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Symbol
Name
ID

Trip13
thyroid hormone receptor interactor 13
MGI:1916966

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Microcephaly	Arthrogryposis multiplex congenita
Disease(s) Associated with TRIP13	Microcephaly	Arthrogryposis multiplex congenita
mosaic variegated aneuploidy syndrome 3

Mouse Phenotypes		abnormal bone structure	decreased bone mineral content	decreased bone mineral density
Availability	Mouse Genotype	abnormal bone structure	decreased bone mineral content	decreased bone mineral density
	Trip13^em1(IMPC)J/Trip13^em1(IMPC)J
	Trip13^{tm1.1(KOMP)Vlcg}/Trip13^{tm1.1(KOMP)Vlcg}

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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