WDR89 - WD repeat domain 89 Gene

Also Known as MSTP050; C14orf150

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 112840

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

WD40: WD domain, G-beta repeat (62 - 98)

WD40

WD40: WD domain, G-beta repeat (167 - 199)

WD40

WD40: WD domain, G-beta repeat (318 - 349)

  • 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

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 Set / 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
Others WDR89 NCBI