2. Gene
  3. WDR89 - WD repeat domain 89 Gene

WDR89 - WD repeat domain 89 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：WD 重复域 89

种属: Homo sapiens

同用名: MSTP050; C14orf150

基因 ID: 112840 | 基因类型: protein coding

关于 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 基因产物(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 蛋白结构

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.
蛋白主名 其他名称

WD repeat-containing protein 89

关联疾病

疾病名称 别名
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
疾病名称 别名
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS15801 WDR89 Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 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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