About Help FAQ

Symbol
Name
ID

Rab27a
RAB27A, member RAS oncogene family
MGI:1861441

Phenotype annotations related to integument

*	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
Availability	Mouse Genotype	integument phenotype	abnormal coat/hair pigmentation	diluted coat color	abnormal skin pigmentation
	Rab27a^ash-N/Rab27a^ash-N
	Rab27a^ash/Rab27a^ash	*
	Rab27a^em1(IMPC)Bay/Rab27a^em1(IMPC)Bay
	Rab27a^m1Anu/Rab27a^m1Anu
	Rab27a^m2Btlr/Rab27a^m2Btlr
	Rab27a^m3Btlr/Rab27a^m3Btlr

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23