Pkd1l1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Pkd1l1
polycystic kidney disease 1 like 1
MGI:2156538

16 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pkd1l1^rks/Pkd1l1⁺ C3H.B6-Pkd1l1^rks	normal renal/urinary system phenotype	J:170490
Pkd1l1^rks/Pkd1l1^rks C3H.B6-Pkd1l1^rks	abnormal direction of embryo turning	J:170490
	abnormal left-right axis patterning	J:170490
	dextrocardia	J:170490
	edema	J:170490
	normal embryo phenotype	J:170490
	embryonic growth arrest	J:170490
	embryonic growth retardation	J:170490
	lethality throughout fetal growth and development, complete penetrance	J:170490
	right pulmonary isomerism	J:170490
	right-sided stomach	J:170490
Pkd1l1^tm1Lex/Pkd1l1^tm1Lex involves: 129S5/SvEvBrd * C57BL/6Brd	normal embryo phenotype	J:171184
	normal nervous system phenotype	J:171184
	postnatal lethality, incomplete penetrance	J:171184
	normal reproductive system phenotype	J:171184
	normal respiratory system phenotype	J:171184
	situs inversus	J:171184

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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