The 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
Associated with diseases ID, MRX-72, WSMN
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants -
Date created December 09, 2013

Links to other resources
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC 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     
00049602 X RAB39B, member RAS oncogene family NM_171998.2 NP_741995.1 -


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