WDR89 (WD repeat domain 89) - Rat Genome Database

Name: WDR89
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: WDR89 (WD repeat domain 89) Homo sapiens

Analyze

Symbol:

WDR89

Name:

WD repeat domain 89

RGD ID:

1316567

HGNC Page

HGNC:20489

Description:

Predicted to act upstream of or within corpus callosum development and ventricular system development; INTERACTS WITH 17beta-estradiol; all-trans-retinoic acid; aristolochic acid A.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C14orf150; MGC9907; MSTP050; WD repeat-containing protein 89

RGD Orthologs

Alliance Genes

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):	Wdr89 (WD repeat domain 89)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Wdr89 (WD repeat domain 89)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Wdr89 (WD repeat domain 89)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	WDR89 (WD repeat domain 89)	NCBI	Ortholog
Canis lupus familiaris (dog):	WDR89 (WD repeat domain 89)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Wdr89 (WD repeat domain 89)	NCBI	Ortholog
Sus scrofa (pig):	WDR89 (WD repeat domain 89)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	WDR89 (WD repeat domain 89)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Wdr89 (WD repeat domain 89)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Wdr89 (WD repeat domain 89)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Wdr89 (WD repeat domain 89)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	wdr89 (WD repeat domain 89)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Drosophila melanogaster (fruit fly):	CG12134	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Saccharomyces cerevisiae (baker's yeast):	YNL035C	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	wdr89.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	wdr89	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB)

Related Pseudogenes:

LOC100130487

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	14	63,597,039 - 63,641,871 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	63,597,039 - 63,641,871 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	64,063,757 - 64,108,589 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	63,133,510 - 63,178,344 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	63,133,510 - 63,178,344	NCBI
Celera	14	44,114,416 - 44,159,247 (-)	NCBI		Celera
Cytogenetic Map	14	q23.2	NCBI
HuRef	14	44,230,434 - 44,274,975 (-)	NCBI		HuRef
CHM1_1	14	64,002,766 - 64,047,647 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(1->4)-beta-D-glucan (ISO)

17beta-estradiol (EXP)

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

all-trans-retinoic acid (EXP)

aristolochic acid A (EXP)

arsenite(3-) (EXP)

benzo[a]pyrene (ISO)

bisphenol A (EXP,ISO)

carbon nanotube (ISO)

chlorpyrifos (ISO)

copper(II) sulfate (EXP)

decabromodiphenyl ether (ISO)

dicrotophos (EXP)

endosulfan (ISO)

ethyl methanesulfonate (EXP)

fenvalerate (ISO)

formaldehyde (EXP)

lead(0) (EXP)

methyl methanesulfonate (EXP)

methylmercury chloride (EXP)

nickel atom (EXP)

ozone (ISO)

paracetamol (ISO)

parathion (ISO)

perfluorooctane-1-sulfonic acid (ISO)

Soman (ISO)

thioacetamide (ISO)

tungsten (ISO)

vorinostat (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

corpus callosum development (IEA,ISO)

ventricular system development (IEA,ISO)

References

References - curated

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

Additional References at PubMed

PMID:12477932	PMID:14702039	PMID:15342556	PMID:15489334	PMID:15635413	PMID:16169070	PMID:16344560	PMID:17207965	PMID:18029348	PMID:21832049	PMID:21988832	PMID:26186194
PMID:26344197	PMID:26673895	PMID:28514442	PMID:29509190	PMID:30804502	PMID:31048545	PMID:31091453	PMID:31527615	PMID:33060197	PMID:33961781	PMID:36604567

Genomics

Comparative Map Data

WDR89
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	14	63,597,039 - 63,641,871 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	63,597,039 - 63,641,871 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	64,063,757 - 64,108,589 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	63,133,510 - 63,178,344 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	63,133,510 - 63,178,344	NCBI
Celera	14	44,114,416 - 44,159,247 (-)	NCBI		Celera
Cytogenetic Map	14	q23.2	NCBI
HuRef	14	44,230,434 - 44,274,975 (-)	NCBI		HuRef
CHM1_1	14	64,002,766 - 64,047,647 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI		T2T-CHM13v2.0

Wdr89
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	12	75,677,368 - 75,716,311 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	12	75,677,370 - 75,716,311 (-)	Ensembl		GRCm39 Ensembl
GRCm38	12	75,630,594 - 75,669,537 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	12	75,630,596 - 75,669,537 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	12	76,731,581 - 76,770,524 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	12	76,549,434 - 76,588,371 (-)	NCBI		MGSCv36	mm8
Celera	12	76,730,938 - 76,769,912 (-)	NCBI		Celera
Cytogenetic Map	12	C3	NCBI
cM Map	12	32.89	NCBI

Wdr89
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	6	100,086,169 - 100,117,796 (-)	NCBI		GRCr8
mRatBN7.2	6	94,350,468 - 94,382,085 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	6	94,350,303 - 94,382,026 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	6	94,744,029 - 94,750,406 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	6	95,042,501 - 95,048,878 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	6	94,471,408 - 94,477,785 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	6	98,599,456 - 98,631,512 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	6	98,599,723 - 98,606,109 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	6	108,017,409 - 108,049,159 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	6	98,231,300 - 98,237,690 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	6	98,234,755 - 98,241,146 (-)	NCBI
Celera	6	92,776,713 - 92,783,104 (-)	NCBI		Celera
Cytogenetic Map	6	q24	NCBI

Wdr89
(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_004955466	6,203,391 - 6,204,548 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955466	6,171,553 - 6,204,818 (+)	NCBI	ChiLan1.0	ChiLan1.0

WDR89
(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	15	64,701,695 - 64,750,622 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	14	63,918,210 - 63,967,136 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	14	44,170,527 - 44,220,090 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	14	62,427,017 - 62,476,018 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	14	62,428,742 - 62,429,905 (-)	Ensembl	panpan1.1		panPan2

WDR89
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	8	38,121,649 - 38,157,178 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	8	38,121,798 - 38,122,961 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	8	37,813,659 - 37,849,642 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	8	38,347,261 - 38,383,287 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	8	38,344,532 - 38,383,145 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	8	37,964,309 - 38,000,279 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	8	38,036,906 - 38,073,061 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	8	38,397,091 - 38,433,470 (-)	NCBI		UU_Cfam_GSD_1.0

Wdr89
(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_024408640	66,684,354 - 66,774,095 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936495	7,417,154 - 7,528,526 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936495	7,417,604 - 7,452,601 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

WDR89
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	1	194,439,820 - 194,475,872 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	1	194,439,825 - 194,475,876 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	1	216,445,622 - 216,461,215 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

WDR89
(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	24	40,793,441 - 40,835,582 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666053	28,965,931 - 29,031,900 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Wdr89
(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_004624734	37,419,141 - 37,420,316 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624734	37,384,138 - 37,420,878 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in WDR89
33 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 14q23.1-23.3(chr14:59917051-66750803)x1	copy number loss	See cases [RCV000050892]	Chr14:59917051..66750803 [GRCh38] Chr14:60383769..67217521 [GRCh37] Chr14:59453522..66287274 [NCBI36] Chr14:14q23.1-23.3	pathogenic
GRCh38/hg38 14q22.3-23.3(chr14:57041036-67208231)x1	copy number loss	See cases [RCV000051521]	Chr14:57041036..67208231 [GRCh38] Chr14:57507754..67674948 [GRCh37] Chr14:56577507..66744701 [NCBI36] Chr14:14q22.3-23.3	pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3	copy number gain	See cases [RCV000135543]	Chr14:20151149..106855263 [GRCh38] Chr14:20619308..107263478 [GRCh37] Chr14:19689148..106334523 [NCBI36] Chr14:14q11.2-32.33	pathogenic
GRCh38/hg38 14q23.2(chr14:63153722-64093651)x3	copy number gain	See cases [RCV000138644]	Chr14:63153722..64093651 [GRCh38] Chr14:63620440..64560369 [GRCh37] Chr14:62690193..63630122 [NCBI36] Chr14:14q23.2	uncertain significance
GRCh38/hg38 14q23.1-23.2(chr14:57653413-64093528)x1	copy number loss	See cases [RCV000138348]	Chr14:57653413..64093528 [GRCh38] Chr14:58120131..64560246 [GRCh37] Chr14:57189884..63629999 [NCBI36] Chr14:14q23.1-23.2	pathogenic
GRCh38/hg38 14q23.2-23.3(chr14:62252700-65753416)x1	copy number loss	See cases [RCV000138250]	Chr14:62252700..65753416 [GRCh38] Chr14:62719418..66220134 [GRCh37] Chr14:61789171..65289887 [NCBI36] Chr14:14q23.2-23.3	pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3	copy number gain	See cases [RCV000143373]	Chr14:20043514..106877229 [GRCh38] Chr14:20511673..107285437 [GRCh37] Chr14:19581513..106356482 [NCBI36] Chr14:14q11.2-32.33	pathogenic
NM_080666.4(WDR89):c.151T>C (p.Ser51Pro)	single nucleotide variant	Inborn genetic diseases [RCV003242821]	Chr14:63599792 [GRCh38] Chr14:64066510 [GRCh37] Chr14:14q23.2	uncertain significance
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3	copy number gain	See cases [RCV000446256]	Chr14:19794561..107234280 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3	copy number gain	See cases [RCV000448557]	Chr14:62493932..107285437 [GRCh37] Chr14:14q23.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437)	copy number gain	See cases [RCV000512041]	Chr14:20511673..107285437 [GRCh37] Chr14:14q11.2-32.33	pathogenic
NM_080666.4(WDR89):c.1061A>G (p.Glu354Gly)	single nucleotide variant	Inborn genetic diseases [RCV003239393]	Chr14:63598882 [GRCh38] Chr14:64065600 [GRCh37] Chr14:14q23.2	uncertain significance
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3	copy number gain	not provided [RCV000738412]	Chr14:19000422..107289053 [GRCh37] Chr14:14q11.1-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3	copy number gain	not provided [RCV000738413]	Chr14:19280733..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3	copy number gain	not provided [RCV000738414]	Chr14:19327823..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q23.2(chr14:63911105-64263364)x1	copy number loss	not provided [RCV000751038]	Chr14:63911105..64263364 [GRCh37] Chr14:14q23.2	benign
GRCh37/hg19 14q23.2(chr14:63916963-64263364)x1	copy number loss	not provided [RCV000751039]	Chr14:63916963..64263364 [GRCh37] Chr14:14q23.2	benign
NM_080666.4(WDR89):c.857C>G (p.Thr286Arg)	single nucleotide variant	Inborn genetic diseases [RCV003271263]	Chr14:63599086 [GRCh38] Chr14:64065804 [GRCh37] Chr14:14q23.2	uncertain significance
NM_080666.4(WDR89):c.824A>G (p.Asp275Gly)	single nucleotide variant	Inborn genetic diseases [RCV003249589]	Chr14:63599119 [GRCh38] Chr14:64065837 [GRCh37] Chr14:14q23.2	uncertain significance
GRCh37/hg19 14q23.1-23.3(chr14:61409856-65742610)x3	copy number gain	not provided [RCV001259780]	Chr14:61409856..65742610 [GRCh37] Chr14:14q23.1-23.3	likely pathogenic
GRCh37/hg19 14q23.2-23.3(chr14:64016496-65834490)x3	copy number gain	See cases [RCV002285053]	Chr14:64016496..65834490 [GRCh37] Chr14:14q23.2-23.3	uncertain significance
GRCh37/hg19 14q22.2-24.3(chr14:54654001-75828024)x3	copy number gain	14q22.2q24.3 duplication [RCV001506967]	Chr14:54654001..75828024 [GRCh37] Chr14:14q22.2-24.3	likely pathogenic
NM_080666.4(WDR89):c.967A>G (p.Thr323Ala)	single nucleotide variant	Inborn genetic diseases [RCV003277445]	Chr14:63598976 [GRCh38] Chr14:64065694 [GRCh37] Chr14:14q23.2	uncertain significance
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2	copy number gain	See cases [RCV002286356]	Chr14:37671058..106985955 [GRCh37] Chr14:14q13.3-32.33	pathogenic
NM_080666.4(WDR89):c.346A>G (p.Asn116Asp)	single nucleotide variant	Inborn genetic diseases [RCV003262641]	Chr14:63599597 [GRCh38] Chr14:64066315 [GRCh37] Chr14:14q23.2	uncertain significance
NM_080666.4(WDR89):c.707C>T (p.Thr236Ile)	single nucleotide variant	Inborn genetic diseases [RCV002660199]	Chr14:63599236 [GRCh38] Chr14:64065954 [GRCh37] Chr14:14q23.2	uncertain significance
NM_080666.4(WDR89):c.595G>A (p.Asp199Asn)	single nucleotide variant	Inborn genetic diseases [RCV002745100]	Chr14:63599348 [GRCh38] Chr14:64066066 [GRCh37] Chr14:14q23.2	uncertain significance
NM_080666.4(WDR89):c.1105G>A (p.Val369Met)	single nucleotide variant	Inborn genetic diseases [RCV002792463]	Chr14:63598838 [GRCh38] Chr14:64065556 [GRCh37] Chr14:14q23.2	uncertain significance
NM_080666.4(WDR89):c.408A>T (p.Lys136Asn)	single nucleotide variant	Inborn genetic diseases [RCV002769871]	Chr14:63599535 [GRCh38] Chr14:64066253 [GRCh37] Chr14:14q23.2	uncertain significance
NM_080666.4(WDR89):c.431T>G (p.Val144Gly)	single nucleotide variant	Inborn genetic diseases [RCV002961845]	Chr14:63599512 [GRCh38] Chr14:64066230 [GRCh37] Chr14:14q23.2	uncertain significance
NM_080666.4(WDR89):c.113G>T (p.Gly38Val)	single nucleotide variant	Inborn genetic diseases [RCV003201070]	Chr14:63599830 [GRCh38] Chr14:64066548 [GRCh37] Chr14:14q23.2	uncertain significance
NM_080666.4(WDR89):c.488G>T (p.Gly163Val)	single nucleotide variant	Inborn genetic diseases [RCV003305357]	Chr14:63599455 [GRCh38] Chr14:64066173 [GRCh37] Chr14:14q23.2	uncertain significance
NM_080666.4(WDR89):c.307A>G (p.Arg103Gly)	single nucleotide variant	Inborn genetic diseases [RCV003371137]	Chr14:63599636 [GRCh38] Chr14:64066354 [GRCh37] Chr14:14q23.2	uncertain significance
GRCh37/hg19 14q22.3-23.2(chr14:55667390-64447598)x1	copy number loss	not provided [RCV003483204]	Chr14:55667390..64447598 [GRCh37] Chr14:14q22.3-23.2	pathogenic
GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3	copy number gain	not provided [RCV003485036]	Chr14:58894502..107227240 [GRCh37] Chr14:14q23.1-32.33	pathogenic
GRCh37/hg19 14q22.3-24.1(chr14:57588965-68334517)x3	copy number gain	not provided [RCV003485034]	Chr14:57588965..68334517 [GRCh37] Chr14:14q22.3-24.1	likely pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1222
Count of miRNA genes:	476
Interacting mature miRNAs:	523
Transcripts:	ENST00000267522, ENST00000394942, ENST00000554717
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

D14S1001

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	64,093,810 - 64,093,980	UniSTS	GRCh37
Build 36	14	63,163,563 - 63,163,733	RGD	NCBI36
Celera	14	44,144,468 - 44,144,636	RGD
Cytogenetic Map	14	q23.2	UniSTS
HuRef	14	44,260,063 - 44,260,235	UniSTS
Marshfield Genetic Map	14	69.18	RGD
Marshfield Genetic Map	14	69.18	UniSTS
Genethon Genetic Map	14	59.0	UniSTS
Whitehead-YAC Contig Map	14		UniSTS

SHGC-36643

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	64,065,334 - 64,065,410	UniSTS	GRCh37
Build 36	14	63,135,087 - 63,135,163	RGD	NCBI36
Celera	14	44,115,993 - 44,116,069	RGD
Cytogenetic Map	14	q23.2	UniSTS
HuRef	14	44,232,011 - 44,232,087	UniSTS
GeneMap99-G3 RH Map	14	2155.0	UniSTS

SHGC-30609

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	64,063,783 - 64,063,907	UniSTS	GRCh37
Build 36	14	63,133,536 - 63,133,660	RGD	NCBI36
Celera	14	44,114,442 - 44,114,566	RGD
Cytogenetic Map	14	q23.2	UniSTS
HuRef	14	44,230,460 - 44,230,584	UniSTS
TNG Radiation Hybrid Map	14	20593.0	UniSTS
Stanford-G3 RH Map	14	2128.0	UniSTS
GeneMap99-GB4 RH Map	14	151.84	UniSTS
Whitehead-RH Map	14	220.7	UniSTS
NCBI RH Map	14	647.8	UniSTS
GeneMap99-G3 RH Map	14	2176.0	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

165

201

766

407

251

193

323

404

Low

2274

2755

1525

547

1007

383

3950

2113

3479

226

1137

1209

166

1160

2691

Below cutoff

204

178

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001008726	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001258272	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001382423	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001382424	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001382425	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001382426	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001382427	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001382428	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001382429	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_080666	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011536383	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375310	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AF115513	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK095324	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL136038	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC010698	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI603622	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP278550	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX248008	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471061	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA882425	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB178690	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000267522 ⟹ ENSP00000267522

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	63,598,502 - 63,641,407 (-)	Ensembl

RefSeq Acc Id:

ENST00000394942 ⟹ ENSP00000378399

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	63,597,039 - 63,641,861 (-)	Ensembl

RefSeq Acc Id:

ENST00000554717 ⟹ ENSP00000451702

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	63,599,263 - 63,641,853 (-)	Ensembl

RefSeq Acc Id:

ENST00000620954 ⟹ ENSP00000480112

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	63,597,039 - 63,641,871 (-)	Ensembl

RefSeq Acc Id:

NM_001008726 ⟹ NP_001008726

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,597,039 - 63,641,871 (-)	NCBI
GRCh37	14	64,063,757 - 64,108,641 (-)	NCBI
Build 36	14	63,133,510 - 63,177,878 (-)	NCBI Archive
Celera	14	44,114,416 - 44,159,247 (-)	RGD
HuRef	14	44,230,434 - 44,274,975 (-)	NCBI
CHM1_1	14	64,002,766 - 64,047,647 (-)	NCBI
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI

Sequence:

show sequence

GTTCCACTTGACCGCTCTAAGCCGCCGCGCAGCCTGCGTTTTCTCCGGTACAGGTTGAGGCTAC
TAAGGCCAGAAAGCAGATTTTCACTTGGGAAGAGACGACCCGTAGTATGGGATGTGGTATGATA
CCAGCAACTGGTCTATTATATCATTTAAACCACATGGCTATCTAAAGAGGTATTTGGCTATTAT
AAATAAAATAGTGATGAACACGTGTACAGGTGTTTGTACGGACATAAGTTGTCATTTCTCTTGA
GTAAATACCTAAAAGTGGGCTTGCTGGAGTTTTACTACCCTTGGATGCTGCTGTTGACATGGAA
AAGATTGAGGAACAATTTGCTAATCTGCACATTGTTAAATGTTCCTTAGGAACCAAAGAGCCCA
CTTACCTTCTTGGTATAGACACATCAAAGACTGTCCAAGCAGGAAAGGAAAACTTGGTTGCTGT
TTTATGTTCTAATGGATCAATCAGAATATATGATAAAGAAAGGTTAAATGTACTACGAGAATTT
AGTGGATATCCTGGACTTCTTAATGGAGTCAGATTTGCAAATTCCTGTGACAGTGTATATTCAG
CATGTACTGATGGCACTGTGAAATGCTGGGATGCTCGAGTAGCCAGAGAAAAACCTGTTCAGCT
CTTCAAGGGTTACCCTTCCAATATTTTTATCAGTTTTGATATTAATTGTAATGATCATATTATT
TGTGCTGGTACAGAAAAAGTTGATGATGATGCATTGTTGGTGTTTTGGGATGCAAGGATGAATT
CTCAGAATTTATCTACAACTAAAGACTCACTTGGTGCATATTCAGAGACACATAGTGATGATGT
CACTCAAGTACGTTTCCATCCCAGCAATCCCAACATGGTAGTCTCAGGTTCATCTGATGGCCTG
GTAAATGTATTTGATATTAATATTGATAATGAGGAGGATGCACTGGTTACAACCTGTAACTCAA
TTTCATCAGTAAGCTGTATTGGTTGGTCTGGGAAAGGTTATAAACAGATTTACTGCATGACACA
TGATGAAGGATTTTATTGGTGGGATCTTAATCATCTGGACACTGATGAACCAGTTACACGTTTG
AACATCCAGGATGTCAGAGAAGTAGTTAACATGAAAGAAGATGCTTTGGACTATTTGATTGGTG
GCCTATATCATGAAAAGACAGACACATTGCATGTTATTGGAGGAACAAACAAAGGAAGGATTCA
TTTGATGAACTGCAGCATGTCAGGACTGACCCATGTGACTAGCCTTCAGGGAGGGCATGCTGCT
ACAGTCCGTTCTTTCTGTTGGAATGTGCAAGATGATTCTTTGTTGACTGGAGGAGAAGATGCAC
AGTTGTTACTTTGGAAACCTGGAGCTATAGAGAAGACCTTTACAAAGAAAGAGAGTATGAAAAT
AGCATCCTCTGTGCACCAACGAGTACGAGTTCATAGTAATGATTCTTATAAAAGAAGGAAAAAG
CAGTGATAATGCATTTGGCACTTTGTTTGGTAGGTTTTATAGTTTCAAATAGTCCTTCTTGTTT
ACTACCCATGGTAGACATGTTTAAAGCTTTATGTAAAAACAAGCCAGTTAGCAAACAGTCCTGG
AAAAATATGGTGAGAATGGTTTAATTCCGGTCTTCACATATTCTAAAAAATTTTAAAGCCTCTA
AGTATAAAATCAGTGAGTTGAAAGTAAAATTTCTTATTTAAAGAACCCATCTGTTAATGTAGTA
AATGTTGGCTTTAAAGAAATAGCTCCGATAAGGACTTTTTAGAAGGAAATACTTGGTAAAACTT
AATAAAACAGGTGGTTGGCTGCATTTTTTAAGCCCAGTTTTTTACATTTTAAATTGTCTTTATT
GTGTATAAAACCAGATTAGACTATATTCTTCATCTGAGGAGCATCTATATGTTTAATACACCTA
ATGTATTATGCTGGAGTATTTAAATGTAAGTATTTTAATGAGTAAATAGAATTAACCTTTTTTA
CAAATGAAATGATAGGCATCTATGTAAAGTGAGAAAAATATGTTTCGTAAATATTTGCATCTTT
AATATTGTTAGTAAGTAGTAAACAGGTGTTTTGCTGATTGAAAGGAAGTTATCTTGGTAAATTG
AGACTCAAAGTGAAATACAAAAATGAAAATATTTATAATAGGACTCGACTTGGAGAAATTGCTA
TTCTTCCTGTTGTCCAAACCATAAATCTGAGGATAACCTGGGCTTTTCTCTTTCCTCTTCTCCT
AACCAGTTTTTCACCAAGTCCTGTGCCATTTCACCTCCTAACGTCTGTCAGCTATCCTTTTGCC
TTTACCTCACCACTATTACCCTAGAGAAGACTTTCATTATTTCTCATCTGGATTACCAGCTCGA
TCTCTAATCTGCTTCAGTTCATCCTTCTTGCTACTTCTAGGCTAAACATCAAAAACAGATCTGG
TAGGGGCGGGGAAATGAGGGGGAAGAAACAAAAACGTGATGGTGCCTCATGCTGCTTAAAATCT
TCAGTACATTGATGTTTTGATGGCGGACTACATAAGCGTTAAAAATTGTGTTTTTCAGAATCTT
TAAAATATAAGACAGTGCTATCTAGTGAATAAAAAAATTAGTTTGAAAGATATCTGGAGAAATC
GCATTCATAAAACAATTGGAAGTGAAACTATTAAAACAATAGGGCTTTTTAAAATTAAAAATAT
TTAAAATTCAAAAGTAATTAATAGTGTTGGAAGATGTAGGTGAGAAAATATTCCTGAAAGTAGA
ACTGAAAGAGACAAAGAGAAAAGATGAAAGCCACAGAAGATAAATACAGGGGTCAAAACCAGAC
TAACAGTTTTAGAAAGTGAAAAAAGTTAAAAAAGAAATGGGGGCAGTGGGTTATTAGAAATAAC
ATAAATGGCTGGTATGGTTTGTCTGTGTCCTCACCCAAATTTCATCTCGAATTGTAATCCCCAT
AATCCCCATGTGTCTAGGGAGAGACCTGGTGGGAGGTGATTGGATCATGGGGGTGGTTTCCCCT
ACGATGTTCTCCTGATAGTGGGTGAGTTCTCACAAGATCTGATGGTTTTATAAAGGGCTCTGCC
CCTTTAACTCCTCACTCTTTCTCCTGAAGCCTTGTGAAGAAGGTGCTTTGCTTCCCCTTTGCGT
TCCCCCATGATTGTAAGTTTCTTGAGGCCTCCCTGGCCATGCTGAACTCTTCAGTCAATTAAAC
ACTTTCCTTTATAAATTA

hide sequence

RefSeq Acc Id:

NM_001258272 ⟹ NP_001245201

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,597,039 - 63,641,871 (-)	NCBI
GRCh37	14	64,063,757 - 64,108,641 (-)	NCBI
HuRef	14	44,230,434 - 44,274,975 (-)	NCBI
CHM1_1	14	64,002,766 - 64,047,647 (-)	NCBI
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI

Sequence:

show sequence

GTTCCACTTGACCGCTCTAAGCCGCCGCGCAGCCTGCGTTTTCTCCGGTACAGGTTGAGGCTAC
TAAGGTACATTTTGCTGGGCCAGGCTGGGCGGGTCCCCGGGATGGGCAGCCCTCTCGACGAGCG
GCGACGCCGTGGTTGAGTCTAGAAAGCTAGAGTTGCTGGACAGCTATCGCGGGAGCGCGGAGGG
AAGTGGGAGGTCTGGACGGAGTGTGCACGTGTTGGCAGTCTCGCTCCGCCGTCGGAGCCACCAG
GTCAAACCTGTGCTGGCCCTGGCCAAAGAAACTTCTGCGGGTCAGGCTGCTGTTGCCGGTGCAG
TTCCCAGTACTTCCTCTGGGGCGTTTTTCAATAAAAGCCAAACGCCCTTGCTCATTTTCAGGGA
AAGACCTGTTTCCTCCTGCTCTTTCCTCTCCACGGATACTCTCCCCACCACTAAAAGGGTTTAG
TATAATCCTTTTGTAGGCCAGAAAGCAGATTTTCACTTGGGAAGAGACGACCCGTAGTATGGGA
TGTGGTATGATACCAGCAACTGGTCTATTATATCATTTAAACCACATGGCTATCTAAAGAGGTA
TTTGGCTATTATAAATAAAATAGTGATGAACACGTGTACAGGTGTTTGTACGGACATAAGTTGT
CATTTCTCTTGAGTAAATACCTAAAAGTGGGCTTGCTGGAGTTTTACTACCCTTGGATGCTGCT
GTTGACATGGAAAAGATTGAGGAACAATTTGCTAATCTGCACATTGTTAAATGTTCCTTAGGAA
CCAAAGAGCCCACTTACCTTCTTGGTATAGACACATCAAAGACTGTCCAAGCAGGAAAGGAAAA
CTTGGTTGCTGTTTTATGTTCTAATGGATCAATCAGAATATATGATAAAGAAAGGTTAAATGTA
CTACGAGAATTTAGTGGATATCCTGGACTTCTTAATGGAGTCAGATTTGCAAATTCCTGTGACA
GTGTATATTCAGCATGTACTGATGGCACTGTGAAATGCTGGGATGCTCGAGTAGCCAGAGAAAA
ACCTGTTCAGCTCTTCAAGGGTTACCCTTCCAATATTTTTATCAGTTTTGATATTAATTGTAAT
GATCATATTATTTGTGCTGGTACAGAAAAAGTTGATGATGATGCATTGTTGGTGTTTTGGGATG
CAAGGATGAATTCTCAGAATTTATCTACAACTAAAGACTCACTTGGTGCATATTCAGAGACACA
TAGTGATGATGTCACTCAAGTACGTTTCCATCCCAGCAATCCCAACATGGTAGTCTCAGGTTCA
TCTGATGGCCTGGTAAATGTATTTGATATTAATATTGATAATGAGGAGGATGCACTGGTTACAA
CCTGTAACTCAATTTCATCAGTAAGCTGTATTGGTTGGTCTGGGAAAGGTTATAAACAGATTTA
CTGCATGACACATGATGAAGGATTTTATTGGTGGGATCTTAATCATCTGGACACTGATGAACCA
GTTACACGTTTGAACATCCAGGATGTCAGAGAAGTAGTTAACATGAAAGAAGATGCTTTGGACT
ATTTGATTGGTGGCCTATATCATGAAAAGACAGACACATTGCATGTTATTGGAGGAACAAACAA
AGGAAGGATTCATTTGATGAACTGCAGCATGTCAGGACTGACCCATGTGACTAGCCTTCAGGGA
GGGCATGCTGCTACAGTCCGTTCTTTCTGTTGGAATGTGCAAGATGATTCTTTGTTGACTGGAG
GAGAAGATGCACAGTTGTTACTTTGGAAACCTGGAGCTATAGAGAAGACCTTTACAAAGAAAGA
GAGTATGAAAATAGCATCCTCTGTGCACCAACGAGTACGAGTTCATAGTAATGATTCTTATAAA
AGAAGGAAAAAGCAGTGATAATGCATTTGGCACTTTGTTTGGTAGGTTTTATAGTTTCAAATAG
TCCTTCTTGTTTACTACCCATGGTAGACATGTTTAAAGCTTTATGTAAAAACAAGCCAGTTAGC
AAACAGTCCTGGAAAAATATGGTGAGAATGGTTTAATTCCGGTCTTCACATATTCTAAAAAATT
TTAAAGCCTCTAAGTATAAAATCAGTGAGTTGAAAGTAAAATTTCTTATTTAAAGAACCCATCT
GTTAATGTAGTAAATGTTGGCTTTAAAGAAATAGCTCCGATAAGGACTTTTTAGAAGGAAATAC
TTGGTAAAACTTAATAAAACAGGTGGTTGGCTGCATTTTTTAAGCCCAGTTTTTTACATTTTAA
ATTGTCTTTATTGTGTATAAAACCAGATTAGACTATATTCTTCATCTGAGGAGCATCTATATGT
TTAATACACCTAATGTATTATGCTGGAGTATTTAAATGTAAGTATTTTAATGAGTAAATAGAAT
TAACCTTTTTTACAAATGAAATGATAGGCATCTATGTAAAGTGAGAAAAATATGTTTCGTAAAT
ATTTGCATCTTTAATATTGTTAGTAAGTAGTAAACAGGTGTTTTGCTGATTGAAAGGAAGTTAT
CTTGGTAAATTGAGACTCAAAGTGAAATACAAAAATGAAAATATTTATAATAGGACTCGACTTG
GAGAAATTGCTATTCTTCCTGTTGTCCAAACCATAAATCTGAGGATAACCTGGGCTTTTCTCTT
TCCTCTTCTCCTAACCAGTTTTTCACCAAGTCCTGTGCCATTTCACCTCCTAACGTCTGTCAGC
TATCCTTTTGCCTTTACCTCACCACTATTACCCTAGAGAAGACTTTCATTATTTCTCATCTGGA
TTACCAGCTCGATCTCTAATCTGCTTCAGTTCATCCTTCTTGCTACTTCTAGGCTAAACATCAA
AAACAGATCTGGTAGGGGCGGGGAAATGAGGGGGAAGAAACAAAAACGTGATGGTGCCTCATGC
TGCTTAAAATCTTCAGTACATTGATGTTTTGATGGCGGACTACATAAGCGTTAAAAATTGTGTT
TTTCAGAATCTTTAAAATATAAGACAGTGCTATCTAGTGAATAAAAAAATTAGTTTGAAAGATA
TCTGGAGAAATCGCATTCATAAAACAATTGGAAGTGAAACTATTAAAACAATAGGGCTTTTTAA
AATTAAAAATATTTAAAATTCAAAAGTAATTAATAGTGTTGGAAGATGTAGGTGAGAAAATATT
CCTGAAAGTAGAACTGAAAGAGACAAAGAGAAAAGATGAAAGCCACAGAAGATAAATACAGGGG
TCAAAACCAGACTAACAGTTTTAGAAAGTGAAAAAAGTTAAAAAAGAAATGGGGGCAGTGGGTT
ATTAGAAATAACATAAATGGCTGGTATGGTTTGTCTGTGTCCTCACCCAAATTTCATCTCGAAT
TGTAATCCCCATAATCCCCATGTGTCTAGGGAGAGACCTGGTGGGAGGTGATTGGATCATGGGG
GTGGTTTCCCCTACGATGTTCTCCTGATAGTGGGTGAGTTCTCACAAGATCTGATGGTTTTATA
AAGGGCTCTGCCCCTTTAACTCCTCACTCTTTCTCCTGAAGCCTTGTGAAGAAGGTGCTTTGCT
TCCCCTTTGCGTTCCCCCATGATTGTAAGTTTCTTGAGGCCTCCCTGGCCATGCTGAACTCTTC
AGTCAATTAAACACTTTCCTTTATAAATTA

hide sequence

RefSeq Acc Id:

NM_001382423 ⟹ NP_001369352

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,597,039 - 63,641,871 (-)	NCBI
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI

Sequence:

show sequence

GTTCCACTTGACCGCTCTAAGCCGCCGCGCAGCCTGCGTTTTCTCCGGTACAGGTTGAGGCTAC
TAAGGTATTTGGCTATTATAAATAAAATAGTGATGAACACGTGTACAGGTGTTTGTACGGACAT
AAGTTGTCATTTCTCTTGAGTAAATACCTAAAAGTGGGCTTGCTGGAAGGCATTTTTGCTGGGT
ACAGAGCTTTGTGTTGAGTTTTACTACCCTTGGATGCTGCTGTTGACATGGAAAAGATTGAGGA
ACAATTTGCTAATCTGCACATTGTTAAATGTTCCTTAGGAACCAAAGAGCCCACTTACCTTCTT
GGTATAGACACATCAAAGACTGTCCAAGCAGGAAAGGAAAACTTGGTTGCTGTTTTATGTTCTA
ATGGATCAATCAGAATATATGATAAAGAAAGGTTAAATGTACTACGAGAATTTAGTGGATATCC
TGGACTTCTTAATGGAGTCAGATTTGCAAATTCCTGTGACAGTGTATATTCAGCATGTACTGAT
GGCACTGTGAAATGCTGGGATGCTCGAGTAGCCAGAGAAAAACCTGTTCAGCTCTTCAAGGGTT
ACCCTTCCAATATTTTTATCAGTTTTGATATTAATTGTAATGATCATATTATTTGTGCTGGTAC
AGAAAAAGTTGATGATGATGCATTGTTGGTGTTTTGGGATGCAAGGATGAATTCTCAGAATTTA
TCTACAACTAAAGACTCACTTGGTGCATATTCAGAGACACATAGTGATGATGTCACTCAAGTAC
GTTTCCATCCCAGCAATCCCAACATGGTAGTCTCAGGTTCATCTGATGGCCTGGTAAATGTATT
TGATATTAATATTGATAATGAGGAGGATGCACTGGTTACAACCTGTAACTCAATTTCATCAGTA
AGCTGTATTGGTTGGTCTGGGAAAGGTTATAAACAGATTTACTGCATGACACATGATGAAGGAT
TTTATTGGTGGGATCTTAATCATCTGGACACTGATGAACCAGTTACACGTTTGAACATCCAGGA
TGTCAGAGAAGTAGTTAACATGAAAGAAGATGCTTTGGACTATTTGATTGGTGGCCTATATCAT
GAAAAGACAGACACATTGCATGTTATTGGAGGAACAAACAAAGGAAGGATTCATTTGATGAACT
GCAGCATGTCAGGACTGACCCATGTGACTAGCCTTCAGGGAGGGCATGCTGCTACAGTCCGTTC
TTTCTGTTGGAATGTGCAAGATGATTCTTTGTTGACTGGAGGAGAAGATGCACAGTTGTTACTT
TGGAAACCTGGAGCTATAGAGAAGACCTTTACAAAGAAAGAGAGTATGAAAATAGCATCCTCTG
TGCACCAACGAGTACGAGTTCATAGTAATGATTCTTATAAAAGAAGGAAAAAGCAGTGATAATG
CATTTGGCACTTTGTTTGGTAGGTTTTATAGTTTCAAATAGTCCTTCTTGTTTACTACCCATGG
TAGACATGTTTAAAGCTTTATGTAAAAACAAGCCAGTTAGCAAACAGTCCTGGAAAAATATGGT
GAGAATGGTTTAATTCCGGTCTTCACATATTCTAAAAAATTTTAAAGCCTCTAAGTATAAAATC
AGTGAGTTGAAAGTAAAATTTCTTATTTAAAGAACCCATCTGTTAATGTAGTAAATGTTGGCTT
TAAAGAAATAGCTCCGATAAGGACTTTTTAGAAGGAAATACTTGGTAAAACTTAATAAAACAGG
TGGTTGGCTGCATTTTTTAAGCCCAGTTTTTTACATTTTAAATTGTCTTTATTGTGTATAAAAC
CAGATTAGACTATATTCTTCATCTGAGGAGCATCTATATGTTTAATACACCTAATGTATTATGC
TGGAGTATTTAAATGTAAGTATTTTAATGAGTAAATAGAATTAACCTTTTTTACAAATGAAATG
ATAGGCATCTATGTAAAGTGAGAAAAATATGTTTCGTAAATATTTGCATCTTTAATATTGTTAG
TAAGTAGTAAACAGGTGTTTTGCTGATTGAAAGGAAGTTATCTTGGTAAATTGAGACTCAAAGT
GAAATACAAAAATGAAAATATTTATAATAGGACTCGACTTGGAGAAATTGCTATTCTTCCTGTT
GTCCAAACCATAAATCTGAGGATAACCTGGGCTTTTCTCTTTCCTCTTCTCCTAACCAGTTTTT
CACCAAGTCCTGTGCCATTTCACCTCCTAACGTCTGTCAGCTATCCTTTTGCCTTTACCTCACC
ACTATTACCCTAGAGAAGACTTTCATTATTTCTCATCTGGATTACCAGCTCGATCTCTAATCTG
CTTCAGTTCATCCTTCTTGCTACTTCTAGGCTAAACATCAAAAACAGATCTGGTAGGGGCGGGG
AAATGAGGGGGAAGAAACAAAAACGTGATGGTGCCTCATGCTGCTTAAAATCTTCAGTACATTG
ATGTTTTGATGGCGGACTACATAAGCGTTAAAAATTGTGTTTTTCAGAATCTTTAAAATATAAG
ACAGTGCTATCTAGTGAATAAAAAAATTAGTTTGAAAGATATCTGGAGAAATCGCATTCATAAA
ACAATTGGAAGTGAAACTATTAAAACAATAGGGCTTTTTAAAATTAAAAATATTTAAAATTCAA
AAGTAATTAATAGTGTTGGAAGATGTAGGTGAGAAAATATTCCTGAAAGTAGAACTGAAAGAGA
CAAAGAGAAAAGATGAAAGCCACAGAAGATAAATACAGGGGTCAAAACCAGACTAACAGTTTTA
GAAAGTGAAAAAAGTTAAAAAAGAAATGGGGGCAGTGGGTTATTAGAAATAACATAAATGGCTG
GTATGGTTTGTCTGTGTCCTCACCCAAATTTCATCTCGAATTGTAATCCCCATAATCCCCATGT
GTCTAGGGAGAGACCTGGTGGGAGGTGATTGGATCATGGGGGTGGTTTCCCCTACGATGTTCTC
CTGATAGTGGGTGAGTTCTCACAAGATCTGATGGTTTTATAAAGGGCTCTGCCCCTTTAACTCC
TCACTCTTTCTCCTGAAGCCTTGTGAAGAAGGTGCTTTGCTTCCCCTTTGCGTTCCCCCATGAT
TGTAAGTTTCTTGAGGCCTCCCTGGCCATGCTGAACTCTTCAGTCAATTAAACACTTTCCTTTA
TAAATTA

hide sequence

RefSeq Acc Id:

NM_001382424 ⟹ NP_001369353

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,597,039 - 63,641,871 (-)	NCBI
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI

Sequence:

show sequence

GTTCCACTTGACCGCTCTAAGCCGCCGCGCAGCCTGCGTTTTCTCCGGTACAGGTTGAGGCTAC
TAAGGTATTTGGCTATTATAAATAAAATAGTGATGAACACGTGTACAGGTGTTTGTACGGACAT
AAGTTGTCATTTCTCTTGAGTAAATACCTAAAAGTGGGCTTGCTGGTAGAGACGGGGTTTTACC
ATGTTGACCAGACTGGTCTCGAACTCCTGACCTCAGTGATCGCTGCCTCGGCCTCCAGAAGTGT
TGGGATTACAGGCATGAGCCACCATGCCTGACCTATTACATCTATTGTAGTTTTACTACCCTTG
GATGCTGCTGTTGACATGGAAAAGATTGAGGAACAATTTGCTAATCTGCACATTGTTAAATGTT
CCTTAGGAACCAAAGAGCCCACTTACCTTCTTGGTATAGACACATCAAAGACTGTCCAAGCAGG
AAAGGAAAACTTGGTTGCTGTTTTATGTTCTAATGGATCAATCAGAATATATGATAAAGAAAGG
TTAAATGTACTACGAGAATTTAGTGGATATCCTGGACTTCTTAATGGAGTCAGATTTGCAAATT
CCTGTGACAGTGTATATTCAGCATGTACTGATGGCACTGTGAAATGCTGGGATGCTCGAGTAGC
CAGAGAAAAACCTGTTCAGCTCTTCAAGGGTTACCCTTCCAATATTTTTATCAGTTTTGATATT
AATTGTAATGATCATATTATTTGTGCTGGTACAGAAAAAGTTGATGATGATGCATTGTTGGTGT
TTTGGGATGCAAGGATGAATTCTCAGAATTTATCTACAACTAAAGACTCACTTGGTGCATATTC
AGAGACACATAGTGATGATGTCACTCAAGTACGTTTCCATCCCAGCAATCCCAACATGGTAGTC
TCAGGTTCATCTGATGGCCTGGTAAATGTATTTGATATTAATATTGATAATGAGGAGGATGCAC
TGGTTACAACCTGTAACTCAATTTCATCAGTAAGCTGTATTGGTTGGTCTGGGAAAGGTTATAA
ACAGATTTACTGCATGACACATGATGAAGGATTTTATTGGTGGGATCTTAATCATCTGGACACT
GATGAACCAGTTACACGTTTGAACATCCAGGATGTCAGAGAAGTAGTTAACATGAAAGAAGATG
CTTTGGACTATTTGATTGGTGGCCTATATCATGAAAAGACAGACACATTGCATGTTATTGGAGG
AACAAACAAAGGAAGGATTCATTTGATGAACTGCAGCATGTCAGGACTGACCCATGTGACTAGC
CTTCAGGGAGGGCATGCTGCTACAGTCCGTTCTTTCTGTTGGAATGTGCAAGATGATTCTTTGT
TGACTGGAGGAGAAGATGCACAGTTGTTACTTTGGAAACCTGGAGCTATAGAGAAGACCTTTAC
AAAGAAAGAGAGTATGAAAATAGCATCCTCTGTGCACCAACGAGTACGAGTTCATAGTAATGAT
TCTTATAAAAGAAGGAAAAAGCAGTGATAATGCATTTGGCACTTTGTTTGGTAGGTTTTATAGT
TTCAAATAGTCCTTCTTGTTTACTACCCATGGTAGACATGTTTAAAGCTTTATGTAAAAACAAG
CCAGTTAGCAAACAGTCCTGGAAAAATATGGTGAGAATGGTTTAATTCCGGTCTTCACATATTC
TAAAAAATTTTAAAGCCTCTAAGTATAAAATCAGTGAGTTGAAAGTAAAATTTCTTATTTAAAG
AACCCATCTGTTAATGTAGTAAATGTTGGCTTTAAAGAAATAGCTCCGATAAGGACTTTTTAGA
AGGAAATACTTGGTAAAACTTAATAAAACAGGTGGTTGGCTGCATTTTTTAAGCCCAGTTTTTT
ACATTTTAAATTGTCTTTATTGTGTATAAAACCAGATTAGACTATATTCTTCATCTGAGGAGCA
TCTATATGTTTAATACACCTAATGTATTATGCTGGAGTATTTAAATGTAAGTATTTTAATGAGT
AAATAGAATTAACCTTTTTTACAAATGAAATGATAGGCATCTATGTAAAGTGAGAAAAATATGT
TTCGTAAATATTTGCATCTTTAATATTGTTAGTAAGTAGTAAACAGGTGTTTTGCTGATTGAAA
GGAAGTTATCTTGGTAAATTGAGACTCAAAGTGAAATACAAAAATGAAAATATTTATAATAGGA
CTCGACTTGGAGAAATTGCTATTCTTCCTGTTGTCCAAACCATAAATCTGAGGATAACCTGGGC
TTTTCTCTTTCCTCTTCTCCTAACCAGTTTTTCACCAAGTCCTGTGCCATTTCACCTCCTAACG
TCTGTCAGCTATCCTTTTGCCTTTACCTCACCACTATTACCCTAGAGAAGACTTTCATTATTTC
TCATCTGGATTACCAGCTCGATCTCTAATCTGCTTCAGTTCATCCTTCTTGCTACTTCTAGGCT
AAACATCAAAAACAGATCTGGTAGGGGCGGGGAAATGAGGGGGAAGAAACAAAAACGTGATGGT
GCCTCATGCTGCTTAAAATCTTCAGTACATTGATGTTTTGATGGCGGACTACATAAGCGTTAAA
AATTGTGTTTTTCAGAATCTTTAAAATATAAGACAGTGCTATCTAGTGAATAAAAAAATTAGTT
TGAAAGATATCTGGAGAAATCGCATTCATAAAACAATTGGAAGTGAAACTATTAAAACAATAGG
GCTTTTTAAAATTAAAAATATTTAAAATTCAAAAGTAATTAATAGTGTTGGAAGATGTAGGTGA
GAAAATATTCCTGAAAGTAGAACTGAAAGAGACAAAGAGAAAAGATGAAAGCCACAGAAGATAA
ATACAGGGGTCAAAACCAGACTAACAGTTTTAGAAAGTGAAAAAAGTTAAAAAAGAAATGGGGG
CAGTGGGTTATTAGAAATAACATAAATGGCTGGTATGGTTTGTCTGTGTCCTCACCCAAATTTC
ATCTCGAATTGTAATCCCCATAATCCCCATGTGTCTAGGGAGAGACCTGGTGGGAGGTGATTGG
ATCATGGGGGTGGTTTCCCCTACGATGTTCTCCTGATAGTGGGTGAGTTCTCACAAGATCTGAT
GGTTTTATAAAGGGCTCTGCCCCTTTAACTCCTCACTCTTTCTCCTGAAGCCTTGTGAAGAAGG
TGCTTTGCTTCCCCTTTGCGTTCCCCCATGATTGTAAGTTTCTTGAGGCCTCCCTGGCCATGCT
GAACTCTTCAGTCAATTAAACACTTTCCTTTATAAATTA

hide sequence

RefSeq Acc Id:

NM_001382425 ⟹ NP_001369354

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,597,039 - 63,641,871 (-)	NCBI
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI

Sequence:

show sequence

GTTCCACTTGACCGCTCTAAGCCGCCGCGCAGCCTGCGTTTTCTCCGGTACAGGTTGAGGCTAC
TAAGTACTTTTCATGCTTGTCTGTCCTCATAGTCAGCATATGAAAATGTTCAGTGACCAGACAT
GAGTAACAGACATTGTGGACTGTGGAAGATCCTGAACGCTAAGTCAAGAAAGTAAACTGTTCCT
GAGGGAGAAAGGAAGAACCACTGATTGTCAGACTTTGCTATCATTCATGGAAATTGGGAGCATG
GGTTGAAGAGAGAAACTAATGAAGTAAATTTTGGATAATCTGAATTTTAAGTTCTGGCAGCACA
TGTAGCAAGCATTTAAGAATACAAGAGCTTCAGAAAGAGAATAAAGAGATGAAGTTTGGAGTTA
AAGATCTGGAAGTGATTATACTAAAGACTTGATCTGGTATTTGGCTATTATAAATAAAATAGTG
ATGAACACGTGTACAGGTGTTTGTACGGACATAAGTTGTCATTTCTCTTGAGTAAATACCTAAA
AGTGGGCTTGCTGGAGTTTTACTACCCTTGGATGCTGCTGTTGACATGGAAAAGATTGAGGAAC
AATTTGCTAATCTGCACATTGTTAAATGTTCCTTAGGAACCAAAGAGCCCACTTACCTTCTTGG
TATAGACACATCAAAGACTGTCCAAGCAGGAAAGGAAAACTTGGTTGCTGTTTTATGTTCTAAT
GGATCAATCAGAATATATGATAAAGAAAGGTTAAATGTACTACGAGAATTTAGTGGATATCCTG
GACTTCTTAATGGAGTCAGATTTGCAAATTCCTGTGACAGTGTATATTCAGCATGTACTGATGG
CACTGTGAAATGCTGGGATGCTCGAGTAGCCAGAGAAAAACCTGTTCAGCTCTTCAAGGGTTAC
CCTTCCAATATTTTTATCAGTTTTGATATTAATTGTAATGATCATATTATTTGTGCTGGTACAG
AAAAAGTTGATGATGATGCATTGTTGGTGTTTTGGGATGCAAGGATGAATTCTCAGAATTTATC
TACAACTAAAGACTCACTTGGTGCATATTCAGAGACACATAGTGATGATGTCACTCAAGTACGT
TTCCATCCCAGCAATCCCAACATGGTAGTCTCAGGTTCATCTGATGGCCTGGTAAATGTATTTG
ATATTAATATTGATAATGAGGAGGATGCACTGGTTACAACCTGTAACTCAATTTCATCAGTAAG
CTGTATTGGTTGGTCTGGGAAAGGTTATAAACAGATTTACTGCATGACACATGATGAAGGATTT
TATTGGTGGGATCTTAATCATCTGGACACTGATGAACCAGTTACACGTTTGAACATCCAGGATG
TCAGAGAAGTAGTTAACATGAAAGAAGATGCTTTGGACTATTTGATTGGTGGCCTATATCATGA
AAAGACAGACACATTGCATGTTATTGGAGGAACAAACAAAGGAAGGATTCATTTGATGAACTGC
AGCATGTCAGGACTGACCCATGTGACTAGCCTTCAGGGAGGGCATGCTGCTACAGTCCGTTCTT
TCTGTTGGAATGTGCAAGATGATTCTTTGTTGACTGGAGGAGAAGATGCACAGTTGTTACTTTG
GAAACCTGGAGCTATAGAGAAGACCTTTACAAAGAAAGAGAGTATGAAAATAGCATCCTCTGTG
CACCAACGAGTACGAGTTCATAGTAATGATTCTTATAAAAGAAGGAAAAAGCAGTGATAATGCA
TTTGGCACTTTGTTTGGTAGGTTTTATAGTTTCAAATAGTCCTTCTTGTTTACTACCCATGGTA
GACATGTTTAAAGCTTTATGTAAAAACAAGCCAGTTAGCAAACAGTCCTGGAAAAATATGGTGA
GAATGGTTTAATTCCGGTCTTCACATATTCTAAAAAATTTTAAAGCCTCTAAGTATAAAATCAG
TGAGTTGAAAGTAAAATTTCTTATTTAAAGAACCCATCTGTTAATGTAGTAAATGTTGGCTTTA
AAGAAATAGCTCCGATAAGGACTTTTTAGAAGGAAATACTTGGTAAAACTTAATAAAACAGGTG
GTTGGCTGCATTTTTTAAGCCCAGTTTTTTACATTTTAAATTGTCTTTATTGTGTATAAAACCA
GATTAGACTATATTCTTCATCTGAGGAGCATCTATATGTTTAATACACCTAATGTATTATGCTG
GAGTATTTAAATGTAAGTATTTTAATGAGTAAATAGAATTAACCTTTTTTACAAATGAAATGAT
AGGCATCTATGTAAAGTGAGAAAAATATGTTTCGTAAATATTTGCATCTTTAATATTGTTAGTA
AGTAGTAAACAGGTGTTTTGCTGATTGAAAGGAAGTTATCTTGGTAAATTGAGACTCAAAGTGA
AATACAAAAATGAAAATATTTATAATAGGACTCGACTTGGAGAAATTGCTATTCTTCCTGTTGT
CCAAACCATAAATCTGAGGATAACCTGGGCTTTTCTCTTTCCTCTTCTCCTAACCAGTTTTTCA
CCAAGTCCTGTGCCATTTCACCTCCTAACGTCTGTCAGCTATCCTTTTGCCTTTACCTCACCAC
TATTACCCTAGAGAAGACTTTCATTATTTCTCATCTGGATTACCAGCTCGATCTCTAATCTGCT
TCAGTTCATCCTTCTTGCTACTTCTAGGCTAAACATCAAAAACAGATCTGGTAGGGGCGGGGAA
ATGAGGGGGAAGAAACAAAAACGTGATGGTGCCTCATGCTGCTTAAAATCTTCAGTACATTGAT
GTTTTGATGGCGGACTACATAAGCGTTAAAAATTGTGTTTTTCAGAATCTTTAAAATATAAGAC
AGTGCTATCTAGTGAATAAAAAAATTAGTTTGAAAGATATCTGGAGAAATCGCATTCATAAAAC
AATTGGAAGTGAAACTATTAAAACAATAGGGCTTTTTAAAATTAAAAATATTTAAAATTCAAAA
GTAATTAATAGTGTTGGAAGATGTAGGTGAGAAAATATTCCTGAAAGTAGAACTGAAAGAGACA
AAGAGAAAAGATGAAAGCCACAGAAGATAAATACAGGGGTCAAAACCAGACTAACAGTTTTAGA
AAGTGAAAAAAGTTAAAAAAGAAATGGGGGCAGTGGGTTATTAGAAATAACATAAATGGCTGGT
ATGGTTTGTCTGTGTCCTCACCCAAATTTCATCTCGAATTGTAATCCCCATAATCCCCATGTGT
CTAGGGAGAGACCTGGTGGGAGGTGATTGGATCATGGGGGTGGTTTCCCCTACGATGTTCTCCT
GATAGTGGGTGAGTTCTCACAAGATCTGATGGTTTTATAAAGGGCTCTGCCCCTTTAACTCCTC
ACTCTTTCTCCTGAAGCCTTGTGAAGAAGGTGCTTTGCTTCCCCTTTGCGTTCCCCCATGATTG
TAAGTTTCTTGAGGCCTCCCTGGCCATGCTGAACTCTTCAGTCAATTAAACACTTTCCTTTATA
AATTA

hide sequence

RefSeq Acc Id:

NM_001382426 ⟹ NP_001369355

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,597,039 - 63,641,871 (-)	NCBI
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI

Sequence:

show sequence

GTTCCACTTGACCGCTCTAAGCCGCCGCGCAGCCTGCGTTTTCTCCGGTACAGGTTGAGGCTAC
TAAGGGAAAGACCTGTTTCCTCCTGCTCTTTCCTCTCCACGGATACTCTCCCCACCACTAAAAG
GGTTTAGTATAATCCTTTTGTAGGCCAGAAAGCAGATTTTCACTTGGGAAGAGACGACCCGTAG
TATGGGATGTGGTATGATACCAGCAACTGGTCTATTATATCATTTAAACCACATGGCTATCTAA
AGAGGTATTTGGCTATTATAAATAAAATAGTGATGAACACGTGTACAGGTGTTTGTACGGACAT
AAGTTGTCATTTCTCTTGAGTAAATACCTAAAAGTGGGCTTGCTGGAGTTTTACTACCCTTGGA
TGCTGCTGTTGACATGGAAAAGATTGAGGAACAATTTGCTAATCTGCACATTGTTAAATGTTCC
TTAGGAACCAAAGAGCCCACTTACCTTCTTGGTATAGACACATCAAAGACTGTCCAAGCAGGAA
AGGAAAACTTGGTTGCTGTTTTATGTTCTAATGGATCAATCAGAATATATGATAAAGAAAGGTT
AAATGTACTACGAGAATTTAGTGGATATCCTGGACTTCTTAATGGAGTCAGATTTGCAAATTCC
TGTGACAGTGTATATTCAGCATGTACTGATGGCACTGTGAAATGCTGGGATGCTCGAGTAGCCA
GAGAAAAACCTGTTCAGCTCTTCAAGGGTTACCCTTCCAATATTTTTATCAGTTTTGATATTAA
TTGTAATGATCATATTATTTGTGCTGGTACAGAAAAAGTTGATGATGATGCATTGTTGGTGTTT
TGGGATGCAAGGATGAATTCTCAGAATTTATCTACAACTAAAGACTCACTTGGTGCATATTCAG
AGACACATAGTGATGATGTCACTCAAGTACGTTTCCATCCCAGCAATCCCAACATGGTAGTCTC
AGGTTCATCTGATGGCCTGGTAAATGTATTTGATATTAATATTGATAATGAGGAGGATGCACTG
GTTACAACCTGTAACTCAATTTCATCAGTAAGCTGTATTGGTTGGTCTGGGAAAGGTTATAAAC
AGATTTACTGCATGACACATGATGAAGGATTTTATTGGTGGGATCTTAATCATCTGGACACTGA
TGAACCAGTTACACGTTTGAACATCCAGGATGTCAGAGAAGTAGTTAACATGAAAGAAGATGCT
TTGGACTATTTGATTGGTGGCCTATATCATGAAAAGACAGACACATTGCATGTTATTGGAGGAA
CAAACAAAGGAAGGATTCATTTGATGAACTGCAGCATGTCAGGACTGACCCATGTGACTAGCCT
TCAGGGAGGGCATGCTGCTACAGTCCGTTCTTTCTGTTGGAATGTGCAAGATGATTCTTTGTTG
ACTGGAGGAGAAGATGCACAGTTGTTACTTTGGAAACCTGGAGCTATAGAGAAGACCTTTACAA
AGAAAGAGAGTATGAAAATAGCATCCTCTGTGCACCAACGAGTACGAGTTCATAGTAATGATTC
TTATAAAAGAAGGAAAAAGCAGTGATAATGCATTTGGCACTTTGTTTGGTAGGTTTTATAGTTT
CAAATAGTCCTTCTTGTTTACTACCCATGGTAGACATGTTTAAAGCTTTATGTAAAAACAAGCC
AGTTAGCAAACAGTCCTGGAAAAATATGGTGAGAATGGTTTAATTCCGGTCTTCACATATTCTA
AAAAATTTTAAAGCCTCTAAGTATAAAATCAGTGAGTTGAAAGTAAAATTTCTTATTTAAAGAA
CCCATCTGTTAATGTAGTAAATGTTGGCTTTAAAGAAATAGCTCCGATAAGGACTTTTTAGAAG
GAAATACTTGGTAAAACTTAATAAAACAGGTGGTTGGCTGCATTTTTTAAGCCCAGTTTTTTAC
ATTTTAAATTGTCTTTATTGTGTATAAAACCAGATTAGACTATATTCTTCATCTGAGGAGCATC
TATATGTTTAATACACCTAATGTATTATGCTGGAGTATTTAAATGTAAGTATTTTAATGAGTAA
ATAGAATTAACCTTTTTTACAAATGAAATGATAGGCATCTATGTAAAGTGAGAAAAATATGTTT
CGTAAATATTTGCATCTTTAATATTGTTAGTAAGTAGTAAACAGGTGTTTTGCTGATTGAAAGG
AAGTTATCTTGGTAAATTGAGACTCAAAGTGAAATACAAAAATGAAAATATTTATAATAGGACT
CGACTTGGAGAAATTGCTATTCTTCCTGTTGTCCAAACCATAAATCTGAGGATAACCTGGGCTT
TTCTCTTTCCTCTTCTCCTAACCAGTTTTTCACCAAGTCCTGTGCCATTTCACCTCCTAACGTC
TGTCAGCTATCCTTTTGCCTTTACCTCACCACTATTACCCTAGAGAAGACTTTCATTATTTCTC
ATCTGGATTACCAGCTCGATCTCTAATCTGCTTCAGTTCATCCTTCTTGCTACTTCTAGGCTAA
ACATCAAAAACAGATCTGGTAGGGGCGGGGAAATGAGGGGGAAGAAACAAAAACGTGATGGTGC
CTCATGCTGCTTAAAATCTTCAGTACATTGATGTTTTGATGGCGGACTACATAAGCGTTAAAAA
TTGTGTTTTTCAGAATCTTTAAAATATAAGACAGTGCTATCTAGTGAATAAAAAAATTAGTTTG
AAAGATATCTGGAGAAATCGCATTCATAAAACAATTGGAAGTGAAACTATTAAAACAATAGGGC
TTTTTAAAATTAAAAATATTTAAAATTCAAAAGTAATTAATAGTGTTGGAAGATGTAGGTGAGA
AAATATTCCTGAAAGTAGAACTGAAAGAGACAAAGAGAAAAGATGAAAGCCACAGAAGATAAAT
ACAGGGGTCAAAACCAGACTAACAGTTTTAGAAAGTGAAAAAAGTTAAAAAAGAAATGGGGGCA
GTGGGTTATTAGAAATAACATAAATGGCTGGTATGGTTTGTCTGTGTCCTCACCCAAATTTCAT
CTCGAATTGTAATCCCCATAATCCCCATGTGTCTAGGGAGAGACCTGGTGGGAGGTGATTGGAT
CATGGGGGTGGTTTCCCCTACGATGTTCTCCTGATAGTGGGTGAGTTCTCACAAGATCTGATGG
TTTTATAAAGGGCTCTGCCCCTTTAACTCCTCACTCTTTCTCCTGAAGCCTTGTGAAGAAGGTG
CTTTGCTTCCCCTTTGCGTTCCCCCATGATTGTAAGTTTCTTGAGGCCTCCCTGGCCATGCTGA
ACTCTTCAGTCAATTAAACACTTTCCTTTATAAATTA

hide sequence

RefSeq Acc Id:

NM_001382427 ⟹ NP_001369356

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,597,039 - 63,641,871 (-)	NCBI
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI

Sequence:

show sequence

GTTCCACTTGACCGCTCTAAGCCGCCGCGCAGCCTGCGTTTTCTCCGGTACAGGTTGAGGCTAC
TAAGGTATTTGGCTATTATAAATAAAATAGTGATGAACACGTGTACAGGTGTTTGTACGGACAT
AAGTTGTCATTTCTCTTGAGTAAATACCTAAAAGTGGGCTTGCTGGTGGAGAGACTCTCTCTGG
GCAGGTGACATATGCTGAGACCTGAATAACAGGAAGGAGTCACTCATGCAGACATGCAGGGAAA
GAATACTCCAGGCAAACAGCTGTTGCTGCAGTCCTGAGGCAGGAGCAAGCCTGACGTGTTCAAG
AGTTTTACTACCCTTGGATGCTGCTGTTGACATGGAAAAGATTGAGGAACAATTTGCTAATCTG
CACATTGTTAAATGTTCCTTAGGAACCAAAGAGCCCACTTACCTTCTTGGTATAGACACATCAA
AGACTGTCCAAGCAGGAAAGGAAAACTTGGTTGCTGTTTTATGTTCTAATGGATCAATCAGAAT
ATATGATAAAGAAAGGTTAAATGTACTACGAGAATTTAGTGGATATCCTGGACTTCTTAATGGA
GTCAGATTTGCAAATTCCTGTGACAGTGTATATTCAGCATGTACTGATGGCACTGTGAAATGCT
GGGATGCTCGAGTAGCCAGAGAAAAACCTGTTCAGCTCTTCAAGGGTTACCCTTCCAATATTTT
TATCAGTTTTGATATTAATTGTAATGATCATATTATTTGTGCTGGTACAGAAAAAGTTGATGAT
GATGCATTGTTGGTGTTTTGGGATGCAAGGATGAATTCTCAGAATTTATCTACAACTAAAGACT
CACTTGGTGCATATTCAGAGACACATAGTGATGATGTCACTCAAGTACGTTTCCATCCCAGCAA
TCCCAACATGGTAGTCTCAGGTTCATCTGATGGCCTGGTAAATGTATTTGATATTAATATTGAT
AATGAGGAGGATGCACTGGTTACAACCTGTAACTCAATTTCATCAGTAAGCTGTATTGGTTGGT
CTGGGAAAGGTTATAAACAGATTTACTGCATGACACATGATGAAGGATTTTATTGGTGGGATCT
TAATCATCTGGACACTGATGAACCAGTTACACGTTTGAACATCCAGGATGTCAGAGAAGTAGTT
AACATGAAAGAAGATGCTTTGGACTATTTGATTGGTGGCCTATATCATGAAAAGACAGACACAT
TGCATGTTATTGGAGGAACAAACAAAGGAAGGATTCATTTGATGAACTGCAGCATGTCAGGACT
GACCCATGTGACTAGCCTTCAGGGAGGGCATGCTGCTACAGTCCGTTCTTTCTGTTGGAATGTG
CAAGATGATTCTTTGTTGACTGGAGGAGAAGATGCACAGTTGTTACTTTGGAAACCTGGAGCTA
TAGAGAAGACCTTTACAAAGAAAGAGAGTATGAAAATAGCATCCTCTGTGCACCAACGAGTACG
AGTTCATAGTAATGATTCTTATAAAAGAAGGAAAAAGCAGTGATAATGCATTTGGCACTTTGTT
TGGTAGGTTTTATAGTTTCAAATAGTCCTTCTTGTTTACTACCCATGGTAGACATGTTTAAAGC
TTTATGTAAAAACAAGCCAGTTAGCAAACAGTCCTGGAAAAATATGGTGAGAATGGTTTAATTC
CGGTCTTCACATATTCTAAAAAATTTTAAAGCCTCTAAGTATAAAATCAGTGAGTTGAAAGTAA
AATTTCTTATTTAAAGAACCCATCTGTTAATGTAGTAAATGTTGGCTTTAAAGAAATAGCTCCG
ATAAGGACTTTTTAGAAGGAAATACTTGGTAAAACTTAATAAAACAGGTGGTTGGCTGCATTTT
TTAAGCCCAGTTTTTTACATTTTAAATTGTCTTTATTGTGTATAAAACCAGATTAGACTATATT
CTTCATCTGAGGAGCATCTATATGTTTAATACACCTAATGTATTATGCTGGAGTATTTAAATGT
AAGTATTTTAATGAGTAAATAGAATTAACCTTTTTTACAAATGAAATGATAGGCATCTATGTAA
AGTGAGAAAAATATGTTTCGTAAATATTTGCATCTTTAATATTGTTAGTAAGTAGTAAACAGGT
GTTTTGCTGATTGAAAGGAAGTTATCTTGGTAAATTGAGACTCAAAGTGAAATACAAAAATGAA
AATATTTATAATAGGACTCGACTTGGAGAAATTGCTATTCTTCCTGTTGTCCAAACCATAAATC
TGAGGATAACCTGGGCTTTTCTCTTTCCTCTTCTCCTAACCAGTTTTTCACCAAGTCCTGTGCC
ATTTCACCTCCTAACGTCTGTCAGCTATCCTTTTGCCTTTACCTCACCACTATTACCCTAGAGA
AGACTTTCATTATTTCTCATCTGGATTACCAGCTCGATCTCTAATCTGCTTCAGTTCATCCTTC
TTGCTACTTCTAGGCTAAACATCAAAAACAGATCTGGTAGGGGCGGGGAAATGAGGGGGAAGAA
ACAAAAACGTGATGGTGCCTCATGCTGCTTAAAATCTTCAGTACATTGATGTTTTGATGGCGGA
CTACATAAGCGTTAAAAATTGTGTTTTTCAGAATCTTTAAAATATAAGACAGTGCTATCTAGTG
AATAAAAAAATTAGTTTGAAAGATATCTGGAGAAATCGCATTCATAAAACAATTGGAAGTGAAA
CTATTAAAACAATAGGGCTTTTTAAAATTAAAAATATTTAAAATTCAAAAGTAATTAATAGTGT
TGGAAGATGTAGGTGAGAAAATATTCCTGAAAGTAGAACTGAAAGAGACAAAGAGAAAAGATGA
AAGCCACAGAAGATAAATACAGGGGTCAAAACCAGACTAACAGTTTTAGAAAGTGAAAAAAGTT
AAAAAAGAAATGGGGGCAGTGGGTTATTAGAAATAACATAAATGGCTGGTATGGTTTGTCTGTG
TCCTCACCCAAATTTCATCTCGAATTGTAATCCCCATAATCCCCATGTGTCTAGGGAGAGACCT
GGTGGGAGGTGATTGGATCATGGGGGTGGTTTCCCCTACGATGTTCTCCTGATAGTGGGTGAGT
TCTCACAAGATCTGATGGTTTTATAAAGGGCTCTGCCCCTTTAACTCCTCACTCTTTCTCCTGA
AGCCTTGTGAAGAAGGTGCTTTGCTTCCCCTTTGCGTTCCCCCATGATTGTAAGTTTCTTGAGG
CCTCCCTGGCCATGCTGAACTCTTCAGTCAATTAAACACTTTCCTTTATAAATTA

hide sequence

RefSeq Acc Id:

NM_001382428 ⟹ NP_001369357

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,597,039 - 63,641,871 (-)	NCBI
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI

Sequence:

show sequence

GTTCCACTTGACCGCTCTAAGCCGCCGCGCAGCCTGCGTTTTCTCCGGTACAGGTTGAGGCTAC
TAAGGTATTTGGCTATTATAAATAAAATAGTGATGAACACGTGTACAGGTGTTTGTACGGACAT
AAGTTGTCATTTCTCTTGAGTAAATACCTAAAAGTGGGCTTGCTGGTGGAGAGACTCTCTCTGG
GCAGGTGACATATGCTGAGACCTGAATAACAGGAAGGAGTCACTCATGCAGACATGCAGGGAAA
GAATACTCCAGGCAAACAGCTGTTGCTGCAGTCCTGAGGCAGGAGCAAGCCTGACGTGTTCAAG
AGACGGGGTTTTACCATGTTGACCAGACTGGTCTCGAACTCCTGACCTCAGTGATCGCTGCCTC
GGCCTCCAGAAGTGTTGGGATTACAGGCATGAGCCACCATGCCTGACCTATTACATCTATTGTA
GTTTTACTACCCTTGGATGCTGCTGTTGACATGGAAAAGATTGAGGAACAATTTGCTAATCTGC
ACATTGTTAAATGTTCCTTAGGAACCAAAGAGCCCACTTACCTTCTTGGTATAGACACATCAAA
GACTGTCCAAGCAGGAAAGGAAAACTTGGTTGCTGTTTTATGTTCTAATGGATCAATCAGAATA
TATGATAAAGAAAGGTTAAATGTACTACGAGAATTTAGTGGATATCCTGGACTTCTTAATGGAG
TCAGATTTGCAAATTCCTGTGACAGTGTATATTCAGCATGTACTGATGGCACTGTGAAATGCTG
GGATGCTCGAGTAGCCAGAGAAAAACCTGTTCAGCTCTTCAAGGGTTACCCTTCCAATATTTTT
ATCAGTTTTGATATTAATTGTAATGATCATATTATTTGTGCTGGTACAGAAAAAGTTGATGATG
ATGCATTGTTGGTGTTTTGGGATGCAAGGATGAATTCTCAGAATTTATCTACAACTAAAGACTC
ACTTGGTGCATATTCAGAGACACATAGTGATGATGTCACTCAAGTACGTTTCCATCCCAGCAAT
CCCAACATGGTAGTCTCAGGTTCATCTGATGGCCTGGTAAATGTATTTGATATTAATATTGATA
ATGAGGAGGATGCACTGGTTACAACCTGTAACTCAATTTCATCAGTAAGCTGTATTGGTTGGTC
TGGGAAAGGTTATAAACAGATTTACTGCATGACACATGATGAAGGATTTTATTGGTGGGATCTT
AATCATCTGGACACTGATGAACCAGTTACACGTTTGAACATCCAGGATGTCAGAGAAGTAGTTA
ACATGAAAGAAGATGCTTTGGACTATTTGATTGGTGGCCTATATCATGAAAAGACAGACACATT
GCATGTTATTGGAGGAACAAACAAAGGAAGGATTCATTTGATGAACTGCAGCATGTCAGGACTG
ACCCATGTGACTAGCCTTCAGGGAGGGCATGCTGCTACAGTCCGTTCTTTCTGTTGGAATGTGC
AAGATGATTCTTTGTTGACTGGAGGAGAAGATGCACAGTTGTTACTTTGGAAACCTGGAGCTAT
AGAGAAGACCTTTACAAAGAAAGAGAGTATGAAAATAGCATCCTCTGTGCACCAACGAGTACGA
GTTCATAGTAATGATTCTTATAAAAGAAGGAAAAAGCAGTGATAATGCATTTGGCACTTTGTTT
GGTAGGTTTTATAGTTTCAAATAGTCCTTCTTGTTTACTACCCATGGTAGACATGTTTAAAGCT
TTATGTAAAAACAAGCCAGTTAGCAAACAGTCCTGGAAAAATATGGTGAGAATGGTTTAATTCC
GGTCTTCACATATTCTAAAAAATTTTAAAGCCTCTAAGTATAAAATCAGTGAGTTGAAAGTAAA
ATTTCTTATTTAAAGAACCCATCTGTTAATGTAGTAAATGTTGGCTTTAAAGAAATAGCTCCGA
TAAGGACTTTTTAGAAGGAAATACTTGGTAAAACTTAATAAAACAGGTGGTTGGCTGCATTTTT
TAAGCCCAGTTTTTTACATTTTAAATTGTCTTTATTGTGTATAAAACCAGATTAGACTATATTC
TTCATCTGAGGAGCATCTATATGTTTAATACACCTAATGTATTATGCTGGAGTATTTAAATGTA
AGTATTTTAATGAGTAAATAGAATTAACCTTTTTTACAAATGAAATGATAGGCATCTATGTAAA
GTGAGAAAAATATGTTTCGTAAATATTTGCATCTTTAATATTGTTAGTAAGTAGTAAACAGGTG
TTTTGCTGATTGAAAGGAAGTTATCTTGGTAAATTGAGACTCAAAGTGAAATACAAAAATGAAA
ATATTTATAATAGGACTCGACTTGGAGAAATTGCTATTCTTCCTGTTGTCCAAACCATAAATCT
GAGGATAACCTGGGCTTTTCTCTTTCCTCTTCTCCTAACCAGTTTTTCACCAAGTCCTGTGCCA
TTTCACCTCCTAACGTCTGTCAGCTATCCTTTTGCCTTTACCTCACCACTATTACCCTAGAGAA
GACTTTCATTATTTCTCATCTGGATTACCAGCTCGATCTCTAATCTGCTTCAGTTCATCCTTCT
TGCTACTTCTAGGCTAAACATCAAAAACAGATCTGGTAGGGGCGGGGAAATGAGGGGGAAGAAA
CAAAAACGTGATGGTGCCTCATGCTGCTTAAAATCTTCAGTACATTGATGTTTTGATGGCGGAC
TACATAAGCGTTAAAAATTGTGTTTTTCAGAATCTTTAAAATATAAGACAGTGCTATCTAGTGA
ATAAAAAAATTAGTTTGAAAGATATCTGGAGAAATCGCATTCATAAAACAATTGGAAGTGAAAC
TATTAAAACAATAGGGCTTTTTAAAATTAAAAATATTTAAAATTCAAAAGTAATTAATAGTGTT
GGAAGATGTAGGTGAGAAAATATTCCTGAAAGTAGAACTGAAAGAGACAAAGAGAAAAGATGAA
AGCCACAGAAGATAAATACAGGGGTCAAAACCAGACTAACAGTTTTAGAAAGTGAAAAAAGTTA
AAAAAGAAATGGGGGCAGTGGGTTATTAGAAATAACATAAATGGCTGGTATGGTTTGTCTGTGT
CCTCACCCAAATTTCATCTCGAATTGTAATCCCCATAATCCCCATGTGTCTAGGGAGAGACCTG
GTGGGAGGTGATTGGATCATGGGGGTGGTTTCCCCTACGATGTTCTCCTGATAGTGGGTGAGTT
CTCACAAGATCTGATGGTTTTATAAAGGGCTCTGCCCCTTTAACTCCTCACTCTTTCTCCTGAA
GCCTTGTGAAGAAGGTGCTTTGCTTCCCCTTTGCGTTCCCCCATGATTGTAAGTTTCTTGAGGC
CTCCCTGGCCATGCTGAACTCTTCAGTCAATTAAACACTTTCCTTTATAAATTA

hide sequence

RefSeq Acc Id:

NM_001382429 ⟹ NP_001369358

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,597,039 - 63,641,871 (-)	NCBI
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI

Sequence:

show sequence

GTTCCACTTGACCGCTCTAAGCCGCCGCGCAGCCTGCGTTTTCTCCGGTACAGGTTGAGGCTAC
TAAGGTATTTGGCTATTATAAATAAAATAGTGATGAACACGTGTACAGGTGTTTGTACGGACAT
AAGTTGTCATTTCTCTTGAGTAAATACCTAAAAGTGGGCTTGCTGGAAGGCATTTTTGCTGGGT
ACAGAGCTTTGTGTTGTGGAGAGACTCTCTCTGGGCAGGTGACATATGCTGAGACCTGAATAAC
AGGAAGGAGTCACTCATGCAGACATGCAGGGAAAGAATACTCCAGGCAAACAGCTGTTGCTGCA
GTCCTGAGGCAGGAGCAAGCCTGACGTGTTCAAGAGTTTTACTACCCTTGGATGCTGCTGTTGA
CATGGAAAAGATTGAGGAACAATTTGCTAATCTGCACATTGTTAAATGTTCCTTAGGAACCAAA
GAGCCCACTTACCTTCTTGGTATAGACACATCAAAGACTGTCCAAGCAGGAAAGGAAAACTTGG
TTGCTGTTTTATGTTCTAATGGATCAATCAGAATATATGATAAAGAAAGGTTAAATGTACTACG
AGAATTTAGTGGATATCCTGGACTTCTTAATGGAGTCAGATTTGCAAATTCCTGTGACAGTGTA
TATTCAGCATGTACTGATGGCACTGTGAAATGCTGGGATGCTCGAGTAGCCAGAGAAAAACCTG
TTCAGCTCTTCAAGGGTTACCCTTCCAATATTTTTATCAGTTTTGATATTAATTGTAATGATCA
TATTATTTGTGCTGGTACAGAAAAAGTTGATGATGATGCATTGTTGGTGTTTTGGGATGCAAGG
ATGAATTCTCAGAATTTATCTACAACTAAAGACTCACTTGGTGCATATTCAGAGACACATAGTG
ATGATGTCACTCAAGTACGTTTCCATCCCAGCAATCCCAACATGGTAGTCTCAGGTTCATCTGA
TGGCCTGGTAAATGTATTTGATATTAATATTGATAATGAGGAGGATGCACTGGTTACAACCTGT
AACTCAATTTCATCAGTAAGCTGTATTGGTTGGTCTGGGAAAGGTTATAAACAGATTTACTGCA
TGACACATGATGAAGGATTTTATTGGTGGGATCTTAATCATCTGGACACTGATGAACCAGTTAC
ACGTTTGAACATCCAGGATGTCAGAGAAGTAGTTAACATGAAAGAAGATGCTTTGGACTATTTG
ATTGGTGGCCTATATCATGAAAAGACAGACACATTGCATGTTATTGGAGGAACAAACAAAGGAA
GGATTCATTTGATGAACTGCAGCATGTCAGGACTGACCCATGTGACTAGCCTTCAGGGAGGGCA
TGCTGCTACAGTCCGTTCTTTCTGTTGGAATGTGCAAGATGATTCTTTGTTGACTGGAGGAGAA
GATGCACAGTTGTTACTTTGGAAACCTGGAGCTATAGAGAAGACCTTTACAAAGAAAGAGAGTA
TGAAAATAGCATCCTCTGTGCACCAACGAGTACGAGTTCATAGTAATGATTCTTATAAAAGAAG
GAAAAAGCAGTGATAATGCATTTGGCACTTTGTTTGGTAGGTTTTATAGTTTCAAATAGTCCTT
CTTGTTTACTACCCATGGTAGACATGTTTAAAGCTTTATGTAAAAACAAGCCAGTTAGCAAACA
GTCCTGGAAAAATATGGTGAGAATGGTTTAATTCCGGTCTTCACATATTCTAAAAAATTTTAAA
GCCTCTAAGTATAAAATCAGTGAGTTGAAAGTAAAATTTCTTATTTAAAGAACCCATCTGTTAA
TGTAGTAAATGTTGGCTTTAAAGAAATAGCTCCGATAAGGACTTTTTAGAAGGAAATACTTGGT
AAAACTTAATAAAACAGGTGGTTGGCTGCATTTTTTAAGCCCAGTTTTTTACATTTTAAATTGT
CTTTATTGTGTATAAAACCAGATTAGACTATATTCTTCATCTGAGGAGCATCTATATGTTTAAT
ACACCTAATGTATTATGCTGGAGTATTTAAATGTAAGTATTTTAATGAGTAAATAGAATTAACC
TTTTTTACAAATGAAATGATAGGCATCTATGTAAAGTGAGAAAAATATGTTTCGTAAATATTTG
CATCTTTAATATTGTTAGTAAGTAGTAAACAGGTGTTTTGCTGATTGAAAGGAAGTTATCTTGG
TAAATTGAGACTCAAAGTGAAATACAAAAATGAAAATATTTATAATAGGACTCGACTTGGAGAA
ATTGCTATTCTTCCTGTTGTCCAAACCATAAATCTGAGGATAACCTGGGCTTTTCTCTTTCCTC
TTCTCCTAACCAGTTTTTCACCAAGTCCTGTGCCATTTCACCTCCTAACGTCTGTCAGCTATCC
TTTTGCCTTTACCTCACCACTATTACCCTAGAGAAGACTTTCATTATTTCTCATCTGGATTACC
AGCTCGATCTCTAATCTGCTTCAGTTCATCCTTCTTGCTACTTCTAGGCTAAACATCAAAAACA
GATCTGGTAGGGGCGGGGAAATGAGGGGGAAGAAACAAAAACGTGATGGTGCCTCATGCTGCTT
AAAATCTTCAGTACATTGATGTTTTGATGGCGGACTACATAAGCGTTAAAAATTGTGTTTTTCA
GAATCTTTAAAATATAAGACAGTGCTATCTAGTGAATAAAAAAATTAGTTTGAAAGATATCTGG
AGAAATCGCATTCATAAAACAATTGGAAGTGAAACTATTAAAACAATAGGGCTTTTTAAAATTA
AAAATATTTAAAATTCAAAAGTAATTAATAGTGTTGGAAGATGTAGGTGAGAAAATATTCCTGA
AAGTAGAACTGAAAGAGACAAAGAGAAAAGATGAAAGCCACAGAAGATAAATACAGGGGTCAAA
ACCAGACTAACAGTTTTAGAAAGTGAAAAAAGTTAAAAAAGAAATGGGGGCAGTGGGTTATTAG
AAATAACATAAATGGCTGGTATGGTTTGTCTGTGTCCTCACCCAAATTTCATCTCGAATTGTAA
TCCCCATAATCCCCATGTGTCTAGGGAGAGACCTGGTGGGAGGTGATTGGATCATGGGGGTGGT
TTCCCCTACGATGTTCTCCTGATAGTGGGTGAGTTCTCACAAGATCTGATGGTTTTATAAAGGG
CTCTGCCCCTTTAACTCCTCACTCTTTCTCCTGAAGCCTTGTGAAGAAGGTGCTTTGCTTCCCC
TTTGCGTTCCCCCATGATTGTAAGTTTCTTGAGGCCTCCCTGGCCATGCTGAACTCTTCAGTCA
ATTAAACACTTTCCTTTATAAATTA

hide sequence

RefSeq Acc Id:

NM_080666 ⟹ NP_542397

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,597,039 - 63,641,871 (-)	NCBI
GRCh37	14	64,063,757 - 64,108,641 (-)	NCBI
Build 36	14	63,133,510 - 63,178,344 (-)	NCBI Archive
Celera	14	44,114,416 - 44,159,247 (-)	RGD
HuRef	14	44,230,434 - 44,274,975 (-)	NCBI
CHM1_1	14	64,002,766 - 64,047,647 (-)	NCBI
T2T-CHM13v2.0	14	57,804,429 - 57,849,265 (-)	NCBI

Sequence:

show sequence

GTTCCACTTGACCGCTCTAAGCCGCCGCGCAGCCTGCGTTTTCTCCGGTACAGGTTGAGGCTAC
TAAGGTATTTGGCTATTATAAATAAAATAGTGATGAACACGTGTACAGGTGTTTGTACGGACAT
AAGTTGTCATTTCTCTTGAGTAAATACCTAAAAGTGGGCTTGCTGGAGTTTTACTACCCTTGGA
TGCTGCTGTTGACATGGAAAAGATTGAGGAACAATTTGCTAATCTGCACATTGTTAAATGTTCC
TTAGGAACCAAAGAGCCCACTTACCTTCTTGGTATAGACACATCAAAGACTGTCCAAGCAGGAA
AGGAAAACTTGGTTGCTGTTTTATGTTCTAATGGATCAATCAGAATATATGATAAAGAAAGGTT
AAATGTACTACGAGAATTTAGTGGATATCCTGGACTTCTTAATGGAGTCAGATTTGCAAATTCC
TGTGACAGTGTATATTCAGCATGTACTGATGGCACTGTGAAATGCTGGGATGCTCGAGTAGCCA
GAGAAAAACCTGTTCAGCTCTTCAAGGGTTACCCTTCCAATATTTTTATCAGTTTTGATATTAA
TTGTAATGATCATATTATTTGTGCTGGTACAGAAAAAGTTGATGATGATGCATTGTTGGTGTTT
TGGGATGCAAGGATGAATTCTCAGAATTTATCTACAACTAAAGACTCACTTGGTGCATATTCAG
AGACACATAGTGATGATGTCACTCAAGTACGTTTCCATCCCAGCAATCCCAACATGGTAGTCTC
AGGTTCATCTGATGGCCTGGTAAATGTATTTGATATTAATATTGATAATGAGGAGGATGCACTG
GTTACAACCTGTAACTCAATTTCATCAGTAAGCTGTATTGGTTGGTCTGGGAAAGGTTATAAAC
AGATTTACTGCATGACACATGATGAAGGATTTTATTGGTGGGATCTTAATCATCTGGACACTGA
TGAACCAGTTACACGTTTGAACATCCAGGATGTCAGAGAAGTAGTTAACATGAAAGAAGATGCT
TTGGACTATTTGATTGGTGGCCTATATCATGAAAAGACAGACACATTGCATGTTATTGGAGGAA
CAAACAAAGGAAGGATTCATTTGATGAACTGCAGCATGTCAGGACTGACCCATGTGACTAGCCT
TCAGGGAGGGCATGCTGCTACAGTCCGTTCTTTCTGTTGGAATGTGCAAGATGATTCTTTGTTG
ACTGGAGGAGAAGATGCACAGTTGTTACTTTGGAAACCTGGAGCTATAGAGAAGACCTTTACAA
AGAAAGAGAGTATGAAAATAGCATCCTCTGTGCACCAACGAGTACGAGTTCATAGTAATGATTC
TTATAAAAGAAGGAAAAAGCAGTGATAATGCATTTGGCACTTTGTTTGGTAGGTTTTATAGTTT
CAAATAGTCCTTCTTGTTTACTACCCATGGTAGACATGTTTAAAGCTTTATGTAAAAACAAGCC
AGTTAGCAAACAGTCCTGGAAAAATATGGTGAGAATGGTTTAATTCCGGTCTTCACATATTCTA
AAAAATTTTAAAGCCTCTAAGTATAAAATCAGTGAGTTGAAAGTAAAATTTCTTATTTAAAGAA
CCCATCTGTTAATGTAGTAAATGTTGGCTTTAAAGAAATAGCTCCGATAAGGACTTTTTAGAAG
GAAATACTTGGTAAAACTTAATAAAACAGGTGGTTGGCTGCATTTTTTAAGCCCAGTTTTTTAC
ATTTTAAATTGTCTTTATTGTGTATAAAACCAGATTAGACTATATTCTTCATCTGAGGAGCATC
TATATGTTTAATACACCTAATGTATTATGCTGGAGTATTTAAATGTAAGTATTTTAATGAGTAA
ATAGAATTAACCTTTTTTACAAATGAAATGATAGGCATCTATGTAAAGTGAGAAAAATATGTTT
CGTAAATATTTGCATCTTTAATATTGTTAGTAAGTAGTAAACAGGTGTTTTGCTGATTGAAAGG
AAGTTATCTTGGTAAATTGAGACTCAAAGTGAAATACAAAAATGAAAATATTTATAATAGGACT
CGACTTGGAGAAATTGCTATTCTTCCTGTTGTCCAAACCATAAATCTGAGGATAACCTGGGCTT
TTCTCTTTCCTCTTCTCCTAACCAGTTTTTCACCAAGTCCTGTGCCATTTCACCTCCTAACGTC
TGTCAGCTATCCTTTTGCCTTTACCTCACCACTATTACCCTAGAGAAGACTTTCATTATTTCTC
ATCTGGATTACCAGCTCGATCTCTAATCTGCTTCAGTTCATCCTTCTTGCTACTTCTAGGCTAA
ACATCAAAAACAGATCTGGTAGGGGCGGGGAAATGAGGGGGAAGAAACAAAAACGTGATGGTGC
CTCATGCTGCTTAAAATCTTCAGTACATTGATGTTTTGATGGCGGACTACATAAGCGTTAAAAA
TTGTGTTTTTCAGAATCTTTAAAATATAAGACAGTGCTATCTAGTGAATAAAAAAATTAGTTTG
AAAGATATCTGGAGAAATCGCATTCATAAAACAATTGGAAGTGAAACTATTAAAACAATAGGGC
TTTTTAAAATTAAAAATATTTAAAATTCAAAAGTAATTAATAGTGTTGGAAGATGTAGGTGAGA
AAATATTCCTGAAAGTAGAACTGAAAGAGACAAAGAGAAAAGATGAAAGCCACAGAAGATAAAT
ACAGGGGTCAAAACCAGACTAACAGTTTTAGAAAGTGAAAAAAGTTAAAAAAGAAATGGGGGCA
GTGGGTTATTAGAAATAACATAAATGGCTGGTATGGTTTGTCTGTGTCCTCACCCAAATTTCAT
CTCGAATTGTAATCCCCATAATCCCCATGTGTCTAGGGAGAGACCTGGTGGGAGGTGATTGGAT
CATGGGGGTGGTTTCCCCTACGATGTTCTCCTGATAGTGGGTGAGTTCTCACAAGATCTGATGG
TTTTATAAAGGGCTCTGCCCCTTTAACTCCTCACTCTTTCTCCTGAAGCCTTGTGAAGAAGGTG
CTTTGCTTCCCCTTTGCGTTCCCCCATGATTGTAAGTTTCTTGAGGCCTCCCTGGCCATGCTGA
ACTCTTCAGTCAATTAAACACTTTCCTTTATAAATTA

hide sequence

RefSeq Acc Id:

XM_011536383 ⟹ XP_011534685

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,597,039 - 63,604,186 (-)	NCBI

Sequence:

show sequence

CATGCTGGGATTACAAGAATGAGCCACTGCACCTGGCCATCATTTTTAATTTTTAAATTAGTGA
AACAGGGTAAGGATGTGATAGGAAATGACAGGGGCTTTTTCACGTTGATTGGCAGTGGAGAGAC
TCTCTCTGGGCAGGTGACATATGCTGAGACCTGAATAACAGGAAGGAGTCACTCATGCAGACAT
GCAGGGAAAGAATACTCCAGGCAAACAGCTGTTGCTGCAGTCCTGAGGCAGGAGCAAGCCTGAC
GTGTTCAAGAGTTTTACTACCCTTGGATGCTGCTGTTGACATGGAAAAGATTGAGGAACAATTT
GCTAATCTGCACATTGTTAAATGTTCCTTAGGAACCAAAGAGCCCACTTACCTTCTTGGTATAG
ACACATCAAAGACTGTCCAAGCAGGAAAGGAAAACTTGGTTGCTGTTTTATGTTCTAATGGATC
AATCAGAATATATGATAAAGAAAGGTTAAATGTACTACGAGAATTTAGTGGATATCCTGGACTT
CTTAATGGAGTCAGATTTGCAAATTCCTGTGACAGTGTATATTCAGCATGTACTGATGGCACTG
TGAAATGCTGGGATGCTCGAGTAGCCAGAGAAAAACCTGTTCAGCTCTTCAAGGGTTACCCTTC
CAATATTTTTATCAGTTTTGATATTAATTGTAATGATCATATTATTTGTGCTGGTACAGAAAAA
GTTGATGATGATGCATTGTTGGTGTTTTGGGATGCAAGGATGAATTCTCAGAATTTATCTACAA
CTAAAGACTCACTTGGTGCATATTCAGAGACACATAGTGATGATGTCACTCAAGTACGTTTCCA
TCCCAGCAATCCCAACATGGTAGTCTCAGGTTCATCTGATGGCCTGGTAAATGTATTTGATATT
AATATTGATAATGAGGAGGATGCACTGGTTACAACCTGTAACTCAATTTCATCAGTAAGCTGTA
TTGGTTGGTCTGGGAAAGGTTATAAACAGATTTACTGCATGACACATGATGAAGGATTTTATTG
GTGGGATCTTAATCATCTGGACACTGATGAACCAGTTACACGTTTGAACATCCAGGATGTCAGA
GAAGTAGTTAACATGAAAGAAGATGCTTTGGACTATTTGATTGGTGGCCTATATCATGAAAAGA
CAGACACATTGCATGTTATTGGAGGAACAAACAAAGGAAGGATTCATTTGATGAACTGCAGCAT
GTCAGGACTGACCCATGTGACTAGCCTTCAGGGAGGGCATGCTGCTACAGTCCGTTCTTTCTGT
TGGAATGTGCAAGATGATTCTTTGTTGACTGGAGGAGAAGATGCACAGTTGTTACTTTGGAAAC
CTGGAGCTATAGAGAAGACCTTTACAAAGAAAGAGAGTATGAAAATAGCATCCTCTGTGCACCA
ACGAGTACGAGTTCATAGTAATGATTCTTATAAAAGAAGGAAAAAGCAGTGATAATGCATTTGG
CACTTTGTTTGGTAGGTTTTATAGTTTCAAATAGTCCTTCTTGTTTACTACCCATGGTAGACAT
GTTTAAAGCTTTATGTAAAAACAAGCCAGTTAGCAAACAGTCCTGGAAAAATATGGTGAGAATG
GTTTAATTCCGGTCTTCACATATTCTAAAAAATTTTAAAGCCTCTAAGTATAAAATCAGTGAGT
TGAAAGTAAAATTTCTTATTTAAAGAACCCATCTGTTAATGTAGTAAATGTTGGCTTTAAAGAA
ATAGCTCCGATAAGGACTTTTTAGAAGGAAATACTTGGTAAAACTTAATAAAACAGGTGGTTGG
CTGCATTTTTTAAGCCCAGTTTTTTACATTTTAAATTGTCTTTATTGTGTATAAAACCAGATTA
GACTATATTCTTCATCTGAGGAGCATCTATATGTTTAATACACCTAATGTATTATGCTGGAGTA
TTTAAATGTAAGTATTTTAATGAGTAAATAGAATTAACCTTTTTTACAAATGAAATGATAGGCA
TCTATGTAAAGTGAGAAAAATATGTTTCGTAAATATTTGCATCTTTAATATTGTTAGTAAGTAG
TAAACAGGTGTTTTGCTGATTGAAAGGAAGTTATCTTGGTAAATTGAGACTCAAAGTGAAATAC
AAAAATGAAAATATTTATAATAGGACTCGACTTGGAGAAATTGCTATTCTTCCTGTTGTCCAAA
CCATAAATCTGAGGATAACCTGGGCTTTTCTCTTTCCTCTTCTCCTAACCAGTTTTTCACCAAG
TCCTGTGCCATTTCACCTCCTAACGTCTGTCAGCTATCCTTTTGCCTTTACCTCACCACTATTA
CCCTAGAGAAGACTTTCATTATTTCTCATCTGGATTACCAGCTCGATCTCTAATCTGCTTCAGT
TCATCCTTCTTGCTACTTCTAGGCTAAACATCAAAAACAGATCTGGTAGGGGCGGGGAAATGAG
GGGGAAGAAACAAAAACGTGATGGTGCCTCATGCTGCTTAAAATCTTCAGTACATTGATGTTTT
GATGGCGGACTACATAAGCGTTAAAAATTGTGTTTTTCAGAATCTTTAAAATATAAGACAGTGC
TATCTAGTGAATAAAAAAATTAGTTTGAAAGATATCTGGAGAAATCGCATTCATAAAACAATTG
GAAGTGAAACTATTAAAACAATAGGGCTTTTTAAAATTAAAAATATTTAAAATTCAAAAGTAAT
TAATAGTGTTGGAAGATGTAGGTGAGAAAATATTCCTGAAAGTAGAACTGAAAGAGACAAAGAG
AAAAGATGAAAGCCACAGAAGATAAATACAGGGGTCAAAACCAGACTAACAGTTTTAGAAAGTG
AAAAAAGTTAAAAAAGAAATGGGGGCAGTGGGTTATTAGAAATAACATAAATGGCTGGTATGGT
TTGTCTGTGTCCTCACCCAAATTTCATCTCGAATTGTAATCCCCATAATCCCCATGTGTCTAGG
GAGAGACCTGGTGGGAGGTGATTGGATCATGGGGGTGGTTTCCCCTACGATGTTCTCCTGATAG
TGGGTGAGTTCTCACAAGATCTGATGGTTTTATAAAGGGCTCTGCCCCTTTAACTCCTCACTCT
TTCTCCTGAAGCCTTGTGAAGAAGGTGCTTTGCTTCCCCTTTGCGTTCCCCCATGATTGTAAGT
TTCTTGAGGCCTCCCTGGCCATGCTGAACTCTTCAGTCAATTAAACACTTTCCTTTATAAATTA

hide sequence

RefSeq Acc Id:

XM_054375310 ⟹ XP_054231285

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	57,804,429 - 57,811,576 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001008726	(Get FASTA)	NCBI Sequence Viewer
	NP_001245201	(Get FASTA)	NCBI Sequence Viewer
	NP_001369352	(Get FASTA)	NCBI Sequence Viewer
	NP_001369353	(Get FASTA)	NCBI Sequence Viewer
	NP_001369354	(Get FASTA)	NCBI Sequence Viewer
	NP_001369355	(Get FASTA)	NCBI Sequence Viewer
	NP_001369356	(Get FASTA)	NCBI Sequence Viewer
	NP_001369357	(Get FASTA)	NCBI Sequence Viewer
	NP_001369358	(Get FASTA)	NCBI Sequence Viewer
	NP_542397	(Get FASTA)	NCBI Sequence Viewer
	XP_011534685	(Get FASTA)	NCBI Sequence Viewer
	XP_054231285	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH10698	(Get FASTA)	NCBI Sequence Viewer
	AAO06950	(Get FASTA)	NCBI Sequence Viewer
	BAC04530	(Get FASTA)	NCBI Sequence Viewer
	CAD62336	(Get FASTA)	NCBI Sequence Viewer
	EAW80831	(Get FASTA)	NCBI Sequence Viewer
	EAW80832	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000267522
	ENSP00000267522.3
	ENSP00000378399.2
	ENSP00000451702.1
	ENSP00000480112
	ENSP00000480112.1
GenBank Protein	Q96FK6	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_542397 ⟸ NM_080666

- UniProtKB:

Q96FK6 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MEKIEEQFANLHIVKCSLGTKEPTYLLGIDTSKTVQAGKENLVAVLCSNGSIRIYDKERLNVLR
EFSGYPGLLNGVRFANSCDSVYSACTDGTVKCWDARVAREKPVQLFKGYPSNIFISFDINCNDH
IICAGTEKVDDDALLVFWDARMNSQNLSTTKDSLGAYSETHSDDVTQVRFHPSNPNMVVSGSSD
GLVNVFDINIDNEEDALVTTCNSISSVSCIGWSGKGYKQIYCMTHDEGFYWWDLNHLDTDEPVT
RLNIQDVREVVNMKEDALDYLIGGLYHEKTDTLHVIGGTNKGRIHLMNCSMSGLTHVTSLQGGH
AATVRSFCWNVQDDSLLTGGEDAQLLLWKPGAIEKTFTKKESMKIASSVHQRVRVHSNDSYKRR
KKQ

hide sequence

RefSeq Acc Id:

NP_001008726 ⟸ NM_001008726

- UniProtKB:

Q96FK6 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MEKIEEQFANLHIVKCSLGTKEPTYLLGIDTSKTVQAGKENLVAVLCSNGSIRIYDKERLNVLR
EFSGYPGLLNGVRFANSCDSVYSACTDGTVKCWDARVAREKPVQLFKGYPSNIFISFDINCNDH
IICAGTEKVDDDALLVFWDARMNSQNLSTTKDSLGAYSETHSDDVTQVRFHPSNPNMVVSGSSD
GLVNVFDINIDNEEDALVTTCNSISSVSCIGWSGKGYKQIYCMTHDEGFYWWDLNHLDTDEPVT
RLNIQDVREVVNMKEDALDYLIGGLYHEKTDTLHVIGGTNKGRIHLMNCSMSGLTHVTSLQGGH
AATVRSFCWNVQDDSLLTGGEDAQLLLWKPGAIEKTFTKKESMKIASSVHQRVRVHSNDSYKRR
KKQ

hide sequence

RefSeq Acc Id:

NP_001245201 ⟸ NM_001258272

- UniProtKB:

Q96FK6 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MEKIEEQFANLHIVKCSLGTKEPTYLLGIDTSKTVQAGKENLVAVLCSNGSIRIYDKERLNVLR
EFSGYPGLLNGVRFANSCDSVYSACTDGTVKCWDARVAREKPVQLFKGYPSNIFISFDINCNDH
IICAGTEKVDDDALLVFWDARMNSQNLSTTKDSLGAYSETHSDDVTQVRFHPSNPNMVVSGSSD
GLVNVFDINIDNEEDALVTTCNSISSVSCIGWSGKGYKQIYCMTHDEGFYWWDLNHLDTDEPVT
RLNIQDVREVVNMKEDALDYLIGGLYHEKTDTLHVIGGTNKGRIHLMNCSMSGLTHVTSLQGGH
AATVRSFCWNVQDDSLLTGGEDAQLLLWKPGAIEKTFTKKESMKIASSVHQRVRVHSNDSYKRR
KKQ

hide sequence

RefSeq Acc Id:

XP_011534685 ⟸ XM_011536383

- Peptide Label:

isoform X1

- Sequence:

show sequence

MQTCRERILQANSCCCSPEAGASLTCSRVLLPLDAAVDMEKIEEQFANLHIVKCSLGTKEPTYL
LGIDTSKTVQAGKENLVAVLCSNGSIRIYDKERLNVLREFSGYPGLLNGVRFANSCDSVYSACT
DGTVKCWDARVAREKPVQLFKGYPSNIFISFDINCNDHIICAGTEKVDDDALLVFWDARMNSQN
LSTTKDSLGAYSETHSDDVTQVRFHPSNPNMVVSGSSDGLVNVFDINIDNEEDALVTTCNSISS
VSCIGWSGKGYKQIYCMTHDEGFYWWDLNHLDTDEPVTRLNIQDVREVVNMKEDALDYLIGGLY
HEKTDTLHVIGGTNKGRIHLMNCSMSGLTHVTSLQGGHAATVRSFCWNVQDDSLLTGGEDAQLL
LWKPGAIEKTFTKKESMKIASSVHQRVRVHSNDSYKRRKKQ

hide sequence

RefSeq Acc Id:	NP_001369353 ⟸ NM_001382424
- UniProtKB:	Q96FK6 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001369356 ⟸ NM_001382427
- UniProtKB:	Q96FK6 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001369357 ⟸ NM_001382428
- UniProtKB:	Q96FK6 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001369352 ⟸ NM_001382423
- UniProtKB:	Q96FK6 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001369358 ⟸ NM_001382429
- UniProtKB:	Q96FK6 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001369354 ⟸ NM_001382425
- UniProtKB:	Q96FK6 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001369355 ⟸ NM_001382426
- UniProtKB:	Q96FK6 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:

ENSP00000480112 ⟸ ENST00000620954

RefSeq Acc Id:

ENSP00000267522 ⟸ ENST00000267522

RefSeq Acc Id:

ENSP00000378399 ⟸ ENST00000394942

RefSeq Acc Id:

ENSP00000451702 ⟸ ENST00000554717

RefSeq Acc Id:	XP_054231285 ⟸ XM_054375310
- Peptide Label:	isoform X1

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96FK6-F1-model_v2	AlphaFold	Q96FK6	1-387	view protein structure

Promoters

RGD ID:

6792035

Promoter ID:

HG_KWN:19550

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:

NM_001008726, NM_080666

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	14	63,178,111 - 63,179,017 (-)	MPROMDB

RGD ID:

7227825

Promoter ID:

EPDNEW_H19658

Type:

multiple initiation site

Name:

WDR89_2

Description:

WD repeat domain 89

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H19659

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,641,492 - 63,641,552	EPDNEW

RGD ID:

7227827

Promoter ID:

EPDNEW_H19659

Type:

initiation region

Name:

WDR89_1

Description:

WD repeat domain 89

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H19658

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	63,641,871 - 63,641,931	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:20489	AgrOrtholog
COSMIC	WDR89	COSMIC
Ensembl Genes	ENSG00000140006	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000267522	ENTREZGENE
	ENST00000267522.7	UniProtKB/Swiss-Prot
	ENST00000394942.2	UniProtKB/Swiss-Prot
	ENST00000554717.1	UniProtKB/TrEMBL
	ENST00000620954	ENTREZGENE
	ENST00000620954.2	UniProtKB/Swiss-Prot
Gene3D-CATH	2.130.10.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000140006	GTEx
HGNC ID	HGNC:20489	ENTREZGENE
Human Proteome Map	WDR89	Human Proteome Map
InterPro	WD40/YVTN_repeat-like_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD40_repeat	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD40_repeat_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WDR89	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:112840	UniProtKB/Swiss-Prot
NCBI Gene	112840	ENTREZGENE
PANTHER	PTHR22889	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD REPEAT-CONTAINING PROTEIN 89	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	WD40	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134871067	PharmGKB
PROSITE	WD_REPEATS_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD_REPEATS_REGION	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	WD40	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF50978	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	G3V4B8_HUMAN	UniProtKB/TrEMBL
	Q96FK6	ENTREZGENE, 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