Usp39 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Usp39
ubiquitin specific peptidase 39
MGI:107622

7 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Grhl3^tm1(cre)Cgh/Grhl3⁺ Usp39^em1Imat/Usp39⁺ involves: 129P2/OlaHsd * CD-1	abnormal hair growth	J:324183
	scaly skin	J:324183
	thick skin	J:324183
Grhl3^tm1(cre)Cgh/Grhl3^tm1(cre)Cgh Usp39^em1Imat/Usp39⁺ involves: 129P2/OlaHsd * CD-1	failure of eyelid fusion	J:324183
Uba1^em1Imat/Uba1⁺ Usp39^em1Imat/Usp39^em1Imat CD1-Usp39^em1Imat Uba1^em1Imat	abnormal primitive streak formation	J:324183
Usp39^em1Imat/Usp39⁺ Vangl2^Lp/Vangl2^Lp involves: A * CD-1	abnormal limb development	J:324183
Usp39^em1Imat/Usp39⁺ Vangl2^Lp/Vangl2^Lp involves: A * CD-1	short rostral-caudal axis	J:324183

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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