Fgfr1 (fibroblast growth factor receptor 1) - Rat Genome Database

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Gene: Fgfr1 (fibroblast growth factor receptor 1) Mus musculus
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Symbol: Fgfr1
Name: fibroblast growth factor receptor 1
RGD ID: 732291
MGI Page MGI
Description: Enables SH2 domain binding activity; fibroblast growth factor binding activity; and fibroblast growth factor receptor activity. Involved in several processes, including cementum mineralization; diphosphate metabolic process; and forebrain development. Acts upstream of or within several processes, including ear development; positive regulation of cell population proliferation; and regulation of animal organ morphogenesis. Located in plasma membrane. Is expressed in several structures, including alimentary system; central nervous system; embryo mesenchyme; genitourinary system; and sensory organ. Used to study Pfeiffer syndrome; atopic dermatitis; and otitis media. Human ortholog(s) of this gene implicated in several diseases, including Jackson-Weiss syndrome; bone disease (multiple); carcinoma (multiple); hematologic cancer (multiple); and hypogonadotropic hypogonadism (multiple). Orthologous to human FGFR1 (fibroblast growth factor receptor 1).
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: AW208770; basic fibroblast growth factor receptor 1; bFGF-R-1; c-fgr; Ea; Eask; FGFR; Fgfr-; Fgfr-1; FGFR-I; FLG; Flt-; Flt-2; Fr; Fr1; Hs; Hspy; MFR; proto-oncogene c-Fgr
RGD Orthologs
Human
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Latest Assembly: GRCm39 - Mouse Genome Assembly GRCm39
Position:
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39826,008,808 - 26,067,819 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl826,003,670 - 26,065,734 (+)EnsemblGRCm39 Ensembl
GRCm38825,518,759 - 25,575,718 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl825,513,654 - 25,575,718 (+)EnsemblGRCm38mm10GRCm38
MGSCv37826,629,244 - 26,686,186 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36826,997,826 - 27,039,466 (+)NCBIMGSCv36mm8
Celera826,986,822 - 27,044,074 (+)NCBICelera
Cytogenetic Map8A2NCBI
cM Map814.12NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View
acoustic neuroma  (ISO)
acrocephalosyndactylia  (ISO)
Acute Lymphoblastic Leukemia, with Lymphomatous Features  (ISO)
acute myeloid leukemia  (ISO)
Acute Otitis Media  (IEP)
Alzheimer's disease  (ISO)
amenorrhea  (ISO)
atypical chronic myeloid leukemia  (ISO)
Breast Neoplasms  (ISO)
Burns  (ISO)
cerebellar hypoplasia  (ISO)
cleft lip  (ISO)
cleft palate  (ISO)
Congenital Foot Deformities  (ISO)
Craniofacial Abnormalities  (IMP,ISO)
craniosynostosis  (IMP,ISO)
Craniosynostosis Syndrome, Autosomal Recessive  (ISO)
Delayed Puberty  (ISO)
demyelinating disease  (IEP)
depressive disorder  (ISO)
disease of cellular proliferation  (ISO)
Encephalocraniocutaneous Lipomatosis  (ISO)
Experimental Arthritis  (IMP)
Experimental Leukemia  (ISO)
Experimental Liver Cirrhosis  (ISO)
fatty liver disease  (ISO)
Femoral Fractures  (ISO)
fibrolamellar carcinoma  (ISO)
gastric adenocarcinoma  (ISO)
genetic disease  (ISO)
glioblastoma  (ISO)
heart valve disease  (ISO)
hepatocellular carcinoma  (ISO)
hereditary spastic paraplegia 54  (ISO)
high grade glioma  (ISO)
holoprosencephaly  (ISO)
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  (ISO)
Hypoglossal Nerve Injuries  (ISO)
hypogonadism  (ISO)
hypogonadotropic hypogonadism  (ISO)
hypogonadotropic hypogonadism 2 with or without anosmia  (ISO)
hypogonadotropic hypogonadism 7 with or without anosmia  (ISO)
Hypogonadotropic Hypogonadism and Anosmia, Autosomal Dominant  (ISO)
infertility  (ISO)
Jackson-Weiss syndrome  (ISO)
Kallmann syndrome  (ISO)
Klinefelter syndrome  (ISO)
limb ischemia  (ISO)
Liver Metastasis  (ISO)
Lung Neoplasms  (ISO)
lung non-small cell carcinoma  (ISO)
lung small cell carcinoma  (ISO)
malignant astrocytoma  (ISO)
Martsolf syndrome 1  (ISO)
medulloblastoma  (ISO)
mesangial proliferative glomerulonephritis  (ISO)
mouth disease  (ISO)
myeloid leukemia  (ISO)
myeloid neoplasm  (ISO)
myocardial infarction  (IEP)
Neointima  (ISO)
Neoplasm Metastasis  (IMP)
neuroblastoma  (ISO)
non-alcoholic fatty liver disease  (IEP)
Nonsyndromic Trigonocephaly  (ISO)
obesity  (ISO)
osteoarthritis  (ISO)
Osteoarthritis, Experimental  (IMP)
osteoglophonic dysplasia  (ISO)
otitis media  (IAGP)
paraplegia  (ISO)
Penetrating Head Injuries  (ISO)
Pfeiffer syndrome  (IAGP,ISO)
pilomyxoid astrocytoma  (ISO)
prostate adenocarcinoma  (IDA,IEP)
prostate cancer  (ISO)
prostate carcinoma in situ  (IDA)
pulmonary hypertension  (ISO)
renal cell carcinoma  (ISO)
retinal detachment  (ISO)
rosette-forming glioneuronal tumor  (ISO)
schizophrenia  (ISO)
sciatic neuropathy  (ISO)
squamous cell carcinoma  (ISO)
Stargardt Disease 3  (IEP)
T-cell non-Hodgkin lymphoma  (ISO)
transient cerebral ischemia  (ISO)
transitional cell carcinoma  (ISO)
Trigonocephaly 1  (ISO)
Tympanic Membrane Perforation  (ISO)
type 2 diabetes mellitus  (IMP)
umbilical hernia  (IMP)
vascular dementia  (ISO)
visual epilepsy  (ISO)

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(S)-amphetamine  (EXP)
1,1-dichloroethene  (EXP)
1,2-dichloroethane  (EXP)
1,2-dimethylhydrazine  (EXP)
17beta-estradiol  (ISO)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,3',4,4',5-Pentachlorobiphenyl  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2-amino-2-deoxy-D-glucopyranose  (ISO)
3,3',5-triiodo-L-thyronine  (EXP,ISO)
3,4-methylenedioxymethamphetamine  (EXP)
3-isobutyl-1-methyl-7H-xanthine  (EXP,ISO)
3-methylcholanthrene  (EXP)
4,4'-sulfonyldiphenol  (ISO)
4-hydroxynon-2-enal  (ISO)
4-hydroxyphenyl retinamide  (EXP)
5-aza-2'-deoxycytidine  (EXP,ISO)
6-propyl-2-thiouracil  (ISO)
acrolein  (ISO)
acrylamide  (ISO)
actinomycin D  (ISO)
Aflatoxin B2 alpha  (ISO)
aldehydo-D-glucosamine  (ISO)
all-trans-retinoic acid  (EXP,ISO)
alpha-pinene  (ISO)
ammonium chloride  (ISO)
antirheumatic drug  (ISO)
AP20187  (EXP)
arsenous acid  (ISO)
benzo[a]pyrene  (ISO)
beta-D-glucosamine  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
Butylparaben  (ISO)
cadmium atom  (ISO)
cadmium dichloride  (ISO)
calcitriol  (ISO)
calcium atom  (ISO)
calcium(0)  (ISO)
capsaicin  (ISO)
carbamazepine  (ISO)
CGP 52608  (ISO)
chlorpromazine  (ISO)
choline  (EXP)
cisplatin  (EXP,ISO)
cocaine  (ISO)
colforsin daropate hydrochloride  (ISO)
copper atom  (ISO)
copper(0)  (ISO)
copper(II) chloride  (ISO)
coumestrol  (ISO)
crizotinib  (ISO)
crocidolite asbestos  (ISO)
Cuprizon  (ISO)
cycloheximide  (ISO)
cyclosporin A  (ISO)
decabromodiphenyl ether  (ISO)
dexamethasone  (EXP,ISO)
dextran sulfate  (EXP)
diarsenic trioxide  (ISO)
diazinon  (ISO)
dibutyl phthalate  (ISO)
diclofenac  (ISO)
dieldrin  (ISO)
dimethylarsinous acid  (ISO)
diuron  (ISO)
dorsomorphin  (ISO)
doxorubicin  (ISO)
ellagic acid  (ISO)
entinostat  (ISO)
enzacamene  (ISO)
ethanol  (EXP,ISO)
ethyl trans-caffeate  (ISO)
fenamidone  (EXP)
folic acid  (EXP,ISO)
formaldehyde  (ISO)
fulvestrant  (ISO)
furan  (ISO)
gamma-tocopherol  (ISO)
heparan sulfate  (EXP,ISO)
heparin  (EXP,ISO)
hydrogen peroxide  (ISO)
indometacin  (ISO)
inulin  (EXP)
isotretinoin  (ISO)
kainic acid  (ISO)
L-methionine  (EXP)
lead diacetate  (ISO)
lenalidomide  (ISO)
malathion  (ISO)
methotrexate  (ISO)
methylmercury chloride  (EXP,ISO)
morphine  (ISO)
N-methyl-N-nitrosourea  (ISO)
N-nitrosodiethylamine  (EXP)
orantinib  (ISO)
oxaliplatin  (ISO)
ozone  (EXP,ISO)
paracetamol  (ISO)
paraoxon  (ISO)
PD-166866  (ISO)
PD173074  (ISO)
perfluorooctane-1-sulfonic acid  (EXP)
peroxynitrous acid  (ISO)
piperine  (ISO)
pirinixic acid  (ISO)
pomalidomide  (ISO)
ponatinib  (ISO)
resveratrol  (ISO)
Salinomycin  (ISO)
SB 431542  (ISO)
sodium arsenate  (EXP)
sodium arsenite  (ISO)
sodium dichromate  (ISO)
streptozocin  (ISO)
sunitinib  (ISO)
tamibarotene  (ISO)
tamoxifen  (ISO)
taurine  (ISO)
testosterone  (EXP)
tetrachloromethane  (EXP)
thalidomide  (ISO)
titanium dioxide  (EXP)
tocopherol  (ISO)
topotecan  (ISO)
trichloroethene  (ISO)
triptonide  (EXP)
urea  (ISO)
urethane  (ISO)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
vorinostat  (ISO)
zinc protoporphyrin  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
angiogenesis  (IGI)
auditory receptor cell development  (IMP)
blood vessel morphogenesis  (IMP)
brain development  (IMP)
branching involved in salivary gland morphogenesis  (IMP)
calcium ion homeostasis  (IGI)
cardiac muscle cell proliferation  (IGI)
cell maturation  (IMP)
cell population proliferation  (IGI)
cellular response to histamine  (ISO)
cellular response to lipopolysaccharide  (ISO)
cellular response to nerve growth factor stimulus  (ISO)
cementum mineralization  (IDA,IMP)
central nervous system neuron development  (ISO)
chondrocyte differentiation  (IGI)
diphosphate metabolic process  (IDA,IMP)
ear development  (IMP)
embryonic limb morphogenesis  (IMP)
epithelial to mesenchymal transition  (ISO)
female pregnancy  (ISO)
fibroblast growth factor receptor signaling pathway  (IGI,ISO)
fibroblast growth factor receptor signaling pathway involved in orbitofrontal cortex development  (IMP)
gene expression  (IDA,IMP)
generation of neurons  (IMP)
in utero embryonic development  (IGI)
inner ear morphogenesis  (IMP)
lung development  (IGI,IMP)
lung-associated mesenchyme development  (IGI)
mesenchymal cell differentiation  (IGI)
mesenchymal cell proliferation  (IGI,IMP)
midbrain development  (IGI,IMP)
middle ear morphogenesis  (IMP)
motogenic signaling involved in postnatal olfactory bulb interneuron migration  (ISO)
negative regulation of fibroblast growth factor production  (IGI)
negative regulation of gene expression  (IGI,IMP)
negative regulation of osteoblast differentiation  (ISO)
negative regulation of transcription by RNA polymerase II  (IMP)
neuron projection development  (IGI,ISO)
orbitofrontal cortex development  (IMP)
organ induction  (IMP)
outer ear morphogenesis  (IMP)
paraxial mesoderm development  (IGI)
peptidyl-tyrosine phosphorylation  (ISO)
phosphorylation  (IEA)
positive regulation of blood vessel endothelial cell migration  (ISO)
positive regulation of cardiac muscle cell proliferation  (IGI,ISO)
positive regulation of cell cycle  (IMP)
positive regulation of cell differentiation  (IBA)
positive regulation of cell population proliferation  (IDA,IGI,IMP,ISO,TAS)
positive regulation of endothelial cell chemotaxis to fibroblast growth factor  (ISO)
positive regulation of fibroblast migration  (ISO)
positive regulation of hepatic stellate cell activation  (ISO)
positive regulation of kinase activity  (IBA)
positive regulation of MAP kinase activity  (ISO)
positive regulation of MAPK cascade  (ISO)
positive regulation of MAPKKK cascade by fibroblast growth factor receptor signaling pathway  (IGI)
positive regulation of mesenchymal cell proliferation  (IGI,IMP,ISO)
positive regulation of mitotic cell cycle DNA replication  (IDA)
positive regulation of neuron differentiation  (ISO)
positive regulation of neuron projection development  (IGI,ISO)
positive regulation of parathyroid hormone secretion  (IGI)
positive regulation of phospholipase C activity  (ISO)
positive regulation of protein kinase B signaling  (ISO)
positive regulation of stem cell proliferation  (IGI,IMP)
positive regulation of transcription by RNA polymerase II  (ISO)
positive regulation of vascular endothelial cell proliferation  (ISO)
protein autophosphorylation  (ISO)
protein phosphorylation  (IEA)
regulation of branching involved in salivary gland morphogenesis by mesenchymal-epithelial signaling  (IDA)
regulation of cell population proliferation  (ISO)
regulation of epithelial cell proliferation  (IMP)
regulation of extrinsic apoptotic signaling pathway in absence of ligand  (IMP)
regulation of gene expression  (IMP)
regulation of lateral mesodermal cell fate specification  (IGI)
regulation of phosphate transport  (IGI)
regulation of phosphorus metabolic process  (IGI)
regulation of stem cell proliferation  (ISO)
response to ischemia  (ISO)
response to nutrient levels  (ISO)
response to sodium phosphate  (IDA,IGI)
salivary gland morphogenesis  (IMP)
sensory perception of sound  (IMP)
stem cell differentiation  (IGI)
stem cell population maintenance  (ISO)
stem cell proliferation  (IGI,IMP)
transmembrane receptor protein tyrosine kinase signaling pathway  (IBA)
ureteric bud development  (IGI)
vasculogenesis involved in coronary vascular morphogenesis  (TAS)
ventricular zone neuroblast division  (IMP)
vitamin D3 metabolic process  (IGI)

Cellular Component

Phenotype Annotations     Click to see Annotation Detail View

Mammalian Phenotype
abnormal alisphenoid bone morphology  (IAGP)
abnormal apical ectodermal ridge morphology  (IAGP)
abnormal astrocyte morphology  (IAGP)
abnormal auditory bulla morphology  (IAGP)
abnormal axial skeleton morphology  (IAGP)
abnormal axon guidance  (IAGP)
abnormal basisphenoid bone morphology  (IAGP)
abnormal blastocyst morphology  (IAGP)
abnormal brain commissure morphology  (IAGP)
abnormal brain morphology  (IAGP)
abnormal carpal bone morphology  (IAGP)
abnormal cartilage development  (IAGP)
abnormal cerebellum development  (IAGP)
abnormal cerebellum morphology  (IAGP)
abnormal cerebellum vermis morphology  (IAGP)
abnormal cervical axis morphology  (IAGP)
abnormal chemokine level  (IAGP)
abnormal chorion morphology  (IAGP)
abnormal cochlea morphology  (IAGP)
abnormal cochlear hair cell development  (IAGP)
abnormal cochlear hair cell morphology  (IAGP)
abnormal cochlear nerve compound action potential  (IAGP)
abnormal cochlear sensory epithelium morphology  (IAGP)
abnormal corpus callosum morphology  (IAGP)
abnormal craniofacial bone morphology  (IAGP)
abnormal craniofacial morphology  (IAGP)
abnormal developmental patterning  (IAGP)
abnormal digestive system physiology  (IAGP)
abnormal digit morphology  (IAGP)
abnormal dorsal telencephalic commissure morphology  (IAGP)
abnormal ear physiology  (IAGP)
abnormal ear position  (IEA)
abnormal ear shape  (IAGP)
abnormal egg cylinder morphology  (IAGP)
abnormal embryo development  (IAGP)
abnormal embryo size  (IEA)
abnormal embryonic autopod plate morphology  (IAGP)
abnormal embryonic epiblast morphology  (IAGP)
abnormal embryonic growth/weight/body size  (IAGP)
abnormal embryonic tissue morphology  (IAGP)
abnormal embryonic-extraembryonic boundary morphology  (IAGP)
abnormal epidermal layer morphology  (IAGP)
abnormal epidermis stratum granulosum morphology  (IAGP)
abnormal extraembryonic tissue morphology  (IAGP)
abnormal fetal cardiomyocyte proliferation  (IAGP)
abnormal forelimb bud morphology  (IAGP)
abnormal forelimb morphology  (IAGP)
abnormal forelimb stylopod morphology  (IAGP)
abnormal forelimb zeugopod morphology  (IAGP)
abnormal frontal lobe morphology  (IAGP)
abnormal gait  (IAGP)
abnormal gastrulation  (IAGP)
abnormal gastrulation movements  (IAGP)
abnormal hair cycle  (IAGP)
abnormal hair follicle morphology  (IAGP)
abnormal head fold morphology  (IAGP)
abnormal head mesenchyme morphology  (IAGP)
abnormal heart development  (IAGP)
abnormal heart tube morphology  (IAGP)
abnormal hindlimb morphology  (IAGP)
abnormal hippocampal commissure morphology  (IAGP)
abnormal hyoid bone lesser horn morphology  (IAGP)
abnormal incudostapedial joint morphology  (IAGP)
abnormal incus body morphology  (IAGP)
abnormal incus long process morphology  (IAGP)
abnormal incus morphology  (IAGP)
abnormal incus short process morphology  (IAGP)
abnormal inner ear morphology  (IAGP)
abnormal kidney development  (IAGP)
abnormal lateral plate mesoderm morphology  (IAGP)
abnormal limb development  (IAGP)
abnormal limb morphology  (IAGP)
abnormal locus ceruleus morphology  (IAGP)
abnormal malleus morphology  (IAGP)
abnormal mast cell morphology  (IAGP)
abnormal maxillary-premaxillary suture morphology  (IAGP)
abnormal medial nasal prominence morphology  (IAGP)
abnormal mesoderm development  (IAGP)
abnormal metanephric mesenchyme morphology  (IAGP)
abnormal midbrain morphology  (IAGP)
abnormal middle ear morphology  (IAGP)
abnormal middle ear ossicle morphology  (IAGP)
abnormal motor neuron morphology  (IAGP)
abnormal myocardial fiber morphology  (IAGP)
abnormal neural crest cell migration  (IAGP)
abnormal neural crest cell morphology  (IAGP)
abnormal neural fold formation  (IAGP)
abnormal neural fold morphology  (IAGP)
abnormal neural plate morphology  (IAGP)
abnormal neural tube closure  (IAGP)
abnormal neural tube morphology  (IAGP)
abnormal neuronal migration  (IAGP)
abnormal notochordal process morphology  (IAGP)
abnormal organ of Corti morphology  (IAGP)
abnormal orientation of inner hair cell stereociliary bundles  (IAGP)
abnormal outer ear morphology  (IAGP)
abnormal palatal mesenchymal cell proliferation  (IAGP)
abnormal palatal rugae morphology  (IAGP)
abnormal palatine bone morphology  (IAGP)
abnormal phalanx morphology  (IAGP)
abnormal pinna reflex  (IAGP)
abnormal posterior primitive streak morphology  (IAGP)
abnormal posture  (IAGP)
abnormal primitive endoderm morphology  (IAGP)
abnormal primitive streak morphology  (IAGP)
abnormal pterygoid bone morphology  (IAGP)
abnormal reproductive system physiology  (IAGP)
abnormal retrotympanic process morphology  (IAGP)
abnormal rib morphology  (IAGP)
abnormal rostral-caudal axis patterning  (IAGP)
abnormal rostral-caudal body axis extension  (IAGP)
abnormal second pharyngeal arch morphology  (IAGP)
abnormal secondary palate development  (IAGP)
abnormal skin adnexa morphology  (IAGP)
abnormal skin appearance  (IAGP)
abnormal small intestine crypts of Lieberkuhn morphology  (IAGP)
abnormal small intestine morphology  (IAGP)
abnormal snout morphology  (IAGP)
abnormal somite development  (IAGP)
abnormal somite size  (IAGP)
abnormal stapes morphology  (IAGP)
abnormal stapes posterior crus morphology  (IAGP)
abnormal sternocostal joint morphology  (IAGP)
abnormal styloid process morphology  (IAGP)
abnormal tail development  (IAGP)
abnormal tail morphology  (IAGP)
abnormal tarsal bone morphology  (IAGP)
abnormal temporal bone squamous part morphology  (IAGP)
abnormal thoracic cage morphology  (IAGP)
abnormal thoracic vertebrae morphology  (IAGP)
abnormal tongue position  (IAGP)
abnormal tooth development  (IAGP)
abnormal trochlear nerve morphology  (IAGP)
abnormal ureteric bud elongation  (IAGP)
abnormal ureteric bud invasion  (IAGP)
abnormal ureteric bud morphology  (IAGP)
abnormal urethra urothelium morphology  (IAGP)
abnormal vascular development  (IAGP)
abnormal vertebrae morphology  (IAGP)
abnormal visceral yolk sac endoderm morphology  (IAGP)
abnormal visceral yolk sac mesenchyme morphology  (IAGP)
abnormal visceral yolk sac morphology  (IAGP)
abnormal viscerocranium morphology  (IAGP)
absent cerebellum vermis  (IAGP)
absent cochlear outer hair cells  (IAGP)
absent gonial bone  (IAGP)
absent hair follicles  (IAGP)
absent incus lenticular process  (IAGP)
absent inferior colliculus  (IAGP)
absent kidney  (IAGP)
absent limb buds  (IAGP)
absent mast cells  (IAGP)
absent metanephric mesenchyme  (IAGP)
absent middle ear ossicles  (IAGP)
absent organ of Corti supporting cells  (IAGP)
absent round window  (IAGP)
absent sebaceous gland  (IAGP)
absent second pharyngeal arch  (IAGP)
absent somites  (IAGP)
absent stapes head  (IAGP)
absent tympanic ring  (IAGP)
absent visceral yolk sac blood islands  (IAGP)
acanthosis  (IAGP)
alopecia  (IAGP)
bleb  (IAGP)
broad limb buds  (IAGP)
caudal body truncation  (IAGP)
cervical vertebral transformation  (IAGP)
cleft palate  (IAGP)
cleft primary palate  (IAGP)
cleft secondary palate  (IAGP)
cleft upper lip  (IAGP)
complete cleft palate  (IAGP)
craniofacial asymmetry  (IAGP)
craniorachischisis  (IAGP)
decreased body size  (IAGP)
decreased body weight  (IAGP)
decreased caudal vertebrae number  (IAGP)
decreased cochlear hair cell number  (IAGP)
decreased cochlear outer hair cell number  (IAGP)
decreased embryo size  (IAGP)
decreased endocochlear potential  (IAGP)
decreased inferior colliculus size  (IAGP)
decreased kidney cell proliferation  (IAGP)
decreased lumbar vertebrae number  (IAGP)
decreased maxillary shelf size  (IAGP)
decreased palatal shelf size  (IAGP)
decreased paraxial mesoderm size  (IAGP)
decreased renal glomerulus number  (IAGP)
decreased somite size  (IAGP)
decreased thoracic vertebrae number  (IAGP)
decreased tympanic ring size  (IAGP)
dermatitis  (IAGP)
dilated heart left ventricle  (IAGP)
dilated heart right ventricle  (IAGP)
dry skin  (IAGP)
ectopic ureteric bud  (IAGP)
embryonic growth arrest  (IAGP)
embryonic growth retardation  (IAGP)
embryonic lethality between implantation and somite formation, complete penetrance  (IAGP)
embryonic lethality between implantation and somite formation, incomplete penetrance  (IAGP)
embryonic lethality between somite formation and embryo turning, complete penetrance  (IAGP)
embryonic lethality between somite formation and embryo turning, incomplete penetrance  (IAGP)
embryonic lethality during organogenesis, complete penetrance  (IAGP)
embryonic lethality during organogenesis, incomplete penetrance  (IAGP)
embryonic lethality prior to tooth bud stage  (IEA)
embryonic lethality, complete penetrance  (IAGP)
enlarged allantois  (IAGP)
enlarged heart  (IAGP)
enlarged heart atrium  (IAGP)
excessive cerumen  (IAGP)
excessive folding of visceral yolk sac  (IAGP)
facial asymmetry  (IAGP)
facial cleft  (IAGP)
failure of heart looping  (IAGP)
failure of palatal shelf elevation  (IAGP)
failure of primitive streak formation  (IAGP)
failure of somite differentiation  (IAGP)
female infertility  (IAGP)
fusion of atlas and occipital bones  (IAGP)
genital tubercle hypoplasia  (IAGP)
heart hypoplasia  (IAGP)
hydronephrosis  (IAGP)
impaired branching involved in ureteric bud morphogenesis  (IAGP)
impaired coordination  (IAGP)
impaired skin barrier function  (IAGP)
increased axial mesoderm size  (IAGP)
increased cochlear inner hair cell number  (IAGP)
increased IgE level  (IAGP)
increased IgG1 level  (IAGP)
increased IgG2a level  (IAGP)
increased keratinocyte proliferation  (IAGP)
increased kidney apoptosis  (IAGP)
increased mast cell number  (IAGP)
increased metanephric mesenchyme apoptosis  (IAGP)
increased or absent threshold for auditory brainstem response  (IEA)
increased osteoblast cell number  (IAGP)
increased osteoblast proliferation  (IAGP)
increased respiratory quotient  (IEA)
increased rib number  (IAGP)
increased susceptibility to otitis media  (IAGP)
increased thoracic vertebrae number  (IAGP)
incus hypoplasia  (IAGP)
kinked neural tube  (IAGP)
lethality throughout fetal growth and development, complete penetrance  (IAGP)
lethality throughout fetal growth and development, incomplete penetrance  (IAGP)
long incisors  (IAGP)
lowered ear position  (IAGP)
lumbar vertebral transformation  (IAGP)
malleus hypoplasia  (IAGP)
micrognathia  (IAGP)
middle ear ossicle hypoplasia  (IAGP)
midface hypoplasia  (IAGP)
midline facial cleft  (IAGP)
neonatal lethality  (IAGP)
neonatal lethality, complete penetrance  (IAGP)
no abnormal phenotype detected  (IAGP)
ocular hypertelorism  (IAGP)
oligodactyly  (IAGP)
palatal shelves fail to meet at midline  (IAGP)
perinatal lethality, incomplete penetrance  (IAGP)
persistence of medial edge epithelium during palatal shelf fusion  (IAGP)
polydipsia  (IAGP)
postaxial polydactyly  (IAGP)
postnatal lethality, complete penetrance  (IAGP)
premature coronal suture closure  (IAGP)
premature cranial suture closure  (IAGP)
premature maxillary-premaxillary suture closure  (IAGP)
premature metopic suture closure  (IAGP)
premature sagittal suture closure  (IAGP)
prenatal lethality, complete penetrance  (IAGP)
prenatal lethality, incomplete penetrance  (IAGP)
preweaning lethality, complete penetrance  (IEA)
progressive hair loss  (IAGP)
reduced male fertility  (IAGP)
rib bifurcation  (IAGP)
rib fusion  (IAGP)
sacral vertebral transformation  (IAGP)
second pharyngeal arch hypoplasia  (IAGP)
short mandible  (IAGP)
short nasal bone  (IAGP)
short snout  (IAGP)
short tail  (IAGP)
short tibia  (IAGP)
skin fibrosis  (IAGP)
skin inflammation  (IAGP)
small cranium  (IAGP)
small ears  (IAGP)
small frontonasal prominence  (IAGP)
small gonial bone  (IAGP)
small hair follicles  (IAGP)
small kidney  (IAGP)
small proamniotic cavity  (IAGP)
small round window  (IAGP)
small second pharyngeal arch  (IAGP)
small ureteric bud  (IAGP)
small visceral yolk sac  (IAGP)
spina bifida  (IAGP)
stapes hypoplasia  (IAGP)
styloid process hypoplasia  (IAGP)
supernumerary teeth  (IAGP)
syndactyly  (IAGP)
thick epidermis  (IAGP)
thin myocardium  (IAGP)
thin ventricular wall  (IAGP)
thoracic vertebral transformation  (IAGP)
tympanic ring hypoplasia  (IAGP)
vertebral transformation  (IAGP)
References

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Additional References at PubMed
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PMID:18533146   PMID:18559345   PMID:18565209   PMID:18566132   PMID:18594511   PMID:18624916   PMID:18625063   PMID:18653561   PMID:18653563   PMID:18670373   PMID:18753255   PMID:18776942  
PMID:18799682   PMID:18799693   PMID:18832392   PMID:18832393   PMID:18937030   PMID:18973581   PMID:19056886   PMID:19097117   PMID:19176828   PMID:19211868   PMID:19218784   PMID:19219044  
PMID:19224984   PMID:19232523   PMID:19238727   PMID:19261810   PMID:19307307   PMID:19386268   PMID:19386269   PMID:19389359   PMID:19389367   PMID:19389374   PMID:19408015   PMID:19502291  
PMID:19515808   PMID:19521500   PMID:19542358   PMID:19544582   PMID:19549074   PMID:19564414   PMID:19574212   PMID:19598249   PMID:19663702   PMID:19666467   PMID:19710172   PMID:19713533  
PMID:19715689   PMID:19728793   PMID:19739251   PMID:19762422   PMID:19800312   PMID:19815519   PMID:19909731   PMID:19923290   PMID:19966287   PMID:20081193   PMID:20103604   PMID:20131355  
PMID:20152827   PMID:20215350   PMID:20299672   PMID:20308431   PMID:20348033   PMID:20392740   PMID:20405041   PMID:20410112   PMID:20436479   PMID:20463222   PMID:20501844   PMID:20501936  
PMID:20553372   PMID:20554972   PMID:20724449   PMID:20732316   PMID:20826535   PMID:20833365   PMID:20847311   PMID:20920500   PMID:20934536   PMID:21074523   PMID:21118511   PMID:21124973  
PMID:21128305   PMID:21156008   PMID:21172336   PMID:21223962   PMID:21223966   PMID:21267068   PMID:21310900   PMID:21389209   PMID:21451043   PMID:21479780   PMID:21515253   PMID:21527526  
PMID:21527531   PMID:21571225   PMID:21596839   PMID:21633168   PMID:21655085   PMID:21693512   PMID:21693575   PMID:21731673   PMID:21750042   PMID:21799763   PMID:21854849   PMID:21873635  
PMID:21876757   PMID:21911092   PMID:21937681   PMID:21939397   PMID:22031906   PMID:22036563   PMID:22076636   PMID:22110055   PMID:22207710   PMID:22235191   PMID:22247553   PMID:22276098  
PMID:22278924   PMID:22278983   PMID:22282599   PMID:22370560   PMID:22434869   PMID:22442730   PMID:22457778   PMID:22465667   PMID:22484060   PMID:22508726   PMID:22514272   PMID:22523080  
PMID:22529382   PMID:22537018   PMID:22573685   PMID:22578469   PMID:22632802   PMID:22643896   PMID:22674535   PMID:22735182   PMID:22751148   PMID:22761819   PMID:22792203   PMID:22802336  
PMID:22819339   PMID:22836867   PMID:22884371   PMID:22893608   PMID:22936024   PMID:22950531   PMID:22992463   PMID:23023126   PMID:23097355   PMID:23133671   PMID:23137310   PMID:23185502  
PMID:23293290   PMID:23308088   PMID:23358455   PMID:23382219   PMID:23451204   PMID:23523568   PMID:23564461   PMID:23592779   PMID:23666531   PMID:23684572   PMID:23715864   PMID:23720040  
PMID:23742896   PMID:23747598   PMID:23754280   PMID:23862974   PMID:24000064   PMID:24024127   PMID:24026051   PMID:24067353   PMID:24145799   PMID:24154525   PMID:24194600   PMID:24198358  
PMID:24259513   PMID:24305876   PMID:24349409   PMID:24361260   PMID:24375670   PMID:24381197   PMID:24427155   PMID:24465223   PMID:24470103   PMID:24496615   PMID:24512770   PMID:24618085  
PMID:24752320   PMID:24796693   PMID:24812002   PMID:24824078   PMID:24859004   PMID:24952961   PMID:24983448   PMID:25002516   PMID:25043058   PMID:25053435   PMID:25089825   PMID:25116473  
PMID:25139991   PMID:25249657   PMID:25285038   PMID:25300351   PMID:25302779   PMID:25344367   PMID:25359900   PMID:25400756   PMID:25419850   PMID:25428587   PMID:25429144   PMID:25453829  
PMID:25467980   PMID:25616962   PMID:25624266   PMID:25641696   PMID:25678108   PMID:25721301   PMID:25766255   PMID:25792827   PMID:25820239   PMID:25843682   PMID:25913734   PMID:25915623  
PMID:25917818   PMID:25923916   PMID:25926357   PMID:25951516   PMID:26024354   PMID:26032417   PMID:26074812   PMID:26075383   PMID:26081170   PMID:26141512   PMID:26234751   PMID:26250517  
PMID:26311115   PMID:26341559   PMID:26441343   PMID:26453795   PMID:26476925   PMID:26487719   PMID:26496610   PMID:26511927   PMID:26550799   PMID:26581390   PMID:26589915   PMID:26685160  
PMID:26718736   PMID:26747503   PMID:26762170   PMID:26764350   PMID:26826126   PMID:26839958   PMID:26847131   PMID:26872365   PMID:26881702   PMID:26903947   PMID:26906157   PMID:26988119  
PMID:27046834   PMID:27052727   PMID:27078042   PMID:27133954   PMID:27134830   PMID:27206683   PMID:27391347   PMID:27436040   PMID:27626380   PMID:27690692   PMID:27732085   PMID:27732850  
PMID:27756203   PMID:27770432   PMID:27787957   PMID:27989801   PMID:28027321   PMID:28031461   PMID:28094278   PMID:28117910   PMID:28131861   PMID:28169396   PMID:28187268   PMID:28193689  
PMID:28336912   PMID:28389228   PMID:28465335   PMID:28467822   PMID:28483978   PMID:28487375   PMID:28489004   PMID:28537241   PMID:28552557   PMID:28552559   PMID:28771231   PMID:28783178  
PMID:28794403   PMID:28813681   PMID:28818950   PMID:28923346   PMID:28938467   PMID:28993502   PMID:29028795   PMID:29031500   PMID:29097598   PMID:29107292   PMID:29132503   PMID:29140246  
PMID:29158323   PMID:29342370   PMID:29360039   PMID:29422515   PMID:29691281   PMID:29718910   PMID:29720668   PMID:29743348   PMID:29796621   PMID:29844125   PMID:29964027   PMID:30026121  
PMID:30061390   PMID:30093411   PMID:30217817   PMID:30283071   PMID:30348976   PMID:30352686   PMID:30352954   PMID:30389913   PMID:30439482   PMID:30499042   PMID:30552867   PMID:30566624  
PMID:30592646   PMID:30720426   PMID:30763736   PMID:30787001   PMID:30838872   PMID:31059863   PMID:31097591   PMID:31175212   PMID:31189094   PMID:31206783   PMID:31208421   PMID:31276493  
PMID:31320324   PMID:31525277   PMID:31613912   PMID:31647919   PMID:31719045   PMID:31758962   PMID:31830366   PMID:32043969   PMID:32127497   PMID:32187553   PMID:32212902   PMID:32325033  
PMID:32385276   PMID:32422143   PMID:32662771   PMID:32715478   PMID:32735383   PMID:32841643   PMID:32857879   PMID:32858001   PMID:33037205   PMID:33131311   PMID:33184218   PMID:33433858  
PMID:33469032   PMID:33580754   PMID:33679600   PMID:34265279   PMID:34484568   PMID:34502405   PMID:34644107   PMID:34757798   PMID:34929174   PMID:34986332   PMID:35020897   PMID:35194044  
PMID:35216141   PMID:35614226   PMID:35729116   PMID:35733256   PMID:35899427   PMID:36002765   PMID:36094016   PMID:36357571   PMID:36382369   PMID:36467073   PMID:36542062   PMID:36861436  


Genomics

Comparative Map Data
Fgfr1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39826,008,808 - 26,067,819 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl826,003,670 - 26,065,734 (+)EnsemblGRCm39 Ensembl
GRCm38825,518,759 - 25,575,718 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl825,513,654 - 25,575,718 (+)EnsemblGRCm38mm10GRCm38
MGSCv37826,629,244 - 26,686,186 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36826,997,826 - 27,039,466 (+)NCBIMGSCv36mm8
Celera826,986,822 - 27,044,074 (+)NCBICelera
Cytogenetic Map8A2NCBI
cM Map814.12NCBI
FGFR1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38838,411,143 - 38,468,635 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl838,400,215 - 38,468,834 (-)EnsemblGRCh38hg38GRCh38
GRCh37838,268,661 - 38,326,153 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36838,387,813 - 38,445,509 (-)NCBINCBI36Build 36hg18NCBI36
Build 34838,389,448 - 38,445,293NCBI
Celera837,221,633 - 37,279,334 (-)NCBICelera
Cytogenetic Map8p11.23NCBI
HuRef836,802,638 - 36,860,684 (-)NCBIHuRef
CHM1_1838,470,562 - 38,528,261 (-)NCBICHM1_1
T2T-CHM13v2.0838,688,107 - 38,745,588 (-)NCBIT2T-CHM13v2.0
Fgfr1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21666,492,445 - 66,546,731 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1666,494,042 - 66,547,350 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1671,773,130 - 71,812,564 (-)NCBIRnor_SHR
UTH_Rnor_SHRSP_BbbUtx_1.01675,179,067 - 75,218,502 (-)NCBIRnor_SHRSP
UTH_Rnor_WKY_Bbb_1.01670,419,796 - 70,459,385 (-)NCBIRnor_WKY
Rnor_6.01671,265,390 - 71,319,046 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1671,266,248 - 71,319,449 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01670,924,716 - 70,977,998 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41670,869,974 - 70,910,045 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11670,870,238 - 70,910,310 (-)NCBI
Celera1664,402,647 - 64,442,189 (-)NCBICelera
Cytogenetic Map16q12.4NCBI
Fgfr1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495546314,013,247 - 14,064,111 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495546314,013,247 - 14,064,354 (-)NCBIChiLan1.0ChiLan1.0
FGFR1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1832,691,569 - 32,751,015 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0837,713,133 - 37,773,098 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1834,890,147 - 34,948,904 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl834,890,147 - 34,948,904 (-)Ensemblpanpan1.1panPan2
FGFR1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11627,029,902 - 27,080,514 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1627,031,588 - 27,078,261 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1627,547,259 - 27,597,845 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01628,928,146 - 28,978,790 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1628,927,382 - 28,977,436 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11627,151,667 - 27,202,222 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01627,728,739 - 27,779,306 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01627,767,626 - 27,818,261 (+)NCBIUU_Cfam_GSD_1.0
Fgfr1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494349,645,976 - 49,698,868 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049367101,760,089 - 1,815,508 (-)EnsemblSpeTri2.0
SpeTri2.0NW_0049367101,760,365 - 1,815,269 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FGFR1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1548,053,340 - 48,106,724 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11548,053,895 - 48,106,634 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21555,216,111 - 55,269,152 (+)NCBISscrofa10.2Sscrofa10.2susScr3
FGFR1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1836,426,116 - 36,485,683 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl836,427,110 - 36,485,508 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660525,502,205 - 5,561,763 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Fgfr1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247805,161,073 - 5,213,870 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247805,161,245 - 5,212,641 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in Fgfr1
2034 total Variants
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
Mir133bmmu-miR-133b-5pOncomiRDBexternal_infoNANA23296701

Predicted Target Of
Summary Value
Count of predictions:5845
Count of miRNA genes:839
Interacting mature miRNAs:1130
Transcripts:ENSMUST00000084027, ENSMUST00000117179, ENSMUST00000119398, ENSMUST00000120106, ENSMUST00000124228, ENSMUST00000126118, ENSMUST00000133936, ENSMUST00000138104, ENSMUST00000138455, ENSMUST00000145218, ENSMUST00000148322, ENSMUST00000155564, ENSMUST00000167764, ENSMUST00000178276, ENSMUST00000179592
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCm39)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
11533914Mts5_mmammary tumor susceptibility 5 (mouse)8130447432Mouse
4140978Nilac5_mnicotine induced locomotor activity 5 (mouse)Not determined8131773288Mouse
27226756Femd2_mfemur midshaft diameter 2, 5 week (mouse)8495000035067154Mouse
1301532Scc8_mcolon tumor susceptibility 8 (mouse)Not determined8721249935110107Mouse
1300906Ap8q_malcohol preference 8 QTL (mouse)Not determined8798418941984342Mouse
10412209Cypr7_mcytokine production 7 (mouse)Not determined8810320142103372Mouse
1301929Eae24_msusceptibility to experimental allergic encephalomyelitis 24 (mouse)Not determined8810320142103372Mouse
1301128Sluc20_msusceptibility to lung cancer 20 (mouse)Not determined8810320142103372Mouse
11532713Sluc42_msusceptibility to lung cancer 42 (mouse)81344721035321225Mouse
1558870Eae36_mexperimental allergic encephalomyelitis susceptibility 36 (mouse)Not determined81477316071498244Mouse
1301088Alcw6_malcohol withdrawal 6 (mouse)Not determined81550657249506729Mouse
1300912Daq19_mdirectional asymmetry QTL 19 (mouse)Not determined81550657249506729Mouse
1301298Pgia4_mproteoglycan induced arthritis 4 (mouse)Not determined81656937350569697Mouse
4142199Poats1_mpost-ovarectomy adrenal tumor susceptibility 1 (mouse)Not determined1708262628849467Mouse
1301550Fembrs2_mfemur breaking strength 2 (mouse)Not determined81832109752321225Mouse
1301160Eae14_msusceptibility to experimental allergic encephalomyelitis 14 (mouse)Not determined81945501853455150Mouse
1300603Cd8ts2_mCD8 T cell subset 2 (mouse)Not determined81945501853455150Mouse

Markers in Region
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38825,572,763 - 25,573,613UniSTSGRCm38
MGSCv37826,684,082 - 26,684,317UniSTSGRCm37
Celera827,041,122 - 27,041,972UniSTS
Cytogenetic Map8A2UniSTS
cM Map810.0UniSTS
cM Map810.0UniSTS
cM Map810.0UniSTS
cM Map810.0UniSTS
cM Map810.0UniSTS
AW208770  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38825,574,313 - 25,574,422UniSTSGRCm38
MGSCv37826,684,785 - 26,684,894UniSTSGRCm37
Celera827,042,672 - 27,042,781UniSTS
Cytogenetic Map8A2UniSTS
cM Map810.0UniSTS
Whitehead/MRC_RH8290.46UniSTS
PMC154461P1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38825,565,927 - 25,566,710UniSTSGRCm38
MGSCv37826,676,399 - 26,677,182UniSTSGRCm37
Celera827,034,152 - 27,034,935UniSTS
Cytogenetic Map8A2UniSTS
cM Map810.0UniSTS
PMC195961P1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38825,565,927 - 25,566,070UniSTSGRCm38
MGSCv37826,676,399 - 26,676,542UniSTSGRCm37
Celera827,034,152 - 27,034,295UniSTS
Cytogenetic Map8A2UniSTS
cM Map810.0UniSTS
MARC_14569-14570:1009480763:3  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38825,573,145 - 25,573,792UniSTSGRCm38
MGSCv37826,683,617 - 26,684,264UniSTSGRCm37
Celera827,041,504 - 27,042,151UniSTS
Cytogenetic Map8A2UniSTS
cM Map810.0UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38825,573,610 - 25,573,845UniSTSGRCm38
MGSCv37826,684,082 - 26,684,317UniSTSGRCm37
Celera827,041,969 - 27,042,204UniSTS
Cytogenetic Map8A2UniSTS
cM Map810.0UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
cM Map810.0UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
cM Map810.0UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
cM Map810.0UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS
Fgfr1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8A2UniSTS


Expression


Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001079908 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001079909 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_010206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC160526 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AEKQ02172397 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF154570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF176552 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI480534 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK028354 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK034295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK049704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK086091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK167639 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC010200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC033447 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC053921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU611199 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB524826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CF532036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH466580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M28998 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M33760 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M65053 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S47233 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S74765 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U22324 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U23445 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X51893 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X57790 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENSMUST00000084027   ⟹   ENSMUSP00000081041
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,008,775 - 26,065,734 (+)Ensembl
GRCm38.p6 Ensembl825,518,759 - 25,575,718 (+)Ensembl
RefSeq Acc Id: ENSMUST00000117179   ⟹   ENSMUSP00000113909
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,008,811 - 26,064,797 (+)Ensembl
GRCm38.p6 Ensembl825,518,795 - 25,574,781 (+)Ensembl
RefSeq Acc Id: ENSMUST00000119398   ⟹   ENSMUSP00000113855
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,008,805 - 26,064,795 (+)Ensembl
GRCm38.p6 Ensembl825,518,789 - 25,574,779 (+)Ensembl
RefSeq Acc Id: ENSMUST00000120106
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,056,866 - 26,064,800 (+)Ensembl
GRCm38.p6 Ensembl825,566,850 - 25,574,784 (+)Ensembl
RefSeq Acc Id: ENSMUST00000124228   ⟹   ENSMUSP00000116564
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,009,853 - 26,045,745 (+)Ensembl
GRCm38.p6 Ensembl825,519,837 - 25,555,729 (+)Ensembl
RefSeq Acc Id: ENSMUST00000126118
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,053,421 - 26,064,801 (+)Ensembl
GRCm38.p6 Ensembl825,563,405 - 25,574,785 (+)Ensembl
RefSeq Acc Id: ENSMUST00000133936
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,059,739 - 26,062,473 (+)Ensembl
GRCm38.p6 Ensembl825,569,723 - 25,572,457 (+)Ensembl
RefSeq Acc Id: ENSMUST00000138104   ⟹   ENSMUSP00000148135
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,045,633 - 26,062,457 (+)Ensembl
GRCm38.p6 Ensembl825,555,617 - 25,572,441 (+)Ensembl
RefSeq Acc Id: ENSMUST00000138455   ⟹   ENSMUSP00000147898
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,048,090 - 26,053,730 (+)Ensembl
GRCm38.p6 Ensembl825,558,074 - 25,563,714 (+)Ensembl
RefSeq Acc Id: ENSMUST00000145218
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,059,502 - 26,062,411 (+)Ensembl
GRCm38.p6 Ensembl825,569,486 - 25,572,395 (+)Ensembl
RefSeq Acc Id: ENSMUST00000148322
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,008,911 - 26,045,674 (+)Ensembl
GRCm38.p6 Ensembl825,518,895 - 25,555,658 (+)Ensembl
RefSeq Acc Id: ENSMUST00000155564   ⟹   ENSMUSP00000117884
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,003,670 - 26,045,584 (+)Ensembl
GRCm38.p6 Ensembl825,513,654 - 25,555,568 (+)Ensembl
RefSeq Acc Id: ENSMUST00000167764   ⟹   ENSMUSP00000131343
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,022,297 - 26,064,593 (+)Ensembl
GRCm38.p6 Ensembl825,532,281 - 25,574,577 (+)Ensembl
RefSeq Acc Id: ENSMUST00000178276   ⟹   ENSMUSP00000137515
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,008,788 - 26,065,730 (+)Ensembl
GRCm38.p6 Ensembl825,518,772 - 25,575,714 (+)Ensembl
RefSeq Acc Id: ENSMUST00000179592   ⟹   ENSMUSP00000136640
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,008,788 - 26,065,730 (+)Ensembl
GRCm38.p6 Ensembl825,518,772 - 25,575,714 (+)Ensembl
RefSeq Acc Id: ENSMUST00000210504
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,056,016 - 26,059,339 (+)Ensembl
GRCm38.p6 Ensembl825,566,000 - 25,569,323 (+)Ensembl
RefSeq Acc Id: ENSMUST00000210778
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,009,360 - 26,048,243 (+)Ensembl
GRCm38.p6 Ensembl825,519,344 - 25,558,227 (+)Ensembl
RefSeq Acc Id: ENSMUST00000210846   ⟹   ENSMUSP00000148032
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,022,141 - 26,045,692 (+)Ensembl
GRCm38.p6 Ensembl825,532,125 - 25,555,676 (+)Ensembl
RefSeq Acc Id: ENSMUST00000211419
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl826,056,882 - 26,058,313 (+)Ensembl
GRCm38.p6 Ensembl825,566,866 - 25,568,297 (+)Ensembl
RefSeq Acc Id: NM_001079908   ⟹   NP_001073377
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39826,008,808 - 26,067,819 (+)NCBI
GRCm38825,518,759 - 25,575,718 (+)NCBI
MGSCv37826,629,244 - 26,686,186 (+)RGD
Celera826,986,809 - 27,044,078 (+)NCBI
cM Map8 ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001079909   ⟹   NP_001073378
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39826,008,808 - 26,067,819 (+)NCBI
GRCm38825,518,759 - 25,575,718 (+)NCBI
MGSCv37826,629,244 - 26,686,186 (+)RGD
Celera826,986,809 - 27,044,078 (+)NCBI
cM Map8 ENTREZGENE
Sequence:
RefSeq Acc Id: NM_010206   ⟹   NP_034336
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39826,008,808 - 26,067,819 (+)NCBI
GRCm38825,518,759 - 25,575,718 (+)NCBI
MGSCv37826,629,244 - 26,686,186 (+)RGD
Celera826,986,809 - 27,044,078 (+)NCBI
cM Map8 ENTREZGENE
Sequence:
Reference Sequences
RefSeq Acc Id: NP_034336   ⟸   NM_010206
- Peptide Label: isoform 1 precursor
- UniProtKB: Q9QZM7 (UniProtKB/Swiss-Prot),   P16092 (UniProtKB/Swiss-Prot),   Q8CBY7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001073377   ⟸   NM_001079908
- Peptide Label: isoform 2 precursor
- UniProtKB: P16092 (UniProtKB/Swiss-Prot),   Q8CBY7 (UniProtKB/TrEMBL),   Q8CIM9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001073378   ⟸   NM_001079909
- Peptide Label: isoform 3 precursor
- UniProtKB: P16092 (UniProtKB/Swiss-Prot),   Q8CBY7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSMUSP00000137515   ⟸   ENSMUST00000178276
RefSeq Acc Id: ENSMUSP00000113855   ⟸   ENSMUST00000119398
RefSeq Acc Id: ENSMUSP00000147898   ⟸   ENSMUST00000138455
RefSeq Acc Id: ENSMUSP00000116564   ⟸   ENSMUST00000124228
RefSeq Acc Id: ENSMUSP00000148135   ⟸   ENSMUST00000138104
RefSeq Acc Id: ENSMUSP00000148032   ⟸   ENSMUST00000210846
RefSeq Acc Id: ENSMUSP00000136640   ⟸   ENSMUST00000179592
RefSeq Acc Id: ENSMUSP00000131343   ⟸   ENSMUST00000167764
RefSeq Acc Id: ENSMUSP00000081041   ⟸   ENSMUST00000084027
RefSeq Acc Id: ENSMUSP00000113909   ⟸   ENSMUST00000117179
RefSeq Acc Id: ENSMUSP00000117884   ⟸   ENSMUST00000155564
Protein Domains
Ig-like   Ig-like C2-type   Protein kinase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P16092-F1-model_v2 AlphaFold P16092 1-822 view protein structure

Promoters
RGD ID:8666755
Promoter ID:EPDNEW_M11409
Type:initiation region
Name:Fgfr1_1
Description:Mus musculus fibroblast growth factor receptor 1 , transcriptvariant 3, mRNA.
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm38825,518,792 - 25,518,852EPDNEW
RGD ID:6843156
Promoter ID:MM_KWN:54004
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Kidney
Transcripts:OTTMUST00000076877
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36826,623,696 - 26,624,196 (+)MPROMDB
RGD ID:6843150
Promoter ID:MM_KWN:54005
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:3T3L1_Day0,   3T3L1_Day1,   3T3L1_Day2,   3T3L1_Day3,   3T3L1_Day4,   3T3L1_Day6,   Brain,   ES_Cell,   Kidney,   Liver,   Lung,   MEF_B4,   MEF_B6
Transcripts:ENSMUST00000084027,   ENSMUST00000117179,   ENSMUST00000118241,   ENSMUST00000119398,   ENSMUST00000120612,   NM_001079908,   NM_001079909,   NM_010206,   OTTMUST00000076878,   OTTMUST00000076879
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36826,629,084 - 26,629,584 (+)MPROMDB
RGD ID:6843157
Promoter ID:MM_KWN:54006
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:3T3L1_Day2,   3T3L1_Day3,   3T3L1_Day4,   Lung
Transcripts:ENSMUST00000120106,   OTTMUST00000076871,   UC009LGB.1,   UC009LGC.1
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36826,642,011 - 26,643,142 (+)MPROMDB
RGD ID:6843158
Promoter ID:MM_KWN:54008
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:3T3L1_Day2,   3T3L1_Day4,   Brain,   Kidney,   Lung
Transcripts:OTTMUST00000076872,   UC009LGE.1
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36826,665,186 - 26,666,022 (+)MPROMDB
RGD ID:6843151
Promoter ID:MM_KWN:54010
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:3T3L1_Day2,   3T3L1_Day3,   3T3L1_Day4,   Brain
Transcripts:OTTMUST00000076873
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36826,667,546 - 26,669,007 (+)MPROMDB
RGD ID:6843152
Promoter ID:MM_KWN:54011
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:3T3L1_Day2,   3T3L1_Day3,   3T3L1_Day4
Transcripts:OTTMUST00000076876
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36826,673,686 - 26,674,907 (+)MPROMDB
RGD ID:6843153
Promoter ID:MM_KWN:54012
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:3T3L1_Day2,   3T3L1_Day3
Transcripts:OTTMUST00000076874,   OTTMUST00000076875
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36826,679,959 - 26,680,459 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene MGI:95522 AgrOrtholog
Ensembl Genes ENSMUSG00000031565 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSMUSP00000081041 ENTREZGENE
  ENSMUSP00000081041.6 UniProtKB/Swiss-Prot
  ENSMUSP00000113855 ENTREZGENE
  ENSMUSP00000113855.3 UniProtKB/Swiss-Prot
  ENSMUSP00000113909 ENTREZGENE
  ENSMUSP00000113909.3 UniProtKB/Swiss-Prot
  ENSMUSP00000116564.2 UniProtKB/TrEMBL
  ENSMUSP00000117884.2 UniProtKB/TrEMBL
  ENSMUSP00000131343.2 UniProtKB/Swiss-Prot
  ENSMUSP00000136640.2 UniProtKB/TrEMBL
  ENSMUSP00000137515.2 UniProtKB/Swiss-Prot
  ENSMUSP00000147898.2 UniProtKB/TrEMBL
  ENSMUSP00000148032.2 UniProtKB/TrEMBL
  ENSMUSP00000148135.2 UniProtKB/TrEMBL
Ensembl Transcript ENSMUST00000084027 ENTREZGENE
  ENSMUST00000084027.13 UniProtKB/Swiss-Prot
  ENSMUST00000117179 ENTREZGENE
  ENSMUST00000117179.9 UniProtKB/Swiss-Prot
  ENSMUST00000119398 ENTREZGENE
  ENSMUST00000119398.10 UniProtKB/Swiss-Prot
  ENSMUST00000124228.2 UniProtKB/TrEMBL
  ENSMUST00000138104.9 UniProtKB/TrEMBL
  ENSMUST00000138455.2 UniProtKB/TrEMBL
  ENSMUST00000155564.8 UniProtKB/TrEMBL
  ENSMUST00000167764.2 UniProtKB/Swiss-Prot
  ENSMUST00000178276.8 UniProtKB/Swiss-Prot
  ENSMUST00000179592.8 UniProtKB/TrEMBL
  ENSMUST00000210846.2 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Transferase(Phosphotransferase) domain 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
InterPro FGF_rcpt_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FGF_rcpt_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_I-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Immunoglobulin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Kinase-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Prot_kinase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Protein_kinase_ATP_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ser-Thr/Tyr_kinase_cat_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Tyr_kinase_AS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Tyr_kinase_cat_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report mmu:14182 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
MGD MGI:95522 ENTREZGENE
NCBI Gene 14182 ENTREZGENE
PANTHER FIBROBLAST GROWTH FACTOR RECEPTOR UniProtKB/TrEMBL
  FIBROBLAST GROWTH FACTOR RECEPTOR UniProtKB/TrEMBL
  FIBROBLAST GROWTH FACTOR RECEPTOR 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TYROSINE-PROTEIN KINASE RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam I-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_3 UniProtKB/TrEMBL
  PF00047 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pkinase_Tyr UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PhenoGen Fgfr1 PhenoGen
PIRSF FGFR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TyrPK_CSF1-R UniProtKB/TrEMBL
PRINTS TYRKINASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE IG_LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_ATP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_DOM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_TYR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART IGc2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00409 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TyrKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48726 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF56112 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A1B0GSD9_MOUSE UniProtKB/TrEMBL