WDR89 - WD repeat domain 89 Gene

Homo sapiens

Also known as MSTP050; C14orf150

Gene ID: 112840 | Gene type: protein coding

About WDR89

This gene has 4 transcripts (splice variants) and 179 orthologues. Ubiquitous expression in lymph node (RPKM 4.5), thyroid (RPKM 4.4) and 25 other tissues.

WDR89 Products(10)

mRNA	Protein	Name
NM_001008726.3	NP_001008726.1	WD repeat-containing protein 89
NM_001258272.2	NP_001245201.1	WD repeat-containing protein 89
NM_001382423.1	NP_001369352.1	WD repeat-containing protein 89
NM_001382424.1	NP_001369353.1	WD repeat-containing protein 89
NM_001382425.1	NP_001369354.1	WD repeat-containing protein 89
NM_001382426.1	NP_001369355.1	WD repeat-containing protein 89
NM_001382427.1	NP_001369356.1	WD repeat-containing protein 89
NM_001382428.1	NP_001369357.1	WD repeat-containing protein 89
NM_001382429.1	NP_001369358.1	WD repeat-containing protein 89
NM_080666.4	NP_542397.1	WD repeat-containing protein 89

WDR89 Protein Structure

WD40

0
100
200
300
387 a.a.

Protein Preferred Names

Protein Names

WD repeat-containing protein 89

Related Diseases

Diseases

Alias

Polyposis, Skin Pigmentation, Alopecia, And Fingernail Changes

Cronkhite-Canada Syndrome	Gastric Cronkhite Canada Polyposis
Cronkhite-Canada Disease	Polyposis Skin Pigmentation Alopecia Fingernail Changes
Gastrointestinal Polyposis-Ectodermal Changes Syndrome	Gastrointestinal Polyposis-Skin Pigmentation-Alopecia-Fingernail Changes Syndrome
Polyposis, Gastrointestinal, With Ectodermal Changes

Erythrocytosis, Familial, 8

Diphosphoglycerate Mutase Deficiency Of Erythrocyte	ECYT8
Bisphosphoglycerate Mutase Deficiency	Bisphosphoglyceromutase Deficiency
Bpgm Deficiency	Dpgm Deficiency
Deficiency Of Bisphosphoglycerate Mutase	Familial Erythrocytosis 8
Hemolytic Anemia Due To Diphosphoglycerate Mutase Deficiency	Erythrocytosis Due To Bisphosphoglycerate Mutase Deficiency
Erythrocytosis, Familial, Type 8

Adamantinous Craniopharyngioma

Adamantinous Rathke'S Pouch Tumor	Craniopharyngioma, Adamantinomatous
Adamantinomatous Craniopharyngioma

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS15801	WDR89 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	WDR89	VGNC	VGNC:48396
Rattus norvegicus	WDR89	RGD	RGD:1307393
Bos taurus	WDR89	VGNC	VGNC:36925
Mus musculus	WDR89	MGD	MGI:1919588
Felis catus	WDR89	VGNC	VGNC:67062
Macaca mulatta	WDR89	VGNC	VGNC:79254

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