Symbol Name ID |
Fgfr1
fibroblast growth factor receptor 1 MGI:95522 |
Darker colors indicate more annotations |
Human Phenotypes | Posterior fossa cyst |
Abnormality of the sense of smell |
Anosmia |
Hyposmia |
Hydrocephalus |
Ventriculomegaly |
Agenesis of corpus callosum |
Absent septum pellucidum |
Megalencephaly |
Abnormal morphology of the limbic system |
Aplasia of the olfactory bulb |
Cerebellar hypoplasia |
Chiari malformation |
Chiari type I malformation |
Arachnoid cyst |
Delayed speech and language development |
Intellectual disability |
Bimanual synkinesia |
Disease(s) Associated with FGFR1 | ||||||||||||||||||
acrocephalosyndactylia | ||||||||||||||||||
hypogonadotropic hypogonadism 2 with or without anosmia | ||||||||||||||||||
hypogonadotropic hypogonadism 7 with or without anosmia | ||||||||||||||||||
osteoglophonic dysplasia | ||||||||||||||||||
Pfeiffer syndrome |
Mouse Phenotypes | abnormal axon guidance |
abnormal neuronal migration |
abnormal neural plate morphology |
abnormal neural tube morphology |
abnormal neural crest cell morphology |
abnormal neural tube closure |
spina bifida |
craniorachischisis |
kinked neural tube |
abnormal cochlear hair cell development |
abnormal cochlear hair cell morphology |
decreased cochlear hair cell number |
decreased cochlear outer hair cell number |
absent cochlear outer hair cells |
increased cochlear inner hair cell number |
abnormal orientation of inner hair cell stereociliary bundles |
abnormal cochlear nerve compound action potential |
abnormal brain morphology |
abnormal cerebellum development |
abnormal brain commissure morphology |
abnormal dorsal telencephalic commissure morphology |
abnormal corpus callosum morphology |
abnormal hippocampal commissure morphology |
abnormal midbrain morphology |
absent inferior colliculus |
decreased inferior colliculus size |
abnormal locus ceruleus morphology |
abnormal frontal lobe morphology |
abnormal cerebellum morphology |
abnormal cerebellum vermis morphology |
absent cerebellum vermis |
abnormal astrocyte morphology |
abnormal neuron morphology |
abnormal motor neuron morphology |
decreased neuron number |
abnormal trochlear nerve morphology |
abnormal hypothalamus secretion |
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Availability | Mouse Genotype | |||||||||||||||||||||||||||||||||||||
Fgfr1tm1.1Upir/Fgfr1tm1.1Upir | ||||||||||||||||||||||||||||||||||||||
Fgfr1tm1Cxd/Fgfr1tm1Cxd | ||||||||||||||||||||||||||||||||||||||
Fgfr1tm1Jrt/Fgfr1tm1Jrt | ||||||||||||||||||||||||||||||||||||||
Fgfr1tm1Led/Fgfr1tm1Led | ||||||||||||||||||||||||||||||||||||||
Fgfr1tm2Jrt/Fgfr1tm2Jrt | ||||||||||||||||||||||||||||||||||||||
Fgfr1tm3.1Sor/Fgfr1tm3.1Sor | ||||||||||||||||||||||||||||||||||||||
Fgfr1tm5.2Sor/Fgfr1tm5.2Sor | ||||||||||||||||||||||||||||||||||||||
Fgfr1tm6Jrt/Fgfr1tm6Jrt | ||||||||||||||||||||||||||||||||||||||
Tg(Gnrh1-Fgfr1)1Tsai/Tg(Gnrh1-Fgfr1)1Tsai | ||||||||||||||||||||||||||||||||||||||
Fgfr1Hspy/Fgfr1+ | ||||||||||||||||||||||||||||||||||||||
En1tm2(cre)Wrst/En1+ Fgfr1tm1Jpa/Fgfr1tm1Jpa (conditional) |
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Fgfr1tm1Jpa/Fgfr1tm1Jpa H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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Fgfr1tm1Upir/Fgfr1tm1Upir Tg(GFAP-cre)25Mes/0 (conditional) |
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Fgfr1tm1Upir/Fgfr1tm1Upir Tg(Nes-cre)1Kln/0 (conditional) |
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Fgfr1tm1Upir/Fgfr1tm1Upir Tg(Mnx1-GFP)1Slp/? Tg(Nes-cre)1Kln/? (conditional) |
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Fgfr1tm3.2Cxd/Fgfr1tm3.2Cxd Tg(T-cre)1Lwd/0 (conditional) |
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Fgfr1tm1Upir/Fgfr1tm1.1Upir Foxg1tm1(cre)Skm/Foxg1+ (conditional) |
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Fgfr1tm3.1Cxd/Fgfr1tm3.2Cxd Tg(T-cre)1Lwd/0 (conditional) |
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 07/05/2024 MGI 6.24 |
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