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Symbol
Name
ID
Atpaf2
ATP synthase mitochondrial F1 complex assembly factor 2
MGI:2180561
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Retrognathia
Microcephaly
Rocker bottom foot
Flexion contracture
Camptodactyly
Disease(s) Associated with ATPAF2
mitochondrial complex V (ATP synthase) deficiency nuclear type 1

Mouse Phenotypes
abnormal maxilla morphology
decreased rib number
decreased thoracic vertebrae number
abnormal vertebrae morphology
Availability Mouse Genotype
Atpaf2tm1a(KOMP)Wtsi/Atpaf2+

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