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Symbol
Name
ID

Ift27
intraflagellar transport 27
MGI:1914292

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Hyposmia	Hypoplasia of the corpus callosum	Delayed speech and language development	Intellectual disability	Global developmental delay	Delayed ability to walk
Disease(s) Associated with IFT27
Bardet-Biedl syndrome 19

Mouse Phenotypes		abnormal vomeronasal organ morphology
Availability	Mouse Genotype	abnormal vomeronasal organ morphology
	Ift27^{tm1b(EUCOMM)Hmgu}/Ift27^{tm1b(EUCOMM)Hmgu}

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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