Bos taurus Gene: BRWD2
Summary
InnateDB Gene IDBG-640422.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BRWD2
Gene Name WD repeat-containing protein 11
Synonyms BRWD2; PHIP
Species Bos taurus
Ensembl Gene ENSBTAG00000021540
Encoded Proteins
WD repeat-containing protein 11
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000120008:
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. This gene is located in the chromosome 10q25-26 region, which is frequently deleted in gliomas and tumors of other tissues, and is disrupted by the t(10;19) translocation rearrangement in glioblastoma cells. The gene location suggests that it is a candidate gene for the tumor suppressor locus. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 26:41212406-41271588
Strand Forward strand
Band
Transcripts
ENSBTAT00000028704 ENSBTAP00000028704
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 4 interaction(s) predicted by orthology.
Predicted by orthology
Total 4 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
Cellular Component
GO:0005737 cytoplasm
GO:0005765 lysosomal membrane
GO:0005929 cilium
GO:0016020 membrane
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL A6QLS8
UniProt Splice Variant
Entrez Gene 525169
UniGene Bt.19088
RefSeq NM_001101122 XM_005225811
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC148072 DAAA02059434
GenPept AAI48073
RNA Seq Atlas 525169