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Proper Citation: RRID:MGI:2176484
Description: Allele Detail: Targeted This is a legacy resource.
Species: Mus musculus
Notes: Allele Detail: Targeted This is a legacy resource.
Phenotype: abnormal hair follicle morphology, thin epidermis, abnormal epidermis stratum basale morphology, abnormal epidermal layer morphology, decreased hair follicle number, abnormal vibrissa number, abnormal keratinocyte morphology, abnormal hair follicle development, ventricular hypoplasia, abnormal left posterior bundle morphology, absent eyelids, decreased fetal size, overriding aortic valve, absent lungs, delayed intramembranous bone ossification, cleft palate, abnormal pancreas development, abnormal adrenal gland development, thin skin, abnormal conotruncal ridge morphology, double outlet right ventricle, atrium hypoplasia, abnormal trabecula carnea morphology, absent pulmonary vein, abnormal pulmonary circulation, absent thyroid gland, abnormal kidney development, absent adenohypophysis, small otic capsule, abnormal stomach glandular region morphology, absent teeth, abnormal skin morphology, decreased nephron number, abnormal heart ventricle morphology, perinatal lethality, complete penetrance, absent pulmonary artery, conotruncal ridge hypoplasia, abnormal interventricular groove morphology, muscular ventricular septal defect, perimembraneous ventricular septal defect, abnormal truncus arteriosus septation, curly tail, abnormal heart development, thin ventricular wall, absent limbs, abnormal hair follicle morphology, small kidney, caudal vertebral fusion, abnormal thymus development, abnormal otic vesicle development, abnormal scapula morphology, abnormal pelvic girdle bone morphology, abnormal apical ectodermal ridge morphology, abnormal salivary gland morphology, hypospadia, abnormal urethra morphology, thin skin
Affected Gene: Fgfr2
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No rating or validation information has been found for Fgfr2tm3Dsn/Fgfr2tm3Dsn.
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Source: Integrated Animals
Source Database: MGI, Mouse Genome Informatics MGI