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Organism Name
RRID:MGI:5447979 RRID Copied  
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RRID:MGI:5447979
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Organism Information

The record is no longer available at this source.

Proper Citation: RRID:MGI:5447979

Description: Allele Detail: Transgenic This is a legacy resource.

Species: Mus musculus

Notes: Allele Detail: Transgenic This is a legacy resource.

Phenotype: absent cornea, absent parietal bone, absent interparietal bone, abnormal palate development, abnormal palatal shelf elevation, abnormal neural crest morphology, abnormal neural crest cell morphology, abnormal mandible morphology, oligodactyly, microphthalmia, failure of bone ossification, abnormal testis development, abnormal fetal Leydig cell differentiation, abnormal testis cord formation, small testis, abnormal testis morphology, abnormal nasal cavity morphology, absent supraoccipital bone, absent tooth placode, acrania, small basioccipital bone, small exoccipital bone, tongue hypoplasia, hemorrhage, abnormal cranium morphology, small frontonasal prominence, abnormal oral cavity morphology, abnormal palatal shelf fusion at midline, edema, diencephalon hypoplasia, decreased embryo size, prenatal lethality, complete penetrance, absent nasal septum, abnormal vertebral column morphology, small embryonic telencephalon, abnormal optic vesicle formation, abnormal nasal capsule morphology, abnormal midbrain morphology, abnormal maxillary prominence morphology, abnormal mandibular prominence morphology, abnormal forebrain morphology, abnormal eye development, abnormal cartilage development, agnathia, absent mandibular angle, absent mandibular condyloid process, absent mandibular coronoid process, arrest of tooth development

Affected Gene: Hhat

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Ratings and Alerts

No rating or validation information has been found for HhatTg(TFAP2A-cre)1Will/HhatTg(TFAP2A-cre)1Will.

No alerts have been found for HhatTg(TFAP2A-cre)1Will/HhatTg(TFAP2A-cre)1Will.

Data and Source Information

Source: Integrated Animals

Source Database: MGI, Mouse Genome Informatics MGI