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

Mouse Phenotypes
domed cranium
abnormal head shape
Availability Mouse Genotype
Mboat7tm1a(KOMP)Wtsi/Mboat7tm1a(KOMP)Wtsi
Mboat7tm1Lex/Mboat7tm1Lex

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