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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Bbs2
Bardet-Biedl syndrome 2 (human)
MGI:2135267
25 phenotypes from 1 allele in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Bbs2tm1Vcs/Bbs2tm1Vcs
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
abnormal abdominal fat pad morphology J:94467
abnormal eye electrophysiology J:94467
abnormal olfaction J:94467
abnormal placing response J:94467
absent sperm flagellum J:94467
decreased aggression J:94467
decreased birth body size J:94467
decreased body size J:94467
decreased salivation J:94467
decreased startle reflex J:94467
disorganized photoreceptor outer segment J:94467
hepatic steatosis J:94467
hyporesponsive to tactile stimuli J:94467
increased body mass index J:94467
increased body weight J:94467
kidney cysts J:94467
normal limbs/digits/tail phenotype J:94467
male infertility J:94467
polyphagia J:94467
retinal degeneration J:94467
Bbs2tm1Vcs/Bbs2tm1Vcs
involves: 129S1/Sv * 129X1/SvJ
abnormal basal ganglion morphology J:128532
enlarged lateral ventricles J:128532
enlarged third ventricle J:128532
small hippocampus J:128532
thin cerebral cortex J:128532

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
11/26/2019
MGI 6.14
The Jackson Laboratory