WDR47 - WD repeat domain 47 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 22911

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.

Summary

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

WDR47 Products (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 Protein Structure

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
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  • 800
  • 919 a.a.
Protein Preferred Names Protein Names

WD repeat-containing protein 47

  • nemitin

WDR47 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
WDR47 O94967 TCL1A Homo sapiens P56279
Y2H Array
25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. 상품명
효과
Purity
Rare Diseases
HY-RS15783 WDR47 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

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
Others WDR47 NCBI