Usp42 Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 11/19/2024 MGI 6.24