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Symbol
Name
ID

Ift140
intraflagellar transport 140
MGI:2146906

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Microcephaly

Photophobia

Ventriculomegaly

Hypoplasia of the corpus callosum

Ataxia

Autistic behavior

Intellectual disability

Intellectual disability, mild

Hyperreflexia

Global developmental delay

Persistent head lag

Seizure

Disease(s) Associated with IFT140

retinitis pigmentosa

short-rib thoracic dysplasia 9 with or without polydactyly

Mouse Phenotypes		abnormal neural tube morphology	abnormal neural tube closure	spina bifida	exencephaly
Availability	Mouse Genotype	abnormal neural tube morphology	abnormal neural tube closure	spina bifida	exencephaly
	Ift140^cauli/Ift140^cauli
	Ift140^{tm1b(KOMP)Wtsi}/Ift140^{tm1b(KOMP)Wtsi}

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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