CRBN
Summary: 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].
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Name | OMIM ID | Ensembl ID | HGNC ID | PHARMGKB ID | Map Location |
---|---|---|---|---|---|
Namecereblon OMIM IDMIM:609262 Ensembl IDEnsembl:ENSG00000113851 HGNC IDHGNC:HGNC:30185 PHARMGKB IDPA134926851 Map Location3p26.2 |
GO terms in CRBN
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Term Type | Evidence Type | GO Term ID | GO Des. |
---|---|---|---|
BP | IEA | GO:0016567 | protein ubiquitination |
BP | IMP | GO:0016567 | protein ubiquitination |
BP | IEA | GO:0032463 | negative regulation of protein homooligomerization |
BP | IEA | GO:0034766 | negative regulation of ion transmembrane transport |
BP | IMP | GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process |
BP | IEA | GO:0090073 | positive regulation of protein homodimerization activity |
Gene expression in normal tissue: CRBN
Gene-model tissue-cancer distribution: Bubble Plot
Gene-drug pathway distribution
Pathways in CRBN
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Database | Pathway ID | Pathway Des. |
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No matching records found |
Gene-Drug: Aster Plot
Gene in drug-gene network: Network Plot

Gene-drug targets distribution
Gene Structure: PDB
Models in CRBN
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Model | Level | Reference ID | Tissue | Cancer | Drug | Clinical Response | Source | |
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No matching records found |