Adcy1tm1Ito/Adcy1tm1.1Ito
Emx1tm1(cre)Ito/Emx1+
B6.129P2-Emx1tm1(cre)Ito Adcy1tm1Ito Adcy1tm1.1Ito
|
abnormal barrel cortex morphology |
J:137123
|
|
decreased miniature excitatory postsynaptic current amplitude |
J:137123
|
|
normal
nervous system phenotype |
J:137123
|
|
reduced long-term potentiation |
J:137123
|
Adcy3tm2.1Drs/Adcy3tm2.1Drs
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129X1/SvJ
|
abnormal depression-related behavior |
J:281839
|
|
abnormal long-term spatial reference memory |
J:281839
|
|
abnormal object recognition memory |
J:281839
|
|
abnormal response to new environment |
J:281839
|
|
behavioral despair |
J:281839
|
|
hypoactivity |
J:281839
|
|
impaired spatial learning |
J:281839
|
Afdntm1c(EUCOMM)Hmgu/Afdntm1c(EUCOMM)Hmgu
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6J * C57BL/6N
|
abnormal cell cycle |
J:215584
|
|
abnormal cerebral cortex morphology |
J:215584
|
|
abnormal cortical ventricular zone morphology |
J:215584
|
|
abnormal embryonic neuroepithelium morphology |
J:215584
|
|
abnormal hippocampus morphology |
J:215584
|
|
abnormal neocortex morphology |
J:215584
|
|
abnormal nervous system tract morphology |
J:215584
|
|
abnormal radial glial cell morphology |
J:215584
|
|
abnormal stratification in cerebral cortex |
J:215584
|
|
abnormal telencephalon development |
J:215584
|
|
ectopic neuron |
J:215584
|
|
increased brain size |
J:215584
|
|
increased neocortex size |
J:215584
|
|
increased neuronal precursor cell number |
J:215584
|
|
increased radial glial cell number |
J:215584
|
|
thin cortical plate |
J:215584
|
Arhgef9tm1Betz/Y
Emx1tm1(cre)Yql/Emx1+
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6
|
abnormal neuron morphology |
J:141850
|
Atrtm2Bal/Atrtm2Bal
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6J
|
abnormal cerebral cortex morphology |
J:181920
|
|
abnormal corpus callosum morphology |
J:181920
|
|
abnormal stratification in cerebral cortex |
J:181920
|
|
hippocampus hypoplasia |
J:181920
|
Atxn1tm2Hzo/Atxn1tm2Hzo
Atxn1ltm2Hzo/Atxn1ltm2Hzo
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129S7/SvEvBrd
|
decreased anxiety-related response |
J:240674
|
|
decreased cerebral cortex cell number |
J:240674
|
|
decreased dentate gyrus size |
J:240674
|
|
impaired contextual conditioning behavior |
J:240674
|
|
increased locomotor activity |
J:240674
|
|
thin cerebral cortex |
J:240674
|
Bdnftm1Krj/Bdnf+
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6J
|
normal
growth/size/body region phenotype |
J:84683
|
Bdnftm1Krj/Bdnftm1Lfr
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6J
|
abnormal cerebral cortex morphology |
J:96903
|
|
abnormal hippocampus morphology |
J:96903
|
|
abnormal medium spiny neuron morphology |
J:96903
|
|
abnormal nest building behavior |
J:84683
|
|
abnormal visual cortex morphology |
J:84683
|
|
decreased body weight |
J:84683
|
|
decreased striatum size |
J:96903
|
|
delayed eyelid opening |
J:84683
|
|
increased aggression |
J:84683
|
|
limb grasping |
J:96903
|
|
obese |
J:84683
|
|
premature death |
J:84683
|
|
reduced fertility |
J:84683
|
|
thin cerebral cortex |
J:84683
|
Bhlhe22tm2.1Meg/Bhlhe22tm2.1Meg
Emx1tm1(cre)Krj/Emx1+
involves: 129/Sv * 129S2/SvPas
|
normal
behavior/neurological phenotype |
J:158273
|
|
normal
integument phenotype |
J:158273
|
Bhlhe22tm2.1Meg/Bhlhe22tm2.1Meg
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J
|
abnormal anterior corticospinal tract morphology |
J:182304
|
|
absent corpus callosum |
J:182304
|
|
absent hippocampal commissure |
J:182304
|
Bicd2tm1Hgrd/Bicd2tm1Hgrd
Emx1tm1(cre)Krj/Emx1+
involves: C57BL/6
|
abnormal hippocampus layer morphology |
J:210236
|
|
abnormal neuronal migration |
J:210236
|
|
abnormal stratification in cerebral cortex |
J:210236
|
|
normal
nervous system phenotype |
J:210236
|
Bptftm1.1Cwu/Bptftm1.1Cwu
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * C57BL/6
|
abnormal cerebral cortex morphology |
J:334252
|
|
abnormal head shape |
J:334252
|
|
abnormal neuron specification |
J:334252
|
|
abnormal neuronal precursor proliferation |
J:334252
|
|
abnormal stratification in cerebral cortex |
J:334252
|
|
normal
behavior/neurological phenotype |
J:334252
|
|
decreased body weight |
J:334252
|
|
decreased brain weight |
J:334252
|
|
decreased forebrain size |
J:334252
|
|
decreased neuronal precursor cell number |
J:334252
|
|
forebrain hypoplasia |
J:334252
|
|
increased neuron apoptosis |
J:334252
|
|
microgliosis |
J:334252
|
|
normal
mortality/aging |
J:334252
|
Brpf1tm1c(EUCOMM)Wtsi/Brpf1tm1c(EUCOMM)Wtsi
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6J * C57BL/6N
|
abnormal behavior |
J:241490
|
|
abnormal cell cycle checkpoint function |
J:224155
|
|
abnormal cell physiology |
J:240552
|
|
abnormal corpus callosum morphology |
J:224155
|
|
abnormal dentate gyrus morphology |
J:224155
|
|
abnormal hippocampal mossy fiber morphology |
J:224155
|
|
abnormal hippocampus CA1 region morphology |
J:224155
|
|
abnormal hippocampus development |
J:224155
|
|
abnormal hippocampus morphology |
J:224155
|
|
abnormal hippocampus neuron morphology |
J:224155
|
|
abnormal hippocampus pyramidal cell layer |
J:224155
|
|
abnormal hippocampus region morphology |
J:224155
|
|
abnormal neocortex morphology |
J:224155,
J:241490
|
|
abnormal nest building behavior |
J:241490
|
|
abnormal neuronal precursor cell migration |
J:224155
|
|
abnormal neuronal stem cell morphology |
J:224155
|
|
abnormal radial glial cell morphology |
J:224155
|
|
decreased body size |
J:241490
|
|
decreased corpus callosum size |
J:241490
|
|
decreased dentate gyrus size |
J:224155
|
|
decreased food intake |
J:241490
|
|
decreased neocortex size |
J:241490
|
|
decreased neuronal precursor cell number |
J:224155
|
|
decreased neuronal precursor proliferation |
J:224155,
J:241490
|
|
decreased radial glial cell number |
J:224155
|
|
increased subiculum size |
J:224155
|
|
limb grasping |
J:241490
|
|
normal
nervous system phenotype |
J:241490
|
|
postnatal lethality, incomplete penetrance |
J:224155,
J:241490
|
|
prenatal growth retardation |
J:241490
|
|
prenatal lethality, incomplete penetrance |
J:241490
|
|
thin cortical plate |
J:241490
|
Btbd9tm1c(EUCOMM)Wtsi/Btbd9tm1c(EUCOMM)Wtsi
Emx1tm1(cre)Yql/Emx1+
involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6N
|
abnormal primary motor cortex morphology |
J:282582
|
|
abnormal primary somatosensory cortex morphology |
J:282582
|
|
abnormal sleep behavior |
J:282582
|
|
hyperactivity |
J:282582
|
|
impaired coordination |
J:282582
|
|
increased thermal nociceptive threshold |
J:282582
|
Cadpstm1.1Tfr/Cadpstm1.2Tfr
Emx1tm1(cre)Ito/Emx1+
B6.Cg-Emx1tm1(cre)Ito Cadpstm1.1Tfr Cadpstm1.2Tfr
|
abnormal dentate gyrus morphology |
J:204664
|
|
abnormal Golgi trans cisterna morphology |
J:204664
|
|
abnormal hippocampus pyramidal cell morphology |
J:204664
|
|
abnormal synaptic bouton morphology |
J:204664
|
|
normal
nervous system phenotype |
J:204664
|
Camk2atm1.1Yelg/Camk2atm1.1Yelg
Emx1tm1.1(cre)Ito/0
B6J.Cg-Camk2atm1.1Yelg Emx1tm1.1(cre)Ito
|
impaired contextual conditioning behavior |
J:216169
|
|
impaired spatial learning |
J:216169
|
Cdh2tm1Glr/Cdh2tm1Glr
Emx1tm1(cre)Krj/Emx1+
involves: 129S6/SvEvTac * C57BL/6
|
abnormal cerebral cortex morphology |
J:215584
|
|
abnormal cortical ventricular zone morphology |
J:215584
|
|
abnormal neocortex morphology |
J:215584
|
|
abnormal nervous system tract morphology |
J:215584
|
|
abnormal radial glial cell morphology |
J:215584
|
|
ectopic neuron |
J:215584
|
|
increased neuronal precursor cell number |
J:215584
|
|
thickened cerebral cortex |
J:215584
|
Cdyltm1.1Yuw/Cdyltm1.1Yuw
Emx1tm1(cre)Yql/Emx1+
involves: 129S2/SvPas * C57BL/6
|
abnormal neuronal migration |
J:251551
|
|
normal
behavior/neurological phenotype |
J:251551
|
|
increased susceptibility to pharmacologically induced seizures |
J:251551
|
Celf4tm1.1Frk/Celf4tm1.1Frk
Emx1tm1(cre)Krj/?
involves: 129 * C57BL/6J
|
increased susceptibility to induction of seizure by inducing agent |
J:19671
|
Celsr1tm1Fati/Celsr1tm1Fati
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ
|
whorled hair |
J:157059
|
Celsr3tm1Agof/Celsr3tm2Agof
Emx1tm1(cre)Krj/Emx1+
involves: 129P2/OlaHsd * 129S2/SvPas
|
abnormal anterior commissure morphology |
J:134879
|
|
abnormal brain internal capsule morphology |
J:134879
|
|
abnormal corticospinal tract morphology |
J:134879
|
Chn1tm1Ito/Chn1tm1.1Ito
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6NSlc
|
normal
behavior/neurological phenotype |
J:209606
|
Chrm1tm2.1Stl/Chrm1tm2.1Stl
Emx1tm1.1(cre)Ito/0
involves: 129P2/OlaHsd
|
abnormal excitatory postsynaptic currents |
J:156540
|
|
abnormal long-term depression |
J:156540
|
|
abnormal miniature excitatory postsynaptic currents |
J:156540
|
|
decreased paired-pulse facilitation |
J:156540
|
Cictm1c(KOMP)Wtsi/Cictm1c(KOMP)Wtsi
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6 * C57BL/6N
|
abnormal cerebral cortex morphology |
J:240674
|
|
abnormal pyramidal neuron dendrite morphology |
J:240674
|
|
decreased anxiety-related response |
J:240674
|
|
decreased cerebral cortex cell number |
J:240674
|
|
decreased dentate gyrus size |
J:240674
|
|
decreased neurotransmitter release |
J:240674
|
|
impaired contextual conditioning behavior |
J:240674
|
|
increased locomotor activity |
J:240674
|
|
thin cerebral cortex |
J:240674
|
Clcn7tm3.1Tjj/Clcn7tm3.1Tjj
Emx1tm1.1(cre)Ito/Emx1+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6
|
abnormal cerebral cortex morphology |
J:155176
|
|
abnormal dentate gyrus morphology |
J:155176
|
|
abnormal hippocampus morphology |
J:155176
|
|
abnormal lysosome physiology |
J:155176
|
|
astrocytosis |
J:155176
|
|
enlarged lateral ventricles |
J:155176
|
|
normal
growth/size/body region phenotype |
J:155176
|
|
hippocampal neuron degeneration |
J:155176
|
|
limb grasping |
J:155176
|
|
loss of cortex neurons |
J:155176
|
|
loss of hippocampal neurons |
J:155176
|
|
microgliosis |
J:155176
|
|
normal
mortality/aging |
J:155176
|
|
neurodegeneration |
J:155176
|
|
normal
skeleton phenotype |
J:155176
|
Cmtr1tm1b(EUCOMM)Hmgu/Cmtr1tm1b(EUCOMM)Hmgu
Emx1tm1(cre)Krj/Emx1+
Tg(Thy1-YFP)HJrs/0
involves: 129S2/SvPas * C57BL/6J * C57BL/6N * CBA
|
abnormal dendrite morphology |
J:300305
|
|
abnormal susceptibility to Riboviria infection |
J:300305
|
|
decreased neocortex size |
J:300305
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem
Emx1tm1(cre)Yql/Emx1+
B6.129-Emx1tm1(cre)Yql Ctnnb1tm2Kem
|
abnormal cerebral cortex morphology |
J:92923
|
|
abnormal hippocampus morphology |
J:92923
|
|
abnormal nursing |
J:92923
|
|
absent corpus callosum |
J:92923
|
|
absent dentate gyrus |
J:92923
|
|
absent hippocampal commissure |
J:92923
|
|
absent hippocampus CA1 region |
J:92923
|
|
absent hippocampus CA2 region |
J:92923
|
|
absent hippocampus CA3 region |
J:92923
|
|
decreased body size |
J:92923
|
|
dilated lateral ventricle |
J:92923
|
|
increased susceptibility to pharmacologically induced seizures |
J:92923
|
|
male infertility |
J:92923
|
|
seizures |
J:92923
|
Dact1tm1.1Bnrc/Dact1tm1.2Bnrc
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas
|
abnormal dendritic spine morphology |
J:159217
|
|
normal
nervous system phenotype |
J:159217
|
Eif4a3tm1.1Dlsi/Eif4a3+
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6J
|
abnormal neocortex morphology |
J:235650
|
|
abnormal neuronal stem cell morphology |
J:235650
|
|
abnormal telencephalon development |
J:235650
|
|
absent telencephalon |
J:235650
|
|
decreased brain size |
J:235650
|
|
decreased forebrain size |
J:235650
|
|
decreased neocortex size |
J:235650
|
|
microcephaly |
J:235650
|
Emx1tm1(cre)Ito/Emx1+
Grin1tm1Stl/Grin1tm2Stl
involves: 129P2/OlaHsd * 129S2/SvPas * 129S4/SvJae * C57BL/6
|
abnormal postnatal growth |
J:64064
|
|
abnormal primary somatosensory cortex morphology |
J:80900
|
|
abnormal somatosensory cortex morphology |
J:64064
|
|
absent barrels in primary somatosensory cortex |
J:64064,
J:80900
|
|
decreased body weight |
J:64064
|
|
reduced NMDA receptor mediated synaptic activity in barrel cortex |
J:64064
|
Emx1tm1(cre)Ito/Emx1+
Hes1tm1Fgu/Hes1tm1Hojo
Hes5tm1Fgu/Hes5tm1Fgu
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
|
abnormal neurohypophysis morphology |
J:121843
|
|
abnormal pituitary diverticulum morphology |
J:121843
|
|
abnormal pituitary gland development |
J:121843
|
|
abnormal pituitary gland morphology |
J:121843
|
|
abnormal pituitary infundibular stalk morphology |
J:121843
|
|
absent pituitary intermediate lobe |
J:121843
|
|
increased somatotroph cell number |
J:121843
|
|
pituitary gland hypoplasia |
J:121843
|
Emx1tm1(cre)Ito/Emx1+
Olig2tm1Qrlu/Olig2tm1Qrlu
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
|
abnormal myelination |
J:105071
|
Emx1tm1(cre)Ito/Emx1+
Htr2atm1Grch/Htr2atm2Grch
129S6.Cg-Htr2atm1Grch Htr2atm2Grch Emx1tm1(cre)Ito
|
normal
behavior/neurological phenotype |
J:110958
|
Emx1tm1(cre)Ito/Emx1+
Rgs9tm1.1(cre)Yql/Rgs9+
Tg(HTT*97Q)IXwy/0
involves: 129P2/OlaHsd * FVB
|
normal
behavior/neurological phenotype |
J:208675
|
|
normal
nervous system phenotype |
J:208675
|
Emx1tm1(cre)Ito/Emx1+
Tg(HTT*97Q)IXwy/0
involves: 129P2/OlaHsd * FVB
|
normal
behavior/neurological phenotype |
J:208675
|
|
decreased locomotor activity |
J:208675
|
|
impaired coordination |
J:208675
|
|
normal
nervous system phenotype |
J:208675
|
Emx1tm1(cre)Ito/Emx1+
Hes1tm1Kag/Hes1tm1Kag
involves: 129P2/OlaHsd * C57BL/6 * CBA
|
normal
nervous system phenotype |
J:139170
|
Emx1tm1(cre)Ito/Emx1+
Hes1tm1Kag/Hes1tm1Kag
Hes3tm1Kag/Hes3tm1Kag
Hes5tm1Fgu/Hes5tm1Fgu
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
|
abnormal brain morphology |
J:139170
|
|
abnormal embryonic neuroepithelium morphology |
J:139170
|
|
abnormal neuron differentiation |
J:139170
|
|
absent choroid plexus |
J:139170
|
|
increased Cajal-Retzius cell number |
J:139170
|
Emx1tm1(cre)Ito/Emx1+
Rac1tm1Atai/Rac1tm1Jms
involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6 * ICR
|
abnormal barrel cortex morphology |
J:140575
|
|
abnormal brain commissure morphology |
J:140575
|
|
abnormal corpus callosum morphology |
J:140575
|
|
abnormal dentate gyrus morphology |
J:140575
|
|
abnormal hippocampus pyramidal cell layer |
J:140575
|
|
abnormal telencephalon morphology |
J:140575
|
|
decreased anterior commissure size |
J:140575
|
|
decreased hippocampal commissure size |
J:140575
|
|
decreased survivor rate |
J:140575
|
|
postnatal lethality, incomplete penetrance |
J:140575
|
|
small hippocampus |
J:140575
|
Emx1tm1(cre)Ito/Emx1+
Tg(CAG-Mtor*)#Atai/0
involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * ICR
|
abnormal cerebral cortex morphology |
J:211789
|
|
decreased neuronal precursor cell number |
J:211789
|
|
increased neuron apoptosis |
J:211789
|
|
small hippocampus |
J:211789
|
Emx1tm1(cre)Ito/?
Gt(ROSA)26Sortm1(HD*103Q)Xwy/?
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
|
normal
nervous system phenotype |
J:99759
|
Emx1tm1(cre)Krj/Emx1+
Numbtm1Ynj/Numbtm1Ynj
involves: 129S2/SvPas * 129X1/SvJ * CD-1
|
no abnormal phenotype detected |
J:87149
|
Emx1tm1(cre)Krj/Emx1+
Numbtm1Ynj/Numbtm1Ynj
Numbltm1Wmz/Numbltm1Wmz
involves: 129S2/SvPas * 129X1/SvJ * CD-1
|
abnormal brain ventricle morphology |
J:87149
|
|
abnormal cerebral cortex morphology |
J:87149
|
|
abnormal cortical marginal zone morphology |
J:87149
|
|
abnormal embryonic neuroepithelium morphology |
J:87149
|
|
abnormal forebrain morphology |
J:87149
|
|
abnormal hearing physiology |
J:87149
|
|
abnormal hippocampus morphology |
J:87149
|
|
abnormal lateral ventricle morphology |
J:87149
|
|
abnormal neuron differentiation |
J:87149
|
|
abnormal neuron specification |
J:87149
|
|
absent corpus callosum |
J:87149
|
|
circling |
J:87149
|
|
decreased body size |
J:87149
|
|
ectopic cortical neuron |
J:87149
|
|
enlarged brain ventricles |
J:87149
|
|
female infertility |
J:87149
|
|
increased neuron apoptosis |
J:87149
|
|
male infertility |
J:87149
|
|
postnatal lethality, incomplete penetrance |
J:87149
|
|
small thalamus |
J:87149
|
|
social withdrawal |
J:87149
|
|
sporadic seizures |
J:87149
|
|
stereotypic behavior |
J:87149
|
Emx1tm1(cre)Krj/Emx1+
Wnt3atm2Eag/Wnt3a+
involves: 129S2/SvPas
|
abnormal cerebral cortex morphology |
J:104373
|
|
abnormal suckling behavior |
J:104373
|
|
absent Cajal-Retzius cell |
J:104373
|
|
absent choroid plexus |
J:104373
|
|
postnatal lethality |
J:104373
|
|
short mandible |
J:104373
|
Emx1tm1(cre)Krj/Emx1+
Mycbp2tm1Adia/Mycbp2tm1Adia
involves: 129S2/SvPas * C57BL/6
|
abnormal axon guidance |
J:125702
|
|
abnormal corpus callosum morphology |
J:125702
|
|
abnormal hippocampus morphology |
J:125702
|
|
decreased corpus callosum size |
J:125702
|
|
enlarged lateral ventricles |
J:125702
|
Emx1tm1(cre)Krj/Emx1+
Ptpn11tm6Bgn/Ptpn11+
B6.129S-Ptpn11tm6Bgn Emx1tm1(cre)Krj
|
abnormal hippocampus neuron morphology |
J:242312
|
|
abnormal spatial learning |
J:242312
|
|
decreased exploration in new environment |
J:242312
|
|
impaired cued conditioning behavior |
J:242312
|
Emx1tm1(cre)Krj/Emx1+
Lhx2tm1.1Ddmo/Lhx2tm1.1Ddmo
involves: 129S2/SvPas * C57BL/6 * SJL
|
abnormal neocortex morphology |
J:154611
|
|
abnormal olfactory bulb morphology |
J:154611
|
|
abnormal olfactory cortex morphology |
J:154611
|
|
abnormal telencephalon morphology |
J:154611
|
|
telencephalon hypoplasia |
J:154611
|
Emx1tm1(cre)Krj/Emx1+
Lhx2tm1.1Ddmo/Lhx2tm1.2Ddmo
involves: 129S2/SvPas * C57BL/6 * SJL
|
abnormal neocortex morphology |
J:154611
|
|
abnormal olfactory bulb morphology |
J:154611
|
|
abnormal olfactory cortex morphology |
J:154611
|
|
abnormal telencephalon morphology |
J:154611
|
|
telencephalon hypoplasia |
J:154611
|
Emx1tm1(cre)Krj/Emx1+
Gsx2tm2.1Kc/Gsx2tm2.1Kc
involves: 129S6/SvEvTac * C57BL/6 * SJL
|
abnormal lateral ganglionic eminence morphology |
J:154936
|
|
abnormal neuron differentiation |
J:154936
|
|
abnormal olfactory bulb morphology |
J:154936
|
Emx1tm1(cre)Krj/Emx1+
Gsx2tm2.1Kc/Gsx2tm2.1Kc
Tg(CAG-cat,-EGFP)1Rbns/0
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL
|
abnormal olfactory bulb development |
J:154936
|
Emx1tm1(cre)Krj/Emx1+
Esco2tm1.1Ge/Esco2tm1.1Ge
involves: 129S2/SvPas * C57BL/6 * SJL
|
abnormal embryonic neuroepithelium morphology |
J:180371
|
|
abnormal hippocampus development |
J:180371
|
|
abnormal neocortex morphology |
J:180371
|
|
abnormal neuronal precursor proliferation |
J:180371
|
|
absent hippocampus |
J:180371
|
|
increased neuron apoptosis |
J:180371
|
|
microcephaly |
J:180371
|
Emx1tm1(cre)Krj/Emx1+
Topbp1tm1Pmc/Topbp1tm1Pmc
involves: 129S2/SvPas * C57BL/6J
|
abnormal cerebral cortex morphology |
J:181920
|
Emx1tm1(cre)Krj/Emx1+
Tg(CMV-GFP,-Smarcc2,-lacZ)#Stoy/0
involves: 129S2/SvPas
|
abnormal DNA methylation |
J:197141
|
|
abnormal neocortex morphology |
J:197141
|
|
abnormal neuron differentiation |
J:197141
|
|
abnormal neuron number |
J:197141
|
|
abnormal neuronal precursor cell number |
J:197141
|
|
thin cerebral cortex |
J:197141
|
Emx1tm1(cre)Krj/Emx1+
Magohtm1c(KOMP)Dlsi/Magoh+
involves: 129S2/SvPas * C57BL/6J
|
microcephaly |
J:235650
|
Emx1tm1(cre)Krj/Emx1+
Rbm8atm1Dlsi/Rbm8a+
involves: 129S2/SvPas * C57BL/6J
|
abnormal cerebral cortex morphology |
J:235650
|
|
decreased neuron number |
J:235650
|
|
microcephaly |
J:235650
|
Emx1tm1(cre)Krj/Emx1+
Rbm8atm1Dlsi/Rbm8a+
involves: C57BL/6J
|
abnormal cerebral cortex morphology |
J:221648
|
|
abnormal radial glial cell apoptosis |
J:221648
|
|
abnormal radial glial cell morphology |
J:221648
|
|
abnormal stratification in cerebral cortex |
J:221648
|
|
abnormal telencephalon development |
J:221648
|
|
decreased brain size |
J:221648
|
|
decreased neocortex size |
J:221648
|
|
decreased neuronal precursor cell number |
J:221648
|
|
decreased radial glial cell number |
J:221648
|
|
ectopic cortical neuron |
J:221648
|
|
impaired neuron differentiation |
J:221648
|
|
increased forebrain apoptosis |
J:221648
|
|
increased neuron apoptosis |
J:221648
|
|
increased neuron number |
J:221648
|
|
increased neuronal precursor proliferation |
J:221648
|
|
microcephaly |
J:221648
|
|
premature neuronal precursor differentiation |
J:221648
|
|
small brain ventricles |
J:221648
|
|
thin cerebral cortex |
J:221648
|
Emx1tm1(cre)Krj/Emx1+
Rcor2tm1c(EUCOMM)Wtsi/Rcor2tm1c(EUCOMM)Wtsi
involves: 129S2/SvPas * C57BL/6N
|
decreased brain size |
J:235702
|
|
thin cerebral cortex |
J:235702
|
Emx1tm1(cre)Krj/?
Kcnq2tm1.1Avtz/Kcnq2tm1.1Avtz
involves: 129S2/SvPas * C57BL/6
|
abnormal action potential |
J:208109
|
|
abnormal afterhyperpolarization |
J:208109
|
|
abnormal brain wave pattern |
J:208109
|
|
abnormal hippocampus morphology |
J:208109
|
|
abnormal nervous system electrophysiology |
J:208109
|
|
postnatal lethality, incomplete penetrance |
J:208109
|
|
premature death |
J:208109
|
|
tonic-clonic seizures |
J:208109
|
Emx1tm1(cre)Krj/?
Kcnq3tm1.1Avtz/Kcnq3tm1.1Avtz
involves: 129S2/SvPas * C57BL/6
|
abnormal hippocampus morphology |
J:208109
|
|
abnormal nervous system electrophysiology |
J:208109
|
Emx1tm1(cre)Krj/?
Rai1tm2.1Luo/Rai1tm2.1Luo
either: (involves: 129S1/Sv * 129S2/SvPas * C57BL/6) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
no abnormal phenotype detected |
J:237687
|
Emx1tm1(cre)Yql/Emx1+
Lhx2tm1Monu/Lhx2tm1Monu
involves: 129P2/OlaHsd * 129S2/SvPas
|
abnormal cerebral cortex morphology |
J:130167
|
Emx1tm1(cre)Yql/Emx1+
Tor1atm2Yql/Tor1atm2Yql
involves: 129S2/SvPas * 129S4/SvJae * C57BL/6
|
abnormal gait |
J:130483
|
|
abnormal motor coordination/balance |
J:130483
|
|
circling |
J:130483
|
|
hyperactivity |
J:130483
|
|
increased stereotypic behavior |
J:130483
|
|
normal
nervous system phenotype |
J:130483
|
Emx1tm1.1(cre)Ito/Emx1+
Tg(Gfap-GFAP*R239H)60TMIke/0
involves: 129P2/OlaHsd * C57BL/6J
|
increased susceptibility to pharmacologically induced seizures |
J:139349
|
Emx1tm1.1(cre)Ito/Emx1+
Scn1atm2.1Kzy/Scn1atm2.1Kzy
involves: 129P2/OlaHsd * C57BL/6
|
abnormal neocortex morphology |
J:202863
|
|
normal
behavior/neurological phenotype |
J:202863
|
Emx1tm1.1(cre)Ito/Emx1+
Scn1atm2.1Kzy/Scn1atm2.1Kzy
Tg(Slc32a1-cre)65Kzy/0
involves: 129P2/OlaHsd * C57BL/6
|
convulsive seizures |
J:202863
|
|
premature death |
J:202863
|
Emx1tm1Sia/Emx1tm1Sia
Emx2tm1Sia/Emx2+
involves: C57BL/6 * CBA
|
abnormal cerebral cortex morphology |
J:163926
|
|
abnormal embryonic/fetal subventricular zone morphology |
J:163926
|
Emx1tm1Sia/Emx1tm1Sia
Emx2tm1Sia/Emx2tm1Sia
involves: C57BL/6 * CBA
|
abnormal pallium development |
J:163926
|
|
absent dentate gyrus |
J:163926
|
|
absent hippocampal fimbria |
J:163926
|
|
absent hippocampus |
J:163926
|
Emx1tm1Sia/Emx1tm1Sia
Otx1tm1Sia/Otx1tm1Sia
Not Specified
|
normal
nervous system phenotype |
J:98539
|
Emx1tm1Sia/Emx1tm1Sia
Otx2tm1Sia/Otx2+
involves: C57BL/6 * CBA
|
normal
nervous system phenotype |
J:98539
|
Emx1tm1Sia/Emx1tm1Sia
Rr103tm3.1Sia/Rr103tm3.1Sia
involves: C57BL/6 * CBA
|
abnormal cerebral cortex morphology |
J:163926
|
|
abnormal pallium development |
J:163926
|
|
absent dentate gyrus |
J:163926
|
|
small hippocampus |
J:163926
|
Emx1tm1Sia/Emx1tm1Sia
Rr103tm3Sia/Rr103tm3Sia
involves: C57BL/6 * CBA
|
abnormal cerebral cortex morphology |
J:163926
|
|
abnormal pallium development |
J:163926
|
|
absent dentate gyrus |
J:163926
|
|
small hippocampus |
J:163926
|
Epha4tm1.1Bzh/Epha4tm1.2Bzh
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129S7/SvEvBrd
|
abnormal corticospinal tract morphology |
J:209606
|
|
normal
behavior/neurological phenotype |
J:209606
|
Fezf2tm1.1Nses/Fezf2tm1.1Nses
Emx1tm1(cre)Ito/Emx1+
involves: 129P2/OlaHsd * 129S1/Sv
|
abnormal corticospinal tract morphology |
J:186632
|
Fgf13tm1Xuzh/Y
Emx1tm1(cre)Yql/Emx1+
involves: 129S2/SvPas
|
abnormal axon morphology |
J:186253
|
|
abnormal cerebral cortex pyramidal cell morphology |
J:186253
|
|
abnormal depression-related behavior |
J:186253
|
|
abnormal object recognition memory |
J:186253
|
|
abnormal spatial learning |
J:186253
|
|
abnormal spatial working memory |
J:186253
|
|
behavioral despair |
J:186253
|
|
hyperactivity |
J:186253
|
|
impaired cued conditioning behavior |
J:186253
|
|
increased anxiety-related response |
J:186253
|
Glultm1.1Ncd/Glultm1.1Ncd
Emx1tm1(cre)Krj/Emx1+
B6.Cg-Glultm1.1Ncd Emx1tm1(cre)Krj
|
abnormal blood vessel physiology |
J:272643
|
|
abnormal brain vasculature morphology |
J:272643
|
|
abnormal locomotor activation |
J:272643
|
|
astrocytosis |
J:272643
|
|
decreased anxiety-related response |
J:272643
|
|
decreased aspartic acid level |
J:272643
|
|
decreased gamma-aminobutyric acid level |
J:272643
|
|
decreased glutamic acid level |
J:272643
|
|
decreased glutamine level |
J:272643
|
|
decreased locomotor activity |
J:272643
|
|
decreased vertical activity |
J:272643
|
|
hippocampus pyramidal cell degeneration |
J:272643
|
|
increased locomotor activity |
J:272643
|
|
neurodegeneration |
J:272643
|
|
premature death |
J:272643
|
|
seizures |
J:272643
|
Gm30731tm1.1Dalm/Gm30731tm1.1Dalm
Emx1tm1(cre)Krj/Emx1+
involves: 129S/SvEv * 129S2/SvPas * C57BL/6
|
abnormal cerebral cortex morphology |
J:281278
|
|
abnormal neocortex morphology |
J:281278
|
|
abnormal neuronal stem cell physiology |
J:281278
|
|
increased neuron number |
J:281278
|
Islr2tm1.1Ddg/Islr2tm2.1Ddg
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6 * SJL
|
abnormal brain internal capsule morphology |
J:210221
|
|
abnormal brain morphology |
J:210221
|
|
abnormal telencephalon development |
J:210221
|
|
premature death |
J:210221
|
Itgb1tm1Mll/Itgb1tm1Mll
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129X1/SvJ
|
abnormal Cajal-Retzius cell morphology |
J:170581
|
|
abnormal radial glial cell morphology |
J:170581
|
|
normal
nervous system phenotype |
J:170581
|
|
radial glial endfoot detachment |
J:170581
|
Kat6atm1c(EUCOMM)Wtsi/Kat6atm1c(EUCOMM)Wtsi
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6J * C57BL/6N * CD-1
|
no abnormal phenotype detected |
J:224155
|
Knl1tm1c(EUCOMM)Hmgu/Knl1tm1c(EUCOMM)Hmgu
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6N
|
decreased neuron number |
J:278483
|
|
microcephaly |
J:278483
|
|
telencephalon hypoplasia |
J:278483
|
Magohtm1c(KOMP)Dlsi/Magoh+
Emx1tm1(cre)Krj/Emx1+
B6.Cg-Magohtm1c(KOMP)Dlsi Emx1tm1(cre)Krj
|
decreased brain size |
J:213515
|
|
thin cerebral cortex |
J:213515
|
Mpp3tm1.1Wij/Mpp3tm1.1Wij
Emx1tm1(cre)Ito/Emx1+
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J
|
abnormal cerebral cortex morphology |
J:198427
|
|
abnormal mitotic spindle morphology |
J:198427
|
|
abnormal neuronal migration |
J:198427
|
|
increased mitotic index |
J:198427
|
Nr2f1tm2.1Mist/Nr2f1tm2.1Mist
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6J
|
abnormal barrel cortex morphology |
J:127387
|
|
abnormal cerebral cortex morphology |
J:127387
|
|
abnormal primary somatosensory cortex morphology |
J:127387
|
|
normal
nervous system phenotype |
J:127387
|
Nrg1tm1Fej/Nrg1tm1Fej
Emx1tm1(cre)Krj/?
involves: 129P2/OlaHsd * 129S2/SvPas
|
normal
nervous system phenotype |
J:145464
|
Orc3tm1.1Zhua/Orc3tm1.1Zhua
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas
|
abnormal radial glial cell morphology |
J:170581
|
|
decreased neuronal precursor proliferation |
J:170581
|
|
decreased radial glial cell number |
J:170581
|
|
normal
nervous system phenotype |
J:170581
|
Pals1tm1Caw/Pals1+
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas
|
abnormal behavior |
J:160624
|
|
abnormal cerebral cortex morphology |
J:160624
|
|
abnormal neuronal precursor proliferation |
J:160624
|
|
premature neuronal precursor differentiation |
J:160624
|
|
small hippocampus |
J:160624
|
Pals1tm1Caw/Pals1tm1Caw
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas
|
abnormal brain morphology |
J:160624
|
|
abnormal cerebral cortex morphology |
J:160624
|
|
abnormal gait |
J:160624
|
|
abnormal neuronal precursor proliferation |
J:160624
|
|
abnormal placing response |
J:160624
|
|
abnormal spatial learning |
J:160624
|
|
normal
behavior/neurological phenotype |
J:160624
|
|
decreased body weight |
J:160624
|
|
decreased exploration in new environment |
J:160624
|
|
decreased grip strength |
J:160624
|
|
decreased locomotor activity |
J:160624
|
|
disheveled coat |
J:160624
|
|
increased neuron apoptosis |
J:160624
|
|
jerky movement |
J:160624
|
|
jumpy |
J:160624
|
|
loss of cortex neurons |
J:160624
|
|
normal
mortality/aging |
J:160624
|
|
premature neuronal precursor differentiation |
J:160624
|
|
normal
reproductive system phenotype |
J:160624
|
|
thin cerebral cortex |
J:160624
|
Pals1tm1Caw/Pals1tm1Caw
Tsc2tm1.1Mjg/Tsc2tm1.1Mjg
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ
|
abnormal cerebral cortex morphology |
J:160624
|
Pax6tm2Pgr/Pax6tm2Pgr
Smarcc2tm1.1Stoy/Smarcc2+
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * C57BL/6
|
abnormal neuron number |
J:197141
|
|
normal
nervous system phenotype |
J:197141
|
Pax6tm2Pgr/Pax6tm2Pgr
Smarcc2tm1.1Stoy/Smarcc2tm1.1Stoy
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * C57BL/6
|
abnormal neocortex morphology |
J:197141
|
|
abnormal neuron number |
J:197141
|
|
abnormal neuronal precursor cell number |
J:197141
|
Pdcd10tm1Wami/Pdcd10tm1Wami
Emx1tm1(cre)Krj/Emx1+
involves: 129 * 129S2/SvPas * C57BL/6
|
abnormal brain vasculature morphology |
J:170480
|
|
astrocytosis |
J:170480
|
|
increased brain size |
J:170480
|
|
increased hemangioma incidence |
J:170480
|
|
normal
mortality/aging |
J:170480
|
Pik3r4mbe/Pik3r4tm1.1Mpnd
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C3H/HeH * C57BL/6
|
abnormal hippocampus pyramidal cell layer |
J:258027
|
|
abnormal hippocampus stratum oriens morphology |
J:258027
|
|
ectopic hippocampus pyramidal cells |
J:258027
|
Pik3r4tm1.1Mpnd/Pik3r4tm1.1Mpnd
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6
|
abnormal cerebral cortex morphology |
J:258027
|
|
abnormal hippocampus morphology |
J:258027
|
|
thin cerebral cortex |
J:258027
|
Pnkptm1.1Pmc/Pnkptm1.1Pmc
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * C57BL/6
|
abnormal cerebellar cortex morphology |
J:226703
|
|
decreased body size |
J:226703
|
|
decreased brain size |
J:226703
|
|
decreased cell proliferation |
J:226703
|
|
increased brain apoptosis |
J:226703
|
Pomt2tm1.1Hhu/Pomt2tm1.1Hhu
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J
|
abnormal Ammon gyrus morphology |
J:179356
|
|
abnormal basement membrane morphology |
J:179356
|
|
abnormal Cajal-Retzius cell morphology |
J:179356
|
|
abnormal dentate gyrus morphology |
J:179356
|
|
abnormal forebrain morphology |
J:179356
|
|
abnormal hippocampus CA3 region morphology |
J:179356
|
|
abnormal hippocampus layer morphology |
J:179356
|
|
abnormal neocortex morphology |
J:179356
|
|
abnormal radial glial cell morphology |
J:179356
|
|
astrocytosis |
J:179356
|
Ppp4r3aem1Qili/Ppp4r3aem1Qili
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6J
|
abnormal miniature excitatory postsynaptic currents |
J:326388
|
|
abnormal sucrose solution preference |
J:326388
|
|
normal
behavior/neurological phenotype |
J:326388
|
|
behavioral despair |
J:326388
|
|
decreased dendritic spine density |
J:326388
|
|
decreased neurotransmitter release |
J:326388
|
|
increased anxiety-related response |
J:326388
|
|
increased thigmotaxis |
J:326388
|
Ptbp1tm1Nobu/Ptbp1tm2Nobu
Emx1tm1(cre)Ito/Emx1+
involves: 129P2/OlaHsd
|
abnormal brain ependyma motile cilium morphology |
J:213479
|
|
abnormal telencephalon morphology |
J:213479
|
|
dilated lateral ventricle |
J:213479
|
|
hydrocephaly |
J:213479
|
Ptbp2tm1.1Dblk/Ptbp2tm1.1Dblk
Emx1tm1(cre)Ito/Emx1+
involves: 129P2/OlaHsd * 129S2/SvPas
|
abnormal mitral cell morphology |
J:207976
|
|
abnormal olfactory bulb layer morphology |
J:207976
|
|
absent corpus callosum |
J:207976
|
|
decreased body size |
J:207976
|
|
enlarged lateral ventricles |
J:207976
|
|
neurodegeneration |
J:207976
|
|
neuron degeneration |
J:207976
|
|
postnatal growth retardation |
J:207976
|
|
postnatal lethality, complete penetrance |
J:207976
|
|
slow postnatal weight gain |
J:207976
|
|
small hippocampus |
J:207976
|
|
thin cerebral cortex |
J:207976
|
Rem2tm1c(EUCOMM)Hmgu/Rem2tm1c(EUCOMM)Hmgu
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6N
|
abnormal visual cortex morphology |
J:263600
|
Rnu11tm1.1Rank/Rnu11tm1.1Rank
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129X1/SvJ
|
abnormal pallium development |
J:266583
|
|
absent hippocampus |
J:266583
|
|
decreased neuron number |
J:266583
|
|
decreased neuronal precursor cell number |
J:266583
|
|
decreased radial glial cell number |
J:266583
|
|
increased cell death |
J:266583
|
|
microcephaly |
J:266583
|
Robo4tm1.1Xby/Robo4tm1.1Xby
Emx1tm1(cre)Ito/Emx1+
involves: 129P2/OlaHsd * C57BL/6
|
normal
nervous system phenotype |
J:202213
|
Slc12a2tm1.1Jheb/Slc12a2tm1.1Jheb
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6
|
normal
behavior/neurological phenotype |
J:201156
|
Slc17a6tm1.1Jder/Slc17a6tm1.1Jder
Emx1tm1(cre)Krj/Emx1+
B6.Cg-Emx1tm1(cre)Krj Slc17a6tm1.1Jder
|
abnormal dendrite morphology |
J:192240
|
|
abnormal dendritic spine morphology |
J:192240
|
|
abnormal glutamate-mediated receptor currents |
J:192240
|
|
abnormal spatial learning |
J:192240
|
|
abnormal spatial reference memory |
J:192240
|
|
decreased body size |
J:192240
|
|
decreased synaptic glutamate release |
J:192240
|
|
increased exploration in new environment |
J:192240
|
|
increased paired-pulse ratio |
J:192240
|
|
reduced long-term depression |
J:192240
|
Smarcc2tm1.1Stoy/Smarcc2tm1.1Stoy
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * C57BL/6
|
abnormal DNA methylation |
J:197141
|
|
abnormal neocortex morphology |
J:197141
|
|
abnormal neuron differentiation |
J:197141
|
|
abnormal neuronal precursor cell number |
J:197141
|
|
abnormal neuronal precursor proliferation |
J:197141
|
|
thickened cerebral cortex |
J:197141
|
Sp2tm1.1Htg/Sp2tm1.1Htg
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas
|
abnormal cortical plate morphology |
J:194076
|
|
abnormal cortical ventricular zone morphology |
J:194076
|
|
abnormal embryonic/fetal subventricular zone morphology |
J:194076
|
|
abnormal neuron differentiation |
J:194076
|
|
prenatal lethality, incomplete penetrance |
J:194076
|
Tor1atm1Wtd/Tor1atm3.1Wtd
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129S6/SvEvTac * C57BL/6J
|
gliosis |
J:213785
|
|
impaired coordination |
J:213785
|
|
limb grasping |
J:288753
|
|
neurodegeneration |
J:213785
|
|
thin cerebral cortex |
J:288753
|
Tor1atm1Wtd/Tor1atm3.1Wtd
Tor1btm1.2Wtd/Tor1btm1.1Wtd
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129S6/SvEvTac * C57BL/6J
|
gliosis |
J:288753
|
|
neurodegeneration |
J:288753
|
|
postnatal growth retardation |
J:288753
|
|
premature death |
J:288753
|
|
thin cerebral cortex |
J:288753
|
Tor1atm2Wtd/Tor1atm3.1Wtd
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129S6/SvEvTac * C57BL/6J
|
normal
nervous system phenotype |
J:288753
|
Tor1atm2Wtd/Tor1atm3.1Wtd
Tor1btm1.2Wtd/Tor1b+
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129S6/SvEvTac * C57BL/6J
|
limb grasping |
J:288753
|
|
thin cerebral cortex |
J:288753
|
Tor1atm2Wtd/Tor1atm3.1Wtd
Tor1btm1.2Wtd/Tor1btm1.2Wtd
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129S6/SvEvTac * C57BL/6J
|
thin cerebral cortex |
J:288753
|
Tsc2tm1.1Kcess/Tsc2tm1.1Kcess
Emx1tm1(cre)Krj/Emx1+
involves: 129S/Sv * C57BL/6J
|
decreased body weight |
J:195049
|
|
environmentally induced seizures |
J:195049
|
|
postnatal growth retardation |
J:195049
|
|
postnatal lethality, complete penetrance |
J:195049
|
Zfp335tm1.1Caw/Zfp335+
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6
|
thin cerebral cortex |
J:193339
|
Zfp335tm1.1Caw/Zfp335tm1.1Caw
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6
|
decreased brain size |
J:193339
|
|
loss of cortex neurons |
J:193339
|
Excel File
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