Prl7b1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Prl7b1
prolactin family 7, subfamily b, member 1
MGI:1922846

6 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Prl7b1^{tm1(KOMP)Vlcg}/Prl7b1^{tm1(KOMP)Vlcg} involves: C57BL/6NTac	abnormal placenta vasculature	J:236336
	increased fetal weight	J:236336
	maternal effect	J:236336
	normal reproductive system phenotype	J:236336
Prl7b1^{tm1.1(KOMP)Vlcg}/Prl7b1^{tm1.1(KOMP)Vlcg} C57BL/6N-Prl7b1^{tm1.1(KOMP)Vlcg}/Ucd	increased circulating alanine transaminase level	J:211773
	increased circulating aspartate transaminase level	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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