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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Pkd1l1rks/Pkd1l1+
C3H.B6-Pkd1l1rks
normal renal/urinary system phenotype J:170490
Pkd1l1rks/Pkd1l1rks
C3H.B6-Pkd1l1rks
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
Pkd1l1tm1Lex/Pkd1l1tm1Lex
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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory