WDR26 - WD repeat domain 26 Gene

Also Known as CDW2; GID7; MIP2; SKDEAS

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 80232

About WDR26

Cytogenetic location: 1q42.11-q42.12 Genomic coordinates (GRCh38): 1:224,385,146-224,434,797 (from NCBI)

This gene has 16 transcripts (splice variants), 275 orthologues, 1 paralogue and is associated with 3 phenotypes. Ubiquitous expression in bone marrow (RPKM 30.1), esophagus (RPKM 28.6) and 25 other tissues.

Summary

This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 Amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, Apoptosis, and gene regulation. Two transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

WDR26 Products (3)

mRNA Protein Name
NM_001115113.3 NP_001108585.2 WD repeat-containing protein 26 isoform b
NM_001379403.1 NP_001366332.1 WD repeat-containing protein 26 isoform c
NM_025160.7 NP_079436.4 WD repeat-containing protein 26 isoform a
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
17510365 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
15378603 GOA
located in nucleus IDA
IDA: Inferred from direct assay
29911972 GOA
part of ubiquitin ligase complex IDA
IDA: Inferred from direct assay
29911972 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

WDR26 Protein Structure

WD40

WD40: WD domain, G-beta repeat (349 - 382)

WD40

WD40: WD domain, G-beta repeat (392 - 424)

WD40

WD40: WD domain, G-beta repeat (443 - 465)

WD40

WD40: WD domain, G-beta repeat (582 - 599)

WD40

WD40: WD domain, G-beta repeat (605 - 641)

  • 0
  • 200
  • 400
  • 600
  • 661 a.a.
Protein Preferred Names Protein Names

WD repeat-containing protein 26

  • CUL4- and DDB1-associated WDR protein 2

WDR26 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
WDR26 Q9H7D7 AXIN1 Homo sapiens O15169 27098453
Intra
WDR26 Q9H7D7 AXIN1 Homo sapiens O15169 27098453
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Skraban-Deardorff Syndrome
  • SKDEAS

  • Intellectual Disability With Seizures, Abnormal Gait, And Distinctive Facial Features

  • Intellectual Disability-Seizures-Abnormal Gait-Facial Dysmorphism Syndrome

  • Intellectual Disability, Seizures, Abnormal Gait And Distinctive Facial Features

Chromosome 1q41-Q42 Deletion Syndrome
  • 1q41-Q42 Microdeletion Syndrome

  • 1q41q42 Microdeletion Syndrome

  • Holoprosencephaly 10, Included

  • Hpe10, Included

  • 1q41-Q42 Deletion Syndrome

  • Deletion 1q41-Q42

  • Monosomy 1q41-Q42

  • Del(1)(Q41q42)

  • Monosomy 1q41q42

  • Chromosome Deletion Syndrome 1q41-Q42

  • Holoprosencephaly 10

Kbg Syndrome
  • KBGS

  • Macrodontia, Mental Retardation, Characteristic Facies, Short Stature, And Skeletal Anomalies

  • Short Stature, Characteristic Facies, Macrodontia, Intellectual Disability, And Skeletal Anomalies

  • Short Stature, Characteristic Facies, Macrodontia, Mental Retardation, And Skeletal Anomalies

  • Short Stature-Characteristic Facies-Mental Retardation-Macrodontia-Skeletal Anomalies Syndrome

  • Short Stature-Facial And Skeletal Anomalies-Intellectual Disability-Macrodontia Syndrome

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

Orthologs Information

Species Symbol Source ID
Canis familiaris WDR26 VGNC VGNC:48358
Macaca mulatta WDR26 VGNC VGNC:79315
Bos taurus WDR26 VGNC VGNC:36889
Rattus norvegicus WDR26 RGD RGD:1565589
Felis catus WDR26 VGNC VGNC:67023
Mus musculus WDR26 MGD MGI:1923825
Others WDR26 NCBI