About   Help   FAQ
Symbol
Name
ID
Abcb6
ATP-binding cassette, sub-family B member 6
MGI:1921354
Phenotype annotations related to integument
Darker colors indicate more annotations
Human Phenotypes
Freckling
Hypermelanotic macule
Multiple cafe-au-lait spots
Hyperpigmented/hypopigmented macules
Hypopigmented skin patches
Spotty hypopigmentation
Cutaneous photosensitivity
Macule
Hypopigmented macule
Disease(s) Associated with ABCB6
dyschromatosis universalis hereditaria

Mouse Phenotypes
abnormal vibrissa morphology
Availability Mouse Genotype
Abcb6tm1a(KOMP)Wtsi/Abcb6tm1a(KOMP)Wtsi

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
03/12/2024
MGI 6.23
The Jackson Laboratory