Rprd2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Rprd2
regulation of nuclear pre-mRNA domain containing 2
MGI:1922387

19 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Rprd2^em1(IMPC)J/Rprd2⁺ C57BL/6NJ-Rprd2^em1(IMPC)J/Mmjax	abnormal coat/hair pigmentation	J:211773
Rprd2^em1(IMPC)J/Rprd2⁺ C57BL/6NJ-Rprd2^em1(IMPC)J/Mmjax	abnormal locomotor behavior	J:211773
Rprd2^em1(IMPC)J/Rprd2^em1(IMPC)J C57BL/6NJ-Rprd2^em1(IMPC)J/Mmjax	abnormal amniotic cavity morphology	J:374598
	abnormal chorioallantoic fusion	J:374598
	abnormal head shape	J:374598
	abnormal heart morphology	J:374598
	abnormal placenta development	J:374598
	abnormal placenta labyrinth morphology	J:374598
	abnormal trophoblast layer morphology	J:374598
	abnormal visceral yolk sac morphology	J:374598
	decreased spongiotrophoblast size	J:374598
	embryonic growth retardation	J:211773, J:374598
	embryonic lethality during organogenesis, complete penetrance	J:374598
	embryonic lethality prior to tooth bud stage	J:211773
	failure of initiation of embryo turning	J:374598
	incomplete embryo turning	J:374598
	incomplete rostral neuropore closure	J:374598
	kinked neural tube	J:374598
	preweaning lethality, complete penetrance	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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