About   Help   FAQ
Due to maintenance, access to MGI may be intermittent 8:00 AM ET Wed, September 18.
Symbol
Name
ID
Cit
citron
MGI:105313
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Spasticity
Hypoplasia of the brainstem
Microlissencephaly
Simplified gyral pattern
Agenesis of corpus callosum
Cerebellar hypoplasia
Ventriculomegaly
Intellectual disability
Hyperreflexia
Global developmental delay
Seizures
Disease(s) Associated with CIT
primary autosomal recessive microcephaly 17

Mouse Phenotypes
increased susceptibility to pharmacologically induced seizures
myoclonus
increased neuron apoptosis
decreased brain weight
decreased midbrain size
abnormal diencephalon morphology
abnormal hippocampus morphology
abnormal dentate gyrus morphology
abnormal cerebral hemisphere morphology
abnormal olfactory bulb morphology
small olfactory bulb
abnormal cerebellum morphology
abnormal cerebellar Purkinje cell layer
thin cerebellar granule layer
abnormal cerebellum lobule morphology
small cerebellum
Availability Mouse Genotype
Cittm1Fdc/Cittm1Fdc

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 & Copyright Notice
Send questions and comments to User Support.
last database update
09/10/2019
MGI 6.14
The Jackson Laboratory