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Symbol
Name
ID
Vps33b
vacuolar protein sorting 33B
MGI:2446237
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Microcephaly
Arthrogryposis multiplex congenita
Delayed skeletal maturation
Hip dysplasia
Reduced bone mineral density
Disease(s) Associated with VPS33B
arthrogryposis, renal dysfunction, and cholestasis 1
progressive familial intrahepatic cholestasis

Mouse Phenotypes
abnormal tendon collagen fibril morphology
abnormal thoracic cage shape
Availability Mouse Genotype
Vps33btm1a(EUCOMM)Wtsi/Vps33b+
Vps33btm1.1Arte/Vps33btm1.1Arte
Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+  (conditional)

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory