Symbol Name ID |
Hhat
hedgehog acyltransferase MGI:2444681 |
Darker colors indicate more annotations |
Human Phenotypes | Severe short stature |
Intrauterine growth retardation |
Disease(s) Associated with HHAT | ||
chondrodysplasia-pseudohermaphroditism syndrome |
Mouse Phenotypes | absent tooth placode |
arrest of tooth development |
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 |
decreased embryo size |
disproportionate dwarf |
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Availability | Mouse Genotype | |||||||||||||
HhatTg(TFAP2A-cre)1Will/HhatTg(TFAP2A-cre)1Will | ||||||||||||||
Hhattm1Ptch/Hhattm1Ptch | ||||||||||||||
Hhattm2Ptch/Hhattm2Ptch |
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 05/21/2024 MGI 6.23 |
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