Symbol Name ID |
Ift27
intraflagellar transport 27 MGI:1914292 |
Darker colors indicate more annotations |
Human Phenotypes | Obesity |
Disease(s) Associated with IFT27 | |
Bardet-Biedl syndrome 19 |
Mouse Phenotypes | abnormal incisor morphology |
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 |
omphalocele |
lung cyst |
abdominal situs ambiguus |
|
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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