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Symbol
Name
ID
Pls3
plastin 3 (T-isoform)
MGI:104807
Phenotype annotations related to skeleton
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Prominent sternum
Osteoporosis
Disease(s) Associated with PLS3
congenital diaphragmatic hernia
osteoporosis

Mouse Phenotypes
skeleton phenotype
decreased femur compact bone thickness
decreased bone mineral density
increased bone mineral density
decreased bone volume
decreased compact bone area
decreased bone trabecula number
increased bone trabecular spacing
osteoporosis
abnormal skeleton physiology
increased bone resorption
decreased bone stiffness
decreased bone strength
Availability Mouse Genotype
Pls3em1Bult/Pls3em1Bult
Pls3em2Bult/Pls3em2Bult
Pls3tm1d(EUCOMM)Wtsi/Pls3tm1d(EUCOMM)Wtsi *
Pls3em1Bult/Y
Pls3em2Bult/Y
Pls3tm1d(EUCOMM)Wtsi/Y *

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
04/16/2024
MGI 6.23
The Jackson Laboratory