CRBN gene homepage

General information
Gene symbol CRBN
Gene name cereblon
Chromosome 3
Chromosomal band p26.3
Imprinted Unknown
Genomic reference NG_016864.1
Transcript reference NM_016302.3
Exon/intron information NM_016302.3 exon/intron table
Associated with diseases ID, MRT-2
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 11
Unique public DNA variants reported 11
Individuals with public variants 2
Hidden variants 1
Download all this gene's data Download all data
Notes Establishment of the database was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created May 01, 2012
Date last updated June 28, 2019
Version CRBN:190628

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_016302.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/CRBN
HGNC 30185
Entrez Gene 51185
PubMed articles CRBN
OMIM - Gene 609262
OMIM - Diseases MRT-2 (mental retardation, autosomal recessive, type 2 (MRT-2))
HGMD CRBN
GeneCards CRBN
GeneTests CRBN


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000009 3 cereblon, transcript variant 1 NM_016302.3 NP_057386.2 11


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