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Symbol
Name
ID

Pth1r
parathyroid hormone 1 receptor
MGI:97801

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Chiari malformation	Intellectual disability	Waddling gait	Motor delay	Febrile seizure (within the age range of 3 months to 6 years)
Disease(s) Associated with PTH1R	Chiari malformation	Intellectual disability	Waddling gait	Motor delay
Eiken syndrome
Jansen's metaphyseal chondrodysplasia

Mouse Phenotypes		anastomosis between internal carotid artery and basilar artery	absent segment of posterior cerebral artery	abnormal brain morphology
Availability	Mouse Genotype
	Pth1r^{tm1a(EUCOMM)Hmgu}/Pth1r^{tm1a(EUCOMM)Hmgu}

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 04/30/2024 MGI 6.23