Symbol Name ID |
Pkd1l1
polycystic kidney disease 1 like 1 MGI:2156538 |
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 |
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 08/02/2024 MGI 6.24 |
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