Nlrp2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Nlrp2
NLR family, pyrin domain containing 2
MGI:3041206

18 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nlrp2^tm1.2Itl/Nlrp2^tm1.2Itl involves: C57BL/6	abnormal blastocyst formation	J:237496
	abnormal preimplantation embryo development	J:237496
	normal cellular phenotype	J:237496
	decreased litter size	J:237496
	normal immune system phenotype	J:237496
	maternal effect	J:237496
	reduced female fertility	J:237496
Nlrp2^{tm1a(KOMP)Wtsi}/Nlrp2^{tm1a(KOMP)Wtsi} Not Specified	abnormal granulosa cell morphology	J:275254
	abnormal oocyte morphology	J:275254
	abnormal ovarian follicle morphology	J:275254
	decreased fertilization frequency	J:275254
	decreased secondary ovarian follicle number	J:275254
	increased atretic ovarian follicle number	J:275254
	maternal effect	J:275254
	normal reproductive system phenotype	J:275254
Nlrp2^{tm1b(KOMP)Wtsi}/Nlrp2^{tm1b(KOMP)Wtsi} C57BL/6N-Nlrp2^{tm1b(KOMP)Wtsi}/BayMmucd	abnormal eye anterior chamber depth	J:211773
	abnormal retina outer nuclear layer morphology	J:211773
	abnormal skin coloration	J:211773
	increased total retina thickness	J:211773

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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