Fgf10Mhdaaey17/Fgf10+
C3HeB/FeJ-Fgf10Mhdaaey17
|
abnormal lens epithelium morphology |
J:154551
|
|
abnormal lens fiber morphology |
J:154551
|
|
abnormal lens morphology |
J:154551
|
|
Harderian gland atrophy |
J:154551
|
|
microphthalmia |
J:86685,
J:154551
|
|
narrow eye opening |
J:154551
|
|
normal
vision/eye phenotype |
J:154551
|
Fgf10Mhdaaey17/Fgf10+
involves: C3HeB/FeJ * C57BL/6
|
abnormal lens fiber morphology |
J:154551
|
|
abnormal retina apoptosis |
J:154551
|
Fgf10Mhdaaey17/Fgf10Mhdaaey17
C3HeB/FeJ-Fgf10Mhdaaey17
|
absent limbs |
J:154551
|
|
prenatal lethality, complete penetrance |
J:154551
|
Fgf10ptls/Fgf10ptls
involves: C57BL/6 * FVB/N
|
absent limb buds |
J:173681
|
|
absent limbs |
J:173681
|
|
absent lungs |
J:173681
|
Fgf10tm1.1(cre/ERT2)Sbel/Fgf10tm1.1(cre/ERT2)Sbel
involves: C57BL/6
|
absent limbs |
J:187831
|
|
absent lung buds |
J:187831
|
|
cecal atresia |
J:187831
|
|
colon atresia |
J:187831
|
Fgf10tm1.1Sms/Fgf10tm1.1Sms
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ
|
abnormal ear morphology |
J:160254
|
|
abnormal embryo development |
J:160254
|
|
abnormal respiratory system morphology |
J:160254
|
Fgf10tm1.1Sms/Fgf10tm1.1Sms
involves: 129S1/Sv * 129X1/SvJ
|
abnormal lung development |
J:150706
|
|
absent lungs |
J:150706
|
|
neonatal lethality, complete penetrance |
J:150706
|
Fgf10tm1.2Sms/Fgf10tm1.2Sms
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ
|
no abnormal phenotype detected |
J:160254
|
Fgf10tm1b(EUCOMM)Wtsi/Fgf10+
C57BL/6N-Fgf10tm1b(EUCOMM)Wtsi/H
|
abnormal behavior |
J:211773
|
|
abnormal cornea morphology |
J:211773
|
|
abnormal iris pigmentation |
J:211773
|
|
abnormal lens morphology |
J:211773
|
|
abnormal optic disk morphology |
J:211773
|
|
abnormal placement of pupils |
J:211773
|
|
abnormal retina blood vessel morphology |
J:211773
|
|
abnormal retina vasculature morphology |
J:211773
|
|
cataract |
J:211773
|
|
cornea opacity |
J:211773
|
|
decreased grip strength |
J:211773
|
|
decreased lean body mass |
J:211773
|
|
decreased leukocyte cell number |
J:211773
|
|
decreased locomotor activity |
J:211773
|
|
decreased thigmotaxis |
J:211773
|
|
fused cornea and lens |
J:211773
|
|
impaired pupillary reflex |
J:211773
|
|
increased circulating cholesterol level |
J:211773
|
|
increased circulating HDL cholesterol level |
J:211773
|
|
increased total body fat amount |
J:211773
|
|
iris synechia |
J:211773
|
|
narrow eye opening |
J:211773
|
|
persistence of hyaloid vascular system |
J:211773
|
Fgf10tm1b(EUCOMM)Wtsi/Fgf10tm1b(EUCOMM)Wtsi
C57BL/6N-Fgf10tm1b(EUCOMM)Wtsi/H
|
preweaning lethality, complete penetrance |
J:211773
|
Fgf10tm1Ska/Fgf10+
involves: C57BL/6 * CBA
|
abnormal forced expiratory flow rates |
J:200882
|
|
abnormal submandibular duct morphology |
J:119849
|
|
decreased body weight |
J:200882
|
|
submandibular gland hypoplasia |
J:119849
|
Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck
involves: C57BL/6 * CBA
|
abnormal colon morphology |
J:115048
|
|
abnormal embryonic tissue morphology |
J:109476
|
|
abnormal enzyme/coenzyme activity |
J:98521
|
|
abnormal intestinal epithelium morphology |
J:115048
|
|
abnormal large intestine crypts of Lieberkuhn morphology |
J:115048
|
|
abnormal mammary placode morphology |
J:109476
|
|
abnormal pulmonary elastic fiber morphology |
J:98521
|
|
impaired branching involved in bronchus morphogenesis |
J:98521
|
|
small lung |
J:98521
|
Fgf10tm1Ska/Fgf10tm1Ska
involves: C57BL/6 * CBA
|
abnormal adipose tissue morphology |
J:108349
|
|
abnormal branching of the mammary ductal tree |
J:73434
|
|
abnormal cecum development |
J:87411,
J:115048
|
|
abnormal colon morphology |
J:115048
|
|
abnormal embryonic tissue morphology |
J:109476
|
|
abnormal gastric chief cell morphology |
J:114183
|
|
abnormal hair follicle morphology |
J:114183
|
|
abnormal hair shaft morphology |
J:114183
|
|
abnormal heart atrium auricular region morphology |
J:111148
|
|
abnormal heart position or orientation |
J:111148
|
|
abnormal hindgut morphology |
J:115048
|
|
abnormal incisor morphology |
J:114183
|
|
abnormal inner ear morphology |
J:114183
|
|
abnormal intestinal epithelium morphology |
J:115048
|
|
abnormal kidney inner medulla morphology |
J:114183
|
|
abnormal kidney medulla morphology |
J:114183
|
|
abnormal kidney outer medulla morphology |
J:114183
|
|
abnormal large intestine crypts of Lieberkuhn morphology |
J:115048
|
|
abnormal limb bud morphology |
J:51966
|
|
abnormal limb development |
J:80685
|
|
abnormal limb muscle morphology |
J:80685
|
|
abnormal lung development |
J:80685
|
|
abnormal mammary fat pad morphology |
J:73434
|
|
abnormal mammary placode morphology |
J:73434,
J:109476
|
|
abnormal metanephric ureteric bud development |
J:114183
|
|
abnormal neurohypophysis development |
J:114183
|
|
abnormal periderm development |
J:109476
|
|
abnormal pulmonary circulation |
J:111148
|
|
abnormal pulmonary trunk morphology |
J:111148
|
|
abnormal Rathke's pouch apoptosis |
J:114183
|
|
abnormal scapula morphology |
J:51966
|
|
abnormal stomach submucosa morphology |
J:114183
|
|
abnormal tooth morphology |
J:114183
|
|
abnormal urethra morphology |
J:94932
|
|
absent adenohypophysis |
J:114183
|
|
absent colon |
J:115048
|
|
absent forelimb |
J:51966,
J:92361,
J:217810
|
|
absent hindlimb |
J:51966,
J:92361
|
|
absent humerus |
J:51966
|
|
absent limbs |
J:51966,
J:94932,
J:114183
|
|
absent lung buds |
J:51966
|
|
absent lungs |
J:51966,
J:80685,
J:92361,
J:114183
|
|
absent pituitary gland |
J:114183
|
|
absent pulmonary artery |
J:111148
|
|
absent pulmonary vein |
J:111148
|
|
absent radius |
J:51966
|
|
absent Rathke's pouch |
J:114183
|
|
absent rectum |
J:92361
|
|
absent salivary gland |
J:114183
|
|
absent submandibular gland |
J:114183,
J:119849
|
|
absent thyroid gland |
J:114183
|
|
absent ulna |
J:51966
|
|
cecal atresia |
J:92361
|
|
decreased colon length |
J:115048
|
|
decreased hair follicle number |
J:114183
|
|
decreased pancreatic beta cell number |
J:114183
|
|
decreased trachea gland number |
J:119848
|
|
dextrocardia |
J:111148
|
|
diaphragmatic hernia |
J:80685
|
|
dilated kidney calyx |
J:114183
|
|
eyelids open at birth |
J:51966
|
|
increased hair follicle apoptosis |
J:114183
|
|
normal
muscle phenotype |
J:80685
|
|
pancreas fibrosis |
J:114183
|
|
perinatal lethality, complete penetrance |
J:51966
|
|
perineal hypospadia |
J:92361
|
|
short incisors |
J:114183
|
|
small hair follicle bulb |
J:114183
|
|
small kidney |
J:114183
|
|
small molars |
J:114183
|
|
small otic capsule |
J:114183
|
|
small pancreas |
J:114183
|
|
small stomach |
J:114183
|
|
small thymus |
J:114183
|
|
submandibular gland hypoplasia |
J:119849
|
|
thin skin |
J:114183
|
|
translucent skin |
J:114183
|
Fgf10tm1Wss/Fgf10+
involves: 129 * 129X1/SvJ * BALB/c * C57BL/6
|
submandibular gland hypoplasia |
J:119849
|
Fgf10tm1Wss/Fgf10+
involves: 129X1/SvJ
|
abnormal lateral nasal gland morphology |
J:237227
|
|
abnormal nasal gland morphology |
J:237227
|
|
abnormal sublingual gland morphology |
J:299375
|
|
abnormal submandibular gland development |
J:299375
|
|
decreased salivation |
J:299375
|
|
decreased submandibular gland size |
J:299375
|
|
polydipsia |
J:299375
|
|
reduced enamel thickness |
J:299375
|
|
small salivary gland |
J:299375
|
|
xerostomia |
J:299375
|
Fgf10tm1Wss/Fgf10tm1.1Sms
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ
|
abnormal ear morphology |
J:160254
|
|
abnormal embryo development |
J:160254
|
|
abnormal respiratory system morphology |
J:160254
|
Fgf10tm1Wss/Fgf10tm1Wss
either: (involves: 129X1/SvJ) or (involves: 129X1/SvJ * Black Swiss)
|
abnormal branching involved in trachea morphogenesis |
J:50768
|
|
abnormal lung development |
J:50768
|
|
abnormal pelvic girdle bone morphology |
J:50768
|
|
absent forelimb |
J:50768
|
|
absent hindlimb |
J:50768
|
|
absent limb buds |
J:50768
|
|
absent limbs |
J:50768
|
|
absent lungs |
J:50768
|
|
decreased fetal size |
J:50768
|
|
impaired branching involved in bronchus morphogenesis |
J:50768
|
|
impaired branching involved in preterminal bronchiole morphogenesis |
J:50768
|
|
impaired lung alveolus development |
J:50768
|
|
perinatal lethality, complete penetrance |
J:50768
|
Fgf10tm1Wss/Fgf10tm1Wss
involves: 129X1/SvJ
|
abnormal epidermal layer morphology |
J:85732
|
|
abnormal lateral nasal gland morphology |
J:237227
|
|
abnormal male reproductive system morphology |
J:85295
|
|
abnormal nasal gland morphology |
J:237227
|
|
abnormal palatal mesenchymal cell proliferation |
J:90909
|
|
abnormal palate morphology |
J:90909
|
|
abnormal primitive urogenital sinus morphology |
J:85295
|
|
abnormal prostate gland morphology |
J:85295
|
|
abnormal secondary palate development |
J:90909
|
|
abnormal tongue morphology |
J:90909
|
|
abnormal Wolffian duct morphology |
J:85295
|
|
absent bulbourethral gland |
J:85295
|
|
absent Harderian gland |
J:64331
|
|
absent lacrimal glands |
J:64331
|
|
absent palatal rugae |
J:90909
|
|
absent prostate gland |
J:85295
|
|
absent seminal vesicle |
J:85295
|
|
cleft secondary palate |
J:90909
|
|
decreased palatal length |
J:90909
|
|
epididymal cyst |
J:85295
|
|
hypospadia |
J:98380
|
|
palatal shelf fusion with tongue or mandible |
J:90909
|
|
thin epidermis |
J:85732
|
|
tongue ankylosis |
J:90909
|
Fgf10tm1Wss/Fgf10tm1Wss
involves: 129X1/SvJ * C57BL/6
|
abnormal cecum development |
J:104353
|
Fgf10tm1Wss/Fgf10tm1Wss
involves: 129X1/SvJ * CF-1
|
abnormal cochlea morphology |
J:83738
|
|
abnormal crista ampullaris morphology |
J:83738
|
|
abnormal inner ear canal morphology |
J:83738
|
|
abnormal inner ear vestibule morphology |
J:83738
|
|
abnormal sensory neuron innervation pattern |
J:83738
|
|
abnormal utricle morphology |
J:83738
|
|
abnormal vestibular hair cell kinocilium morphology |
J:83738
|
|
abnormal vestibular hair cell stereociliary bundle morphology |
J:83738
|
|
absent posterior semicircular canal |
J:83738
|
|
absent superior semicircular canal |
J:83738
|
|
decreased lateral semicircular canal size |
J:83738
|
|
small ears |
J:83738
|
|
small vestibular saccule |
J:83738
|
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