Symbol Name ID |
Rab27a
RAB27A, member RAS oncogene family MGI:1861441 |
* | 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 |
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 |
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