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Gene : BRWD3 Homo sapiens

Name  ? bromodomain and WD repeat domain containing 3 Cytological Location  Xq21.1
Brief Description  bromodomain and WD repeat domain containing 3
Description  The protein encoded by this gene contains a bromodomain and several WD repeats. It is thought to have a chromatin-modifying function, and may thus play a role in transcription. Mutations in this gene are associated with a spectrum of cognitive disabilities and X-linked macrocephaly. This gene is also associated with translocations in patients with B-cell chronic lymphocytic leukemia. [provided by RefSeq, Jul 2017]
  • synonyms:
  • OTTHUMG00000021908,
  • MRX93,
  • HGNC:17342,
  • BRWD3,
  • NM_153252,
  • BRODL,
  • MRX93,
  • FLJ38568,
  • uc004edt.4
  • identifiers:
  • 254065,
  • ENSG00000165288,
  • BRWD3

Genome feature

Region: gene ? Length: 140375  
Location: X:80669503-80809877 reverse strand Cyto location: Xq21.1

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

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Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

3756 SN Ps

5 Cross References

18 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results