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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Hhat
hedgehog acyltransferase
MGI:2444681
57 phenotypes from 3 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
HhatTg(TFAP2A-cre)1Will/HhatTg(TFAP2A-cre)1Will
Not Specified 		abnormal cartilage development J:190013
abnormal cranium morphology J:190013
abnormal eye development J:190013
abnormal fetal Leydig cell differentiation J:226657
abnormal forebrain morphology J:190013
abnormal mandible morphology J:190013
abnormal mandibular prominence morphology J:190013
abnormal maxillary prominence morphology J:190013
abnormal midbrain morphology J:190013
abnormal nasal cartilage morphology J:190013
abnormal nasal cavity morphology J:190013
abnormal neural crest cell morphology J:190013
abnormal neural crest morphology J:190013
abnormal optic vesicle formation J:190013
abnormal oral cavity morphology J:190013
abnormal palatal shelf elevation J:190013
abnormal palatal shelf fusion at midline J:190013
abnormal palate development J:190013
abnormal testis cord formation J:226657
abnormal testis development J:226657
abnormal testis morphology J:226657
abnormal vertebral column morphology J:190013
absent cornea J:190013
absent interparietal bone J:190013
absent mandibular angle J:190013
absent mandibular condyloid process J:190013
absent mandibular coronoid process J:190013
absent nasal septum J:190013
absent parietal bone J:190013
absent supraoccipital bone J:190013
absent tooth placode J:190013
acrania J:190013
agnathia J:190013
arrest of tooth development J:190013
decreased embryo size J:190013
diencephalon hypoplasia J:190013
edema J:190013
failure of bone ossification J:190013
hemorrhage J:190013
microphthalmia J:190013
nasal cartilage hypoplasia J:190013
oligodactyly J:190013
prenatal lethality, complete penetrance J:190013
small basioccipital bone J:190013
small embryonic telencephalon J:190013
small exoccipital bone J:190013
small frontonasal prominence J:190013
small testis J:226657
tongue hypoplasia J:190013
Hhattm1Ptch/Hhattm1Ptch
involves: 129P2/OlaHsd * FVB/N * various 		abnormal ventral interneuron 2 morphology J:89228
abnormal ventral interneuron 3 morphology J:89228
absent floor plate J:89228
chondrodystrophy J:89228
decreased embryo size J:89228
decreased motor neuron number J:89228
disproportionate dwarf J:89228
holoprosencephaly J:89228
neonatal lethality, complete penetrance J:89228
oligodactyly J:89228
Hhattm2Ptch/Hhattm2Ptch
involves: 129P2/OlaHsd * FVB/N * various 		abnormal ventral interneuron 2 morphology J:89228
abnormal ventral interneuron 3 morphology J:89228
absent floor plate J:89228
chondrodystrophy J:89228
decreased embryo size J:89228
decreased motor neuron number J:89228
disproportionate dwarf J:89228
holoprosencephaly J:89228
neonatal lethality, complete penetrance J:89228
oligodactyly J:89228
Contributing Projects:
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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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory