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Symbol
Name
ID
Mboat7
membrane bound O-acyltransferase domain containing 7
MGI:1924832
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Disease(s) Associated with MBOAT7
autosomal recessive intellectual developmental disorder 57

Mouse Phenotypes
domed cranium
Availability Mouse Genotype
Mboat7tm1a(KOMP)Wtsi/Mboat7tm1a(KOMP)Wtsi

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
04/09/2024
MGI 6.23
The Jackson Laboratory