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URL: https://www.mmrrc.org/catalog/sds.php?mmrrc_id=11202
Proper Citation: RRID:MMRRC_011202-UCD
Description: Mus musculus with name STOCK Fgf8tm1.3Mrt/Mmucd from MMRRC.
Species: Mus musculus
Notes: Research areas: Apoptosis, Developmental Biology, Neurobiology; Mutation Type: Targeted Mutation ; Collection:
Phenotype: abnormal heart morphology [MP:0000266]| abnormal heart development [MP:0000267]| abnormal heart tube morphology [MP:0000270]| double outlet right ventricle [MP:0000284]| abnormal craniofacial morphology [MP:0000428]| abnormal maxilla morphology [MP:0000455]| abnormal mandible morphology [MP:0000458]| abnormal kidney development [MP:0000527]| absent radius [MP:0000553]| oligodactyly [MP:0000565]| abnormal thymus morphology [MP:0000703]| small thymus [MP:0000706]| abnormal substantia nigra morphology [MP:0000836]| small cerebellum [MP:0000852]| abnormal midbrain morphology [MP:0000897]| abnormal rhombomere morphology [MP:0000933]| abnormal trigeminal nerve morphology [MP:0001065]| abnormal eyelid morphology [MP:0001340]| postnatal growth retardation [MP:0001732]| abnormal cardiovascular system morphology [MP:0002127]| abnormal neural tube morphology [MP:0002151]| abnormal reproductive system morphology [MP:0002160]| no abnormal phenotype detected [MP:0002169]| persistent truncus arteriosis [MP:0002633]| dilated heart left ventricle [MP:0002753]| abnormal pharyngeal arch morphology [MP:0002884]| dilated heart atrium [MP:0003140]| abnormal pillar cell differentiation [MP:0003152]| increased neuron apoptosis [MP:0003203]| abnormal forebrain development [MP:0003232]| abnormal cochlear sensory epithelium morphology [MP:0003308]| kidney failure [MP:0003606]| abnormal pillar cell morphology [MP:0003825]| abnormal forelimb stylopod morphology [MP:0003854]| abnormal forelimb zeugopod morphology [MP:0003855]| abnormal hindlimb stylopod morphology [MP:0003856]| abnormal hindlimb zeugopod morphology [MP:0003857]| absent heart right ventricle [MP:0003872]| pharyngeal arch hypoplasia [MP:0003873]| abnormal serotonergic neuron morphology [MP:0003877]| absent molars [MP:0003931]| abnormal craniofacial development [MP:0003935]| aortic dissection [MP:0004044]| polysyndactyly [MP:0004083]| transposition of great arteries [MP:0004110]| abnormal aortic arch morphology [MP:0004113]| interrupted aortic arch [MP:0004157]| cervical aortic arch [MP:0004161]| absent pillar cells [MP:0004312]| absent incus [MP:0004318]| absent Meckel's cartilage [MP:0004439]| small limb buds [MP:0004575]| decreased mitotic index [MP:0004759]| abnormal Raphe nucleus morphology [MP:0004861]| impaired branching involved in ureteric bud morphogenesis [MP:0004936]| abnormal vascular smooth muscle morphology [MP:0005592]| abnormal limb bud morphology [MP:0005650]| abnormal ureteric bud morphology [MP:0006032]| increased apoptosis [MP:0006042]| abnormal cardiac outflow tract development [MP:0006126]| abnormal limb development [MP:0006279]| abnormal digit development [MP:0006280]| abnormal patterning of the organ of Corti [MP:0006331]| small first pharyngeal arch [MP:0006341]| fused tarsal bones [MP:0008919]| abnormal neural crest cell morphology [MP:0009845]| decreased tongue size [MP:0009907]| atrial septal defect [MP:0010403]| perimembraneous ventricular septal defect [MP:0010418]| neonatal lethality [MP:0011087]| complete penetrance [MP:0011089]| perinatal lethality [MP:0011090]| complete penetrance [MP:0011098]| perinatal lethality [MP:0011262]| incomplete penetrance [MP:0011354]| embryonic lethality during organogenesis [MP:0011368]| complete penetrance [MP:0011448]| abnormal pharyngeal arch mesenchyme morphology [MP:0012179]| absent renal glomerulus [MP:0012730]| increased kidney apoptosis [MP:0014044]
Affected Gene: Fgf8
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Source: Integrated Animals
Source Database: Mutant Mouse Resource and Research Center (MMRRC)
