2. Gene
  3. WDR47 - WD repeat domain 47 Gene

WDR47 - WD repeat domain 47 Gene

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

中文名称：WD 重复域 47

种属: Homo sapiens

基因 ID: 22911 | 基因类型: protein coding

关于 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.

功能概要

预测位于细胞质和微管中。 [由基因组资源联盟提供，2022 年 4 月]

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

WDR47 基因产物(3)

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

WDR47 蛋白结构

WD40

WD40: WD domain, G-beta repeat (606 - 632)

WD40

WD40: WD domain, G-beta repeat (658 - 687)

WD40

WD40: WD domain, G-beta repeat (746 - 782)

WD40

WD40: WD domain, G-beta repeat (794 - 828)

WD40

WD40: WD domain, G-beta repeat (835 - 868)

WD40

WD40: WD domain, G-beta repeat (881 - 915)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 919 a.a.
蛋白主名 其他名称

WD repeat-containing protein 47

nemitin

WDR47 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
WDR47 O94967 TCL1A Homo sapiens P56279
Y2H Array
25416956
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
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
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-RS15783 WDR47 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 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
嗨！很高兴为您提供帮助！

尊敬的 MCE 客户您好，
请您选择所在区域，我们将转接对应客服为您服务！

热门区域

A

B

C

F

G

H

J

L

N

Q

S

T

X

Y

Z

热 A B C F G H J L N Q S T X Y Z