RAB39B gene homepage

General information
Gene symbol RAB39B
Gene name RAB39B, member RAS oncogene family
Chromosome X
Chromosomal band q28
Imprinted Unknown
Genomic reference NG_012626.2
Transcript reference NM_171998.2
Exon/intron information NM_171998.2 exon/intron table
Associated with diseases ID, MRX-72, WSMN
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Yujing Gao
Total number of public variants reported 15
Unique public DNA variants reported 5
Individuals with public variants 18
Hidden variants 0
Download all this gene's data Download all data
Notes This gene sequence variant database has been initiated based on the data reported by Tarpey et al. (2009) A systematic, large-scale resequencing screen of the X-chromosome coding exons in mental retardation. Nat.Genet. 41: 535-543. 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 March 06, 2009
Date last updated July 30, 2018
Version RAB39B:180730

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_171998.2.
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/RAB39B
External URL Orphanet
HGNC 16499
Entrez Gene 116442
PubMed articles RAB39B
OMIM - Gene 300774
OMIM - Diseases MRX-72 (mental retardation, X-linked, type 72 (MRX-72))
WSMN (Waisman syndrome? (WSMN))
HGMD RAB39B
GeneCards RAB39B
GeneTests RAB39B


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00017327 X RAB39B, member RAS oncogene family NM_171998.2 NP_741995.1 15


Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective curator(s). Any unauthorised use, copying, storage or distribution of this material without written permission from the curator(s) will lead to copyright infringement with possible ensuing litigation. Copyright © 2009-2018. All Rights Reserved. For further details, refer to Directive 96/9/EC of the European Parliament and the Council of March 11 (1996) on the legal protection of databases.

We have used all reasonable efforts to ensure that the information displayed on these pages and contained in the databases is of high quality. We make no warranty, express or implied, as to its accuracy or that the information is fit for a particular purpose, and will not be held responsible for any consequences arising out of any inaccuracies or omissions. Individuals, organisations and companies which use this database do so on the understanding that no liability whatsoever either direct or indirect shall rest upon the curator(s) or any of their employees or agents for the effects of any product, process or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided.