Symbol Name ID |
Ift140
intraflagellar transport 140 MGI:2146906 |
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 |
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Availability | Mouse Genotype | ||||
Ift140cauli/Ift140cauli | |||||
Ift140tm1b(KOMP)Wtsi/Ift140tm1b(KOMP)Wtsi |
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 05/28/2024 MGI 6.13 |
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