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Symbol
Name
ID
Rab27a
RAB27A, member RAS oncogene family
MGI:1861441
Phenotype annotations related to vision/eye
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Iris hypopigmentation
Disease(s) Associated with RAB27A
Griscelli syndrome type 2

Mouse Phenotypes
vision/eye phenotype
increased cornea thickness
abnormal retina inner nuclear layer morphology
Availability Mouse Genotype
Rab27aash/Rab27aash *
Rab27aem1(IMPC)Bay/Rab27aem1(IMPC)Bay

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory