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Symbol
Name
ID
Dhcr7
7-dehydrocholesterol reductase
MGI:1298378
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Disease(s) Associated with DHCR7
Smith-Lemli-Opitz syndrome

Mouse Phenotypes
abnormal placenta vasculature
embryonic growth retardation
abnormal placenta morphology
Availability Mouse Genotype
Dhcr7em1(IMPC)Mbp/Dhcr7em1(IMPC)Mbp
Dhcr7em1(IMPC)Mbp/Dhcr7+

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
04/16/2024
MGI 6.23
The Jackson Laboratory