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Symbol
Name
ID
Dhcr7
7-dehydrocholesterol reductase
MGI:1298378
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Feeding difficulties
Poor suck
Autism
Aggressive behavior
Hyperactivity
Self-mutilation
Disease(s) Associated with DHCR7
Smith-Lemli-Opitz syndrome

Mouse Phenotypes
absent gastric milk in neonates
abnormal suckling behavior
absent suckling reflex
no swallowing reflex
weakness
decreased locomotor activity
no spontaneous movement
abnormal vocalization
Availability Mouse Genotype
Dhcr7tm1Fdp/Dhcr7tm1Fdp
Dhcr7tm1Gst/Dhcr7tm1Gst

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
03/19/2024
MGI 6.23
The Jackson Laboratory