Symbol Name ID |
Pkd1l1
polycystic kidney disease 1 like 1 MGI:2156538 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Polyhydramnios |
Disease(s) Associated with PKD1L1 | |
visceral heterotaxy |
Mouse Phenotypes | embryo phenotype |
abnormal direction of embryo turning |
abnormal left-right axis patterning |
embryonic growth arrest |
embryonic growth retardation |
|
Availability | Mouse Genotype | |||||
Pkd1l1rks/Pkd1l1rks | * | |||||
Pkd1l1tm1Lex/Pkd1l1tm1Lex | * |
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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