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Symbol
Name
ID
C1qbp
complement component 1, q subcomponent binding protein
MGI:1194505
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Oligohydramnios
Disease(s) Associated with C1QBP
combined oxidative phosphorylation deficiency 33

Mouse Phenotypes
embryonic growth retardation
decreased embryo size
Availability Mouse Genotype
C1qbptm1.1Tuch/C1qbptm1.1Tuch

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