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Gene: THAP5 (THAP domain containing 5) Canis lupus familiaris

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Symbol:

THAP5

Name:

THAP domain containing 5

RGD ID:

12134939

Description:

ENCODES a protein that exhibits protease binding (ortholog); INVOLVED IN negative regulation of cell cycle (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH pleomorphic xanthoastrocytoma (ortholog); FOUND IN chromatin (ortholog); nucleoplasm (ortholog)

Type:

protein-coding

RefSeq Status:

MODEL

Previously known as:

THAP domain-containing protein 5

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 ...
Homo sapiens (human):	THAP5 (THAP domain containing 5)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Thap5 (THAP domain containing 5)	Transitive Ortholog Pipeline	Transitive Ortholog Pipeline
Pan paniscus (bonobo/pygmy chimpanzee):	THAP5 (THAP domain containing 5)	Transitive Ortholog Pipeline	Transitive Ortholog Pipeline
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Thap5 (THAP domain containing 5)	Transitive Ortholog Pipeline	Transitive Ortholog Pipeline
Sus scrofa (pig):	THAP5 (THAP domain containing 5)	Transitive Ortholog Pipeline	Transitive Ortholog Pipeline
Chlorocebus sabaeus (green monkey):	THAP5 (THAP domain containing 5)	Transitive Ortholog Pipeline	Transitive Ortholog Pipeline
Heterocephalus glaber (naked mole-rat):	Thap5 (THAP domain containing 5)	Transitive Ortholog Pipeline	Transitive Ortholog Pipeline

Latest Assembly:

CanFam3.1 - Dog CanFam3.1 Assembly

Position:

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	14	48,738,882 - 48,880,295 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	14	48,873,990 - 48,880,266 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	14	48,183,037 - 48,324,132 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	14	48,681,884 - 48,829,752 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	14	48,822,741 - 48,829,735 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	14	48,786,690 - 48,926,847 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	14	48,466,945 - 48,610,709 (-)	NCBI		UNSW_CanFamBas_1.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
THAP5	Dog	pleomorphic xanthoastrocytoma		ISO	RGD:1353274	8554872	ClinVar Annotator: match by term: Pleomorphic xanthoastrocytoma	ClinVar	PMID:28299358

Biological Process

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
THAP5	Dog	negative regulation of cell cycle	involved_in	ISO	RGD:1353274	9068941	PMID:19502560	UniProt	PMID:19502560
THAP5	Dog	negative regulation of transcription by RNA polymerase II	involved_in	ISO	RGD:1353274	9068941	PMID:21110952	ARUK-UCL	PMID:21110952

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
THAP5	Dog	chromatin	located_in	ISO	RGD:1353274	9068941	PMID:21110952	ARUK-UCL	PMID:21110952
THAP5	Dog	nucleoplasm	located_in	ISO	RGD:1353274	9068941		HPA	GO_REF:0000052
THAP5	Dog	nucleus	located_in	IEA	UniProtKB-SubCell:SL-0191	150520179		UniProt	GO_REF:0000044
THAP5	Dog	nucleus	is_active_in	IBA	PANTHER:PTN002930720\|UniProtKB:Q7Z6K1	150520179		GO_Central	GO_REF:0000033

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
THAP5	Dog	DNA binding	enables	IEA	UniProtKB-KW:KW-0238	150520179		UniProt	GO_REF:0000043
THAP5	Dog	DNA binding	enables	IEA	UniRule:UR000415608	150520179		UniProt	GO_REF:0000104
THAP5	Dog	metal ion binding	enables	IEA	UniProtKB-KW:KW-0479	150520179		UniProt	GO_REF:0000043
THAP5	Dog	protease binding	enables	ISO	UniProtKB:O43464	9068941	PMID:19502560	UniProt	PMID:19502560
THAP5	Dog	zinc ion binding	enables	IEA	UniProtKB-KW:KW-0863	150520179		UniProt	GO_REF:0000043

THAP5
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	14	48,738,882 - 48,880,295 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	14	48,873,990 - 48,880,266 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	14	48,183,037 - 48,324,132 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	14	48,681,884 - 48,829,752 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	14	48,822,741 - 48,829,735 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	14	48,786,690 - 48,926,847 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	14	48,466,945 - 48,610,709 (-)	NCBI		UNSW_CanFamBas_1.0

THAP5
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	7	108,541,759 - 108,569,768 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	7	108,554,543 - 108,569,750 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	7	108,202,576 - 108,210,212 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	7	107,991,766 - 107,997,133 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	7	107,798,482 - 107,803,848	NCBI
Celera	7	103,016,042 - 103,023,538 (-)	NCBI		Celera
Cytogenetic Map	7	q31.1	NCBI
HuRef	7	102,570,894 - 102,578,384 (-)	NCBI		HuRef
CHM1_1	7	108,135,971 - 108,143,453 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	7	109,865,676 - 109,894,376 (-)	NCBI		T2T-CHM13v2.0
CRA_TCAGchr7v2	7	107,569,889 - 107,577,381 (-)	NCBI

Thap5
(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_004955410	12,808,700 - 12,815,193 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955410	12,808,700 - 12,814,915 (-)	NCBI	ChiLan1.0	ChiLan1.0

THAP5
(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	6	145,412,123 - 145,419,606 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	7	193,682,093 - 193,689,576 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	7	100,547,874 - 100,555,416 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	7	113,266,499 - 113,274,038 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	7	113,266,499 - 113,274,033 (-)	Ensembl	panpan1.1		panPan2

Thap5
(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_024405118	68,395,316 - 68,402,923 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936653	1,544,613 - 1,554,216 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936653	1,546,682 - 1,554,347 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

THAP5
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	18	36,584,373 - 36,592,252 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	18	36,584,359 - 36,592,255 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	18	40,224,757 - 40,232,666 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

THAP5
(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	21	77,469,566 - 77,477,190 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	21	77,471,631 - 77,477,733 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666042	26,386,093 - 26,393,350 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Thap5
(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_004624739	21,193,484 - 21,199,103 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624739	21,193,399 - 21,220,936 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in THAP5
1808 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	copy number gain	See cases [RCV000052925]	Chr19:49907832..58557889 [GRCh38] Chr19:50411089..59069256 [GRCh37] Chr19:55102901..63761068 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	copy number gain	See cases [RCV000052914]	Chr19:47908540..58539965 [GRCh38] Chr19:48411797..59051332 [GRCh37] Chr19:53103609..63743144 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	copy number gain	See cases [RCV000052915]	Chr19:47929575..58572206 [GRCh38] Chr19:48432832..59083573 [GRCh37] Chr19:53124644..63775385 [NCBI36] Chr19:19q13.33-13.43	pathogenic
NM_016553.5(NUP62):c.848G>C (p.Ser283Thr)	single nucleotide variant	Infantile bilateral striatal necrosis [RCV001787922]\|NUP62-related disorder [RCV003975031]\|not provided [RCV001514104]\|not specified [RCV000117866]	Chr19:49908960 [GRCh38] Chr19:50412217 [GRCh37] Chr19:19q13.33	benign\|likely benign
NM_001193646.1(ATF5):c.440C>T (p.Ser147Phe)	single nucleotide variant	Malignant melanoma [RCV000063600]	Chr19:49932683 [GRCh38] Chr19:50435940 [GRCh37] Chr19:55127752 [NCBI36] Chr19:19q13.33	not provided
NM_016553.5(NUP62):c.1172A>C (p.Gln391Pro)	single nucleotide variant	Infantile bilateral striatal necrosis [RCV000005018]	Chr19:49908636 [GRCh38] Chr19:50411893 [GRCh37] Chr19:19q13.33	pathogenic
NM_001193646.1(ATF5):c.807C>T (p.Ile269=)	single nucleotide variant	Malignant melanoma [RCV000063601]	Chr19:49933050 [GRCh38] Chr19:50436307 [GRCh37] Chr19:55128119 [NCBI36] Chr19:19q13.33	not provided
NM_016553.5(NUP62):c.648C>T (p.Ser216=)	single nucleotide variant	Infantile bilateral striatal necrosis [RCV001787921]\|not provided [RCV001519352]\|not specified [RCV000117865]	Chr19:49909160 [GRCh38] Chr19:50412417 [GRCh37] Chr19:19q13.33	benign\|likely benign
NM_016553.5(NUP62):c.1323T>C (p.Asp441=)	single nucleotide variant	Infantile bilateral striatal necrosis [RCV001787920]\|not provided [RCV001519351]\|not specified [RCV000117863]	Chr19:49908485 [GRCh38] Chr19:50411742 [GRCh37] Chr19:19q13.33	benign\|likely benign
NM_016553.5(NUP62):c.549G>A (p.Thr183=)	single nucleotide variant	NUP62-related disorder [RCV003915156]\|not provided [RCV001521717]\|not specified [RCV000117864]	Chr19:49909259 [GRCh38] Chr19:50412516 [GRCh37] Chr19:19q13.33	benign\|likely benign
NM_016553.5(NUP62):c.700A>G (p.Thr234Ala)	single nucleotide variant	Infantile bilateral striatal necrosis [RCV001333016]\|not provided [RCV001871845]	Chr19:49909108 [GRCh38] Chr19:50412365 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.413C>G (p.Thr138Ser)	single nucleotide variant	not provided [RCV003730445]\|not specified [RCV004255948]	Chr19:49909395 [GRCh38] Chr19:50412652 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.192C>T (p.Thr64=)	single nucleotide variant	NUP62-related disorder [RCV003937703]\|not provided [RCV000955042]\|not specified [RCV000194217]	Chr19:49909616 [GRCh38] Chr19:50412873 [GRCh37] Chr19:19q13.33	benign\|likely benign\|uncertain significance
NM_016553.5(NUP62):c.337G>A (p.Gly113Ser)	single nucleotide variant	not provided [RCV001854924]\|not specified [RCV000239227]	Chr19:49909471 [GRCh38] Chr19:50412728 [GRCh37] Chr19:19q13.33	conflicting interpretations of pathogenicity\|uncertain significance
GRCh37/hg19 19q13.33(chr19:50391979-50665993)x3	copy number gain	See cases [RCV000446903]	Chr19:50391979..50665993 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.560C>T (p.Thr187Met)	single nucleotide variant	not provided [RCV000428843]	Chr19:49909248 [GRCh38] Chr19:50412505 [GRCh37] Chr19:19q13.33	benign\|likely benign
NM_152899.2(IL4I1):c.79G>C (p.Glu27Gln)	single nucleotide variant	not specified [RCV004328694]	Chr19:49895988 [GRCh38] Chr19:50399245 [GRCh37] Chr19:19q13.33	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	copy number gain	See cases [RCV000511289]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic\|uncertain significance
NM_016553.5(NUP62):c.1444A>T (p.Met482Leu)	single nucleotide variant	not specified [RCV004312173]	Chr19:49908364 [GRCh38] Chr19:50411621 [GRCh37] Chr19:19q13.33	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	copy number gain	See cases [RCV000512296]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3	copy number gain	not provided [RCV000752444]	Chr19:260912..59097160 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3	copy number gain	not provided [RCV000752439]	Chr19:68029..59110290 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
NM_016553.5(NUP62):c.582G>A (p.Thr194=)	single nucleotide variant	NUP62-related disorder [RCV003912877]\|not provided [RCV000901825]	Chr19:49909226 [GRCh38] Chr19:50412483 [GRCh37] Chr19:19q13.33	benign\|likely benign
NM_016553.5(NUP62):c.1209G>A (p.Leu403=)	single nucleotide variant	not provided [RCV000915448]	Chr19:49908599 [GRCh38] Chr19:50411856 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1338C>T (p.Arg446=)	single nucleotide variant	NUP62-related disorder [RCV003922973]\|not provided [RCV000901316]	Chr19:49908470 [GRCh38] Chr19:50411727 [GRCh37] Chr19:19q13.33	benign
NM_016553.5(NUP62):c.1483C>T (p.Leu495=)	single nucleotide variant	not provided [RCV000904821]	Chr19:49908325 [GRCh38] Chr19:50411582 [GRCh37] Chr19:19q13.33	benign
NM_016553.5(NUP62):c.835G>A (p.Ala279Thr)	single nucleotide variant	not provided [RCV000903463]	Chr19:49908973 [GRCh38] Chr19:50412230 [GRCh37] Chr19:19q13.33	benign
NM_016553.5(NUP62):c.848GCA[5] (p.Ser286_Thr287insSer)	microsatellite	not provided [RCV000879188]	Chr19:49908948..49908949 [GRCh38] Chr19:50412205..50412206 [GRCh37] Chr19:19q13.33	benign
NM_016553.5(NUP62):c.1482G>C (p.Leu494=)	single nucleotide variant	not provided [RCV000894493]	Chr19:49908326 [GRCh38] Chr19:50411583 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.494C>T (p.Thr165Met)	single nucleotide variant	NUP62-related disorder [RCV003950504]\|not provided [RCV000897986]	Chr19:49909314 [GRCh38] Chr19:50412571 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.548C>T (p.Thr183Met)	single nucleotide variant	Infantile bilateral striatal necrosis [RCV000984939]\|not provided [RCV002549633]	Chr19:49909260 [GRCh38] Chr19:50412517 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1518C>T (p.Cys506=)	single nucleotide variant	not provided [RCV000893169]	Chr19:49908290 [GRCh38] Chr19:50411547 [GRCh37] Chr19:19q13.33	benign
GRCh37/hg19 19q13.33(chr19:49600909-51366070)x3	copy number gain	not provided [RCV000847250]	Chr19:49600909..51366070 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.102C>T (p.Phe34=)	single nucleotide variant	not provided [RCV000914091]	Chr19:49909706 [GRCh38] Chr19:50412963 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.796G>A (p.Gly266Ser)	single nucleotide variant	not provided [RCV002559221]\|not specified [RCV001193313]	Chr19:49909012 [GRCh38] Chr19:50412269 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.933C>T (p.Thr311=)	single nucleotide variant	not provided [RCV003121702]	Chr19:49908875 [GRCh38] Chr19:50412132 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.59C>T (p.Thr20Ile)	single nucleotide variant	not specified [RCV004306429]	Chr19:49909749 [GRCh38] Chr19:50413006 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1048C>T (p.His350Tyr)	single nucleotide variant	not specified [RCV004322885]	Chr19:49908760 [GRCh38] Chr19:50412017 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.795C>T (p.Ser265=)	single nucleotide variant	not provided [RCV000927193]	Chr19:49909013 [GRCh38] Chr19:50412270 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.663C>G (p.Leu221=)	single nucleotide variant	not provided [RCV000885752]	Chr19:49909145 [GRCh38] Chr19:50412402 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.171C>T (p.Thr57=)	single nucleotide variant	not provided [RCV000915449]	Chr19:49909637 [GRCh38] Chr19:50412894 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.990C>T (p.Tyr330=)	single nucleotide variant	not provided [RCV000907432]	Chr19:49908818 [GRCh38] Chr19:50412075 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.894G>A (p.Ala298=)	single nucleotide variant	not provided [RCV000909640]	Chr19:49908914 [GRCh38] Chr19:50412171 [GRCh37] Chr19:19q13.33	likely benign
GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3	copy number gain	not provided [RCV001007050]	Chr19:44738088..53621561 [GRCh37] Chr19:19q13.31-13.42	pathogenic
NM_016553.5(NUP62):c.811A>T (p.Thr271Ser)	single nucleotide variant	not specified [RCV001193314]	Chr19:49908997 [GRCh38] Chr19:50412254 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1383C>T (p.Ser461=)	single nucleotide variant	not provided [RCV000891305]	Chr19:49908425 [GRCh38] Chr19:50411682 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.900C>T (p.Ala300=)	single nucleotide variant	not provided [RCV000934477]	Chr19:49908908 [GRCh38] Chr19:50412165 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.277G>A (p.Gly93Ser)	single nucleotide variant	not provided [RCV000891069]	Chr19:49909531 [GRCh38] Chr19:50412788 [GRCh37] Chr19:19q13.33	benign
GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871)	copy number gain	not provided [RCV001249294]	Chr19:47939842..54626871 [GRCh37] Chr19:19q13.32-13.42	not provided
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3	copy number gain	not provided [RCV001259944]	Chr19:48463931..57095254 [GRCh37] Chr19:19q13.33-13.43	pathogenic
NM_016553.5(NUP62):c.175C>G (p.Leu59Val)	single nucleotide variant	not provided [RCV001317849]	Chr19:49909633 [GRCh38] Chr19:50412890 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1089C>T (p.Arg363=)	single nucleotide variant	not provided [RCV003112579]	Chr19:49908719 [GRCh38] Chr19:50411976 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.581C>T (p.Thr194Met)	single nucleotide variant	not provided [RCV001874414]	Chr19:49909227 [GRCh38] Chr19:50412484 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1045C>T (p.Arg349Trp)	single nucleotide variant	not provided [RCV002030185]	Chr19:49908763 [GRCh38] Chr19:50412020 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.595A>G (p.Thr199Ala)	single nucleotide variant	not provided [RCV002001469]	Chr19:49909213 [GRCh38] Chr19:50412470 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.822_830del (p.Ala275_Ala277del)	deletion	not provided [RCV002014254]	Chr19:49908978..49908986 [GRCh38] Chr19:50412235..50412243 [GRCh37] Chr19:19q13.33	uncertain significance
GRCh37/hg19 19q13.33-13.41(chr19:49911081-53127438)	copy number gain	not specified [RCV002052689]	Chr19:49911081..53127438 [GRCh37] Chr19:19q13.33-13.41	likely pathogenic
NM_016553.5(NUP62):c.455C>G (p.Ala152Gly)	single nucleotide variant	not provided [RCV002023793]\|not specified [RCV004046851]	Chr19:49909353 [GRCh38] Chr19:50412610 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.385G>A (p.Val129Ile)	single nucleotide variant	not provided [RCV002028429]	Chr19:49909423 [GRCh38] Chr19:50412680 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.823GCCACC[2] (p.275AT[2])	microsatellite	not provided [RCV002033200]	Chr19:49908968..49908973 [GRCh38] Chr19:50412225..50412230 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1279G>A (p.Asp427Asn)	single nucleotide variant	not provided [RCV002048441]\|not specified [RCV004046826]	Chr19:49908529 [GRCh38] Chr19:50411786 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.124T>C (p.Phe42Leu)	single nucleotide variant	not provided [RCV002022352]	Chr19:49909684 [GRCh38] Chr19:50412941 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.841A>G (p.Thr281Ala)	single nucleotide variant	NUP62-related disorder [RCV003948880]\|not provided [RCV002036902]	Chr19:49908967 [GRCh38] Chr19:50412224 [GRCh37] Chr19:19q13.33	likely benign\|uncertain significance
GRCh37/hg19 19q13.33(chr19:50355646-50552140)	copy number gain	not specified [RCV002052690]	Chr19:50355646..50552140 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.626C>T (p.Thr209Ile)	single nucleotide variant	not provided [RCV002044757]	Chr19:49909182 [GRCh38] Chr19:50412439 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.622C>G (p.Pro208Ala)	single nucleotide variant	not provided [RCV001913205]\|not specified [RCV004042525]	Chr19:49909186 [GRCh38] Chr19:50412443 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.249G>A (p.Ser83=)	single nucleotide variant	not provided [RCV001979049]	Chr19:49909559 [GRCh38] Chr19:50412816 [GRCh37] Chr19:19q13.33	likely benign\|uncertain significance
NM_016553.5(NUP62):c.305C>T (p.Thr102Ile)	single nucleotide variant	not provided [RCV001953381]	Chr19:49909503 [GRCh38] Chr19:50412760 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.77C>T (p.Thr26Ile)	single nucleotide variant	not provided [RCV001949172]	Chr19:49909731 [GRCh38] Chr19:50412988 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.935C>T (p.Ala312Val)	single nucleotide variant	not provided [RCV001897164]	Chr19:49908873 [GRCh38] Chr19:50412130 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.395G>A (p.Ser132Asn)	single nucleotide variant	not provided [RCV001897679]	Chr19:49909413 [GRCh38] Chr19:50412670 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.425T>C (p.Phe142Ser)	single nucleotide variant	not provided [RCV001958475]\|not specified [RCV004043764]	Chr19:49909383 [GRCh38] Chr19:50412640 [GRCh37] Chr19:19q13.33	uncertain significance
NC_000019.9:g.(?_50411496)_(50413064_?)dup	duplication	not provided [RCV004579787]	Chr19:50411496..50413064 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1088G>A (p.Arg363His)	single nucleotide variant	not provided [RCV001986034]	Chr19:49908720 [GRCh38] Chr19:50411977 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.373A>T (p.Ile125Leu)	single nucleotide variant	not provided [RCV001881042]	Chr19:49909435 [GRCh38] Chr19:50412692 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.665T>C (p.Phe222Ser)	single nucleotide variant	not provided [RCV001981835]\|not specified [RCV004042018]	Chr19:49909143 [GRCh38] Chr19:50412400 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.322A>G (p.Met108Val)	single nucleotide variant	not provided [RCV001928615]	Chr19:49909486 [GRCh38] Chr19:50412743 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.991G>A (p.Ala331Thr)	single nucleotide variant	not provided [RCV001974619]\|not specified [RCV004042937]	Chr19:49908817 [GRCh38] Chr19:50412074 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.823GCCACC[4] (p.Thr280_Thr281insAlaThr)	microsatellite	not provided [RCV001957652]	Chr19:49908967..49908968 [GRCh38] Chr19:50412224..50412225 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1436A>G (p.Asn479Ser)	single nucleotide variant	not provided [RCV001878647]\|not specified [RCV004641712]	Chr19:49908372 [GRCh38] Chr19:50411629 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1098C>G (p.Ile366Met)	single nucleotide variant	not provided [RCV001881230]\|not specified [RCV004837818]	Chr19:49908710 [GRCh38] Chr19:50411967 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1366G>A (p.Glu456Lys)	single nucleotide variant	not provided [RCV001881517]\|not specified [RCV004041397]	Chr19:49908442 [GRCh38] Chr19:50411699 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.661C>T (p.Leu221Phe)	single nucleotide variant	not provided [RCV001903856]	Chr19:49909147 [GRCh38] Chr19:50412404 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1357G>A (p.Asp453Asn)	single nucleotide variant	not provided [RCV001883214]	Chr19:49908451 [GRCh38] Chr19:50411708 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.842C>G (p.Thr281Ser)	single nucleotide variant	not provided [RCV001885754]\|not specified [RCV004041062]	Chr19:49908966 [GRCh38] Chr19:50412223 [GRCh37] Chr19:19q13.33	likely benign\|uncertain significance
NM_016553.5(NUP62):c.836CCA[2] (p.Thr281_Thr282del)	microsatellite	not provided [RCV001908944]	Chr19:49908961..49908966 [GRCh38] Chr19:50412218..50412223 [GRCh37] Chr19:19q13.33	uncertain significance
NC_000019.9:g.(?_48618906)_(50921204_?)dup	duplication	Developmental and epileptic encephalopathy, 12 [RCV001939968]\|not provided [RCV001916178]	Chr19:48618906..50921204 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1525C>T (p.Arg509Trp)	single nucleotide variant	not provided [RCV001972101]	Chr19:49908283 [GRCh38] Chr19:50411540 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.564G>A (p.Leu188=)	single nucleotide variant	not provided [RCV002107202]	Chr19:49909244 [GRCh38] Chr19:50412501 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.378G>A (p.Ser126=)	single nucleotide variant	not provided [RCV002112532]	Chr19:49909430 [GRCh38] Chr19:50412687 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1134G>A (p.Glu378=)	single nucleotide variant	not provided [RCV002075409]	Chr19:49908674 [GRCh38] Chr19:50411931 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.864C>T (p.Thr288=)	single nucleotide variant	not provided [RCV002220460]	Chr19:49908944 [GRCh38] Chr19:50412201 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.756G>C (p.Gly252=)	single nucleotide variant	NUP62-related disorder [RCV003973336]\|not provided [RCV002201894]	Chr19:49909052 [GRCh38] Chr19:50412309 [GRCh37] Chr19:19q13.33	benign
NM_016553.5(NUP62):c.201G>A (p.Pro67=)	single nucleotide variant	not provided [RCV002162841]	Chr19:49909607 [GRCh38] Chr19:50412864 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.927C>T (p.Ala309=)	single nucleotide variant	not provided [RCV002091077]	Chr19:49908881 [GRCh38] Chr19:50412138 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1395C>T (p.Ala465=)	single nucleotide variant	not provided [RCV002216207]	Chr19:49908413 [GRCh38] Chr19:50411670 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.828C>G (p.Thr276=)	single nucleotide variant	not provided [RCV002111509]	Chr19:49908980 [GRCh38] Chr19:50412237 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.663C>T (p.Leu221=)	single nucleotide variant	NUP62-related disorder [RCV003978655]\|not provided [RCV002112693]	Chr19:49909145 [GRCh38] Chr19:50412402 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.828C>T (p.Thr276=)	single nucleotide variant	not provided [RCV002136858]	Chr19:49908980 [GRCh38] Chr19:50412237 [GRCh37] Chr19:19q13.33	benign
NM_016553.5(NUP62):c.190A>C (p.Thr64Pro)	single nucleotide variant	not provided [RCV002175325]	Chr19:49909618 [GRCh38] Chr19:50412875 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.415G>A (p.Gly139Ser)	single nucleotide variant	not provided [RCV002190313]	Chr19:49909393 [GRCh38] Chr19:50412650 [GRCh37] Chr19:19q13.33	benign
NM_016553.5(NUP62):c.504C>T (p.Pro168=)	single nucleotide variant	not provided [RCV002071840]	Chr19:49909304 [GRCh38] Chr19:50412561 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.336C>T (p.Ser112=)	single nucleotide variant	not provided [RCV002127203]	Chr19:49909472 [GRCh38] Chr19:50412729 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.276C>T (p.Ile92=)	single nucleotide variant	not provided [RCV002175321]	Chr19:49909532 [GRCh38] Chr19:50412789 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.123G>T (p.Gly41=)	single nucleotide variant	NUP62-related disorder [RCV003913626]\|not provided [RCV002081141]	Chr19:49909685 [GRCh38] Chr19:50412942 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.642C>A (p.Ile214=)	single nucleotide variant	not provided [RCV002097352]	Chr19:49909166 [GRCh38] Chr19:50412423 [GRCh37] Chr19:19q13.33	likely benign
NC_000019.9:g.(?_50411496)_(50766697_?)dup	duplication	not provided [RCV003122710]	Chr19:50411496..50766697 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1132G>A (p.Glu378Lys)	single nucleotide variant	not provided [RCV003121346]	Chr19:49908676 [GRCh38] Chr19:50411933 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.184C>A (p.Leu62Ile)	single nucleotide variant	not specified [RCV004310289]	Chr19:49909624 [GRCh38] Chr19:50412881 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.766A>G (p.Arg256Gly)	single nucleotide variant	not specified [RCV004145927]	Chr19:49890978 [GRCh38] Chr19:50394235 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.965C>T (p.Ala322Val)	single nucleotide variant	not provided [RCV002800359]\|not specified [RCV004064702]	Chr19:49908843 [GRCh38] Chr19:50412100 [GRCh37] Chr19:19q13.33	likely benign\|uncertain significance
NM_016553.5(NUP62):c.1547G>C (p.Ser516Thr)	single nucleotide variant	not provided [RCV002971543]	Chr19:49908261 [GRCh38] Chr19:50411518 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1404dup (p.Asp469Ter)	duplication	not provided [RCV002862989]	Chr19:49908403..49908404 [GRCh38] Chr19:50411660..50411661 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1489G>A (p.Ala497Thr)	single nucleotide variant	not specified [RCV004151644]	Chr19:49889885 [GRCh38] Chr19:50393142 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1388C>T (p.Ala463Val)	single nucleotide variant	not provided [RCV002975662]	Chr19:49908420 [GRCh38] Chr19:50411677 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.955G>A (p.Ala319Thr)	single nucleotide variant	not specified [RCV004106361]	Chr19:49908853 [GRCh38] Chr19:50412110 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1393G>A (p.Glu465Lys)	single nucleotide variant	not specified [RCV004151717]	Chr19:49889981 [GRCh38] Chr19:50393238 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1186G>A (p.Ala396Thr)	single nucleotide variant	not specified [RCV004137080]	Chr19:49890188 [GRCh38] Chr19:50393445 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.220T>C (p.Phe74Leu)	single nucleotide variant	not provided [RCV002972264]\|not specified [RCV004837861]	Chr19:49909588 [GRCh38] Chr19:50412845 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.838A>G (p.Thr280Ala)	single nucleotide variant	not specified [RCV004108468]	Chr19:49908970 [GRCh38] Chr19:50412227 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.814T>C (p.Ser272Pro)	single nucleotide variant	not provided [RCV002614172]	Chr19:49908994 [GRCh38] Chr19:50412251 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.538G>C (p.Glu180Gln)	single nucleotide variant	not specified [RCV004078171]	Chr19:49894297 [GRCh38] Chr19:50397554 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1085C>T (p.Pro362Leu)	single nucleotide variant	not specified [RCV004146755]	Chr19:49890289 [GRCh38] Chr19:50393546 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.247T>C (p.Ser83Pro)	single nucleotide variant	not provided [RCV002618357]	Chr19:49909561 [GRCh38] Chr19:50412818 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1108G>A (p.Glu370Lys)	single nucleotide variant	not specified [RCV004140043]	Chr19:49890266 [GRCh38] Chr19:50393523 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.802_804del (p.Ser268del)	deletion	not provided [RCV002637555]	Chr19:49909004..49909006 [GRCh38] Chr19:50412261..50412263 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.238G>A (p.Asp80Asn)	single nucleotide variant	not specified [RCV004163801]	Chr19:49895829 [GRCh38] Chr19:50399086 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.455T>G (p.Val152Gly)	single nucleotide variant	not specified [RCV004093055]	Chr19:49894380 [GRCh38] Chr19:50397637 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1445T>A (p.Met482Lys)	single nucleotide variant	not specified [RCV004139369]	Chr19:49908363 [GRCh38] Chr19:50411620 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.188C>T (p.Ala63Val)	single nucleotide variant	not provided [RCV003778013]\|not specified [RCV004190594]	Chr19:49909620 [GRCh38] Chr19:50412877 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1236G>T (p.Glu412Asp)	single nucleotide variant	not provided [RCV005098975]\|not specified [RCV004190665]	Chr19:49908572 [GRCh38] Chr19:50411829 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.993G>A (p.Ala331=)	single nucleotide variant	not provided [RCV002659014]	Chr19:49908815 [GRCh38] Chr19:50412072 [GRCh37] Chr19:19q13.33	likely benign
NM_152899.2(IL4I1):c.1256C>T (p.Ala419Val)	single nucleotide variant	not specified [RCV004179657]	Chr19:49890118 [GRCh38] Chr19:50393375 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.454G>A (p.Ala152Thr)	single nucleotide variant	not specified [RCV004118756]	Chr19:49909354 [GRCh38] Chr19:50412611 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1665A>C (p.Leu555Phe)	single nucleotide variant	not specified [RCV004199772]	Chr19:49889709 [GRCh38] Chr19:50392966 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.820G>A (p.Ala274Thr)	single nucleotide variant	not provided [RCV002890777]\|not specified [RCV004066032]	Chr19:49908988 [GRCh38] Chr19:50412245 [GRCh37] Chr19:19q13.33	likely benign\|uncertain significance
NM_152899.2(IL4I1):c.1612T>G (p.Ser538Ala)	single nucleotide variant	not specified [RCV004211832]	Chr19:49889762 [GRCh38] Chr19:50393019 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.68C>T (p.Thr23Met)	single nucleotide variant	not provided [RCV002780191]	Chr19:49909740 [GRCh38] Chr19:50412997 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1170C>T (p.Asp390=)	single nucleotide variant	not provided [RCV002948743]	Chr19:49908638 [GRCh38] Chr19:50411895 [GRCh37] Chr19:19q13.33	likely benign
NM_152899.2(IL4I1):c.637G>A (p.Glu213Lys)	single nucleotide variant	not specified [RCV004080718]	Chr19:49891107 [GRCh38] Chr19:50394364 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.381C>G (p.Ser127Arg)	single nucleotide variant	not provided [RCV002912689]	Chr19:49909427 [GRCh38] Chr19:50412684 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1046G>A (p.Arg349Gln)	single nucleotide variant	not specified [RCV004100673]	Chr19:49908762 [GRCh38] Chr19:50412019 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.952G>A (p.Ala318Thr)	single nucleotide variant	not provided [RCV003052834]	Chr19:49908856 [GRCh38] Chr19:50412113 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.731C>A (p.Thr244Asn)	single nucleotide variant	not provided [RCV003019055]	Chr19:49909077 [GRCh38] Chr19:50412334 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1645C>T (p.Pro549Ser)	single nucleotide variant	not specified [RCV004076121]	Chr19:49889729 [GRCh38] Chr19:50392986 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.851CCA[3] (p.Ser283_Ser284insThrThrThr)	microsatellite	not provided [RCV002645820]	Chr19:49908957..49908958 [GRCh38] Chr19:50412214..50412215 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.819C>T (p.Thr273=)	single nucleotide variant	not provided [RCV002626910]	Chr19:49908989 [GRCh38] Chr19:50412246 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.893C>T (p.Ala298Val)	single nucleotide variant	not provided [RCV002957374]\|not specified [RCV004067203]	Chr19:49908915 [GRCh38] Chr19:50412172 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.192_206del (p.Pro67_Thr71del)	deletion	not provided [RCV003005159]	Chr19:49909602..49909616 [GRCh38] Chr19:50412859..50412873 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.517C>G (p.Gln173Glu)	single nucleotide variant	not specified [RCV004121171]	Chr19:49894318 [GRCh38] Chr19:50397575 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.901G>A (p.Gly301Arg)	single nucleotide variant	not provided [RCV002594852]	Chr19:49908907 [GRCh38] Chr19:50412164 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.838A>C (p.Thr280Pro)	single nucleotide variant	not provided [RCV002914530]\|not specified [RCV004066280]	Chr19:49908970 [GRCh38] Chr19:50412227 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.172G>A (p.Gly58Ser)	single nucleotide variant	not provided [RCV002800607]	Chr19:49909636 [GRCh38] Chr19:50412893 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.313A>G (p.Thr105Ala)	single nucleotide variant	not provided [RCV002742032]\|not specified [RCV004067913]	Chr19:49909495 [GRCh38] Chr19:50412752 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1288C>T (p.Arg430Cys)	single nucleotide variant	not provided [RCV002595900]	Chr19:49908520 [GRCh38] Chr19:50411777 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.757A>T (p.Thr253Ser)	single nucleotide variant	not provided [RCV003059414]	Chr19:49909051 [GRCh38] Chr19:50412308 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.652G>A (p.Glu218Lys)	single nucleotide variant	not specified [RCV004196145]	Chr19:49891092 [GRCh38] Chr19:50394349 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.575C>T (p.Pro192Leu)	single nucleotide variant	not provided [RCV002890778]\|not specified [RCV004066033]	Chr19:49909233 [GRCh38] Chr19:50412490 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.778G>T (p.Ala260Ser)	single nucleotide variant	not provided [RCV002599066]	Chr19:49909030 [GRCh38] Chr19:50412287 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1094G>T (p.Arg365Leu)	single nucleotide variant	not specified [RCV004114820]	Chr19:49890280 [GRCh38] Chr19:50393537 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.738G>A (p.Ala246=)	single nucleotide variant	not provided [RCV002579013]	Chr19:49909070 [GRCh38] Chr19:50412327 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.377C>T (p.Ser126Leu)	single nucleotide variant	not provided [RCV003009406]	Chr19:49909431 [GRCh38] Chr19:50412688 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.256A>T (p.Thr86Ser)	single nucleotide variant	not provided [RCV002963138]	Chr19:49909552 [GRCh38] Chr19:50412809 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.737C>T (p.Ala246Val)	single nucleotide variant	not provided [RCV002941895]	Chr19:49909071 [GRCh38] Chr19:50412328 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.654G>A (p.Gly218=)	single nucleotide variant	not provided [RCV003027866]	Chr19:49909154 [GRCh38] Chr19:50412411 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.363C>T (p.Leu121=)	single nucleotide variant	not provided [RCV003091292]	Chr19:49909445 [GRCh38] Chr19:50412702 [GRCh37] Chr19:19q13.33	benign
NM_016553.5(NUP62):c.823GCCACC[1] (p.275AT[1])	microsatellite	not provided [RCV002581626]	Chr19:49908968..49908979 [GRCh38] Chr19:50412225..50412236 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.589G>A (p.Ala197Thr)	single nucleotide variant	not specified [RCV004100131]	Chr19:49909219 [GRCh38] Chr19:50412476 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1237G>A (p.Glu413Lys)	single nucleotide variant	not specified [RCV004155311]	Chr19:49890137 [GRCh38] Chr19:50393394 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.778G>A (p.Ala260Thr)	single nucleotide variant	not provided [RCV002631696]\|not specified [RCV004066626]	Chr19:49909030 [GRCh38] Chr19:50412287 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.836CCA[3] (p.Thr282del)	microsatellite	not provided [RCV002600840]	Chr19:49908961..49908963 [GRCh38] Chr19:50412218..50412220 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.749C>A (p.Thr250Asn)	single nucleotide variant	not provided [RCV002597578]\|not specified [RCV004065624]	Chr19:49909059 [GRCh38] Chr19:50412316 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.572C>G (p.Thr191Ser)	single nucleotide variant	not provided [RCV002832988]	Chr19:49909236 [GRCh38] Chr19:50412493 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.939A>T (p.Pro313=)	single nucleotide variant	not provided [RCV002833578]	Chr19:49908869 [GRCh38] Chr19:50412126 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1321G>A (p.Asp441Asn)	single nucleotide variant	not provided [RCV002602297]	Chr19:49908487 [GRCh38] Chr19:50411744 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.858C>T (p.Ser286=)	single nucleotide variant	not provided [RCV002653778]	Chr19:49908950 [GRCh38] Chr19:50412207 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1176G>C (p.Glu392Asp)	single nucleotide variant	not provided [RCV002653998]\|not specified [RCV004652010]	Chr19:49908632 [GRCh38] Chr19:50411889 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.673A>G (p.Ile225Val)	single nucleotide variant	not provided [RCV002587921]	Chr19:49909135 [GRCh38] Chr19:50412392 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.889C>T (p.Leu297=)	single nucleotide variant	not provided [RCV002610050]	Chr19:49908919 [GRCh38] Chr19:50412176 [GRCh37] Chr19:19q13.33	likely benign
NM_172374.3(IL4I1):c.44T>G (p.Met15Arg)	single nucleotide variant	not specified [RCV004078058]	Chr19:49901674 [GRCh38] Chr19:50404931 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.813_821del (p.Ser272_Ala274del)	deletion	not provided [RCV002654394]	Chr19:49908987..49908995 [GRCh38] Chr19:50412244..50412252 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.237G>A (p.Ala79=)	single nucleotide variant	NUP62-related disorder [RCV003926624]\|not provided [RCV002944290]	Chr19:49909571 [GRCh38] Chr19:50412828 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.704C>G (p.Thr235Ser)	single nucleotide variant	not provided [RCV003730446]\|not specified [RCV004255949]	Chr19:49909104 [GRCh38] Chr19:50412361 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.249G>T (p.Ser83=)	single nucleotide variant	not provided [RCV003415370]	Chr19:49909559 [GRCh38] Chr19:50412816 [GRCh37] Chr19:19q13.33	likely benign
NM_152899.2(IL4I1):c.289C>T (p.Arg97Cys)	single nucleotide variant	not specified [RCV004350273]	Chr19:49895144 [GRCh38] Chr19:50398401 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.7G>A (p.Gly3Arg)	single nucleotide variant	not provided [RCV003717302]	Chr19:49909801 [GRCh38] Chr19:50413058 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1029G>A (p.Glu343=)	single nucleotide variant	not provided [RCV003733418]	Chr19:49908779 [GRCh38] Chr19:50412036 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1232A>G (p.Glu411Gly)	single nucleotide variant	not provided [RCV003718879]	Chr19:49908576 [GRCh38] Chr19:50411833 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1544G>A (p.Arg515His)	single nucleotide variant	not provided [RCV003734092]	Chr19:49908264 [GRCh38] Chr19:50411521 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.436A>T (p.Thr146Ser)	single nucleotide variant	not provided [RCV003684510]	Chr19:49909372 [GRCh38] Chr19:50412629 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.371C>G (p.Ala124Gly)	single nucleotide variant	not provided [RCV003715277]	Chr19:49909437 [GRCh38] Chr19:50412694 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.832A>G (p.Thr278Ala)	single nucleotide variant	not provided [RCV003673432]	Chr19:49908976 [GRCh38] Chr19:50412233 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.827C>T (p.Thr276Ile)	single nucleotide variant	not provided [RCV003675189]	Chr19:49908981 [GRCh38] Chr19:50412238 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1077C>T (p.Asn359=)	single nucleotide variant	not provided [RCV003670036]	Chr19:49908731 [GRCh38] Chr19:50411988 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1254C>T (p.Ser418=)	single nucleotide variant	not provided [RCV003724964]	Chr19:49908554 [GRCh38] Chr19:50411811 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1130G>A (p.Arg377His)	single nucleotide variant	not provided [RCV003725339]\|not specified [RCV004374071]	Chr19:49908678 [GRCh38] Chr19:50411935 [GRCh37] Chr19:19q13.33	uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	copy number gain	not provided [RCV003485200]	Chr19:49625130..57647352 [GRCh37] Chr19:19q13.33-13.43	likely pathogenic
NM_016553.5(NUP62):c.402C>A (p.Gly134=)	single nucleotide variant	not provided [RCV003546254]	Chr19:49909406 [GRCh38] Chr19:50412663 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.507C>T (p.Ser169=)	single nucleotide variant	not provided [RCV003560804]	Chr19:49909301 [GRCh38] Chr19:50412558 [GRCh37] Chr19:19q13.33	benign
NM_016553.5(NUP62):c.271G>A (p.Gly91Arg)	single nucleotide variant	not provided [RCV003566199]	Chr19:49909537 [GRCh38] Chr19:50412794 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1235A>G (p.Glu412Gly)	single nucleotide variant	not provided [RCV003545669]	Chr19:49908573 [GRCh38] Chr19:50411830 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.254G>A (p.Gly85Glu)	single nucleotide variant	not provided [RCV003553879]	Chr19:49909554 [GRCh38] Chr19:50412811 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.770G>T (p.Ser257Ile)	single nucleotide variant	not provided [RCV003838581]	Chr19:49909038 [GRCh38] Chr19:50412295 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1387G>A (p.Ala463Thr)	single nucleotide variant	not provided [RCV003855984]	Chr19:49908421 [GRCh38] Chr19:50411678 [GRCh37] Chr19:19q13.33	uncertain significance
GRCh37/hg19 19q13.33-13.41(chr19:48905537-51614930)x3	copy number gain	not specified [RCV003986127]	Chr19:48905537..51614930 [GRCh37] Chr19:19q13.33-13.41	likely pathogenic
NM_016553.5(NUP62):c.457A>G (p.Thr153Ala)	single nucleotide variant	not provided [RCV003853103]	Chr19:49909351 [GRCh38] Chr19:50412608 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1111A>G (p.Lys371Glu)	single nucleotide variant	not specified [RCV004488605]	Chr19:49908697 [GRCh38] Chr19:50411954 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1412T>C (p.Leu471Pro)	single nucleotide variant	not specified [RCV004488607]	Chr19:49908396 [GRCh38] Chr19:50411653 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1520A>T (p.Glu507Val)	single nucleotide variant	not specified [RCV004488610]	Chr19:49908288 [GRCh38] Chr19:50411545 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.561G>A (p.Thr187=)	single nucleotide variant	NUP62-related disorder [RCV003919499]	Chr19:49909247 [GRCh38] Chr19:50412504 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1259C>T (p.Thr420Ile)	single nucleotide variant	not specified [RCV004488606]	Chr19:49908549 [GRCh38] Chr19:50411806 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1146G>A (p.Val382=)	single nucleotide variant	NUP62-related disorder [RCV003949658]	Chr19:49908662 [GRCh38] Chr19:50411919 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1503G>C (p.Glu501Asp)	single nucleotide variant	not specified [RCV004488609]	Chr19:49908305 [GRCh38] Chr19:50411562 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.992C>T (p.Ala331Val)	single nucleotide variant	not specified [RCV004488611]	Chr19:49908816 [GRCh38] Chr19:50412073 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1529C>A (p.Pro510His)	single nucleotide variant	not specified [RCV004405299]	Chr19:49889845 [GRCh38] Chr19:50393102 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.296T>C (p.Leu99Ser)	single nucleotide variant	Familial infantile bilateral striatal necrosis [RCV003133095]	Chr19:49909512 [GRCh38] Chr19:50412769 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.765C>T (p.Gly255=)	single nucleotide variant	not provided [RCV003663829]	Chr19:49909043 [GRCh38] Chr19:50412300 [GRCh37] Chr19:19q13.33	likely benign
NM_152899.2(IL4I1):c.1112G>A (p.Gly371Asp)	single nucleotide variant	not specified [RCV004405294]	Chr19:49890262 [GRCh38] Chr19:50393519 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.51C>A (p.Ser17Arg)	single nucleotide variant	not specified [RCV004405295]	Chr19:49896016 [GRCh38] Chr19:50399273 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1415C>T (p.Pro472Leu)	single nucleotide variant	not specified [RCV004405296]	Chr19:49889959 [GRCh38] Chr19:50393216 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.82C>T (p.Arg28Cys)	single nucleotide variant	not specified [RCV004405297]	Chr19:49895985 [GRCh38] Chr19:50399242 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1525G>C (p.Gly509Arg)	single nucleotide variant	not specified [RCV004405298]	Chr19:49889849 [GRCh38] Chr19:50393106 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.161A>G (p.Asn54Ser)	single nucleotide variant	not specified [RCV004405300]	Chr19:49895906 [GRCh38] Chr19:50399163 [GRCh37] Chr19:19q13.33	uncertain significance
NC_000019.9:g.(?_49713446)_(50413064_?)dup	duplication	Developmental and epileptic encephalopathy, 12 [RCV004581120]	Chr19:49713446..50413064 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.122G>A (p.Gly41Glu)	single nucleotide variant	not specified [RCV004652755]	Chr19:49909686 [GRCh38] Chr19:50412943 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.895C>T (p.Pro299Ser)	single nucleotide variant	not specified [RCV004652756]	Chr19:49908913 [GRCh38] Chr19:50412170 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1309G>C (p.Gly437Arg)	single nucleotide variant	not specified [RCV004628073]	Chr19:49890065 [GRCh38] Chr19:50393322 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.576A>C (p.Lys192Asn)	single nucleotide variant	not specified [RCV004628074]	Chr19:49891465 [GRCh38] Chr19:50394722 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.322T>C (p.Trp108Arg)	single nucleotide variant	not specified [RCV004628075]	Chr19:49895111 [GRCh38] Chr19:50398368 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.656G>C (p.Gly219Ala)	single nucleotide variant	not specified [RCV004628071]	Chr19:49891088 [GRCh38] Chr19:50394345 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1508A>G (p.Lys503Arg)	single nucleotide variant	not specified [RCV004628072]	Chr19:49889866 [GRCh38] Chr19:50393123 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1324G>A (p.Ala442Thr)	single nucleotide variant	not specified [RCV004835482]	Chr19:49908484 [GRCh38] Chr19:50411741 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.365C>T (p.Thr122Ile)	single nucleotide variant	not specified [RCV004835479]	Chr19:49909443 [GRCh38] Chr19:50412700 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.355A>G (p.Ser119Gly)	single nucleotide variant	not specified [RCV004835478]	Chr19:49909453 [GRCh38] Chr19:50412710 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1465G>A (p.Asp489Asn)	single nucleotide variant	not specified [RCV004835483]	Chr19:49908343 [GRCh38] Chr19:50411600 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.977C>T (p.Ser326Phe)	single nucleotide variant	not specified [RCV004835485]	Chr19:49908831 [GRCh38] Chr19:50412088 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.251G>C (p.Gly84Ala)	single nucleotide variant	not specified [RCV004835484]	Chr19:49909557 [GRCh38] Chr19:50412814 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1393G>A (p.Ala465Thr)	single nucleotide variant	not specified [RCV004835481]	Chr19:49908415 [GRCh38] Chr19:50411672 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.31G>T (p.Ala11Ser)	single nucleotide variant	not specified [RCV004835480]	Chr19:49909777 [GRCh38] Chr19:50413034 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1190T>C (p.Leu397Pro)	single nucleotide variant	not specified [RCV004832736]	Chr19:49908618 [GRCh38] Chr19:50411875 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1323_1324inv (p.Ala442Thr)	inversion	not provided [RCV005168927]	Chr19:49908484..49908485 [GRCh38] Chr19:50411741..50411742 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.51G>A (p.Thr17=)	single nucleotide variant	not provided [RCV005193664]	Chr19:49909757 [GRCh38] Chr19:50413014 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1224C>T (p.Ser408=)	single nucleotide variant	not provided [RCV005149443]	Chr19:49908584 [GRCh38] Chr19:50411841 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.963G>T (p.Gly321=)	single nucleotide variant	not provided [RCV005109610]	Chr19:49908845 [GRCh38] Chr19:50412102 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.996G>C (p.Gln332His)	single nucleotide variant	not provided [RCV005066672]	Chr19:49908812 [GRCh38] Chr19:50412069 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1245G>A (p.Lys415=)	single nucleotide variant	not provided [RCV005061937]	Chr19:49908563 [GRCh38] Chr19:50411820 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.978C>T (p.Ser326=)	single nucleotide variant	not provided [RCV005081264]	Chr19:49908830 [GRCh38] Chr19:50412087 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.979G>T (p.Ala327Ser)	single nucleotide variant	not provided [RCV005131604]	Chr19:49908829 [GRCh38] Chr19:50412086 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1108G>C (p.Glu370Gln)	single nucleotide variant	not provided [RCV005150896]	Chr19:49908700 [GRCh38] Chr19:50411957 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.703A>G (p.Thr235Ala)	single nucleotide variant	not provided [RCV005069116]	Chr19:49909105 [GRCh38] Chr19:50412362 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1098C>T (p.Ile366=)	single nucleotide variant	not provided [RCV005081248]	Chr19:49908710 [GRCh38] Chr19:50411967 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1519G>A (p.Glu507Lys)	single nucleotide variant	not provided [RCV005180714]	Chr19:49908289 [GRCh38] Chr19:50411546 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.836CCA[1] (p.Thr280_Thr282del)	microsatellite	not provided [RCV005062855]	Chr19:49908961..49908969 [GRCh38] Chr19:50412218..50412226 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.495G>A (p.Thr165=)	single nucleotide variant	not provided [RCV005065706]	Chr19:49909313 [GRCh38] Chr19:50412570 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.213G>A (p.Thr71=)	single nucleotide variant	not provided [RCV005060760]	Chr19:49909595 [GRCh38] Chr19:50412852 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.274A>G (p.Ile92Val)	single nucleotide variant	not provided [RCV005159065]	Chr19:49909534 [GRCh38] Chr19:50412791 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.680C>G (p.Thr227Ser)	single nucleotide variant	not provided [RCV005084157]	Chr19:49909128 [GRCh38] Chr19:50412385 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1436A>T (p.Asn479Ile)	single nucleotide variant	not provided [RCV005120546]	Chr19:49908372 [GRCh38] Chr19:50411629 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.1386G>A (p.Gly462=)	single nucleotide variant	not provided [RCV005088716]	Chr19:49908422 [GRCh38] Chr19:50411679 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.923C>G (p.Ala308Gly)	single nucleotide variant	not provided [RCV005066673]	Chr19:49908885 [GRCh38] Chr19:50412142 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.850_851insCCA (p.Ser283_Ser284insThr)	insertion	not provided [RCV005067820]	Chr19:49908957..49908958 [GRCh38] Chr19:50412214..50412215 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.791C>T (p.Ala264Val)	single nucleotide variant	not provided [RCV005083837]	Chr19:49909017 [GRCh38] Chr19:50412274 [GRCh37] Chr19:19q13.33	uncertain significance
NM_016553.5(NUP62):c.945C>T (p.Gly315=)	single nucleotide variant	not provided [RCV005195634]	Chr19:49908863 [GRCh38] Chr19:50412120 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.1386G>C (p.Gly462=)	single nucleotide variant	not provided [RCV005174989]	Chr19:49908422 [GRCh38] Chr19:50411679 [GRCh37] Chr19:19q13.33	likely benign
NM_016553.5(NUP62):c.753T>G (p.Ala251=)	single nucleotide variant	not provided [RCV005177677]	Chr19:49909055 [GRCh38] Chr19:50412312 [GRCh37] Chr19:19q13.33	likely benign
NM_152899.2(IL4I1):c.1688C>G (p.Thr563Arg)	single nucleotide variant	not specified [RCV004929243]	Chr19:49889686 [GRCh38] Chr19:50392943 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.1633G>C (p.Glu545Gln)	single nucleotide variant	not specified [RCV004929248]	Chr19:49889741 [GRCh38] Chr19:50392998 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.686T>C (p.Leu229Pro)	single nucleotide variant	not specified [RCV004929247]	Chr19:49891058 [GRCh38] Chr19:50394315 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.782G>T (p.Arg261Leu)	single nucleotide variant	not specified [RCV004929246]	Chr19:49890592 [GRCh38] Chr19:50393849 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.877G>A (p.Gly293Arg)	single nucleotide variant	not specified [RCV004929245]	Chr19:49890497 [GRCh38] Chr19:50393754 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.75G>C (p.Lys25Asn)	single nucleotide variant	not specified [RCV004929244]	Chr19:49895992 [GRCh38] Chr19:50399249 [GRCh37] Chr19:19q13.33	uncertain significance
NM_152899.2(IL4I1):c.402C>A (p.Asn134Lys)	single nucleotide variant	not specified [RCV004405301]	Chr19:49894433 [GRCh38] Chr19:50397690 [GRCh37] Chr19:19q13.33	uncertain significance

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

adipose tissue	alimentary part of gastrointestinal system	circulatory system	ectoderm	endocrine system	endoderm	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	nervous system	reproductive system	respiratory system
6	5	5	23	22	16	6	6	6	6	33	22	12	14	10


RefSeq Transcripts	XM_005628731	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005628732	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005628733	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_022427579	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_022427580	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_022427581	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_022427582	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_022427583	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038445056	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038445112	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038495074	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038495075	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038495076	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038495077	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038495078	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038495079	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038495080	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038495081	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038495082	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038495083	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038495084	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038621288	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038621289	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038621290	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038621291	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038621292	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038621293	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038621294	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038621295	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038621296	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038621297	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038621298	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038686973	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038686974	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038686975	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038686976	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038686977	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038686978	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038686979	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038686980	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038686981	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038686982	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_038686983	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_539521	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_002633103	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_005335964	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_005404023	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_005437474	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AAEX04000014	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	JAAQRD010000017	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	JAAUVH010000208	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	REHQ01000014	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENSCAFT00000005270 ⟹ ENSCAFP00000032124

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1 Ensembl	14	48,873,990 - 48,880,266 (-)	Ensembl

Ensembl Acc Id:

ENSCAFT00845052860 ⟹ ENSCAFP00845041503

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0 Ensembl	14	48,822,741 - 48,829,735 (-)	Ensembl

RefSeq Acc Id:

XM_005628731 ⟹ XP_005628788

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1	14	48,873,299 - 48,879,845 (-)	NCBI
Dog10K_Boxer_Tasha	14	48,317,131 - 48,323,662 (-)	NCBI

Sequence:

show sequence

CTGGCGCGTGGGGGCGGCGCTCCGCGGTTTTCAGAGCGTTTCCCGCCCTCGCCTGGTCTCTGTTGGACGAGGACTTCCGCCTCAGGTTTCCTCTACATGACAAAGAAAGACTTGAAAAATGGTTAAAG
AATATGAAACGAGATTCATGGGTACCCAGTAAATACCAGTTCCTGTGTAGTGACCATTTTACTCCTGACTCTCTTGACATCAGATGGGGTATTCGATATTTGAAACAAACTGCAATTCCAACAATATT
TTCTTTGCCTGAAGACGATCAGGAAAAAGACCCTTCCAAAAAAAAATCTCAGAAGAAAAAATTAGATGATGAGAAAGAAGTGTGCCTAAAAGCCAAGTCACAAGAATCATTTGCTTCAAATGAGTTAA
AGAAAAATACAGTTAATACAAATATTCTCCTTGAACACACAGAATTATGTAATTCATCTACTTTGGTGAAGCCACCAGCTCCCAAACCAGAATGTATACAAAATAACGTATTAACTCTTAATCTGCTT
AAACAAGATATTGGAATACCAGTATCTACCTTGGAAACTTCAGTTACCCAAGACATAGATATAGGTGGTTTTCACACATCTTTTGAGAATCTAAATTCTACAACTATTACCTTGACAACTTCAAACTC
AGAAGATGTTCAGCCATCTTTGGAAACCCAAGAAGTGTTTGAAATAACTGCGAATCATCTTGCTAACCCAAACTTTACAAATAATTCCATGGAAATTAAGTCCGCACAGGAAAGTCCATTTTTACTCA
GCACAATTACTCAAACAGTCGAAGAGTTAAATACAAATAAAGAATCTGTTATTGCCATTTTTGTACCCACAGAAAATTCCAAACCAATTAATTCATTTGTATCTGCTGAAAAAGAAACTGTGGAAATG
GAAGATCTAGACATTGAAGACTCCTTATATAAGGATGTAGACTATGAGACAGAAGTTTTACAAATTGAACATTCTTATTGCAGACAAGATATAAATAAGGAACATCTTTGGCAGAAAGTTTCTAAACT
ACATTCAAAGATAACTCTTCTCGAGCTACAAGAACAACAAACTCTTGGAAGATTGAAGTCTTTGGAAGCTCTTATAAGGCAGCTAAAACAAGAAAACTGGCTATCCGAAGAAAATGTCAAGATTATAG
AAAATCATTTCACAACATATGAAGTTACTATGATATAGAGTGTAAAGAGTTTAACACTATGACTTTTATATAAGCTTTTTGCAGCCAAACTAAATTATATGTAACTTTTTCCGGTATAAAGTTCTCAT
CTTAAGCTAAGAAAATGTTCTAATGTTAAAAACTGCATCCCGTTCTTGTAGTGTTCATTGTTAAGAAAAACAAGAGAGTTGTTGGACTGTAGAGAAGAAGTTTCACCACTTGGTAATCTTCTAAATTA
AAGTTAAAATAGAGTGAATAAGTAATATGATTCATAAAATGGGAGAACATGGAGATGGTGAAAGGAGCCCAGAAGAGAAATCAGGCTTGGATATCAGTGCCAGTTCTACCTTTGGCATGTGATTTGGG
CGAATTACTTTGAAGCCTCAGTCTGTAATCTGTACAATAAGGGCACTTACAAAATCTAGTCTGTTTATAGTTCCTTTCCTTTGTATTAAGATACTTTTTTAATAGAACAACTTTTTGGTAAGATAATA
CATACTTACATAATACTAGATGTTGGCTAGTATTTGATGTTATTTGCTATTGGATTATCCTCAGAATTGAATTCTGTGGTATTTGACTTGTTGACTATAGTTATTTGTAATAATAGTACTCCTTTTAT
AATTTTATTCCACTTGAGTGATAATAACCATTAGTCCGGTTCATAGGGGAAGTACTTTAAACTTCAAAGAATATGTATTTCAATACCCTATATGTAGCTGACCATCATAATACATAGTCAGGTAATCT
CCTTAACATTCTATATTTAAAAAAAAATTCTATATTTAAGGTTATAATTTATAAACCAAAAATTGTAATGAGGTTAATTTTTAAAACTATGTAGATTACTATATTTTAGAAATCATAACTTATATATA
ATGTGTAGCTTTTTTAAATGTGTGCTTTTGTCATTTTTAAATTCCAGAATGATAGAGTACTATTTAATATTATACATGCCCACTTACATATATGTATTTTATTAAAATTTATAAGCAAGAAACTGTAT
ATCTGGAGTGATCTTAGACAAGCAAGAAAGGAATGATGGTGATGTAAATAAAAATATTGCTTATACCCATGAGAATTTTTTTTTAAGTGTGAAAAAGACAGTGGGAACAGCAGAAATGTAGAAAATAA
TGATTTAAAATTGACAGTTAATATAATTGAATATGTTACTGATTATAGTATTGAGCAAGTTCCTATCAGTTCTTATCACACTTTTCCTTGCCTTTTTTATAAAAAAATACTACTACTTAATCTCAAAG
GAGTGTTTTGAGAATTCAATGAAGTAACATGTTTTTGGTTCTGGAAAATAGGAGGTGCTCAATAAACATTAGTTGACTGCACAGCAGATAGTATACTAATTGTTTTGTAAATTCATGGTGATTATTTT
TGGCCACACTTTATTTTTTTCAAGCTAATACAATTCATTGGTATTATATAATATGTATCTTAAATATGAAAAGTTAATTTATTGGTATCTTTATTATGGGAGAAAAAAACCATAGATTTTTGCATAAA
TTAGGTACAGATAATTGGTAGAATTAATGTATTTAAGTATTCCCATGCTCCATTTTACAATATTTATTTGAAATAATTATTGTAGATGAAAATAACTTTAATAAGTCATTATAAAATAATGTTTCAAC
TCTGTTTTTACCTGTGCGTATTGTATTTATTTTCTCTTTATTTAAAGTTGTAGTCTACTCAGGAATAATTTAAACTGGTTGTATTTCTTTAAACTTAATAAATTATAAATATTTAAGATA

hide sequence

RefSeq Acc Id:

XM_005628732 ⟹ XP_005628789

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1	14	48,797,689 - 48,880,293 (-)	NCBI
Dog10K_Boxer_Tasha	14	48,241,611 - 48,324,131 (-)	NCBI

Sequence:

show sequence

GTGGCGCAGGCGCAGTGGCTCGGCGACGCGCCGGGGGTGGTAGCCCGCTCCGCCTTGGCGGACGGGGTCACGCCAGCGCCCCTCGCCGGCCCGGCCCCTCCGGGCCGCCGCGGAGGGAGCGATGCCTC
GCTACTGCGCGGCGATTTGCTGTAAGAACCGTCGGGGACGGAACAGTAAGGACCGGAAGCTGAGTTTTTACCCGTTTCCTCTACATGACAAAGAAAGACTTGAAAAATGGTTAAAGAATATGAAACGA
GATTCATGGGTACCCAGTAAATACCAGTTCCTGTGTAGTGACCATTTTACTCCTGACTCTCTTGACATCAGATGGGGTATTCGATATTTGAAACAAACTGCAATTCCAACAATATTTTCTTTGCCTGA
AGACGATCAGAATCTATGTCATTCTGAAGAAATTGACTCCATGTCTCAACTCCAAAGATGGGACTCTAACCTGAGGCTAAGACTGCCGTATGTTCAACTGGCACATAGTGGGCTTCATAACTGTTCTC
TTGCCAGCCACAGTGCATAAAATTTCCCAGGCTCCTCAGGAATTTGCCTGAGTGACTACAGATTGCCTGGAAGTGTGAGTGCCTATAGCCGGTTATAATCTTGAAGGACACATTGTTCTGAAATGAAT
TTTAAGCTTGTATGCTCACTCATTTTAAGTTTTGGAGTCTTGTTAATCCAGTCAACAATTCCTACCTTAACGGAATCATTACAAACAAAATGATCTC

hide sequence

RefSeq Acc Id:

XM_005628733 ⟹ XP_005628790

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1	14	48,802,568 - 48,880,293 (-)	NCBI
Dog10K_Boxer_Tasha	14	48,246,637 - 48,324,130 (-)	NCBI

Sequence:

show sequence

GTGGCGCAGGCGCAGTGGCTCGGCGACGCGCCGGGGGTGGTAGCCCGCTCCGCCTTGGCGGACGGGGTCACGCCAGCGCCCCTCGCCGGCCCGGCCCCTCCGGGCCGCCGCGGAGGGAGCGATGCCTC
GCTACTGCGCGGCGATTTGCTGTAAGAACCGTCGGGGACGGAACAGTAAGGACCGGAAGCTGAGTTTTTACCCGTTTCCTCTACATGACAAAGAAAGACTTGAAAAATGGTTAAAGAATATGAAACGA
GATTCATGGGTACCCAGTAAATACCAGTTCCTGTGTAGTGACCATTTTACTCCTGACTCTCTTGACATCAGATGGGGTATTCGATATTTGAAACAAACTGCAATTCCAACAATATTTTCTTTGCCTGA
AGACGATCAGAATCTATGTCATTCTGAAGAAATTGACTCCATGTCTCAACTCCAAAGATGGGACTCTAACCTGAGGCTAAGGGATTCATCCAGAACTCCAGGAAATGCTTCTGTGTGCTCAGACCTGT
GAAATGATATCTCTTTATACTGTGGTTGTTTTTTTTAAAAAAAGAACTGTCTCCACATCTCCTCCATCCTGTGCTTTTGGAACCAAGAGAAGACCTTTGCATTGATCTTGCCTAAATTTTATTTTGCT
ACACGGGTTTTCAGAACTTTTTAGATCCTAAATACGACCACTACGTCTTTATTCAAGATGTGCAACAGAACTGAAGTCCAAGGTCTCTGCCCATCCAGAAGTTTCCATTTGAACATCAGTCCTTCAGA
AAAGTTACTCTCTAGACACCAGACAGCCTGTGTTTCCAGAATGTCAATATTGCCAACAGCAACCTTGCCAGATGCCTAGATGAAAACCACATACCTATGTCTAATGAATATTGTTCAATTTCATTCTG
GTAACCTGTGCAAGGTATCCCTGTCGCAATGTAACTTTCCAGCCACATGAATTAGGATTTGGATTCTTCATTCACAGTAGAATGCAAAGATTTGGAAATTCAGCTGCATTCCAAGTTCCTCTCTTTTA
TCTAGTGAACTAGATGCCCTTAGACCACATAGACTCCCTGAGCCCCCATTTTACTAATTAAGACAATGGGATAATGCCTGTGCCTCTAATGCAAAAATTTTTTAAATTTGCTTGTTTTATGATTTGTA
TGGCCTTTATCTAGAGCAGTACTTTCGCTTTAAGGTATTCCATGAATTTCAAACTCCACAAGTAGAATATTCTGAAACAGAGACCATCAAACATCCTCATCAGTGCAGAAGCCCAAGGTTTTCACCAT
TTAATGCATCCACACATTATACTTATTTAAAAAAAAATTGTCACCTGTAAAGAAATCCCTTGTAAAGATGGTGATAATGATGATGATGATGGCAATGATGATGATGACGTCCTGATATCCAAACTGGG
GCTTCACCCTAAAGTGAAGTGTTGCTAGAATAACTGATGTTATTCACTTGGCTTCCTCCAGACTTTGAGGTGTTCTATTTATATGCATGTCTGGATATTATAAGGTATTTTAGGGTAGTTGCTAGGGT
TGACAGATGAATTTTATGGAGGAACATGAGTACACCTCAAACCTATACTTCCTCTCAGCAAGGAACTAGATTCAAGGCCTATGTAATTCTCACGAAACAATTTCTACAGTACTATTTTTAAAGCACAA
CTTGTTTTTCTAGAAGCAGAGCAGGAGTCCCTGTATTTTGGAAGACCACACTCCTATAGAGAAGAAATCTAATGGCATTATAACTTAAGAAATCTTAGCATATGGGGGAAGAATTCCAATCTCCCATG
TTTTTATTCGCCAGTAATTTACACACACACCAGATAGATCTAGTAACTGAATCACCAGGCAAAAACGTTTATTCCAGGTTAAGCCAGGCCAACACCTAATTTTAAGCTTCAAGCATCCTGACCCTGTT
TACAGAAATAGTCTTATTTTCTCTGACCTTAACCTTAATTTCCTTGCTTACTTTCCATTTCTGCATCCACTTAGCTCTTAACTGTTTTGCTTTGTCTCCCGTGAAGGACCCTGTGCTTGCTTTTTGTA
GTTAAGGGTGGATTTGACTTCTTTAGTTCCAGGTAGACTTCCCACCTGATTGAGCCCTAGCCAACTCATCATCTATGATGGTTTCCTTAGTTCCTTAATACTCACGCCTCAAGTGAGAGGTTCACAGT
TCTCCTGAGAATGACCAGCTCTTTCCAGAGAAACTTAATAGATAGTTATAGTGGGTCTTTACTTTAGCTGCTCCTAATGTTGCATTTTTATTTTTTAAAAAAATCATCCCATGTTTTCCTGTTTCCTT
AACATTTGTGTTTCCGTCCTCATTTTGGTTACTGCATCTCTACAGTACATTTTTTTTCTTGGAGGATGAGTTTGTTTATTTTAAAGATTGATTTATTTGAGAGAGTGTGTGTGTGCACATGAGCAGAT
GGTGGGGTAAGGGGAGAGAGAATGTCCAGCAAACTTTTTGCTGAGTACAGAGCCTAAGGTGGTGCTCGTTCCCAAGACCCTGAAATCATGACCTGAGCTGAAATCAAGAGTCAGATACTTAACTGACT
GAGCCACCCAGGCGCCTCTTAGAGGATGAATTTATTAATTTACTCAGCAAATGCCTATTTTACCATTGTATTTATACTTACCAGCACAGCTCCAGAAGCTGCCTATTAATTTGATTCTACCTTTGCTG
GGGAACTTGTCATCTCCTTGTACTACAGCATAGGCCTCATCATACTGGCCAGCAGTCGGCTGGATGCTATTTATTTCTGAATTCCTTAGCCTTGGTACACAAGTCTCCTCATTCACACACAATCTCTC
ATTTGCTATCATTCCCAATTTGTAAATAAAAACCTTAATTTATCTACTGTAATAAAGTCAAATTTAAGTCAATATACATATTTTGTTTATAATTTAACAGAAAATAAATTCTATGAAATTACAGAGTA
TAATTTATATACAGTGACTGACCAACACTTAGCACAGTAGCACAAAACACGTTGCATATGCTCAATAATTGTTTGCTTAGTGGGAAGATGGATGGTTGGATTGATGTATAGATGGATGGATGGATGCT
CAGTATGTGCCAGACTGATATTAAGAATTTCATATAAAATAAATAAGCCCTGGAGATGTATTGTACGGCGTGATGAGTATAGCTAATACTGTATTATATATTTGAAAATGGGTAGAAGAGTAAATCTT
CGAAAAGAAAACTATAACTGTGTTTGATGGATGTTAAAGTAGAATTATTGTGGTGACAATTTCACTATATATGCAAATGTTGAATCATTATGTTATACATATGAAACCAACATAAGGTTATATGTCAG
TTGTATCTCAAATAAATAAATAAGAATTTAATA

hide sequence

RefSeq Acc Id:

XM_022427579 ⟹ XP_022283287

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1	14	48,873,299 - 48,880,070 (-)	NCBI
Dog10K_Boxer_Tasha	14	48,317,131 - 48,324,089 (-)	NCBI

Sequence:

show sequence

GCGTCCGCCTTTACGGTGAGGCCACGGGGCTGTGGCGTTTGGGGCCGGCGGTACCTGGAGAGTC
GTCCTCGGCCCCACCGGCGCGTCCCGTCACAGCGCGGGAGGACGACGTGGAGGCTCGAGTTCAGGTTTCCTCTACATGACAAAGAAAGACTTGAAAAATGGTTAAAGAATATGAAACGAGATTCATGG
GTACCCAGTAAATACCAGTTCCTGTGTAGTGACCATTTTACTCCTGACTCTCTTGACATCAGATGGGGTATTCGATATTTGAAACAAACTGCAATTCCAACAATATTTTCTTTGCCTGAAGACGATCA
GGAAAAAGACCCTTCCAAAAAAAAATCTCAGAAGAAAAAATTAGATGATGAGAAAGAAGTGTGCCTAAAAGCCAAGTCACAAGAATCATTTGCTTCAAATGAGTTAAAGAAAAATACAGTTAATACAA
ATATTCTCCTTGAACACACAGAATTATGTAATTCATCTACTTTGGTGAAGCCACCAGCTCCCAAACCAGAATGTATACAAAATAACGTATTAACTCTTAATCTGCTTAAACAAGATATTGGAATACCA
GTATCTACCTTGGAAACTTCAGTTACCCAAGACATAGATATAGGTGGTTTTCACACATCTTTTGAGAATCTAAATTCTACAACTATTACCTTGACAACTTCAAACTCAGAAGATGTTCAGCCATCTTT
GGAAACCCAAGAAGTGTTTGAAATAACTGCGAATCATCTTGCTAACCCAAACTTTACAAATAATTCCATGGAAATTAAGTCCGCACAGGAAAGTCCATTTTTACTCAGCACAATTACTCAAACAGTCG
AAGAGTTAAATACAAATAAAGAATCTGTTATTGCCATTTTTGTACCCACAGAAAATTCCAAACCAATTAATTCATTTGTATCTGCTGAAAAAGAAACTGTGGAAATGGAAGATCTAGACATTGAAGAC
TCCTTATATAAGGATGTAGACTATGAGACAGAAGTTTTACAAATTGAACATTCTTATTGCAGACAAGATATAAATAAGGAACATCTTTGGCAGAAAGTTTCTAAACTACATTCAAAGATAACTCTTCT
CGAGCTACAAGAACAACAAACTCTTGGAAGATTGAAGTCTTTGGAAGCTCTTATAAGGCAGCTAAAACAAGAAAACTGGCTATCCGAAGAAAATGTCAAGATTATAGAAAATCATTTCACAACATATG
AAGTTACTATGATATAGAGTGTAAAGAGTTTAACACTATGACTTTTATATAAGCTTTTTGCAGCCAAACTAAATTATATGTAACTTTTTCCGGTATAAAGTTCTCATCTTAAGCTAAGAAAATGTTCT
AATGTTAAAAACTGCATCCCGTTCTTGTAGTGTTCATTGTTAAGAAAAACAAGAGAGTTGTTGGACTGTAGAGAAGAAGTTTCACCACTTGGTAATCTTCTAAATTAAAGTTAAAATAGAGTGAATAA
GTAATATGATTCATAAAATGGGAGAACATGGAGATGGTGAAAGGAGCCCAGAAGAGAAATCAGGCTTGGATATCAGTGCCAGTTCTACCTTTGGCATGTGATTTGGGCGAATTACTTTGAAGCCTCAG
TCTGTAATCTGTACAATAAGGGCACTTACAAAATCTAGTCTGTTTATAGTTCCTTTCCTTTGTATTAAGATACTTTTTTAATAGAACAACTTTTTGGTAAGATAATACATACTTACATAATACTAGAT
GTTGGCTAGTATTTGATGTTATTTGCTATTGGATTATCCTCAGAATTGAATTCTGTGGTATTTGACTTGTTGACTATAGTTATTTGTAATAATAGTACTCCTTTTATAATTTTATTCCACTTGAGTGA
TAATAACCATTAGTCCGGTTCATAGGGGAAGTACTTTAAACTTCAAAGAATATGTATTTCAATACCCTATATGTAGCTGACCATCATAATACATAGTCAGGTAATCTCCTTAACATTCTATATTTAAA
AAAAAATTCTATATTTAAGGTTATAATTTATAAACCAAAAATTGTAATGAGGTTAATTTTTAAAACTATGTAGATTACTATATTTTAGAAATCATAACTTATATATAATGTGTAGCTTTTTTAAATGT
GTGCTTTTGTCATTTTTAAATTCCAGAATGATAGAGTACTATTTAATATTATACATGCCCACTTACATATATGTATTTTATTAAAATTTATAAGCAAGAAACTGTATATCTGGAGTGATCTTAGACAA
GCAAGAAAGGAATGATGGTGATGTAAATAAAAATATTGCTTATACCCATGAGAATTTTTTTTTAAGTGTGAAAAAGACAGTGGGAACAGCAGAAATGTAGAAAATAATGATTTAAAATTGACAGTTAA
TATAATTGAATATGTTACTGATTATAGTATTGAGCAAGTTCCTATCAGTTCTTATCACACTTTTCCTTGCCTTTTTTATAAAAAAATACTACTACTTAATCTCAAAGGAGTGTTTTGAGAATTCAATG
AAGTAACATGTTTTTGGTTCTGGAAAATAGGAGGTGCTCAATAAACATTAGTTGACTGCACAGCAGATAGTATACTAATTGTTTTGTAAATTCATGGTGATTATTTTTGGCCACACTTTATTTTTTTC
AAGCTAATACAATTCATTGGTATTATATAATATGTATCTTAAATATGAAAAGTTAATTTATTGGTATCTTTATTATGGGAGAAAAAAACCATAGATTTTTGCATAAATTAGGTACAGATAATTGGTAG
AATTAATGTATTTAAGTATTCCCATGCTCCATTTTACAATATTTATTTGAAATAATTATTGTAGATGAAAATAACTTTAATAAGTCATTATAAAATAATGTTTCAACTCTGTTTTTACCTGTGCGTAT
TGTATTTATTTTCTCTTTATTTAAAGTTGTAGTCTACTCAGGAATAATTTAAACTGGTTGTATTTCTTTAAACTTAATAAATTATAAATATTTAAGATA

hide sequence

RefSeq Acc Id:

XM_022427580 ⟹ XP_022283288

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1	14	48,873,299 - 48,879,810 (-)	NCBI
Dog10K_Boxer_Tasha	14	48,317,131 - 48,323,635 (-)	NCBI

Sequence:

show sequence

GCGTTTCCCGCCCTCGCCTGGTCTCTGTTGGACGAGGACTTCCGCCTCAGGTGAGCCTCAGGCCGGCCGCAGTCGCGCTCACGCTCACCTCACGCCTTCTGGGAGGTTTCCTCTACATGACAAAGAAA
GACTTGAAAAATGGTTAAAGAATATGAAACGAGATTCATGGGTACCCAGTAAATACCAGTTCCTGTGTAGTGACCATTTTACTCCTGACTCTCTTGACATCAGATGGGGTATTCGATATTTGAAACAA
ACTGCAATTCCAACAATATTTTCTTTGCCTGAAGACGATCAGGAAAAAGACCCTTCCAAAAAAAAATCTCAGAAGAAAAAATTAGATGATGAGAAAGAAGTGTGCCTAAAAGCCAAGTCACAAGAATC
ATTTGCTTCAAATGAGTTAAAGAAAAATACAGTTAATACAAATATTCTCCTTGAACACACAGAATTATGTAATTCATCTACTTTGGTGAAGCCACCAGCTCCCAAACCAGAATGTATACAAAATAACG
TATTAACTCTTAATCTGCTTAAACAAGATATTGGAATACCAGTATCTACCTTGGAAACTTCAGTTACCCAAGACATAGATATAGGTGGTTTTCACACATCTTTTGAGAATCTAAATTCTACAACTATT
ACCTTGACAACTTCAAACTCAGAAGATGTTCAGCCATCTTTGGAAACCCAAGAAGTGTTTGAAATAACTGCGAATCATCTTGCTAACCCAAACTTTACAAATAATTCCATGGAAATTAAGTCCGCACA
GGAAAGTCCATTTTTACTCAGCACAATTACTCAAACAGTCGAAGAGTTAAATACAAATAAAGAATCTGTTATTGCCATTTTTGTACCCACAGAAAATTCCAAACCAATTAATTCATTTGTATCTGCTG
AAAAAGAAACTGTGGAAATGGAAGATCTAGACATTGAAGACTCCTTATATAAGGATGTAGACTATGAGACAGAAGTTTTACAAATTGAACATTCTTATTGCAGACAAGATATAAATAAGGAACATCTT
TGGCAGAAAGTTTCTAAACTACATTCAAAGATAACTCTTCTCGAGCTACAAGAACAACAAACTCTTGGAAGATTGAAGTCTTTGGAAGCTCTTATAAGGCAGCTAAAACAAGAAAACTGGCTATCCGA
AGAAAATGTCAAGATTATAGAAAATCATTTCACAACATATGAAGTTACTATGATATAGAGTGTAAAGAGTTTAACACTATGACTTTTATATAAGCTTTTTGCAGCCAAACTAAATTATATGTAACTTT
TTCCGGTATAAAGTTCTCATCTTAAGCTAAGAAAATGTTCTAATGTTAAAAACTGCATCCCGTTCTTGTAGTGTTCATTGTTAAGAAAAACAAGAGAGTTGTTGGACTGTAGAGAAGAAGTTTCACCA
CTTGGTAATCTTCTAAATTAAAGTTAAAATAGAGTGAATAAGTAATATGATTCATAAAATGGGAGAACATGGAGATGGTGAAAGGAGCCCAGAAGAGAAATCAGGCTTGGATATCAGTGCCAGTTCTA
CCTTTGGCATGTGATTTGGGCGAATTACTTTGAAGCCTCAGTCTGTAATCTGTACAATAAGGGCACTTACAAAATCTAGTCTGTTTATAGTTCCTTTCCTTTGTATTAAGATACTTTTTTAATAGAAC
AACTTTTTGGTAAGATAATACATACTTACATAATACTAGATGTTGGCTAGTATTTGATGTTATTTGCTATTGGATTATCCTCAGAATTGAATTCTGTGGTATTTGACTTGTTGACTATAGTTATTTGT
AATAATAGTACTCCTTTTATAATTTTATTCCACTTGAGTGATAATAACCATTAGTCCGGTTCATAGGGGAAGTACTTTAAACTTCAAAGAATATGTATTTCAATACCCTATATGTAGCTGACCATCAT
AATACATAGTCAGGTAATCTCCTTAACATTCTATATTTAAAAAAAAATTCTATATTTAAGGTTATAATTTATAAACCAAAAATTGTAATGAGGTTAATTTTTAAAACTATGTAGATTACTATATTTTA
GAAATCATAACTTATATATAATGTGTAGCTTTTTTAAATGTGTGCTTTTGTCATTTTTAAATTCCAGAATGATAGAGTACTATTTAATATTATACATGCCCACTTACATATATGTATTTTATTAAAAT
TTATAAGCAAGAAACTGTATATCTGGAGTGATCTTAGACAAGCAAGAAAGGAATGATGGTGATGTAAATAAAAATATTGCTTATACCCATGAGAATTTTTTTTTAAGTGTGAAAAAGACAGTGGGAAC
AGCAGAAATGTAGAAAATAATGATTTAAAATTGACAGTTAATATAATTGAATATGTTACTGATTATAGTATTGAGCAAGTTCCTATCAGTTCTTATCACACTTTTCCTTGCCTTTTTTATAAAAAAAT
ACTACTACTTAATCTCAAAGGAGTGTTTTGAGAATTCAATGAAGTAACATGTTTTTGGTTCTGGAAAATAGGAGGTGCTCAATAAACATTAGTTGACTGCACAGCAGATAGTATACTAATTGTTTTGT
AAATTCATGGTGATTATTTTTGGCCACACTTTATTTTTTTCAAGCTAATACAATTCATTGGTATTATATAATATGTATCTTAAATATGAAAAGTTAATTTATTGGTATCTTTATTATGGGAGAAAAAA
ACCATAGATTTTTGCATAAATTAGGTACAGATAATTGGTAGAATTAATGTATTTAAGTATTCCCATGCTCCATTTTACAATATTTATTTGAAATAATTATTGTAGATGAAAATAACTTTAATAAGTCA
TTATAAAATAATGTTTCAACTCTGTTTTTACCTGTGCGTATTGTATTTATTTTCTCTTTATTTAAAGTTGTAGTCTACTCAGGAATAATTTAAACTGGTTGTATTTCTTTAAACTTAATAAATTATAA
ATATTTAAGATA

hide sequence

RefSeq Acc Id:

XM_022427581 ⟹ XP_022283289

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1	14	48,873,299 - 48,879,681 (-)	NCBI
Dog10K_Boxer_Tasha	14	48,317,131 - 48,323,415 (-)	NCBI

Sequence:

show sequence

CTTCCTTCCGTTTTTTTCCCCCCGAAGAAACGGAGGCCCTTCAGGAAGTAGGCCACGCTGGAAG
CGTCGTGACCTCGCGCAGGCCTCCCCGTGACGCCCTCCCGACCGTCCCGGGAGCAGGTTTCCTCTACATGACAAAGAAAGACTTGAAAAATGGTTAAAGAATATGAAACGAGATTCATGGGTACCCAG
TAAATACCAGTTCCTGTGTAGTGACCATTTTACTCCTGACTCTCTTGACATCAGATGGGGTATTCGATATTTGAAACAAACTGCAATTCCAACAATATTTTCTTTGCCTGAAGACGATCAGGAAAAAG
ACCCTTCCAAAAAAAAATCTCAGAAGAAAAAATTAGATGATGAGAAAGAAGTGTGCCTAAAAGCCAAGTCACAAGAATCATTTGCTTCAAATGAGTTAAAGAAAAATACAGTTAATACAAATATTCTC
CTTGAACACACAGAATTATGTAATTCATCTACTTTGGTGAAGCCACCAGCTCCCAAACCAGAATGTATACAAAATAACGTATTAACTCTTAATCTGCTTAAACAAGATATTGGAATACCAGTATCTAC
CTTGGAAACTTCAGTTACCCAAGACATAGATATAGGTGGTTTTCACACATCTTTTGAGAATCTAAATTCTACAACTATTACCTTGACAACTTCAAACTCAGAAGATGTTCAGCCATCTTTGGAAACCC
AAGAAGTGTTTGAAATAACTGCGAATCATCTTGCTAACCCAAACTTTACAAATAATTCCATGGAAATTAAGTCCGCACAGGAAAGTCCATTTTTACTCAGCACAATTACTCAAACAGTCGAAGAGTTA
AATACAAATAAAGAATCTGTTATTGCCATTTTTGTACCCACAGAAAATTCCAAACCAATTAATTCATTTGTATCTGCTGAAAAAGAAACTGTGGAAATGGAAGATCTAGACATTGAAGACTCCTTATA
TAAGGATGTAGACTATGAGACAGAAGTTTTACAAATTGAACATTCTTATTGCAGACAAGATATAAATAAGGAACATCTTTGGCAGAAAGTTTCTAAACTACATTCAAAGATAACTCTTCTCGAGCTAC
AAGAACAACAAACTCTTGGAAGATTGAAGTCTTTGGAAGCTCTTATAAGGCAGCTAAAACAAGAAAACTGGCTATCCGAAGAAAATGTCAAGATTATAGAAAATCATTTCACAACATATGAAGTTACT
ATGATATAGAGTGTAAAGAGTTTAACACTATGACTTTTATATAAGCTTTTTGCAGCCAAACTAAATTATATGTAACTTTTTCCGGTATAAAGTTCTCATCTTAAGCTAAGAAAATGTTCTAATGTTAA
AAACTGCATCCCGTTCTTGTAGTGTTCATTGTTAAGAAAAACAAGAGAGTTGTTGGACTGTAGAGAAGAAGTTTCACCACTTGGTAATCTTCTAAATTAAAGTTAAAATAGAGTGAATAAGTAATATG
ATTCATAAAATGGGAGAACATGGAGATGGTGAAAGGAGCCCAGAAGAGAAATCAGGCTTGGATATCAGTGCCAGTTCTACCTTTGGCATGTGATTTGGGCGAATTACTTTGAAGCCTCAGTCTGTAAT
CTGTACAATAAGGGCACTTACAAAATCTAGTCTGTTTATAGTTCCTTTCCTTTGTATTAAGATACTTTTTTAATAGAACAACTTTTTGGTAAGATAATACATACTTACATAATACTAGATGTTGGCTA
GTATTTGATGTTATTTGCTATTGGATTATCCTCAGAATTGAATTCTGTGGTATTTGACTTGTTGACTATAGTTATTTGTAATAATAGTACTCCTTTTATAATTTTATTCCACTTGAGTGATAATAACC
ATTAGTCCGGTTCATAGGGGAAGTACTTTAAACTTCAAAGAATATGTATTTCAATACCCTATATGTAGCTGACCATCATAATACATAGTCAGGTAATCTCCTTAACATTCTATATTTAAAAAAAAATT
CTATATTTAAGGTTATAATTTATAAACCAAAAATTGTAATGAGGTTAATTTTTAAAACTATGTAGATTACTATATTTTAGAAATCATAACTTATATATAATGTGTAGCTTTTTTAAATGTGTGCTTTT
GTCATTTTTAAATTCCAGAATGATAGAGTACTATTTAATATTATACATGCCCACTTACATATATGTATTTTATTAAAATTTATAAGCAAGAAACTGTATATCTGGAGTGATCTTAGACAAGCAAGAAA
GGAATGATGGTGATGTAAATAAAAATATTGCTTATACCCATGAGAATTTTTTTTTAAGTGTGAAAAAGACAGTGGGAACAGCAGAAATGTAGAAAATAATGATTTAAAATTGACAGTTAATATAATTG
AATATGTTACTGATTATAGTATTGAGCAAGTTCCTATCAGTTCTTATCACACTTTTCCTTGCCTTTTTTATAAAAAAATACTACTACTTAATCTCAAAGGAGTGTTTTGAGAATTCAATGAAGTAACA
TGTTTTTGGTTCTGGAAAATAGGAGGTGCTCAATAAACATTAGTTGACTGCACAGCAGATAGTATACTAATTGTTTTGTAAATTCATGGTGATTATTTTTGGCCACACTTTATTTTTTTCAAGCTAAT
ACAATTCATTGGTATTATATAATATGTATCTTAAATATGAAAAGTTAATTTATTGGTATCTTTATTATGGGAGAAAAAAACCATAGATTTTTGCATAAATTAGGTACAGATAATTGGTAGAATTAATG
TATTTAAGTATTCCCATGCTCCATTTTACAATATTTATTTGAAATAATTATTGTAGATGAAAATAACTTTAATAAGTCATTATAAAATAATGTTTCAACTCTGTTTTTACCTGTGCGTATTGTATTTA
TTTTCTCTTTATTTAAAGTTGTAGTCTACTCAGGAATAATTTAAACTGGTTGTATTTCTTTAAACTTAATAAATTATAAATATTTAAGATA

hide sequence

RefSeq Acc Id:

XM_022427582 ⟹ XP_022283290

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1	14	48,873,299 - 48,876,562 (-)	NCBI
Dog10K_Boxer_Tasha	14	48,317,131 - 48,320,368 (-)	NCBI

Sequence:

show sequence

TAGTGACCATTTTACTCCTGACTCTCTTGACATCAGATGGGGTATTCGATATTTGAAACAAACTGCAATTCCAACAATATTTTCTTTGCCTGAAGACGATCAGGTATTGGAGGCAGCACATAGGGGAG
AGGGGGACAATGCTGAGCAGGATGGAAAAAGACCCTTCCAAAAAAAAATCTCAGAAGAAAAAATTAGATGATGAGAAAGAAGTGTGCCTAAAAGCCAAGTCACAAGAATCATTTGCTTCAAATGAGTT
AAAGAAAAATACAGTTAATACAAATATTCTCCTTGAACACACAGAATTATGTAATTCATCTACTTTGGTGAAGCCACCAGCTCCCAAACCAGAATGTATACAAAATAACGTATTAACTCTTAATCTGC
TTAAACAAGATATTGGAATACCAGTATCTACCTTGGAAACTTCAGTTACCCAAGACATAGATATAGGTGGTTTTCACACATCTTTTGAGAATCTAAATTCTACAACTATTACCTTGACAACTTCAAAC
TCAGAAGATGTTCAGCCATCTTTGGAAACCCAAGAAGTGTTTGAAATAACTGCGAATCATCTTGCTAACCCAAACTTTACAAATAATTCCATGGAAATTAAGTCCGCACAGGAAAGTCCATTTTTACT
CAGCACAATTACTCAAACAGTCGAAGAGTTAAATACAAATAAAGAATCTGTTATTGCCATTTTTGTACCCACAGAAAATTCCAAACCAATTAATTCATTTGTATCTGCTGAAAAAGAAACTGTGGAAA
TGGAAGATCTAGACATTGAAGACTCCTTATATAAGGATGTAGACTATGAGACAGAAGTTTTACAAATTGAACATTCTTATTGCAGACAAGATATAAATAAGGAACATCTTTGGCAGAAAGTTTCTAAA
CTACATTCAAAGATAACTCTTCTCGAGCTACAAGAACAACAAACTCTTGGAAGATTGAAGTCTTTGGAAGCTCTTATAAGGCAGCTAAAACAAGAAAACTGGCTATCCGAAGAAAATGTCAAGATTAT
AGAAAATCATTTCACAACATATGAAGTTACTATGATATAGAGTGTAAAGAGTTTAACACTATGACTTTTATATAAGCTTTTTGCAGCCAAACTAAATTATATGTAACTTTTTCCGGTATAAAGTTCTC
ATCTTAAGCTAAGAAAATGTTCTAATGTTAAAAACTGCATCCCGTTCTTGTAGTGTTCATTGTTAAGAAAAACAAGAGAGTTGTTGGACTGTAGAGAAGAAGTTTCACCACTTGGTAATCTTCTAAAT
TAAAGTTAAAATAGAGTGAATAAGTAATATGATTCATAAAATGGGAGAACATGGAGATGGTGAAAGGAGCCCAGAAGAGAAATCAGGCTTGGATATCAGTGCCAGTTCTACCTTTGGCATGTGATTTG
GGCGAATTACTTTGAAGCCTCAGTCTGTAATCTGTACAATAAGGGCACTTACAAAATCTAGTCTGTTTATAGTTCCTTTCCTTTGTATTAAGATACTTTTTTAATAGAACAACTTTTTGGTAAGATAA
TACATACTTACATAATACTAGATGTTGGCTAGTATTTGATGTTATTTGCTATTGGATTATCCTCAGAATTGAATTCTGTGGTATTTGACTTGTTGACTATAGTTATTTGTAATAATAGTACTCCTTTT
ATAATTTTATTCCACTTGAGTGATAATAACCATTAGTCCGGTTCATAGGGGAAGTACTTTAAACTTCAAAGAATATGTATTTCAATACCCTATATGTAGCTGACCATCATAATACATAGTCAGGTAAT
CTCCTTAACATTCTATATTTAAAAAAAAATTCTATATTTAAGGTTATAATTTATAAACCAAAAATTGTAATGAGGTTAATTTTTAAAACTATGTAGATTACTATATTTTAGAAATCATAACTTATATA
TAATGTGTAGCTTTTTTAAATGTGTGCTTTTGTCATTTTTAAATTCCAGAATGATAGAGTACTATTTAATATTATACATGCCCACTTACATATATGTATTTTATTAAAATTTATAAGCAAGAAACTGT
ATATCTGGAGTGATCTTAGACAAGCAAGAAAGGAATGATGGTGATGTAAATAAAAATATTGCTTATACCCATGAGAATTTTTTTTTAAGTGTGAAAAAGACAGTGGGAACAGCAGAAATGTAGAAAAT
AATGATTTAAAATTGACAGTTAATATAATTGAATATGTTACTGATTATAGTATTGAGCAAGTTCCTATCAGTTCTTATCACACTTTTCCTTGCCTTTTTTATAAAAAAATACTACTACTTAATCTCAA
AGGAGTGTTTTGAGAATTCAATGAAGTAACATGTTTTTGGTTCTGGAAAATAGGAGGTGCTCAATAAACATTAGTTGACTGCACAGCAGATAGTATACTAATTGTTTTGTAAATTCATGGTGATTATT
TTTGGCCACACTTTATTTTTTTCAAGCTAATACAATTCATTGGTATTATATAATATGTATCTTAAATATGAAAAGTTAATTTATTGGTATCTTTATTATGGGAGAAAAAAACCATAGATTTTTGCATA
AATTAGGTACAGATAATTGGTAGAATTAATGTATTTAAGTATTCCCATGCTCCATTTTACAATATTTATTTGAAATAATTATTGTAGATGAAAATAACTTTAATAAGTCATTATAAAATAATGTTTCA
ACTCTGTTTTTACCTGTGCGTATTGTATTTATTTTCTCTTTATTTAAAGTTGTAGTCTACTCAGGAATAATTTAAACTGGTTGTATTTCTTTAAACTTAATAAATTATAAATATTTAAGATA

hide sequence

RefSeq Acc Id:

XM_022427583 ⟹ XP_022283291

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1	14	48,831,121 - 48,880,293 (-)	NCBI
Dog10K_Boxer_Tasha	14	48,275,029 - 48,324,131 (-)	NCBI

Sequence:

show sequence

GTGGCGCAGGCGCAGTGGCTCGGCGACGCGCCGGGGGTGGTAGCCCGCTCCGCCTTGGCGGACGGGGTCACGCCAGCGCCCCTCGCCGGCCCGGCCCCTCCGGGCCGCCGCGGAGGGAGCGATGCCTC
GCTACTGCGCGGCGATTTGCTGTAAGAACCGTCGGGGACGGAACAGTAAGGACCGGAAGCTGAGTTTTTACCCGTTTCCTCTACATGACAAAGAAAGACTTGAAAAATGGTTAAAGAATATGAAACGA
GATTCATGGGTACCCAGTAAATACCAGTTCCTGTGTAGTGACCATTTTACTCCTGACTCTCTTGACATCAGATGGGGTATTCGATATTTGAAACAAACTGCAATTCCAACAATATTTTCTTTGCCTGA
AGACGATCAGAATCTATGTCATTCTGAAGAAATTGACTCCATGTCTCAACTCCAAAGATGGGACTCTAACCTGAGGCTAAGCACGAGAAGAGCATACTGGGCTAGCCCCTGGTCCCAAGAAGAGGATG
GAAGACACATGGAGTGGAACTAAACCATCCAATAGATC

hide sequence

RefSeq Acc Id:

XM_038445056 ⟹ XP_038300984

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
Dog10K_Boxer_Tasha	14	48,317,131 - 48,323,608 (-)	NCBI

RefSeq Acc Id:

XM_038445112 ⟹ XP_038301040

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
Dog10K_Boxer_Tasha	14	48,219,639 - 48,324,130 (-)	NCBI

RefSeq Acc Id:

XM_038495074 ⟹ XP_038351002

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,919,832 - 48,926,837 (-)	NCBI

RefSeq Acc Id:

XM_038495075 ⟹ XP_038351003

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,919,832 - 48,926,804 (-)	NCBI

RefSeq Acc Id:

XM_038495076 ⟹ XP_038351004

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,919,832 - 48,926,259 (-)	NCBI

RefSeq Acc Id:

XM_038495077 ⟹ XP_038351005

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,919,832 - 48,926,324 (-)	NCBI

RefSeq Acc Id:

XM_038495078 ⟹ XP_038351006

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,919,832 - 48,926,383 (-)	NCBI

RefSeq Acc Id:

XM_038495079 ⟹ XP_038351007

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,919,832 - 48,926,114 (-)	NCBI

RefSeq Acc Id:

XM_038495080 ⟹ XP_038351008

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,919,832 - 48,923,067 (-)	NCBI

RefSeq Acc Id:

XM_038495081 ⟹ XP_038351009

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,874,589 - 48,926,846 (-)	NCBI

RefSeq Acc Id:

XM_038495082 ⟹ XP_038351010

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,841,162 - 48,926,846 (-)	NCBI

RefSeq Acc Id:

XM_038495083 ⟹ XP_038351011

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,846,046 - 48,926,845 (-)	NCBI

RefSeq Acc Id:

XM_038495084 ⟹ XP_038351012

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,819,192 - 48,926,845 (-)	NCBI

RefSeq Acc Id:

XM_038621288 ⟹ XP_038477216

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,603,709 - 48,610,699 (-)	NCBI

RefSeq Acc Id:

XM_038621289 ⟹ XP_038477217

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,603,709 - 48,610,666 (-)	NCBI

RefSeq Acc Id:

XM_038621290 ⟹ XP_038477218

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,603,709 - 48,610,137 (-)	NCBI

RefSeq Acc Id:

XM_038621291 ⟹ XP_038477219

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,603,709 - 48,610,192 (-)	NCBI

RefSeq Acc Id:

XM_038621292 ⟹ XP_038477220

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,603,709 - 48,610,251 (-)	NCBI

RefSeq Acc Id:

XM_038621293 ⟹ XP_038477221

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,603,709 - 48,609,993 (-)	NCBI

RefSeq Acc Id:

XM_038621294 ⟹ XP_038477222

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,603,709 - 48,606,946 (-)	NCBI

RefSeq Acc Id:

XM_038621295 ⟹ XP_038477223

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,558,561 - 48,610,708 (-)	NCBI

RefSeq Acc Id:

XM_038621296 ⟹ XP_038477224

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,525,862 - 48,610,708 (-)	NCBI

RefSeq Acc Id:

XM_038621297 ⟹ XP_038477225

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,530,153 - 48,610,707 (-)	NCBI

RefSeq Acc Id:

XM_038621298 ⟹ XP_038477226

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,502,734 - 48,610,707 (-)	NCBI

RefSeq Acc Id:

XM_038686973 ⟹ XP_038542901

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,822,740 - 48,829,742 (-)	NCBI

RefSeq Acc Id:

XM_038686974 ⟹ XP_038542902

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,822,740 - 48,829,709 (-)	NCBI

RefSeq Acc Id:

XM_038686975 ⟹ XP_038542903

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,822,740 - 48,829,253 (-)	NCBI

RefSeq Acc Id:

XM_038686976 ⟹ XP_038542904

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,822,740 - 48,829,226 (-)	NCBI

RefSeq Acc Id:

XM_038686977 ⟹ XP_038542905

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,822,740 - 48,829,280 (-)	NCBI

RefSeq Acc Id:

XM_038686978 ⟹ XP_038542906

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,822,740 - 48,829,033 (-)	NCBI

RefSeq Acc Id:

XM_038686979 ⟹ XP_038542907

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,822,740 - 48,825,977 (-)	NCBI

RefSeq Acc Id:

XM_038686980 ⟹ XP_038542908

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,780,539 - 48,829,751 (-)	NCBI

RefSeq Acc Id:

XM_038686981 ⟹ XP_038542909

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,740,652 - 48,829,751 (-)	NCBI

RefSeq Acc Id:

XM_038686982 ⟹ XP_038542910

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,745,669 - 48,829,750 (-)	NCBI

RefSeq Acc Id:

XM_038686983 ⟹ XP_038542911

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,717,539 - 48,829,750 (-)	NCBI

RefSeq Acc Id:

XM_539521 ⟹ XP_539521

Type:

CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1	14	48,873,299 - 48,880,286 (-)	NCBI
Dog10K_Boxer_Tasha	14	48,317,131 - 48,324,122 (-)	NCBI

Sequence:

show sequence

AGGCGCAGTGGCTCGGCGACGCGCCGGGGGTGGTAGCCCGCTCCGCCTTGGCGGACGGGGTCAC
GCCAGCGCCCCTCGCCGGCCCGGCCCCTCCGGGCCGCCGCGGAGGGAGCGATGCCTCGCTACTGCGCGGCGATTTGCTGTAAGAACCGTCGGGGACGGAACAGTAAGGACCGGAAGCTGAGTTTTTAC
CCGTTTCCTCTACATGACAAAGAAAGACTTGAAAAATGGTTAAAGAATATGAAACGAGATTCATGGGTACCCAGTAAATACCAGTTCCTGTGTAGTGACCATTTTACTCCTGACTCTCTTGACATCAG
ATGGGGTATTCGATATTTGAAACAAACTGCAATTCCAACAATATTTTCTTTGCCTGAAGACGATCAGGAAAAAGACCCTTCCAAAAAAAAATCTCAGAAGAAAAAATTAGATGATGAGAAAGAAGTGT
GCCTAAAAGCCAAGTCACAAGAATCATTTGCTTCAAATGAGTTAAAGAAAAATACAGTTAATACAAATATTCTCCTTGAACACACAGAATTATGTAATTCATCTACTTTGGTGAAGCCACCAGCTCCC
AAACCAGAATGTATACAAAATAACGTATTAACTCTTAATCTGCTTAAACAAGATATTGGAATACCAGTATCTACCTTGGAAACTTCAGTTACCCAAGACATAGATATAGGTGGTTTTCACACATCTTT
TGAGAATCTAAATTCTACAACTATTACCTTGACAACTTCAAACTCAGAAGATGTTCAGCCATCTTTGGAAACCCAAGAAGTGTTTGAAATAACTGCGAATCATCTTGCTAACCCAAACTTTACAAATA
ATTCCATGGAAATTAAGTCCGCACAGGAAAGTCCATTTTTACTCAGCACAATTACTCAAACAGTCGAAGAGTTAAATACAAATAAAGAATCTGTTATTGCCATTTTTGTACCCACAGAAAATTCCAAA
CCAATTAATTCATTTGTATCTGCTGAAAAAGAAACTGTGGAAATGGAAGATCTAGACATTGAAGACTCCTTATATAAGGATGTAGACTATGAGACAGAAGTTTTACAAATTGAACATTCTTATTGCAG
ACAAGATATAAATAAGGAACATCTTTGGCAGAAAGTTTCTAAACTACATTCAAAGATAACTCTTCTCGAGCTACAAGAACAACAAACTCTTGGAAGATTGAAGTCTTTGGAAGCTCTTATAAGGCAGC
TAAAACAAGAAAACTGGCTATCCGAAGAAAATGTCAAGATTATAGAAAATCATTTCACAACATATGAAGTTACTATGATATAGAGTGTAAAGAGTTTAACACTATGACTTTTATATAAGCTTTTTGCA
GCCAAACTAAATTATATGTAACTTTTTCCGGTATAAAGTTCTCATCTTAAGCTAAGAAAATGTTCTAATGTTAAAAACTGCATCCCGTTCTTGTAGTGTTCATTGTTAAGAAAAACAAGAGAGTTGTT
GGACTGTAGAGAAGAAGTTTCACCACTTGGTAATCTTCTAAATTAAAGTTAAAATAGAGTGAATAAGTAATATGATTCATAAAATGGGAGAACATGGAGATGGTGAAAGGAGCCCAGAAGAGAAATCA
GGCTTGGATATCAGTGCCAGTTCTACCTTTGGCATGTGATTTGGGCGAATTACTTTGAAGCCTCAGTCTGTAATCTGTACAATAAGGGCACTTACAAAATCTAGTCTGTTTATAGTTCCTTTCCTTTG
TATTAAGATACTTTTTTAATAGAACAACTTTTTGGTAAGATAATACATACTTACATAATACTAGATGTTGGCTAGTATTTGATGTTATTTGCTATTGGATTATCCTCAGAATTGAATTCTGTGGTATT
TGACTTGTTGACTATAGTTATTTGTAATAATAGTACTCCTTTTATAATTTTATTCCACTTGAGTGATAATAACCATTAGTCCGGTTCATAGGGGAAGTACTTTAAACTTCAAAGAATATGTATTTCAA
TACCCTATATGTAGCTGACCATCATAATACATAGTCAGGTAATCTCCTTAACATTCTATATTTAAAAAAAAATTCTATATTTAAGGTTATAATTTATAAACCAAAAATTGTAATGAGGTTAATTTTTA
AAACTATGTAGATTACTATATTTTAGAAATCATAACTTATATATAATGTGTAGCTTTTTTAAATGTGTGCTTTTGTCATTTTTAAATTCCAGAATGATAGAGTACTATTTAATATTATACATGCCCAC
TTACATATATGTATTTTATTAAAATTTATAAGCAAGAAACTGTATATCTGGAGTGATCTTAGACAAGCAAGAAAGGAATGATGGTGATGTAAATAAAAATATTGCTTATACCCATGAGAATTTTTTTT
TAAGTGTGAAAAAGACAGTGGGAACAGCAGAAATGTAGAAAATAATGATTTAAAATTGACAGTTAATATAATTGAATATGTTACTGATTATAGTATTGAGCAAGTTCCTATCAGTTCTTATCACACTT
TTCCTTGCCTTTTTTATAAAAAAATACTACTACTTAATCTCAAAGGAGTGTTTTGAGAATTCAATGAAGTAACATGTTTTTGGTTCTGGAAAATAGGAGGTGCTCAATAAACATTAGTTGACTGCACA
GCAGATAGTATACTAATTGTTTTGTAAATTCATGGTGATTATTTTTGGCCACACTTTATTTTTTTCAAGCTAATACAATTCATTGGTATTATATAATATGTATCTTAAATATGAAAAGTTAATTTATT
GGTATCTTTATTATGGGAGAAAAAAACCATAGATTTTTGCATAAATTAGGTACAGATAATTGGTAGAATTAATGTATTTAAGTATTCCCATGCTCCATTTTACAATATTTATTTGAAATAATTATTGT
AGATGAAAATAACTTTAATAAGTCATTATAAAATAATGTTTCAACTCTGTTTTTACCTGTGCGTATTGTATTTATTTTCTCTTTATTTAAAGTTGTAGTCTACTCAGGAATAATTTAAACTGGTTGTA
TTTCTTTAAACTTAATAAATTATAAATATTTAAGATA

hide sequence

RefSeq Acc Id:

XR_002633103

Type:

NON-CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1	14	48,738,882 - 48,880,295 (-)	NCBI
Dog10K_Boxer_Tasha	14	48,183,037 - 48,324,132 (-)	NCBI

Sequence:

show sequence

TTGTGGCGCAGGCGCAGTGGCTCGGCGACGCGCCGGGGGTGGTAGCCCGCTCCGCCTTGGCGGA
CGGGGTCACGCCAGCGCCCCTCGCCGGCCCGGCCCCTCCGGGCCGCCGCGGAGGGAGCGATGCCTCGCTACTGCGCGGCGATTTGCTGTAAGAACCGTCGGGGACGGAACAGTAAGGACCGGAAGCTG
AGTTTTTACCCGTTTCCTCTACATGACAAAGAAAGACTTGAAAAATGGTTAAAGAATATGAAACGAGATTCATGGGTACCCAGTAAATACCAGTTCCTGTGTAGTGACCATTTTACTCCTGACTCTCT
TGACATCAGATGGGGTATTCGATATTTGAAACAAACTGCAATTCCAACAATATTTTCTTTGCCTGAAGACGATCAGAATCTATGTCATTCTGAAGAAATTGACTCCATGTCTCAACTCCAAAGATGGG
ACTCTAACCTGAGGCTAAGATCTCAGACCACTGCAGACAGCAGAGCTGTTCCACTTGTCACACCAAGGCTCTTTTCAGCTTGTGATGCTAGGAGCTCAGAGGCAACATCTTCAATAAGCCTCCAAGGC
CACTGTGGATGAGCTCCTGAGAGGACAGGCCTGGAAGGAATGTGTGTGCATCACTTCTGCTGATGTTCATGGACTCGATTTCAGTCACAGAGTTACTCTAAAGGAATGCCAGCTGCCATGTCAAGATG
ACACTCAATTCAACAGCCCTATAGAGAGGTTGAAGTGATATGGATTTAGAACTCCTCTCAACAGCTAACAACAACTGAGGCAGACTTCCTTTTACCAGCCATGTGAGAGGGCCATCTTGAAATTCATC
TTCCAGCCCCAGCCCAGCCTTCAGATGATTGTAGCCCTAGCCAACATTATGACTGCAACCTCATAAGAGATCCAAACTAGAAACACCTAGCTAAGCTACTTAGATTTTG

hide sequence

RefSeq Acc Id:

XR_005335964

Type:

NON-CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UMICH_Zoey_3.1	14	48,786,690 - 48,926,847 (-)	NCBI

RefSeq Acc Id:

XR_005404023

Type:

NON-CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
UNSW_CanFamBas_1.0	14	48,466,945 - 48,610,709 (-)	NCBI

RefSeq Acc Id:

XR_005437474

Type:

NON-CODING

Position:

Dog Assembly	Chr	Position (strand)	Source
ROS_Cfam_1.0	14	48,681,884 - 48,829,752 (-)	NCBI


Protein RefSeqs	XP_005628788	(Get FASTA)	NCBI Sequence Viewer
	XP_005628789	(Get FASTA)	NCBI Sequence Viewer
	XP_005628790	(Get FASTA)	NCBI Sequence Viewer
	XP_022283287	(Get FASTA)	NCBI Sequence Viewer
	XP_022283288	(Get FASTA)	NCBI Sequence Viewer
	XP_022283289	(Get FASTA)	NCBI Sequence Viewer
	XP_022283290	(Get FASTA)	NCBI Sequence Viewer
	XP_022283291	(Get FASTA)	NCBI Sequence Viewer
	XP_038300984	(Get FASTA)	NCBI Sequence Viewer
	XP_038301040	(Get FASTA)	NCBI Sequence Viewer
	XP_038351002	(Get FASTA)	NCBI Sequence Viewer
	XP_038351003	(Get FASTA)	NCBI Sequence Viewer
	XP_038351004	(Get FASTA)	NCBI Sequence Viewer
	XP_038351005	(Get FASTA)	NCBI Sequence Viewer
	XP_038351006	(Get FASTA)	NCBI Sequence Viewer
	XP_038351007	(Get FASTA)	NCBI Sequence Viewer
	XP_038351008	(Get FASTA)	NCBI Sequence Viewer
	XP_038351009	(Get FASTA)	NCBI Sequence Viewer
	XP_038351010	(Get FASTA)	NCBI Sequence Viewer
	XP_038351011	(Get FASTA)	NCBI Sequence Viewer
	XP_038351012	(Get FASTA)	NCBI Sequence Viewer
	XP_038477216	(Get FASTA)	NCBI Sequence Viewer
	XP_038477217	(Get FASTA)	NCBI Sequence Viewer
	XP_038477218	(Get FASTA)	NCBI Sequence Viewer
	XP_038477219	(Get FASTA)	NCBI Sequence Viewer
	XP_038477220	(Get FASTA)	NCBI Sequence Viewer
	XP_038477221	(Get FASTA)	NCBI Sequence Viewer
	XP_038477222	(Get FASTA)	NCBI Sequence Viewer
	XP_038477223	(Get FASTA)	NCBI Sequence Viewer
	XP_038477224	(Get FASTA)	NCBI Sequence Viewer
	XP_038477225	(Get FASTA)	NCBI Sequence Viewer
	XP_038477226	(Get FASTA)	NCBI Sequence Viewer
	XP_038542901	(Get FASTA)	NCBI Sequence Viewer
	XP_038542902	(Get FASTA)	NCBI Sequence Viewer
	XP_038542903	(Get FASTA)	NCBI Sequence Viewer
	XP_038542904	(Get FASTA)	NCBI Sequence Viewer
	XP_038542905	(Get FASTA)	NCBI Sequence Viewer
	XP_038542906	(Get FASTA)	NCBI Sequence Viewer
	XP_038542907	(Get FASTA)	NCBI Sequence Viewer
	XP_038542908	(Get FASTA)	NCBI Sequence Viewer
	XP_038542909	(Get FASTA)	NCBI Sequence Viewer
	XP_038542910	(Get FASTA)	NCBI Sequence Viewer
	XP_038542911	(Get FASTA)	NCBI Sequence Viewer
	XP_539521	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSCAFP00000032124.3
	ENSCAFP00030007994.1
	ENSCAFP00040022926.1
	ENSCAFP00845041503
	ENSCAFP00845041503.1

RefSeq Acc Id:	XP_005628789 ⟸ XM_005628732
- Peptide Label:	isoform X5
- Sequence:	show sequence MPRYCAAICCKNRRGRNSKDRKLSFYPFPLHDKERLEKWLKNMKRDSWVPSKYQFLCSDHFTPDSLDIRWGIRYLKQTAIPTIFSLPEDDQNLCHSEEIDSMSQLQRWDSNLRLRLPYVQLAHSGLHN CSLASHSA hide sequence

RefSeq Acc Id:	XP_005628790 ⟸ XM_005628733
- Peptide Label:	isoform X6
- Sequence:	show sequence MPRYCAAICCKNRRGRNSKDRKLSFYPFPLHDKERLEKWLKNMKRDSWVPSKYQFLCSDHFTPD SLDIRWGIRYLKQTAIPTIFSLPEDDQNLCHSEEIDSMSQLQRWDSNLRLRDSSRTPGNASVCSDL hide sequence

RefSeq Acc Id:	XP_539521 ⟸ XM_539521
- Peptide Label:	isoform X1
- UniProtKB:	A0A8C0JZQ6 (UniProtKB/TrEMBL), A0A8I3Q8Q1 (UniProtKB/TrEMBL), A0A8P0SPS3 (UniProtKB/TrEMBL), A0A8C0QX27 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPRYCAAICCKNRRGRNSKDRKLSFYPFPLHDKERLEKWLKNMKRDSWVPSKYQFLCSDHFTPDSLDIRWGIRYLKQTAIPTIFSLPEDDQEKDPSKKKSQKKKLDDEKEVCLKAKSQESFASNELKK NTVNTNILLEHTELCNSSTLVKPPAPKPECIQNNVLTLNLLKQDIGIPVSTLETSVTQDIDIGGFHTSFENLNSTTITLTTSNSEDVQPSLETQEVFEITANHLANPNFTNNSMEIKSAQESPFLLST ITQTVEELNTNKESVIAIFVPTENSKPINSFVSAEKETVEMEDLDIEDSLYKDVDYETEVLQIEHSYCRQDINKEHLWQKVSKLHSKITLLELQEQQTLGRLKSLEALIRQLKQENWLSEENVKIIEN HFTTYEVTMI hide sequence

RefSeq Acc Id:	XP_005628788 ⟸ XM_005628731
- Peptide Label:	isoform X2
- UniProtKB:	A0A8C0MDI1 (UniProtKB/TrEMBL), A0A8C0QX27 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKRDSWVPSKYQFLCSDHFTPDSLDIRWGIRYLKQTAIPTIFSLPEDDQEKDPSKKKSQKKKLD DEKEVCLKAKSQESFASNELKKNTVNTNILLEHTELCNSSTLVKPPAPKPECIQNNVLTLNLLKQDIGIPVSTLETSVTQDIDIGGFHTSFENLNSTTITLTTSNSEDVQPSLETQEVFEITANHLAN PNFTNNSMEIKSAQESPFLLSTITQTVEELNTNKESVIAIFVPTENSKPINSFVSAEKETVEMEDLDIEDSLYKDVDYETEVLQIEHSYCRQDINKEHLWQKVSKLHSKITLLELQEQQTLGRLKSLE ALIRQLKQENWLSEENVKIIENHFTTYEVTMI hide sequence

RefSeq Acc Id:	XP_022283291 ⟸ XM_022427583
- Peptide Label:	isoform X4
- Sequence:	show sequence MPRYCAAICCKNRRGRNSKDRKLSFYPFPLHDKERLEKWLKNMKRDSWVPSKYQFLCSDHFTPD SLDIRWGIRYLKQTAIPTIFSLPEDDQNLCHSEEIDSMSQLQRWDSNLRLSTRRAYWASPWSQEEDGRHMEWN hide sequence

Protein Domains

THAP-type

RGD ID:

13685811

Promoter ID:

EPDNEW_C3878

Type:

initiation region

Name:

THAP5_1

Description:

THAP domain containing 5

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Dog Assembly	Chr	Position (strand)	Source
CanFam3.1	14	48,880,255 - 48,880,315	EPDNEW

Database	Acc Id	Source(s)
Ensembl Genes	ENSCAFG00000003290	Ensembl, UniProtKB/TrEMBL
	ENSCAFG00030004961	UniProtKB/TrEMBL
	ENSCAFG00040014311	UniProtKB/TrEMBL
	ENSCAFG00845029849	Ensembl, ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript	ENSCAFT00000005270.4	UniProtKB/TrEMBL
	ENSCAFT00030009111.1	UniProtKB/TrEMBL
	ENSCAFT00040026381.1	UniProtKB/TrEMBL
	ENSCAFT00845052860	ENTREZGENE
	ENSCAFT00845052860.1	UniProtKB/TrEMBL
InterPro	THAP_domain_protein	UniProtKB/TrEMBL
	THAP_Znf	UniProtKB/TrEMBL
KEGG Report	cfa:482404	UniProtKB/TrEMBL
NCBI Gene	THAP5	ENTREZGENE
PANTHER	AGAP005574-PA	UniProtKB/TrEMBL
	THAP DOMAIN-CONTAINING PROTEIN 5	UniProtKB/TrEMBL
Pfam	THAP	UniProtKB/TrEMBL
PROSITE	ZF_THAP	UniProtKB/TrEMBL
SMART	DM3	UniProtKB/TrEMBL
	THAP	UniProtKB/TrEMBL
Superfamily-SCOP	Glucocorticoid receptor-like (DNA-binding domain)	UniProtKB/TrEMBL
UniProt	A0A8C0JZQ6	ENTREZGENE
	A0A8C0MDI1	ENTREZGENE, UniProtKB/TrEMBL
	A0A8C0QX27	ENTREZGENE
	A0A8I3Q8Q1	ENTREZGENE, UniProtKB/TrEMBL
	A0A8P0SPS3	ENTREZGENE, UniProtKB/TrEMBL
VGNC ID	VGNC:47329	ENTREZGENE

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


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


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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Imported Disease Annotations - ClinVar