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Symbol
Name
ID

Fgfr3
fibroblast growth factor receptor 3
MGI:95524

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Feeding difficulties	Feeding difficulties in infancy	Bowel incontinence	Urinary incontinence	Autism	Attention deficit hyperactivity disorder
Disease(s) Associated with FGFR3	Decreased fetal movement	Feeding difficulties	Feeding difficulties in infancy	Bowel incontinence	Urinary incontinence	Autism	Attention deficit hyperactivity disorder
achondroplasia
craniosynostosis
Muenke Syndrome
SADDAN
thanatophoric dysplasia

Mouse Phenotypes		abnormal behavior	absent gastric milk in neonates	abnormal gait
Availability	Mouse Genotype	abnormal behavior	absent gastric milk in neonates	abnormal gait
	Fgfr3^tm1Dor/Fgfr3^tm1Dor
	Fgfr3^tm1Led/Fgfr3^tm1Led
	Fgfr3^tm3Cxd/Fgfr3^tm3Cxd
	Fgfr3^tm5Cxd/Fgfr3^tm5Cxd

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 04/16/2024 MGI 6.23