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Symbol Name ID |
Ift27
intraflagellar transport 27 MGI:1914292 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hyposmia |
| Disease(s) Associated with IFT27 | |
| Bardet-Biedl syndrome 19 |
| Mouse Phenotypes | abnormal jaw morphology |
abnormal incisor morphology |
small mandible |
micrognathia |
midface hypoplasia |
abnormal mouth morphology |
abnormal palate morphology |
abnormal tongue morphology |
absent tongue |
decreased tongue size |
abnormal nose morphology |
abnormal nasal septum morphology |
abnormal vomeronasal organ morphology |
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| Availability | Mouse Genotype | |||||||||||||
| Ift27tm1b(EUCOMM)Hmgu/Ift27tm1b(EUCOMM)Hmgu | ||||||||||||||
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 07/05/2024 MGI 6.24 |
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