About   Help   FAQ
Symbol
Name
ID
Ifng
interferon gamma
MGI:107656
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Intracranial hemorrhage
Intraventricular hemorrhage
Microcephaly
Anorexia
Meningitis
Cerebral calcification
Astrocytoma
Subependymal giant-cell astrocytoma
Ependymoma
Optic nerve glioma
Subependymal nodules
Cortical tubers
Hemimegalencephaly
Ataxia
Dysdiadochokinesis
Progressive cerebellar ataxia
Slurred speech
Choreoathetosis
Myoclonus
Tremor
Intention tremor
Delayed speech and language development
Dysarthria
Depression
Irritability
Autism
Polyphagia
Hyperactivity
Attention deficit hyperactivity disorder
Intellectual disability
Hyperreflexia
Reduced tendon reflexes
Dystonia
Inability to walk
Headache
Migraine
Specific learning disability
Peripheral neuropathy
Seizure
Epileptic spasm
Infantile spasms
Paresthesia
Disease(s) Associated with IFNG
ataxia telangiectasia
chronic granulomatous disease
factor VIII deficiency
graft-versus-host disease
Graves' disease
temporal arteritis
tuberous sclerosis 2
vesicoureteral reflux

Mouse Phenotypes
CNS inflammation
increased medulloblastoma incidence
abnormal cerebellum development
abnormal cerebellum external granule cell layer morphology
abnormal cerebellum morphology
enlarged cerebellum
decreased prepulse inhibition
Availability Mouse Genotype
Ifngtm1.1(KOMP)Vlcg/Ifng+
Tg(GFAP-tTA)67Pop/0
Tg(tetO-Ifng)184Pop/0
Tg(GFAP-tTA)78Pop/0
Tg(tetO-Ifng)184Pop/0

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
04/23/2024
MGI 6.23
The Jackson Laboratory