2. Gene
  3. WDR20 - WD repeat domain 20 Gene

WDR20 - WD repeat domain 20 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as DMR; Bun107

Gene ID: 91833 | Gene type: protein coding

About WDR20

Cytogenetic location: 14q32.31 Genomic coordinates (GRCh38): 14:102,139,423-102,224,839 (from NCBI)

This gene has 20 transcripts (splice variants), 285 orthologues and 1 paralogue. Ubiquitous expression in testis (RPKM 5.3), thyroid (RPKM 3.2) and 25 other tissues.

Summary

This gene encodes a WD repeat-containing protein that functions to preserve and regulate the activity of the USP12-UAF1 deubiquitinating Enzyme complex. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2011]

WDR20 Products(36)

mRNA Protein Name
NM_001242414.2 NP_001229343.1 WD repeat-containing protein 20 isoform 4
NM_001242415.2 NP_001229344.1 WD repeat-containing protein 20 isoform 5
NM_001242416.2 NP_001229345.1 WD repeat-containing protein 20 isoform 6
NM_001242417.2 NP_001229346.1 WD repeat-containing protein 20 isoform 7
NM_001242418.2 NP_001229347.1 WD repeat-containing protein 20 isoform 8
NM_001320130.2 NP_001307059.1 WD repeat-containing protein 20 isoform 10
NM_001330228.3 NP_001317157.1 WD repeat-containing protein 20 isoform 11
NM_001353656.2 NP_001340585.1 WD repeat-containing protein 20 isoform 12
NM_001353657.2 NP_001340586.1 WD repeat-containing protein 20 isoform 13
NM_001353658.2 NP_001340587.1 WD repeat-containing protein 20 isoform 14
NM_001353659.2 NP_001340588.1 WD repeat-containing protein 20 isoform 15
NM_001353660.2 NP_001340589.1 WD repeat-containing protein 20 isoform 16
NM_001353661.2 NP_001340590.1 WD repeat-containing protein 20 isoform 17
NM_001353662.2 NP_001340591.1 WD repeat-containing protein 20 isoform 18
NM_001353663.2 NP_001340592.1 WD repeat-containing protein 20 isoform 18
NM_001353664.2 NP_001340593.1 WD repeat-containing protein 20 isoform 18
NM_001353665.2 NP_001340594.1 WD repeat-containing protein 20 isoform 18
NM_001353666.2 NP_001340595.1 WD repeat-containing protein 20 isoform 18
NM_001353667.2 NP_001340596.1 WD repeat-containing protein 20 isoform 19
NM_001353668.2 NP_001340597.1 WD repeat-containing protein 20 isoform 20
NM_001353669.2 NP_001340598.1 WD repeat-containing protein 20 isoform 20
NM_001353670.2 NP_001340599.1 WD repeat-containing protein 20 isoform 20
NM_001353671.2 NP_001340600.1 WD repeat-containing protein 20 isoform 20
NM_001353672.2 NP_001340601.1 WD repeat-containing protein 20 isoform 20
NM_001353673.2 NP_001340602.1 WD repeat-containing protein 20 isoform 20
NM_001353674.2 NP_001340603.1 WD repeat-containing protein 20 isoform 20
NM_001353675.2 NP_001340604.1 WD repeat-containing protein 20 isoform 21
NM_001353676.2 NP_001340605.1 WD repeat-containing protein 20 isoform 22
NM_001353677.2 NP_001340606.1 WD repeat-containing protein 20 isoform 22
NM_001353678.2 NP_001340607.1 WD repeat-containing protein 20 isoform 22
NM_001353679.2 NP_001340608.1 WD repeat-containing protein 20 isoform 23
NM_001353680.2 NP_001340609.1 WD repeat-containing protein 20 isoform 24
NM_001353681.2 NP_001340610.1 WD repeat-containing protein 20 isoform 4
NM_144574.4 NP_653175.2 WD repeat-containing protein 20 isoform 2
NM_181291.3 NP_851808.1 WD repeat-containing protein 20 isoform 1
NM_181308.3 NP_851825.1 WD repeat-containing protein 20 isoform 3
Gene Ontology
  • Molecular Function
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables deubiquitinase activator activity IDA
IDA: Inferred from direct assay
20147737 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
19615732 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cytoplasm IDA
IDA: Inferred from direct assay
30466959 GOA
located in nucleus IDA
IDA: Inferred from direct assay
30466959 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

WDR20 Protein Structure

WD40

WD40: WD domain, G-beta repeat (215 - 248)

WD40

WD40: WD domain, G-beta repeat (265 - 290)

  • 0
  • 100
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  • 400
  • 500
  • 569 a.a.
Protein Preferred Names Protein Names

WD repeat-containing protein 20

WDR20 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
WDR20 Q8TBZ3 USP12 Homo sapiens O75317
Anti Tag CoIP
19615732
Intra
WDR20 Q8TBZ3 USP12 Homo sapiens O75317
Anti Tag CoIP
33961781
Intra
WDR20 Q8TBZ3 USP46 Homo sapiens P62068
Anti Tag CoIP
33961781
Intra
WDR20 Q8TBZ3 DAPP1 Homo sapiens Q9UN19
Validated Y2H
25814554
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Temple Syndrome

Uniparental Disomy, Maternal, Chromosome 14

Temple Syndrome Due To Paternal 14q32.2 Microdeletion

Paternal Del(14)(Q32.2)

Temple Syndrome Due To Paternal 14q32.2 Hypomethylation

Temple Syndrome Due To Maternal Uniparental Disomy Of Chromosome 14

Upd(14)Mat
Kagami-Ogata Syndrome

Paternal Uniparental Disomy Of Chromosome 14

Uniparental Disomy, Paternal, Chromosome 14

Kos

Mca Due To 14q32.2 Maternally Expressed Gene Defect

Paternal Uniparental Disomy 14

Kagami-Ogata Syndrome Due To Maternal 14q32.2 Microdeletion

Maternal Del(14)(Q32.2)

Maternal Monosomy 14q32.2

Kagami-Ogata Syndrome Due To Maternal 14q32.2 Hypermethylation

Kagami-Ogata Syndrome Due To Paternal Uniparental Disomy Of Chromosome 14

Upd(14)Pat
Silver-Russell Syndrome 1

Silver-Russell Syndrome

Russell-Silver Syndrome

Silver-Russell Dwarfism

Rss

SRS1

Srs

Silver Russell Dwarfism

Russell Silver Syndrome

Silver Russell Syndrome
Transient Neonatal Diabetes Mellitus

Diabetes Mellitus, Transient Neonatal

Tndm

Chromosome 6-Associated Transient Diabetes Mellitus

Dmtn

Diabetes Mellitus, 6q24-Related Transient Neonatal

Tndm1

Neonatal Diabetes Mellitus, Transient

Tndm -[Transient Neonatal Diabetes Mellitus]
Osteogenesis Imperfecta, Type Iii

Osteogenesis Imperfecta Type Iii

OI3

Oi, Type Iii

Osteogenesis Imperfecta Type 3

Oi Type Iii

Oi Type 3

Progressive Deforming Osteogenesis Imperfecta

Severe Osteogenesis Imperfecta

Osteogenesis Imperfecta, Progressively Deforming, With Normal Sclerae

Progressively Deforming Osteogenesis Imperfecta With Normal Sclera

Osteogenesis Imperfecta, Progressively Deforming With Normal Sclerae

Progressively Deforming Oi

Osteogenesis Imperfecta 3

Oi-Iii

Progressively Deforming Osteogenesis Imperfecta With Normal Sclerae
Beckwith-Wiedemann Syndrome

Wiedemann-Beckwith Syndrome

BWS

Exomphalos-Macroglossia-Gigantism Syndrome

Emg Syndrome

Beckwith-Wiedemann Syndrome Due To Cdkn1c Mutation

Emg Abnormality

Wbs

Exomphalos Macroglossia Gigantism Syndrome

Beckwith-Wiedemann Syndrome Due To Nsd1 Mutation

Macroglossia Exomphalos Gigantism
Polyhydramnios
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-RS15767 WDR20 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Macaca mulatta WDR20 VGNC VGNC:79196
Felis catus WDR20 VGNC VGNC:67020
Rattus norvegicus WDR20 RGD RGD:1306499
Bos taurus WDR20 VGNC VGNC:50061
Canis familiaris WDR20 VGNC VGNC:49741
Mus musculus WDR20 MGD MGI:1916891