Lpin2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Lpin2
lipin 2
MGI:1891341

23 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Lpin2^{tm1b(KOMP)Wtsi}/Lpin2^{tm1b(KOMP)Wtsi} C57BL/6N-Lpin2^{tm1b(KOMP)Wtsi}/Tcp	decreased hemoglobin content	J:211773
	decreased mean corpuscular hemoglobin	J:211773
	decreased mean corpuscular hemoglobin concentration	J:211773
	decreased prepulse inhibition	J:211773
	enlarged lymph nodes	J:211773
	hydrometra	J:211773
	increased mean platelet volume	J:211773
	increased red blood cell distribution width	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Lpin2^tm1Reue/Lpin2⁺ involves: C57BL/6J	abnormal gonadal fat pad morphology	J:189894
Lpin2^tm1Reue/Lpin2^tm1Reue involves: C57BL/6J	abnormal cerebellar Purkinje cell layer	J:189894
	abnormal cerebellum morphology	J:189894
	abnormal enzyme/coenzyme activity	J:189894
	abnormal erythrocyte morphology	J:189894
	anemia	J:189894
	ataxia	J:189894
	decreased circulating free fatty acids level	J:189894
	decreased circulating triglyceride level	J:189894
	decreased fasting circulating glucose level	J:189894
	decreased hemoglobin content	J:189894
	normal immune system phenotype	J:189894
	impaired balance	J:189894
	increased liver triglyceride level	J:189894
	increased red blood cell distribution width	J:189894
	tremors	J:189894

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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