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 | Petechiae |
Jaundice |
Hypopigmentation of hair |
Silver-gray hair |
Melanin pigment aggregation in hair shafts |
Premature graying of hair |
Accumulation of melanosomes in melanocytes |
Hypopigmentation of the skin |
Partial albinism |
Disease(s) Associated with RAB27A | |||||||||
Griscelli syndrome type 2 |
Mouse Phenotypes | integument phenotype |
abnormal coat/hair pigmentation |
diluted coat color |
abnormal skin pigmentation |
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Availability | Mouse Genotype | ||||
Rab27aash-N/Rab27aash-N | |||||
Rab27aash/Rab27aash | * | ||||
Rab27aem1(IMPC)Bay/Rab27aem1(IMPC)Bay | |||||
Rab27am1Anu/Rab27am1Anu | |||||
Rab27am2Btlr/Rab27am2Btlr | |||||
Rab27am3Btlr/Rab27am3Btlr |
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 06/12/2024 MGI 6.13 |
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