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Symbol
Name
ID
Fgfr3
fibroblast growth factor receptor 3
MGI:95524
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Increased nuchal translucency
Short neck
Rhizomelia
Hepatosplenomegaly
Protuberant abdomen
Inguinal hernia
Umbilical hernia
Short stature
Disproportionate short stature
Disproportionate short-limb short stature
Childhood onset short-limb short stature
Lethal short-limbed short stature
Neonatal short-limb short stature
Severe short stature
Tall stature
Intrauterine growth retardation
Disease(s) Associated with FGFR3
achondroplasia
camptodactyly-tall stature-scoliosis-hearing loss syndrome
craniosynostosis
hypochondroplasia
Muenke Syndrome
SADDAN
thanatophoric dysplasia

Mouse Phenotypes
long incisors
misaligned incisors
malocclusion
short nasal bone
abnormal palatine bone horizontal plate morphology
midface hypoplasia
abnormal snout morphology
small snout
short snout
round head
decreased body weight
small thoracic cavity
abnormal head size
megacephaly
abnormal postnatal growth/weight/body size
decreased body length
decreased body size
disproportionate dwarf
proportional dwarf
Availability Mouse Genotype
Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw
Fgfr3tm1Cxd/Fgfr3tm1Cxd
Fgfr3tm1Dor/Fgfr3tm1Dor
Fgfr3tm1Led/Fgfr3tm1Led
Fgfr3tm3.1Cxd/Fgfr3tm3.1Cxd
Fgfr3tm3Cxd/Fgfr3tm3Cxd
Fgfr3tm5Cxd/Fgfr3tm5Cxd
Tg(Col2a1-Fgfr3/GH)ADor/Tg(Col2a1-Fgfr3/GH)ADor
Fgfr3tm1.1Aomw/Fgfr3+
Fgfr3tm1.1Iwa/Fgfr3+
Fgfr3tm1Cxd/Fgfr3+
Fgfr3tm1Llm/Fgfr3+
Fgfr3tm2Wei/Fgfr3+
Fgfr3tm3.1Cxd/Fgfr3+
Fgfr3tm3.1Llm/Fgfr3+
Fgfr3tm4.1Cxd/Fgfr3+
Fgfr3tm5.1Cxd/Fgfr3+
Tg(Col2a1-Fgfr3/GH)BDor/0
Fgfr3tm2Llm/Fgfr3+
Tg(CMV-cre)1Ipc/?  (conditional)
Fgfr3tm2Llm/Fgfr3+
Tg(Col2a1-cre)1Bhr/?  (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
05/21/2024
MGI 6.23
The Jackson Laboratory