|
Symbol Name ID |
Hhat
hedgehog acyltransferase MGI:2444681 |
| Darker colors indicate more annotations |
| Human Phenotypes | Increased skull ossification |
Microcephaly |
Blepharophimosis |
Upslanted palpebral fissure |
Telecanthus |
| Disease(s) Associated with HHAT | |||||
| chondrodysplasia-pseudohermaphroditism syndrome |
| Mouse Phenotypes | abnormal cranium morphology |
small basioccipital bone |
absent interparietal bone |
small exoccipital bone |
absent supraoccipital bone |
absent parietal bone |
absent tooth placode |
arrest of tooth development |
abnormal mandible morphology |
absent mandibular angle |
absent mandibular condyloid process |
absent mandibular coronoid process |
agnathia |
acrania |
small frontonasal prominence |
abnormal mandibular prominence morphology |
abnormal maxillary prominence morphology |
abnormal palate development |
abnormal palatal shelf elevation |
abnormal palatal shelf fusion at midline |
abnormal oral cavity morphology |
tongue hypoplasia |
abnormal nasal cartilage morphology |
nasal cartilage hypoplasia |
abnormal nasal cavity morphology |
absent nasal septum |
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| Availability | Mouse Genotype | ||||||||||||||||||||||||||
| HhatTg(TFAP2A-cre)1Will/HhatTg(TFAP2A-cre)1Will | |||||||||||||||||||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/30/2024 MGI 6.23 |
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