Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+ Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi
involves: 129S4/SvJae * C57BL/6N * FVB/NJ
|
abnormal spontaneous fetal mouth movement |
J:278485
|
Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+ Rdh10tm1c(KOMP)Wtsi/Rdh10tm1d(KOMP)Wtsi
involves: 129S4/SvJae * C57BL/6N * FVB/NJ
|
abnormal cricoid cartilage morphology |
J:278485
|
abnormal hyoid bone morphology |
J:278485
|
abnormal hypoglossal nerve morphology |
J:278485
|
abnormal motor neuron morphology |
J:278485
|
abnormal palatal shelf elevation |
J:278485
|
abnormal thyroid cartilage morphology |
J:278485
|
abnormal tongue muscle morphology |
J:278485
|
abnormal tongue position |
J:278485
|
cleft secondary palate |
J:278485
|
normal
craniofacial phenotype |
J:278485
|
decreased palatine bone horizontal plate size |
J:278485
|
decreased tongue size |
J:278485
|
palatal shelves fail to meet at midline |
J:278485
|
Rdh10m366Asp/Rdh10m366Asp
involves: C57BL/6J
|
abnormal cerebral cortex morphology |
J:157301
|
abnormal craniofacial morphology |
J:157301
|
abnormal eye morphology |
J:157301
|
abnormal forebrain morphology |
J:157301
|
abnormal limb morphology |
J:157301
|
normal
nervous system phenotype |
J:157301
|
Rdh10m366Asp/Rdh10m366Asp Tg(Rr291-lacZ)#Mekk/0
involves: C57BL/6J * FVB/N
|
thin cerebral cortex |
J:136795
|
Rdh10tm1.1Ics/Rdh10tm1.1Ics
involves: C57BL/6 * SJL
|
abnormal cardiovascular system physiology |
J:177362
|
abnormal craniofacial development |
J:177362
|
abnormal embryo development |
J:177362
|
abnormal eye development |
J:177362
|
abnormal heart development |
J:177362
|
abnormal heart tube morphology |
J:177362
|
abnormal hindbrain development |
J:177362
|
abnormal intestine morphology |
J:177362
|
abnormal limb morphology |
J:177362
|
abnormal mesoderm development |
J:177362
|
abnormal otic vesicle morphology |
J:177362
|
abnormal pharyngeal arch morphology |
J:177362
|
abnormal stomach morphology |
J:177362
|
absent lungs |
J:177362
|
brachydactyly |
J:177362
|
caudal body truncation |
J:177362
|
circling |
J:177362
|
decreased ventral retina size |
J:177362
|
normal
embryo phenotype |
J:177362
|
embryo tissue necrosis |
J:177362
|
embryonic growth retardation |
J:177362
|
embryonic lethality during organogenesis, complete penetrance |
J:177362
|
facial cleft |
J:177362
|
incomplete embryo turning |
J:177362
|
lethality during fetal growth through weaning, complete penetrance |
J:177362
|
liver hypoplasia |
J:177362
|
pancreas hypoplasia |
J:177362
|
persistent truncus arteriosus |
J:177362
|
renal hypoplasia |
J:177362
|
small forelimb buds |
J:177362
|
small lens |
J:177362
|
small otic vesicle |
J:177362
|
syndactyly |
J:177362
|
Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi
involves: C57BL/6J * C57BL/6N
|
abnormal embryo turning |
J:185330
|
abnormal heart tube morphology |
J:185330
|
abnormal rostral-caudal body axis extension |
J:185330
|
absent pharyngeal arches |
J:185330
|
decreased embryo size |
J:185330
|
decreased somite size |
J:185330
|
embryonic growth retardation |
J:185330
|
failure of heart looping |
J:185330
|
small otic vesicle |
J:185330
|
Rdh10tm1a(KOMP)Wtsi/Rdh10trex
involves: 129S1/Sv * C57BL/6J * C57BL/6N
|
abnormal embryonic tissue morphology |
J:185330
|
decreased embryo size |
J:185330
|
decreased somite size |
J:185330
|
Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi Tg(Amh-cre)8815Reb/0
involves: C57BL/6 * C57BL/6N * FVB/N * SJL
|
abnormal male reproductive system physiology |
J:193281
|
decreased testis weight |
J:193281
|
seminiferous tubule degeneration |
J:193281
|
Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi Tg(Amh-cre)8815Reb/0 Tg(RARE-Hspa1b/lacZ)12Jrt/0 Tg(Stra8-icre)1Reb/0
involves: C57BL/6 * C57BL/6N * CD-1 * FVB/N * SJL
|
abnormal male reproductive system physiology |
J:193281
|
small testis |
J:193281
|
Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi Tg(Amh-cre)8815Reb/0 Tg(Stra8-icre)1Reb/0
involves: C57BL/6 * C57BL/6N * FVB/N * SJL
|
abnormal male reproductive system physiology |
J:193281
|
abnormal seminiferous tubule morphology |
J:193281
|
abnormal spermatogenesis |
J:193281
|
abnormal spermatogonia morphology |
J:193281
|
arrest of male meiosis |
J:193281
|
decreased testis weight |
J:193281
|
reduced male fertility |
J:193281
|
seminiferous tubule degeneration |
J:193281
|
small testis |
J:193281
|
Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi Tg(Stra8-icre)1Reb/0
involves: C57BL/6 * C57BL/6N * FVB/NJ * SJL
|
normal
reproductive system phenotype |
J:193281
|
Rdh10tm1d(KOMP)Wtsi/Rdh10tm1d(KOMP)Wtsi
involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
|
abnormal embryo turning |
J:185330
|
abnormal heart tube morphology |
J:185330
|
abnormal vitamin A metabolism |
J:185330
|
decreased embryo size |
J:185330
|
decreased somite size |
J:185330
|
embryonic growth arrest |
J:185330
|
embryonic growth retardation |
J:185330
|
embryonic lethality during organogenesis, complete penetrance |
J:185330
|
failure of heart looping |
J:185330
|
small otic vesicle |
J:185330
|
Rdh10tm1Ics/Rdh10tm1Ics
Not Specified
|
no abnormal phenotype detected |
J:177362
|
Rdh10tm2Ics/Rdh10tm2Ics
Not Specified
|
abnormal cardiovascular system physiology |
J:177362
|
abnormal craniofacial development |
J:177362
|
abnormal embryo development |
J:177362
|
abnormal eye development |
J:177362
|
abnormal heart development |
J:177362
|
abnormal heart tube morphology |
J:177362
|
abnormal hindbrain development |
J:177362
|
abnormal intestine morphology |
J:177362
|
abnormal limb morphology |
J:177362
|
abnormal mesoderm development |
J:177362
|
abnormal otic vesicle morphology |
J:177362
|
abnormal pharyngeal arch morphology |
J:177362
|
abnormal stomach morphology |
J:177362
|
absent lungs |
J:177362
|
brachydactyly |
J:177362
|
caudal body truncation |
J:177362
|
circling |
J:177362
|
decreased ventral retina size |
J:177362
|
normal
embryo phenotype |
J:177362
|
embryo tissue necrosis |
J:177362
|
embryonic growth retardation |
J:177362
|
embryonic lethality during organogenesis, complete penetrance |
J:177362
|
facial cleft |
J:177362
|
incomplete embryo turning |
J:177362
|
lethality during fetal growth through weaning, complete penetrance |
J:177362
|
liver hypoplasia |
J:177362
|
pancreas hypoplasia |
J:177362
|
persistent truncus arteriosus |
J:177362
|
renal hypoplasia |
J:177362
|
small forelimb buds |
J:177362
|
small lens |
J:177362
|
small otic vesicle |
J:177362
|
syndactyly |
J:177362
|
Rdh10trex/Rdh10trex
involves: 129S1/Sv * C57BL/6
|
abnormal fourth pharyngeal arch morphology |
J:185330
|
abnormal heart looping |
J:185330
|
abnormal otic vesicle morphology |
J:185330
|
abnormal pharyngeal arch morphology |
J:185330
|
abnormal sixth pharyngeal arch morphology |
J:185330
|
abnormal third pharyngeal arch morphology |
J:185330
|
abnormal vitamin A metabolism |
J:185330
|
absent fourth pharyngeal arch |
J:185330
|
absent pharyngeal arches |
J:185330
|
absent sixth pharyngeal arch |
J:185330
|
absent third pharyngeal arch |
J:185330
|
cardiac edema |
J:185330
|
fused pharyngeal arches |
J:185330
|
small forelimb buds |
J:185330
|
small otic vesicle |
J:185330
|
Rdh10trex/Rdh10trex
involves: 129S1/Sv * C57BL/6 * FVB/NJ
|
abnormal cardiac outflow tract development |
J:171522
|
abnormal cranial ganglia morphology |
J:121229,
J:171522
|
abnormal craniofacial morphology |
J:121229
|
abnormal digit development |
J:121229
|
abnormal dorsal aorta morphology |
J:171522
|
abnormal eye development |
J:121229,
J:171522
|
abnormal forelimb bud morphology |
J:121229
|
abnormal forelimb morphology |
J:121229
|
abnormal frontonasal prominence morphology |
J:121229
|
abnormal geniculate ganglion morphology |
J:121229,
J:171522
|
abnormal glossopharyngeal ganglion morphology |
J:121229,
J:171522
|
abnormal lateral nasal prominence morphology |
J:171522
|
abnormal liver parenchyma morphology |
J:121229
|
abnormal lung development |
J:121229
|
abnormal maxillary prominence morphology |
J:171522
|
abnormal medial nasal prominence morphology |
J:171522
|
abnormal metanephros morphology |
J:121229
|
abnormal midgut morphology |
J:121229
|
abnormal nasal placode morphology |
J:171522
|
abnormal optic vesicle formation |
J:121229,
J:171522
|
abnormal otic vesicle development |
J:171522
|
abnormal otic vesicle morphology |
J:121229
|
abnormal pharyngeal arch morphology |
J:171522
|
abnormal reproductive system development |
J:121229
|
abnormal retina morphology |
J:121229
|
abnormal second pharyngeal arch artery morphology |
J:171522
|
abnormal third pharyngeal arch morphology |
J:171522
|
abnormal trigeminal ganglion morphology |
J:121229,
J:171522
|
abnormal vagus ganglion morphology |
J:171522
|
abnormal vestibulocochlear ganglion morphology |
J:121229,
J:171522
|
absent cornea |
J:121229
|
absent fourth pharyngeal arch |
J:171522
|
absent lung buds |
J:121229
|
absent nasal cavity |
J:121229
|
absent nasal septum |
J:121229
|
absent pancreas |
J:121229
|
absent pharyngeal arches |
J:121229
|
absent radius |
J:121229
|
absent sixth pharyngeal arch artery |
J:171522
|
absent third pharyngeal arch artery |
J:171522
|
decreased autopod size |
J:121229
|
normal
embryo phenotype |
J:121229
|
embryonic lethality during organogenesis, complete penetrance |
J:121229,
J:171522
|
facial cleft |
J:121229
|
frontonasal prominence hypoplasia |
J:171522
|
fused pharyngeal arches |
J:171522
|
hemorrhage |
J:121229
|
impaired branching involved in trachea morphogenesis |
J:121229
|
midline facial cleft |
J:171522
|
pulmonary hypoplasia |
J:121229
|
small gonad |
J:121229
|
small lens |
J:121229
|
small liver |
J:121229
|
small otic vesicle |
J:121229
|
small stomach |
J:121229
|