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Symbol
Name
ID
Hhat
hedgehog acyltransferase
MGI:2444681
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Thin corpus callosum
Cerebral hypoplasia
Cerebellar vermis hypoplasia
Dysarthria
Intellectual disability
Bilateral tonic-clonic seizure
Focal-onset seizure
Disease(s) Associated with HHAT
chondrodysplasia-pseudohermaphroditism syndrome

Mouse Phenotypes
absent floor plate
abnormal neural crest morphology
abnormal neural crest cell morphology
small embryonic telencephalon
holoprosencephaly
abnormal midbrain morphology
abnormal forebrain morphology
diencephalon hypoplasia
decreased motor neuron number
abnormal ventral interneuron 2 morphology
abnormal ventral interneuron 3 morphology
Availability Mouse Genotype
HhatTg(TFAP2A-cre)1Will/HhatTg(TFAP2A-cre)1Will
Hhattm1Ptch/Hhattm1Ptch
Hhattm2Ptch/Hhattm2Ptch

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory