The CUL4B gene homepage

General information
Gene symbol CUL4B
Gene name cullin 4B
Chromosome X
Chromosomal band q23
Imprinted Unknown
Genomic reference NG_009388.1
Transcript reference NM_003588.3
Exon/intron information NM_003588.3 exon/intron table
Associated with diseases ID, MRX15
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 97
Unique public DNA variants reported 82
Individuals with public variants 72
Hidden variants 11
Date created March 06, 2009
Date last updated October 31, 2021
Version CUL4B:211031

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_003588.3.
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
HGNC 2555
Entrez Gene 8450
PubMed articles CUL4B
OMIM - Gene 300304
OMIM - Diseases MRX15 (mental retardation, X-linked, syndromic, type 15 (MRX15, Cabezas type))
GeneCards CUL4B
GeneTests CUL4B
Orphanet CUL4B

Active transcripts




NCBI ID     

NCBI Protein ID     

00001071 X transcript variant 1 NM_003588.3 NP_003579.3 97

Copyright & disclaimer
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