Pex10 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Pex10
peroxisomal biogenesis factor 10
MGI:2684988

18 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Pex10^m1Nisw/Pex10⁺ 129S1.B6-Pex10^m1Nisw	abnormal bile salt homeostasis	J:216140
Pex10^m1Nisw/Pex10⁺ 129S1.B6-Pex10^m1Nisw	decreased plasmalogen level	J:216140
Pex10^m1Nisw/Pex10^m1Nisw 129S1.B6-Pex10^m1Nisw	abnormal axon extension	J:216140
	abnormal axon fasciculation	J:216140
	abnormal axon morphology	J:216140
	abnormal bile salt homeostasis	J:216140
	abnormal endplate potential	J:216140
	abnormal neuromuscular synapse morphology	J:216140
	abnormal prenatal movement	J:216140
	ataxia	J:216140
	cyanosis	J:216140
	decreased body size	J:216140
	decreased body weight	J:216140
	decreased plasmalogen level	J:216140
	decreased Schwann cell number	J:216140
	forelimb paralysis	J:216140
	hindlimb paralysis	J:216140
	increased fatty acids level	J:216140
	perinatal lethality, incomplete penetrance	J:216140
	respiratory distress	J:216140

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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