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Symbol
Name
ID
Pkd1
polycystin 1, transient receptor potential channel interacting
MGI:97603
Phenotype annotations related to craniofacial
Darker colors indicate more annotations

Mouse Phenotypes
abnormal craniofacial bone morphology
abnormal sagittal suture morphology
abnormal basicranium morphology
abnormal Meckel's cartilage morphology
abnormal presphenoid synchondrosis
premature presphenoid synchondrosis closure
abnormal sphenooccipital synchondrosis
premature sphenooccipital synchondrosis closure
premature cranial synchondrosis closure
short frontal bone
abnormal sphenoid bone morphology
short presphenoid bone
malocclusion
short mandible
short premaxilla
maxilla hypoplasia
short maxilla
micrognathia
nasal bone hypoplasia
short nasal bone
domed cranium
short snout
Availability Mouse Genotype
Pkd1b2b1585Clo/Pkd1b2b1585Clo
Pkd1tm1Rsa/Pkd1tm1Rsa
Tg(Pkd1)26Mtru/0
Pkd1tm3Jzh/Pkd1tm3Jzh
H2az2Tg(Wnt1-cre)11Rth/H2az2+  (conditional)
Pkd1tm3Jzh/Pkd1tm3Jzh  (conditional)
Pkd1tm3Jzh/Pkd1tm3Jzh
Tg(Col2a1-cre)10Amc/0  (conditional)

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
04/16/2024
MGI 6.23
The Jackson Laboratory