Pkd1l1 Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 11/12/2024 MGI 6.24