCCTCCATCAGAGGTGCTCTGACCCTAGGTTACACGGGAAAGTGCCCCACATG
CAAGTCTCCCTGAGGGTTCTGCCCCTAAAGGCAGACTGCCTCATGCCCGCTAGCTGTGAGGTTC
ATTGCTACCCTCGGCCCTACTAGCCCTCTCTTCCCCCTTGTGCAGCGGACCACTTGCCCAGTTT
GCTGTGGTGCTAGCCTTCCCCATCATCCACCGGGTGATTTCTGGGTCCCAGGGAAAGAAAGAGA
GAGCTGATGCAGGTTTCTACAGTGAGGAACAGGCGTTTCCCAGGCCCCACACCCAGATTTCTCT
ATCTTTGCTGTGTTTTATGGCCTGGGACTGAGTCCACACGGATAGATTTTTCCTTGTAACCTTG
AGACGAGAATTCCAAGGAGTGTCACCATCAGAGGCTTCTCTTCATTGTGTCAAAGAAGCCCCTA
GCTGCTCTCGTGGCCTCCTTCCCCCACTCCCTATCCCTTCACCTGTGAAATGCCTTTGCTTTGC
ATATTGTGTGTGGATGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTATGTGTGTGCTTCTGTGTG
TGCCTAATGCTCTGTCTCTTGGTCACTGAAGCATCCAAATAAAGAATTTCCCTCATGGGCCAGA
CTACAACTTAACAGACCTAGGGTTTTGAGCCATATTGCCATTGGATCTAGTATGTCTGTCTTGA
CCCCTCACCCCCACCCCATTCAGACCTCAGTAGTCCCCAGTAGTCACTTTAGGAGTTGGGACAG
AGTCGAGCACCCTGTGAAAGTCTCCCTTGAGTTCAGGTGCCCTGAACTCAGTACAGCCTCATCT
TCTCATCCACCACCTTCTCCTGCTTCTCCTGTCACATAGGGCCTCATGAAGGTCTTTAAAGGGT
TTAAGCTGGGGATCTGCTTTATGTTTGAGAGAACTGTTCTGGCTGTTATGTAAAGGAGTGCAGG
GAGGGGCAGGAAAGGAGACAAGGAGGCCAGTATGGACACTGTGTCCAGTATGGCTTTCCAGGCT
AATCACTTAGGGCAGAGACCCAGCCTTATTCATCTCTACTTCCTGATGTCCATAGTGGTGTGTC
ATGAATTTTTATTGAATGAACAAATGAGGTGTATGAGGAGAGATGGTTTTCTCCTGCTCAGCTC
TTACACAGTGATAGGTTTGTTCCATGGGACTTATCATAGGCCTGGTGATTCTTGAAAGAGCATT
TTTCATGACTCAAAAATGAGCTGAGAAGGAGTGTTATGGCCAGGTGCGGCGTCATGCACCTATA
GTCCCAGCTGCTCAGGAGGCTAAGGCAGAAAGACCATTCAAGCCCAGGAGTTCCAGCCTGAAGT
ATGCTGTGATCATGCCTGTGAATAACCACTGCACTCCAGCCAGGGCAACATAACAAGACTCTAT
C

hide sequence

RefSeq Acc Id:

XM_011534496 ⟹ XP_011532798

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI

Sequence:

show sequence

GAAGATGGAGTATCCCGCGCCGGCCACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTAC
AGCAGCTCGGAGTTGCTGGAGGGCCAGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGC
GCCGCCTGTGGGAAGCCGTGTCCGGTGCCCAGCCGGTGGGTAGAGAGGAAGCGCAGTTTTTCCC
ACATTCGAGGACTGTCATCCCTATACTCGTCCTGTCGGAGACCTACAGTCTTTGCCATCCCGTG
GAGCACATGATCCAGAAGAACCAATGTCTCTTCACCAACACCCAGTGTAAGGTTTGCTGCGCCT
TGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACCAGAGCAAAAAACATGCCAACAAAGTGAA
GAGATACCTAGCAATCCATGGAATGGAGACATTAAAGGGGGAAACGAAGAAGCTAGACTCAGAT
CAGAAGAGCAGCAGAAGCAAAGACAAGAACCAGTGCTGCCCCATCTGTAACATGACCTTTTCCT
CCCCTGTCGTGGCCCAGTCGCACTACCTGGGGAAGACCCACGCAAAGAACTTAAAGCTGAAGCA
GCAGTCCACTAAGGTGGAAGCCTTGCACCAGAATAGAGAGATGATAGACCCAGACAAGTTCTGC
AGCCTCTGCCATGCAACTTTCAACGACCCTGTCATGGCTCAACAACATTATGTGGGCAAGAAAC
ACAGAAAACAGGAGACCAAGCTCAAACTAATGGCACGCTATGGGCGGCTGGCGGACCCTGCTGT
CACTGACTTTCCAGGTCACCAAAAACAGTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGC
AACCCATTCAGAAAGACTCAACCACCTTGGAAGACTAGAGGTGATTCTGCCCAGCATCCCATAT
TGGGCCAGCCATGAGCCAGCTTCCCGTGACTGCTCAGCCCTTGGCTCCCTCTTGCTCGTTGTTC
TCACCAGGAAAGTACACGGGCCTGAGGCAGGATTGGGCCACAGACAGCCTCTCATTGGTCCGGG
CTAATTCACTCCTGCTGCTCCCCTTTGGCAGGGGTCCTGTAGGTCATGACAGGGGAGGCAAGGG
TATTGAGAGACTCGGGGTCTCGCGGGGTGGTAGTTTGGAGGGTGGCTTTCCCCATTTCCCAACC
CCTCTGGGCCTTAGGTGCTGAGGCCCCTGCCACCTGTCTTTCCTCTAAAGGTCAGTTTTGGGCC
AGTTCTTGCAACTAAAGAGCAGAGATCTCTCTGGGCCCTAGACATTTCCAGCAAAACCTGGAAC
TTTCATGCCAAACCTGGGGCAGGGCAGGAAACAGAGGAAATGGCTGCAACATGGGAGCTTGGAG
CTAATACGACACTCTGCCTTCCCCCAGAAGGTGCAGGCTTTCCTGAGTCTTAGACCAGATATGG
CCAGTTGCGCAGGTTTCTGCCAACTGTGAAGTATCCTCCTGGAGCAGTGACACAATCTTGGCGG
AGCATTGCTACCCCCGCTGCCCCCTCCACAGTTCCTGAATGGTGCTAAGGATCTGCAGCAGTTG
GCAACGAGCTGGGGCTGGGGGCGGCCTCCATGTCCACTGAGATCATAGGACACTCCAATGGGGA
TGGGACCTTTCCCCTCCTCCATCAGAGGTGCTCTGACCCTAGGTTACACGGGAAAGTGCCCCAC
ATGCAAGTCTCCCTGAGGGTTCTGCCCCTAAAGGCAGACTGCCTCATGCCCGCTAGCTGTGAGG
TTCATTGCTACCCTCGGCCCTACTAGCCCTCTCTTCCCCCTTGTGCAGCGGACCACTTGCCCAG
TTTGCTGTGGTGCTAGCCTTCCCCATCATCCACCGGGTGATTTCTGGGTCCCAGGGAAAGAAAG
AGAGAGCTGATGCAGGTTTCTACAGTGAGGAACAGGCGTTTCCCAGGCCCCACACCCAGATTTC
TCTATCTTTGCTGTGTTTTATGGCCTGGGACTGAGTCCACACGGATAGATTTTTCCTTGTAACC
TTGAGACGAGAATTCCAAGGAGTGTCACCATCAGAGGCTTCTCTTCATTGTGTCAAAGAAGCCC
CTAGCTGCTCTCGTGGCCTCCTTCCCCCACTCCCTATCCCTTCACCTGTGAAATGCCTTTGCTT
TGCATATTGTGTGTGGATGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTATGTGTGTGCTTCTGT
GTGTGCCTAATGCTCTGTCTCTTGGTCACTGAAGCATCCAAATAAAGAATTTCCCTCATGGGCC
AGACTACAACTTAACAGACCTAGGGTTTTGAGCCATATTGCCATTGGATCTAGTATGTCTGTCT
TGACCCCTCACCCCCACCCCATTCAGACCTCAGTAGTCCCCAGTAGTCACTTTAGGAGTTGGGA
CAGAGTCGAGCACCCTGTGAAAGTCTCCCTTGAGTTCAGGTGCCCTGAACTCAGTACAGCCTCA
TCTTCTCATCCACCACCTTCTCCTGCTTCTCCTGTCACATAGGGCCTCATGAAGGTCTTTAAAG
GGTTTAAGCTGGGGATCTGCTTTATGTTTGAGAGAACTGTTCTGGCTGTTATGTAAAGGAGTGC
AGGGAGGGGCAGGAAAGGAGACAAGGAGGCCAGTATGGACACTGTGTCCAGTATGGCTTTCCAG
GCTAATCACTTAGGGCAGAGACCCAGCCTTATTCATCTCTACTTCCTGATGTCCATAGTGGTGT
GTCATGAATTTTTATTGAATGAACAAATGAGGTGTATGAGGAGAGATGGTTTTCTCCTGCTCAG
CTCTTACACAGTGATAGGTTTGTTCCATGGGACTTATCATAGGCCTGGTGATTCTTGAAAGAGC
ATTTTTCATGACTCAAAAATGAGCTGAGAAGGAGTGTTATGGCCAGGTGCGGCGTCATGCACCT
ATAGTCCCAGCTGCTCAGGAGGCTAAGGCAGAAAGACCATTCAAGCCCAGGAGTTCCAGCCTGA
AGTATGCTGTGATCATGCCTGTGAATAACCACTGCACTCCAGCCAGGGCAACATAACAAGACTC
TATC

hide sequence

RefSeq Acc Id:

XM_017009297 ⟹ XP_016864786

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI

Sequence:

show sequence

GCGATACCTAGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCC
GCGCCGGCCACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGC
TGGAGGGCCAGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGC
CGTGTCCGGTGCCCAGCCGGTGGGTAGAGAGGAAGTGGAGCACATGATCCAGAAGAACCAATGT
CTCTTCACCAACACCCAGTGTAAGGTTTGCTGCGCCTTGCTTATTTCTGAGTCCCAGAAGCTGG
CACATTACCAGAGCAAAAAACATGCCAACAAAGTGAAGAGATACCTAGCAATCCATGGAATGGA
GACATTAAAGGGGGAAACGAAGAAGCTAGACTCAGATCAGAAGAGCAGCAGAAGCAAAGACAAG
AACCAGTGCTGCCCCATCTGTAACATGACCTTTTCCTCCCCTGTCGTGGCCCAGTCGCACTACC
TGGGGAAGACCCACGCAAAGAACTTAAAGCTGAAGCAGCAGTCCACTAAGGTGGAAGCTCTGTC
AAAACGCCTTACAAATCCTTTCCTTGTGGCCTCCACCTTAGCCTTGCACCAGAATAGAGAGATG
ATAGACCCAGACAAGTTCTGCAGCCTCTGCCATGCAACTTTCAACGACCCTGTCATGGCTCAAC
AACATTATGTGGGCAAGAAACACAGAAAACAGGAGACCAAGCTCAAACTAATGGCACGCTATGG
GCGGCTGGCGGACCCTGCTGTCACTGACTTTCCAGGTCACCAAAAACAGTGGCATCATCCCTGG
GCCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGACTCAACCACCTTGGAAGACTAGAGGTG
ATTCTGCCCAGCATCCCATATTGGGCCAGCCATGAGCCAGCTTCCCGTGACTGCTCAGCCCTTG
GCTCCCTCTTGCTCGTTGTTCTCACCAGGAAAGTACACGGGCCTGAGGCAGGATTGGGCCACAG
ACAGCCTCTCATTGGTCCGGGCTAATTCACTCCTGCTGCTCCCCTTTGGCAGGGGTCCTGTAGG
TCATGACAGGGGAGGCAAGGGTATTGAGAGACTCGGGGTCTCGCGGGGTGGTAGTTTGGAGGGT
GGCTTTCCCCATTTCCCAACCCCTCTGGGCCTTAGGTGCTGAGGCCCCTGCCACCTGTCTTTCC
TCTAAAGGTCAGTTTTGGGCCAGTTCTTGCAACTAAAGAGCAGAGATCTCTCTGGGCCCTAGAC
ATTTCCAGCAAAACCTGGAACTTTCATGCCAAACCTGGGGCAGGGCAGGAAACAGAGGAAATGG
CTGCAACATGGGAGCTTGGAGCTAATACGACACTCTGCCTTCCCCCAGAAGGTGCAGGCTTTCC
TGAGTCTTAGACCAGATATGGCCAGTTGCGCAGGTTTCTGCCAACTGTGAAGTATCCTCCTGGA
GCAGTGACACAATCTTGGCGGAGCATTGCTACCCCCGCTGCCCCCTCCACAGTTCCTGAATGGT
GCTAAGGATCTGCAGCAGTTGGCAACGAGCTGGGGCTGGGGGCGGCCTCCATGTCCACTGAGAT
CATAGGACACTCCAATGGGGATGGGACCTTTCCCCTCCTCCATCAGAGGTGCTCTGACCCTAGG
TTACACGGGAAAGTGCCCCACATGCAAGTCTCCCTGAGGGTTCTGCCCCTAAAGGCAGACTGCC
TCATGCCCGCTAGCTGTGAGGTTCATTGCTACCCTCGGCCCTACTAGCCCTCTCTTCCCCCTTG
TGCAGCGGACCACTTGCCCAGTTTGCTGTGGTGCTAGCCTTCCCCATCATCCACCGGGTGATTT
CTGGGTCCCAGGGAAAGAAAGAGAGAGCTGATGCAGGTTTCTACAGTGAGGAACAGGCGTTTCC
CAGGCCCCACACCCAGATTTCTCTATCTTTGCTGTGTTTTATGGCCTGGGACTGAGTCCACACG
GATAGATTTTTCCTTGTAACCTTGAGACGAGAATTCCAAGGAGTGTCACCATCAGAGGCTTCTC
TTCATTGTGTCAAAGAAGCCCCTAGCTGCTCTCGTGGCCTCCTTCCCCCACTCCCTATCCCTTC
ACCTGTGAAATGCCTTTGCTTTGCATATTGTGTGTGGATGTGTGTGTGTGTGTGTGTGTGTTTG
TGTGTATGTGTGTGCTTCTGTGTGTGCCTAATGCTCTGTCTCTTGGTCACTGAAGCATCCAAAT
AAAGAATTTCCCTCATGGGCCAGACTACAACTTAACAGACCTAGGGTTTTGAGCCATATTGCCA
TTGGATCTAGTATGTCTGTCTTGACCCCTCACCCCCACCCCATTCAGACCTCAGTAGTCCCCAG
TAGTCACTTTAGGAGTTGGGACAGAGTCGAGCACCCTGTGAAAGTCTCCCTTGAGTTCAGGTGC
CCTGAACTCAGTACAGCCTCATCTTCTCATCCACCACCTTCTCCTGCTTCTCCTGTCACATAGG
GCCTCATGAAGGTCTTTAAAGGGTTTAAGCTGGGGATCTGCTTTATGTTTGAGAGAACTGTTCT
GGCTGTTATGTAAAGGAGTGCAGGGAGGGGCAGGAAAGGAGACAAGGAGGCCAGTATGGACACT
GTGTCCAGTATGGCTTTCCAGGCTAATCACTTAGGGCAGAGACCCAGCCTTATTCATCTCTACT
TCCTGATGTCCATAGTGGTGTGTCATGAATTTTTATTGAATGAACAAATGAGGTGTATGAGGAG
AGATGGTTTTCTCCTGCTCAGCTCTTACACAGTGATAGGTTTGTTCCATGGGACTTATCATAGG
CCTGGTGATTCTTGAAAGAGCATTTTTCATGACTCAAAAATGAGCTGAGAAGGAGTGTTATGGC
CAGGTGCGGCGTCATGCACCTATAGTCCCAGCTGCTCAGGAGGCTAAGGCAGAAAGACCATTCA
AGCCCAGGAGTTCCAGCCTGAAGTATGCTGTGATCATGCCTGTGAATAACCACTGCACTCCAGC
CAGGGCAACATAACAAGACTCTATC

hide sequence

RefSeq Acc Id:

XM_017009298 ⟹ XP_016864787

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,060,242 (+)	NCBI

Sequence:

show sequence

GAAGATGGAGTATCCCGCGCCGGCCACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTAC
AGCAGCTCGGAGTTGCTGGAGGGCCAGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGC
GCCGCCTGTGGGAAGCCGTGTCCGGTGCCCAGCCGGTGGGTAGAGAGGAAGCGCAGTTTTTCCC
ACATTCGAGGACTGTCATCCCTATACTCGTCCTGTCGGAGACCTACAGTCTTTGCCATCCCGTG
GAGCACATGATCCAGAAGAACCAATGTCTCTTCACCAACACCCAGTGTAAGGTTTGCTGCGCCT
TGCTTATTTCTGAGTCCCAGAAGCTGGCACATTACCAGAGCAAAAAACATGCCAACAAAGTGAA
GAGATACCTAGCAATCCATGGAATGGAGACATTAAAGGGGGAAACGAAGAAGCTAGACTCAGAT
CAGAAGAGCAGCAGAAGCAAAGACAAGAACCAGTGCTGCCCCATCTGTAACATGACCTTTTCCT
CCCCTGTCGTGGCCCAGTCGCACTACCTGGGGAAGACCCACGCAAAGAACTTAAAGCTGAAGCA
GCAGTCCACTAAGGTGGAAGCTCTGTCAAAACGCCTTACAAATCCTTTCCTTGTGGCCTCCACC
TTAGCCTTGCACCAGAATAGAGAGATGATAGACCCAGACAAGTTCTGCAGCCTCTGCCATGCAA
CTTTCAACGACCCTGTCATGGCTCAACAACATTATGTGGGCAAGAAACACAGAAAACAGGAGAC
CAAGCTCAAACTAATGGCACGCTATGGGCGGCTGGCGGACCCTGCTGTCACTGACTTTCCAGAT
GAGGATATTAAAACCAGAAAGGTGAAGTGATTTTCCAGGGTTCCACACTAAAGAGTGGCAGAGC
CAGAGCCCACATTGAAACCCAATGTAGTTCTGTGTTGGATCCAGAGAATAGTTCCTGAGGGTCC
CTGACAAGTGTCTCATGGCAAGTATGGACCTACTGTAAGATTACCCAGGGTATCCAAATCCCAC
CAGGGGCAAATGCATCATCTACCACGCAGATCAAATAAGCCTTAGAGTGGTTTTATACTCCAGG
CTTGTGTTTCTCTCATATTCACCCAAGAAGGCCAGAACTAAAACCTACATAGCATTCAGGCAAA
TCCTTCTTGCCCCCAGAGCATTGAATGTCCCCTCCAGGTTACTGAAATCCTCTGCTTCACCCCA
TTACTTTCCCTAATTAGGGTCTTATCTCCCACTCAGTAGAGCTGCTTTCTGAGCCCCATGCTGG
TCCCCCAGTTTCTTCAGCTTTTATATACAGGACAAGTTTTCAAGTCTTACTAAATTCATATATA
GTCAATAAGTATTTATTGGACTTTTACCTAATATGTGCCAGGCATTGTGGTAAATACGTAGTAA
ACAAGACAGGTATTGTCTGTGTTCTTATGGAGCTTACAGTCTAGCAGAGAAGACAGGCATTGAG
CAAACAGTTACAACTGTGACAAACTTCAGAAAAAAAGACAAATGCAAGACTGTGGGCACATAAA
ATGAGAGGAGATAAGATGGGGGAGCAGGGATCAAGAAAGGCACCCCAGAGGGCAAGTAGGATAG
TATGGGACGTAGTGACGCGGAGGACATGAGCAGGTGTCCACGCATGGCTTTGTGGGTCATGTTA
GGGCAGCGGGCCTTCACCCTGAGAGCACTGGGACTGGGAAGCCGCTGCCAGTTTGAGCTTTACG
GGCGGATCATCCTGGTTCCAGCGTGAGGAGGTTTGGAGCCTGGGCAACATGGCACAACCCCACC
TCTACAAAAAGAAGAAAATACAAAAATTACCCAGGTGTGG

hide sequence

RefSeq Acc Id:

XM_017009299 ⟹ XP_016864788

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI

Sequence:

show sequence

GCGATACCTAGGCGCCTGAGAGGCTCTCTACCGGTGAGGGTTTGCGGGGAAGATGGAGTATCCC
GCGCCGGCCACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACAGCAGCTCGGAGTTGC
TGGAGGGCCAGGAGCCGGACGGGGTGCGCTTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGC
CGTGTCCGGTGCCCAGCCGGTGGGTAGAGAGGAAGTGGAGCACATGATCCAGAAGAACCAATGT
CTCTTCACCAACACCCAGTGTAAGGTTTGCTGCGCCTTGCTTATTTCTGAGTCCCAGAAGCTGG
CACATTACCAGAGCAAAAAACATGCCAACAAAGTGAAGAGATACCTAGCAATCCATGGAATGGA
GACATTAAAGGGGGAAACGAAGAAGCTAGACTCAGATCAGAAGAGCAGCAGAAGCAAAGACAAG
AACCAGTGCTGCCCCATCTGTAACATGACCTTTTCCTCCCCTGTCGTGGCCCAGTCGCACTACC
TGGGGAAGACCCACGCAAAGAACTTAAAGCTGAAGCAGCAGTCCACTAAGGTGGAAGCCTTGCA
CCAGAATAGAGAGATGATAGACCCAGACAAGTTCTGCAGCCTCTGCCATGCAACTTTCAACGAC
CCTGTCATGGCTCAACAACATTATGTGGGCAAGAAACACAGAAAACAGGAGACCAAGCTCAAAC
TAATGGCACGCTATGGGCGGCTGGCGGACCCTGCTGTCACTGACTTTCCAGGTCACCAAAAACA
GTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGCAACCCATTCAGAAAGACTCAACCACCT
TGGAAGACTAGAGGTGATTCTGCCCAGCATCCCATATTGGGCCAGCCATGAGCCAGCTTCCCGT
GACTGCTCAGCCCTTGGCTCCCTCTTGCTCGTTGTTCTCACCAGGAAAGTACACGGGCCTGAGG
CAGGATTGGGCCACAGACAGCCTCTCATTGGTCCGGGCTAATTCACTCCTGCTGCTCCCCTTTG
GCAGGGGTCCTGTAGGTCATGACAGGGGAGGCAAGGGTATTGAGAGACTCGGGGTCTCGCGGGG
TGGTAGTTTGGAGGGTGGCTTTCCCCATTTCCCAACCCCTCTGGGCCTTAGGTGCTGAGGCCCC
TGCCACCTGTCTTTCCTCTAAAGGTCAGTTTTGGGCCAGTTCTTGCAACTAAAGAGCAGAGATC
TCTCTGGGCCCTAGACATTTCCAGCAAAACCTGGAACTTTCATGCCAAACCTGGGGCAGGGCAG
GAAACAGAGGAAATGGCTGCAACATGGGAGCTTGGAGCTAATACGACACTCTGCCTTCCCCCAG
AAGGTGCAGGCTTTCCTGAGTCTTAGACCAGATATGGCCAGTTGCGCAGGTTTCTGCCAACTGT
GAAGTATCCTCCTGGAGCAGTGACACAATCTTGGCGGAGCATTGCTACCCCCGCTGCCCCCTCC
ACAGTTCCTGAATGGTGCTAAGGATCTGCAGCAGTTGGCAACGAGCTGGGGCTGGGGGCGGCCT
CCATGTCCACTGAGATCATAGGACACTCCAATGGGGATGGGACCTTTCCCCTCCTCCATCAGAG
GTGCTCTGACCCTAGGTTACACGGGAAAGTGCCCCACATGCAAGTCTCCCTGAGGGTTCTGCCC
CTAAAGGCAGACTGCCTCATGCCCGCTAGCTGTGAGGTTCATTGCTACCCTCGGCCCTACTAGC
CCTCTCTTCCCCCTTGTGCAGCGGACCACTTGCCCAGTTTGCTGTGGTGCTAGCCTTCCCCATC
ATCCACCGGGTGATTTCTGGGTCCCAGGGAAAGAAAGAGAGAGCTGATGCAGGTTTCTACAGTG
AGGAACAGGCGTTTCCCAGGCCCCACACCCAGATTTCTCTATCTTTGCTGTGTTTTATGGCCTG
GGACTGAGTCCACACGGATAGATTTTTCCTTGTAACCTTGAGACGAGAATTCCAAGGAGTGTCA
CCATCAGAGGCTTCTCTTCATTGTGTCAAAGAAGCCCCTAGCTGCTCTCGTGGCCTCCTTCCCC
CACTCCCTATCCCTTCACCTGTGAAATGCCTTTGCTTTGCATATTGTGTGTGGATGTGTGTGTG
TGTGTGTGTGTGTTTGTGTGTATGTGTGTGCTTCTGTGTGTGCCTAATGCTCTGTCTCTTGGTC
ACTGAAGCATCCAAATAAAGAATTTCCCTCATGGGCCAGACTACAACTTAACAGACCTAGGGTT
TTGAGCCATATTGCCATTGGATCTAGTATGTCTGTCTTGACCCCTCACCCCCACCCCATTCAGA
CCTCAGTAGTCCCCAGTAGTCACTTTAGGAGTTGGGACAGAGTCGAGCACCCTGTGAAAGTCTC
CCTTGAGTTCAGGTGCCCTGAACTCAGTACAGCCTCATCTTCTCATCCACCACCTTCTCCTGCT
TCTCCTGTCACATAGGGCCTCATGAAGGTCTTTAAAGGGTTTAAGCTGGGGATCTGCTTTATGT
TTGAGAGAACTGTTCTGGCTGTTATGTAAAGGAGTGCAGGGAGGGGCAGGAAAGGAGACAAGGA
GGCCAGTATGGACACTGTGTCCAGTATGGCTTTCCAGGCTAATCACTTAGGGCAGAGACCCAGC
CTTATTCATCTCTACTTCCTGATGTCCATAGTGGTGTGTCATGAATTTTTATTGAATGAACAAA
TGAGGTGTATGAGGAGAGATGGTTTTCTCCTGCTCAGCTCTTACACAGTGATAGGTTTGTTCCA
TGGGACTTATCATAGGCCTGGTGATTCTTGAAAGAGCATTTTTCATGACTCAAAAATGAGCTGA
GAAGGAGTGTTATGGCCAGGTGCGGCGTCATGCACCTATAGTCCCAGCTGCTCAGGAGGCTAAG
GCAGAAAGACCATTCAAGCCCAGGAGTTCCAGCCTGAAGTATGCTGTGATCATGCCTGTGAATA
ACCACTGCACTCCAGCCAGGGCAACATAACAAGACTCTATC

hide sequence

RefSeq Acc Id:

XM_017009303 ⟹ XP_016864792

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,043,727 - 177,067,985 (+)	NCBI

Sequence:

show sequence

TGCACTCCAGCCTGGGCAACAGAGTGAGACCCTGTCTTAAAAAAAAAAAACCTAATGGTCCACT
TGTTCAGCAAACTCTGAGCATCTACTGTGTGCCAGACTCCAGCTGGGTGTGAAGGATAAGAAAC
AAAAATGAGTCAAATAGTCCGTGTTCCAATGTCACACTTGAGTTCACAGAAAAGTCTCCTAAGC
TATGACACTGTCAGTTTAGGGTGGCAAGTGGTATGACAGAGGTCTATTTAATGTACTCTGGGAG
CACAGAAGAGGAGCAGGGTTAATTCTTCCTGGAATACACAAAGGGACTTGACAGTTGTTTACTG
AATGATGTTTTTTTTTTTTTGAGAGAAAGTCCCCCAGAGGAAAAGCTTATATTTAAATTGGGTC
TTGAAGGCTAAGCAGACACGCTGCCAAGCAGGAAAGGAAGGAAGCACATTTTAGACAGCAGGAA
TGGCCAAAGCAAAGCAAGGAAGCATCAGAGAATAAAGTGGGGGATGAAGAGCAGCAGAAGCAAA
GACAAGAACCAGTGCTGCCCCATCTGTAACATGACCTTTTCCTCCCCTGTCGTGGCCCAGTCGC
ACTACCTGGGGAAGACCCACGCAAAGAACTTAAAGCTGAAGCAGCAGTCCACTAAGGTGGAAGC
TCTGTCAAAACGCCTTACAAATCCTTTCCTTGTGGCCTCCACCTTAGCCTTGCACCAGAATAGA
GAGATGATAGACCCAGACAAGTTCTGCAGCCTCTGCCATGCAACTTTCAACGACCCTGTCATGG
CTCAACAACATTATGTGGGCAAGAAACACAGAAAACAGGAGACCAAGCTCAAACTAATGGCACG
CTATGGGCGGCTGGCGGACCCTGCTGTCACTGACTTTCCAGCTGGAAAGGGCTACCCCTGCAAA
ACATGTAAGATAGTGCTGAACTCCATAGAACAGTACCAAGCTCATGTCAGCGGCTTCAAACACA
AGAACCAGTCACCAAAAACAGTGGCATCATCCCTGGGCCAGATTCCAATGCAAAGGCAACCCAT
TCAGAAAGACTCAACCACCTTGGAAGACTAGAGGTGATTCTGCCCAGCATCCCATATTGGGCCA
GCCATGAGCCAGCTTCCCGTGACTGCTCAGCCCTTGGCTCCCTCTTGCTCGTTGTTCTCACCAG
GAAAGTACACGGGCCTGAGGCAGGATTGGGCCACAGACAGCCTCTCATTGGTCCGGGCTAATTC
ACTCCTGCTGCTCCCCTTTGGCAGGGGTCCTGTAGGTCATGACAGGGGAGGCAAGGGTATTGAG
AGACTCGGGGTCTCGCGGGGTGGTAGTTTGGAGGGTGGCTTTCCCCATTTCCCAACCCCTCTGG
GCCTTAGGTGCTGAGGCCCCTGCCACCTGTCTTTCCTCTAAAGGTCAGTTTTGGGCCAGTTCTT
GCAACTAAAGAGCAGAGATCTCTCTGGGCCCTAGACATTTCCAGCAAAACCTGGAACTTTCATG
CCAAACCTGGGGCAGGGCAGGAAACAGAGGAAATGGCTGCAACATGGGAGCTTGGAGCTAATAC
GACACTCTGCCTTCCCCCAGAAGGTGCAGGCTTTCCTGAGTCTTAGACCAGATATGGCCAGTTG
CGCAGGTTTCTGCCAACTGTGAAGTATCCTCCTGGAGCAGTGACACAATCTTGGCGGAGCATTG
CTACCCCCGCTGCCCCCTCCACAGTTCCTGAATGGTGCTAAGGATCTGCAGCAGTTGGCAACGA
GCTGGGGCTGGGGGCGGCCTCCATGTCCACTGAGATCATAGGACACTCCAATGGGGATGGGACC
TTTCCCCTCCTCCATCAGAGGTGCTCTGACCCTAGGTTACACGGGAAAGTGCCCCACATGCAAG
TCTCCCTGAGGGTTCTGCCCCTAAAGGCAGACTGCCTCATGCCCGCTAGCTGTGAGGTTCATTG
CTACCCTCGGCCCTACTAGCCCTCTCTTCCCCCTTGTGCAGCGGACCACTTGCCCAGTTTGCTG
TGGTGCTAGCCTTCCCCATCATCCACCGGGTGATTTCTGGGTCCCAGGGAAAGAAAGAGAGAGC
TGATGCAGGTTTCTACAGTGAGGAACAGGCGTTTCCCAGGCCCCACACCCAGATTTCTCTATCT
TTGCTGTGTTTTATGGCCTGGGACTGAGTCCACACGGATAGATTTTTCCTTGTAACCTTGAGAC
GAGAATTCCAAGGAGTGTCACCATCAGAGGCTTCTCTTCATTGTGTCAAAGAAGCCCCTAGCTG
CTCTCGTGGCCTCCTTCCCCCACTCCCTATCCCTTCACCTGTGAAATGCCTTTGCTTTGCATAT
TGTGTGTGGATGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTATGTGTGTGCTTCTGTGTGTGCC
TAATGCTCTGTCTCTTGGTCACTGAAGCATCCAAATAAAGAATTTCCCTCATGGGCCAGACTAC
AACTTAACAGACCTAGGGTTTTGAGCCATATTGCCATTGGATCTAGTATGTCTGTCTTGACCCC
TCACCCCCACCCCATTCAGACCTCAGTAGTCCCCAGTAGTCACTTTAGGAGTTGGGACAGAGTC
GAGCACCCTGTGAAAGTCTCCCTTGAGTTCAGGTGCCCTGAACTCAGTACAGCCTCATCTTCTC
ATCCACCACCTTCTCCTGCTTCTCCTGTCACATAGGGCCTCATGAAGGTCTTTAAAGGGTTTAA
GCTGGGGATCTGCTTTATGTTTGAGAGAACTGTTCTGGCTGTTATGTAAAGGAGTGCAGGGAGG
GGCAGGAAAGGAGACAAGGAGGCCAGTATGGACACTGTGTCCAGTATGGCTTTCCAGGCTAATC
ACTTAGGGCAGAGACCCAGCCTTATTCATCTCTACTTCCTGATGTCCATAGTGGTGTGTCATGA
ATTTTTATTGAATGAACAAATGAGGTGTATGAGGAGAGATGGTTTTCTCCTGCTCAGCTCTTAC
ACAGTGATAGGTTTGTTCCATGGGACTTATCATAGGCCTGGTGATTCTTGAAAGAGCATTTTTC
ATGACTCAAAAATGAGCTGAGAAGGAGTGTTATGGCCAGGTGCGGCGTCATGCACCTATAGTCC
CAGCTGCTCAGGAGGCTAAGGCAGAAAGACCATTCAAGCCCAGGAGTTCCAGCCTGAAGTATGC
TGTGATCATGCCTGTGAATAACCACTGCACTCCAGCCAGGGCAACATAACAAGACTCTATC

hide sequence

RefSeq Acc Id:

XM_047417051 ⟹ XP_047273007

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI

RefSeq Acc Id:

XM_047417052 ⟹ XP_047273008

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI

RefSeq Acc Id:

XM_047417053 ⟹ XP_047273009

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,065,983 (+)	NCBI

RefSeq Acc Id:

XM_047417054 ⟹ XP_047273010

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI

RefSeq Acc Id:

XM_047417055 ⟹ XP_047273011

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI

RefSeq Acc Id:

XM_047417056 ⟹ XP_047273012

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,060,242 (+)	NCBI

RefSeq Acc Id:

XM_047417057 ⟹ XP_047273013

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	177,022,696 - 177,067,985 (+)	NCBI

RefSeq Acc Id:

XM_054352256 ⟹ XP_054208231

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

RefSeq Acc Id:

XM_054352257 ⟹ XP_054208232

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,624,397 (+)	NCBI

RefSeq Acc Id:

XM_054352258 ⟹ XP_054208233

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,609,186 (+)	NCBI

RefSeq Acc Id:

XM_054352259 ⟹ XP_054208234

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

RefSeq Acc Id:

XM_054352260 ⟹ XP_054208235

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

RefSeq Acc Id:

XM_054352261 ⟹ XP_054208236

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

RefSeq Acc Id:

XM_054352262 ⟹ XP_054208237

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,603,448 (+)	NCBI

RefSeq Acc Id:

XM_054352263 ⟹ XP_054208238

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

RefSeq Acc Id:

XM_054352264 ⟹ XP_054208239

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,609,186 (+)	NCBI

RefSeq Acc Id:

XM_054352265 ⟹ XP_054208240

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

RefSeq Acc Id:

XM_054352266 ⟹ XP_054208241

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

RefSeq Acc Id:

XM_054352267 ⟹ XP_054208242

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

RefSeq Acc Id:

XM_054352268 ⟹ XP_054208243

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,603,448 (+)	NCBI

RefSeq Acc Id:

XM_054352269 ⟹ XP_054208244

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,565,869 - 177,611,193 (+)	NCBI

RefSeq Acc Id:

XM_054352270 ⟹ XP_054208245

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	5	177,586,922 - 177,611,193 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001295142	(Get FASTA)	NCBI Sequence Viewer
	NP_001295143	(Get FASTA)	NCBI Sequence Viewer
	NP_001295144	(Get FASTA)	NCBI Sequence Viewer
	NP_001295145	(Get FASTA)	NCBI Sequence Viewer
	NP_001295147	(Get FASTA)	NCBI Sequence Viewer
	NP_001295148	(Get FASTA)	NCBI Sequence Viewer
	NP_001295150	(Get FASTA)	NCBI Sequence Viewer
	NP_001295152	(Get FASTA)	NCBI Sequence Viewer
	NP_001350642	(Get FASTA)	NCBI Sequence Viewer
	NP_036411	(Get FASTA)	NCBI Sequence Viewer
	XP_005265921	(Get FASTA)	NCBI Sequence Viewer
	XP_011532796	(Get FASTA)	NCBI Sequence Viewer
	XP_011532797	(Get FASTA)	NCBI Sequence Viewer
	XP_011532798	(Get FASTA)	NCBI Sequence Viewer
	XP_016864786	(Get FASTA)	NCBI Sequence Viewer
	XP_016864787	(Get FASTA)	NCBI Sequence Viewer
	XP_016864788	(Get FASTA)	NCBI Sequence Viewer
	XP_016864792	(Get FASTA)	NCBI Sequence Viewer
	XP_047273007	(Get FASTA)	NCBI Sequence Viewer
	XP_047273008	(Get FASTA)	NCBI Sequence Viewer
	XP_047273009	(Get FASTA)	NCBI Sequence Viewer
	XP_047273010	(Get FASTA)	NCBI Sequence Viewer
	XP_047273011	(Get FASTA)	NCBI Sequence Viewer
	XP_047273012	(Get FASTA)	NCBI Sequence Viewer
	XP_047273013	(Get FASTA)	NCBI Sequence Viewer
	XP_054208231	(Get FASTA)	NCBI Sequence Viewer
	XP_054208232	(Get FASTA)	NCBI Sequence Viewer
	XP_054208233	(Get FASTA)	NCBI Sequence Viewer
	XP_054208234	(Get FASTA)	NCBI Sequence Viewer
	XP_054208235	(Get FASTA)	NCBI Sequence Viewer
	XP_054208236	(Get FASTA)	NCBI Sequence Viewer
	XP_054208237	(Get FASTA)	NCBI Sequence Viewer
	XP_054208238	(Get FASTA)	NCBI Sequence Viewer
	XP_054208239	(Get FASTA)	NCBI Sequence Viewer
	XP_054208240	(Get FASTA)	NCBI Sequence Viewer
	XP_054208241	(Get FASTA)	NCBI Sequence Viewer
	XP_054208242	(Get FASTA)	NCBI Sequence Viewer
	XP_054208243	(Get FASTA)	NCBI Sequence Viewer
	XP_054208244	(Get FASTA)	NCBI Sequence Viewer
	XP_054208245	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAD52018	(Get FASTA)	NCBI Sequence Viewer
	AAH07775	(Get FASTA)	NCBI Sequence Viewer
	BAD18614	(Get FASTA)	NCBI Sequence Viewer
	BAH12103	(Get FASTA)	NCBI Sequence Viewer
	BAH12584	(Get FASTA)	NCBI Sequence Viewer
	BAH12620	(Get FASTA)	NCBI Sequence Viewer
	BAH13202	(Get FASTA)	NCBI Sequence Viewer
	BAH13338	(Get FASTA)	NCBI Sequence Viewer
	CAH18475	(Get FASTA)	NCBI Sequence Viewer
	EAW85038	(Get FASTA)	NCBI Sequence Viewer
	EAW85039	(Get FASTA)	NCBI Sequence Viewer
	EAW85040	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000350869
	ENSP00000350869.3
	ENSP00000421089
	ENSP00000421089.1
	ENSP00000421212
	ENSP00000421212.1
	ENSP00000421388.1
	ENSP00000423515
	ENSP00000423515.1
	ENSP00000423690.1
	ENSP00000424495
	ENSP00000424495.1
	ENSP00000425725
	ENSP00000425725.1
GenBank Protein	Q9UL40	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_036411 ⟸ NM_012279
- Peptide Label:	isoform a
- UniProtKB:	Q68CV9 (UniProtKB/Swiss-Prot), B7Z367 (UniProtKB/Swiss-Prot), Q6ZMW1 (UniProtKB/Swiss-Prot), Q9UL40 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEVEHMIQ KNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKRYLAIHGMETLKGETKKLDSDQKSSR SKDKNQCCPICNMTFSSPVVAQSHYLGKTHAKNLKLKQQSTKVEALHQNREMIDPDKFCSLCHA TFNDPVMAQQHYVGKKHRKQETKLKLMARYGRLADPAVTDFPAGKGYPCKTCKIVLNSIEQYQA HVSGFKHKNQSPKTVASSLGQIPMQRQPIQKDSTTLED hide sequence

RefSeq Acc Id:

XP_005265921 ⟸ XM_005265864

- Peptide Label:

isoform X11

- Sequence:

show sequence

MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEAQFFPH
SRTVIPILVLSETYSLCHPVEHMIQKNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKR
YLAIHGMETLKGETKKLDSDQKSSRSKDKNQCCPICNMTFSSPVVAQSHYLGKTHAKNLKLKQQ
STKVEAGKGYPCKTCKIVLNSIEQYQAHVSGFKHKNQSPKTVASSLGQIPMQRQPIQKDSTTLE
D

hide sequence

RefSeq Acc Id:

XP_011532796 ⟸ XM_011534494

- Peptide Label:

isoform X2

- Sequence:

show sequence

MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEAQFFPH
SRTVIPILVLSETYSLCHPVEHMIQKNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKR
YLAIHGMETLKGETKKLDSDQKSSRSKDKNQCCPICNMTFSSPVVAQSHYLGKTHAKNLKLKQQ
STKVEALSKRLTNPFLVASTLALHQNREMIDPDKFCSLCHATFNDPVMAQQHYVGKKHRKQETK
LKLMARYGRLADPAVTDFPGHQKQWHHPWARFQCKGNPFRKTQPPWKTRARGGRVTVWPRK

hide sequence

RefSeq Acc Id:

XP_011532797 ⟸ XM_011534495

- Peptide Label:

isoform X3

- Sequence:

show sequence

MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEAQFFPH
SRTVIPILVLSETYSLCHPVEHMIQKNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKR
YLAIHGMETLKGETKKLDSDQKSSRSKDKNQCCPICNMTFSSPVVAQSHYLGKTHAKNLKLKQQ
STKVEALSKRLTNPFLVASTLALHQNREMIDPDKFCSLCHATFNDPVMAQQHYVGKKHRKQETK
LKLMARYGRLADPAVTDFPGHQKQWHHPWARFQCKGNPFRKTQPPWKTREGAGFPES

hide sequence

RefSeq Acc Id:

XP_011532798 ⟸ XM_011534496

- Peptide Label:

isoform X5

- Sequence:

show sequence

MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEAQFFPH
SRTVIPILVLSETYSLCHPVEHMIQKNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKR
YLAIHGMETLKGETKKLDSDQKSSRSKDKNQCCPICNMTFSSPVVAQSHYLGKTHAKNLKLKQQ
STKVEALHQNREMIDPDKFCSLCHATFNDPVMAQQHYVGKKHRKQETKLKLMARYGRLADPAVT
DFPGHQKQWHHPWARFQCKGNPFRKTQPPWKTRGDSAQHPILGQP

hide sequence

RefSeq Acc Id:	NP_001295142 ⟸ NM_001308213
- Peptide Label:	isoform b
- UniProtKB:	Q9UL40 (UniProtKB/Swiss-Prot), B7Z4N4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEAQFFPH SRTVIPILVLSETYSLCHPVEHMIQKNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKR YLAIHGMETLKGETKKLDSDQKSSRSKDKNQCCPICNMTFSSPVVAQSHYLGKTHAKNLKLKQQ STKVEALHQNREMIDPDKFCSLCHATFNDPVMAQQHYVGKKHRKQETKLKLMARYGRLADPAVT DFPAGKGYPCKTCKIVLNSIEQYQAHVSGFKHKNQSPKTVASSLGQIPMQRQPIQKDSTTLED hide sequence

RefSeq Acc Id:	NP_001295148 ⟸ NM_001308219
- Peptide Label:	isoform g
- UniProtKB:	Q9UL40 (UniProtKB/Swiss-Prot), B7Z4N4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEVEHMIQ KNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKRYLAIHGMETLKGETKKLDSDQVTKN SGIIPGPDSNAKATHSERLNHLGRLELGVAVSQSGQGNEIGSCCVETQLSGTSSFLLPLHKCDG SS hide sequence

RefSeq Acc Id:	NP_001295152 ⟸ NM_001308223
- Peptide Label:	isoform h
- UniProtKB:	B7Z4N4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEAGKGYP CKTCKIVLNSIEQYQAHVSGFKHKNQSPKTVASSLGQIPMQRQPIQKDSTTLED hide sequence

RefSeq Acc Id:

NP_001295144 ⟸ NM_001308215

- Peptide Label:

isoform d

- Sequence:

show sequence

MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEVEHMIQ
KNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKRYLAIHGMETLKGETKKLDSDQKSSR
SKDKNQCCPICNMTFSSPVVAQSHYLGKTHAKNLKLKQQSTKVEAGKGYPCKTCKIVLNSIEQY
QAHVSGFKHKNQSPKTVASSLGQIPMQRQPIQKDSTTLED

hide sequence

RefSeq Acc Id:

NP_001295145 ⟸ NM_001308216

- Peptide Label:

isoform e

- Sequence:

show sequence

MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEVEHMIQ
KNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKRYLAIHGMETLKGETKKLDSDQVTKN
SGIIPGPDSNAKATHSERLNHLGRLEVILPSIPYWASHEPASRDCSALGSLLLVVLTRKVHGPE
AGLGHRQPLIGPG

hide sequence

RefSeq Acc Id:	NP_001295143 ⟸ NM_001308214
- Peptide Label:	isoform c
- UniProtKB:	Q9UL40 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEVEHMIQ KNQCLFTNTQCKVCCALLISESQKLAHYQSSRSKDKNQCCPICNMTFSSPVVAQSHYLGKTHAK NLKLKQQSTKVEALHQNREMIDPDKFCSLCHATFNDPVMAQQHYVGKKHRKQETKLKLMARYGR LADPAVTDFPAGKGYPCKTCKIVLNSIEQYQAHVSGFKHKNQSPKTVASSLGQIPMQRQPIQKD STTLED hide sequence

RefSeq Acc Id:	NP_001295147 ⟸ NM_001308218
- Peptide Label:	isoform f
- UniProtKB:	B7Z4J8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEALSKRL TNPFLVASTLALHQNREMIDPDKFCSLCHATFNDPVMAQQHYVGKKHRKQETKLKLMARYGRLA DPAVTDFPAGKGYPCKTCKIVLNSIEQYQAHVSGFKHKNQSPKTVASSLGQIPMQRQPIQKDST TLED hide sequence

RefSeq Acc Id:	NP_001295150 ⟸ NM_001308221
- Peptide Label:	isoform h
- UniProtKB:	B7Z4N4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEAGKGYP CKTCKIVLNSIEQYQAHVSGFKHKNQSPKTVASSLGQIPMQRQPIQKDSTTLED hide sequence

RefSeq Acc Id:

XP_016864786 ⟸ XM_017009297

- Peptide Label:

isoform X6

- Sequence:

show sequence

MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEVEHMIQ
KNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKRYLAIHGMETLKGETKKLDSDQKSSR
SKDKNQCCPICNMTFSSPVVAQSHYLGKTHAKNLKLKQQSTKVEALSKRLTNPFLVASTLALHQ
NREMIDPDKFCSLCHATFNDPVMAQQHYVGKKHRKQETKLKLMARYGRLADPAVTDFPGHQKQW
HHPWARFQCKGNPFRKTQPPWKTRGDSAQHPILGQP

hide sequence

RefSeq Acc Id:

XP_016864788 ⟸ XM_017009299

- Peptide Label:

isoform X8

- Sequence:

show sequence

MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEVEHMIQ
KNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKRYLAIHGMETLKGETKKLDSDQKSSR
SKDKNQCCPICNMTFSSPVVAQSHYLGKTHAKNLKLKQQSTKVEALHQNREMIDPDKFCSLCHA
TFNDPVMAQQHYVGKKHRKQETKLKLMARYGRLADPAVTDFPGHQKQWHHPWARFQCKGNPFRK
TQPPWKTRGDSAQHPILGQP

hide sequence

RefSeq Acc Id:

XP_016864787 ⟸ XM_017009298

- Peptide Label:

isoform X7

- Sequence:

show sequence

MEYPAPATVQAADGGAAGPYSSSELLEGQEPDGVRFDRERARRLWEAVSGAQPVGREEAQFFPH
SRTVIPILVLSETYSLCHPVEHMIQKNQCLFTNTQCKVCCALLISESQKLAHYQSKKHANKVKR
YLAIHGMETLKGETKKLDSDQKSSRSKDKNQCCPICNMTFSSPVVAQSHYLGKTHAKNLKLKQQ
STKVEALSKRLTNPFLVASTLALHQNREMIDPDKFCSLCHATFNDPVMAQQHYVGKKHRKQETK
LKLMARYGRLADPAVTDFPDEDIKTRKVK

hide sequence

RefSeq Acc Id:	XP_016864792 ⟸ XM_017009303
- Peptide Label:	isoform X15
- Sequence:	show sequence MKSSRSKDKNQCCPICNMTFSSPVVAQSHYLGKTHAKNLKLKQQSTKVEALSKRLTNPFLVAST LALHQNREMIDPDKFCSLCHATFNDPVMAQQHYVGKKHRKQETKLKLMARYGRLADPAVTDFPA GKGYPCKTCKIVLNSIEQYQAHVSGFKHKNQSPKTVASSLGQIPMQRQPIQKDSTTLED hide sequence

RefSeq Acc Id:	NP_001350642 ⟸ NM_001363713
- Peptide Label:	isoform i
- UniProtKB:	D6RJ07 (UniProtKB/TrEMBL)

RefSeq Acc Id:

ENSP00000424495 ⟸ ENST00000503039

RefSeq Acc Id:

ENSP00000421212 ⟸ ENST00000503425

RefSeq Acc Id:

ENSP00000423515 ⟸ ENST00000506693

RefSeq Acc Id:

ENSP00000421388 ⟸ ENST00000508155

RefSeq Acc Id:

ENSP00000425725 ⟸ ENST00000511834

RefSeq Acc Id:

ENSP00000421089 ⟸ ENST00000512315

RefSeq Acc Id:

ENSP00000423690 ⟸ ENST00000513587

RefSeq Acc Id:

ENSP00000350869 ⟸ ENST00000358149

RefSeq Acc Id:	XP_047273010 ⟸ XM_047417054
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_047273011 ⟸ XM_047417055
- Peptide Label:	isoform X12

RefSeq Acc Id:	XP_047273013 ⟸ XM_047417057
- Peptide Label:	isoform X14

RefSeq Acc Id:	XP_047273007 ⟸ XM_047417051
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047273008 ⟸ XM_047417052
- Peptide Label:	isoform X4
- UniProtKB:	D6RJ07 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047273009 ⟸ XM_047417053
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_047273012 ⟸ XM_047417056
- Peptide Label:	isoform X13

RefSeq Acc Id:	XP_054208232 ⟸ XM_054352257
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054208240 ⟸ XM_054352265
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_054208242 ⟸ XM_054352267
- Peptide Label:	isoform X12

RefSeq Acc Id:	XP_054208244 ⟸ XM_054352269
- Peptide Label:	isoform X14

RefSeq Acc Id:	XP_054208231 ⟸ XM_054352256
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054208235 ⟸ XM_054352260
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054208241 ⟸ XM_054352266
- Peptide Label:	isoform X11

RefSeq Acc Id:	XP_054208234 ⟸ XM_054352259
- Peptide Label:	isoform X4
- UniProtKB:	D6RJ07 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054208236 ⟸ XM_054352261
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054208238 ⟸ XM_054352263
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_054208233 ⟸ XM_054352258
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054208239 ⟸ XM_054352264
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_054208237 ⟸ XM_054352262
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054208243 ⟸ XM_054352268
- Peptide Label:	isoform X13

RefSeq Acc Id:	XP_054208245 ⟸ XM_054352270
- Peptide Label:	isoform X15

Protein Domains

C2H2-type U1-type

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9UL40-F1-model_v2	AlphaFold	Q9UL40	1-294	view protein structure

Promoters

RGD ID:

6803719

Promoter ID:

HG_KWN:51890

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000261948, NM_012279, UC003MFJ.1, UC003MFK.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	5	176,381,676 - 176,382,392 (+)	MPROMDB

RGD ID:

6871660

Promoter ID:

EPDNEW_H8994

Type:

initiation region

Name:

ZNF346_1

Description:

zinc finger protein 346

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	5	177,022,696 - 177,022,756	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:16403	AgrOrtholog
COSMIC	ZNF346	COSMIC
Ensembl Genes	ENSG00000113761	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000358149	ENTREZGENE
	ENST00000358149.8	UniProtKB/Swiss-Prot
	ENST00000503039	ENTREZGENE
	ENST00000503039.1	UniProtKB/Swiss-Prot
	ENST00000503425	ENTREZGENE
	ENST00000503425.5	UniProtKB/Swiss-Prot
	ENST00000506693	ENTREZGENE
	ENST00000506693.5	UniProtKB/TrEMBL
	ENST00000508155.5	UniProtKB/TrEMBL
	ENST00000511834	ENTREZGENE
	ENST00000511834.5	UniProtKB/TrEMBL
	ENST00000512315	ENTREZGENE
	ENST00000512315.5	UniProtKB/TrEMBL
	ENST00000513587.5	UniProtKB/TrEMBL
Gene3D-CATH	Classic Zinc Finger	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000113761	GTEx
HGNC ID	HGNC:16403	ENTREZGENE
Human Proteome Map	ZNF346	Human Proteome Map
InterPro	Matrin/U1-like-C_Znf_C2H2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_C2H2_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_C2H2_type	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:23567	UniProtKB/Swiss-Prot
NCBI Gene	23567	ENTREZGENE
OMIM	605308	OMIM
PANTHER	ZINC FINGER PROTEIN 346	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC FINGER PROTEIN 385B-LIKE	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	zf-met	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134898181	PharmGKB
PROSITE	ZINC_FINGER_C2H2_1	UniProtKB/TrEMBL
SMART	ZnF_C2H2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZnF_U1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF57667	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	B7Z367	ENTREZGENE
	B7Z4J8	ENTREZGENE, UniProtKB/TrEMBL
	B7Z4N4	ENTREZGENE, UniProtKB/TrEMBL
	B7Z6B6_HUMAN	UniProtKB/TrEMBL
	B7Z6Q2_HUMAN	UniProtKB/TrEMBL
	D6RJ07	ENTREZGENE, UniProtKB/TrEMBL
	Q68CV9	ENTREZGENE
	Q6ZMW1	ENTREZGENE
	Q9UL40	ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary	B7Z367	UniProtKB/Swiss-Prot
	Q68CV9	UniProtKB/Swiss-Prot
	Q6ZMW1	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