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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Bbs7
Bardet-Biedl syndrome 7
MGI:1918742
8 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Bbs7tm1Vcs/Bbs7tm1Vcs
Ift88Tg737Rpw/Ift88Tg737Rpw
involves: FVB/N
abnormal limb development J:181886
anophthalmia J:181886
broad limb buds J:181886
cleft palate J:181886
delayed limb development J:181886
embryonic lethality during organogenesis, complete penetrance J:181886
exencephaly J:181886
pericardial edema J:181886

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
04/30/2024
MGI 6.23
The Jackson Laboratory