3billion
back to listBack to List

RAP1B

RAP1B, member of RAS oncogene family

HCNC Approved Symbol
RAP1B (HGNC:9857)
Genomic Coordinates
12:68,610,899 - 68,671,901 (12q15)
Synonyms
K-REV, RAL1B, DKFZp586H0723
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies
620654AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the RAP1B gene.

Frequently observed phenotypes

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

No Results