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Symbol
Name
ID

Ift172
intraflagellar transport 172
MGI:2682064

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes	Orofacial cleft
Disease(s) Associated with IFT172	Orofacial cleft
short-rib thoracic dysplasia 10 with or without polydactyly

Mouse Phenotypes		abnormal craniofacial morphology	abnormal pharyngeal arch morphology	cleft secondary palate	short snout
Availability	Mouse Genotype	abnormal craniofacial morphology	abnormal pharyngeal arch morphology	cleft secondary palate	short snout
	Ift172^avc1/Ift172^avc1
	Ift172^{tm2b(EUCOMM)Hmgu}/Ift172^{tm2b(EUCOMM)Hmgu}
	Ift172^avc1/Ift172^wim

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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