About   Help   FAQ
Symbol
Name
ID
Ift122
intraflagellar transport 122
MGI:1932386
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Intellectual disability
Disease(s) Associated with IFT122
cranioectodermal dysplasia 1

Mouse Phenotypes
abnormal neural tube morphology
open neural tube
exencephaly
increased motor neuron number
abnormal ventral interneuron 3 morphology
abnormal spinal cord morphology
Availability Mouse Genotype
Ift122sopb/Ift122sopb
Mbd4/Ift122tm1Abc/Mbd4/Ift122tm1Abc

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory