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RAB39B

RAB39B, member RAS oncogene family

HCNC Approved Symbol
RAB39B (HGNC:16499)
Genomic Coordinates
23:155,258,235 - 155,264,491 (Xq28)
Synonyms
MRX72, WSN
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Intellectual developmental disorder, X-linked 72
300271X-linked recessive
Waisman syndrome
311510X-linked recessive

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the RAB39B gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results