Bhlhe22tm3.1(cre)Meg/Bhlhe22+
Gata3tm1Jfz/Gata3tm1Jfz
involves: 129S1/Sv * 129X1/SvJ
|
abnormal cochlear ganglion morphology |
J:207904
|
Gata3jal/Gata3+
C3H/HeJ-Gata3jal/J
|
abnormal hair texture |
J:186383
|
Gata3jal/Gata3jal
C3H/HeJ-Gata3jal/J
|
abnormal hair cuticle |
J:77437
|
|
abnormal hair cycle |
J:77437
|
|
abnormal hair follicle morphology |
J:77437
|
|
abnormal hair shaft melanin granule distribution |
J:77437
|
|
abnormal hair shaft morphology |
J:77437
|
|
abnormal hair texture |
J:77437,
J:186383
|
|
abnormal vibrissa morphology |
J:77437
|
|
alopecia |
J:186383
|
|
curly vibrissae |
J:186383
|
|
decreased body size |
J:186383
|
|
focal dorsal hair loss |
J:77437
|
|
short vibrissae |
J:186383
|
|
waved hair |
J:77437,
J:186383
|
Gata3tm1.1Gan/Gata3+
Tg(Pax2-cre)1Akg/0
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6Ncr
|
decreased body weight |
J:199588
|
Gata3tm1.1Gan/Gata3tm1.1Gan
Tg(Pax2-cre)1Akg/0
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6Ncr
|
abnormal cochlea morphology |
J:199588
|
|
abnormal cochlear ganglion morphology |
J:199588
|
|
abnormal cochlear hair cell morphology |
J:199588
|
|
abnormal crista ampullaris morphology |
J:199588
|
|
abnormal inner ear development |
J:199588
|
|
abnormal organ of Corti morphology |
J:199588
|
|
abnormal vestibular ganglion morphology |
J:199588
|
|
absent cochlear hair cells |
J:199588
|
|
cochlear ganglion degeneration |
J:199588
|
|
decreased cochlea coiling |
J:199588
|
|
decreased cochlear hair cell number |
J:199588
|
|
decreased organ of Corti supporting cell number |
J:199588
|
|
increased apoptosis |
J:199588
|
|
inner ear hypoplasia |
J:199588
|
|
neonatal lethality, complete penetrance |
J:199588
|
Gata3tm1.1Mbu/Gata3tm1.1Mbu
involves: 129P2/OlaHsd * C57BL/6 * SJL
|
abnormal humoral immune response |
J:123631
|
|
decreased interleukin-4 secretion |
J:123631
|
|
increased interferon-gamma secretion |
J:123631
|
Gata3tm1.2Mbu/Gata3tm1.2Mbu
C3.129P2-Gata3tm1.2Mbu
|
abnormal mesonephros morphology |
J:104408
|
|
abnormal Wolffian duct morphology |
J:104408
|
|
absent ureteric bud |
J:104408
|
|
absent Wolffian ducts |
J:104408
|
|
embryonic lethality during organogenesis, complete penetrance |
J:104408
|
Gata3tm1Gsv/Gata3+
either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal axon guidance |
J:66227
|
|
abnormal sensory neuron innervation pattern |
J:66227
|
Gata3tm1Gsv/Gata3+
FVB.129(B6)-Gata3tm1Gsv
|
abnormal cochlear outer hair cell morphology |
J:104653
|
|
absent distortion product otoacoustic emissions |
J:104653
|
|
cochlear outer hair cell degeneration |
J:104653
|
Gata3tm1Gsv/Gata3+
involves: 129S7/SvEvBrd * C57BL/6 * FVB/N
|
cochlear hair cell degeneration |
J:116235
|
|
cochlear inner hair cell degeneration |
J:116235
|
|
cochlear outer hair cell degeneration |
J:116235
|
|
degeneration of organ of Corti supporting cells |
J:116235
|
|
increased or absent threshold for auditory brainstem response |
J:116235
|
|
organ of Corti degeneration |
J:116235
|
|
pillar cell degeneration |
J:116235
|
|
sensorineural hearing loss |
J:116235
|
Gata3tm1Gsv/Gata3tm1Gsv
either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal aortic arch morphology |
J:144855
|
|
abnormal aorticopulmonary septum morphology |
J:144855
|
|
abnormal axon guidance |
J:66227
|
|
abnormal cardiac outflow tract development |
J:144855
|
|
abnormal cochlear sensory epithelium morphology |
J:66227
|
|
abnormal conotruncal ridge morphology |
J:144855
|
|
abnormal endolymphatic duct morphology |
J:66227
|
|
abnormal facial morphology |
J:144855
|
|
abnormal first pharyngeal arch artery morphology |
J:144855
|
|
abnormal first pharyngeal arch morphology |
J:144855
|
|
abnormal heart morphology |
J:144855
|
|
abnormal heart tube morphology |
J:144855
|
|
abnormal inner ear morphology |
J:66227
|
|
abnormal mandible morphology |
J:144855
|
|
abnormal otic vesicle development |
J:66227
|
|
abnormal pharyngeal arch artery morphology |
J:144855
|
|
abnormal pharynx morphology |
J:144855
|
|
abnormal second pharyngeal arch artery morphology |
J:144855
|
|
abnormal sensory neuron innervation pattern |
J:66227
|
|
absent common crus |
J:66227
|
|
absent semicircular canals |
J:66227
|
|
absent utricle |
J:66227
|
|
absent vestibular saccule |
J:66227
|
|
cervical aortic arch |
J:144855
|
|
decreased cochlea coiling |
J:66227
|
|
delayed inner ear development |
J:66227,
J:93820
|
|
double outlet right ventricle |
J:144855
|
|
embryonic lethality during organogenesis, complete penetrance |
J:66227,
J:144855
|
|
hemorrhage |
J:144855
|
|
inner ear cyst |
J:66227
|
|
interrupted aortic arch |
J:144855
|
|
persistent truncus arteriosus |
J:144855
|
|
pharyngeal arch hypoplasia |
J:144855
|
|
small otic vesicle |
J:66227
|
|
ventricular septal defect |
J:144855
|
Gata3tm1Gsv/Gata3tm1Gsv
involves: 129
|
abnormal pyloric sphincter morphology |
J:228275
|
|
abnormal stomach smooth muscle circular layer morphology |
J:228275
|
|
abnormal stomach smooth muscle outer longitudinal layer morphology |
J:228275
|
Gata3tm1Gsv/Gata3tm1Gsv
involves: 129 * FVB
|
abnormal facial nerve morphology |
J:310312
|
|
abnormal first pharyngeal arch morphology |
J:310312
|
|
abnormal gonial bone morphology |
J:310312
|
|
abnormal incus morphology |
J:310312
|
|
abnormal jaw morphology |
J:310312
|
|
abnormal malleus morphology |
J:310312
|
|
abnormal mandible morphology |
J:310312
|
|
abnormal Meckel's cartilage morphology |
J:310312
|
|
abnormal middle ear ossicle morphology |
J:310312
|
|
abnormal molar morphology |
J:310312
|
|
abnormal neural crest cell migration |
J:310312
|
|
abnormal oral cavity morphology |
J:310312
|
|
abnormal secondary palate development |
J:310312
|
|
abnormal stapes morphology |
J:310312
|
|
abnormal tympanic ring morphology |
J:310312
|
|
absent temporomandibular joint |
J:310312
|
|
bony syngnathia |
J:310312
|
|
cleft palate |
J:310312
|
|
decreased mouth size |
J:310312
|
|
hemifacial hypoplasia |
J:310312
|
|
mandible hypoplasia |
J:310312
|
|
maxilla hypoplasia |
J:310312
|
|
micrognathia |
J:310312
|
|
prenatal lethality, complete penetrance |
J:310312
|
|
small lower incisors |
J:310312
|
|
small mandible |
J:310312
|
|
small maxilla |
J:310312
|
|
small trigeminal ganglion |
J:310312
|
|
small zygomatic bone |
J:310312
|
|
tongue hypoplasia |
J:310312
|
Gata3tm1Iho/Gata3tm1Iho
Il13tm1(YFP/cre)Lky/Il13+
involves: 129S4/SvJae
|
decreased eosinophil cell number |
J:178986
|
|
increased susceptibility to parasitic infection |
J:178986
|
Gata3tm1Iho/Gata3tm1Iho
Tg(Cd4-cre)1Cwi/0
involves: C57BL/6 * DBA/2
|
abnormal T cell differentiation |
J:86996
|
|
decreased CD4-positive, alpha-beta T cell number |
J:86996
|
Gata3tm1Iho/Gata3tm1Iho
Tg(Lck-cre)1Cwi/0
involves: BALB/c
|
abnormal CD8-positive, alpha-beta T cell number |
J:86996
|
|
abnormal T cell subpopulation ratio |
J:86996
|
|
arrested T cell differentiation |
J:86996
|
|
decreased CD4-positive, alpha-beta T cell number |
J:86996
|
|
decreased double-positive T cell number |
J:86996
|
|
decreased thymocyte number |
J:86996
|
|
increased T cell apoptosis |
J:86996
|
|
prenatal lethality, incomplete penetrance |
J:86996
|
|
small thymus |
J:86996
|
Gata3tm1Jeng/Gata3+
involves: 129S7/SvEvBrd
|
no abnormal phenotype detected |
J:28393
|
Gata3tm1Jeng/Gata3tm1Jeng
involves: 129S7/SvEvBrd
|
abnormal blood coagulation |
J:28393
|
|
abnormal brain morphology |
J:28393
|
|
abnormal cardiovascular system physiology |
J:62552
|
|
abnormal craniofacial bone morphology |
J:28393
|
|
abnormal definitive hematopoiesis |
J:28393
|
|
abnormal embryonic growth/weight/body size |
J:28393
|
|
abnormal erythrocyte morphology |
J:28393
|
|
abnormal immune system organ morphology |
J:62552
|
|
abnormal neural tube morphology |
J:28393
|
|
prenatal lethality |
J:28393
|
Gata3tm1Jfz/Gata3tm1Jfz
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
|
no abnormal phenotype detected |
J:93538
|
Gata3tm1Jfz/Gata3tm1Jfz
Tg(Cd4-cre)1Cwi/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2
|
abnormal CD4-positive, alpha beta T cell morphology |
J:93538
|
|
abnormal T cell differentiation |
J:141145
|
|
decreased CD4-positive, alpha-beta T cell number |
J:141145
|
|
decreased interleukin-13 secretion |
J:172134
|
Gata3tm1Jfz/Gata3tm1Jfz
Tg(Fev-cre)1Esd/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
|
abnormal Raphe nucleus morphology |
J:165266
|
|
decreased serotonin level |
J:165266
|
Gata3tm1Jfz/Gata3tm1Jfz
Tg(LGB-cre)74Acl/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
|
abnormal mammary gland growth during lactation |
J:184505
|
|
lactation failure |
J:184505
|
Gata3tm1Jfz/Gata3tm1Jfz
Tg(Tnfrsf4-cre)1Nik/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
|
abnormal CD4-positive, alpha beta T cell morphology |
J:93538
|
|
decreased IgE level |
J:93538
|
|
decreased T-helper 2 cell number |
J:93538
|
|
increased susceptibility to parasitic infection |
J:93538
|
|
increased T-helper 1 cell number |
J:93538
|
Gata3tm1Jml/Gata3tm1Jml
involves: 129S/SvEv * C57BL/6
|
abnormal immune system cell morphology |
J:37093
|
Gata3tm2Gsv/Gata3+
either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal axon guidance |
J:66227
|
|
abnormal sensory neuron innervation pattern |
J:66227
|
Gata3tm2Gsv/Gata3tm2Gsv
either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal axon guidance |
J:66227
|
|
abnormal cochlear sensory epithelium morphology |
J:66227
|
|
abnormal endolymphatic duct morphology |
J:66227
|
|
abnormal inner ear morphology |
J:66227
|
|
abnormal otic vesicle development |
J:66227
|
|
abnormal sensory neuron innervation pattern |
J:66227
|
|
absent common crus |
J:66227
|
|
absent semicircular canals |
J:66227
|
|
absent utricle |
J:66227
|
|
absent vestibular saccule |
J:66227
|
|
decreased cochlea coiling |
J:66227
|
|
delayed inner ear development |
J:66227
|
|
embryonic lethality during organogenesis, complete penetrance |
J:66227
|
|
inner ear cyst |
J:66227
|
|
small otic vesicle |
J:66227
|
Gata3tm2Jeng/Gata3tm2Jeng
Not Specified
|
abnormal double-positive T cell morphology |
J:155686
|
|
abnormal T cell differentiation |
J:155686
|
|
abnormal T cell number |
J:155686
|
|
decreased double-negative T cell number |
J:155686
|
|
decreased gamma-delta T cell number |
J:155686
|
|
decreased thymocyte number |
J:155686
|
|
perinatal lethality |
J:155686
|
Gata3tm3Gsv/Gata3tm3Gsv
Tg(Dbh-cre/ERT2)198.1Hroh/0
involves: 129P2/OlaHsd * C57BL/6
|
abnormal sympathetic ganglion morphology |
J:163233
|
|
abnormal sympathetic neuron innervation pattern |
J:163233
|
|
blepharoptosis |
J:163233
|
|
normal
endocrine/exocrine gland phenotype |
J:163233
|
|
small superior cervical ganglion |
J:163233
|
Gata3tm3Gsv/Gata3tm3Gsv
Tg(Dbh-icre)1Gsc/0
involves: 129P2/OlaHsd * C57BL/6
|
abnormal embryo development |
J:163233
|
|
abnormal nervous system development |
J:163233
|
|
abnormal sympathetic ganglion morphology |
J:163233
|
Gata3tm3Gsv/Gata3tm3Gsv
Tg(KRT14-cre)8Brn/0
involves: 129P2/OlaHsd * FVB/N
|
abnormal epidermal layer morphology |
J:117058
|
|
abnormal epidermis stratum basale morphology |
J:117058
|
|
abnormal hair cycle |
J:117058
|
|
abnormal hair follicle inner root sheath morphology |
J:117058
|
|
abnormal hair follicle melanin granule morphology |
J:117058
|
|
abnormal hair follicle morphology |
J:117058
|
|
abnormal hair follicle orientation |
J:117058
|
|
abnormal hair follicle outer root sheath morphology |
J:117058
|
|
abnormal hair growth |
J:117058
|
|
abnormal hair texture |
J:117058
|
|
abnormal skin condition |
J:117058
|
|
abnormal skin morphology |
J:117058
|
|
absent nipple |
J:117058
|
|
absent subcutaneous adipose tissue |
J:117058
|
|
decreased body size |
J:117058
|
|
decreased T cell number |
J:117058
|
|
delayed hair appearance |
J:117058
|
|
enlarged sebaceous gland |
J:117058
|
|
epidermal hyperplasia |
J:117058
|
|
hyperkeratosis |
J:117058
|
|
impaired skin barrier function |
J:117058
|
|
narrow eye opening |
J:117058
|
|
postnatal growth retardation |
J:117058
|
|
progressive hair loss |
J:117058
|
|
scaly skin |
J:117058
|
|
short hair |
J:117058
|
|
short vibrissae |
J:117058
|
|
sparse hair |
J:117058
|
|
thick epidermis |
J:117058
|
|
thick hair follicle outer root sheath |
J:117058
|
|
thin dermal layer |
J:117058
|
|
weight loss |
J:117058
|
|
wrinkled skin |
J:117058
|
Excel File
Analysis Tools