En1tm2(cre)Wrst/En1+
Fgfr1tm1Jpa/Fgfr1tm1Jpa
involves: 129S1/Sv * 129X1/SvJ
|
abnormal cerebellum morphology |
J:83004
|
|
abnormal gait |
J:83004
|
|
abnormal locus ceruleus morphology |
J:83004
|
|
abnormal midbrain morphology |
J:83004
|
|
abnormal posture |
J:83004
|
|
abnormal trochlear nerve morphology |
J:83004
|
|
absent cerebellum vermis |
J:83004
|
|
absent inferior colliculus |
J:83004
|
|
impaired coordination |
J:83004
|
Fgfr1Eask/Fgfr1+
BALB/cByJ-Fgfr1Eask/GrsrJ
|
abnormal ear position |
J:179274
|
|
abnormal ear shape |
J:179274
|
|
abnormal outer ear morphology |
J:179274
|
|
increased or absent threshold for auditory brainstem response |
J:179274
|
|
lowered ear position |
J:179274
|
|
normal
vision/eye phenotype |
J:179274
|
Fgfr1Eask/Fgfr1Eask
BALB/cByJ-Fgfr1Eask/GrsrJ
|
prenatal lethality, complete penetrance |
J:179274
|
Fgfr1Hspy/Fgfr1+
(C3HeB/FeJ-Fgfr1Hspy x C57BL/6J)F1
|
abnormal outer ear morphology |
J:171915
|
|
abnormal stapes morphology |
J:171915
|
|
normal
hearing/vestibular/ear phenotype |
J:171915
|
Fgfr1Hspy/Fgfr1+
C3HeB/FeJ-Fgfr1Hspy
|
abnormal incus morphology |
J:171915
|
|
abnormal outer ear morphology |
J:171915
|
|
abnormal snout morphology |
J:171915
|
|
abnormal stapes morphology |
J:171915
|
|
normal
hearing/vestibular/ear phenotype |
J:171915
|
|
short snout |
J:171915
|
|
small ears |
J:171915
|
Fgfr1Hspy/Fgfr1+
C3HeB/FeJ-Hspy
|
abnormal auditory bulla morphology |
J:95895
|
|
abnormal cochlear nerve compound action potential |
J:95895
|
|
abnormal ear physiology |
J:95895
|
|
abnormal ear shape |
J:95895
|
|
abnormal incudostapedial joint morphology |
J:95895
|
|
abnormal incus body morphology |
J:95895
|
|
abnormal incus long process morphology |
J:95895
|
|
abnormal incus morphology |
J:95895
|
|
abnormal incus short process morphology |
J:95895
|
|
abnormal inner ear morphology |
J:95895
|
|
abnormal middle ear morphology |
J:95895
|
|
abnormal outer ear morphology |
J:95895
|
|
abnormal pinna reflex |
J:95895
|
|
abnormal stapes morphology |
J:95895
|
|
abnormal stapes posterior crus morphology |
J:95895
|
|
absent incus lenticular process |
J:95895
|
|
absent round window |
J:95895
|
|
absent stapes head |
J:95895
|
|
decreased cochlear outer hair cell number |
J:95895
|
|
decreased endocochlear potential |
J:95895
|
|
decreased round window size |
J:95895
|
|
excessive cerumen |
J:95895
|
|
increased susceptibility to otitis media |
J:95895
|
|
lowered ear position |
J:95895
|
|
short mandible |
J:95895
|
|
short nasal bone |
J:95895
|
|
small cranium |
J:95895
|
|
small ears |
J:95895
|
Fgfr1Hspy/Fgfr1Hspy
C3HeB/FeJ-Fgfr1Hspy
|
abnormal embryonic-extraembryonic boundary morphology |
J:171915
|
|
embryonic growth retardation |
J:171915
|
|
embryonic lethality between somite formation and embryo turning, complete penetrance |
J:171915
|
Fgfr1tm1.1(KOMP)Vlcg/Fgfr1+
C57BL/6N-Fgfr1tm1.1(KOMP)Vlcg/Ucd
|
increased respiratory quotient |
J:211773
|
Fgfr1tm1.1(KOMP)Vlcg/Fgfr1tm1.1(KOMP)Vlcg
C57BL/6N-Fgfr1tm1.1(KOMP)Vlcg/Ucd
|
abnormal embryo size |
J:211773
|
|
embryonic growth retardation |
J:211773
|
|
embryonic lethality prior to tooth bud stage |
J:211773
|
|
preweaning lethality, complete penetrance |
J:211773
|
Fgfr1tm1.1Jpa/Fgfr1tm1.1Jpa
involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * ICR
|
abnormal gastrulation |
J:83004
|
|
embryonic lethality, complete penetrance |
J:83004
|
Fgfr1tm1.1Upir/Fgfr1tm1.1Upir
involves: ICR
|
abnormal brain morphology |
J:78879
|
|
abnormal craniofacial morphology |
J:78879
|
|
abnormal developmental patterning |
J:78879
|
|
abnormal embryonic growth/weight/body size |
J:78879
|
|
abnormal embryonic tissue morphology |
J:78879
|
|
abnormal extraembryonic tissue morphology |
J:78879
|
|
abnormal heart development |
J:78879
|
|
abnormal neural tube morphology |
J:78879
|
|
embryonic lethality, complete penetrance |
J:78879
|
Fgfr1tm1Cxd/Fgfr1tm1Cxd
involves: 129S6/SvEvTac * NIH Black Swiss
|
abnormal axial skeleton morphology |
J:54222
|
|
abnormal developmental patterning |
J:54222
|
|
abnormal embryonic tissue morphology |
J:54222
|
|
abnormal neural tube morphology |
J:54222
|
|
embryonic lethality, complete penetrance |
J:54222
|
Fgfr1tm1Jpa/Fgfr1tm1.1Jpa
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * ICR
|
abnormal craniofacial bone morphology |
J:81179
|
|
cleft palate |
J:81179
|
|
normal
craniofacial phenotype |
J:81179
|
Fgfr1tm1Jpa/Fgfr1tm1Jpa
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
|
abnormal cerebellum development |
J:83004
|
|
abnormal cerebellum vermis morphology |
J:83004
|
|
absent inferior colliculus |
J:83004
|
|
neonatal lethality |
J:83004
|
Fgfr1tm1Jpa/Fgfr1tm1Jpa
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * ICR
|
abnormal hyoid bone lesser horn morphology |
J:81179
|
|
cleft palate |
J:81179
|
|
normal
craniofacial phenotype |
J:81179
|
Fgfr1tm1Jpa/Fgfr1tm1Jpa
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J
|
abnormal medial nasal prominence morphology |
J:298139
|
|
abnormal palatal mesenchymal cell proliferation |
J:298139
|
|
abnormal palatal rugae morphology |
J:298139
|
|
abnormal secondary palate development |
J:298139
|
|
abnormal tongue position |
J:298139
|
|
abnormal tooth development |
J:298139
|
|
cleft primary palate |
J:298139
|
|
cleft secondary palate |
J:298139
|
|
cleft upper lip |
J:298139
|
|
complete cleft palate |
J:298139
|
|
decreased palatal shelf size |
J:298139
|
|
failure of palatal shelf elevation |
J:298139
|
|
micrognathia |
J:298139
|
|
palatal shelves fail to meet at midline |
J:298139
|
|
persistence of medial edge epithelium during palatal shelf fusion |
J:298139
|
Fgfr1tm1Jrt/Fgfr1tm1Jrt
either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal chorion morphology |
J:22117
|
|
abnormal egg cylinder morphology |
J:22117
|
|
abnormal extraembryonic tissue morphology |
J:22117
|
|
abnormal gastrulation movements |
J:22117
|
|
abnormal head fold morphology |
J:22117
|
|
abnormal head mesenchyme morphology |
J:22117
|
|
abnormal heart tube morphology |
J:22117
|
|
abnormal mesoderm development |
J:22117
|
|
abnormal midbrain morphology |
J:22117
|
|
abnormal neural fold morphology |
J:22117
|
|
abnormal neural plate morphology |
J:22117
|
|
abnormal notochordal process morphology |
J:22117
|
|
abnormal posterior primitive streak morphology |
J:22117
|
|
abnormal primitive streak morphology |
J:22117
|
|
abnormal rostral-caudal body axis extension |
J:22117
|
|
abnormal visceral yolk sac endoderm morphology |
J:22117
|
|
abnormal visceral yolk sac mesenchyme morphology |
J:22117
|
|
abnormal visceral yolk sac morphology |
J:22117
|
|
absent somites |
J:22117
|
|
absent visceral yolk sac blood islands |
J:22117
|
|
decreased embryo size |
J:22117
|
|
decreased paraxial mesoderm size |
J:22117
|
|
embryonic growth retardation |
J:22117
|
|
embryonic lethality between implantation and somite formation, incomplete penetrance |
J:22117
|
|
embryonic lethality between somite formation and embryo turning, incomplete penetrance |
J:22117
|
|
embryonic lethality during organogenesis, incomplete penetrance |
J:22117
|
|
enlarged allantois |
J:22117
|
|
excessive folding of visceral yolk sac |
J:22117
|
|
failure of primitive streak formation |
J:22117
|
|
increased axial mesoderm size |
J:22117
|
|
kinked neural tube |
J:22117
|
Fgfr1tm1Jrt/Fgfr1tm2Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
abnormal axial skeleton morphology |
J:49154
|
|
abnormal carpal bone morphology |
J:49154
|
|
abnormal craniofacial bone morphology |
J:49154
|
|
abnormal digit morphology |
J:49154
|
|
abnormal limb morphology |
J:49154
|
|
abnormal sternocostal joint morphology |
J:49154
|
|
abnormal tarsal bone morphology |
J:49154
|
|
caudal body truncation |
J:49154
|
|
cervical vertebral transformation |
J:49154
|
|
decreased caudal vertebrae number |
J:49154
|
|
lumbar vertebral transformation |
J:49154
|
|
neonatal lethality, complete penetrance |
J:49154
|
|
oligodactyly |
J:49154
|
|
prenatal lethality, incomplete penetrance |
J:49154
|
|
rib fusion |
J:49154
|
|
sacral vertebral transformation |
J:49154
|
|
short tibia |
J:49154
|
|
syndactyly |
J:49154
|
|
vertebral transformation |
J:49154
|
Fgfr1tm1Jrt/Fgfr1tm4Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
abnormal tail development |
J:49154
|
|
prenatal lethality, complete penetrance |
J:49154
|
Fgfr1tm1Jrt/Fgfr1tm6.1Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
abnormal axial skeleton morphology |
J:49154
|
|
abnormal vertebrae morphology |
J:49154
|
|
cervical vertebral transformation |
J:49154
|
|
lumbar vertebral transformation |
J:49154
|
|
rib fusion |
J:49154
|
|
sacral vertebral transformation |
J:49154
|
|
thoracic vertebral transformation |
J:49154
|
Fgfr1tm1Led/Fgfr1tm1Led
involves: 129S4/SvJae * NIH Black Swiss
|
abnormal developmental patterning |
J:22118
|
|
abnormal egg cylinder morphology |
J:22118
|
|
abnormal extraembryonic tissue morphology |
J:22118
|
|
abnormal mesoderm development |
J:22118
|
|
abnormal neural tube morphology |
J:22118
|
|
abnormal primitive streak morphology |
J:22118
|
|
abnormal rostral-caudal axis patterning |
J:22118
|
|
abnormal rostral-caudal body axis extension |
J:22118
|
|
absent limb buds |
J:22118
|
|
absent somites |
J:22118
|
|
decreased embryo size |
J:22118
|
|
embryonic growth retardation |
J:22118
|
|
embryonic lethality between implantation and somite formation, incomplete penetrance |
J:22118
|
|
embryonic lethality during organogenesis, complete penetrance |
J:22118
|
|
excessive folding of visceral yolk sac |
J:22118
|
|
small proamniotic cavity |
J:22118
|
|
small visceral yolk sac |
J:22118
|
Fgfr1tm1Swnr/Fgfr1tm1Swnr
involves: 129S7/SvEvBrd * C57BL/6
|
normal
integument phenotype |
J:101854
|
Fgfr1tm1Upir/Fgfr1tm1.1Upir
involves: C57BL/6J
|
abnormal fetal cardiomyocyte proliferation |
J:95803
|
|
abnormal heart development |
J:95803
|
|
abnormal myocardial fiber morphology |
J:95803
|
|
dilated heart left ventricle |
J:95803
|
|
dilated heart right ventricle |
J:95803
|
|
heart hypoplasia |
J:95803
|
|
increased heart atrium size |
J:95803
|
|
thin myocardium |
J:95803
|
Fgfr1tm1Upir/Fgfr1tm1.1Upir
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * ICR
|
abnormal cochlea morphology |
J:78879
|
|
abnormal cochlear hair cell development |
J:78879
|
|
abnormal cochlear sensory epithelium morphology |
J:78879
|
|
abnormal organ of Corti morphology |
J:78879
|
|
abnormal orientation of inner hair cell stereociliary bundles |
J:78879
|
|
absent cochlear outer hair cells |
J:78879
|
|
absent organ of Corti supporting cells |
J:78879
|
|
decreased cochlear hair cell number |
J:78879
|
|
increased cochlear inner hair cell number |
J:78879
|
|
neonatal lethality, complete penetrance |
J:78879
|
Fgfr1tm1Upir/Fgfr1tm1Upir
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * ICR
|
abnormal cochlear sensory epithelium morphology |
J:78879
|
|
abnormal organ of Corti morphology |
J:78879
|
|
neonatal lethality, complete penetrance |
J:78879
|
Fgfr1tm1Upir/Fgfr1tm1Upir
Tg(GFAP-cre)25Mes/0
involves: FVB/N
|
abnormal astrocyte morphology |
J:110263
|
|
abnormal brain commissure morphology |
J:110263
|
|
abnormal corpus callosum morphology |
J:110263
|
|
abnormal hippocampal commissure morphology |
J:110263
|
|
abnormal neuronal migration |
J:110263
|
Fgfr1tm1Upir/Fgfr1tm1Upir
Tg(KRT5-cre)5132Jlj/0
involves: C57BL/6 * C57BL/6J * DBA/2J
|
no abnormal phenotype detected |
J:158802
|
Fgfr1tm1Upir/Fgfr1tm1Upir
Tg(Mnx1-GFP)1Slp/?
Tg(Nes-cre)1Kln/?
Not Specified
|
abnormal axon guidance |
J:122940
|
|
abnormal motor neuron morphology |
J:122940
|
Fgfr1tm1Upir/Fgfr1tm1Upir
Tg(Nes-cre)1Kln/0
involves: C57BL/6 * SJL
|
abnormal corpus callosum morphology |
J:110263
|
|
abnormal dorsal telencephalic commissure morphology |
J:110263
|
|
abnormal frontal lobe morphology |
J:110263
|
Fgfr1tm2.1Cxd/Fgfr1+
B6J.129S6(Cg)-Fgfr1tm2.1Cxd
|
abnormal maxillary-premaxillary suture morphology |
J:228708
|
|
abnormal palatine bone morphology |
J:228708
|
|
abnormal viscerocranium morphology |
J:228708
|
Fgfr1tm2.1Cxd/Fgfr1+
D2.129S6(Cg)-Fgfr1tm2.1Cxd
|
abnormal basisphenoid bone morphology |
J:228708
|
|
abnormal maxillary-premaxillary suture morphology |
J:228708
|
|
abnormal palatine bone morphology |
J:228708
|
|
abnormal viscerocranium morphology |
J:228708
|
|
midface hypoplasia |
J:228708
|
|
premature maxillary-premaxillary suture closure |
J:228708
|
Fgfr1tm2.1Cxd/Fgfr1+
involves: 129S6/SvEvTac * FVB/N
|
abnormal craniofacial bone morphology |
J:63959
|
|
facial asymmetry |
J:63959
|
|
increased osteoblast cell number |
J:63959
|
|
increased osteoblast proliferation |
J:63959
|
|
long incisors |
J:63959
|
|
midface hypoplasia |
J:63959
|
|
ocular hypertelorism |
J:63959
|
|
premature coronal suture closure |
J:63959
|
|
premature cranial suture closure |
J:63959
|
|
premature metopic suture closure |
J:63959
|
|
premature sagittal suture closure |
J:63959
|
Fgfr1tm2.1Cxd/Fgfr1tm2.1Cxd
involves: 129S6/SvEvTac * FVB/N
|
abnormal craniofacial bone morphology |
J:63959
|
|
craniofacial asymmetry |
J:63959
|
|
decreased body size |
J:63959
|
|
ocular hypertelorism |
J:63959
|
|
premature cranial suture closure |
J:63959
|
|
short tail |
J:63959
|
Fgfr1tm2.1Jrt/Fgfr1tm2.1Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
no abnormal phenotype detected |
J:49154
|
Fgfr1tm2Jrt/Fgfr1tm2Jrt
involves: 129S1/Sv * 129X1/SvJ
|
abnormal cerebellum vermis morphology |
J:83004
|
|
decreased inferior colliculus size |
J:83004
|
Fgfr1tm2Jrt/Fgfr1tm2Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
abnormal axial skeleton morphology |
J:49154
|
|
abnormal carpal bone morphology |
J:49154
|
|
abnormal cervical axis morphology |
J:49154
|
|
abnormal craniofacial bone morphology |
J:49154
|
|
abnormal digit morphology |
J:49154
|
|
abnormal limb morphology |
J:49154
|
|
abnormal phalanx morphology |
J:49154
|
|
abnormal rostral-caudal axis patterning |
J:49154
|
|
abnormal sternocostal joint morphology |
J:49154
|
|
abnormal tail development |
J:49154
|
|
abnormal tarsal bone morphology |
J:49154
|
|
caudal body truncation |
J:49154
|
|
cervical vertebral transformation |
J:49154
|
|
decreased caudal vertebrae number |
J:49154
|
|
increased rib number |
J:49154
|
|
lumbar vertebral transformation |
J:49154
|
|
neonatal lethality, complete penetrance |
J:49154
|
|
oligodactyly |
J:49154
|
|
rib fusion |
J:49154
|
|
sacral vertebral transformation |
J:49154
|
|
small second pharyngeal arch |
J:49154
|
|
syndactyly |
J:49154
|
|
thoracic vertebral transformation |
J:49154
|
|
vertebral transformation |
J:49154
|
Fgfr1tm2Jrt/Fgfr1tm2Jrt
involves: 129S1/Sv * 129X1/SvJ * ICR
|
abnormal alisphenoid bone morphology |
J:81179
|
|
abnormal cochlear sensory epithelium morphology |
J:78879
|
|
abnormal hyoid bone lesser horn morphology |
J:81179
|
|
abnormal incus morphology |
J:81179
|
|
abnormal malleus morphology |
J:81179
|
|
abnormal middle ear ossicle morphology |
J:81179
|
|
abnormal neural crest cell migration |
J:81179
|
|
abnormal neural crest cell morphology |
J:81179
|
|
abnormal organ of Corti morphology |
J:78879
|
|
abnormal pterygoid bone morphology |
J:81179
|
|
abnormal retrotympanic process morphology |
J:81179
|
|
abnormal second pharyngeal arch morphology |
J:81179
|
|
abnormal secondary palate development |
J:81179
|
|
abnormal styloid process morphology |
J:81179
|
|
abnormal tongue position |
J:81179
|
|
absent gonial bone |
J:81179
|
|
absent middle ear ossicles |
J:81179
|
|
absent tympanic ring |
J:81179
|
|
cleft palate |
J:81179
|
|
decreased cochlear outer hair cell number |
J:78879
|
|
decreased tympanic ring size |
J:81179
|
|
failure of palatal shelf elevation |
J:81179
|
|
neonatal lethality, complete penetrance |
J:78879,
J:81179
|
|
small ears |
J:81179
|
|
small gonial bone |
J:81179
|
Fgfr1tm2Jrt/Fgfr1tm2Jrt
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * ICR
|
abnormal alisphenoid bone morphology |
J:81179
|
|
abnormal incus morphology |
J:81179
|
|
abnormal malleus morphology |
J:81179
|
|
abnormal middle ear ossicle morphology |
J:81179
|
|
abnormal pterygoid bone morphology |
J:81179
|
|
abnormal second pharyngeal arch morphology |
J:81179
|
|
abnormal temporal bone squamous part morphology |
J:81179
|
|
normal
craniofacial phenotype |
J:81179
|
|
decreased tympanic ring size |
J:81179
|
|
small gonial bone |
J:81179
|
Fgfr1tm3.1Cxd/Fgfr1tm3.1Cxd
involves: 129S6/SvEvTac * Black Swiss
|
embryonic lethality, complete penetrance |
J:75137
|
Fgfr1tm3.1Cxd/Fgfr1tm3.2Cxd
Shhtm1(EGFP/cre)Cjt/Shh+
involves: 129S6/SvEvTac
|
abnormal embryonic autopod plate morphology |
J:101736
|
|
oligodactyly |
J:101736
|
Fgfr1tm3.1Cxd/Fgfr1tm3.2Cxd
Tg(T-cre)1Lwd/0
involves: 129S6/SvEvTac * C3H * C57BL/6
|
abnormal apical ectodermal ridge morphology |
J:101736
|
|
abnormal axial skeleton morphology |
J:101736
|
|
abnormal cartilage development |
J:101736
|
|
abnormal forelimb bud morphology |
J:101736
|
|
abnormal forelimb stylopod morphology |
J:101736
|
|
abnormal forelimb zeugopod morphology |
J:101736
|
|
abnormal hindlimb morphology |
J:101736
|
|
abnormal neural plate morphology |
J:101736
|
|
abnormal somite size |
J:101736
|
|
forelimb oligodactyly |
J:101736
|
|
neonatal lethality, complete penetrance |
J:101736
|
Fgfr1tm3.1Jrt/Fgfr1tm3.1Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
abnormal gastrulation |
J:49154
|
|
abnormal somite development |
J:49154
|
|
absent somites |
J:49154
|
|
decreased paraxial mesoderm size |
J:49154
|
|
embryonic lethality during organogenesis, incomplete penetrance |
J:49154
|
Fgfr1tm3.1Sor/Fgfr1tm3.1Sor
involves: 129S4/SvJaeSor * C57BL/6J
|
abnormal neural tube closure |
J:105920
|
|
embryonic growth retardation |
J:105920
|
|
lethality throughout fetal growth and development, complete penetrance |
J:105920
|
|
spina bifida |
J:105920
|
Fgfr1tm3.2Cxd/Fgfr1tm3.2Cxd
Shhtm1(EGFP/cre)Cjt/Shh+
involves: 129S6/SvEvTac
|
abnormal embryonic autopod plate morphology |
J:101736
|
|
oligodactyly |
J:101736
|
Fgfr1tm3.2Cxd/Fgfr1tm3.2Cxd
Tg(T-cre)1Lwd/0
involves: 129S6/SvEvTac * C3H * C57BL/6
|
abnormal apical ectodermal ridge morphology |
J:101736
|
|
abnormal axial skeleton morphology |
J:101736
|
|
abnormal cartilage development |
J:101736
|
|
abnormal forelimb bud morphology |
J:101736
|
|
abnormal forelimb stylopod morphology |
J:101736
|
|
abnormal forelimb zeugopod morphology |
J:101736
|
|
abnormal hindlimb morphology |
J:101736
|
|
abnormal neural plate morphology |
J:101736
|
|
abnormal somite size |
J:101736
|
|
forelimb oligodactyly |
J:101736
|
|
neonatal lethality, complete penetrance |
J:101736
|
Fgfr1tm3Cxd/Fgfr1tm3Cxd
involves: 129S6/SvEvTac * Black Swiss
|
embryonic lethality between implantation and somite formation, complete penetrance |
J:75137
|
Fgfr1tm3Jrt/Fgfr1tm3Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
abnormal gastrulation |
J:49154
|
|
abnormal somite development |
J:49154
|
|
absent somites |
J:49154
|
|
decreased paraxial mesoderm size |
J:49154
|
|
embryonic lethality during organogenesis, incomplete penetrance |
J:49154
|
Fgfr1tm3Sor/Fgfr1tm3Sor
involves: 129S4/SvJaeSor * C57BL/6J
|
embryonic lethality, complete penetrance |
J:105920
|
Fgfr1tm4.1Jrt/Fgfr1tm4.1Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
no abnormal phenotype detected |
J:49154
|
Fgfr1tm4.1Jrt/Fgfr1tm4.1Jrt
involves: 129S1/Sv * 129X1/SvJ * ICR
|
normal
hearing/vestibular/ear phenotype |
J:78879
|
Fgfr1tm4.1Sor/Fgfr1tm4.1Sor
involves: 129S4/SvJaeSor * C57BL/6J
|
abnormal digit morphology |
J:105920
|
|
decreased embryo size |
J:105920
|
|
lethality throughout fetal growth and development, incomplete penetrance |
J:105920
|
Fgfr1tm4Jrt/Fgfr1tm4Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
abnormal axial skeleton morphology |
J:49154
|
|
abnormal carpal bone morphology |
J:49154
|
|
abnormal cartilage development |
J:49154
|
|
abnormal cervical axis morphology |
J:49154
|
|
abnormal craniofacial bone morphology |
J:49154
|
|
abnormal forelimb morphology |
J:49154
|
|
abnormal limb morphology |
J:49154
|
|
abnormal phalanx morphology |
J:49154
|
|
abnormal rostral-caudal axis patterning |
J:49154
|
|
abnormal sternocostal joint morphology |
J:49154
|
|
abnormal tail morphology |
J:49154
|
|
abnormal tarsal bone morphology |
J:49154
|
|
cervical vertebral transformation |
J:49154
|
|
decreased caudal vertebrae number |
J:49154
|
|
embryonic lethality during organogenesis, incomplete penetrance |
J:49154
|
|
lethality throughout fetal growth and development, incomplete penetrance |
J:49154
|
|
lumbar vertebral transformation |
J:49154
|
|
neonatal lethality, complete penetrance |
J:49154
|
|
sacral vertebral transformation |
J:49154
|
|
small second pharyngeal arch |
J:49154
|
|
vertebral transformation |
J:49154
|
Fgfr1tm4Sor/Fgfr1tm4Sor
involves: 129S4/SvJaeSor * C57BL/6J
|
embryonic lethality, complete penetrance |
J:105920
|
Fgfr1tm5.1Jrt/Fgfr1tm5.1Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
no abnormal phenotype detected |
J:49154
|
Fgfr1tm5.1Sor/Fgfr1tm5.1Sor
H2az2Tg(Wnt1-cre)11Rth/H2az2+
129S4.Cg-Fgfr1tm5.1Sor H2az2Tg(Wnt1-cre)11Rth
|
midline facial cleft |
J:226497
|
Fgfr1tm5.1Sor/Fgfr1tm9.1Sor
H2az2Tg(Wnt1-cre)11Rth/H2az2+
129S4.Cg-Fgfr1tm5.1Sor Fgfr1tm9.1Sor H2az2Tg(Wnt1-cre)11Rth
|
cleft palate |
J:226497
|
Fgfr1tm5.1Sor/Fgfr1tm10.1Sor
H2az2Tg(Wnt1-cre)11Rth/H2az2+
129S4.Cg-Fgfr1tm5.1Sor Fgfr1tm10.1Sor H2az2Tg(Wnt1-cre)11Rth
|
cleft palate |
J:226497
|
Fgfr1tm5.2Sor/Fgfr1tm5.2Sor
129S4/SvJaeSor-Fgfr1tm5.2Sor
|
abnormal blastocyst morphology |
J:226497
|
|
abnormal developmental patterning |
J:226497
|
|
abnormal embryonic epiblast morphology |
J:226497
|
|
abnormal primitive endoderm morphology |
J:226497
|
|
embryonic lethality, complete penetrance |
J:226497
|
Fgfr1tm5.2Sor/Fgfr1tm5.2Sor
involves: 129S4/SvJaeSor * C57BL/6J
|
abnormal developmental patterning |
J:105920
|
|
abnormal gastrulation movements |
J:105920
|
|
abnormal mesoderm development |
J:105920
|
|
caudal body truncation |
J:105920
|
|
craniorachischisis |
J:105920
|
|
decreased paraxial mesoderm size |
J:105920
|
|
embryonic growth retardation |
J:105920
|
|
embryonic lethality during organogenesis, complete penetrance |
J:105920
|
|
enlarged heart |
J:105920
|
|
failure of heart looping |
J:105920
|
|
failure of somite differentiation |
J:105920
|
|
increased axial mesoderm size |
J:105920
|
Fgfr1tm5Jrt/Fgfr1tm5Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
abnormal axial skeleton morphology |
J:49154
|
|
abnormal craniofacial bone morphology |
J:49154
|
|
abnormal lateral plate mesoderm morphology |
J:49154
|
|
abnormal limb morphology |
J:49154
|
|
abnormal neural fold morphology |
J:49154
|
|
abnormal somite development |
J:49154
|
|
abnormal sternocostal joint morphology |
J:49154
|
|
abnormal tail morphology |
J:49154
|
|
broad limb buds |
J:49154
|
|
caudal body truncation |
J:49154
|
|
cervical vertebral transformation |
J:49154
|
|
decreased caudal vertebrae number |
J:49154
|
|
fusion of atlas and occipital bones |
J:49154
|
|
neonatal lethality |
J:49154
|
|
prenatal lethality, incomplete penetrance |
J:49154
|
|
rib fusion |
J:49154
|
|
small second pharyngeal arch |
J:49154
|
|
thoracic vertebral transformation |
J:49154
|
Fgfr1tm6.1Jrt/Fgfr1tm6.1Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
abnormal axial skeleton morphology |
J:49154
|
|
abnormal sternocostal joint morphology |
J:49154
|
|
abnormal vertebrae morphology |
J:49154
|
|
cervical vertebral transformation |
J:49154
|
|
lumbar vertebral transformation |
J:49154
|
|
rib fusion |
J:49154
|
|
sacral vertebral transformation |
J:49154
|
|
thoracic vertebral transformation |
J:49154
|
Fgfr1tm6Jrt/Fgfr1tm6Jrt
involves: 129S1/Sv * 129X1/SvJ
|
abnormal cerebellum vermis morphology |
J:83004
|
|
decreased inferior colliculus size |
J:83004
|
Fgfr1tm6Jrt/Fgfr1tm6Jrt
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
abnormal axial skeleton morphology |
J:49154
|
|
abnormal craniofacial bone morphology |
J:49154
|
|
abnormal lateral plate mesoderm morphology |
J:49154
|
|
abnormal limb morphology |
J:49154
|
|
abnormal neural fold formation |
J:49154
|
|
abnormal somite development |
J:49154
|
|
abnormal sternocostal joint morphology |
J:49154
|
|
broad limb buds |
J:49154
|
|
caudal body truncation |
J:49154
|
|
cervical vertebral transformation |
J:49154
|
|
decreased caudal vertebrae number |
J:49154
|
|
decreased somite size |
J:49154
|
|
embryonic lethality during organogenesis, incomplete penetrance |
J:49154
|
|
fusion of atlas and occipital bones |
J:49154
|
|
neonatal lethality, complete penetrance |
J:49154
|
|
perinatal lethality, incomplete penetrance |
J:49154
|
|
rib fusion |
J:49154
|
|
small second pharyngeal arch |
J:49154
|
|
thoracic vertebral transformation |
J:49154
|
|
vertebral transformation |
J:49154
|
Fgfr1tm6Jrt/Fgfr1tm6Jrt
involves: 129S1/Sv * 129X1/SvJ * ICR
|
abnormal cochlear hair cell development |
J:78879
|
|
abnormal cochlear hair cell morphology |
J:78879
|
|
abnormal cochlear sensory epithelium morphology |
J:78879
|
|
abnormal orientation of inner hair cell stereociliary bundles |
J:78879
|
|
absent cochlear outer hair cells |
J:78879
|
|
absent organ of Corti supporting cells |
J:78879
|
|
increased cochlear inner hair cell number |
J:78879
|
|
neonatal lethality, complete penetrance |
J:78879
|
Fgfr1tm7.1Sor/Fgfr1tm7.1Sor
129S4/SvJaeSor-Fgfr1tm7.1Sor
|
normal
no abnormal phenotype detected |
J:226497
|
Fgfr1tm8.1Sor/Fgfr1tm8.1Sor
129S4/SvJaeSor-Fgfr1tm8.1Sor
|
abnormal axial skeleton morphology |
J:226497
|
|
abnormal rib morphology |
J:226497
|
|
abnormal thoracic cage morphology |
J:226497
|
|
abnormal thoracic vertebrae morphology |
J:226497
|
|
decreased lumbar vertebrae number |
J:226497
|
|
decreased thoracic vertebrae number |
J:226497
|
|
normal
growth/size/body region phenotype |
J:226497
|
|
normal
homeostasis/metabolism phenotype |
J:226497
|
|
rib bifurcation |
J:226497
|
Fgfr1tm9.1Sor/Fgfr1tm9.1Sor
129S4/SvJaeSor-Fgfr1tm9.1Sor
|
cleft palate |
J:226497
|
|
increased thoracic vertebrae number |
J:226497
|
|
incus hypoplasia |
J:226497
|
|
lumbar vertebral transformation |
J:226497
|
|
malleus hypoplasia |
J:226497
|
|
middle ear ossicle hypoplasia |
J:226497
|
|
postaxial polydactyly |
J:226497
|
|
postnatal lethality, complete penetrance |
J:226497
|
|
second pharyngeal arch hypoplasia |
J:226497
|
|
stapes hypoplasia |
J:226497
|
|
styloid process hypoplasia |
J:226497
|
|
tympanic ring hypoplasia |
J:226497
|
Fgfr1tm10.1Sor/Fgfr1tm10.1Sor
129S4/SvJaeSor-Fgfr1tm10.1Sor
|
abnormal embryo development |
J:226497
|
|
abnormal neural crest cell migration |
J:226497
|
|
abnormal somite development |
J:226497
|
|
absent second pharyngeal arch |
J:226497
|
|
bleb |
J:226497
|
|
caudal body truncation |
J:226497
|
|
decreased somite size |
J:226497
|
|
embryonic growth arrest |
J:226497
|
|
embryonic growth retardation |
J:226497
|
|
embryonic lethality, complete penetrance |
J:226497
|
Tg(Gnrh1-Fgfr1)1Tsai/Tg(Gnrh1-Fgfr1)1Tsai
involves: C57BL/6J * DBA/2J
|
abnormal hypothalamus secretion |
J:95057
|
|
abnormal neuron morphology |
J:95057
|
|
decreased litter size |
J:95057
|
|
decreased neuron number |
J:95057
|
|
decreased testis weight |
J:95057
|
|
delayed vaginal opening |
J:95057
|
|
early reproductive senescence |
J:95057
|
|
normal
homeostasis/metabolism phenotype |
J:95057
|
Excel File
Analysis Tools