WDR47 - WD repeat domain 47 Gene

Homo sapiens

Gene ID: 22911 | Gene type: protein coding

About WDR47

Cytogenetic location: 1p13.3 Genomic coordinates (GRCh38): 1:108,970,214-109,042,102 (from NCBI)

This gene has 8 transcripts (splice variants) and 208 orthologues. Broad expression in brain (RPKM 29.8), testis (RPKM 15.2) and 22 other tissues.

Predicted to be located in cytoplasm and microtubule. [provided by Alliance of Genome Resources, Apr 2022]

mRNA	Protein	Name
NM_001142550.2	NP_001136022.1	WD repeat-containing protein 47 isoform 1
NM_001142551.2	NP_001136023.1	WD repeat-containing protein 47 isoform 3
NM_014969.6	NP_055784.3	WD repeat-containing protein 47 isoform 2

WD40

Protein Preferred Names

Protein Names

WD repeat-containing protein 47

nemitin

Type Cross Intra	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	Reference
Intra	WDR47	O94967	TCL1A	Homo sapiens	P56279	Y2H Array	25416956

Cross: Cross-species interaction Intra: Intraspecies interaction

Diseases

Alias

Myopathy, X-Linked, With Excessive Autophagy

X-Linked Myopathy With Excessive Autophagy	Xmea
MEAX	Vacuolar Myopathy

Lissencephaly

Pachygyria	Broad Gyri Of Cerebrum
Large Gyri Of Cerebrum	Macrogyria

Lissencephaly 1

LIS1	Classic Lissencephaly
Ils	Subcortical Laminar Heterotopia
Lissencephaly Due To Lis1 Mutation	Lissencephaly Sequence, Isolated
Lissencephaly, Classic	Pafah1b1-Related Lissencephaly
Classical Lissencephaly	Lissencephaly Type 1
Lissencephaly-1	Subcortical Band Heterotopia
Double Cortex	Lissencephaly Classic
Lissencephaly Sequence Isolated	Isolated Lissencephaly Sequence
Type 1 Lissencephaly	Lissencephaly Syndrome Type 1
SBH	Sclh
Lissencephaly, Type 1	Type I Lissencephaly

Primary Ciliary Dyskinesia

Immotile Cilia Syndrome	Kartagener Syndrome
Dextrocardia Bronchiectasis And Sinusitis	Pcd
Ciliary Motility Disorders	Ciliary Motility Disorder
Immotile Ciliary Syndrome	Ciliary Dyskinesia Primary
Ics	Polynesian Bronchiectasis
Dextrocardia-Bronchiectasis-Sinusitis Syndrome	Immotile Cilia Syndrome, Kartagener Type
Primary Ciliary Dyskinesia And Situs Inversus	Primary Ciliary Dyskinesia, Kartagener Type
Siewert Syndrome	Dyskinesia, Ciliary, Primary

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS15783	WDR47 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Species	Symbol	Source	ID
Rattus norvegicus	WDR47	RGD	RGD:1309181
Bos taurus	WDR47	VGNC	VGNC:36903
Canis familiaris	WDR47	VGNC	VGNC:48370
Mus musculus	WDR47	MGD	MGI:2139593
Macaca mulatta	WDR47	VGNC	VGNC:79780
Felis catus	WDR47	VGNC	VGNC:67037

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