ENSMUSG00000031074


Mus musculus

Features
Gene ID: ENSMUSG00000031074
  
Biological name :Fgf3
  
Synonyms : Fgf3 / fibroblast growth factor 3
  
Possible biological names infered from orthology : P11487
  
Species: Mus musculus
  
Chr. number: 7
Strand: 1
Band: F5
Gene start: 144838083
Gene end: 144844436
  
Corresponding Affymetrix probe sets: 10559361 (MoGene1.0st)   1422923_at (Mouse Genome 430 2.0 Array)   1441350_at (Mouse Genome 430 2.0 Array)   1441914_x_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000115205
Ensembl peptide - ENSMUSP00000101518
NCBI entrez gene - 14174     See in Manteia.
MGI - MGI:95517
RefSeq - NM_008007
RefSeq - XM_011241980
RefSeq Peptide - NP_032033
swissprot - D3YWD4
swissprot - Q0VG15
Ensembl - ENSMUSG00000031074
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 fgf3ENSDARG00000101540Danio rerio
 FGF3ENSGALG00000026853Gallus gallus
 FGF3ENSG00000186895Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Fgf10 / O35565 / Fibroblast growth factor 10 / O15520*ENSMUSG0000002173232
Fgf20 / Q9ESL9 / Fibroblast growth factor 20 / Q9NP95*ENSMUSG0000003160330
Fgf5 / P15656 / Fibroblast growth factor 5 / P12034*ENSMUSG0000002933729
Fgf16 / Q9ESL8 / Fibroblast growth factor 16 / O43320*ENSMUSG0000003123029
Fgf9 / P54130 / Fibroblast growth factor 9 / P31371*ENSMUSG0000002197428
Fgf22 / Q9ESS2 / Fibroblast growth factor 22 / Q9HCT0*ENSMUSG0000002032728
Fgf7 / P36363 / Fibroblast growth factor 7 / P21781*ENSMUSG0000002720827
Fgf6 / P21658 / Fibroblast growth factor 6 / P10767*ENSMUSG0000000018326
Fgf13 / P70377 / Mus musculus fibroblast growth factor 13 (Fgf13), transcript variant 4, mRNA. / Q92913* / fibroblast growth factor 13*ENSMUSG0000003113724
Fgf12 / P61329 / Fibroblast growth factor 12 / P61328*ENSMUSG0000002252323
Fgf14 / fibroblast growth factor 14 / Q92915*ENSMUSG0000002555123
Fgf4 / P11403 / Fibroblast growth factor 4 / P08620*ENSMUSG0000005091722
Fgf11 / P70378 / Fibroblast growth factor 11 / Q92914*ENSMUSG0000004282622


Protein motifs (from Interpro)
Interpro ID Name
 IPR002209  Fibroblast growth factor family
 IPR008996  Cytokine IL1/FGF
 IPR028232  Fibroblast growth factor 3


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0008284 positive regulation of cell proliferation IEA
 biological_processGO:0008543 fibroblast growth factor receptor signaling pathway IEA
 biological_processGO:0010469 regulation of signaling receptor activity IEA
 biological_processGO:0055026 negative regulation of cardiac muscle tissue development IEA
 cellular_componentGO:0005576 extracellular region IEA
 molecular_functionGO:0005104 fibroblast growth factor receptor binding IEA
 molecular_functionGO:0008083 growth factor activity IEA


Pathways (from Reactome)
Pathway description
PI3K Cascade
PIP3 activates AKT signaling
FGFR1b ligand binding and activation
FGFR2b ligand binding and activation
Phospholipase C-mediated cascade: FGFR1
Phospholipase C-mediated cascade; FGFR2
Downstream signaling of activated FGFR1
SHC-mediated cascade:FGFR1
PI-3K cascade:FGFR1
FRS-mediated FGFR1 signaling
PI-3K cascade:FGFR2
SHC-mediated cascade:FGFR2
FRS-mediated FGFR2 signaling
FRS-mediated FGFR3 signaling
FRS-mediated FGFR4 signaling
Negative regulation of FGFR1 signaling
Negative regulation of FGFR2 signaling
FGFRL1 modulation of FGFR1 signaling
RAF/MAP kinase cascade
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000026 abnormal inner ear morphology "malformation or malfunction of any components of the labyrinth, including the semicircular canals, vestibule and cochlea" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776]
Show

Allelic Composition: F9tm1Dws/Y
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Fgf3tm2Mrc/Fgf3tm2Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0000031 abnormal cochlea morphology "any anomaly, deformity, malformation, impairment or dysfunction of the cochlea" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, cml:Cathleen M. Lutz , Mouse Genome Informatics Curator, J:21484]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0000034 abnormal vestibule morphology "malformed cavity between the semicircular canals and the cochlea of the inner ear" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0000035 abnormal membranous labyrinth "malformations in the complex arrangement of communicating canaliculi and sacs suspended within the cavity of the bony labyrinth of the inner ear" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23837]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0000041 absent endolymphatic duct "missing small membranous canal of the inner ear; connecting membranous labyrinth with the endolymphatic sac" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0000549 absent limbs "missing extremities" [J:51966, J:50768]
Show

Allelic Composition: Fgf3tm2Mrc/Fgf3tm2Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf10tm1.1Sms/Fgf10tm1.1Sms,Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 MP:0000585 kinked tail "a sharp bend or zig-zag in the tail" [J:61295]
Show

Allelic Composition: F9tm1Dws/Y
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Fgf3tm2Mrc/Fgf3tm2Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm2.1Sms/Fgf3tm2.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ

 MP:0000588 thick tail "a tail with a greater diameter than the norm " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Slc4a1tm1Llp/Slc4a1wan
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J

 MP:0000592 short tail "reduced length of tail compared to control " [J:55583]
Show

Allelic Composition: Slc4a1tm1Llp/Slc4a1wan
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm2Mrc/Fgf3tm2Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Fgf10tm1.1Sms/Fgf10tm1.1Sms,Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

Allelic Composition: Fgf3tm1Lwd/Fgf3tm1Lwd,Fgf4tm1.1Lwd/Fgf4tm1.1Lwd
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6 * NIH Swiss Webster * SJL/J

 MP:0000702 enlarged lymph nodes "lymph nodes of increased size" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Fgf3tm4b(EUCOMM)Hmgu/Fgf3tm4b(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Fgf3tm4b(EUCOMM)Hmgu/Bay

 MP:0001081 abnormal cranial ganglia morphology "any anomaly, deformity, or malformation of the groups of nerve cell bodies associated with the twelve cranial nerves" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:45302]
Show

Allelic Composition: Fgf3tm2Mrc/Fgf3tm2Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0001265 reduced body size "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170]
Show

Allelic Composition: Casc3Gt(RRU345)Byg/Casc3tm1(KOMP)Vlcg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac

 MP:0001394 circling "repeated, compulsive movement in a circle; often associated with inner ear defects" [MGI:CLS, J:61295]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Fgf3tm1Lwd/Fgf3tm1Lwd,Fgf4tm1.1Lwd/Fgf4tm1.1Lwd
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6 * NIH Swiss Webster * SJL/J

 MP:0001399 hyperactivity "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125]
Show

Allelic Composition: F9tm1Dws/Y
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001404 no spontaneous movement "failure to make any change in position or posture" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:60159]
Show

Allelic Composition: Fgf3tm4b(EUCOMM)Hmgu/Fgf3tm4b(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Fgf3tm4b(EUCOMM)Hmgu/Bay

 MP:0001489 decreased startle reflex "greater threshold or less severe reflex response to variable stimuli, often auditory; usually measured by amplitude of whole body flinch" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, What s Wrong With My Mouse?:ISBN 0-471-31639-3]
Show

Allelic Composition: F9tm1Dws/Y
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001523 impaired righting response "reduced ability or greater amount of time needed to recover from supine position" [J:25565]
Show

Allelic Composition: F9tm1Dws/Y
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001539 decreased number of caudal vertebrae "reduced number of the bony segments of the tail" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1Lwd/Fgf3tm1Lwd,Fgf4tm1.1Lwd/Fgf4tm1.2Lwd
Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6 * C57BL/6 * NIH Swiss Webster * SJL/J

 MP:0001672 abnormal embryogenesis/ development "anomaly in the establishment of the characteristic configuration of the embryonic body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Fgf10tm1.2Sms/Fgf10tm1.2Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 MP:0001688 abnormal somite development "anomalous formation of any of the paired, metamerically arranged cell masses formed in the embryonic paraxial mesoderm" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0001697 abnormal embryo size "anomalous proportions of embryo compared to littermates" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator]
Show

Allelic Composition: Fgf3tm4b(EUCOMM)Hmgu/Fgf3tm4b(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Fgf3tm4b(EUCOMM)Hmgu/Bay

 MP:0001698 reduced embryo size "smaller proportions of embryo compared to littermates" [J:61790]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm2Mrc/Fgf3tm2Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0002082 postnatal lethality "premature death anytime after postnatal day 1 to weaning age (3 weeks)" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0002102 abnormal ear morphology "structural or developmental anomaly of any of the structures involved in the ear or vestibular system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Fgf10tm1.2Sms/Fgf10tm1.2Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 MP:0002111 abnormal tail morphology "abnormal development of the tail resulting in structural abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Slc4a1tm1Llp/Slc4a1wan
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J

Allelic Composition: Fgf3tm4b(EUCOMM)Hmgu/Fgf3tm4b(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Fgf3tm4b(EUCOMM)Hmgu/Bay

 MP:0002151 abnormal neural tube morphology/development "anomalous structure of or development of the embryonic neural tube resulting in structural anomaly" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: F9tm1Dws/Y
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0002169 no phenotype detected "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Fgf3tm2.1Sms/Fgf3tm2.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ

Allelic Composition: Fgf10tm1.2Sms/Fgf10tm1.2Sms,Fgf3tm1.2Sms/Fgf3tm1.2Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ

 MP:0002428 abnormal semicircular canal "anomaly of the organ of balance composed of three long bony tubes of the labyrinth" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0002759 abnormal caudal vertebrae morphology "malformed bony segments of the tail, usually 27-30 present" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:82849]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm2Mrc/Fgf3tm2Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0003051 curly tail "a loop or corkscrew-like curl in the tail" [csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm2Mrc/Fgf3tm2Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0003148 reduced cochlear coiling "a reduction in cochlear coiling or number of turns; in wild-type mice, the cochlea most commonly exhibits one and three-fourth turns" [J:56294, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0003163 absent posterior semicircular canal 
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0003165 absent superior semicircular canal 
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0003168 abnormal scala vestibuli morphology "any malformation or absence of the division of the spiral canal of the cochlea lying on the apical side of the spiral lamina and vestibular membrane" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0003169 abnormal scala media morphology "any malformation or absence of the division of the spiral canal of the cochlea that contains the organ of Corti (the neuroepithelial receptor organ for hearing)" [J:23837, J:46972, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0003637 cochlear ganglion hypoplasia "reduced numbers of the group of nerve cell bodies that conveys auditory sensation from the organ of Corti to the hindbrain and resides on the cochlear part of the vestibulocochlear nerve (eighth cranial nerve)" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0003703 abnormal vestibulocochlear ganglion morphology "malformed group of neuron cell bodies associated with the eighth cranial nerve during embryogenesis; splits in later development to form the cochlear and vestibular ganglia" [smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0003938 abnormal ear development "developmental anomaly of any of the structures involved in the ear or vestibular system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Slc4a1tm1Llp/Slc4a1wan
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J

 MP:0003984 embryonic growth retardation "slow or limited development before birth" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0004309 absent otic vesicle "absence of the simple epithelial sac formed from the otic placode that gives rise to the structures of the inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

Allelic Composition: Fgf10tm1.1Sms/Fgf10tm1.1Sms,Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 MP:0004310 small otic vesicle "reduced size of the simple epithelial sac formed from the otic placode that gives rise to the structures of the inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Slc4a1tm1Llp/Slc4a1wan
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J

Allelic Composition: Fgf3tm1Sng/Fgf3tm1Sng,Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * CBA

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10+
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

Allelic Composition: Fgf3tm1Mrc/Fgf3+,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

Allelic Composition: Fgf10tm1.1Sms/Fgf10tm1.1Sms,Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 MP:0004313 absent vestibulocochlear ganglion "absence of the group of neuron cell bodies associated with the eighth cranial nerve during embryogenesis; splits in later development to form the cochlear and vestibular ganglia" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Fgf3tm1Sng/Fgf3tm1Sng,Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * CBA

 MP:0004493 dilated cochlea "the luminal space of the cochlea is increased in volume or area, usually with an increase in contained fluid" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0004619 caudal vertebral fusion "the union of one or more caudal vertebrae into a single structure in species where this does not normally occur" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0004923 absent common crus "absence of the united, nonampullary ends of the superior and posterior semicircular ducts in the inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0005191 head tilt "condition in which the portion of the body containing the brain and organs of sight, hearing, taste, and smell lists to the side" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Fgf3tm1Lwd/Fgf3tm1Lwd,Fgf4tm1.1Lwd/Fgf4tm1.1Lwd
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6 * NIH Swiss Webster * SJL/J

 MP:0006013 absent endolymphatic sac "absence of the dilated blind extremity of the endolymphatic duct, which lies external to the dura on the posterior aspect of the petrous part of the temporal bone" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, smb:Susan M Bello, Mouse Genome Informatics Curator, J:1776:]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0006030 abnormal otic vesicle formation "anomalous formation of the simple epithelial sac formed from the otic placode that gives rise to the structures of the inner ear" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:57313:]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd

 MP:0006089 abnormal saccule morphology "malformation in the smaller of the two sacs in the vestibule" [smb:Susan M Bello, Mouse Genome Informatics Curator, Taber s Cyclopedic Medical Dictionary:19th edition: ISBN N 0-8036-0655-99, J:92940]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0006090 abnormal utricle morphology "malformation in the larger of the two sacs in the vestibule" [smb:Susan M Bello, Mouse Genome Informatics Curator, Taber s Cyclopedic Medical Dictionary:19th edition: ISBN N 0-8036-0655-99, J:92940]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0006285 absent inner ear "absence of all components of the labyrinth, including the semicircular canals, vestibule and cochlea" [J:86619, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

 MP:0006358 absent pinna reflex "complete failure to respond to an auditory stimulus by a characteristic ear twitch" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0008065 short endolymphatic duct "length reduction or truncation of the small membranous canal which connects with both saccule and utricle of the membranous labyrinth, passes through the aqueduct of vestibule, and terminates in the endolymphatic sac" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0008309 dilated scala media "stretched or widened aperture of the luminal space of the spirally arranged membranous tube suspended within the cochlea, lying between and separating the scala vestibuli and scala tympani" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0011086 partial postnatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms anytime between the neonatal period and weaning age (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0011088 partial neonatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms within the neonatal period after birth (Mus: P0)" [MGI:csmith]
Show

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0011098 complete embryonic lethality during organogenesis "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
Show

Allelic Composition: Fgf3tm1Sng/Fgf3tm1Sng,Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * CBA

 MP:0011100 complete preweaning lethality "death of all organisms of a given genotype in a population between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Fgf3tm4b(EUCOMM)Hmgu/Fgf3tm4b(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Fgf3tm4b(EUCOMM)Hmgu/Bay

 MP:0011967 increased or absent threshold for auditory brainstem response "increase in the value at which one or more sound frequencies or broadband clicks first elicits a recordable response generated by electrical activity of neurons in the ascending auditory system, or complete lack of a recordable response at any frequency or broadband click" [MGI:csmith]
Show

Allelic Composition: Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0012173 short rostral-caudal axis "length reduction or truncation of the axis that runs from the head to the tail of the body" [MGI:anna]
Show

Allelic Composition: Fgf3tm1Lwd/Fgf3tm1Lwd,Fgf4tm1.1Lwd/Fgf4tm1.2Lwd
Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6 * C57BL/6 * NIH Swiss Webster * SJL/J

 MP:0012182 abnormal presomitic mesoderm morphology "any structural anomaly of the unsegmented field of paraxial mesoderm present posterior to the most recently formed somite pair, from which somites will form" [MGI:anna]
Show

Allelic Composition: Fgf3tm1Lwd/Fgf3tm1Lwd,Fgf4tm1.1Lwd/Fgf4tm1.1Lwd
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6 * NIH Swiss Webster * SJL/J

Allelic Composition: Fgf3tm1Lwd/Fgf3tm1Lwd,Fgf4tm1.1Lwd/Fgf4tm1.2Lwd
Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6 * C57BL/6 * NIH Swiss Webster * SJL/J

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

0 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2024
contact: otassy@igbmc.fr