Usp42 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Usp42
ubiquitin specific peptidase 42
MGI:1924050

16 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} B6JTyr;B6N-Usp42^{tm2a(EUCOMM)Wtsi}/Wtsi	abnormal behavior	J:175295
	decreased body length	J:175295
	decreased body weight	J:175295
	decreased lean body mass	J:175295
	decreased lumbar vertebrae number	J:175295
	hyperactivity	J:175295
	increased sacral vertebrae number	J:175295
	male infertility	J:211773
	thrombocytopenia	J:175295
Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} involves: C57BL/6 * C57BL/6N	abnormal behavior	J:213427
	abnormal fertility/fecundity	J:213427
	abnormal lens morphology	J:213427
	cataract	J:213427
	hyperactivity	J:213427
	increased CD4-positive, alpha-beta T cell number	J:213427
	increased T cell number	J:213427
	oligozoospermia	J:213427
	testis degeneration	J:213427

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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