WDR41 (WD repeat domain 41) - Rat Genome Database

Name: WDR41
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

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Gene: WDR41 (WD repeat domain 41) Homo sapiens

Analyze

Symbol:

WDR41

Name:

WD repeat domain 41

RGD ID:

1314938

HGNC Page

HGNC:25601

Description:

Contributes to guanyl-nucleotide exchange factor activity. Involved in positive regulation of GTPase activity and regulation of autophagy. Located in cytoplasm. Part of guanyl-nucleotide exchange factor complex. Colocalizes with Atg1/ULK1 kinase complex.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FLJ10904; MSTP048; WD repeat-containing protein 41

RGD Orthologs

Mouse

Rat

Chinchilla

Bonobo

Dog

Squirrel

Pig

Green Monkey

Naked Mole-Rat

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Wdr41 (WD repeat domain 41)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Wdr41 (WD repeat domain 41)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Wdr41 (WD repeat domain 41)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	WDR41 (WD repeat domain 41)	NCBI	Ortholog
Canis lupus familiaris (dog):	WDR41 (WD repeat domain 41)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Wdr41 (WD repeat domain 41)	NCBI	Ortholog
Sus scrofa (pig):	WDR41 (WD repeat domain 41)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	WDR41 (WD repeat domain 41)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Wdr41 (WD repeat domain 41)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Wdr41 (WD repeat domain 41)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Wdr41 (WD repeat domain 41)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	wdr41 (WD repeat domain 41)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	5	77,430,933 - 77,620,577 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p13 Ensembl	5	77,425,970 - 77,620,611 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	5	76,726,758 - 76,788,141 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	5	76,763,825 - 76,824,088 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	5	76,763,825 - 76,824,088	NCBI
Celera	5	72,622,605 - 72,682,854 (-)	NCBI		Celera
Cytogenetic Map	5	q13.3-q14.1	NCBI
HuRef	5	71,934,855 - 71,995,126 (-)	NCBI		HuRef
CHM1_1	5	76,161,811 - 76,222,105 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	5	77,913,542 - 77,974,918 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

Neurodevelopmental Disorders (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

2,2',4,4',5,5'-hexachlorobiphenyl (ISO)

2,2',5,5'-tetrachlorobiphenyl (ISO)

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

aristolochic acid A (EXP)

arsenous acid (EXP)

benzo[a]pyrene (EXP)

bisphenol A (ISO)

cisplatin (EXP)

cyclosporin A (EXP)

diarsenic trioxide (EXP)

dibutyl phthalate (ISO)

dicrotophos (EXP)

doxorubicin (EXP)

epoxiconazole (ISO)

erastin (EXP)

folic acid (ISO)

fonofos (EXP)

furan (ISO)

methylmercury chloride (EXP)

paracetamol (ISO)

parathion (EXP)

PCB138 (ISO)

potassium chromate (EXP)

potassium dichromate (ISO)

quercetin (EXP)

sodium arsenite (EXP)

terbufos (EXP)

testosterone (EXP)

triptonide (ISO)

valproic acid (EXP,ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

autophagy (IEA)

negative regulation of exocytosis (NAS)

negative regulation of immune response (NAS)

positive regulation of GTPase activity (IMP)

regulation of autophagy (IEA,IMP,NAS)

Cellular Component

Atg1/ULK1 kinase complex (IDA)

cytoplasm (IDA,IEA,NAS)

guanyl-nucleotide exchange factor complex (IDA,IPI)

lysosomal membrane (HDA)

Molecular Function

guanyl-nucleotide exchange factor activity (IDA)

protein binding (IPI)

References

References - curated

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
2.	Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.	Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.

Additional References at PubMed

PMID:14702039	PMID:15342556	PMID:15489334	PMID:16341674	PMID:17897319	PMID:19913121	PMID:20379614	PMID:20628086	PMID:21502949	PMID:22678362	PMID:26186194	PMID:26638075
PMID:26871637	PMID:27103069	PMID:27193190	PMID:27617292	PMID:28195531	PMID:28514442	PMID:29395067	PMID:29568061	PMID:29950492	PMID:29995611	PMID:30669939	PMID:31056421
PMID:31091453	PMID:31871319	PMID:32303654	PMID:32394588	PMID:32848248	PMID:32877691	PMID:33597295	PMID:33957083	PMID:33961781	PMID:34079125	PMID:34226595	PMID:34432599
PMID:34672954	PMID:34709727	PMID:35241646	PMID:35256949	PMID:35509820	PMID:35844135

Genomics

Comparative Map Data

WDR41
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	5	77,430,933 - 77,620,577 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p13 Ensembl	5	77,425,970 - 77,620,611 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	5	76,726,758 - 76,788,141 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	5	76,763,825 - 76,824,088 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	5	76,763,825 - 76,824,088	NCBI
Celera	5	72,622,605 - 72,682,854 (-)	NCBI		Celera
Cytogenetic Map	5	q13.3-q14.1	NCBI
HuRef	5	71,934,855 - 71,995,126 (-)	NCBI		HuRef
CHM1_1	5	76,161,811 - 76,222,105 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	5	77,913,542 - 77,974,918 (-)	NCBI		T2T-CHM13v2.0

Wdr41
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	13	95,112,226 - 95,161,800 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	13	95,112,852 - 95,159,822 (+)	Ensembl		GRCm39 Ensembl
GRCm38	13	94,976,329 - 95,023,316 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	13	94,976,344 - 95,023,314 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	13	95,746,303 - 95,793,269 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	13	96,077,043 - 96,115,230 (+)	NCBI		MGSCv36	mm8
Celera	13	98,594,444 - 98,641,510 (+)	NCBI		Celera
Cytogenetic Map	13	C3- D1	NCBI

Wdr41
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
mRatBN7.2	2	26,222,797 - 26,273,840 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	2	26,224,495 - 26,273,836 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	2	33,260,068 - 33,309,248 (+)	NCBI	Rnor_SHR
UTH_Rnor_SHRSP_BbbUtx_1.0	2	31,360,307 - 31,409,491 (+)	NCBI	Rnor_SHRSP
UTH_Rnor_WKY_Bbb_1.0	2	26,178,985 - 26,227,815 (+)	NCBI	Rnor_WKY
Rnor_6.0	2	24,668,108 - 24,717,280 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	2	24,668,116 - 24,717,267 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	2	43,827,385 - 43,876,540 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	2	25,299,797 - 25,349,926 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	2	25,264,929 - 25,270,296 (+)	NCBI
Celera	2	22,294,024 - 22,343,220 (+)	NCBI		Celera
Cytogenetic Map	2	q12	NCBI

Wdr41
(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_004955425	23,470,278 - 23,514,638 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955425	23,366,130 - 23,510,897 (+)	NCBI	ChiLan1.0	ChiLan1.0

WDR41
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
PanPan1.1	5	38,338,267 - 38,398,503 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	5	38,214,273 - 38,398,503 (+)	Ensembl	panpan1.1		panPan2
Mhudiblu_PPA_v0	5	37,809,767 - 37,870,039 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3

WDR41
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	3	29,082,481 - 29,286,632 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	3	29,073,073 - 29,286,681 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	3	30,322,335 - 30,526,500 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	3	29,003,543 - 29,208,015 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	3	28,994,217 - 29,208,226 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	3	28,940,203 - 29,142,315 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	3	28,918,819 - 29,123,031 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	3	29,249,596 - 29,454,033 (+)	NCBI		UU_Cfam_GSD_1.0

Wdr41
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024407213	185,240,144 - 185,405,769 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936549	5,453,913 - 5,494,533 (-)	Ensembl	SpeTri2.0
SpeTri2.0	NW_004936549	5,453,824 - 5,494,809 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

WDR41
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	2	86,319,014 - 86,380,588 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	2	86,322,933 - 86,380,619 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	87,933,152 - 88,028,663 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

WDR41
(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	4	71,672,474 - 71,719,507 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	4	71,673,369 - 71,719,491 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666049	20,510,784 - 20,557,831 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Wdr41
(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_004624869	1,938,925 - 1,981,045 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624869	1,936,960 - 1,980,932 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in WDR41
4 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 5q13.3-22.1(chr5:74163186-110809453)x3	copy number gain	See cases [RCV000051839]	Chr5:74163186..110809453 [GRCh38] Chr5:73459011..110145153 [GRCh37] Chr5:73494767..110173052 [NCBI36] Chr5:5q13.3-22.1	pathogenic
GRCh38/hg38 5q13.3-14.1(chr5:77018109-78190068)x1	copy number loss	See cases [RCV000053473]	Chr5:77018109..78190068 [GRCh38] Chr5:76313934..77485892 [GRCh37] Chr5:76349690..77521648 [NCBI36] Chr5:5q13.3-14.1	pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)	copy number gain	See cases [RCV000510723]	Chr5:113577..180719789 [GRCh37] Chr5:5p15.33-q35.3	pathogenic
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1	copy number loss	See cases [RCV000511978]	Chr5:17628741..176575720 [GRCh37] Chr5:5p15.1-q35.2	pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3	copy number gain	See cases [RCV000512039]	Chr5:113577..180719789 [GRCh37] Chr5:5p15.33-q35.3	pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3	copy number gain	not provided [RCV000744317]	Chr5:13648..180905029 [GRCh37] Chr5:5p15.33-q35.3	pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3	copy number gain	not provided [RCV000744323]	Chr5:25328..180693344 [GRCh37] Chr5:5p15.33-q35.3	pathogenic
Single allele	deletion	Neurodevelopmental disorder [RCV000787436]	Chr5:14685137..149511942 [GRCh37] Chr5:5p15.2-q32	uncertain significance
GRCh37/hg19 5q13.3(chr5:76683620-76810358)x3	copy number gain	not provided [RCV000850000]	Chr5:76683620..76810358 [GRCh37] Chr5:5q13.3	uncertain significance
GRCh37/hg19 5q13.2-15(chr5:72790061-97478870)x3	copy number gain	not provided [RCV001005683]	Chr5:72790061..97478870 [GRCh37] Chr5:5q13.2-15	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	4000
Count of miRNA genes:	1125
Interacting mature miRNAs:	1376
Transcripts:	ENST00000296679, ENST00000414719, ENST00000502528, ENST00000503035, ENST00000504895, ENST00000505129, ENST00000506307, ENST00000506474, ENST00000507029, ENST00000507239, ENST00000507452, ENST00000507654, ENST00000508154, ENST00000509701, ENST00000509858, ENST00000509892, ENST00000509971, ENST00000511036, ENST00000511630, ENST00000511791, ENST00000512033, ENST00000512168, ENST00000513417, ENST00000513917, ENST00000514451, ENST00000514559, ENST00000514878, ENST00000515253, ENST00000515321
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

SHGC-57669

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	76,747,537 - 76,747,632	UniSTS	GRCh37
Build 36	5	76,783,293 - 76,783,388	RGD	NCBI36
Celera	5	72,642,081 - 72,642,176	RGD
Cytogenetic Map	5	q13.3	UniSTS
HuRef	5	71,954,327 - 71,954,422	UniSTS
TNG Radiation Hybrid Map	5	35854.0	UniSTS

SHGC-36700

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	76,728,888 - 76,728,973	UniSTS	GRCh37
Build 36	5	76,764,644 - 76,764,729	RGD	NCBI36
Celera	5	72,623,424 - 72,623,509	RGD
Cytogenetic Map	5	q13.3	UniSTS
HuRef	5	71,935,674 - 71,935,759	UniSTS
Stanford-G3 RH Map	5	2775.0	UniSTS
NCBI RH Map	5	363.9	UniSTS
GeneMap99-G3 RH Map	5	2770.0	UniSTS

RH80473

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	76,728,094 - 76,728,193	UniSTS	GRCh37
Build 36	5	76,763,850 - 76,763,949	RGD	NCBI36
Celera	5	72,622,630 - 72,622,729	RGD
Cytogenetic Map	5	q13.3	UniSTS
HuRef	5	71,934,880 - 71,934,979	UniSTS
GeneMap99-GB4 RH Map	5	376.16	UniSTS

SHGC-133093

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	76,728,089 - 76,728,367	UniSTS	GRCh37
Build 36	5	76,763,845 - 76,764,123	RGD	NCBI36
Celera	5	72,622,625 - 72,622,903	RGD
Cytogenetic Map	5	q13.3	UniSTS
HuRef	5	71,934,875 - 71,935,153	UniSTS
TNG Radiation Hybrid Map	5	35846.0	UniSTS

SHGC-36223

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	76,762,673 - 76,762,795	UniSTS	GRCh37
Build 36	5	76,798,429 - 76,798,551	RGD	NCBI36
Celera	5	72,657,218 - 72,657,340	RGD
Cytogenetic Map	5	q13.3	UniSTS
HuRef	5	71,969,470 - 71,969,592	UniSTS
Stanford-G3 RH Map	5	2786.0	UniSTS
NCBI RH Map	5	363.9	UniSTS
GeneMap99-G3 RH Map	5	2781.0	UniSTS

RH44392

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	76,728,203 - 76,728,338	UniSTS	GRCh37
Build 36	5	76,763,959 - 76,764,094	RGD	NCBI36
Celera	5	72,622,739 - 72,622,874	RGD
Cytogenetic Map	5	q13.3	UniSTS
HuRef	5	71,934,989 - 71,935,124	UniSTS
GeneMap99-GB4 RH Map	5	368.59	UniSTS
NCBI RH Map	5	363.9	UniSTS

RH44320

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	76,728,161 - 76,728,398	UniSTS	GRCh37
Build 36	5	76,763,917 - 76,764,154	RGD	NCBI36
Celera	5	72,622,697 - 72,622,934	RGD
Cytogenetic Map	5	q13.3	UniSTS
HuRef	5	71,934,947 - 71,935,184	UniSTS
GeneMap99-GB4 RH Map	5	368.59	UniSTS
NCBI RH Map	5	363.9	UniSTS

D5S2319

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	76,728,924 - 76,729,074	UniSTS	GRCh37
Build 36	5	76,764,680 - 76,764,830	RGD	NCBI36
Celera	5	72,623,460 - 72,623,610	RGD
Cytogenetic Map	5	q13.3	UniSTS
HuRef	5	71,935,710 - 71,935,860	UniSTS
GeneMap99-GB4 RH Map	5	368.49	UniSTS
Whitehead-RH Map	5	269.9	UniSTS
Whitehead-YAC Contig Map	5		UniSTS
NCBI RH Map	5	363.9	UniSTS

SHGC-64313

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	76,728,236 - 76,728,359	UniSTS	GRCh37
Build 36	5	76,763,992 - 76,764,115	RGD	NCBI36
Celera	5	72,622,772 - 72,622,895	RGD
Cytogenetic Map	5	q13.3	UniSTS
HuRef	5	71,935,022 - 71,935,145	UniSTS

WI-20907

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	76,728,196 - 76,728,473	UniSTS	GRCh37
Build 36	5	76,763,952 - 76,764,229	RGD	NCBI36
Celera	5	72,622,732 - 72,623,009	RGD
Cytogenetic Map	5	q13.3	UniSTS
HuRef	5	71,934,982 - 71,935,259	UniSTS
GeneMap99-GB4 RH Map	5	368.39	UniSTS
Whitehead-RH Map	5	268.9	UniSTS
NCBI RH Map	5	363.9	UniSTS

Expression

RNA-SEQ Expression

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

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

801

1354

872

125

895

3090

333

1927

237

1194

1463

910

1782

Low

1638

1628

854

499

1050

400

1266

1861

1807

182

266

150

102

294

1006

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_018268	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005248551	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005248552	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011543505	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011543507	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017009606	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047417349	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047417350	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047417351	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001742140	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001742141	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC010234	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC108173	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF115511	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK001766	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK021855	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK023977	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK293316	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK295249	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK296423	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300058	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK304329	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL834138	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC001807	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC040241	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BG113002	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM818066	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP276774	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ000743	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CD656920	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471084	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068273	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC403958	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU178690	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU178691	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Reference Sequences

RefSeq Acc Id:

ENST00000296679 ⟹ ENSP00000296679

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,430,933 - 77,492,316 (-)	Ensembl

RefSeq Acc Id:

ENST00000502528

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,432,244 - 77,452,873 (-)	Ensembl

RefSeq Acc Id:

ENST00000503035 ⟹ ENSP00000421166

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,451,291 - 77,492,477 (-)	Ensembl

RefSeq Acc Id:

ENST00000504895 ⟹ ENSP00000426141

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,453,866 - 77,491,285 (-)	Ensembl

RefSeq Acc Id:

ENST00000505129 ⟹ ENSP00000425249

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,440,817 - 77,492,496 (-)	Ensembl

RefSeq Acc Id:

ENST00000506307 ⟹ ENSP00000424327

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,440,931 - 77,492,223 (-)	Ensembl

RefSeq Acc Id:

ENST00000506474 ⟹ ENSP00000425813

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,453,889 - 77,492,220 (-)	Ensembl

RefSeq Acc Id:

ENST00000507029 ⟹ ENSP00000424287

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,432,893 - 77,492,316 (-)	Ensembl

RefSeq Acc Id:

ENST00000507239

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,458,859 - 77,492,222 (-)	Ensembl

RefSeq Acc Id:

ENST00000507452

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,449,765 - 77,492,215 (-)	Ensembl

RefSeq Acc Id:

ENST00000507654 ⟹ ENSP00000427291

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,436,379 - 77,492,203 (-)	Ensembl

RefSeq Acc Id:

ENST00000508154

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,426,654 - 77,433,159 (-)	Ensembl

RefSeq Acc Id:

ENST00000509701 ⟹ ENSP00000427652

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,437,407 - 77,492,220 (-)	Ensembl

RefSeq Acc Id:

ENST00000509858

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,463,093 - 77,620,576 (-)	Ensembl

RefSeq Acc Id:

ENST00000509892 ⟹ ENSP00000427219

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,449,804 - 77,492,215 (-)	Ensembl

RefSeq Acc Id:

ENST00000509971 ⟹ ENSP00000422922

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,453,879 - 77,620,611 (-)	Ensembl

RefSeq Acc Id:

ENST00000511036 ⟹ ENSP00000422510

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,451,324 - 77,492,487 (-)	Ensembl

RefSeq Acc Id:

ENST00000511630 ⟹ ENSP00000425563

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,436,360 - 77,451,353 (-)	Ensembl

RefSeq Acc Id:

ENST00000511791 ⟹ ENSP00000423540

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,438,258 - 77,492,287 (-)	Ensembl

RefSeq Acc Id:

ENST00000512033

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,426,652 - 77,436,279 (-)	Ensembl

RefSeq Acc Id:

ENST00000512168

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,463,124 - 77,492,507 (-)	Ensembl

RefSeq Acc Id:

ENST00000513417 ⟹ ENSP00000423462

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,449,831 - 77,492,220 (-)	Ensembl

RefSeq Acc Id:

ENST00000513917

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,463,106 - 77,499,636 (-)	Ensembl

RefSeq Acc Id:

ENST00000514451

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,463,106 - 77,492,003 (-)	Ensembl

RefSeq Acc Id:

ENST00000514559 ⟹ ENSP00000426937

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,451,291 - 77,492,222 (-)	Ensembl

RefSeq Acc Id:

ENST00000514878

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,425,970 - 77,432,955 (-)	Ensembl

RefSeq Acc Id:

ENST00000515253 ⟹ ENSP00000426499

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,432,813 - 77,492,199 (-)	Ensembl

RefSeq Acc Id:

ENST00000515321

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	5	77,449,815 - 77,492,221 (-)	Ensembl

RefSeq Acc Id:

NM_018268 ⟹ NP_060738

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	77,430,933 - 77,492,316 (-)	NCBI
GRCh37	5	76,727,622 - 76,788,332 (-)	NCBI
Build 36	5	76,763,825 - 76,824,088 (-)	NCBI Archive
Celera	5	72,622,605 - 72,682,854 (-)	RGD
HuRef	5	71,934,855 - 71,995,126 (-)	RGD
CHM1_1	5	76,160,501 - 76,222,138 (-)	NCBI
T2T-CHM13v2.0	5	77,913,542 - 77,974,918 (-)	NCBI

Sequence:

show sequence

AGTTGCGCTGCAGCCGGGGAGGAAGGAGGAGGCCGAGCCTGGGGCGGAGTTTGGGCTGACTGGG
GCTGGACCGGGCAAGACGCCGCCGCTGCCCGGATGTTGCGATGGCTGATCGGGGGAGGCCGAGA
ACCGCAGGGACTGGCCGAGAAATCTCCTTTACAGACAATAGGTGAAGAACAAACCCAGAATCCC
TACACTGAACTGCTAGTACTGAAGGCTCATCATGATATTGTACGATTTCTGGTACAGTTAGATG
ACTACAGATTTGCATCTGCTGGTGATGATGGAATTGTAGTTGTGTGGAATGCCCAGACAGGGGA
AAAACTTTTAGAACTGAATGGACACACTCAAAAGATAACAGCTATTATTACATTTCCTTCCTTG
GAATCTTGTGAAGAGAAAAATCAACTCATCTTGACAGCCTCTGCTGATAGAACAGTTATTGTGT
GGGATGGTGATACTACCAGACAAGTTCAGAGAATATCATGCTTCCAGTCTACTGTAAAGTGTTT
AACTGTTCTTCAGAGACTAGATGTTTGGCTTTCTGGTGGGAATGACCTGTGTGTGTGGAACCGA
AAATTAGATCTCCTGTGTAAGACTAGCCACCTTTCTGATACAGGTATTAGTGCTTTGGTTGAAA
TACCTAAGAACTGTGTTGTGGCAGCAGTTGGCAAAGAACTGATAATTTTCAGGTTGGTAGCACC
CACAGAAGGATCACTAGAATGGGATATTCTTGAAGTTAAGCGCCTCCTTGATCACCAGGATAAT
ATTCTCTCATTGATTAATGTCAATGATTTGAGTTTTGTCACCGGCTCCCACGTCGGAGAGCTGA
TCATCTGGGATGCCCTGGACTGGACCATGCAGGCCTATGAACGCAACTTCTGGGACCCATCTCC
ACAACTGGACACCCAACAAGAAATAAAACTCTGTCAAAAATCAAATGACATTTCTATTCATCAT
TTCACATGTGATGAAGAGAATGTATTTGCTGCAGTTGGAAGGGGTTTATACGTGTATAGCCTTC
AAATGAAGCGTGTGATTGCCTGCCAGAAAACTGCACATGACTCCAATGTCCTGCACGTTGCCAG
ACTTCCAAACAGGCAGTTAATCTCATGCTCAGAAGATGGCAGTGTACGCATTTGGGAGTTAAGA
GAAAAACAGCAGCTTGCAGCTGAGCCTGTACCAACAGGTTTTTTTAACATGTGGGGATTTGGAA
GAGTCAGCAAACAAGCCAGCCAACCTGTTAAAAAGCAGCAAGAAAATGCTACTTCATGTTCACT
GGAGCTTATTGGAGATTTGATTGGACACTCATCATCTGTGGAGATGTTTCTATACTTTGAAGAT
CATGGACTAGTGACGTGCTCCGCTGATCATCTCATTATTTTGTGGAAAAATGGAGAGCGAGAAT
CTGGATTGCGCAGTTTAAGATTATTTCAAAAATTAGAGGAGAATGGTGACTTATACCTTGCTGT
CTAGTTTAAGGAATTAAAAATACACATGCATGAACCTTGAACATCAAATATCGGGTACTACTCT
GAAAACCATTAATATATTGATCACTTAAATTGGTAATTTTTTTTGTCAGTCCATAAAATTCTAC
ATGTTTAAATTTTTTGTGGACCTACCAACCAGGAACATGTTGCTTCTCAGGTCCTAGTATATCC
TCCAAAGAATATACCACAAGTTTTTCCATTTGACTTTGAGCTGCTGTTGAAGTGGTGAGTGCTG
TGTTTTGAGCTTATTTTGAACCTAGATCCTTGTGAAAGGTACAAATAGAGGTAATAGTTAAGTT
ATGGCATTTATTAGAAGTTTTATTATTTGGCTTCCTTTAGAATTATTGTGAAGTTTAAAAATAG
CCTTTCTCCTGCAAATTTTCCTAGTCTTTAGTAACTGTTAGTGTTCTATATAGCACAAACTTGA
ATCTCTCAGCCAAAAAAGGGAACATATATACTGTTTAAGTATGGCAAGTTTTCTTTGGTACCAA
TTTGTTTAGATAATTTTAAAAATGTTTTTTAGTTCTAGCTACTAAAACCTGTATGAACTCAAAT
GGATAGGCATCTTGTGAGGGTGTGTTTTTCCCAGTGTGAATTGGCTTGAAGAGCCATGGGCTAA
ATGGGTACTAGAACAACAACTGCCCCTCATGTACGCCAAGGATGAGCTCTAGATCATTTGAGAG
GCACAGTGTTTCCGGAGTCAGGGACTGCAGCTGAGCGCAACTGCCCCATCTGACCACTGACTCA
AATACGAACTGCTTGAGACAGACTTCTTTTATGTAGTTCTTTGCAGTGTCCATTGAGACACTAT
AACCAGCCTTGTAACAATATGTTTTCTCCTTTTGGTGCTAAAAAATGAAAATATTAGAAAGTAG
TCTACACATTAAAGATTGAAATTCTTAAACTACTGATGAAGAAAGGGCAACGTGACAGATGTTA
GCAGACTGACCCTTCTTACAGAAAACCTACAGATTTATTTGTTCATTATACAAATATACTACAA
ATATACCCTAAAGGGAATCTCCATAAGTTCTTTTACTAGTTTTAGCTTTGACAGTTGCTTCCAC
AACTACCTACAAAGACTGGAAGAGTTAAGGTCATCTGAGTAGACCAGTGGCATAATGTTACAAA
TGAGGAAACTGAGGCCCAGTGCAGTAAGGCCTTGCAATTAAATCTGTAGTGCCCAGTATCACCA
AGCAGCTCTAAAAACAGGAACTGAAGACTGAATGAGAAAAGGCTTATATGACTACTTTAAATCC
AAACAACATTGAGTCATGAAAAGTTCTATGGAGAAATATTAAAACTTAAGCTACCTCAATTACA
GAAGACTTTCTCCCATTATTCACGTGCTTTTTCCTTTAGAAATTCTGCATTGGCCCATACATTT
GTAAAGTTGTTTTCTGAAGTTGTATGACACAAGGGAGCCATAGACTTAACTGTTTTACTTCCTA
GCCTGTTCTAGGCTAGTATTTTGTGATAGTAATCTATTCAAATGGAGTGGTAGAAATCACATGA
ATTTTGGAAGCAAATGGTACCGTAAGTACCACAGCAAATTCCTTCTGGTCATTATACAGGCGTA
CCTCAGAGATACTACAGGTTAGGTTTCAGACCACATCAAAAAAGCAACTATTGCAAATAGAGTG
AGTCACATCTAGTTTTTGGTTTCCCAGTGCCTATAAAACTTGTGTTTATACTACAGTCTTAAAT
TTCTAAAAAATGTACATACCTTAAGAATACTTTATTGCTAAAAAATGCTAACAATCATCTGAGC
CTTCAGCGAGTCATAATCTTTTTGCTGGTGGAGGGTCTTGATACTGCTGGCTGTTGACTAAGGT
GGTTACTGAAGGTTGGGGTGGCTGTGGCAGTTCCTTAAAATAAGATAGCGATGAAGTTTTCCAA
ATCAATTGACTTCCTTTCACAAATGAGATCTCTGTAACATGTAATACTATTTAATAGCATTTTA
CCCACAGTAGAACTTCTTTCAAAATTTAGAGTCTGTCATCTCAAATCCTGATGCTCCTTTATGA
ACTAAGTTTATAGAATATTCTAAATCCTTTGTTGTCATTTCAACTATGTTTACAGCATCTTCAC
TGTGGAAATGACTGTCTCCAGAAACCACTTTCTATACACATTCTTAAGCAACTTCTCATCTATT
AAAGTTTGATCATGAGATTACAGCAATTCA

hide sequence

RefSeq Acc Id:

XM_005248551 ⟹ XP_005248608

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	77,430,933 - 77,492,316 (-)	NCBI

Sequence:

show sequence

ACTCGGAGCAGCGCGCGCCCCGCAATCGCCGCAGCCGCCCCCGCCGTCGGCCGCCGCACCCCAA
GCGACTGCCCAAACTAAGCCTCCGTGGCTGGGTACGGGAGCGCTTTGGGGACAAAAATTCTCCC
TCAACTGTGGTCTGCATTCCTTCGGCCCGTGGGCTGATCTGGGGCGGGAAGTATTAGCGTCTCA
GTTGCGCTGCAGCCGGGGAGGAAGGAGGAGGCCGAGCCTGGGGCGGAGTTTGGGCTGACTGGGG
CTGGACCGGGCAAGACGCCGCCGCTGCCCGGATGTTGCGATGGCTGATCGGGGGAGGCCGAGAA
CCGCAGGGACTGGCCGAGAAATCTCCTTTACAGACAATAGGTGAAGAACAAACCCAGAATCCCT
ACACTGAACTGCTAGTACTGAAGGCTCATCATGATATTGTACGATTTCTGGTACAGTTAGATGA
CTACAGATTTGCATCTGCTGGTGATGATGGAATTGTAGTTGTGTGGAATGCCCAGACAGGGGAA
AAACTTTTAGAACTGAATGGACACACTCAAAAGATAACAGCTATTATTACATTTCCTTCCTTGG
AATCTTGTGAAGAGAAAAATCAACTCATCTTGACAGCCTCTGCTGATAGAACAGTTATTGTGTG
GGATGGTGATACTACCAGACAAGTTCAGAGAATATCATGCTTCCAGTCTACTGTAAAGTGTTTA
ACTGTTCTTCAGAGACTAGATGTTTGGCTTTCTGGTGGGAATGACCTGTGTGTGTGGAACCGAA
AATTAGATCTCCTGTGTAAGACTAGCCACCTTTCTGATACAGATTTGAGTTTTGTCACCGGCTC
CCACGTCGGAGAGCTGATCATCTGGGATGCCCTGGACTGGACCATGCAGGCCTATGAACGCAAC
TTCTGGGACCCATCTCCACAACTGGACACCCAACAAGAAATAAAACTCTGTCAAAAATCAAATG
ACATTTCTATTCATCATTTCACATGTGATGAAGAGAATGTATTTGCTGCAGTTGGAAGGGGTTT
ATACGTGTATAGCCTTCAAATGAAGCGTGTGATTGCCTGCCAGAAAACTGCACATGACTCCAAT
GTCCTGCACGTTGCCAGACTTCCAAACAGGCAGTTAATCTCATGCTCAGAAGATGGCAGTGTAC
GCATTTGGGAGTTAAGAGAAAAACAGCAGCTTGCAGCTGAGCCTGTACCAACAGGTTTTTTTAA
CATGTGGGGATTTGGAAGAGTCAGCAAACAAGCCAGCCAACCTGTTAAAAAGCAGCAAGAAAAT
GCTACTTCATGTTCACTGGAGCTTATTGGAGATTTGATTGGACACTCATCATCTGTGGAGATGT
TTCTATACTTTGAAGATCATGGACTAGTGACGTGCTCCGCTGATCATCTCATTATTTTGTGGAA
AAATGGAGAGCGAGAATCTGGATTGCGCAGTTTAAGATTATTTCAAAAATTAGAGGAGAATGGT
GACTTATACCTTGCTGTCTAGTTTAAGGAATTAAAAATACACATGCATGAACCTTGAACATCAA
ATATCGGGTACTACTCTGAAAACCATTAATATATTGATCACTTAAATTGGTAATTTTTTTTGTC
AGTCCATAAAATTCTACATGTTTAAATTTTTTGTGGACCTACCAACCAGGAACATGTTGCTTCT
CAGGTCCTAGTATATCCTCCAAAGAATATACCACAAGTTTTTCCATTTGACTTTGAGCTGCTGT
TGAAGTGGTGAGTGCTGTGTTTTGAGCTTATTTTGAACCTAGATCCTTGTGAAAGGTACAAATA
GAGGTAATAGTTAAGTTATGGCATTTATTAGAAGTTTTATTATTTGGCTTCCTTTAGAATTATT
GTGAAGTTTAAAAATAGCCTTTCTCCTGCAAATTTTCCTAGTCTTTAGTAACTGTTAGTGTTCT
ATATAGCACAAACTTGAATCTCTCAGCCAAAAAAGGGAACATATATACTGTTTAAGTATGGCAA
GTTTTCTTTGGTACCAATTTGTTTAGATAATTTTAAAAATGTTTTTTAGTTCTAGCTACTAAAA
CCTGTATGAACTCAAATGGATAGGCATCTTGTGAGGGTGTGTTTTTCCCAGTGTGAATTGGCTT
GAAGAGCCATGGGCTAAATGGGTACTAGAACAACAACTGCCCCTCATGTACGCCAAGGATGAGC
TCTAGATCATTTGAGAGGCACAGTGTTTCCGGAGTCAGGGACTGCAGCTGAGCGCAACTGCCCC
ATCTGACCACTGACTCAAATACGAACTGCTTGAGACAGACTTCTTTTATGTAGTTCTTTGCAGT
GTCCATTGAGACACTATAACCAGCCTTGTAACAATATGTTTTCTCCTTTTGGTGCTAAAAAATG
AAAATATTAGAAAGTAGTCTACACATTAAAGATTGAAATTCTTAAACTACTGATGAAGAAAGGG
CAACGTGACAGATGTTAGCAGACTGACCCTTCTTACAGAAAACCTACAGATTTATTTGTTCATT
ATACAAATATACTACAAATATACCCTAAAGGGAATCTCCATAAGTTCTTTTACTAGTTTTAGCT
TTGACAGTTGCTTCCACAACTACCTACAAAGACTGGAAGAGTTAAGGTCATCTGAGTAGACCAG
TGGCATAATGTTACAAATGAGGAAACTGAGGCCCAGTGCAGTAAGGCCTTGCAATTAAATCTGT
AGTGCCCAGTATCACCAAGCAGCTCTAAAAACAGGAACTGAAGACTGAATGAGAAAAGGCTTAT
ATGACTACTTTAAATCCAAACAACATTGAGTCATGAAAAGTTCTATGGAGAAATATTAAAACTT
AAGCTACCTCAATTACAGAAGACTTTCTCCCATTATTCACGTGCTTTTTCCTTTAGAAATTCTG
CATTGGCCCATACATTTGTAAAGTTGTTTTCTGAAGTTGTATGACACAAGGGAGCCATAGACTT
AACTGTTTTACTTCCTAGCCTGTTCTAGGCTAGTATTTTGTGATAGTAATCTATTCAAATGGAG
TGGTAGAAATCACATGAATTTTGGAAGCAAATGGTACCGTAAGTACCACAGCAAATTCCTTCTG
GTCATTATACAGGCGTACCTCAGAGATACTACAGGTTAGGTTTCAGACCACATCAAAAAAGCAA
CTATTGCAAATAGAGTGAGTCACATCTAGTTTTTGGTTTCCCAGTGCCTATAAAACTTGTGTTT
ATACTACAGTCTTAAATTTCTAAAAAATGTACATACCTTAAGAATACTTTATTGCTAAAAAATG
CTAACAATCATCTGAGCCTTCAGCGAGTCATAATCTTTTTGCTGGTGGAGGGTCTTGATACTGC
TGGCTGTTGACTAAGGTGGTTACTGAAGGTTGGGGTGGCTGTGGCAGTTCCTTAAAATAAGATA
GCGATGAAGTTTTCCAAATCAATTGACTTCCTTTCACAAATGAGATCTCTGTAACATGTAATAC
TATTTAATAGCATTTTACCCACAGTAGAACTTCTTTCAAAATTTAGAGTCTGTCATCTCAAATC
CTGATGCTCCTTTATGAACTAAGTTTATAGAATATTCTAAATCCTTTGTTGTCATTTCAACTAT
GTTTACAGCATCTTCACTGTGGAAATGACTGTCTCCAGAAACCACTTTCTATACACATTCTTAA
GCAACTTCTCATCTATTAAAGTTTGATCATGAGATTACAGCAATTCATTCACATCTTCAGGCTC
CACTTCTTCCAGACTCCTTTTAATGCTGGAATTTTGACCGCCTCCCATGAATCAGAATGTTCTT
AGTGGCATCTAGAATGCTAAATGCTTCCCAGAAGGTTTTCAATTGACTTTGCCCAGACTCTTCA
GAGGAATCACTAGTTAGGGCAGCTACAGCCTTATTAAATGTATTTCTTAAATAAATAAGACTTA
AAAGTCAAAGTGACTCCTTGACCCATGGACTGCAGCATAGATGTTGTGGTAGCTGGCACGAAGA
CAACATGAACCTCCTTGTACATCTCCATCAGAACTCTTAGGTGACCAGGTAACATTGTAATGGG
CAGTAATATTTGGAAAGAAATTTGAGCAGGTCTCAACCATAGGCTTAAATATTCAATAAACCAT
GCTATAAACAGA

hide sequence

RefSeq Acc Id:

XM_005248552 ⟹ XP_005248609

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	77,436,283 - 77,492,316 (-)	NCBI
GRCh37	5	76,727,622 - 76,788,332 (-)	NCBI

Sequence:

show sequence

ACTCGGAGCAGCGCGCGCCCCGCAATCGCCGCAGCCGCCCCCGCCGTCGGCCGCCGCACCCCAA
GCGACTGCCCAAACTAAGCCTCCGTGGCTGGGTACGGGAGCGCTTTGGGGACAAAAATTCTCCC
TCAACTGTGGTCTGCATTCCTTCGGCCCGTGGGCTGATCTGGGGCGGGAAGTATTAGCGTCTCA
GTTGCGCTGCAGCCGGGGAGGAAGGAGGAGGCCGAGCCTGGGGCGGAGTTTGGGCTGACTGGGG
CTGGACCGGGCAAGACGCCGCCGCTGCCCGGATGTTGCGATGGCTGATCGGGGGAGGCCGAGAA
CCGCAGGGACTGGCCGAGAAATCTCCTTTACAGACAATAGGTGAAGAACAAACCCAGAATCCCT
ACACTGAACTGCTAGTACTGAAGGCTCATCATGATATTGTACGATTTCTGGTACAGTTAGATGA
CTACAGATTTGCATCTGCTGGTGATGATGGAATTGTAGTTGTGTGGAATGCCCAGACAGGGGAA
AAACTTTTAGAACTGAATGGACACACTCAAAAGATAACAGCTATTATTACATTTCCTTCCTTGG
AATCTTGTGAAGAGAAAAATCAACTCATCTTGACAGCCTCTGCTGATAGAACAGTTATTGTGTG
GGATGGTGATACTACCAGACAAGTTCAGAGAATATCATGCTTCCAGTCTACTGTAAAGTGTTTA
ACTGTTCTTCAGAGACTAGATGTTTGGCTTTCTGGTGGGAATGACCTGTGTGTGTGGAACCGAA
AATTAGATCTCCTGTGTAAGACTAGCCACCTTTCTGATACAGGTATTAGTGCTTTGGTTGAAAT
ACCTAAGAACTGTGTTGTGGCAGCAGTTGGCAAAGAACTGATAATTTTCAGGTTGGTAGCACCC
ACAGAAGGATCACTAGAATGGGATATTCTTGAAGTTAAGCGCCTCCTTGATCACCAGGATAATA
TTCTCTCATTGATTAATGTCAATGATTTGAGTTTTGTCACCGGCTCCCACGTCGGAGAGCTGAT
CATCTGGGATGCCCTGGACTGGACCATGCAGGCCTATGAACGCAACTTCTGGGACCCATCTCCA
CAACTGGACACCCAACAAGAAATAAAACTCTGTCAAAAATCAAATGACATTTCTATTCATCATT
TCACATGTGATGAAGAGAATGTATTTGCTGCAGTTGGAAGGGGTTTATACGTGTATAGCCTTCA
AATGAAGCGTGTGATTGCCTGCCAGAAAACTGCACATGACTCCAATGTCCTGCACGTTGCCAGA
CTTCCAAACAGGCAGTTAATCTCATGCTCAGAAGATGGCAGTGTACGCATTTGGGAGTTAAGAG
AAAAACAGCAGCTTGCAGCTGAGCCTGTACCAACAGGTTTTTTTTAACATGTGGGGATTTGGAA
GAGTCAGCAAACAAGCCAGCCAACCTGTTAAAAAGCAGCAAGAAAATGCTACTTCATGTTCACT
GGAGCTTATTGGAGATTTGAT

hide sequence

RefSeq Acc Id:

XM_011543505 ⟹ XP_011541807

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	77,430,933 - 77,620,577 (-)	NCBI

Sequence:

show sequence

AGAATGAAAAGAATGGGCAGCCTAGTGGTTGCTCAGGTGAGCGCAGGTACACAGACCAGGAAGT
ATCTCTGCTCCTAACCTCTCTTTATGTATGCATGAAGCTAATTGTTCAAGTCCAGGGGAAACTG
GTGAGAAATCTCCTTTACAGACAATAGGTGAAGAACAAACCCAGAATCCCTACACTGAACTGCT
AGTACTGAAGGCTCATCATGATATTGTACGATTTCTGGTACAGTTAGATGACTACAGATTTGCA
TCTGCTGGTGATGATGGAATTGTAGTTGTGTGGAATGCCCAGACAGGGGAAAAACTTTTAGAAC
TGAATGGACACACTCAAAAGATAACAGCTATTATTACATTTCCTTCCTTGGAATCTTGTGAAGA
GAAAAATCAACTCATCTTGACAGCCTCTGCTGATAGAACAGTTATTGTGTGGGATGGTGATACT
ACCAGACAAGTTCAGAGAATATCATGCTTCCAGTCTACTGTAAAGTGTTTAACTGTTCTTCAGA
GACTAGATGTTTGGCTTTCTGGTGGGAATGACCTGTGTGTGTGGAACCGAAAATTAGATCTCCT
GTGTAAGACTAGCCACCTTTCTGATACAGGTATTAGTGCTTTGGTTGAAATACCTAAGAACTGT
GTTGTGGCAGCAGTTGGCAAAGAACTGATAATTTTCAGGTTGGTAGCACCCACAGAAGGATCAC
TAGAATGGGATATTCTTGAAGTTAAGCGCCTCCTTGATCACCAGGATAATATTCTCTCATTGAT
TAATGTCAATGATTTGAGTTTTGTCACCGGCTCCCACGTCGGAGAGCTGATCATCTGGGATGCC
CTGGACTGGACCATGCAGGCCTATGAACGCAACTTCTGGGACCCATCTCCACAACTGGACACCC
AACAAGAAATAAAACTCTGTCAAAAATCAAATGACATTTCTATTCATCATTTCACATGTGATGA
AGAGAATGTATTTGCTGCAGTTGGAAGGGGTTTATACGTGTATAGCCTTCAAATGAAGCGTGTG
ATTGCCTGCCAGAAAACTGCACATGACTCCAATGTCCTGCACGTTGCCAGACTTCCAAACAGGC
AGTTAATCTCATGCTCAGAAGATGGCAGTGTACGCATTTGGGAGTTAAGAGAAAAACAGCAGCT
TGCAGCTGAGCCTGTACCAACAGGTTTTTTTAACATGTGGGGATTTGGAAGAGTCAGCAAACAA
GCCAGCCAACCTGTTAAAAAGCAGCAAGAAAATGCTACTTCATGTTCACTGGAGCTTATTGGAG
ATTTGATTGGACACTCATCATCTGTGGAGATGTTTCTATACTTTGAAGATCATGGACTAGTGAC
GTGCTCCGCTGATCATCTCATTATTTTGTGGAAAAATGGAGAGCGAGAATCTGGATTGCGCAGT
TTAAGATTATTTCAAAAATTAGAGGAGAATGGTGACTTATACCTTGCTGTCTAGTTTAAGGAAT
TAAAAATACACATGCATGAACCTTGAACATCAAATATCGGGTACTACTCTGAAAACCATTAATA
TATTGATCACTTAAATTGGTAATTTTTTTTGTCAGTCCATAAAATTCTACATGTTTAAATTTTT
TGTGGACCTACCAACCAGGAACATGTTGCTTCTCAGGTCCTAGTATATCCTCCAAAGAATATAC
CACAAGTTTTTCCATTTGACTTTGAGCTGCTGTTGAAGTGGTGAGTGCTGTGTTTTGAGCTTAT
TTTGAACCTAGATCCTTGTGAAAGGTACAAATAGAGGTAATAGTTAAGTTATGGCATTTATTAG
AAGTTTTATTATTTGGCTTCCTTTAGAATTATTGTGAAGTTTAAAAATAGCCTTTCTCCTGCAA
ATTTTCCTAGTCTTTAGTAACTGTTAGTGTTCTATATAGCACAAACTTGAATCTCTCAGCCAAA
AAAGGGAACATATATACTGTTTAAGTATGGCAAGTTTTCTTTGGTACCAATTTGTTTAGATAAT
TTTAAAAATGTTTTTTAGTTCTAGCTACTAAAACCTGTATGAACTCAAATGGATAGGCATCTTG
TGAGGGTGTGTTTTTCCCAGTGTGAATTGGCTTGAAGAGCCATGGGCTAAATGGGTACTAGAAC
AACAACTGCCCCTCATGTACGCCAAGGATGAGCTCTAGATCATTTGAGAGGCACAGTGTTTCCG
GAGTCAGGGACTGCAGCTGAGCGCAACTGCCCCATCTGACCACTGACTCAAATACGAACTGCTT
GAGACAGACTTCTTTTATGTAGTTCTTTGCAGTGTCCATTGAGACACTATAACCAGCCTTGTAA
CAATATGTTTTCTCCTTTTGGTGCTAAAAAATGAAAATATTAGAAAGTAGTCTACACATTAAAG
ATTGAAATTCTTAAACTACTGATGAAGAAAGGGCAACGTGACAGATGTTAGCAGACTGACCCTT
CTTACAGAAAACCTACAGATTTATTTGTTCATTATACAAATATACTACAAATATACCCTAAAGG
GAATCTCCATAAGTTCTTTTACTAGTTTTAGCTTTGACAGTTGCTTCCACAACTACCTACAAAG
ACTGGAAGAGTTAAGGTCATCTGAGTAGACCAGTGGCATAATGTTACAAATGAGGAAACTGAGG
CCCAGTGCAGTAAGGCCTTGCAATTAAATCTGTAGTGCCCAGTATCACCAAGCAGCTCTAAAAA
CAGGAACTGAAGACTGAATGAGAAAAGGCTTATATGACTACTTTAAATCCAAACAACATTGAGT
CATGAAAAGTTCTATGGAGAAATATTAAAACTTAAGCTACCTCAATTACAGAAGACTTTCTCCC
ATTATTCACGTGCTTTTTCCTTTAGAAATTCTGCATTGGCCCATACATTTGTAAAGTTGTTTTC
TGAAGTTGTATGACACAAGGGAGCCATAGACTTAACTGTTTTACTTCCTAGCCTGTTCTAGGCT
AGTATTTTGTGATAGTAATCTATTCAAATGGAGTGGTAGAAATCACATGAATTTTGGAAGCAAA
TGGTACCGTAAGTACCACAGCAAATTCCTTCTGGTCATTATACAGGCGTACCTCAGAGATACTA
CAGGTTAGGTTTCAGACCACATCAAAAAAGCAACTATTGCAAATAGAGTGAGTCACATCTAGTT
TTTGGTTTCCCAGTGCCTATAAAACTTGTGTTTATACTACAGTCTTAAATTTCTAAAAAATGTA
CATACCTTAAGAATACTTTATTGCTAAAAAATGCTAACAATCATCTGAGCCTTCAGCGAGTCAT
AATCTTTTTGCTGGTGGAGGGTCTTGATACTGCTGGCTGTTGACTAAGGTGGTTACTGAAGGTT
GGGGTGGCTGTGGCAGTTCCTTAAAATAAGATAGCGATGAAGTTTTCCAAATCAATTGACTTCC
TTTCACAAATGAGATCTCTGTAACATGTAATACTATTTAATAGCATTTTACCCACAGTAGAACT
TCTTTCAAAATTTAGAGTCTGTCATCTCAAATCCTGATGCTCCTTTATGAACTAAGTTTATAGA
ATATTCTAAATCCTTTGTTGTCATTTCAACTATGTTTACAGCATCTTCACTGTGGAAATGACTG
TCTCCAGAAACCACTTTCTATACACATTCTTAAGCAACTTCTCATCTATTAAAGTTTGATCATG
AGATTACAGCAATTCATTCACATCTTCAGGCTCCACTTCTTCCAGACTCCTTTTAATGCTGGAA
TTTTGACCGCCTCCCATGAATCAGAATGTTCTTAGTGGCATCTAGAATGCTAAATGCTTCCCAG
AAGGTTTTCAATTGACTTTGCCCAGACTCTTCAGAGGAATCACTAGTTAGGGCAGCTACAGCCT
TATTAAATGTATTTCTTAAATAAATAAGACTTAAAAGTCAAAGTGACTCCTTGACCCATGGACT
GCAGCATAGATGTTGTGGTAGCTGGCACGAAGACAACATGAACCTCCTTGTACATCTCCATCAG
AACTCTTAGGTGACCAGGTAACATTGTAATGGGCAGTAATATTTGGAAAGAAATTTGAGCAGGT
CTCAACCATAGGCTTAAATATTCAATAAACCATGCTATAAACAGA

hide sequence

RefSeq Acc Id:

XM_011543507 ⟹ XP_011541809

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	77,436,283 - 77,492,316 (-)	NCBI

Sequence:

show sequence

ACTCGGAGCAGCGCGCGCCCCGCAATCGCCGCAGCCGCCCCCGCCGTCGGCCGCCGCACCCCAA
GCGACTGCCCAAACTAAGCCTCCGTGGCTGGGTACGGGAGCGCTTTGGGGACAAAAATTCTCCC
TCAACTGTGGTCTGCATTCCTTCGGCCCGTGGGCTGATCTGGGGCGGGAAGTATTAGCGTCTCA
GTTGCGCTGCAGCCGGGGAGGAAGGAGGAGGCCGAGCCTGGGGCGGAGTTTGGGCTGACTGGGG
CTGGACCGGGCAAGACGCCGCCGCTGCCCGGATGTTGCGATGGCTGATCGGGGGAGGCCGAGAA
CCGCAGGGACTGGCCGAGAAATCTCCTTTACAGACAATAGGTGAAGAACAAACCCAGAATCCCT
ACACTGAACTGCTAGTACTGAAGGCTCATCATGATATTGTACGATTTCTGGTACAGTTAGATGA
CTACAGATTTGCATCTGCTGGTGATGATGGAATTGTAGTTGTGTGGAATGCCCAGACAGGGGAA
AAACTTTTAGAACTGAATGGACACACTCAAAAGATAACAGCTATTATTACATTTCCTTCCTTGG
AATCTTGTGAAGAGAAAAATCAACTCATCTTGACAGCCTCTGCTGATAGAACAGTTATTGTGTG
GGATGGTGATACTACCAGACAAGTTCAGAGAATATCATGCTTCCAGTCTACTGTAAAGTGTTTA
ACTGTTCTTCAGAGACTAGATGTTTGGCTTTCTGGTGGGAATGACCTGTGTGTGTGGAACCGAA
AATTAGATCTCCTGTGTAAGACTAGCCACCTTTCTGATACAGGTATTAGTGCTTTGGTTGAAAT
ACCTAAGAACTGTGTTGTGGCAGCAGTTGGCAAAGAACTGATAATTTTCAGGTTGGTAGCACCC
ACAGAAGGATCACTAGAATGGGATATTCTTGAAGTTAAGCGCCTCCTTGATCACCAGGATAATA
TTCTCTCATTGATTAATGTCAATGATTTGAGTTTTGTCACCGGCTCCCACGTCGGAGAGCTGAT
CATCTGGGATGCCCTGGACTGGACCATGCAGGCCTATGAACGCAACTTCTGGGACCCATCTCCA
CAACTGGACACCCAACAAGAAATAAAACTCTGTCAAAAATCAAATGACATTTCTATTCATCATT
TCACATGTGATGAAGAGAATGTATTTGCTGCAGTTGGAAGGGGTTTATACGTGTATAGCCTTCA
AATGAAGCGTGTGATTGCCTGCCAGAAAACTGCACATGACTCCAATGTCCTGCACGTTGCCAGA
CTTCCAAACAGGTTTTTTTAACATGTGGGGATTTGGAAGAGTCAGCAAACAAGCCAGCCAACCT
GTTAAAAAGCAGCAAGAAAATGCTACTTCATGTTCACTGGAGCTTATTGGAGATTTGAT

hide sequence

RefSeq Acc Id:

XM_017009606 ⟹ XP_016865095

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	77,430,933 - 77,491,997 (-)	NCBI

Sequence:

show sequence

GAACCGCAGGGACTGGCCGAGGTAAACCCCGGGTGGGTCTGCTCTGCGTCCGTCGAGCTTGCTG
GAGGGGCGGCTTCGTTCCGGTTCGGCCTTCCTGGGTTCCGACCGCGGGGACCCGGGCGGAGGCG
GGGCTGGCTGCTGAGCTCGTGCCACGCGCTGTTCTCACGACGGTGGGGGCGGAGGGCGCGGGAG
CCGGAGCTCCTCAGACCCGGCGGGACCCCAGGCGCACCCTGGAGCTGCAGACCCCCGGCCCCGT
CCCACGGCTAGCTGAATCGTGAGATCCTGGCTCAGGGACGCTCAGCTGGTCAGCAGTCCTATTG
GGACCTGTGACAACTTAGGGCTTCTGGCTACCGAAACTATCTTCATTTCCACTTAAAAAGTATA
CGATTTAGCTAGAAACGAACGAGTTGTGACCGCAGCTTTCCACTTTTGGTTTATTTGAATTGGT
GTCTCTTCCTGGCGTCTACTGATACTTGGTCAGGGAATATAAAATTAATTTACTTATCCAACAA
CCGAAAAAGGATATAATTATTTTTAAAAAGTAATCTGCTTCAAGGTCAAGAACATGATTTTCTA
ATTAACTGCTGTTTTTGGTTTCATAGTCACACTTTCTTCATGGGCCCGAATAATTGAATAGACC
GTGTGTAATGAAATTTACATTTGAAATGTGAATAAAATAATTTTTGCAGTCTTGGAAATTTTGA
GGTCCCAAATTTATTTCGTATGCCACACAAGAACTTTCATGCGCGTCCGTGTGAAGAGACCACC
AAACAGGCTTTGTAAATCTCCTTTACAGACAATAGGTGAAGAACAAACCCAGAATCCCTACACT
GAACTGCTAGTACTGAAGGCTCATCATGATATTGTACGATTTCTGGTACAGTTAGATGACTACA
GATTTGCATCTGCTGGTGATGATGGAATTGTAGTTGTGTGGAATGCCCAGACAGGGGAAAAACT
TTTAGAACTGAATGGACACACTCAAAAGATAACAGCTATTATTACATTTCCTTCCTTGGAATCT
TGTGAAGAGAAAAATCAACTCATCTTGACAGCCTCTGCTGATAGAACAGTTATTGTGTGGGATG
GTGATACTACCAGACAAGTTCAGAGAATATCATGCTTCCAGTCTACTGTAAAGTGTTTAACTGT
TCTTCAGAGACTAGATGTTTGGCTTTCTGGTGGGAATGACCTGTGTGTGTGGAACCGAAAATTA
GATCTCCTGTGTAAGACTAGCCACCTTTCTGATACAGGTATTAGTGCTTTGGTTGAAATACCTA
AGAACTGTGTTGTGGCAGCAGTTGGCAAAGAACTGATAATTTTCAGGTTGGTAGCACCCACAGA
AGGATCACTAGAATGGGATATTCTTGAAGTTAAGCGCCTCCTTGATCACCAGGATAATATTCTC
TCATTGATTAATGTCAATGATTTGAGTTTTGTCACCGGCTCCCACGTCGGAGAGCTGATCATCT
GGGATGCCCTGGACTGGACCATGCAGGCCTATGAACGCAACTTCTGGGACCCATCTCCACAACT
GGACACCCAACAAGAAATAAAACTCTGTCAAAAATCAAATGACATTTCTATTCATCATTTCACA
TGTGATGAAGAGAATGTATTTGCTGCAGTTGGAAGGGGTTTATACGTGTATAGCCTTCAAATGA
AGCGTGTGATTGCCTGCCAGAAAACTGCACATGACTCCAATGTCCTGCACGTTGCCAGACTTCC
AAACAGGCAGTTAATCTCATGCTCAGAAGATGGCAGTGTACGCATTTGGGAGTTAAGAGAAAAA
CAGCAGCTTGCAGCTGAGCCTGTACCAACAGGTTTTTTTAACATGTGGGGATTTGGAAGAGTCA
GCAAACAAGCCAGCCAACCTGTTAAAAAGCAGCAAGAAAATGCTACTTCATGTTCACTGGAGCT
TATTGGAGATTTGATTGGACACTCATCATCTGTGGAGATGTTTCTATACTTTGAAGATCATGGA
CTAGTGACGTGCTCCGCTGATCATCTCATTATTTTGTGGAAAAATGGAGAGCGAGAATCTGGAT
TGCGCAGTTTAAGATTATTTCAAAAATTAGAGGAGAATGGTGACTTATACCTTGCTGTCTAGTT
TAAGGAATTAAAAATACACATGCATGAACCTTGAACATCAAATATCGGGTACTACTCTGAAAAC
CATTAATATATTGATCACTTAAATTGGTAATTTTTTTTGTCAGTCCATAAAATTCTACATGTTT
AAATTTTTTGTGGACCTACCAACCAGGAACATGTTGCTTCTCAGGTCCTAGTATATCCTCCAAA
GAATATACCACAAGTTTTTCCATTTGACTTTGAGCTGCTGTTGAAGTGGTGAGTGCTGTGTTTT
GAGCTTATTTTGAACCTAGATCCTTGTGAAAGGTACAAATAGAGGTAATAGTTAAGTTATGGCA
TTTATTAGAAGTTTTATTATTTGGCTTCCTTTAGAATTATTGTGAAGTTTAAAAATAGCCTTTC
TCCTGCAAATTTTCCTAGTCTTTAGTAACTGTTAGTGTTCTATATAGCACAAACTTGAATCTCT
CAGCCAAAAAAGGGAACATATATACTGTTTAAGTATGGCAAGTTTTCTTTGGTACCAATTTGTT
TAGATAATTTTAAAAATGTTTTTTAGTTCTAGCTACTAAAACCTGTATGAACTCAAATGGATAG
GCATCTTGTGAGGGTGTGTTTTTCCCAGTGTGAATTGGCTTGAAGAGCCATGGGCTAAATGGGT
ACTAGAACAACAACTGCCCCTCATGTACGCCAAGGATGAGCTCTAGATCATTTGAGAGGCACAG
TGTTTCCGGAGTCAGGGACTGCAGCTGAGCGCAACTGCCCCATCTGACCACTGACTCAAATACG
AACTGCTTGAGACAGACTTCTTTTATGTAGTTCTTTGCAGTGTCCATTGAGACACTATAACCAG
CCTTGTAACAATATGTTTTCTCCTTTTGGTGCTAAAAAATGAAAATATTAGAAAGTAGTCTACA
CATTAAAGATTGAAATTCTTAAACTACTGATGAAGAAAGGGCAACGTGACAGATGTTAGCAGAC
TGACCCTTCTTACAGAAAACCTACAGATTTATTTGTTCATTATACAAATATACTACAAATATAC
CCTAAAGGGAATCTCCATAAGTTCTTTTACTAGTTTTAGCTTTGACAGTTGCTTCCACAACTAC
CTACAAAGACTGGAAGAGTTAAGGTCATCTGAGTAGACCAGTGGCATAATGTTACAAATGAGGA
AACTGAGGCCCAGTGCAGTAAGGCCTTGCAATTAAATCTGTAGTGCCCAGTATCACCAAGCAGC
TCTAAAAACAGGAACTGAAGACTGAATGAGAAAAGGCTTATATGACTACTTTAAATCCAAACAA
CATTGAGTCATGAAAAGTTCTATGGAGAAATATTAAAACTTAAGCTACCTCAATTACAGAAGAC
TTTCTCCCATTATTCACGTGCTTTTTCCTTTAGAAATTCTGCATTGGCCCATACATTTGTAAAG
TTGTTTTCTGAAGTTGTATGACACAAGGGAGCCATAGACTTAACTGTTTTACTTCCTAGCCTGT
TCTAGGCTAGTATTTTGTGATAGTAATCTATTCAAATGGAGTGGTAGAAATCACATGAATTTTG
GAAGCAAATGGTACCGTAAGTACCACAGCAAATTCCTTCTGGTCATTATACAGGCGTACCTCAG
AGATACTACAGGTTAGGTTTCAGACCACATCAAAAAAGCAACTATTGCAAATAGAGTGAGTCAC
ATCTAGTTTTTGGTTTCCCAGTGCCTATAAAACTTGTGTTTATACTACAGTCTTAAATTTCTAA
AAAATGTACATACCTTAAGAATACTTTATTGCTAAAAAATGCTAACAATCATCTGAGCCTTCAG
CGAGTCATAATCTTTTTGCTGGTGGAGGGTCTTGATACTGCTGGCTGTTGACTAAGGTGGTTAC
TGAAGGTTGGGGTGGCTGTGGCAGTTCCTTAAAATAAGATAGCGATGAAGTTTTCCAAATCAAT
TGACTTCCTTTCACAAATGAGATCTCTGTAACATGTAATACTATTTAATAGCATTTTACCCACA
GTAGAACTTCTTTCAAAATTTAGAGTCTGTCATCTCAAATCCTGATGCTCCTTTATGAACTAAG
TTTATAGAATATTCTAAATCCTTTGTTGTCATTTCAACTATGTTTACAGCATCTTCACTGTGGA
AATGACTGTCTCCAGAAACCACTTTCTATACACATTCTTAAGCAACTTCTCATCTATTAAAGTT
TGATCATGAGATTACAGCAATTCATTCACATCTTCAGGCTCCACTTCTTCCAGACTCCTTTTAA
TGCTGGAATTTTGACCGCCTCCCATGAATCAGAATGTTCTTAGTGGCATCTAGAATGCTAAATG
CTTCCCAGAAGGTTTTCAATTGACTTTGCCCAGACTCTTCAGAGGAATCACTAGTTAGGGCAGC
TACAGCCTTATTAAATGTATTTCTTAAATAAATAAGACTTAAAAGTCAAAGTGACTCCTTGACC
CATGGACTGCAGCATAGATGTTGTGGTAGCTGGCACGAAGACAACATGAACCTCCTTGTACATC
TCCATCAGAACTCTTAGGTGACCAGGTAACATTGTAATGGGCAGTAATATTTGGAAAGAAATTT
GAGCAGGTCTCAACCATAGGCTTAAATATTCAATAAACCATGCTATAAACAGA

hide sequence

RefSeq Acc Id:

XM_047417349 ⟹ XP_047273305

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	77,430,933 - 77,620,577 (-)	NCBI

RefSeq Acc Id:

XM_047417350 ⟹ XP_047273306

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	77,430,933 - 77,620,577 (-)	NCBI

RefSeq Acc Id:

XM_047417351 ⟹ XP_047273307

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	77,436,283 - 77,492,316 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_060738	(Get FASTA)	NCBI Sequence Viewer
	XP_005248608	(Get FASTA)	NCBI Sequence Viewer
	XP_005248609	(Get FASTA)	NCBI Sequence Viewer
	XP_011541807	(Get FASTA)	NCBI Sequence Viewer
	XP_011541809	(Get FASTA)	NCBI Sequence Viewer
	XP_016865095	(Get FASTA)	NCBI Sequence Viewer
	XP_047273305	(Get FASTA)	NCBI Sequence Viewer
	XP_047273306	(Get FASTA)	NCBI Sequence Viewer
	XP_047273307	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH40241	(Get FASTA)	NCBI Sequence Viewer
	AAO06948	(Get FASTA)	NCBI Sequence Viewer
	ALQ34148	(Get FASTA)	NCBI Sequence Viewer
	ALQ34149	(Get FASTA)	NCBI Sequence Viewer
	BAA91895	(Get FASTA)	NCBI Sequence Viewer
	BAB13915	(Get FASTA)	NCBI Sequence Viewer
	BAB14749	(Get FASTA)	NCBI Sequence Viewer
	BAG56835	(Get FASTA)	NCBI Sequence Viewer
	BAG58240	(Get FASTA)	NCBI Sequence Viewer
	BAG59085	(Get FASTA)	NCBI Sequence Viewer
	BAG61867	(Get FASTA)	NCBI Sequence Viewer
	BAG65176	(Get FASTA)	NCBI Sequence Viewer
	CAD38853	(Get FASTA)	NCBI Sequence Viewer
	EAW95805	(Get FASTA)	NCBI Sequence Viewer
	EAW95806	(Get FASTA)	NCBI Sequence Viewer
	EAW95807	(Get FASTA)	NCBI Sequence Viewer
	Q9HAD4	(Get FASTA)	NCBI Sequence Viewer

Reference Sequences

RefSeq Acc Id:

NP_060738 ⟸ NM_018268

- UniProtKB:

Q9NV62 (UniProtKB/Swiss-Prot), Q9HAD4 (UniProtKB/Swiss-Prot), A0A0S2Z5E0 (UniProtKB/TrEMBL)

- Sequence:

show sequence

MLRWLIGGGREPQGLAEKSPLQTIGEEQTQNPYTELLVLKAHHDIVRFLVQLDDYRFASAGDDG
IVVVWNAQTGEKLLELNGHTQKITAIITFPSLESCEEKNQLILTASADRTVIVWDGDTTRQVQR
ISCFQSTVKCLTVLQRLDVWLSGGNDLCVWNRKLDLLCKTSHLSDTGISALVEIPKNCVVAAVG
KELIIFRLVAPTEGSLEWDILEVKRLLDHQDNILSLINVNDLSFVTGSHVGELIIWDALDWTMQ
AYERNFWDPSPQLDTQQEIKLCQKSNDISIHHFTCDEENVFAAVGRGLYVYSLQMKRVIACQKT
AHDSNVLHVARLPNRQLISCSEDGSVRIWELREKQQLAAEPVPTGFFNMWGFGRVSKQASQPVK
KQQENATSCSLELIGDLIGHSSSVEMFLYFEDHGLVTCSADHLIILWKNGERESGLRSLRLFQK
LEENGDLYLAV

hide sequence

RefSeq Acc Id:

XP_005248608 ⟸ XM_005248551

- Peptide Label:

isoform X4

- Sequence:

show sequence

MLRWLIGGGREPQGLAEKSPLQTIGEEQTQNPYTELLVLKAHHDIVRFLVQLDDYRFASAGDDG
IVVVWNAQTGEKLLELNGHTQKITAIITFPSLESCEEKNQLILTASADRTVIVWDGDTTRQVQR
ISCFQSTVKCLTVLQRLDVWLSGGNDLCVWNRKLDLLCKTSHLSDTDLSFVTGSHVGELIIWDA
LDWTMQAYERNFWDPSPQLDTQQEIKLCQKSNDISIHHFTCDEENVFAAVGRGLYVYSLQMKRV
IACQKTAHDSNVLHVARLPNRQLISCSEDGSVRIWELREKQQLAAEPVPTGFFNMWGFGRVSKQ
ASQPVKKQQENATSCSLELIGDLIGHSSSVEMFLYFEDHGLVTCSADHLIILWKNGERESGLRS
LRLFQKLEENGDLYLAV

hide sequence

RefSeq Acc Id:

XP_005248609 ⟸ XM_005248552

- Peptide Label:

isoform X6

- Sequence:

show sequence

MLRWLIGGGREPQGLAEKSPLQTIGEEQTQNPYTELLVLKAHHDIVRFLVQLDDYRFASAGDDG
IVVVWNAQTGEKLLELNGHTQKITAIITFPSLESCEEKNQLILTASADRTVIVWDGDTTRQVQR
ISCFQSTVKCLTVLQRLDVWLSGGNDLCVWNRKLDLLCKTSHLSDTGISALVEIPKNCVVAAVG
KELIIFRLVAPTEGSLEWDILEVKRLLDHQDNILSLINVNDLSFVTGSHVGELIIWDALDWTMQ
AYERNFWDPSPQLDTQQEIKLCQKSNDISIHHFTCDEENVFAAVGRGLYVYSLQMKRVIACQKT
AHDSNVLHVARLPNRQLISCSEDGSVRIWELREKQQLAAEPVPTGFF

hide sequence

RefSeq Acc Id:

XP_011541807 ⟸ XM_011543505

- Peptide Label:

isoform X1

- Sequence:

show sequence

MHEANCSSPGETGEKSPLQTIGEEQTQNPYTELLVLKAHHDIVRFLVQLDDYRFASAGDDGIVV
VWNAQTGEKLLELNGHTQKITAIITFPSLESCEEKNQLILTASADRTVIVWDGDTTRQVQRISC
FQSTVKCLTVLQRLDVWLSGGNDLCVWNRKLDLLCKTSHLSDTGISALVEIPKNCVVAAVGKEL
IIFRLVAPTEGSLEWDILEVKRLLDHQDNILSLINVNDLSFVTGSHVGELIIWDALDWTMQAYE
RNFWDPSPQLDTQQEIKLCQKSNDISIHHFTCDEENVFAAVGRGLYVYSLQMKRVIACQKTAHD
SNVLHVARLPNRQLISCSEDGSVRIWELREKQQLAAEPVPTGFFNMWGFGRVSKQASQPVKKQQ
ENATSCSLELIGDLIGHSSSVEMFLYFEDHGLVTCSADHLIILWKNGERESGLRSLRLFQKLEE
NGDLYLAV

hide sequence

RefSeq Acc Id:

XP_011541809 ⟸ XM_011543507

- Peptide Label:

isoform X7

- Sequence:

show sequence

MLRWLIGGGREPQGLAEKSPLQTIGEEQTQNPYTELLVLKAHHDIVRFLVQLDDYRFASAGDDG
IVVVWNAQTGEKLLELNGHTQKITAIITFPSLESCEEKNQLILTASADRTVIVWDGDTTRQVQR
ISCFQSTVKCLTVLQRLDVWLSGGNDLCVWNRKLDLLCKTSHLSDTGISALVEIPKNCVVAAVG
KELIIFRLVAPTEGSLEWDILEVKRLLDHQDNILSLINVNDLSFVTGSHVGELIIWDALDWTMQ
AYERNFWDPSPQLDTQQEIKLCQKSNDISIHHFTCDEENVFAAVGRGLYVYSLQMKRVIACQKT
AHDSNVLHVARLPNRFF

hide sequence

RefSeq Acc Id:

XP_016865095 ⟸ XM_017009606

- Peptide Label:

isoform X2

- Sequence:

show sequence

MRVRVKRPPNRLCKSPLQTIGEEQTQNPYTELLVLKAHHDIVRFLVQLDDYRFASAGDDGIVVV
WNAQTGEKLLELNGHTQKITAIITFPSLESCEEKNQLILTASADRTVIVWDGDTTRQVQRISCF
QSTVKCLTVLQRLDVWLSGGNDLCVWNRKLDLLCKTSHLSDTGISALVEIPKNCVVAAVGKELI
IFRLVAPTEGSLEWDILEVKRLLDHQDNILSLINVNDLSFVTGSHVGELIIWDALDWTMQAYER
NFWDPSPQLDTQQEIKLCQKSNDISIHHFTCDEENVFAAVGRGLYVYSLQMKRVIACQKTAHDS
NVLHVARLPNRQLISCSEDGSVRIWELREKQQLAAEPVPTGFFNMWGFGRVSKQASQPVKKQQE
NATSCSLELIGDLIGHSSSVEMFLYFEDHGLVTCSADHLIILWKNGERESGLRSLRLFQKLEEN
GDLYLAV

hide sequence

RefSeq Acc Id:

ENSP00000421166 ⟸ ENST00000503035

RefSeq Acc Id:

ENSP00000426141 ⟸ ENST00000504895

RefSeq Acc Id:

ENSP00000425249 ⟸ ENST00000505129

RefSeq Acc Id:

ENSP00000425813 ⟸ ENST00000506474

RefSeq Acc Id:

ENSP00000424327 ⟸ ENST00000506307

RefSeq Acc Id:

ENSP00000296679 ⟸ ENST00000296679

RefSeq Acc Id:

ENSP00000424287 ⟸ ENST00000507029

RefSeq Acc Id:

ENSP00000427291 ⟸ ENST00000507654

RefSeq Acc Id:

ENSP00000427652 ⟸ ENST00000509701

RefSeq Acc Id:

ENSP00000422922 ⟸ ENST00000509971

RefSeq Acc Id:

ENSP00000427219 ⟸ ENST00000509892

RefSeq Acc Id:

ENSP00000423540 ⟸ ENST00000511791

RefSeq Acc Id:

ENSP00000425563 ⟸ ENST00000511630

RefSeq Acc Id:

ENSP00000422510 ⟸ ENST00000511036

RefSeq Acc Id:

ENSP00000423462 ⟸ ENST00000513417

RefSeq Acc Id:

ENSP00000426937 ⟸ ENST00000514559

RefSeq Acc Id:

ENSP00000426499 ⟸ ENST00000515253

RefSeq Acc Id:	XP_047273306 ⟸ XM_047417350
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047273305 ⟸ XM_047417349
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047273307 ⟸ XM_047417351
- Peptide Label:	isoform X5

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9HAD4-F1-model_v2	AlphaFold	Q9HAD4	1-459	view protein structure

Promoters

RGD ID:

6803702

Promoter ID:

HG_KWN:50519

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

OTTHUMT00000220014

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	5	76,823,651 - 76,824,151 (-)	MPROMDB

RGD ID:

6869952

Promoter ID:

EPDNEW_H8141

Type:

initiation region

Name:

WDR41_2

Description:

WD repeat domain 41

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H8142

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	77,492,224 - 77,492,284	EPDNEW

RGD ID:

6869954

Promoter ID:

EPDNEW_H8142

Type:

initiation region

Name:

WDR41_1

Description:

WD repeat domain 41

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H8141

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	5	77,492,507 - 77,492,567	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:25601	AgrOrtholog
COSMIC	WDR41	COSMIC
Ensembl Genes	ENSG00000164253	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein	ENSP00000296679	ENTREZGENE
	ENSP00000296679.4	UniProtKB/Swiss-Prot
	ENSP00000421166.1	UniProtKB/TrEMBL
	ENSP00000422510.1	UniProtKB/TrEMBL
	ENSP00000422922.1	UniProtKB/TrEMBL
	ENSP00000423462.1	UniProtKB/TrEMBL
	ENSP00000423540.1	UniProtKB/TrEMBL
	ENSP00000424287.1	UniProtKB/Swiss-Prot
	ENSP00000424327.1	UniProtKB/TrEMBL
	ENSP00000425249.1	UniProtKB/TrEMBL
	ENSP00000425563.2	UniProtKB/TrEMBL
	ENSP00000425813.1	UniProtKB/TrEMBL
	ENSP00000426141.1	UniProtKB/TrEMBL
	ENSP00000426499	ENTREZGENE
	ENSP00000426499.1	UniProtKB/TrEMBL
	ENSP00000426937.1	UniProtKB/TrEMBL
	ENSP00000427219.1	UniProtKB/TrEMBL
	ENSP00000427291.1	UniProtKB/TrEMBL
	ENSP00000427652.1	UniProtKB/TrEMBL
Ensembl Transcript	ENST00000296679	ENTREZGENE
	ENST00000296679.9	UniProtKB/Swiss-Prot
	ENST00000503035.5	UniProtKB/TrEMBL
	ENST00000504895.5	UniProtKB/TrEMBL
	ENST00000505129.5	UniProtKB/TrEMBL
	ENST00000506307.5	UniProtKB/TrEMBL
	ENST00000506474.5	UniProtKB/TrEMBL
	ENST00000507029.5	UniProtKB/Swiss-Prot
	ENST00000507654.5	UniProtKB/TrEMBL
	ENST00000509701.5	UniProtKB/TrEMBL
	ENST00000509892.5	UniProtKB/TrEMBL
	ENST00000509971.5	UniProtKB/TrEMBL
	ENST00000511036.5	UniProtKB/TrEMBL
	ENST00000511630.6	UniProtKB/TrEMBL
	ENST00000511791.1	UniProtKB/TrEMBL
	ENST00000513417.5	UniProtKB/TrEMBL
	ENST00000514559.5	UniProtKB/TrEMBL
	ENST00000515253	ENTREZGENE
	ENST00000515253.5	UniProtKB/TrEMBL
Gene3D-CATH	2.130.10.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000164253	GTEx
HGNC ID	HGNC:25601	ENTREZGENE
Human Proteome Map	WDR41	Human Proteome Map
InterPro	G-protein_beta_WD-40_rep	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD40/YVTN_repeat-like_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD40_repeat	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD40_repeat_CS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD40_repeat_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WDR41	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:55255	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	55255	ENTREZGENE
OMIM	617502	OMIM
PANTHER	PTHR22805	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	WD40	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134906058	PharmGKB
PRINTS	GPROTEINBRPT	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	WD_REPEATS_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD_REPEATS_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD_REPEATS_REGION	UniProtKB/Swiss-Prot
SMART	WD40	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF50978	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A024RAK0_HUMAN	UniProtKB/TrEMBL
	A0A0S2Z5D8_HUMAN	UniProtKB/TrEMBL
	A0A0S2Z5E0	ENTREZGENE, UniProtKB/TrEMBL
	B4DHS8_HUMAN	UniProtKB/TrEMBL
	B4DK73_HUMAN	UniProtKB/TrEMBL
	D6R9E7_HUMAN	UniProtKB/TrEMBL
	D6R9M1_HUMAN	UniProtKB/TrEMBL
	D6RA22_HUMAN	UniProtKB/TrEMBL
	D6RB94_HUMAN	UniProtKB/TrEMBL
	D6RBY6_HUMAN	UniProtKB/TrEMBL
	D6RE66_HUMAN	UniProtKB/TrEMBL
	D6RGW4_HUMAN	UniProtKB/TrEMBL
	D6RH33_HUMAN	UniProtKB/TrEMBL
	D6RIX6_HUMAN	UniProtKB/TrEMBL
	D6RJA5_HUMAN	UniProtKB/TrEMBL
	H0Y9Z3_HUMAN	UniProtKB/TrEMBL
	H0YAA3_HUMAN	UniProtKB/TrEMBL
	H0YAI6_HUMAN	UniProtKB/TrEMBL
	Q9HAD4	ENTREZGENE
	Q9NV62	ENTREZGENE
	WDR41_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	B4DT55	UniProtKB/Swiss-Prot
	Q7Z792	UniProtKB/Swiss-Prot
	Q8IWG3	UniProtKB/Swiss-Prot
	Q8IXA9	UniProtKB/Swiss-Prot
	Q8NDA7	UniProtKB/Swiss-Prot
	Q9NV62	UniProtKB/Swiss-Prot

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

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

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

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

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Imported Disease Annotations - ClinVar