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Gene : CRBN Homo sapiens

Name  ? cereblon Cytological Location  3p26.2
Brief Description  cereblon
Description  This gene encodes a protein related to the Lon protease protein family. In rodents and other mammals this gene product is found in the cytoplasm localized with a calcium channel membrane protein, and is thought to play a role in brain development. Mutations in this gene are associated with autosomal recessive nonsyndromic cognitive disability. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]
  • synonyms:
  • MRT2,
  • mental retardation, non-syndromic, autosomal recessive, 2A,
  • HGNC:30185,
  • NM_016302,
  • uc003bpq.4,
  • MRT2,
  • CRBN,
  • BC017419,
  • OTTHUMG00000090261,
  • MRT2A,
  • MRT2A
  • identifiers:
  • 51185,
  • ENSG00000113851,
  • CRBN

Genome feature

Region: gene ? Length: 31228  
Location: 3:3148490-3179717 reverse strand Cyto location: 3p26.2


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

1580 SN Ps

5 Cross References

19 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results