Gt(ROSA)26Sortm1(Hoxa2)Fmr/Gt(ROSA)26Sor+
Olig2tm2(TVA,cre)Rth/Olig2+
involves: 129P2/OlaHsd
|
abnormal brain development |
J:193058
|
|
decreased oligodendrocyte progenitor number |
J:193058
|
Hoxa2tm1(tetO)Mllo/Hoxa2tm1(tetO)Mllo
involves: 129S1/Sv
|
abnormal rhombomere 2 morphology |
J:80131
|
|
abnormal rhombomere 3 morphology |
J:80131
|
|
abnormal rhombomere morphology |
J:80131
|
Hoxa2tm1(tetO)Mllo/Hoxa2tm1(tetO)Mllo
involves: 129S1/Sv * C57BL/6J
|
abnormal hyoid bone lesser horn morphology |
J:71951
|
|
abnormal incudostapedial joint morphology |
J:71951
|
|
abnormal middle ear ossicle morphology |
J:71951
|
|
abnormal stapes morphology |
J:71951
|
|
abnormal styloid process morphology |
J:71951
|
|
abnormal temporal bone squamous part morphology |
J:71951
|
|
abnormal tongue muscle morphology |
J:71951
|
|
absent stapedial artery |
J:71951
|
|
bifid tongue |
J:71951
|
|
normal
hearing/vestibular/ear phenotype |
J:71951
|
|
neonatal lethality, complete penetrance |
J:71951
|
|
normal
nervous system phenotype |
J:71951
|
|
small malleus processus brevis |
J:71951
|
Hoxa2tm1(tetO)Mllo/Hoxa2tm1Grid
involves: 129S1/Sv * C57BL/6J
|
abnormal facial nerve morphology |
J:71951
|
|
abnormal hyoid bone lesser horn morphology |
J:71951
|
|
abnormal malleus morphology |
J:71951
|
|
abnormal middle ear ossicle morphology |
J:71951
|
|
abnormal outer ear morphology |
J:71951
|
|
abnormal stapedial artery morphology |
J:71951
|
|
abnormal temporal bone squamous part morphology |
J:71951
|
|
abnormal tongue muscle morphology |
J:71951
|
|
abnormal tympanic ring morphology |
J:71951
|
|
absent oval window |
J:71951
|
|
absent stapes |
J:71951
|
|
absent styloid process |
J:71951
|
|
cleft palate |
J:71951
|
|
normal
nervous system phenotype |
J:71951
|
Hoxa2tm1.1Fmr/Hoxa2tm1.1Fmr
involves: 129/Sv * C57BL/6 * SJL
|
no abnormal phenotype detected |
J:75130,
J:80131
|
Hoxa2tm1.1Fmr/Hoxa2tm1.1Fmr
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129/Sv * C57BL/6J * CBA/J
|
abnormal craniofacial bone morphology |
J:102845
|
|
abnormal gonial bone morphology |
J:102845
|
|
abnormal hyoid bone morphology |
J:102845
|
|
abnormal incus morphology |
J:102845
|
|
abnormal malleus morphology |
J:102845
|
|
abnormal Meckel's cartilage morphology |
J:102845
|
|
abnormal tympanic ring morphology |
J:102845
|
|
absent outer ear |
J:102845
|
|
absent stapes |
J:102845
|
|
absent styloid process |
J:102845
|
Hoxa2tm1.1Fmr/Hoxa2tm1.1Fmr
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S2/SvPas * C57BL/6 * SJL
|
abnormal cochlear VIII nucleus morphology |
J:197162
|
|
lethality throughout fetal growth and development |
J:197162
|
Hoxa2tm1.1Fmr/Hoxa2tm1.1Fmr
Tg(CAG-cre/ERT2)F34Fmr/0
involves: 129 * CD-1
|
abnormal brain development |
J:193058
|
|
increased oligodendrocyte progenitor number |
J:193058
|
Hoxa2tm1.1Fmr/Hoxa2tm1.1Fmr
Tg(CAG-cre/ERT2)F34Fmr/0
involves: 129/Sv * C57BL/6 * CD-1
|
abnormal craniofacial bone morphology |
J:102845
|
|
abnormal gonial bone morphology |
J:102845
|
|
abnormal middle ear morphology |
J:102845
|
|
abnormal stapes morphology |
J:102845
|
|
abnormal styloid process morphology |
J:102845
|
|
absent hyoid bone lesser horns |
J:102845
|
|
absent outer ear |
J:102845
|
|
perinatal lethality, complete penetrance |
J:102845
|
Hoxa2tm1.2Fmr/Hoxa2tm1.2Fmr
involves: 129/Sv * C57BL/6 * SJL
|
abnormal behavior |
J:75130
|
|
abnormal craniofacial morphology |
J:75130
|
|
abnormal ear morphology |
J:75130
|
|
abnormal nervous system morphology |
J:75130
|
|
abnormal skeleton morphology |
J:75130
|
|
neonatal lethality, complete penetrance |
J:75130
|
Hoxa2tm1b(EUCOMM)Wtsi/Hoxa2+
C57BL/6N-Hoxa2tm1b(EUCOMM)Wtsi/Ieg
|
abnormal auditory brainstem response |
J:211773
|
|
abnormal gait |
J:211773
|
|
abnormal snout morphology |
J:211773
|
|
decreased circulating creatinine level |
J:211773
|
|
decreased prepulse inhibition |
J:211773
|
|
decreased respiratory quotient |
J:211773
|
|
improved glucose tolerance |
J:211773
|
Hoxa2tm1b(EUCOMM)Wtsi/Hoxa2tm1b(EUCOMM)Wtsi
C57BL/6N-Hoxa2tm1b(EUCOMM)Wtsi/Ieg
|
preweaning lethality, complete penetrance |
J:211773
|
Hoxa2tm1Fmr/Hoxa2+
involves: 129/Sv * C57BL/6
|
no abnormal phenotype detected |
J:80131
|
Hoxa2tm1Fmr/Hoxa2tm1Fmr
involves: 129/Sv * C57BL/6
|
abnormal hyoid bone lesser horn morphology |
J:80131
|
|
abnormal rhombomere 2 morphology |
J:80131
|
|
abnormal stapes morphology |
J:80131
|
|
abnormal styloid process morphology |
J:80131
|
|
lethality at weaning, complete penetrance |
J:80131
|
|
postnatal growth retardation |
J:80131
|
Hoxa2tm1Grid/Hoxa2+
involves: 129S1/Sv
|
abnormal malleus morphology |
J:71951
|
|
abnormal retrotympanic process morphology |
J:71951
|
|
abnormal rhombomere boundary morphology |
J:71951
|
|
abnormal styloid process morphology |
J:71951
|
Hoxa2tm1Grid/Hoxa2tm1Grid
involves: 129S1/Sv
|
abnormal basisphenoid bone morphology |
J:71951
|
|
abnormal external auditory canal morphology |
J:30826
|
|
abnormal facial nerve morphology |
J:71951
|
|
abnormal gonial bone morphology |
J:71951
|
|
abnormal rhombomere boundary morphology |
J:71951
|
|
abnormal stapedial artery morphology |
J:71951
|
|
abnormal temporal bone squamous part morphology |
J:71951
|
|
abnormal tympanic ring morphology |
J:30826
|
|
absent outer ear |
J:71951
|
|
aphagia |
J:71951
|
|
decreased rhombomere 3 size |
J:71951
|
|
neonatal lethality, complete penetrance |
J:71951
|
Hoxa2tm1Grid/Hoxa2tm1Grid
involves: 129S1/Sv * C57BL/6J
|
abnormal basioccipital bone morphology |
J:16389
|
|
abnormal facial nerve morphology |
J:16389
|
|
abnormal glossopharyngeal nerve morphology |
J:16389
|
|
abnormal hyoid bone morphology |
J:16389
|
|
abnormal Meckel's cartilage morphology |
J:16389
|
|
abnormal middle ear ossicle morphology |
J:16389
|
|
abnormal outer ear morphology |
J:16389
|
|
abnormal palatal shelf fusion at midline |
J:151467
|
|
abnormal secondary palate development |
J:151467,
J:316149
|
|
abnormal styloid process morphology |
J:16389
|
|
abnormal temporal bone morphology |
J:16389
|
|
abnormal tubotympanic recess morphology |
J:16389
|
|
abnormal tympanic ring morphology |
J:16389
|
|
abnormal vagus nerve morphology |
J:16389
|
|
absent stapes |
J:16389
|
|
cleft secondary palate |
J:16389
|
|
failure of palatal shelf elevation |
J:151467,
J:316149
|
|
meteorism |
J:16389
|
|
neonatal lethality, complete penetrance |
J:16389
|
|
normal
nervous system phenotype |
J:16389
|
|
palatal shelves fail to meet at midline |
J:151467
|
|
persistence of medial edge epithelium during palatal shelf fusion |
J:316149
|
Hoxa2tm1Grid/Hoxa2tm1Grid
involves: 129S/SvEv * 129S1/Sv * C57BL/6 * DBA/2
|
abnormal incus morphology |
J:100238
|
|
abnormal malleus morphology |
J:100238
|
|
abnormal otic capsule morphology |
J:100238
|
Hoxa2tm1Ipc/Hoxa2tm1.1Fmr
Tg(CAG-cre/ERT2)F34Fmr/0
involves: 129/Sv * 129S2/SvPas * C57BL/6 * CD-1
|
abnormal craniofacial bone morphology |
J:102845
|
|
small ears |
J:102845
|
Hoxa2tm1Ipc/Hoxa2tm1Ipc
involves: 129S2/SvPas
|
abnormal basioccipital bone morphology |
J:16388
|
|
abnormal cartilage development |
J:16388
|
|
abnormal craniofacial bone morphology |
J:102845
|
|
abnormal facial motor nucleus morphology |
J:16388
|
|
abnormal facial nerve morphology |
J:16388
|
|
abnormal gonial bone morphology |
J:102845
|
|
abnormal incus morphology |
J:16388,
J:102845
|
|
abnormal malleus morphology |
J:16388,
J:102845
|
|
abnormal Meckel's cartilage morphology |
J:16388,
J:102845
|
|
abnormal neuron differentiation |
J:54652
|
|
abnormal otic capsule morphology |
J:16388
|
|
abnormal retrotympanic process morphology |
J:16388
|
|
abnormal rhombomere 2 morphology |
J:54652
|
|
abnormal rhombomere 3 morphology |
J:54652
|
|
abnormal scala vestibuli morphology |
J:16388
|
|
abnormal skeleton development |
J:16388
|
|
abnormal stapes morphology |
J:16388
|
|
abnormal suckling behavior |
J:16388
|
|
abnormal temporal bone morphology |
J:16388
|
|
abnormal temporal bone squamous part morphology |
J:16388
|
|
abnormal temporal bone tympanic part morphology |
J:16388
|
|
abnormal tensor tympani muscle morphology |
J:16388
|
|
abnormal tympanic cavity morphology |
J:16388
|
|
abnormal tympanic membrane morphology |
J:16388
|
|
abnormal tympanic ring morphology |
J:102845
|
|
absent hyoid bone lesser horns |
J:16388,
J:102845
|
|
absent malleus processus brevis |
J:16388
|
|
absent outer ear |
J:16388,
J:102845
|
|
absent stapedius muscle |
J:16388
|
|
absent stapes |
J:102845
|
|
absent stylohyoid muscle |
J:16388
|
|
absent styloid process |
J:102845
|
|
bifid tongue |
J:16388
|
|
cleft secondary palate |
J:16388
|
|
enlarged gonial bone |
J:16388
|
|
increased rhombomere 1 size |
J:54652
|
|
neonatal lethality, complete penetrance |
J:16388
|
Hoxa2tm1Mrc/Hoxa2tm1Mrc
involves: 129S1/Sv * 129X1/SvJ
|
abnormal basioccipital bone morphology |
J:58093
|
|
abnormal cranium morphology |
J:58093
|
|
abnormal middle ear ossicle morphology |
J:58093
|
|
abnormal styloglossus muscle morphology |
J:58093
|
|
abnormal suckling behavior |
J:58093
|
|
abnormal tongue muscle morphology |
J:58093
|
|
absent outer ear |
J:58093
|
|
cleft secondary palate |
J:58093
|
|
neonatal lethality, complete penetrance |
J:58093
|
Hoxa2tm2(cre)Mrc/Hoxa2tm2(cre)Mrc
Not Specified
|
decreased sensory neuron number |
J:88581
|
Hoxa2tm2.1Fmr/Hoxa2tm2.1Fmr
involves: 129S2/SvPas
|
abnormal brain development |
J:193058
|
|
increased oligodendrocyte progenitor number |
J:193058
|
Hoxa2tm2.1Fmr/Hoxa2tm2.1Fmr
involves: 129S2/SvPas * C57BL/6
|
normal
nervous system phenotype |
J:197162
|
Hoxa2tm2.1Fmr/Hoxa2tm2.1Fmr
involves: 129S2/SvPas * C57BL/6 * SJL
|
abnormal behavior |
J:75129
|
|
abnormal craniofacial morphology |
J:75129
|
|
abnormal ear morphology |
J:75129
|
|
abnormal nervous system morphology |
J:75129
|
|
abnormal skeleton morphology |
J:75129
|
|
neonatal lethality, complete penetrance |
J:75129
|
Hoxa2tm2Fmr/Hoxa2tm2Fmr
involves: 129S2/SvPas
|
abnormal behavior |
J:75129
|
|
abnormal craniofacial morphology |
J:75129
|
|
abnormal ear morphology |
J:75129
|
|
abnormal nervous system morphology |
J:75129
|
|
abnormal skeleton morphology |
J:75129
|
|
neonatal lethality, complete penetrance |
J:75129
|
Excel File
Analysis Tools