Symbol Name ID |
Ift88
intraflagellar transport 88 MGI:98715 |
Allelic Composition Genetic Background |
Annotated Term | Reference |
Ankmy2tm1b(EUCOMM)Hmgu/Ankmy2tm1b(EUCOMM)Hmgu Ift88tm1Bky/Ift88tm1Bky involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N |
abnormal heart looping | J:297055 |
absent embryonic cilia | J:297055 | |
normal embryo phenotype | J:297055 | |
embryonic lethality prior to organogenesis | J:297055 | |
pericardial effusion | J:297055 | |
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 | |
Omptm4(cre)Mom/Omp+ Gucy1b2tm3Mom Ift88tm1Bky/Gucy1b2tm3Mom Ift88tm1Bky involves: 129P2/OlaHsd * C57BL/6J |
abnormal homeostasis | J:307157 |
abnormal response to novel odor | J:307157 |
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 11/12/2024 MGI 6.24 |
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