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Symbol
Name
ID
Rab39b
RAB39B, member RAS oncogene family
MGI:1915040
Phenotype annotations related to integument
Darker colors indicate more annotations
Human Phenotypes
Synophrys
Low posterior hairline
Disease(s) Associated with RAB39B
non-syndromic X-linked intellectual disability

Mouse Phenotypes
abnormal skin morphology
Availability Mouse Genotype
Rab39bem1(IMPC)Tcp/Y

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/13/2019
MGI 6.13
The Jackson Laboratory