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Symbol
Name
ID

Atp6v1b1
ATPase, H+ transporting, lysosomal V1 subunit B1
MGI:103285

Phenotype annotations related to nervous system

!	Indicates phenotype varies with strain background.
	Darker colors indicate more annotations

Human Phenotypes	Periodic paralysis
Disease(s) Associated with ATP6V1B1	Periodic paralysis
renal tubular acidosis

Mouse Phenotypes		decreased cochlear outer hair cell number
Availability	Mouse Genotype	decreased cochlear outer hair cell number
	Atp6v1b1^vtx/Atp6v1b1^vtx	!

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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