Mnx1tm4(cre)Tmj/Mnx1+
Rettm2(RET)Heno/Rettm2(RET)Heno
involves: 129S1/Sv * C57BL/6 * SJL
|
normal
nervous system phenotype |
J:132854
|
Mnx1tm4(cre)Tmj/Mnx1+
Rettm2(RET)Heno/Rettm2(RET)Heno
involves: C57BL/6 * SJL
|
abnormal motor neuron innervation pattern |
J:132854
|
|
decreased motor neuron number |
J:132854
|
Nkx6-2tm2(cre)Ercs/Nkx6-2+
Rettm1.1Pern/Rettm1.1Pern
involves: 129P2/OlaHsd * C57BL/6 * SJL
|
abnormal facial motor nucleus morphology |
J:131770
|
|
abnormal hypoglossal nucleus morphology |
J:131770
|
|
abnormal neuromuscular synapse morphology |
J:131770
|
|
normal
renal/urinary system phenotype |
J:131770
|
Rettm1.1Ddg/Rettm1.1Ddg
involves: 129
|
abnormal neuron morphology |
J:154926
|
Rettm1.1Kln/Rettm1.1Kln
involves: 129/Sv * BALB/c * C57BL/6 * CBA/J
|
abnormal innervation pattern to muscle |
J:110955
|
Rettm1.1Pern/Rettm1.1Pern
involves: 129P2/OlaHsd * C57BL/6 * SJL
|
no abnormal phenotype detected |
J:131770
|
Rettm1.1Vlcg/Rettm1.1Vlcg
involves: 129S6/SvEvTac * C57BL/6NTac
|
no abnormal phenotype detected |
J:200671
|
Rettm1.2Pern/Rettm1.2Pern
involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
|
abnormal kidney development |
J:131770
|
|
abnormal neuromuscular synapse morphology |
J:131770
|
|
perinatal lethality, complete penetrance |
J:131770
|
Rettm1Cos/Ret+
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ
|
decreased renal glomerulus number |
J:117753
|
|
single kidney |
J:117753
|
Rettm1Cos/Ret+
involves: 129S/SvEv * C57BL/6
|
abnormal enteric neuron morphology |
J:82456
|
|
abnormal neurotransmitter secretion |
J:82456
|
|
intestinal hypoperistalsis |
J:82456
|
Rettm1Cos/Rettm1Cos
involves: 129S/Sv * C57BL/6
|
abnormal enteric ganglia morphology |
J:135153
|
|
abnormal enteric nervous system morphology |
J:135153
|
|
absent kidney |
J:135153
|
Rettm1Cos/Rettm1Cos
involves: 129S/SvEv
|
normal
endocrine/exocrine gland phenotype |
J:82111
|
Rettm1Cos/Rettm1Cos
involves: 129S/SvEv * MF1
|
abnormal branching involved in ureteric bud morphogenesis |
J:84282
|
|
abnormal cardiac ganglion morphology |
J:64539
|
|
abnormal enteric neural crest cell migration |
J:30830
|
|
abnormal kidney collecting duct morphology |
J:23852
|
|
abnormal kidney mesenchyme morphology |
J:23852
|
|
abnormal kidney morphology |
J:23852,
J:30389
|
|
abnormal lung development |
J:30389
|
|
abnormal mesonephros morphology |
J:84282
|
|
abnormal metanephric mesenchyme morphology |
J:84282
|
|
abnormal parasympathetic postganglionic fiber morphology |
J:64539
|
|
abnormal stellate ganglion morphology |
J:30830
|
|
abnormal ureter development |
J:23852
|
|
abnormal ureter morphology |
J:23852,
J:30389
|
|
abnormal ureteric bud elongation |
J:84282
|
|
abnormal ureteric bud invasion |
J:84282
|
|
absent enteric neurons |
J:23852,
J:30389,
J:30830
|
|
absent kidney |
J:23852,
J:30389
|
|
absent nephrogenic zone |
J:23852
|
|
absent superior cervical ganglion |
J:30830
|
|
absent ureter |
J:23852,
J:30389
|
|
blind ureter |
J:23852,
J:30389
|
|
normal
cardiovascular system phenotype |
J:64539
|
|
dilated renal glomerular capsule |
J:30389
|
|
dilated renal tubule |
J:30389
|
|
increased metanephric mesenchyme apoptosis |
J:84282
|
|
intestinal hypoperistalsis |
J:23852,
J:30389
|
|
neonatal lethality, complete penetrance |
J:23852,
J:30389
|
|
oligohydramnios |
J:30389
|
|
small kidney |
J:30389
|
Rettm1Cos/Rettm2.1Cos
involves: 129S/SvEv * 129S1/Sv * C57BL/6J * FVB/N * MF1
|
normal
endocrine/exocrine gland phenotype |
J:60659
|
|
normal
neoplasm |
J:60659
|
|
normal
reproductive system phenotype |
J:60659
|
Rettm1Cti/Ret+
involves: 129S/SvEv * C57BL/6J
|
abnormal enteric neuron morphology |
J:107335
|
|
abnormal large intestine morphology |
J:107335
|
|
abnormal small intestine morphology |
J:107335
|
Rettm1Cti/Rettm1Cti
involves: 129S/SvEv * C57BL/6J
|
abnormal enteric ganglia morphology |
J:107335
|
|
abnormal urinary bladder morphology |
J:107335
|
|
absent enteric neurons |
J:107335
|
|
absent kidney |
J:107335
|
|
neonatal lethality, complete penetrance |
J:107335
|
Rettm1Ddg/Rettm1Ddg
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129 * C57BL/6 * C57BL/6J * CBA/J
|
abnormal jejunum morphology |
J:126484
|
|
abnormal neuron morphology |
J:126484
|
|
absent enteric neurons |
J:126484
|
|
aganglionic megacolon |
J:126484
|
|
distended abdomen |
J:126484
|
|
enlarged ileum |
J:126484
|
|
postnatal lethality, incomplete penetrance |
J:126484
|
|
small dorsal root ganglion |
J:126484
|
|
weakness |
J:126484
|
Rettm1Giro/Ret+
129.129P2-Rettm1Giro
|
abnormal thyroid gland morphology |
J:141658
|
|
adrenal cortical hyperplasia |
J:141658
|
|
increased thyroid adenoma incidence |
J:141658
|
Rettm1Giro/Ret+
involves: 129/Sv * 129P2/OlaHsd * C57BL/6
|
adrenal cortical hyperplasia |
J:141658
|
Rettm1Giro/Rettm1Giro
involves: 129/Sv * 129P2/OlaHsd * C57BL/6
|
abnormal enteric ganglia morphology |
J:141658
|
|
abnormal neuron differentiation |
J:141658
|
|
absent kidney |
J:141658
|
|
neonatal lethality, complete penetrance |
J:141658
|
|
normal
nervous system phenotype |
J:141658
|
Rettm1Heno/Rettm1Heno
Not Specified
|
abnormal gastrocnemius morphology |
J:132854
|
|
abnormal hypaxial muscle morphology |
J:132854
|
|
abnormal motor neuron innervation pattern |
J:132854
|
|
abnormal muscle spindle morphology |
J:132854
|
|
decreased motor neuron number |
J:132854
|
Rettm1Heno/Rettm2(RET)Heno
Tg(CAG-cre/Esr1*)5Amc/0
involves: 129X1/SvJ * C57BL/6 * CBA
|
abnormal enteric neuron morphology |
J:159854
|
Rettm1Jmi/Ret+
involves: 129X1/SvJ
|
impaired branching involved in ureteric bud morphogenesis |
J:213514
|
Rettm1Jmi/Rettm1Jmi
involves: 129X1/SvJ
|
abnormal innervation |
J:106244
|
|
abnormal prevertebral ganglion morphology |
J:71881
|
|
abnormal submandibular gland morphology |
J:71881
|
|
abnormal sympathetic ganglion morphology |
J:71881
|
|
abnormal sympathetic neuron morphology |
J:71881
|
|
abnormal sympathetic postganglionic fiber morphology |
J:71881
|
|
absent enteric neurons |
J:71881
|
|
absent kidney |
J:71881
|
|
increased cell proliferation |
J:71881
|
|
increased neuron apoptosis |
J:71881
|
|
neonatal lethality, complete penetrance |
J:71881
|
|
small superior cervical ganglion |
J:71881
|
Rettm1Kln/Rettm1Kln
Slc6a3tm1(cre)Xz/Slc6a3+
involves: 129S1/Sv
|
abnormal synaptic dopamine release |
J:188348
|
|
loss of dopaminergic neurons |
J:188348
|
Rettm1Kln/Rettm1Kln
Tg(Nes-cre)1Kln/0
involves: 129/Sv * BALB/c * C57BL/6 * CBA/J * SJL
|
abnormal innervation pattern to muscle |
J:110955
|
|
clubfoot |
J:110955
|
Rettm1Mat/Rettm1Mat
involves: 129X1/SvJ * C57BL/6J
|
abnormal colon morphology |
J:92802
|
|
abnormal enteric ganglia morphology |
J:92802
|
|
abnormal enteric nervous system morphology |
J:92802
|
|
abnormal small intestine morphology |
J:92802
|
|
abnormal ureteric bud morphology |
J:92802
|
|
decreased kidney weight |
J:92802
|
|
distended abdomen |
J:92802
|
|
kidney cyst |
J:92802
|
|
postnatal growth retardation |
J:92802
|
|
postnatal lethality, complete penetrance |
J:92802
|
Rettm2(cre/ERT2)Ddg/Ret+
Not Specified
|
no abnormal phenotype detected |
J:157722
|
Rettm2(RET)Heno/Rettm1Cos
Tg(CAG-cre/Esr1*)5Amc/0
involves: 129S/Sv * C57BL/6 * CBA
|
abnormal enteric ganglia morphology |
J:135153
|
Rettm2.1Cos/Ret+
involves: 129S1/Sv * C57BL/6J * FVB/N
|
adrenergic chromaffin cell hyperplasia |
J:60659
|
|
thyroid gland hyperplasia |
J:60659
|
Rettm2.1Cos/Rettm2.1Cos
involves: 129S1/Sv
|
normal
immune system phenotype |
J:195828
|
Rettm2.1Cos/Rettm2.1Cos
involves: 129S1/Sv * C57BL/6J
|
increased pheochromocytoma incidence |
J:148708
|
Rettm2.1Cos/Rettm2.1Cos
involves: 129S1/Sv * C57BL/6J * FVB/N
|
abnormal adrenal gland morphology |
J:60659
|
|
abnormal adrenal medulla morphology |
J:60659
|
|
abnormal sympathetic ganglion morphology |
J:60659
|
|
adrenergic chromaffin cell hyperplasia |
J:60659
|
|
increased ganglioneuroma incidence |
J:60659
|
|
increased pheochromocytoma incidence |
J:60659
|
|
male infertility |
J:60659
|
|
thyroid gland hyperplasia |
J:60659
|
Rettm2.1Heno/Rettm2.1Heno
involves: 129S/Sv * C57BL/6 * FVB/N
|
abnormal enteric nervous system morphology |
J:135153
|
|
absent kidney |
J:135153
|
|
increased neuron apoptosis |
J:135153
|
Rettm2.1Heno/Rettm2.1Heno
involves: C57BL/6 * FVB/N * SJL
|
abnormal gastrocnemius morphology |
J:132854
|
|
abnormal hypaxial muscle morphology |
J:132854
|
|
abnormal motor neuron innervation pattern |
J:132854
|
|
abnormal muscle spindle morphology |
J:132854
|
|
decreased motor neuron number |
J:132854
|
|
muscular atrophy |
J:132854
|
Rettm2Cos/Rettm2Cos
involves: 129S1/Sv
|
abnormal intestinal peristalsis |
J:60659
|
|
absent kidney |
J:60659
|
|
neonatal lethality, complete penetrance |
J:60659
|
Rettm3(RET)Jmi/Ret+
Not Specified
|
no abnormal phenotype detected |
J:93262
|
Rettm3.1(RET)Jmi/Ret+
Not Specified
|
abnormal colon morphology |
J:93262
|
|
abnormal enteric ganglia morphology |
J:93262
|
|
abnormal enteric nervous system morphology |
J:93262
|
|
abnormal kidney development |
J:93262
|
|
abnormal pterygopalatine ganglion morphology |
J:93262
|
|
abnormal spermatogenesis |
J:93262
|
|
arrest of spermatogenesis |
J:93262
|
|
decreased renal glomerulus number |
J:93262
|
|
distended ileum |
J:93262
|
|
kidney cyst |
J:93262
|
|
premature death |
J:93262
|
|
renal cast |
J:93262
|
|
renal hypoplasia |
J:93262
|
|
seminiferous tubule degeneration |
J:93262
|
Rettm3Cos/Rettm3Cos
involves: 129S1/Sv * FVB/N
|
abnormal colon morphology |
J:116089
|
|
abnormal enteric ganglia morphology |
J:116089
|
|
abnormal enteric neural crest cell migration |
J:116089
|
|
abnormal enteric neural crest cell morphology |
J:116089
|
|
abnormal enteric neuron morphology |
J:116089
|
|
abnormal enzyme/coenzyme activity |
J:116089
|
|
absent enteric neurons |
J:116089
|
Rettm4(RET)Jmi/Rettm4(RET)Jmi
involves: 129X1/SvJ * 129S1/Sv * C57BL/6
|
dilated ureter |
J:105047
|
|
hydronephrosis |
J:105047
|
Rettm6.1Vpa/Rettm6.2Vpa
Tg(CD2-icre)4Kio/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/10 * CBA/Ca
|
normal
hematopoietic system phenotype |
J:195828
|
|
normal
immune system phenotype |
J:195828
|
Rettm7(RET)Jmi/Rettm7(RET)Jmi
involves: 129X1/SvJ * 129S1/Sv * C57BL/6
|
large ureter |
J:105047
|
Rettm8(RET)Jmi/Rettm8(RET)Jmi
involves: 129X1/SvJ * 129S1/Sv * C57BL/6
|
abnormal kidney morphology |
J:105047
|
|
abnormal ureter morphology |
J:105047
|
|
abnormal ureteric bud morphology |
J:105047
|
|
abnormal vas deferens morphology |
J:105047
|
|
dilated ureter |
J:105047
|
|
ectopic ovary |
J:105047
|
|
ectopic testis |
J:105047
|
|
ectopic ureteric bud |
J:105047
|
|
impaired branching involved in ureteric bud morphogenesis |
J:105047
|
|
kidney cyst |
J:105047
|
|
large ureter |
J:105047
|
|
renal hypoplasia |
J:105047
|
Rettm9(RET)Jmi/Rettm9(RET)Jmi
involves: 129X1/SvJ * 129S1/Sv * C57BL/6
|
abnormal kidney development |
J:105047
|
|
abnormal kidney morphology |
J:105047
|
|
absent kidney |
J:105047
|
|
absent nephrogenic zone |
J:105047
|
|
decreased renal glomerulus number |
J:105047
|
|
kidney cyst |
J:105047
|
|
single kidney |
J:105047
|
Rettm9(RET)Jmi/Rettm12(RET)Jmi
involves: 129X1/SvJ * 129S1/Sv * C57BL/6
|
normal
renal/urinary system phenotype |
J:105047
|
Rettm10(RET)Jmi/Rettm10(RET)Jmi
involves: 129X1/SvJ * 129S1/Sv * C57BL/6
|
normal
renal/urinary system phenotype |
J:105047
|
Rettm11(RET)Jmi/Rettm11(RET)Jmi
involves: 129S1/Sv * 129X1/SvJ
|
normal
nervous system phenotype |
J:132854
|
Rettm11(RET)Jmi/Rettm11(RET)Jmi
involves: 129X1/SvJ * 129S1/Sv * C57BL/6
|
abnormal kidney development |
J:105047
|
|
abnormal kidney medulla development |
J:105047
|
|
abnormal kidney morphology |
J:105047
|
|
abnormal renal glomerulus morphology |
J:105047
|
|
abnormal ureter morphology |
J:105047
|
|
abnormal ureteric bud morphology |
J:105047
|
|
absent kidney cortex |
J:105047
|
|
absent kidney medulla |
J:105047
|
|
cryptorchism |
J:105047
|
|
decreased renal glomerulus number |
J:105047
|
|
dilated ureter |
J:105047
|
|
ectopic kidney |
J:105047
|
|
ectopic ovary |
J:105047
|
|
ectopic ureteric bud |
J:105047
|
|
glomerulosclerosis |
J:105047
|
|
hydronephrosis |
J:105047
|
|
impaired branching involved in ureteric bud morphogenesis |
J:105047
|
|
increased kidney apoptosis |
J:105047
|
|
kidney atrophy |
J:105047
|
|
kidney cyst |
J:105047
|
|
large ureter |
J:105047
|
|
premature death |
J:105047
|
|
renal hypoplasia |
J:105047
|
|
ureter obstruction |
J:105047
|
|
ureter stenosis |
J:105047
|
Rettm11(RET)Jmi/Rettm12(RET)Jmi
involves: 129S1/Sv * 129X1/SvJ
|
abnormal hypaxial muscle morphology |
J:132854
|
|
abnormal motor neuron innervation pattern |
J:132854
|
|
abnormal muscle spindle morphology |
J:132854
|
|
decreased motor neuron number |
J:132854
|
|
muscular atrophy |
J:132854
|
Rettm12(RET)Jmi/Rettm12(RET)Jmi
involves: 129S1/Sv * 129X1/SvJ
|
abnormal hypaxial muscle morphology |
J:132854
|
|
abnormal motor neuron innervation pattern |
J:132854
|
|
abnormal muscle spindle morphology |
J:132854
|
|
decreased motor neuron number |
J:132854
|
|
muscular atrophy |
J:132854
|
Rettm12(RET)Jmi/Rettm12(RET)Jmi
involves: 129X1/SvJ * 129S1/Sv * C57BL/6
|
dilated ureter |
J:105047
|
Rettm13.1Jmi/Rettm13.1Jmi
involves: 129S1/Sv * 129X1/SvJ * FVB/N
|
abnormal enteric neuron morphology |
J:114682
|
|
absent enteric neurons |
J:114682
|
|
absent kidney |
J:114682
|
|
normal
nervous system phenotype |
J:114682
|
Rettm14(Gfra1)Jmi/Ret+
involves: 129X1/SvJ
|
no abnormal phenotype detected |
J:130616
|
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