Uchl1 Phenotype Annotations - Multigenic Genotypes

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Uchl1
ubiquitin carboxy-terminal hydrolase L1
MGI:103149

13 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Tg(Thy1-Snca)1S13Putt/0 Uchl1^tm1Dgen/Uchl1^tm1Dgen involves: 129P2/OlaHsd * C57BL/6	alpha-synuclein inclusion body	J:207278
	astrocytosis	J:207278
	decreased grip strength	J:207278
	impaired coordination	J:207278
	premature death	J:207278
Uchl1^gad/Uchl1^gad Uchl3^tm1Tilg/Uchl3^tm1Tilg involves: 129S1/Sv * C57BL/6J * CBA/Nga * RFM/Nga	abnormal dorsal root ganglion morphology	J:71819
	abnormal gait	J:71819
	ataxia	J:71819
	axon degeneration	J:71819
	axonal dystrophy	J:71819
	decreased body weight	J:71819
	dysphagia	J:71819
	paralysis	J:71819
	premature death	J:71819

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 11/12/2024 MGI 6.24